Andrea Carmine Belin

Om mig
Publikationer
Forskningsbidrag
CV
Populärvetenskap och samverkan

Forskningsbeskrivning

Syftet med vår forskning är att öka förståelsen av patofysiologin bakom
neurologiska sjukdomar med fokus på huvudvärk, främst Hortons
huvudvärk/klusterhuvudvärk, genom att identifiera, karakterisera och
modellera genetiska markörer inom det mänskliga genomet.

Artiklar

Article: NEUROLOGY. 2024;103(3):e209620
Association of Body Mass Index and Parkinson Disease A Bidirectional Mendelian Randomization Study
Domenighetti C; Sugier P-E; Ashok Kumar Sreelatha A; Schulte C; Grover S; Portugal B; Lee P-C; May P; Bobbili D; Radivojkov Blagojevic M; Lichtner P; Singleton AB; Hernandez D; Edsall C; Mellick GD; Zimprich AA; Pirker W; Rogaeva EA; Lang AE; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlander AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Straniero L; Zecchinelli AL; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Matsuo H; Nakayama A; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; Van De Warrenburg BPC; Bloem BR; Toft M; Pihlstrm L; Correia Guedes L; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Hellberg C; Clarke CE; Morrison KE; Tan MM; Krainc D; Burbulla LF; Farrer M; Kruger R; Gasser T; Sharma M; Elbaz A
Article: THE JOURNAL OF HEADACHE AND PAIN. 2024;25(1):121
Elevated cytokine levels in the central nervous system of cluster headache patients in bout and in remission
Ran C; Olofsgard FJ; Wellfelt K; Steinberg A; Belin AC
Journal article: LANCET NEUROLOGY. 2024;23(7):712-724
Recent advances in diagnosing, managing, and understanding the pathophysiology of cluster headache.
Petersen AS; Lund N; Goadsby PJ; Belin AC; Wang S-J; Fronczek R; Burish M; Cho S-J; Peres MFP; Jensen RH
Article: THE JOURNAL OF HEADACHE AND PAIN. 2024;25(1):85
MERTK in the rat trigeminal system: a potential novel target for cluster headache?
Edvinsson JCA; Ran C; Olofsgard FJ; Steinberg A; Edvinsson L; Belin AC
Article: JOURNAL OF MOLECULAR NEUROSCIENCE. 2024;74(2):45
Genetic and Phenotypic Profiling of Triptan Users in a Swedish Cluster Headache Cohort
Olofsgard FJ; Ran C; Qin Y; Fourier C; Waldenlind E; Steinberg A; Sjostrand C; Belin AC
Article: BRAIN SCIENCES. 2024;14(4):348
Use of Prescribed and Non-Prescribed Treatments for Cluster Headache in a Swedish Cohort
Smedfors G; Olofsgard FJ; Steinberg A; Waldenlind E; Ran C; Belin AC
Article: ANNALS OF NEUROLOGY. 2023;94(4):713-726
Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor
Winsvold B; Harder AVEA; Ran C; Chalmer M; Dalmasso MC; Ferkingstad E; Tripathi KP; Bacchelli E; Borte S; Fourier CS; Petersen AH; Vijfhuizen L; Magnusson S; O'Connor E; Bjornsdottir G; Happola P; Wang Y-F; Callesen I; Kelderman T; Gallardo VJ; de Boer I; Olofsgard FJ; Heinze K; Lund N; Thomas LF; Hsu C-L; Pirinen M; Hautakangas H; Ribases M; Guerzoni S; Sivakumar P; Yip J; Heinze A; Kucukali FB; Ostrowski SS; Pedersen OE; Kristoffersen ES; Martinsen AE; Artigas MS; Lagrata S; Cainazzo MM; Adebimpe J; Quinn O; Goebel CE; Cirkel A; Volk A; Heilmann-Heimbach SE; Skogholt AH; Gabrielsen ME; Wilbrink LA; Danno D; Mehta DR; Guobjartsson DF; Rosendaal FR; van Dijk KW; Fronczek RA; Wagner M; Scherer M; Goebel HA; Sleegers K; Sveinsson O; Pani L; Zoli M; Ramos-Quiroga JA; Dardiotis E; Steinberg A; Riedel-Heller S; Sjostrand C; Thorgeirsson TE; Stefansson H; Southgate L; Trembath RC; Vandrovcova J; Noordam R; Paemeleire KH; Stefansson K; Fann CS-J; Waldenlind E; Tronvik E; Jensen RH; Chen S-P; Houlden H; Terwindt GC; Kubisch C; Maestrini E; Vikelis M; Pozo-Rosich P; Belin AC; Matharu M; van den Maagdenberg AMJM; Hansen TF; Ramirez A; Zwart J-A
Article: THE JOURNAL OF HEADACHE AND PAIN. 2023;24(1):121
Current treatment options for cluster headache: limitations and the unmet need for better and specific treatments-a consensus article
Lund NLT; Petersen AS; Fronczek R; Tfelt-Hansen J; Belin AC; Meisingset T; Tronvik E; Steinberg A; Gaul C; Jensen RH
Article: THE JOURNAL OF HEADACHE AND PAIN. 2023;24(1):114
Patients with cluster headache show signs of insomnia and sleep related stress: results from an actigraphy and self-assessed sleep study
Ran C; Olofsgard FJ; Steinberg A; Sjoestrand C; Waldenlind E; Dahlgren A; Belin AC
Article: HUMAN GENETICS. 2023;142(8):1185-1200
Migraine, chronic kidney disease and kidney function: observational and genetic analyses
Zhang W; Zhang L; Yang LM; Xiao C; Wu X; Yan P; Cui H; Yang C; Zhu J; Wu X; Tang MR; Wang Y; Chen L; Liu YA; Zou YM; Zhang LE; Yang C; Yao Y; Li J; Liu ZS; Zhang B; Jiang X
Article: MOVEMENT DISORDERS. 2023;38(4):604-615
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers
Sugier P-E; Lucotte EA; Domenighetti C; Law MH; Iles MM; Brown K; Amos C; McKay JD; Hung RJ; Karimi M; Bacq-Daian D; Boland-Auge A; Olaso R; Deleuze J-F; Lesueur F; Ostroumova E; Kesminiene A; de Vathaire F; Guenel P; Sreelatha AAK; Schulte C; Grover S; May P; Bobbili DR; Radivojkov-Blagojevic M; Lichtner P; Singleton AB; Hernandez DG; Edsall C; Mellick GD; Zimprich A; Pirker W; Rogaeva E; Lang AE; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlaender AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Matsuo H; Nakayama A; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; van de Warrenburg BPC; Bloem BR; Aasly J; Toft M; Pihlstrom L; Guedes LC; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen N; Ran C; Belin AC; Puschmann A; Roedstroem EY; Clarke CE; Morrison KE; Tan M; Krainc D; Burbulla LF; Farrer MJ; Kruger R; Gasser T; Sharma M; Truong T; Elbaz A
Article: NEUROLOGY. 2023;100(12):e1207-e1220
Sex Differences in Clinical Features, Treatment, and Lifestyle Factors in Patients With Cluster Headache
Fourier C; Ran C; Steinberg A; Sjoestrand C; Waldenlind E; Belin AC
Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2023;24(6):5950
Investigating Vitamin D Receptor Genetic Markers in a Cluster Headache Meta-Analysis
Jennysdotter Olofsgard F; Ran C; Qin Y; Fourier C; Sjoestrand C; Waldenlind E; Steinberg A; Belin AC
Article: NEUROLOGY. 2023;100(10):e1083-e1094
Multimorbidity and Sickness Absence/Disability Pension in Patients With Cluster Headache and Matched References A Swedish Register-Based Study
Ran C; Alexanderson K; Belin AC; Almondo G; Steinberg A; Sjoestrand C
Article: STROKE. 2023;54(3):810-818
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Bakker MK; Kanning JP; Abraham G; Martinsen AE; Winsvold BS; Zwart J-A; Bourcier R; Sawada T; Koido M; Kamatani Y; Morel S; Amouyel P; Debette S; Bijlenga P; Berrandou T; Ganesh SK; Bouatia-Naji N; Jones G; Bown M; Rinkel GJE; Veldink JH; Ruigrok YM; HUNT All-In Stroke, CADISP group, International Co
Article: MOVEMENT DISORDERS. 2023;38(2):286-303
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Vollstedt E-J; Schaake S; Lohmann K; Padmanabhan S; Brice A; Lesage S; Tesson C; Vidailhet M; Wurster I; Hentati F; Mirelman A; Giladi N; Marder K; Waters C; Fahn S; Kasten M; Bruggemann N; Borsche M; Foroud T; Tolosa E; Garrido A; Annesi G; Gagliardi M; Bozi M; Stefanis L; Ferreira JJ; Guedes LC; Avenali M; Petrucci S; Clark L; Fedotova EY; Abramycheva NY; Alvarez V; Menendez-Gonzalez M; Maestre SJ; Gomez-Garre P; Mir P; Belin AC; Ran C; Lin C-H; Kuo M-C; Crosiers D; Wszolek ZK; Ross OA; Jankovic J; Nishioka K; Funayama M; Clarimon J; Williams-Gray CH; Camacho M; Cornejo-Olivas M; Torres-Ramirez L; Wu Y-R; Lee-Chen G-J; Morgadinho A; Pulkes T; Termsarasab P; Berg D; Kuhlenbaumer G; Kuhn AA; Borngraeber F; de Michele G; De Rosa A; Zimprich A; Puschmann A; Mellick GD; Dorszewska J; Carr J; Ferese R; Gambardella S; Chase B; Markopoulou K; Satake W; Toda T; Rossi M; Merello M; Lynch T; Olszewska DA; Lim S-Y; Ahmad-Annuar A; Tan AH; Al-Mubarak B; Hanagasi H; Koziorowski D; Ertan S; Genc G; Aguiar PDC; Barkhuizen M; Pimentel MMG; Saunders-Pullman R; van de Warrenburg B; Bressman S; Toft M; Appel-Cresswell S; Lang AE; Skorvanek M; Boon AJW; Kruger R; Sammler EM; Tumas V; Zhang B-R; Garraux G; Chung SJ; Kim YJ; Winkelmann J; Sue CM; Tan E-K; Damasio J; Klivenyi P; Kostic VS; Arkadir D; Martikainen M; Borges V; Hertz JM; Brighina L; Spitz M; Suchowersky O; Riess O; Das P; Mollenhauer B; Gatto EM; Petersen MS; Hattori N; Wu R-M; Illarioshkin SN; Valente EM; Aasly JO; Aasly A; Alcalay RN; Thaler A; Farrer MJ; Brockmann K; Corvol J-C; Klein C
Article: PLOS ONE. 2023;18(10):e0292180
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
Vollstedt E-J; Madoev H; Aasly A; Ahmad-Annuar A; Al-Mubarak B; Alcalay RN; Alvarez V; Amorin I; Annesi G; Arkadir D; Bardien S; Barker RA; Barkhuizen M; Basak AN; Bonifati V; Boon A; Brighina L; Brockmann K; Belin AC; Carr J; Clarimon J; Cornejo-Olivas M; Guedes LC; Corvol J-C; Crosiers D; Damasio J; Das P; de Carvalho Aguiar P; De Rosa A; Dorszewska J; Ertan S; Ferese R; Ferreira J; Gatto E; Genc G; Giladi N; Gomez-Garre P; Hanagasi H; Hattori N; Hentati F; Hoffman-Zacharska D; Illarioshkin SN; Jankovic J; Jesus S; Kaasinen V; Kievit A; Klivenyi P; Kostic V; Koziorowski D; Kuehn AA; Lang AE; Lim S-Y; Lin C-H; Lohmann K; Markovic V; Martikainen MH; Mellick G; Merello M; Milanowski L; Mir P; oeztop-cakmak O; Pimentel MMG; Pulkes T; Puschmann A; Rogaeva E; Sammler EM; Skaalum Petersen M; Skorvanek M; Spitz M; Suchowersky O; Tan AH; Termsarasab P; Thaler A; Tumas V; Valente EM; van de Warrenburg B; Williams-Gray CH; Wu R-M; Zhang B; Zimprich A; Solle J; Padmanabhan S; Klein C
Article: MOVEMENT DISORDERS. 2022;37(9):1929-1937
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited
Domenighetti C; Douillard V; Sugier P-E; Sreelatha AAK; Schulte C; Grover S; May P; Bobbili DR; Radivojkov-Blagojevic M; Lichtner P; Singleton AB; Hernandez DG; Edsall C; Gourraud P-A; Mellick GD; Zimprich A; Pirker W; Rogaeva E; Lang AE; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlander AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Duga S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Matsuo H; Nakayama A; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; van de Warrenburg BPC; Bloem BR; Aasly J; Toft M; Pihlstrom L; Correia Guedes L; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Ygland Rodstrom E; Clarke CE; Morrison KE; Tan M; KraincMD D; Burbulla LF; Farrer MJ; Kruger R; Gasser T; Sharma M; Vince N; Elbaz A
Article: NEUROLOGY. 2022;99(7):e698-e710
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium
Grover S; Kumar Sreelatha AA; Pihlstrom L; Domenighetti C; Schulte C; Sugier P-E; Radivojkov-Blagojevic M; Lichtner P; Mohamed O; Portugal B; Landoulsi Z; May P; Bobbili D; Edsall C; Bartusch F; Hanussek M; Krueger J; Hernandez DG; Blauwendraat C; Mellick GD; Zimprich A; Pirker W; Tan M; Rogaeva E; Lang A; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlaender AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Burbulla LF; Matsuo H; Kawamura Y; Hattori N; Nishioka K; Chung SJ; Kim YJ; Pavelka L; van de Warrenburg BPC; Bloem BR; Singleton AB; Aasly J; Toft M; Guedes LC; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Hellberg C; Clarke CE; Morrison KE; Krainc D; Farrer MJ; Kruger R; Elbaz A; Gasser T; Sharma M
Article: ANNALS OF NEUROLOGY. 2022;92(2):270-278
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.
Liu H; Dehestani M; Blauwendraat C; Makarious MB; Leonard H; Kim JJ; Schulte C; Noyce A; Jacobs BM; Foote I; Sharma M; International Parkinson's Disease Genomics Consort; Nalls M; Singleton A; Gasser T; Bandres-Ciga S
Article: MOVEMENT DISORDERS. 2022;37(4):857-864
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study
Domenighetti C; Sugier P-E; Sreelatha AAK; Schulte C; Grover S; Mohamed O; Portugal B; May P; Bobbili DR; Radivojkov-Blagojevic M; Lichtner P; Singleton AB; Hernandez DG; Edsall C; Mellick GD; Zimprich A; Pirker W; Rogaeva E; Lang AE; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlaender AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Duga S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Matsuo H; Kawamura Y; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; van de Warrenburg BPC; Bloem BR; Aasly J; Toft M; Pihlstrom L; Guedes LC; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Hellberg C; Clarke CE; Morrison KE; Tan M; Krainc D; Burbulla LF; Farrer MJ; Kruger R; Gasser T; Sharma M; Elbaz A
Article: NATURE GENETICS. 2022;54(2):152-160
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Hautakangas H; Winsvold BS; Ruotsalainen SE; Bjornsdottir G; Harder AVE; Kogelman LJA; Thomas LF; Noordam R; Benner C; Gormley P; Artto V; Banasik K; Bjornsdottir A; Boomsma DI; Brumpton BM; Burgdorf KS; Buring JE; Chalmer MA; de Boer I; Dichgans M; Erikstrup C; Farkkila M; Garbrielsen ME; Ghanbari M; Hagen K; Happola P; Hottenga J-J; Hrafnsdottir MG; Hveem K; Johnsen MB; Kahonen M; Kristoffersen ES; Kurth T; Lehtimaki T; Lighart L; Magnusson SH; Malik R; Pedersen OB; Pelzer N; Penninx BWJH; Ran C; Ridker PM; Rosendaal FR; Sigurdardottir GR; Skogholt AH; Sveinsson OA; Thorgeirsson TE; Ullum H; Vijfhuizen LS; Widen E; van Dijk KW; Aromaa A; Belin AC; Freilinger T; Ikram MA; Jarvelin M-R; Raitakari OT; Terwindt GM; Kallela M; Wessman M; Olesen J; Chasman DI; Nyholt DR; Stefansson H; Stefansson K; van den Maagdenberg AMJM; Hansen TF; Ripatti S; Zwart J-A; Palotie A; Pirinen M
Article: JOURNAL OF PARKINSON’S DISEASE. 2022;12(1):267-282
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease
Domenighetti C; Sugier P-E; Sreelatha AAK; Schulte C; Grover S; Mohamed O; Portugal B; May P; Bobbili DR; Radivojkov-Blagojevic M; Lichtner P; Singleton AB; Hernandez DG; Edsall C; Mellick GD; Zimprich A; Pirker W; Rogaeva E; Lang AE; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlaender AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Duga S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Matsuo H; Kawamura Y; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; van de Warrenburg BP; Bloem BR; Aasly J; Toft M; Pihlstrom L; Guedes LC; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Hellberg C; Clarke CE; Morrison KE; Tan M; Krainc D; Burbulla LF; Farrer MJ; Krueger R; Gasser T; Sharma M; Elbaz A
Article: CEPHALALGIA. 2022;42(1):87
Board Walk - January 2022.
Belin AC
Journal article: THE JOURNAL OF HEADACHE AND PAIN. 2022;23(SUPPL 1)
Cluster headache genome-wide association study identifies seven loci and implicates smoking as causal risk factor
Winsvold BS; Harder A; Ran C; Chalmer MA; Dalmasso MC; Ferkingstad E; Belin A; Matharu M; Van den Maagdenberg A; Hansen TF; Ramirez A; Zwart JA
Article: CEPHALALGIA. 2021;41(13):1374-1381
The molecular clock gene cryptochrome 1 (CRY1) and its role in cluster headache
Fourier C; Ran C; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Article: BRAIN SCIENCES. 2021;11(8):1108
PER Gene Family Polymorphisms in Relation to Cluster Headache and Circadian Rhythm in Sweden
Olofsgard FJ; Ran C; Fourier C; Wirth C; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Article: ANNALS OF NEUROLOGY. 2021;90(2):193-202
Genome-Wide Association Study Identifies Risk Loci for Cluster Headache
O'Connor E; Fourier C; Ran C; Sivakumar P; Liesecke F; Southgate L; Harder AVE; Vijfhuizen LS; Yip J; Giffin N; Silver N; Ahmed F; Hostettler IC; Davies B; Cader MZ; Simpson BS; Sullivan R; Efthymiou S; Adebimpe J; Quinn O; Campbell C; Cavalleri GL; Vikelis M; Kelderman T; Paemeleire K; Kilbride E; Grangeon L; Lagrata S; Danno D; Trembath R; Wood NW; Kockum I; Winsvold BS; Steinberg A; Sjostrand C; Waldenlind E; Vandrovcova J; Houlden H; Matharu M; Belin AC
Article: BRAIN SCIENCES. 2020;11(1):34
Analysis of NOS Gene Polymorphisms in Relation to Cluster Headache and Predisposing Factors in Sweden
Ran C; Michalska JM; Fourier C; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Article: NATURE COMMUNICATIONS. 2020;11(1):3368
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine
Guo Y; Rist PM; Daghlas I; Giulianini F; Kurth T; Chasman DI
Article: NATURE GENETICS. 2020;52(5):482-493
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease
Bryois J; Skene NG; Hansen TF; Kogelman LJA; Watson HJ; Liu Z; Brueggeman L; Breen G; Bulik CM; Arenas E; Hjerling-Leffler J; Sullivan PF
Article: BRAIN SCIENCES. 2019;10(1):5
Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine
Smedfors G; Liesecke F; Ran C; Olson L; Karlsson TE; Belin AC
Article: NEUROLOGY: GENETICS. 2019;5(6):e364
Migraine polygenic risk score associates with efficacy of migraine-specific drugs
Kogelman LJA; Esserlind A-L; Christensen AF; Awasthi S; Ripke S; Ingason A; Davidsson OB; Erikstrup C; Hjalgrim H; Ullum H; Olesen J; Hansen TF; Gudbjartsson D; Gastafsson O; Stefansson K; Stefansson H; Porsteinsdottir U; Andersen S; Banasik K; Brunak S; Buil A; Burgdorf K; Gregor J; Jennum P; Nielsen KR; Nyegaard M; Paarup HM; Pedersen OB; Sorensen E; Werge T; Anttila V; Artto V; Belin AC; de Boer I; Boomsma DI; Borte S; Chasman DI; Cherkas L; Cormand B; Cuenca-Leon E; Davey-Smith G; Dichgans M; van Duijn C; Esko T; Ferrari M; Frants RR; Freilinger T; Furlotte N; Gormley P; Griffiths L; Hamalainen E; Hiekkala M; Ikram MA; Jarvelin M-R; Kajanne R; Kallela M; Kaprio J; Kaunisto M; Kubisch C; Kurki M; Kurth T; Launer L; Lehtimaki T; Lessel D; Ligthart L; Litterman N; van den Maagdenberg A; Macaya A; Malik R; Mangino M; McMahon G; Muller-Myhsok B; Neale BM; Northover C; Nyholt DR; Palotie A; Palta P; Pedersen L; Pedersen N; Posthuma D; Pozo-Rosich P; Pressman A; Raitakari O; Schurks M; Sintas C; Steinberg S; Strachan D; Terwindt G; Vila-Pueyo M; Wessman M; Winsvold BS; Zhao H; Zwart J-A
Article: PARKINSONISM AND RELATED DISORDERS. 2019;66:158-165
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study
Puschmann A; Jimenez-Ferrer I; Lundblad-Andersson E; Martensson E; Hansson O; Odin P; Widner H; Brolin K; Mzezewa R; Kristensen J; Soller M; Rodstrom EY; Ross OA; Toft M; Breedveld GJ; Bonifati V; Brodin L; Zettergren A; Sydow O; Linder J; Wirdefeldt K; Svenningsson P; Nissbrandt H; Belin AC; Forsgren L; Swanberg M
Article: BRAIN SCIENCES. 2019;9(8):E184-184
Anoctamin 3: A Possible Link between Cluster Headache and Ca²⁺ Signaling
Ran C; Fourier C; Arafa D; Liesecke F; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Article: HEADACHE. 2019;59(3):410-417
Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden
Fourier C; Ran C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Journal article: CEPHALALGIA REPORTS. 2019;2:2515816319879886
Involvement of CGRP receptor RAMP1 in cluster headache: A Swedish case-control study
Michalska JM; Ran C; Fourier C; Steinberg A; Sjöstrand C; Waldenlind E; Belin AC
Article: THE JOURNAL OF HEADACHE AND PAIN. 2018;19(1):100
Implications for the migraine SNP rs1835740 in a Swedish cluster headache population
Ran C; Fourier C; Zinnegger M; Steinberg A; Sjoestrand C; Waldenlind E; Belin AC
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2018;26(8):1202-1216
Molecular genetic overlap between migraine and major depressive disorder
Yang Y; Zhao H; Boomsma DI; Ligthart L; Belin AC; Smith GD; Esko T; Freilinger TM; Hansen TF; Ikram MA; Kallela M; Kubisch C; Paraskevi C; Strachan DP; Wessman M; van den Maagdenberg AMJM; Terwindt GM; Nyholt DR
Article: SCIENCE. 2018;360(6395):1313
Analysis of shared heritability in common disorders of the brain
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Article: CEPHALALGIA. 2018;38(7):1286-1295
Cluster headache - clinical pattern and a new severity scale in a Swedish cohort
Steinberg A; Fourier C; Ran C; Waldenlind E; Sjostrand C; Belin AC
Article: NEURON. 2018;98(4):743-753.e4
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
Gormley P; Kurki MI; Hiekkala ME; Veerapen K; Happola P; Mitchell AA; Lal D; Palta P; Surakka I; Kaunisto MA; Hamalainen E; Vepsalainen S; Havanka H; Harno H; Ilmavirta M; Nissila M; Sako E; Sumelahti M-L; Liukkonen J; Sillanpaa M; Metsahonkala L; Koskinen S; Lehtimaki T; Raitakari O; Mannikko M; Ran C; Belin AC; Jousilahti P; Anttila V; Salomaa V; Artto V; Farkkila M; Runz H; Daly MJ; Neale BM; Ripatti S; Kallela M; Wessman M; Palotie A
Article: BMC MEDICAL GENETICS. 2018;19(1):42
S100B polymorphisms are associated with age of onset of Parkinson's disease
Fardell C; Zettergren A; Ran C; Belin AC; Ekman A; Sydow O; Backman L; Holmberg B; Dizdar N; Soderkvist P; Nissbrandt H
Article: CEPHALALGIA. 2018;38(3):496-502
A genetic CLOCK variant associated with cluster headache causing increased mRNA levels
Fourier C; Ran C; Zinnegger M; Johansson A-S; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Article: CHRONOBIOLOGY INTERNATIONAL. 2018;35(2):270-279
The choroid plexus harbors a circadian oscillator modulated by estrogens
Quintela T; Albuquerque T; Lundkvist G; Belin AC; Talhada D; Goncalves I; Carro E; Santos CRA
Article: THE JOURNAL OF HEADACHE AND PAIN. 2017;18(1):88
Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort
Ran C; Fourier C; Michalska JM; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Article: PLOS ONE. 2017;12(9):e0185663
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants
Winsvold BS; Bettella F; Witoelar A; Anttila V; Gormley P; Kurth T; Terwindt GM; Freilinger TM; Frei O; Shadrin A; Wang Y; Dale AM; van den Maagdenberg AMJM; Chasman DI; Nyholt DR; Palotie A; Andreassen OA; Zwart J-A
Article: PARKINSON'S DISEASE. 2017;2017:4020198-7
Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease
Ran C; Wirdefeldt K; Brodin L; Ramezani M; Westerlund M; Xiang F; Anvret A; Willows T; Sydow O; Johansson A; Galter D; Svenningsson P; Belin AC
Article: EUROPEAN JOURNAL OF NEUROSCIENCE. 2016;44(7):2504-2514
Ryanodine-sensitive intracellular Ca²⁺ channels are involved in the output from the SCN circadian clock
Aguilar-Roblero R; Quinto D; Baez-Ruiz A; Luis Chavez J; Carmine Belin A; Diaz-Munoz M; Michel S; Lundkvist G
Article: NEUROBIOLOGY OF AGING. 2016;45:212.e5-212.e11
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden
Ran C; Brodin L; Forsgren L; Westerlund M; Ramezani M; Gellhaar S; Xiang F; Fardell C; Nissbrandt H; Soderkvist P; Puschmann A; Ygland E; Olson L; Willows T; Johansson A; Sydow O; Wirdefeldt K; Galter D; Svenningsson P; Belin AC
Article: NATURE GENETICS. 2016;48(8):856-866
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P; Anttila V; Winsvold BS; Palta P; Esko T; Pers TH; Farh K-H; Cuenca-Leon E; Muona M; Furlotte NA; Kurth T; Ingason A; McMahon G; Ligthart L; Terwindt GM; Kallela M; Freilinger TM; Ran C; Gordon SG; Stam AH; Steinberg S; Borck G; Koiranen M; Quaye L; Adams HHH; Lehtimaki T; Sarin A-P; Wedenoja J; Hinds DA; Buring JE; Schurks M; Ridker PM; Hrafnsdottir MG; Stefansson H; Ring SM; Hottenga J-J; Penninx BWJH; Farkkila M; Artto V; Kaunisto M; Vepsalainen S; Malik R; Heath AC; Madden PAF; Martin NG; Montgomery GW; Kurki MI; Kals M; Magi R; Parn K; Hamalainen E; Huang H; Byrnes AE; Franke L; Huang J; Stergiakouli E; Lee PH; Sandor C; Webber C; Cader Z; Muller-Myhsok B; Schreiber S; Meitinger T; Eriksson JG; Salomaa V; Heikkila K; Loehrer E; Uitterlinden AG; Hofman A; van Duijn CM; Cherkas L; Pedersen LM; Stubhaug A; Nielsen CS; Mannikko M; Mihailov E; Milani L; Gobel H; Esserlind A-L; Christensen AF; Hansen TF; Werge T; Kaprio J; Aromaa AJ; Raitakari O; Ikram MA; Spector T; Jarvelin M-R; Metspalu A; Kubisch C; Strachan DP; Ferrari MD; Belin AC; Dichgans M; Wessman M; van den Maagdenberg AMJM; Zwart J-A; Boomsma DI; Smith GD; Stefansson K; Eriksson N; Daly MJ; Neale BM; Olesen J; Chasman DI; Nyholt DR; Palotie A
Article: OPEN NEUROLOGY JOURNAL. 2016;10:25-29
No Association Between rs7077361 in ITGA8 and Parkinson's Disease in Sweden.
Ran C; Mehdi RN; Fardell C; Xiang F; Nissbrandt H; Sydow O; Wirdefeldt K; Belin AC
Article: HEADACHE. 2016;56(5):835-840
Screening of Two ADH4 Variations in a Swedish Cluster Headache Case-Control Material
Fourier C; Ran C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Journal article: NEUROLOGY: GENETICS. 2015;1(1):&na
Genetic analysis for a shared biological basis between migraine and coronary artery disease.
Winsvold BS; Nelson CP; Malik R; Gormley P; Anttila V; Vander Heiden J; Elliott KS; Jacobsen LM; Palta P; Amin N; de Vries B; Hämäläinen E; Freilinger T; Ikram MA; Kessler T; Koiranen M; Ligthart L; McMahon G; Pedersen LM; Willenborg C; Won H-H; Olesen J; Artto V; Assimes TL; Blankenberg S; Boomsma DI; Cherkas L; Davey Smith G; Epstein SE; Erdmann J; Ferrari MD; Göbel H; Hall AS; Jarvelin M-R; Kallela M; Kaprio J; Kathiresan S; Lehtimäki T; McPherson R; März W; Nyholt DR; O'Donnell CJ; Quaye L; Rader DJ; Raitakari O; Roberts R; Schunkert H; Schürks M; Stewart AFR; Terwindt GM; Thorsteinsdottir U; van den Maagdenberg AMJM; van Duijn C; Wessman M; Kurth T; Kubisch C; Dichgans M; Chasman DI; Cotsapas C; Zwart J-A; Samani NJ; Palotie A; CARDIoGRAM Consortium and the International Headac
Article: GENETICS RESEARCH. 2015;97:e8
ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide
Graae L; Paddock S; Belin AC
Article: NEUROLOGY. 2014;83(21):1906-1913
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Theuns J; Verstraeten A; Sleegers K; Wauters E; Gijselinck I; Smolders S; Crosiers D; Corsmit E; Elinck E; Sharma M; Krüger R; Lesage S; Brice A; Chung SJ; Kim M-J; Kim YJ; Ross OA; Wszolek ZK; Rogaeva E; Xi Z; Lang AE; Klein C; Weissbach A; Mellick GD; Silburn PA; Hadjigeorgiou GM; Dardiotis E; Hattori N; Ogaki K; Tan E-K; Zhao Y; Aasly J; Valente EM; Petrucci S; Annesi G; Quattrone A; Ferrarese C; Brighina L; Deutschländer A; Puschmann A; Nilsson C; Garraux G; LeDoux MS; Pfeiffer RF; Boczarska-Jedynak M; Opala G; Maraganore DM; Engelborghs S; De Deyn PP; Cras P; Cruts M; Van Broeckhoven C; GEO-PD Consortium
Article: BMC MEDICAL GENETICS. 2014;15:38
A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample
Ran C; Graae L; Magnusson PKE; Pedersen NL; Olson L; Belin AC
Article: NEUROBIOLOGY OF AGING. 2014;35(1):266.e5-266.14
The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
Heckman MG; Elbaz A; Soto-Ortolaza AI; Serie DJ; Aasly JO; Annesi G; Auburger G; Bacon JA; Boczarska-Jedynak M; Bozi M; Brighina L; Chartier-Harlin M-C; Dardiotism E; Destee A; Ferrarese C; Ferraris A; Fiske B; Gispert S; Hadjigeorgioum GM; Hattori N; Ioannidis JPA; Jasinska-Myga B; Jeon BS; Kim YJ; Klein C; Kruger R; Kyratzi E; Lin C-H; Lohmann K; Loriot M-A; Lynch T; Mellick GD; Mutez E; Opala G; Park SS; Petrucci S; Quattrone A; Sharma M; Silburn PA; Sohn YH; Stefanis L; Tadic V; Tomiyama H; Uitti RJ; Valente EM; Vassilatis DK; Vilarino-Guell C; White LR; Wirdefeldt K; Wszolek ZK; Wu R-M; Xiromerisiou G; Maraganore DM; Farrer MJ; Ross OA
Article: NEUROLOGY. 2012;79(7):659-667
Large-scale replication and heterogeneity in Parkinson disease genetic loci
Sharma M; Ioannidis JPA; Aasly JO; Annesi G; Brice A; Van Broeckhoven C; Bertram L; Bozi M; Crosiers D; Clarke C; Facheris M; Farrer M; Garraux G; Gispert S; Auburger G; Vilarino-Gueell C; Hadjigeorgiou GM; Hicks AA; Hattori N; Jeon B; Lesage S; Lill CM; Lin J-J; Lynch T; Lichtner P; Lang AE; Mok V; Jasinska-Myga B; Mellick GD; Morrison KE; Opala G; Pramstaller PP; Pichler I; Park SS; Quattrone A; Rogaeva E; Ross OA; Stefanis L; Stockton JD; Satake W; Silburn PA; Theuns J; Tan E-K; Toda T; Tomiyama H; Uitti RJ; Wirdefeldt K; Wszolek Z; Xiromerisiou G; Yueh K-C; Zhao Y; Gasser T; Maraganore D; Krueger R
Article: NEUROSCIENCE LETTERS. 2012;522(1):30-35
Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease
Belin AC; Ran C; Anvret A; Paddock S; Westerlund M; Hakansson A; Nissbrandt H; Soderkvist P; Dizdar N; Ahmadi A; Anvret M; Willows T; Sydow O; Galter D
Article: BIOLOGICAL PSYCHIATRY. 2012;71(10):922-930
MAGI1 Copy Number Variation in Bipolar Affective Disorder and Schizophrenia
Karlsson R; Graae L; Lekman M; Wang D; Favis R; Axelsson T; Galter D; Belin AC; Paddock S
Article: OPEN NEUROLOGY JOURNAL. 2012;6:1-5
Genetic Screening of the Mitochondrial Rho GTPases MIRO1 and MIRO2 in Parkinson's Disease.
Anvret A; Ran C; Westerlund M; Sydow O; Willows T; Olson L; Galter D; Belin AC
Article: BEHAVIOURAL BRAIN RESEARCH. 2012;227(1):252-257
Adh1 and Adh1/4 knockout mice as possible rodent models for presymptomatic Parkinson's disease
Anvret A; Ran C; Westerlund M; Gellhaar S; Lindqvist E; Pernold K; Lundstromer K; Duester G; Felder MR; Galter D; Belin AC
Article: LANCET NEUROLOGY. 2011;10(10):898-908
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
Ross OA; Soto-Ortolaza AI; Heckman MG; Aasly JO; Abahuni N; Annesi G; Bacon JA; Bardien S; Bozi M; Brice A; Brighina L; Van Broeckhoven C; Carr J; Chartier-Harlin M-C; Dardiotis E; Dickson DW; Diehl NN; Elbaz A; Ferrarese C; Ferraris A; Fiske B; Gibson JM; Gibson R; Hadjigeorgiou GM; Hattori N; Ioannidis JPA; Jasinska-Myga B; Jeon BS; Kim YJ; Klein C; Kruger R; Kyratzi E; Lesage S; Lin C-H; Lynch T; Maraganore DM; Mellick GD; Mutez E; Nilsson C; Opala G; Park SS; Puschmann A; Quattrone A; Sharma M; Silburn PA; Sohn YH; Stefanis L; Tadic V; Theuns J; Tomiyama H; Uitti RJ; Valente EM; van de Loo S; Vassilatis DK; Vilarino-Gueell C; White LR; Wirdefeldt K; Wszolek ZK; Wu R-M; Farrer MJ
Article: NEUROSCIENCE LETTERS. 2011;501(1):41-44
Genetic studies of the protein kinase AKT1 in Parkinson's disease
Ran C; Westerlund M; Anvret A; Willows T; Sydow O; Galter D; Belin AC
Article: THE FASEB JOURNAL. 2011;25(4):1345-1352
Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease
Westerlund M; Behbahani H; Gellhaar S; Forsell C; Belin AC; Anvret A; Zettergren A; Nissbrandt H; Lind C; Sydow O; Graff C; Olson L; Ankarcrona M; Galter D
Article: OPEN NEUROLOGY JOURNAL. 2011;5:8-11
DJ-1 Mutations are Rare in a Swedish Parkinson Cohort.
Anvret A; Blackinton JG; Westerlund M; Ran C; Sydow O; Willows T; Håkansson A; Nissbrandt H; Belin AC
Article: BEHAVIOURAL BRAIN RESEARCH. 2011;217(2):439-445
Modeling Parkinson's disease genetics: Altered function of the dopamine system in Adh4 knockout mice
Belin AC; Westerlund M; Anvret A; Lindqvist E; Pernold K; Ogren SO; Duester G; Galter D
Article: NEUROBIOLOGY OF AGING. 2011;32(3):548.e9-548.18
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
Krueger R; Sharma M; Riess O; Gasser T; Van Broeckhoven C; Theuns J; Aasly J; Annesi G; Bentivoglio AR; Brice A; Djarmati A; Elbaz A; Farrer M; Ferrarese C; Gibson JM; Hadjigeorgiou GM; Hattori N; Ioannidis JPA; Jasinska-Myga B; Klein C; Lambert J-C; Lesage S; Lin J-J; Lynch T; Mellick GD; de Nigris F; Opala G; Prigione A; Quattrone A; Ross OA; Satake W; Silburn PA; Tan EK; Toda T; Tomiyama H; Wirdefeldt K; Wszolek Z; Xiromerisiou G; Maraganore DM
Article: NEUROSCIENCE LETTERS. 2010;485(2):117-120
Variations of the CAG trinucleotide repeat in DNA polymerase gamma (POLG1) is associated with Parkinson's disease in Sweden
Anvret A; Westerlund M; Sydow O; Willows T; Lind C; Galter D; Belin AC
Article: PARKINSON'S DISEASE. 2010;2010:491751-5
Possible Involvement of a Mitochondrial Translation Initiation Factor 3 Variant Causing Decreased mRNA Levels in Parkinson's Disease
Anvret A; Ran C; Westerlund M; Thelander A-C; Sydow O; Lind C; Hakansson A; Nissbrandt H; Galter D; Belin AC
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2010;153B(1):220-228
Non-Replication of Association for Six Polymorphisms From Meta-Analysis of Genome-Wide Association Studies of Parkinson's Disease: Large-Scale Collaborative Study
Evangelou E; Maraganore DM; Annesi G; Brijhina L; Brice A; Elbaz A; Ferrarese C; Hadjigeorgiou GM; Krueger R; Lambert J-C; Lesage S; Markopoulou K; Mellick GD; Meeus B; Pedersen NL; Quattrone A; Van Broeckhoven C; Sharma M; Silburn PA; Tan E-K; Wirdefeldt K; Ioannidis JPA
Article: NEUROBIOLOGY OF AGING. 2010;31(1):114-117
PITX3 polymorphism is associated with early onset Parkinson's disease
Bergman O; Hakansson A; Westberg L; Nordenstrom K; Belin AC; Sydow O; Olson L; Holmberg B; Eriksson E; Nissbrandt H
Article: PARKINSONISM AND RELATED DISORDERS. 2009;15(6):422-424
Association of a polymorphism in the ABCB1 gene with Parkinson's disease
Westerlund M; Belin AC; Anvret A; Hakansson A; Nissbrandt H; Lind C; Sydow O; Olson L; Galter D
Article: JOURNAL OF NEURAL TRANSMISSION. 2009;116(5):567-573
Cytochrome P450 2E1 gene polymorphisms/haplotypes and Parkinson's disease in a Swedish population
Shahabi HN; Westberg L; Melke J; Hakansson A; Belin AC; Sydow O; Olson L; Holmberg B; Nissbrandt H
Article: JOURNAL OF NEURAL TRANSMISSION. 2009;116(3):333-338
Do polymorphisms in transcription factors LMX1A and LMX1B influence the risk for Parkinson's disease?
Bergman O; Hayenkansson A; Westberg L; Belin AC; Sydow O; Olson L; Holmberg B; Fratiglioni L; Baeckman L; Eriksson E; Nissbrandt H
Article: CELL AND TISSUE RESEARCH. 2008;334(2):179-185
Expression of multi-drug resistance 1 mRNA in human and rodent tissues: reduced levels in Parkinson patients
Westerlund M; Belin AC; Olson L; Galter D
Article: THE FASEB JOURNAL. 2008;22(10):3509-3514
Cerebellar α-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material
Westerlund M; Belin AC; Anvret A; Hakansson A; Nissbrandt H; Lind C; Sydow O; Olson L; Galter D
Article: NEUROSCIENCE. 2008;152(2):429-436
Developmental regulation of leucine-rich repeat kinase 1 and 2 expression in the brain and other rodent and human organs: Implications for Parkinson's disease
Westerlund M; Belin AC; Anvret A; Bickford P; Olson L; Galter D
Journal article: EUROPEAN NEUROLOGICAL REVIEW. 2008;3(2):41
S18Y, UCH-L1 and Parkinson’s Disease
Belin AC; Galter D
Article: PHYSIOLOGY AND BEHAVIOR. 2007;92(1-2):46-53
DJ-1 and UCH-L1 gene activity patterns in the brains of controls, Parkinson and schizophrenia patients and in rodents
Galter D; Westerlund M; Belin AC; Olson L
Article: PARKINSONISM AND RELATED DISORDERS. 2007;13(5):295-298
S18Y in ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) associated with decreased risk of Parkinson's disease in Sweden
Belin AC; Westerlund M; Bergman O; Nissbrandt H; Lind C; Sydow O; Galter D
Article: NEUROSCIENCE LETTERS. 2007;420(3):257-262
Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease
Belin AC; Bjork BF; Westerlund M; Galter D; Sydow O; Lind C; Pernold K; Rosvall L; Hakansson A; Winblad B; Nissbrandt H; Graff C; Olson L
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2007;144B(3):367-369
Cyclooxygenase-2 polymorphisms in Parkinson's disease
Hakansson A; Bergman O; Chrapkowska C; Westberg L; Belin AC; Sydow O; Johnels B; Olson L; Holmberg B; Nissbrandt H
Article: THE FEBS JOURNAL. 2007;274(5):1212-1223
High and complementary expression patterns of alcohol and aldehyde dehydrogenases in the gastrointestinal tract - Implications for Parkinson's disease
Westerlund M; Belin AC; Felder MR; Olson L; Galter D
Article: LANCET NEUROLOGY. 2006;5(11):917-923
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease:: a large-scale international study
Elbaz A; Nelson LM; Payami H; Ioannidis JPA; Fiske BK; Annesi G; Belin AC; Factor SA; Ferrarese C; Hadjigeorgiou GM; Higgins DS; Kawakami H; Krueger R; Marder KS; Mayeux RP; Mellick GD; Nutt JG; Ritz B; Samii A; Tanner CM; Van Broeckhoven C; Van Den Eeden SK; Wirdefeldt K; Zabetian CP; Dehem M; Montimurro JS; Southwick A; Myers RM; Trikalinos TA
Article: MOVEMENT DISORDERS. 2006;21(10):1731-1734
Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish Parkinson cohort and a healthy nonagenarian
Belin AC; Westerlund M; Sydow O; Lundstromer K; Hakansson A; Nissbrandt H; Olson L; Galter D
Article: ANNALS OF NEUROLOGY. 2006;59(4):714-719
LRRK2 expression linked to dopamine-innervated areas
Galter D; Westerlund M; Carmine A; Lindqvist E; Sydow O; Olson L
Article: CELL AND TISSUE RESEARCH. 2005;322(2):227-236
Tissue- and species-specific expression patterns of class I, III, and IV Adh and Aldh1 mRNAs in rodent embryos
Westerlund M; Galter D; Carmine A; Olson L
Article: MOVEMENT DISORDERS. 2005;20(5):569-573
Investigation of genes coding for inflammatory components in Parkinson's disease
Håkansson A; Westberg L; Nilsson S; Buervenich S; Carmine A; Holmberg B; Sydow O; Olson L; Johnels B; Eriksson E; Nissbrandt H
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2005;133B(1):88-92
Interaction of polymorphisms in the genes encoding interleukin-6 and estrogen receptor beta on the susceptibility to Parkinson's disease
Håkansson A; Westberg L; Nilsson S; Buervenich S; Carmine A; Holmberg B; Sydow O; Olson L; Johnels B; Eriksson E; Nissbrandt H
Article: ARCHIVES OF NEUROLOGY. 2005;62(1):74-78
A rare truncating mutation in ADH1C (G 78Stop) shows significant association with Parkinson disease in a large international sample
Buervenich S; Carmine A; Galter D; Shahabi HN; Johnels B; Holmberg B; Ahlberg J; Nissbrandt H; Eerola J; Hellström O; Tienari P; Matsuura T; Ashizawa T; Wüllner U; Klockgether T; Zimprich A; Gasser T; Hanson M; Waseem S; Singleton A; McMahon FJ; Anvret M; Sydow O; Olson L
Article: PSYCHONEUROENDOCRINOLOGY. 2004;29(8):993-998
Association between the estrogen receptor beta gene and age of onset of Parkinson's disease
Westberg L; Håkansson A; Melke J; Shahabi HN; Nilsson S; Buervenich S; Carmine A; Ahlberg J; Grundell MB; Schulhof B; Klingborg K; Holmberg B; Sydow O; Olson L; Johnels EB; Eriksson E; Nissbrandt H
Article: NEUROBIOLOGY OF DISEASE. 2003;14(3):637-647
ALDH1 mRNA: presence in human dopamine neurons and decreases in substantia nigra in Parkinson's disease and in the ventral tegmental area in schizophrenia
Galter D; Buervenich S; Carmine A; Anvret M; Olson L
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2003;120B(1):51-57
NURR1 promoter polymorphisms:: Parkinson's disease, schizophrenia, and personality traits
Carmine A; Buervenich S; Galter D; Jönsson EG; Sedvall GC; Farde L; Gustavsson JP; Bergman H; Chowdari KV; Nimgaonkar VL; Anvret M; Sydow O; Olson L
Article: EUROPEAN JOURNAL OF NEUROSCIENCE. 2003;17(11):2418-2424
Decreased ethanol preference and wheel running in Nurr1-deficient mice
Werme M; Hermanson E; Carmine A; Buervenich S; Zetterström RH; Thorén P; Ögren SO; Olson L; Perlmann T; Brené S
Article: PSYCHIATRIC GENETICS. 2003;13(1):23-28
Two NOTCH4 polymorphisms and their relation to schizophrenia susceptibility and different personality traits
Carmine A; Chheda MG; Jönsson EG; Sedvall GC; Farde L; Gustavsson JP; Bergman H; Anvret M; Buervenich S; Olson L
Article: THE FEBS JOURNAL. 2003;270(6):1316-1326
Distribution of class I, III and IV alcohol dehydrogenase mRNAs in the adult rat, mouse and human brain
Galter D; Carmine A; Buervenich S; Duester G; Olson L
Article: MOVEMENT DISORDERS. 2002;17(4):764-766
Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease
Carmine A; Buervenich S; Sydow O; Anvret M; Olson L
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART A. 2000;96(6):808-813
NURR1 mutations in cases of schizophrenia and manic-depressive disorder
Buervenich S; Carmine A; Arvidsson M; Xiang FQ; Zhang ZP; Sydow O; Jönsson EG; Sedvall GC; Leonard S; Ross RG; Freedman R; Chowdari KV; Nimgaonkar VL; Perlmann T; Anvret M; Olson L
Article: MOVEMENT DISORDERS. 2000;15(5):813-818
Alcohol dehydrogenase alleles in Parkinson's disease
Buervenich S; Sydow O; Carmine A; Zhang ZP; Anvret M; Olson L
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Alla övriga publikationer

Preprint: MEDRXIV. 2024;MEDRXIV
Genome-wide association study of copy number variations in Parkinson's disease.
Landoulsi Z; Sreelatha AAK; Schulte C; Bobbili DR; Montanucci L; Leu C; Niestroj L-M; Hassanin E; Domenighetti C; Pavelka L; Sugier P-E; Radivojkov-Blagojevic M; Lichtner P; Portugal B; Edsall C; Kru Ger J; Hernandez DG; Blauwendraat C; Mellick GD; Zimprich A; Pirker W; Tan M; Rogaeva E; Lang AE; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschländer AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Burbulla LF; Matsuo H; Nakayama A; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; van de Warrenburg BP; Bloem BR; Singleton AB; Toft M; Pihlstrom L; Guedes LC; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Clarke CE; Morrison KE; Krainc D; Farrer MJ; Lal D; Elbaz A; Gasser T; Krüger R; Sharma M; May P
Review: LANCET NEUROLOGY. 2024;23(7):712-724
Recent advances in diagnosing, managing, and understanding the pathophysiology of cluster headache
Petersen AS; Lund N; Goadsby PJ; Belin AC; Wang S-J; Fronczek R; Burish M; Cho S-J; Peres MFP; Jensen RH
Preprint: RESEARCH SQUARE. 2024
MERTK in the trigeminal system: a novel target for cluster headache and other headache disorders?
Edvinsson JCA; Edvinsson L; Ran C; Olofsgård FJ; Steinberg A; Belin AC
Review: CEPHALALGIA. 2023;43(10):3331024231208126
The genetics and chronobiology of cluster headache
Belin AC; Barloese MC
Conference publication: CEPHALALGIA. 2023;43(1supp):84
Disease Characteristics in Triptan Users and Non-users in a Swedish Cluster Headache Cohort
Olofsgard FJ; Ran C; Wellfelt K; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Conference publication: CEPHALALGIA. 2023;43(1supp):100
Actigraphy and self-assessed sleep study show increased sleep latency and sleep related stress in cluster headache
Ran C; Olofsgard FJ; Steinberg A; Wellfelt K; Sjostrand C; Waldenlind E; Dahlgren A; Belin AC
Conference publication: CEPHALALGIA. 2022;42(1_SUPPL):11-12
Investigating the Impact of Genetic Variants on Triptan Response in Cluster Headache
Olofsgard FMEJ; Ran C; Qin Y; Fourier C; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Preprint: MEDRXIV. 2021
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Hautakangas H; Winsvold BS; Ruotsalainen SE; Bjornsdottir G; Harder AVE; Kogelman LJA; Thomas LF; Noordam R; Benner C; Gormley P; Artto V; Banasik K; Bjornsdottir A; Boomsma DI; Brumpton BM; Burgdorf KS; Buring JE; Chalmer MA; de Boer I; Dichgans M; Erikstrup C; Färkkilä M; Garbrielsen ME; Ghanbari M; Hagen K; Häppölä P; Hottenga J-J; Hrafnsdottir MG; Hveem K; Johnsen MB; Kähönen M; Kristoffersen ES; Kurth T; Lehtimäki T; Lighart L; Magnusson SH; Malik R; Pedersen OB; Pelzer N; Penninx BWJH; Ran C; Ridker PM; Rosendaal FR; Sigurdardottir GR; Skogholt AH; Sveinsson OA; Thorgeirsson TE; Ullum H; Vijfhuizen LS; Widén E; van Dijk KW; Consortium IHG; Headache HA-I; Cohort DBDSG; Aromaa A; Belin AC; Freilinger T; Ikram MA; Järvelin M-R; Raitakari OT; Terwindt GM; Kallela M; Wessman M; Olesen J; Chasman DI; Nyholt DR; Stefánsson H; Stefansson K; van den Maagdenberg AMJM; Hansen TF; Ripatti S; Zwart J-A; Palotie A; Pirinen M
Conference publication: MOVEMENT DISORDERS. 2021;36:S327
The MJFF Global Genetic Parkinson's Disease Research Resource
Vollstedt EJ; Aasly JO; Al Mubarak B; Alcalay R; Alvarez V; Amorin I; Annesi G; Arkadir D; Barkhuizen M; Berg D; Bonifati V; Boon A; Brighina L; Brockmann K; Belin AC; Carr J; Clarimon J; Cornejo-Olivas M; Corvol JC; Crosiers D; Damasio J; Das P; Aguiar PC; De Rosa A; Dorszewska J; Ertan S; Ferese R; Ferreira J; Gatto E; Giladi N; Hanagasi H; Hattori N; Hentati F; Illarioshkin S; Jankovic J; Klivenyi P; Kostic V; Koziorowski D; Lang A; Lim SY; Lin CH; Lohmann K; Martikainen M; Mellick G; Merello M; Mir P; Pimentel M; Pulkes T; Puschmann A; Sammler E; Petersen MS; Skorvanek M; Spitz M; Stefanis L; Suchowersky O; Tumas V; Valente EM; de Warrenburg B; Williams-Gray C; Wu R; Zhang B; Zimprich A; Klein C
Conference publication: CEPHALALGIA. 2021;41(1_SUPPL):232
International Consortium for Cluster Headache Genetics: two initiatives report first genome-wide association hits
Winsvold BS; Harder AVE; Fourier C; Noordam R; O'Connor E; Ran C; Vandrovcova J; Zwart JA; Houlden H; Terwindt GM; Matharu M; van den Maagdenberg A; Belin AC
Conference publication: THE JOURNAL OF HEADACHE AND PAIN. 2021;22(SUPPL 1):25
Sleep assessment in patients with Cluster headache - self reported vs observed data
Ran C; Fourier C; Olofsgard FJ; Wirth C; Steinberg A; Sjostrand C; Waldenlind E; Dahlgren A; Belin AC
Conference publication: CEPHALALGIA. 2021;41(1_SUPPL):38
Sleep assessment in patients with Cluster headache - self reported vs observed data
Ran C; Fourier C; Olofsgard FJ; Wirth C; Steinberg A; Sjostrand C; Waldenlind E; Dahlgren A; Belin AC
Review: BRAIN SCIENCES. 2020;10(1):E30-30
Calcitonin Gene-Related Peptide (CGRP) and Cluster Headache
Belin AC; Ran C; Edvinsson L
Conference publication: CEPHALALGIA. 2020;40:36
INVESTIGATING THE LINK BETWEEN CLUSTER HEADACHE AND GENETIC VARIANTS IN THE BIOLOGICAL CLOCK GENE PER3
Olofsgard FMEJ; Ran C; Fourier C; Sjostrand C; Waldenlind E; Steinberg A; Belin AC
Editorial comment: ANNALS OF NEUROLOGY. 2019;86(2):153-157
Using global team science to identify genetic parkinson's disease worldwide
Vollstedt E-J; Kasten M; Klein C
Conference publication: CEPHALALGIA. 2019;39:18
Circadian rhythm gene expression in cluster headache
Ran C; Liesecke F; Fourier C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Conference publication: CEPHALALGIA. 2019;39:17-18
Gender differences in cluster headache in Sweden
Fourier C; Ran C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Book chapter: BLOOD-BRAIN BARRIER: NEUROMETHODS. 2019;p. 205-230
Experimental Tools to Study the Regulation and Function of the Choroid Plexus
Gonçalves I; Quintela T; Duarte AC; Hubbard P; Baltazar G; Schwerk C; Belin AC; Tomás J; Santos CRA
Other: NEURON. 2018;99(5):1098
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (vol 98, pg 743, 2018)
Gormley P; Kurki MI; Hiekkala ME; Veerapen K; Happola P; Mitchell AA; Lal D; Palta P; Surakka I; Kaunisto MA; Hamalainen E; Vepsalainen S; Havanka H; Harno H; Ilmavirta M; Nissila M; Sako E; Sumelahti M-L; Liukkonen J; Sillanpaa M; Metsahonkala L; Koskinen S; Lehtimaki T; Raitakari O; Mannikko M; Ran C; Belin AC; Jousilahti P; Anttila V; Salomaa V; Artto V; Farkkila M; Runz H; Daly MJ; Neale BM; Ripatti S; Kallela M; Wessman M; Palotie A
Conference publication: CEPHALALGIA. 2018;38:24
INVOLVEMENT OF CGRP RECEPTOR RAMP1 IN CLUSTER HEADACHE - A SWEDISH CASE-CONTROL STUDY
Michalska J; Fourier C; Steinberg A; Sjostrand C; Waldenlind E; Ran C; Belin AC
Conference publication: CEPHALALGIA. 2018;38:23
POTENTIAL CANDIDATE GENES FOR CLUSTER HEADACHE INVOLVED IN CA2+SIGNALING AND T-CELL DIFFERENTIATION
Ran C; Fourier C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Conference publication: CEPHALALGIA. 2017;37:240-241
INVOLVEMENT OF THE MIGRAINE SNP rs1835740 IN CLUSTER HEADACHE
Ran C; Fourier C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Conference publication: CEPHALALGIA. 2017;37:212
Cluster Headache - Clinical pattern and a new severity scale in a Swedish cohort
Steinberg A; Fourier C; Ran C; Waldenlind E; Sjostrand C; Belin AC
Conference publication: CEPHALALGIA. 2017;37:21-22
The clock gene CRY1 is associated with cluster headache in Sweden
Fourier C; Ran C; Steinberg A; Sjostrand C; Waldenlind E; Belin AC
Other: NATURE GENETICS. 2016;48(10):1296
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (vol 48, pg 856, 2016)
Gormley P; Anttila V; Winsvold BS; Palta P; Esko T; Pers TH; Farh K-H; Cuenca-Leon E; Muona M; Furlotte NA; Kurth T; Ingason A; McMahon G; Ligthart L; Terwindt GM; Kallela M; Freilinger TM; Ran C; Gordon SG; Stam AH; Steinberg S; Borck G; Koiranen M; Quaye L; Adams HHH; Lehtimaki T; Sarin A-P; Wedenoja J; Hinds DA; Buring JE; Schurks M; Ridker PM; Hrafnsdottir MG; Stefansson H; Ring SM; Hottenga J-J; Penninx BWJH; Farkkila M; Artto V; Kaunisto M; Vepsalainen S; Malik R; Heath AC; Madden PAF; Martin NG; Montgomery GW; Kurki MI; Kals M; Magi R; Parn K; Hamalainen E; Huang H; Byrnes AE; Franke L; Huang J; Stergiakouli E; Lee PH; Sandor C; Webber C; Cader Z; Muller-Myhsok B; Schreiber S; Meitinger T; Eriksson JG; Salomaa V; Heikkila K; Loehrer E; Uitterlinden AG; Hofman A; van Duijn CM; Cherkas L; Pedersen LM; Stubhaug A; Nielsen CS; Mannikko M; Mihailov E; Milani L; Gobel H; Esserlind A-L; Christensen AF; Hansen TF; Werge T; Kaprio J; Aromaa AJ; Raitakari O; Ikram MA; Spector T; Jarvelin M-R; Metspalu A; Kubisch C; Strachan DP; Ferrari MD; Belin AC; Dichgans M; Wessman M; van den Maagdenberg AMJM; Zwart J-A; Boomsma DI; Smith GD; Stefansson K; Eriksson N; Jdaly M; Neale BM; Olesen J; Chasman DI; Nyholt DR; Palotie A
Other: NATURE GENETICS. 2016;48(8)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (vol 48, pg 856, 2016)
Gormley P; Anttila V; Winsvold BS; Palta P; Esko T; Pers TH; Farh K-H; Cuenca-Leon E; Muona M; Furlotte NA; Kurth T; Ingason A; McMahon G; Ligthart L; Terwindt GM; Kallela M; Freilinger TM; Ran C; Gordon SG; Stam AH; Steinberg S; Borck G; Koiranen M; Quaye L; Adams HHH; Lehtimaki T; Sarin A-P; Wedenoja J; Hinds DA; Buring JE; Schurks M; Ridker PM; Hrafnsdottir MG; Stefansson H; Ring SM; Hottenga J-J; Penninx BWJH; Farkkila M; Artto V; Kaunisto M; Vepsalainen S; Malik R; Heath AC; Madden PAF; Martin NG; Montgomery GW; Kurki MI; Kals M; Magi R; Parn K; Hamalainen E; Huang H; Byrnes AE; Franke L; Huang J; Stergiakouli E; Lee PH; Sandor C; Webber C; Cader Z; Muller-Myhsok B; Schreiber S; Meitinger T; Eriksson JG; Salomaa V; Heikkila K; Loehrer E; Uitterlinden AG; Hofman A; van Duijn CM; Cherkas L; Pedersen LM; Stubhaug A; Nielsen CS; Mannikko M; Mihailov E; Milani L; Gobel H; Esserlind A-L; Christensen AF; Hansen TF; Werge T; Kaprio J; Aromaa AJ; Raitakari O; Ikram MA; Spector T; Jarvelin M-R; Metspalu A; Kubisch C; Strachan DP; Ferrari MD; Belin AC; Dichgans M; Wessman M; van den Maagdenberg AMJM; Zwart J-A; Boomsma DI; Smith GD; Stefansson K; Eriksson N; Daly MJ; Neale BM; Olesen J; Chasman DI; Nyholt DR; Palotie A
Conference publication: CEPHALALGIA. 2016;36:79
GENETIC SCREENING OF CLOCK IN A SWEDISH CLUSTER HEADACHE CASE-CONTROL MATERIAL
Fourier C; Zinnegger M; Steinberg A; Sjostrand C; Waldenlind E; Ran C; Belin AC
Preprint: BIORXIV. 2015
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P; Anttila V; Winsvold BS; Palta P; Esko T; Pers TH; Farh K-H; Cuenca-Leon E; Muona M; Furlotte NA; Kurth T; Ingason A; McMahon G; Ligthart L; Terwindt GM; Kallela M; Freilinger TM; Ran C; Gordon SG; Stam AH; Steinberg S; Borck G; Koiranen M; Quaye L; Adams HH; Lehtimäki T; Sarin A-P; Wedenoja J; Hinds DA; Buring JE; Schürks M; Ridker PM; Hrafnsdottir MG; Stefansson H; Ring SM; Hottenga J-J; Penninx BW; Färkkilä M; Artto V; Kaunisto M; Vepsäläinen S; Malik R; Heath AC; Madden PAF; Martin NG; Montgomery GW; Hämäläinen E; Huang H; Byrnes AE; Franke L; Huang J; Stergiakouli E; Lee PH; Sandor C; Webber C; Cader Z; Muller-Myhsok B; Schreiber S; Meitinger T; Eriksson JG; Salomaa V; Heikkilä K; Loehrer E; Uitterlinden AG; Hofman A; van Duijn CM; Cherkas L; Pedersen LM; Stubhaug A; Nielsen CS; Männikkö M; Mihailov E; Milani L; Göbel H; Esserlind A-L; Christensen AF; Hansen TF; Werge T; Kaprio J; Aromaa AJ; Raitakari O; Ikram MA; Spector T; Järvelin M-R; Metspalu A; Kubisch C; Strachan DP; Ferrari MD; Belin AC; Dichgans M; Wessman M; van den Maagdenberg AM; Zwart J-A; Boomsma DI; Smith GD; Stefansson K; Eriksson N; Daly MJ; Neale BM; Olesen J; Chasman DI; Nyholt DR; Palotie A; Consortium OBOTIHG
Conference publication: CEPHALALGIA. 2015;35:262
Genetic screening and characterization of hyporcretin receptor 2 in cluster headache in Sweden
Ran C; Xiang F; Mattsson A; Sjostrand C; Steinberg A; Waldenlind E; Belin AC
Review: JOURNAL OF PARKINSONISM AND RESTLESS LEGS SYNDROME. 2014;Volume 4:63-75
The genetics of Parkinson’s disease: review of current and emerging candidates
Belin A; Ran C
Conference publication: MOVEMENT DISORDERS. 2014;29:S60
Glucocerebrosidase (GBA) mutations in Parkinson's disease in Sweden and tissue expression of GBA mRNA
Ran C; Westerlund MO; Ramezani M; Gellhaar S; Xiang F; Fardell C; Nissbrandt H; Soderkvist P; Willows T; Willows T; Johansson AC; Wirdefeldt K; Sydow O; Olson L; Galter D; Belin AC
Letter: PARKINSONISM AND RELATED DISORDERS. 2013;19(7):701-702
The HLA-DRA variation rs3129882 is not associated with Parkinson's disease in Sweden
Ran C; Willows T; Sydow O; Johansson A; Soderkvist P; Dizdar N; Ahmadi A; Olson L; Belin C
Meeting abstract: EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2010;20:S57
Alcohol dehydrogenase 4 knock-out mice as a model of dopamine-system related dysfunction
Westerlund M; Belin AC; Anvret A; Lindqvist E; Pernold K; Ogren SO; Duester G; Galter D
Conference publication: MOVEMENT DISORDERS. 2010;25:S632
Modeling Parkinson's Disease in Adh1 and Adh1/4 Knockout Mice
Anvret A; Ran C; Westerlund M; Lindqvist E; Pernold K; Lundstromer K; Duester G; Felder MR; Galter D; Belin AC
Letter: PARKINSONISM AND RELATED DISORDERS. 2008;14(6):520-522
Investigation of genes related to familial forms of Parkinson's disease -: With focus on the Parkin gene
Hakansson A; Belin AC; Stiller C; Sydow O; Johnels B; Olson L; Holmberg B; Nissbrandt H
Corrigendum: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2008;147B(4):541
Uyclooxygenase-2 polymorphisms in Parkinson's disease (vol 144B, 367, 2008)
Hakansson A; Bergman O; Chrapkowska C; Westberg L; Belin AC; Sydow O; Johnels B; Olson L; Holmberg B; Nissbrandt H
Review: THE FEBS JOURNAL. 2008;275(7):1377-1383
Parkinson's disease: A genetic perspective
Belin AC; Westerlund M
Meeting abstract: EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2007;17:S59
Modeling genetic risk in Parkinson's disease:: changed response to challenge of the dopamine system in ADH4 knockout mice
Belin AC; Westerlund M; Paddock S; Lindqvist E; Pernold K; Duester G; Ogren SO; Olson L; Galter D
Conference publication: MOVEMENT DISORDERS. 2006;21:S607
Protective effects of the S18Y polymorphism in Ubiquitin Carboxyterminal Hydrolase L1 (UCH-L1) in a Swedish parkinson material
Belin AC; Westerlund M; Bergman O; Nissbrandt H; Lind C; Sydow O; Galter D
Conference publication: MOVEMENT DISORDERS. 2006;21:S572
Association of an intronic polymorphism in SNCA with Parkinson's disease in a Swedish material
Westerlund M; Belin AC; Galter D; Lind C; Sydow O; Olson L
Thesis / dissertation: 2003
On Parkinson's disease and schizophrenia : case control studies, cellular localization and modelling of candidate genes
Carmine, Andrea
Letter: ANNALS OF NEUROLOGY. 2003;53(6):823
Lack of association between the BDNF Val66Met polymorphism and Parkinson's disease in a Swedish population
Håkansson A; Melke J; Westberg L; Shahabi HN; Buervenich S; Carmine A; Klingborg K; Grundell MB; Schulhof B; Holmberg B; Ahlberg J; Eriksson E; Sydow O; Olson L; Johnels B; Nissbrandt H
Conference publication: AMERICAN JOURNAL OF HUMAN GENETICS. 1999;65(4):A266
Identification of a new polymorphism in intron 6 of the human NURR1 gene and investigation of association with Parkinson's disease and schizophrenia.
Buervenich S; Carmine A; Xiang F; Zhang Z; Sydow O; Jonsson EG; Sedvall GC; Anvret M; Olson L
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Forskningsbidrag

Mapping of the mechanisms behind cluster headache with a focus on inflammation
Hjärnfonden
1 July 2023 - 31 December 2025
In depth characterization of genetic markers behind primary headache disorders with a focus on cluster headache
Hjärnfonden
1 July 2022 - 31 December 2024
Validering av läkemedelsrespons vid Hortons huvudvärk kopplat till genetik och dygnsrytm.
Region Stockholm
1 January 2021 - 31 December 2023
Deciphering the mechanisms behind primary headache disorders with focus on genetics and circadian rhythm
Karolinska Institutet
1 January 2021 - 31 December 2024
Genetic screening of Cluster headache in relation to treatment and circadian rhythm
Hjärnfonden
1 July 2020 - 31 December 2022
Cluster (“suicide”) headache and circadian rhythm - A multifaceted approach to reveal causes based on a world leading biobank and animal studies
Swedish Research Council
1 January 2018 - 31 December 2020
GENEPARK - The build-up and use of a unique biobank to help identifying, characterizing and modelling genetic factors in Parkinson´s disease
Swedish Research Council
1 January 2013 - 31 December 2015

Anställningar

Senior Forskare, Neurovetenskap, Karolinska Institutet, 2022-

Examina och utbildning

Docent, Neurovetenskap, Karolinska Institutet, 2011
MEDICINE DOKTORSEXAMEN, Neurovetenskap, On Parkinson’s Disease and Schizophrenia: Case Control Studies, Cellular Localization and Modelling of Candidate Genes, Institutionen för neurovetenskap, Karolinska Institutet, 2003
Medicine Magisterexamen, Karolinska Institutet, 1999

Uppdrag

Director, Centrum för Klusterhuvudvärk, Karolinska Institute, https://ki.se/en/research/research-areas-centres-and-networks/research-centres/centre-for-cluster-headache, 2023-
Forskargruppsledare, Carmine Belin Lab, Karolinska Institute, https://ki.se/en/research/research-areas-centres-and-networks/research-groups/genetic-and-molecular-basis-of-nervous-system-disorders-andrea-carmine-belin-group#tab-start, 2011-

Priser och utmärkelser

Svenska Migränsällskapets stipendium, Swedish Headache Society, 2014
Top-Cited Paper Award, Top-cited paper award for “Parkinson's disease: a genetic perspective“ published in the FEBS Journal Volume 275, issue 7, 2008., Federation of European Biochemical Societies, 2008
Special grant for younger scientists, Awarded with the special grants available for young scientists, establishing their own research projects., Karolinska Institutet, 2008
Postdoc-stipend, Hjärnfonden, 2005

Handledare

Carmen Fourier, 2022
Gabriella Smedfors, 2021
Felicia Jennysdotter Olofsgård, 2021
Franziska Liesecke, 2018
Anna Mattsson, 2014
Caroline Ran, 2014
Anna Anvret, 2011
Telma Quintela
Marie Westlund, On the roles of genes in Parkinson's disease, https://openarchive.ki.se/xmlui/handle/10616/37742
Anna Anvret, Genes involved in Parkinson's disease : focus on mitochondrial and detoxifying enzymes, https://openarchive.ki.se/xmlui/handle/10616/40551
Sandra Gellhaar, Neurodegenerative diseases studied in human brain and rodent models, https://openarchive.ki.se/xmlui/handle/10616/44514
Lisette Graae, Genetic analysis and software development for studies on complex human traits, https://openarchive.ki.se/xmlui/handle/10616/41854
Caroline Ran, On genes involved in common neurological disorders : focus on Parkinson's disease, https://openarchive.ki.se/xmlui/handle/10616/41854
Carmen Fourier, Deciphering the role of genetics and circadian rhythm in cluster headache, https://openarchive.ki.se/xmlui/handle/10616/47618
Lovisa Brodin, Parkinson's disease and Gaucher disease : focus on the GBA1 link, https://openarchive.ki.se/xmlui/handle/10616/48972

Uppdrag i kommitté

Ordförande, International Consortium for Cluster Headache Genetics, https://www.clusterheadachegenetics.org/, 2023-
Ordförande, Centrum för Klusterhuvudvärk, Karolinska Institute, https://ki.se/en/research/research-areas-centres-and-networks/research-centres/centre-for-cluster-headache, 2023-
Annat, Swedish Headache Society, https://huvudvarkssallskapet.se/, 2021-
Medlem, International Consortium for Cluster Headache Genetics, https://www.clusterheadachegenetics.org/, 2021-
Annat, International Headache Society, International Headache Society, https://ihs-headache.org/en/, 2021-2025
Vice ordförande, Junior Faculty, Karolinska Institutet, https://staff.ki.se/our-ki/junior-faculty-at-karolinska-institutet, 2018-2018
Medlem, Svenska Huvudvärkssällskapet, https://huvudvarkssallskapet.se/, 2016-
Medlem, Junior Faculty, Karolinska Institutet, https://staff.ki.se/our-ki/junior-faculty-at-karolinska-institutet, 2016-2020
Medlem, Genetic Epidemiology of Parkinson's Disesase, https://www.geopd.net/home-page, 2005-

Utvärdering av avhandlingsarbete

Elliot Glotfelty, Defence chairperson, Neuroscience, Karolinska Institutet, Mitigating neuroinflammation : new potential therapeutics and targets, https://openarchive.ki.se/xmlui/handle/10616/48691, 2023
Karin Westin, Examination board member, Karolinska Institutet, On mapping epilepsy : magneto- and electroencephalographic characterizations of epileptic activities, https://openarchive.ki.se/xmlui/handle/10616/47901, 2022
Ourania Tzortzi, Examination board member, Karolinska Institutet, Organization of brain circuits that control motivated behaviors, https://openarchive.ki.se/xmlui/handle/10616/46981, 2020
Sigrid Børte, Opponent, University of Oslo, Genetic and environmental causes of migraine, https://www.med.uio.no/klinmed/english/research/news-and-events/events/disputations/2020/borte-sigrid.html, 2020
Susanna Ylönen, External thesis reviewer, University of Oulu, Genetic risk factors for movement disorders in Finland, https://oulurepo.oulu.fi/handle/10024/36459, 2019
Bianca Migliori, Examination board member, Karolinska Institutet, Novel technologies for studies of structural and functional connections, https://openarchive.ki.se/xmlui/handle/10616/46560, 2018
Parvin Kumar, Examination board member, Karolinska Institute, Novel blood markers in psychosis, https://openarchive.ki.se/xmlui/handle/10616/46535, 2018
Saket Nigam, Examination board member, Karolinska Institute, Alzheimer's disease : uncovering mechanisms for amyloid precursor protein processing and trafficking, https://openarchive.ki.se/xmlui/handle/10616/45907, 2017
Carl-Henrik Andersson, Examination board member, University of Gothenburg, The role of microglia in Alzheimer's disease - Investigating mechansims regulating amyloid-β clearance, https://gup.ub.gu.se/publication/244166, 2016
Nadine Schweizer, Examination board member, Uppsala University, Across Borders : A Histological and Physiological Study of the Subthalamic Nucleus in Reward and Movement, https://uu.diva-portal.org/smash/get/diva2:899108/FULLTEXT01.pdf, 2016

Redaktör för vetenskaplig tidskrift

Confinia Cephalalgica et Neurologica, Medlem i redaktionskommittén, https://www.confiniacephalalgica.com/site/board, 2024
International Journal of Molecular Sciences, Gästredaktör, https://www.mdpi.com/journal/ijms/special_issues/mechanisms_primary_headache, 2023
Headache and Pain Research, Medlem i redaktionskommittén, https://www.e-hpr.org/about/editorial.php, 2023
Brain Sciences, Gästredaktör, https://www.mdpi.com/journal/brainsci/special_issues/Genetic_Headache, 2021-2021
Brain Sciences, Section editor / academic editor, https://www.mdpi.com/journal/brainsci/sectioneditors/Molecular_Cellular_Neuroscience, 2019

Sakkunniggranskning för vetenskaplig tidskrift

Movement Disorders
Brain Research
Journal of Neurology
Environment International
Neuroscience Letters
Microarrays, MDPI
Genetics Research
The Journal of Biomedical Science
Scientific Reports
Neuropsychiatric Disease and Treatment
BioMed research international
Journal of Pain Research
Neurotoxicology
EBioMedicine
Cephalalgia Reports
PLOS ONE
The Journal of Headache and Pain
JAMA Neurology
Expert Opinion On Pharmacotherapy
Frontiers in Neurology
Cephalalgia
Headache
Neurology
Current Medical Research & Opinion
Brain Sciences

Expert

Evaluator of major research grant applications in local competition, Karolinska Institutet Research Funds, Karolinska Institute, 2022-2024
Evaluator of major research grant applications in local competition, Grant reviewer of KID-applications, KID funding is a block grant for partial financing of doctoral education at KI., Karolinska Institute, 2021-2022

Konferenser och events

Ordförande, International Headache Congress, Update on trigeminal autonomic cephalalgias, 2023
Inbjuden föredragshållare, International Headache Congress, Recent developments in the genetics of cluster headache, 2023
Ordförande, International Headache Congress, Headache Trainees Excellence Tournament, 2023
Inbjuden föredragshållare, European Headache Congress, https://headache-congress.org/, Genetics in migraine, 2023
Inbjuden föredragshållare, Lundbeck R&D oragnization – Idea Forum, Cluster Headache – The alarm clock of pain, 2023
Inbjuden föredragshållare, Regional Headache Conference, https://ihs-headache.org/en/resources/ihs-regional-headache-conference/, The genetics of cluster headache, 2022
Inbjuden föredragshållare, Nordic Migraine Symposium, https://www.nordicmigrainesymposium.com/, Biomarkers - with focus on genetics, 2022
Inbjuden föredragshållare, Framtidens migränvård - danska och svenska lärdomar, Hur bli världsledande inom klusterhuvudvärk och genetikforskning, 2022
Muntliga presentationer av egna accepterade abstract, International Headache Congress, Circadian rhythm gene expression in cluster headache, 2019
Ordförande, Nordic Neuroscience Meeting, https://www.helsinki.fi/en/conferences/3rd-nordic-neuroscience-meeting-2019, Cluster headache and migraine genetics - new insights, 2019
Muntliga presentationer av egna accepterade abstract, Migraine Trust International Symposium, Involvement of CGRP receptor RAMP1 in cluster headache – A Swedish case-control study, 2018
Poster-presentationer av egna accepterade abstract, International Headache Congress, Cluster Headache – Clinical pattern and a new severity scale in a Swedish cohort, 2017

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