Andrea Carmine Belin

About me
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Research

Visit my research group Carmine Belin Laboratory [1].
[1] https://ki.se/en/neuro/carmine-belin-laboratory

Articles

Journal 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
Journal 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
Journal 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
Journal 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
Journal 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; 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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
Journal 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: 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: 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: 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
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All other publications

Review: CEPHALALGIA. 2023;43(10):3331024231208126

The genetics and chronobiology of cluster headache.

Belin AC; Barloese MC
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
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
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
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
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Grants

Mapping of the mechanisms behind cluster headache with a focus on inflammation

Swedish Brain Foundation

1 July 2023 - 31 December 2025
In depth characterization of genetic markers behind primary headache disorders with a focus on cluster headache

Swedish Brain Foundation

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
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

Employments

Principal Researcher, Department of Neuroscience, Karolinska Institutet, 2022-

Degrees and Education

Docent, Karolinska Institutet, 2011
Doctor Of Philosophy, Neuroscience, On Parkinson’s Disease and Schizophrenia: Case Control Studies, Cellular Localization and Modelling of Candidate Genes, Department of neuroscience, Karolinska Institutet, 2003
Master Of Medical Science, Karolinska Institutet, 1999

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