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

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: 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; Olofsgård 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.

Jennysdotter Olofsgård F; Ran C; Qin Y; Fourier C; Waldenlind E; Steinberg A; Sjöstrand 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; Jennysdotter Olofsgård F; 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 BS; Harder AVE; Ran C; Chalmer MA; Dalmasso MC; Ferkingstad E; Tripathi KP; Bacchelli E; Børte S; Fourier C; Petersen AS; Vijfhuizen LS; Magnusson SH; O'Connor E; Bjornsdottir G; Häppölä P; Wang Y-F; Callesen I; Kelderman T; Gallardo VJ; de Boer I; Olofsgård FJ; Heinze K; Lund N; Thomas LF; Hsu C-L; Pirinen M; Hautakangas H; Ribasés M; Guerzoni S; Sivakumar P; Yip J; Heinze A; Küçükali F; Ostrowski SR; Pedersen OB; Kristoffersen ES; Martinsen AE; Artigas MS; Lagrata S; Cainazzo MM; Adebimpe J; Quinn O; Göbel C; Cirkel A; Volk AE; Heilmann-Heimbach S; Skogholt AH; Gabrielsen ME; Wilbrink LA; Danno D; Mehta D; Guðbjartsson DF; HUNT All-In Headache, The International Headache G; Rosendaal FR; Willems van Dijk K; Fronczek R; Wagner M; Scherer M; Göbel H; Sleegers K; Sveinsson OA; Pani L; Zoli M; Ramos-Quiroga JA; Dardiotis E; Steinberg A; Riedel-Heller S; Sjöstrand C; Thorgeirsson TE; Stefansson H; Southgate L; Trembath RC; Vandrovcova J; Noordam R; Paemeleire K; Stefansson K; Fann CS-J; Waldenlind E; Tronvik E; Jensen RH; Chen S-P; Houlden H; Terwindt GM; Kubisch C; Maestrini E; Vikelis M; Pozo-Rosich P; Belin AC; Matharu M; van den Maagdenberg AMJM; Hansen TF; Ramirez A; Zwart J-A; International Consortium for Cluster Headache Gene
Article: 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: 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; Jennysdotter Olofsgård F; Steinberg A; Sjöstrand 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 L; Xiao C; Wu X; Yan P; Cui H; Yang C; Zhu J; Wu X; Tang M; Wang Y; Chen L; Liu Y; Zou Y; Zhang L; Yang C; Yao Y; Li J; Liu Z; Zhang B; Jiang X; International Headache Genetics Consortium
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-Augé A; Olaso R; Deleuze J-F; Lesueur F; Ostroumova E; Kesminiene A; de Vathaire F; Guénel P; EPITHYR consortium; 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; 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; Matsuo H; Nakayama A; Hattori N; Nishioka K; Chung SJ; Kim YJ; Kolber P; van de Warrenburg BPC; Bloem BR; Aasly J; Toft M; Pihlstrøm 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; Rödström EY; Clarke CE; Morrison KE; Tan M; Krainc D; Burbulla LF; Farrer MJ; Kruger R; Gasser T; Sharma M; Comprehensive Unbiased Risk Factor Assessment for ; 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; Sjöstrand 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 Olofsgård F; Ran C; Qin Y; Fourier C; Sjöstrand 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; Sjöstrand 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; Brüggemann N; Borsche M; Foroud T; Tolosa E; Garrido A; Annesi G; Gagliardi M; Bozi M; Stefanis L; Ferreira JJ; Correia Guedes L; Avenali M; Petrucci S; Clark L; Fedotova EY; Abramycheva NY; Alvarez V; Menéndez-González M; Jesús Maestre S; Gómez-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; Kuhlenbäumer G; Kühn AA; Borngräber 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; Genç G; de Carvalho Aguiar P; Barkhuizen M; Pimentel MMG; Saunders-Pullman R; van de Warrenburg B; Bressman S; Toft M; Appel-Cresswell S; Lang AE; Skorvanek M; Boon AJW; Krüger R; Sammler EM; Tumas V; Zhang B-R; Garraux G; Chung SJ; Kim YJ; Winkelmann J; Sue CM; Tan E-K; Damásio J; Klivényi 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; MJFF Global Genetic Parkinson's Disease Study Grou
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; Carmine Belin A; Carr J; Clarimon J; Cornejo-Olivas M; Correia Guedes L; Corvol J-C; Crosiers D; Damásio J; Das P; de Carvalho Aguiar P; De Rosa A; Dorszewska J; Ertan S; Ferese R; Ferreira J; Gatto E; Genç G; Giladi N; Gómez-Garre P; Hanagasi H; Hattori N; Hentati F; Hoffman-Zacharska D; Illarioshkin SN; Jankovic J; Jesús S; Kaasinen V; Kievit A; Klivenyi P; Kostic V; Koziorowski D; Kühn AA; Lang AE; Lim S-Y; Lin C-H; Lohmann K; Markovic V; Martikainen MH; Mellick G; Merello M; Milanowski L; Mir P; Öztop-Çakmak Ö; 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; Deutschländer 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; Pihlstrøm 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 Rödström E; Clarke CE; Morrison KE; Tan M; Krainc D; Burbulla LF; Farrer MJ; Krüger R; Gasser T; Sharma M; Vince N; Elbaz A; Comprehensive Unbiased Risk Factor Assessment for
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; Krüger 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; 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; 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; and the Comprehensive Unbiased Risk Factor Assessm
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; Ashok Kumar Sreelatha A; 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; Deutschländer 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; Pihlstrøm 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 M; Krainc D; Burbulla LF; Farrer MJ; Krüger R; Gasser T; Sharma M; Elbaz A; Comprehensive Unbiased Risk Factor Assessment for
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; 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; International Headache Genetics Consortium; HUNT All-in Headache; Danish Blood Donor Study Genomic Cohort; 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
Article: JOURNAL OF PARKINSONS 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; Deutschländer 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; Pihlstrøm 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; Krüger R; Gasser T; Sharma M; Elbaz A; Comprehensive Unbiaised Risk Factor Assessment for
Article: CEPHALALGIA. 2022;42(1):87

Board Walk - January 2022.

Belin AC
Journal article: 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; Sjöstrand 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.

Jennysdotter Olofsgård F; Ran C; Fourier C; Wirth C; Sjöstrand 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; Sjöstrand 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; Sjöstrand 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; International Headache Genetics Consortium; 23andMe Research Team; 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; Eating Disorders Working Group of the Psychiatric ; International Headache Genetics Consortium; 23andMe Research Team; 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; Carmine Belin A
Article: NEUROLOGY-GENETICS. 2019;5(6):e364

Migraine polygenic risk score associates with efficacy of migraine-specific drugs.

Kogelman LJA; Esserlind A-L; Francke Christensen A; Awasthi S; Ripke S; Ingason A; Davidsson OB; Erikstrup C; Hjalgrim H; Ullum H; Olesen J; Folkmann Hansen T; DBDS Genomic Consortium, The International Headach
Article: PARKINSONISM & RELATED DISORDERS. 2019;66:158-165

Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study.

Puschmann A; Jiménez-Ferrer I; Lundblad-Andersson E; Mårtensson E; Hansson O; Odin P; Widner H; Brolin K; Mzezewa R; Kristensen J; Soller M; Rödström 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; Sjöstrand 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; Sjöstrand C; Waldenlind E; Belin AC
Journal article: CEPHALALGIA REPORTS. 2019;2:2515816319879886-251581631987988

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: 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; Sjöstrand 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; International Headache Genetics Consortium; van den Maagdenberg AMJM; Terwindt GM; Nyholt DR
Article: SCIENCE. 2018;360(6395):1313

Analysis of shared heritability in common disorders of the brain.

Brainstorm Consortium; Anttila V; Bulik-Sullivan B; Finucane HK; Walters RK; Bras J; Duncan L; Escott-Price V; Falcone GJ; Gormley P; Malik R; Patsopoulos NA; Ripke S; Wei Z; Yu D; Lee PH; Turley P; Grenier-Boley B; Chouraki V; Kamatani Y; Berr C; Letenneur L; Hannequin D; Amouyel P; Boland A; Deleuze J-F; Duron E; Vardarajan BN; Reitz C; Goate AM; Huentelman MJ; Kamboh MI; Larson EB; Rogaeva E; St George-Hyslop P; Hakonarson H; Kukull WA; Farrer LA; Barnes LL; Beach TG; Demirci FY; Head E; Hulette CM; Jicha GA; Kauwe JSK; Kaye JA; Leverenz JB; Levey AI; Lieberman AP; Pankratz VS; Poon WW; Quinn JF; Saykin AJ; Schneider LS; Smith AG; Sonnen JA; Stern RA; Van Deerlin VM; Van Eldik LJ; Harold D; Russo G; Rubinsztein DC; Bayer A; Tsolaki M; Proitsi P; Fox NC; Hampel H; Owen MJ; Mead S; Passmore P; Morgan K; Nöthen MM; Rossor M; Lupton MK; Hoffmann P; Kornhuber J; Lawlor B; McQuillin A; Al-Chalabi A; Bis JC; Ruiz A; Boada M; Seshadri S; Beiser A; Rice K; van der Lee SJ; De Jager PL; Geschwind DH; Riemenschneider M; Riedel-Heller S; Rotter JI; Ransmayr G; Hyman BT; Cruchaga C; Alegret M; Winsvold B; Palta P; Farh K-H; Cuenca-Leon E; Furlotte N; Kurth T; Ligthart L; Terwindt GM; Freilinger T; Ran C; Gordon SD; Borck G; Adams HHH; Lehtimäki T; Wedenoja J; Buring JE; Schürks M; Hrafnsdottir M; Hottenga J-J; Penninx B; Artto V; Kaunisto M; Vepsäläinen S; Martin NG; Montgomery GW; Kurki MI; Hämäläinen E; Huang H; Huang J; Sandor C; Webber C; Muller-Myhsok B; Schreiber S; Salomaa V; Loehrer E; Göbel H; Macaya A; Pozo-Rosich P; Hansen T; Werge T; Kaprio J; Metspalu A; Kubisch C; Ferrari MD; Belin AC; van den Maagdenberg AMJM; Zwart J-A; Boomsma D; Eriksson N; Olesen J; Chasman DI; Nyholt DR; Avbersek A; Baum L; Berkovic S; Bradfield J; Buono RJ; Catarino CB; Cossette P; De Jonghe P; Depondt C; Dlugos D; Ferraro TN; French J; Hjalgrim H; Jamnadas-Khoda J; Kälviäinen R; Kunz WS; Lerche H; Leu C; Lindhout D; Lo W; Lowenstein D; McCormack M; Møller RS; Molloy A; Ng P-W; Oliver K; Privitera M; Radtke R; Ruppert A-K; Sander T; Schachter S; Schankin C; Scheffer I; Schoch S; Sisodiya SM; Smith P; Sperling M; Striano P; Surges R; Thomas GN; Visscher F; Whelan CD; Zara F; Heinzen EL; Marson A; Becker F; Stroink H; Zimprich F; Gasser T; Gibbs R; Heutink P; Martinez M; Morris HR; Sharma M; Ryten M; Mok KY; Pulit S; Bevan S; Holliday E; Attia J; Battey T; Boncoraglio G; Thijs V; Chen W-M; Mitchell B; Rothwell P; Sharma P; Sudlow C; Vicente A; Markus H; Kourkoulis C; Pera J; Raffeld M; Silliman S; Boraska Perica V; Thornton LM; Huckins LM; William Rayner N; Lewis CM; Gratacos M; Rybakowski F; Keski-Rahkonen A; Raevuori A; Hudson JI; Reichborn-Kjennerud T; Monteleone P; Karwautz A; Mannik K; Baker JH; O'Toole JK; Trace SE; Davis OSP; Helder SG; Ehrlich S; Herpertz-Dahlmann B; Danner UN; van Elburg AA; Clementi M; Forzan M; Docampo E; Lissowska J; Hauser J; Tortorella A; Maj M; Gonidakis F; Tziouvas K; Papezova H; Yilmaz Z; Wagner G; Cohen-Woods S; Herms S; Julià A; Rabionet R; Dick DM; Ripatti S; Andreassen OA; Espeseth T; Lundervold AJ; Steen VM; Pinto D; Scherer SW; Aschauer H; Schosser A; Alfredsson L; Padyukov L; Halmi KA; Mitchell J; Strober M; Bergen AW; Kaye W; Szatkiewicz JP; Cormand B; Ramos-Quiroga JA; Sánchez-Mora C; Ribasés M; Casas M; Hervas A; Arranz MJ; Haavik J; Zayats T; Johansson S; Williams N; Dempfle A; Rothenberger A; Kuntsi J; Oades RD; Banaschewski T; Franke B; Buitelaar JK; Arias Vasquez A; Doyle AE; Reif A; Lesch K-P; Freitag C; Rivero O; Palmason H; Romanos M; Langley K; Rietschel M; Witt SH; Dalsgaard S; Børglum AD; Waldman I; Wilmot B; Molly N; Bau CHD; Crosbie J; Schachar R; Loo SK; McGough JJ; Grevet EH; Medland SE; Robinson E; Weiss LA; Bacchelli E; Bailey A; Bal V; Battaglia A; Betancur C; Bolton P; Cantor R; Celestino-Soper P; Dawson G; De Rubeis S; Duque F; Green A; Klauck SM; Leboyer M; Levitt P; Maestrini E; Mane S; De-Luca DM; Parr J; Regan R; Reichenberg A; Sandin S; Vorstman J; Wassink T; Wijsman E; Cook E; Santangelo S; Delorme R; Rogé B; Magalhaes T; Arking D; Schulze TG; Thompson RC; Strohmaier J; Matthews K; Melle I; Morris D; Blackwood D; McIntosh A; Bergen SE; Schalling M; Jamain S; Maaser A; Fischer SB; Reinbold CS; Fullerton JM; Guzman-Parra J; Mayoral F; Schofield PR; Cichon S; Mühleisen TW; Degenhardt F; Schumacher J; Bauer M; Mitchell PB; Gershon ES; Rice J; Potash JB; Zandi PP; Craddock N; Ferrier IN; Alda M; Rouleau GA; Turecki G; Ophoff R; Pato C; Anjorin A; Stahl E; Leber M; Czerski PM; Cruceanu C; Jones IR; Posthuma D; Andlauer TFM; Forstner AJ; Streit F; Baune BT; Air T; Sinnamon G; Wray NR; MacIntyre DJ; Porteous D; Homuth G; Rivera M; Grove J; Middeldorp CM; Hickie I; Pergadia M; Mehta D; Smit JH; Jansen R; de Geus E; Dunn E; Li QS; Nauck M; Schoevers RA; Beekman AT; Knowles JA; Viktorin A; Arnold P; Barr CL; Bedoya-Berrio G; Bienvenu OJ; Brentani H; Burton C; Camarena B; Cappi C; Cath D; Cavallini M; Cusi D; Darrow S; Denys D; Derks EM; Dietrich A; Fernandez T; Figee M; Freimer N; Gerber G; Grados M; Greenberg E; Hanna GL; Hartmann A; Hirschtritt ME; Hoekstra PJ; Huang A; Huyser C; Illmann C; Jenike M; Kuperman S; Leventhal B; Lochner C; Lyon GJ; Macciardi F; Madruga-Garrido M; Malaty IA; Maras A; McGrath L; Miguel EC; Mir P; Nestadt G; Nicolini H; Okun MS; Pakstis A; Paschou P; Piacentini J; Pittenger C; Plessen K; Ramensky V; Ramos EM; Reus V; Richter MA; Riddle MA; Robertson MM; Roessner V; Rosário M; Samuels JF; Sandor P; Stein DJ; Tsetsos F; Van Nieuwerburgh F; Weatherall S; Wendland JR; Wolanczyk T; Worbe Y; Zai G; Goes FS; McLaughlin N; Nestadt PS; Grabe H-J; Depienne C; Konkashbaev A; Lanzagorta N; Valencia-Duarte A; Bramon E; Buccola N; Cahn W; Cairns M; Chong SA; Cohen D; Crespo-Facorro B; Crowley J; Davidson M; DeLisi L; Dinan T; Donohoe G; Drapeau E; Duan J; Haan L; Hougaard D; Karachanak-Yankova S; Khrunin A; Klovins J; Kučinskas V; Lee Chee Keong J; Limborska S; Loughland C; Lönnqvist J; Maher B; Mattheisen M; McDonald C; Murphy KC; Nenadic I; van Os J; Pantelis C; Pato M; Petryshen T; Quested D; Roussos P; Sanders AR; Schall U; Schwab SG; Sim K; So H-C; Stögmann E; Subramaniam M; Toncheva D; Waddington J; Walters J; Weiser M; Cheng W; Cloninger R; Curtis D; Gejman PV; Henskens F; Mattingsdal M; Oh S-Y; Scott R; Webb B; Breen G; Churchhouse C; Bulik CM; Daly M; Dichgans M; Faraone SV; Guerreiro R; Holmans P; Kendler KS; Koeleman B; Mathews CA; Price A; Scharf J; Sklar P; Williams J; Wood NW; Cotsapas C; Palotie A; Smoller JW; Sullivan P; Rosand J; Corvin A; Neale BM; Schott JM; Anney R; Elia J; Grigoroiu-Serbanescu M; Edenberg HJ; Murray R
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; Sjöstrand 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; Häppölä P; Mitchell AA; Lal D; Palta P; Surakka I; Kaunisto MA; Hämäläinen E; Vepsäläinen S; Havanka H; Harno H; Ilmavirta M; Nissilä M; Säkö E; Sumelahti M-L; Liukkonen J; Sillanpää M; Metsähonkala L; Koskinen S; Lehtimäki T; Raitakari O; Männikkö M; Ran C; Belin AC; Jousilahti P; Anttila V; Salomaa V; Artto V; Färkkilä M; 23andMe Research Team; International Headache Genetics Consortium (IHGC); 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; Carmine Belin A; Ekman A; Sydow O; Bäckman L; Holmberg B; Dizdar N; Söderkvist 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; Sjöstrand 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; Carmine Belin A; Talhada D; Gonçalves I; Carro E; Santos CRA
Article: 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; Sjöstrand C; Waldenlind E; Belin AC
Article: PARKINSONS 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: 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; International Headache Genetics Consortium
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; Báez-Ruíz A; Chávez JL; Belin AC; Díaz-Muñoz 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; Söderkvist 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; 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 BWJH; Färkkilä M; Artto V; Kaunisto M; Vepsäläinen S; Malik R; Heath AC; Madden PAF; Martin NG; Montgomery GW; Kurki MI; Kals M; Mägi R; Pärn K; 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; International Headache Genetics Consortium; 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 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; Sjöstrand C; Waldenlind E; Carmine Belin A
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

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; Dardiotis E; Destée A; Ferrarese C; Ferraris A; Fiske B; Gispert S; Hadjigeorgiou 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; Vilariño-Güell C; White LR; Wirdefeldt K; Wszolek ZK; Wu R-M; Xiromerisiou G; Maraganore DM; Farrer MJ; Ross OA; Genetic Epidemiology Of Parkinson's Disease (GEO-P
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; Vilariño-Güell 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; Krüger R; GEO-PD Consortium
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; Håkansson A; Nissbrandt H; Söderkvist 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; Lundströmer 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; Vilariño-Güell C; White LR; Wirdefeldt K; Wszolek ZK; Wu R-M; Farrer MJ; Genetic Epidemiology Of Parkinson's Disease (GEO-P
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: 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.

Krüger 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; Genetic Epidemiology of Parkinson's disease consor
Article: NEUROSCIENCE LETTERS. 2010;485(2):117-120

Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden.

Anvret A; Westerlund M; Sydow O; Willows T; Lind C; Galter D; Belin AC
Article: PARKINSONS 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; Håkansson 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; Brighina 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; Genetic Epidemiology of Parkinson's Disease (GEOPD
Article: NEUROBIOLOGY OF AGING. 2010;31(1):114-117

PITX3 polymorphism is associated with early onset Parkinson's disease.

Bergman O; Håkansson A; Westberg L; Nordenström K; Carmine Belin A; Sydow O; Olson L; Holmberg B; Eriksson E; Nissbrandt H
Article: PARKINSONISM & 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; Håkansson 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; Håkansson 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; Håkansson A; Westberg L; Belin AC; Sydow O; Olson L; Holmberg B; Fratiglioni L; Bäckman 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: FASEB JOURNAL. 2008;22(10):3509-3514

Cerebellar alpha-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; Håkansson 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 & 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 & 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.

Carmine Belin A; 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; Björk BF; Westerlund M; Galter D; Sydow O; Lind C; Pernold K; Rosvall L; Håkansson 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.

Håkansson A; Bergman O; Chrapkowska C; Westberg L; Belin AC; Sydow O; Johnels B; Olson L; Holmberg B; Nissbrandt H
Article: 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; Carmine Belin A; Factor SA; Ferrarese C; Hadjigeorgiou GM; Higgins DS; Kawakami H; Krüger 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.

Carmine Belin A; Westerlund M; Sydow O; Lundströmer K; Håkansson 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 Aldh 1 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 (G78Stop) 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 PJ; 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; Ogren SO; Olson L; Perlmann T; Brené S
Article: 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: 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: 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 F; Zhang Z; 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 Z; Anvret M; Olson L
Visa fler

Alla övriga publikationer

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: 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.

Carmine Belin A; 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; MJFF Global Genetic Parkinson's Disease Study Grou
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.

Gormley P; Kurki MI; Hiekkala ME; Veerapen K; Häppölä P; Mitchell AA; Lal D; Palta P; Surakka I; Kaunisto MA; Hämäläinen E; Vepsäläinen S; Havanka H; Harno H; Ilmavirta M; Nissilä M; Säkö E; Sumelahti M-L; Liukkonen J; Sillanpää M; Metsähonkala L; Koskinen S; Lehtimäki T; Raitakari O; Männikkö M; Ran C; Belin AC; Jousilahti P; Anttila V; Salomaa V; Artto V; Färkkilä M; 23andMe Research Team; International Headache Genetics Consortium (IHGC); 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

Corrigendum: 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; 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 BWJH; Färkkilä M; Artto V; Kaunisto M; Vepsäläinen S; Malik R; Heath AC; Madden PAF; Martin NG; Montgomery GW; Kurki MI; Kals M; Mägi R; Pärn K; 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; International Headache Genetics Consortium; 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 AMJM; Zwart J-A; Boomsma DI; Smith GD; Stefansson K; Eriksson N; Daly MJ; 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 & 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; Söderkvist P; Dizdar N; Ahmadi A; Olson L; Belin AC
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 & RELATED DISORDERS. 2008;14(6):520-522

Investigation of genes related to familial forms of Parkinson's disease--with focus on the Parkin gene.

Håkansson 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: 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
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 M-B; 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
Visa fler

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
Deciphering the mechanisms behind primary headache disorders with focus on genetics and circadian rhythm

Vetenskapsrådet

1 January 2021 - 31 December 2024
Validering av läkemedelsrespons vid Hortons huvudvärk kopplat till genetik och dygnsrytm.

Region Stockholm

1 January 2021 - 31 December 2023
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

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
Bianca Migliori, Examination board member, Karolinska Institute, 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

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