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Andrea Carmine Belin - Publications

Affiliations: 
Karolinska Institute, Stockholm, Sweden 
Area:
Parkinson genetics
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47 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Landoulsi Z, Sreelatha AAK, Schulte C, Bobbili DR, Montanucci L, Leu C, Niestroj LM, Hassanin E, Domenighetti C, Pavelka L, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Portugal B, Edsall C, ... ... Belin AC, et al. Genome-wide association study of copy number variations in Parkinson's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 39228715 DOI: 10.1101/2024.08.21.24311915  0.38
2024 Domenighetti C, Sugier PE, Ashok Kumar Sreelatha A, Schulte C, Grover S, Portugal B, Lee PC, May P, Bobbili D, Radivojkov Blagojevic M, Lichtner P, Singleton AB, Hernandez D, Edsall C, Mellick GD, ... ... Belin AC, et al. Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study. Neurology. 103: e209620. PMID 38986057 DOI: 10.1212/WNL.0000000000209620  0.355
2023 Sugier PE, 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 JF, Lesueur F, ... ... Belin AC, et al. Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36788297 DOI: 10.1002/mds.29337  0.359
2023 Vollstedt EJ, 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, ... ... Belin AC, et al. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36692014 DOI: 10.1002/mds.29288  0.389
2022 Grover S, Kumar Sreelatha AA, Pihlstrom L, Domenighetti C, Schulte C, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Mohamed O, Portugal B, Landoulsi Z, May P, Bobbili D, Edsall C, Bartusch F, ... ... Belin AC, et al. Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium. Neurology. 99: e698-e710. PMID 35970579 DOI: 10.1212/WNL.0000000000200699  0.389
2022 Grover S, Ashwin AKS, Pihlstrom L, Domenighetti C, Schulte C, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Mohamed O, Portugal B, Landoulsi Z, May P, Bobbili D, Edsall C, Bartusch F, ... ... Belin AC, et al. Genome-wide Association and Meta-analysis of Age-at-Onset in Parkinson Disease: Evidence From COURAGE-PD Consortium. Neurology. PMID 35618440 DOI: 10.1212/WNL.0000000000200699  0.399
2022 Domenighetti C, Sugier PE, 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, ... ... Belin AC, et al. Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 34997937 DOI: 10.1002/mds.28902  0.367
2021 Jennysdotter Olofsgård F, Ran C, Fourier C, Wirth C, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. Gene Family Polymorphisms in Relation to Cluster Headache and Circadian Rhythm in Sweden. Brain Sciences. 11. PMID 34439727 DOI: 10.3390/brainsci11081108  0.307
2019 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, ... ... Belin AC, et al. Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study. Parkinsonism & Related Disorders. PMID 31422003 DOI: 10.1016/J.Parkreldis.2019.07.032  0.45
2019 Ran C, Fourier C, Arafa D, Liesecke F, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. Anoctamin 3: A Possible Link between Cluster Headache and Ca Signaling. Brain Sciences. 9. PMID 31366133 DOI: 10.3390/Brainsci9080184  0.328
2019 Fourier C, Ran C, Steinberg A, Sjöstrand C, Waldenlind E, Belin AC. Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden. Headache. PMID 30652302 DOI: 10.1111/Head.13462  0.388
2018 Ran C, Fourier C, Zinnegger M, Steinberg A, Sjöstrand C, Waldenlind E, Belin AC. Implications for the migraine SNP rs1835740 in a Swedish cluster headache population. The Journal of Headache and Pain. 19: 100. PMID 30382894 DOI: 10.1186/S10194-018-0937-0  0.322
2018 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, et al. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics : Ejhg. PMID 29995844 DOI: 10.1038/S41431-018-0150-2  0.405
2018 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, ... ... Belin AC, et al. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron. PMID 29731251 DOI: 10.1016/J.Neuron.2018.04.014  0.307
2017 Ran C, Fourier C, Michalska JM, Steinberg A, Sjöstrand C, Waldenlind E, Belin AC. Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort. The Journal of Headache and Pain. 18: 88. PMID 28831700 DOI: 10.1186/S10194-017-0798-Y  0.386
2017 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. Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease. Parkinson's Disease. 2017: 4020198. PMID 28540099 DOI: 10.1155/2017/4020198  0.485
2017 Fourier C, Ran C, Zinnegger M, Johansson AS, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. A genetic CLOCK variant associated with cluster headache causing increased mRNA levels. Cephalalgia : An International Journal of Headache. 333102417698709. PMID 28466652 DOI: 10.1177/0333102417698709  0.406
2016 Ran C, Mehdi RN, Fardell C, Xiang F, Nissbrandt H, Sydow O, Wirdefeldt K, Belin AC. No Association Between rs7077361 in ITGA8 and Parkinson's Disease in Sweden. The Open Neurology Journal. 10: 25-9. PMID 27583043 DOI: 10.2174/1874205X01610010025  0.401
2016 Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Belin AC, et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. PMID 27322543 DOI: 10.1038/Ng.3598  0.388
2016 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, ... ... Belin AC, et al. Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden. Neurobiology of Aging. PMID 27255555 DOI: 10.1016/J.Neurobiolaging.2016.04.022  0.594
2015 Graae L, Paddock S, Belin AC. ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide. Genetics Research. 97: e8. PMID 25882789 DOI: 10.1017/S0016672315000051  0.34
2014 Ran C, Graae L, Magnusson PK, Pedersen NL, Olson L, Belin AC. A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample. Bmc Medical Genetics. 15: 38. PMID 24674449 DOI: 10.1186/1471-2350-15-38  0.522
2013 Ran C, Willows T, Sydow O, Johansson A, Söderkvist P, Dizdar N, Ahmadi A, Olson L, Belin AC. The HLA-DRA variation rs3129882 is not associated with Parkinson's disease in Sweden. Parkinsonism & Related Disorders. 19: 701-2. PMID 23579001 DOI: 10.1016/J.Parkreldis.2013.03.001  0.575
2012 Belin AC, Ran C, Anvret A, Paddock S, Westerlund M, HÃ¥kansson A, Nissbrandt H, Söderkvist P, Dizdar N, Ahmadi A, Anvret M, Willows T, Sydow O, Galter D. Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease. Neuroscience Letters. 522: 30-5. PMID 22704918 DOI: 10.1016/J.Neulet.2012.06.007  0.56
2012 Anvret A, Ran C, Westerlund M, Sydow O, Willows T, Olson L, Galter D, Belin AC. Genetic Screening of the Mitochondrial Rho GTPases MIRO1 and MIRO2 in Parkinson's Disease. The Open Neurology Journal. 6: 1-5. PMID 22496713 DOI: 10.2174/1874205X01206010001  0.603
2012 Karlsson R, Graae L, Lekman M, Wang D, Favis R, Axelsson T, Galter D, Belin AC, Paddock S. MAGI1 copy number variation in bipolar affective disorder and schizophrenia. Biological Psychiatry. 71: 922-30. PMID 22381734 DOI: 10.1016/J.Biopsych.2012.01.020  0.343
2012 Anvret A, Ran C, Westerlund M, Gellhaar S, Lindqvist E, Pernold K, Lundströmer K, Duester G, Felder MR, Galter D, Belin AC. Adh1 and Adh1/4 knockout mice as possible rodent models for presymptomatic Parkinson's disease. Behavioural Brain Research. 227: 252-7. PMID 22079585 DOI: 10.1016/J.Bbr.2011.10.040  0.367
2011 Ran C, Westerlund M, Anvret A, Willows T, Sydow O, Galter D, Belin AC. Genetic studies of the protein kinase AKT1 in Parkinson's disease. Neuroscience Letters. 501: 41-4. PMID 21741444 DOI: 10.1016/J.Neulet.2011.06.038  0.491
2011 Anvret A, Blackinton JG, Westerlund M, Ran C, Sydow O, Willows T, Håkansson A, Nissbrandt H, Belin AC. DJ-1 Mutations are Rare in a Swedish Parkinson Cohort. The Open Neurology Journal. 5: 8-11. PMID 21532868 DOI: 10.2174/1874205X01105010008  0.47
2011 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. Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1345-52. PMID 21163861 DOI: 10.1096/Fj.10-163402  0.514
2011 Belin AC, Westerlund M, Anvret A, Lindqvist E, Pernold K, Ogren SO, Duester G, Galter D. Modeling Parkinson's disease genetics: altered function of the dopamine system in Adh4 knockout mice. Behavioural Brain Research. 217: 439-45. PMID 21075145 DOI: 10.1016/J.Bbr.2010.11.023  0.411
2010 Anvret A, Ran C, Westerlund M, Thelander AC, Sydow O, Lind C, Håkansson A, Nissbrandt H, Galter D, Belin AC. Possible involvement of a mitochondrial translation initiation factor 3 variant causing decreased mRNA levels in Parkinson's disease. Parkinson's Disease. 2010: 491751. PMID 20976088 DOI: 10.4061/2010/491751  0.535
2010 Anvret A, Westerlund M, Sydow O, Willows T, Lind C, Galter D, Belin AC. Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden. Neuroscience Letters. 485: 117-20. PMID 20826197 DOI: 10.1016/J.Neulet.2010.08.082  0.398
2009 Shahabi HN, Westberg L, Melke J, HÃ¥kansson A, Belin AC, Sydow O, Olson L, Holmberg B, Nissbrandt H. Cytochrome P450 2E1 gene polymorphisms/haplotypes and Parkinson's disease in a Swedish population. Journal of Neural Transmission (Vienna, Austria : 1996). 116: 567-73. PMID 19381774 DOI: 10.1007/s00702-009-0221-1  0.588
2009 Westerlund M, Belin AC, Anvret A, HÃ¥kansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Association of a polymorphism in the ABCB1 gene with Parkinson's disease. Parkinsonism & Related Disorders. 15: 422-4. PMID 19196542 DOI: 10.1016/J.Parkreldis.2008.11.010  0.592
2009 Bergman O, HÃ¥kansson A, Westberg L, Belin AC, Sydow O, Olson L, Holmberg B, Fratiglioni L, Bäckman L, Eriksson E, Nissbrandt H. Do polymorphisms in transcription factors LMX1A and LMX1B influence the risk for Parkinson's disease? Journal of Neural Transmission (Vienna, Austria : 1996). 116: 333-8. PMID 19189040 DOI: 10.1007/S00702-009-0187-Z  0.617
2008 Westerlund M, Belin AC, Olson L, Galter D. Expression of multi-drug resistance 1 mRNA in human and rodent tissues: reduced levels in Parkinson patients. Cell and Tissue Research. 334: 179-85. PMID 18855017 DOI: 10.1007/S00441-008-0686-5  0.448
2008 Westerlund M, Belin AC, Anvret A, HÃ¥kansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 22: 3509-14. PMID 18606870 DOI: 10.1096/Fj.08-110148  0.604
2008 HÃ¥kansson A, Belin AC, Stiller C, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Investigation of genes related to familial forms of Parkinson's disease--with focus on the Parkin gene. Parkinsonism & Related Disorders. 14: 520-2. PMID 18321758 DOI: 10.1016/J.Parkreldis.2007.10.013  0.496
2008 Belin AC, Westerlund M. Parkinson's disease: a genetic perspective. The Febs Journal. 275: 1377-83. PMID 18279377 DOI: 10.1111/J.1742-4658.2008.06301.X  0.496
2008 Westerlund M, Belin AC, Anvret A, Bickford P, Olson L, Galter D. 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. Neuroscience. 152: 429-36. PMID 18272292 DOI: 10.1016/J.Neuroscience.2007.10.062  0.506
2008 Håkansson A, Bergman O, Chrapkowska C, Westberg L, Belin AC, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Cyclooxygenase-2 polymorphisms in Parkinson's disease (American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 144B, (367-369)) American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147: 541. DOI: 10.1002/ajmg.b.30790  0.428
2007 Galter D, Westerlund M, Belin AC, Olson L. DJ-1 and UCH-L1 gene activity patterns in the brains of controls, Parkinson and schizophrenia patients and in rodents. Physiology & Behavior. 92: 46-53. PMID 17599367 DOI: 10.1016/J.Physbeh.2007.05.046  0.527
2007 Belin AC, Björk BF, Westerlund M, Galter D, Sydow O, Lind C, Pernold K, Rosvall L, HÃ¥kansson A, Winblad B, Nissbrandt H, Graff C, Olson L. Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease. Neuroscience Letters. 420: 257-62. PMID 17537576 DOI: 10.1016/J.Neulet.2007.05.010  0.572
2007 Westerlund M, Belin AC, Felder MR, Olson L, Galter D. High and complementary expression patterns of alcohol and aldehyde dehydrogenases in the gastrointestinal tract: implications for Parkinson's disease. The Febs Journal. 274: 1212-23. PMID 17257171 DOI: 10.1111/J.1742-4658.2007.05665.X  0.536
2007 HÃ¥kansson A, Bergman O, Chrapkowska C, Westberg L, Belin AC, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Cyclooxygenase-2 polymorphisms in Parkinson's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 367-9. PMID 17171651 DOI: 10.1002/Ajmg.B.30449  0.621
2007 Belin A, Westerlund M, Paddock S, Lindqvist E, Pernold K, Duester G, Ögren S, Olson L, Galter D. P.2.25 Modeling genetic risk in Parkinson's disease: changed response to challenge of the dopamine system in ADH4 knockout mice European Neuropsychopharmacology. 17: S59. DOI: 10.1016/S0924-977X(07)70070-6  0.355
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