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, Zimprich AA, Pirker W, Rogaeva EA, Lang AE, Koks S, Taba P, Lesage S, Brice A, Corvol JC, Chartier-Harlin MC et al. (2024)
Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study
Neurology, 103 (3), e209620
DOI 10.1212/WNL.0000000000209620, PubMed 38986057
Faouzi J, Tan M, Casse F, Lesage S, Tesson C, Brice A, Mangone G, Mariani LL, Iwaki H, Colliot O, Pihlstrøm L, Corvol JC (2024)
Proxy-analysis of the genetics of cognitive decline in Parkinson's disease through polygenic scores
NPJ Parkinsons Dis, 10 (1), 8
DOI 10.1038/s41531-023-00619-5, PubMed 38177146
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, Kru Ger J, Hernandez DG, Blauwendraat C, Mellick GD, Zimprich A, Pirker W, Tan M, Rogaeva E, Lang AE, Koks S et al. (2024)
Genome-wide association study of copy number variations in Parkinson's disease
medRxiv
DOI 10.1101/2024.08.21.24311915, PubMed 39228715
Manzoni C, Kia DA, Ferrari R, Leonenko G, Costa B, Saba V, Jabbari E, Tan MM, Albani D, Alvarez V, Alvarez I, Andreassen OA, Angiolillo A, Arighi A, Baker M, Benussi L, Bessi V, Binetti G, Blackburn DJ, Boada M, Boeve BF, Borrego-Ecija S, Borroni B, Bråthen G, Brooks WS et al. (2024)
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Am J Hum Genet, 111 (7), 1316-1329
DOI 10.1016/j.ajhg.2024.05.017, PubMed 38889728
Tan MMX, Lawton MA, Pollard MI, Brown E, Real R, Carrasco AM, Bekadar S, Jabbari E, Reynolds RH, Iwaki H, Blauwendraat C, Kanavou S, Hubbard L, Malek N, Grosset KA, Bajaj N, Barker RA, Burn DJ, Bresner C, Foltynie T, Wood NW, Williams-Gray CH, Andreassen OA, Toft M, Elbaz A et al. (2024)
Genome-wide determinants of mortality and motor progression in Parkinson's disease
NPJ Parkinsons Dis, 10 (1), 113
DOI 10.1038/s41531-024-00729-8, PubMed 38849413
Towns C, Fang ZH, Tan MMX, Jasaityte S, Schmaderer TM, Stafford EJ, Pollard M, Tilney R, Hodgson M, Wu L, Labrum R, Hehir J, Polke J, Lange LM, Schapira AHV, Bhatia KP, Parkinson’s Families Project (PFP) Study Group, Global Parkinson’s Genetics Program (GP2), Singleton AB, Blauwendraat C, Klein C, Houlden H, Wood NW, Jarman PR, Morris HR et al. (2024)
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease
NPJ Parkinsons Dis, 10 (1), 188
DOI 10.1038/s41531-024-00778-z, PubMed 39420034
Leonard HL, Murtadha R, Martinez-Carrasco A, Jama A, Müller-Nedebock AC, Gil-Martinez AL, Illarionova A, Moore A, Bustos BI, Jadhav B, Huxford B, Storm C, Towns C, Vitale D, Chetty D, Yu E, Grenn FP, Salazar G, Rateau G, Iwaki H, Elsayed I, Foote IF, Jansen van Rensburg Z, Kim JJ, Yuan J et al. (2023)
The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data
NPJ Parkinsons Dis, 9 (1), 33
DOI 10.1038/s41531-023-00472-6, PubMed 36871034
Leonard HL, Murtadha R, Martinez-Carrasco A, Jama A, Müller-Nedebock AC, Gil-Martinez AL, Illarionova A, Moore A, Bustos BI, Jadhav B, Huxford B, Storm C, Towns C, Vitale D, Chetty D, Yu E, Grenn FP, Salazar G, Rateau G, Iwaki H, Elsayed I, Foote IF, Jansen van Rensburg Z, Kim JJ, Yuan J et al. (2023)
Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data
NPJ Parkinsons Dis, 9 (1), 77
DOI 10.1038/s41531-023-00529-6, PubMed 37225742
Martínez Carrasco A, Real R, Lawton M, Hertfelder Reynolds R, Tan M, Wu L, Williams N, Carroll C, Corvol JC, Hu M, Grosset D, Hardy J, Ryten M, Ben-Shlomo Y, Shoai M, Morris HR (2023)
Genome-wide Analysis of Motor Progression in Parkinson Disease
Neurol Genet, 9 (5), e200092
DOI 10.1212/NXG.0000000000200092, PubMed 37560120
Martinez-Carrasco A, Real R, Lawton M, Iwaki H, Tan MMX, Wu L, Williams NM, Carroll C, Hu MTM, Grosset DG, Hardy J, Ryten M, Foltynie T, Ben-Shlomo Y, Shoai M, Morris HR (2023)
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease
medRxiv
DOI 10.1101/2023.05.24.23290362, PubMed 37425912
Martinez-Carrasco A, Real R, Lawton M, Iwaki H, Tan MMX, Wu L, Williams NM, Carroll C, Hu MTM, Grosset DG, Hardy J, Ryten M, Foltynie T, Ben-Shlomo Y, Shoai M, Morris HR (2023)
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease
NPJ Parkinsons Dis, 9 (1), 128
DOI 10.1038/s41531-023-00573-2, PubMed 37652906
Real R, Martinez-Carrasco A, Reynolds RH, Lawton MA, Tan MMX, Shoai M, Corvol JC, Ryten M, Bresner C, Hubbard L, Brice A, Lesage S, Faouzi J, Elbaz A, Artaud F, Williams N, Hu MTM, Ben-Shlomo Y, Grosset DG, Hardy J, Morris HR (2023)
Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia
Brain, 146 (5), 1873-1887
DOI 10.1093/brain/awac414, PubMed 36348503
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, Ostroumova E, Kesminiene A, de Vathaire F, Guénel P, EPITHYR consortium, Sreelatha AAK, Schulte C, Grover S, May P, Bobbili DR et al. (2023)
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers
Mov Disord, 38 (4), 604-615
DOI 10.1002/mds.29337, PubMed 36788297
Towns C, Richer M, Jasaityte S, Stafford EJ, Joubert J, Antar T, Martinez-Carrasco A, Makarious MB, Casey B, Vitale D, Levine K, Leonard H, Pantazis CB, Screven LA, Hernandez DG, Wegel CE, Solle J, Nalls MA, Blauwendraat C, Singleton AB, Tan MMX, Iwaki H, Morris HR, Global Parkinson’s Genetics Program (GP2) (2023)
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)
NPJ Parkinsons Dis, 9 (1), 131
DOI 10.1038/s41531-023-00533-w, PubMed 37699923
Tunold JA, Tan MMX, Koga S, Geut H, Rozemuller AJM, Valentino R, Sekiya H, Martin NB, Heckman MG, Bras J, Guerreiro R, Dickson DW, Toft M, van de Berg WDJ, Ross OA, Pihlstrøm L (2023)
Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease
Brain, 146 (10), 4077-4087
DOI 10.1093/brain/awad183, PubMed 37247383
Tunold JA, Tan MMX, Toft M, Ross O, van de Berg WDJ, Pihlstrøm L (2023)
Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk
Mov Disord, 39 (3), 596-601
DOI 10.1002/mds.29698, PubMed 38124396
Domenighetti C, Douillard V, Sugier PE, Sreelatha AAK, Schulte C, Grover S, May P, Bobbili DR, Radivojkov-Blagojevic M, Lichtner P, Singleton AB, Hernandez DG, Edsall C, Gourraud PA, Mellick GD, Zimprich A, Pirker W, Rogaeva E, Lang AE, Koks S, Taba P, Lesage S, Brice A, Corvol JC, Chartier-Harlin MC et al. (2022)
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited
Mov Disord, 37 (9), 1929-1937
DOI 10.1002/mds.29133, PubMed 35810454
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, Zimprich A, Pirker W, Rogaeva E, Lang AE, Koks S, Taba P, Lesage S, Brice A, Corvol JC, Chartier-Harlin MC et al. (2022)
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study
Mov Disord, 37 (4), 857-864
DOI 10.1002/mds.28902, PubMed 34997937
Domenighetti C, Sugier PE, 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 JC, Chartier-Harlin MC et al. (2022)
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease
J Parkinsons Dis, 12 (1), 267-282
DOI 10.3233/JPD-212851, PubMed 34633332
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, Hanussek M, Krüger J, Hernandez DG, Blauwendraat C, Mellick GD, Zimprich A, Pirker W, Tan M, Rogaeva E, Lang A et al. (2022)
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium
Neurology, 99 (7), e698-e710
DOI 10.1212/WNL.0000000000200699, PubMed 35970579
Lawton M, Tan MM, Ben-Shlomo Y, Baig F, Barber T, Klein JC, Evetts SG, Millin S, Malek N, Grosset K, Barker RA, Williams N, Burn DJ, Foltynie T, Morris HR, Wood N, Grosset DG, Hu MT (2022)
Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts
J Neurol Neurosurg Psychiatry, 93 (9), 952-9 (in press)
DOI 10.1136/jnnp-2021-327376, PubMed 35732412
Stolp Andersen M, Tan M, Holtman IR, Hardy J, International Parkinson's Disease Genomics Consortium, Pihlstrøm L (2022)
Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease
Ann Clin Transl Neurol, 9 (8), 1289-1295
DOI 10.1002/acn3.51606, PubMed 35684951
Vijiaratnam N, Lawton M, Heslegrave AJ, Guo T, Tan M, Jabbari E, Real R, Woodside J, Grosset K, Chelban V, Athauda D, Girges C, Barker RA, Hardy J, Wood N, Houlden H, Williams N, Ben-Shlomo Y, Zetterberg H, Grosset DG, Foltynie T, Morris HR, PRoBaND clinical consortium (2022)
Combining biomarkers for prognostic modelling of Parkinson's disease
J Neurol Neurosurg Psychiatry, 93 (7), 707-15 (in press)
DOI 10.1136/jnnp-2021-328365, PubMed 35577512
Alfradique-Dunham I, Al-Ouran R, von Coelln R, Blauwendraat C, Hill E, Luo L, Stillwell A, Young E, Kaw A, Tan M, Liao C, Hernandez D, Pihlstrom L, Grosset D, Shulman LM, Liu Z, Rouleau GA, Nalls M, Singleton AB, Morris H, Jankovic J, Shulman JM (2021)
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes
Neurol Genet, 7 (2), e557
DOI 10.1212/NXG.0000000000000557, PubMed 33987465
Blauwendraat C, Iwaki H, Makarious MB, Bandres-Ciga S, Leonard HL, Grenn FP, Lake J, Krohn L, Tan M, Kim JJ, Gibbs JR, Hernandez DG, Ruskey JA, Pihlstrøm L, Toft M, van Hilten JJ, Marinus J, Schulte C, Brockmann K, Sharma M, Siitonen A, Majamaa K, Eerola-Rautio J, Tienari PJ, Grosset DG et al. (2021)
Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
Ann Neurol, 90 (1), 35-42
DOI 10.1002/ana.26090, PubMed 33901317
Brolin K, Bandres-Ciga S, Leonard H, Makarious MB, Blauwendraat C, Mata IF, Foo JN, Pihlstrøm L, Swanberg M, Gan-Or Z, Tan MM, International Parkinson's Disease Genomics Consortium (2021)
RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts
Neurobiol Aging, 109, 264-268
DOI 10.1016/j.neurobiolaging.2021.08.009, PubMed 34538707
Lubbe SJ, Bustos BI, Hu J, Krainc D, Joseph T, Hehir J, Tan M, Zhang W, Escott-Price V, Williams NM, Blauwendraat C, Singleton AB, Morris HR, for International Parkinson’s Disease Genomics Consortium (IPDGC) (2021)
Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk
Hum Mol Genet, 30 (1), 78-86
DOI 10.1093/hmg/ddaa273, PubMed 33448283
Oxtoby NP, Leyland LA, Aksman LM, Thomas GEC, Bunting EL, Wijeratne PA, Young AL, Zarkali A, Tan MMX, Bremner FD, Keane PA, Morris HR, Schrag AE, Alexander DC, Weil RS (2021)
Sequence of clinical and neurodegeneration events in Parkinson's disease progression
Brain, 144 (3), 975-988
DOI 10.1093/brain/awaa461, PubMed 33543247
Pihlstrøm L, Fan CC, Frei O, Tan M, Karunamuni RA, Blauwendraat C, Bandres-Ciga S, Gan-Or Z, Grosset DG, International Parkinson's Disease Genomics Consortium (IPDGC), Dale AM, Seibert TM, Andreassen OA (2021)
Genetic Stratification of Age-Dependent Parkinson's Disease Risk by Polygenic Hazard Score
Mov Disord, 37 (1), 62-69
DOI 10.1002/mds.28808, PubMed 34612543
Blauwendraat C, Reed X, Krohn L, Heilbron K, Bandres-Ciga S, Tan M, Gibbs JR, Hernandez DG, Kumaran R, Langston R, Bonet-Ponce L, Alcalay RN, Hassin-Baer S, Greenbaum L, Iwaki H, Leonard HL, Grenn FP, Ruskey JA, Sabir M, Ahmed S, Makarious MB, Pihlstrøm L, Toft M, van Hilten JJ, Marinus J et al. (2020)
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Brain, 143 (1), 234-248
DOI 10.1093/brain/awz350, PubMed 31755958
Brown EE, Blauwendraat C, Trinh J, Rizig M, Nalls MA, Leveille E, Ruskey JA, Jonvik H, Tan MMX, Bandres-Ciga S, Hassin-Baer S, Brockmann K, Infante J, Tolosa E, Ezquerra M, Ben Romdhan S, Benmahdjoub M, Arezki M, Mhiri C, Hardy J, Singleton AB, Alcalay RN, Gasser T, Grosset DG, Williams NM et al. (2020)
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease
Neurobiol Aging, 97, 148.e17-148.e24
DOI 10.1016/j.neurobiolaging.2020.07.002, PubMed 32873436
Jabbari E, Holland N, Chelban V, Jones PS, Lamb R, Rawlinson C, Guo T, Costantini AA, Tan MMX, Heslegrave AJ, Roncaroli F, Klein JC, Ansorge O, Allinson KSJ, Jaunmuktane Z, Holton JL, Revesz T, Warner TT, Lees AJ, Zetterberg H, Russell LL, Bocchetta M, Rohrer JD, Williams NM, Grosset DG et al. (2020)
Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome
JAMA Neurol, 77 (3), 377-387
DOI 10.1001/jamaneurol.2019.4347, PubMed 31860007
Jabbari E, Koga S, Valentino RR, Reynolds RH, Ferrari R, Tan MMX, Rowe JB, Dalgard CL, Scholz SW, Dickson DW, Warner TT, Revesz T, Höglinger GU, Ross OA, Ryten M, Hardy J, Shoai M, Morris HR, PSP Genetics Group (2020)
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Lancet Neurol, 20 (2), 107-116
DOI 10.1016/S1474-4422(20)30394-X, PubMed 33341150
Tan MMX, Lawton MA, Jabbari E, Reynolds RH, Iwaki H, Blauwendraat C, Kanavou S, Pollard MI, Hubbard L, Malek N, Grosset KA, Marrinan SL, Bajaj N, Barker RA, Burn DJ, Bresner C, Foltynie T, Wood NW, Williams-Gray CH, Hardy J, Nalls MA, Singleton AB, Williams NM, Ben-Shlomo Y, Hu MTM et al. (2020)
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease
Mov Disord, 36 (2), 424-433
DOI 10.1002/mds.28342, PubMed 33111402
Bandres-Ciga S, Ahmed S, Sabir MS, Blauwendraat C, Adarmes-Gómez AD, Bernal-Bernal I, Bonilla-Toribio M, Buiza-Rueda D, Carrillo F, Carrión-Claro M, Gómez-Garre P, Jesús S, Labrador-Espinosa MA, Macias D, Méndez-Del-Barrio C, Periñán-Tocino T, Tejera-Parrado C, Vargas-González L, Diez-Fairen M, Alvarez I, Tartari JP, Buongiorno M, Aguilar M, Gorostidi A, Bergareche JA et al. (2019)
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Mov Disord, 34 (12), 1851-1863
DOI 10.1002/mds.27864, PubMed 31660654
Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R, Pihlstrøm L, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Siitonen A, Iwaki H, Leonard H, Noyce AJ, Tan M, Gibbs JR, Hernandez DG, Scholz SW, Jankovic J, Shulman LM, Lesage S, Corvol JC, Brice A, van Hilten JJ, Marinus J et al. (2019)
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms
Mov Disord, 34 (6), 866-875
DOI 10.1002/mds.27659, PubMed 30957308
Fernandez-Santiago R, Martin-Flores N, Antonelli F, Cerquera C, Moreno V, Bandres-Ciga S, Manduchi E, Tolosa E, Singleton AB, Moore JH, Noyce AJ, Kaiyrzhanov R, Middlehurst B, Kia DA, Tan M, Houlden H, Morris HR, Plun-Favreau H, Holmans P, Hardy J, Trabzuni D, Bras J, Quinn J, Mok KY, Kinghorn KJ et al. (2019)
SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
Mov. Disord., 34 (9), 1333-1344
DOI 10.1002/mds.27770
Jabbari E, Woodside J, Tan MMX, Pavese N, Bandmann O, Ghosh BCP, Massey LA, Capps E, Warner TT, Lees AJ, Revesz T, Holton JL, Williams NM, Grosset DG, Morris HR (2019)
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy
Mov Disord, 34 (9), 1307-1314
DOI 10.1002/mds.27786, PubMed 31299107
Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Pihlstrøm L, Siitonen A, Iwaki H, Leonard H, Faghri F, Gibbs JR, Hernandez DG, Scholz SW et al. (2019)
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Lancet Neurol, 18 (12), 1091-1102
DOI 10.1016/S1474-4422(19)30320-5, PubMed 31701892
Tan MMX, Malek N, Lawton MA, Hubbard L, Pittman AM, Joseph T, Hehir J, Swallow DMA, Grosset KA, Marrinan SL, Bajaj N, Barker RA, Burn DJ, Bresner C, Foltynie T, Hardy J, Wood N, Ben-Shlomo Y, Grosset DG, Williams NM, Morris HR (2019)
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study
Brain, 142 (9), 2828-2844
DOI 10.1093/brain/awz191, PubMed 31324919
Jabbari E, Woodside J, Tan MMX, Shoai M, Pittman A, Ferrari R, Mok KY, Zhang D, Reynolds RH, de Silva R, Grimm MJ, Respondek G, Müller U, Al-Sarraj S, Gentleman SM, Lees AJ, Warner TT, Hardy J, Revesz T, Höglinger GU, Holton JL, Ryten M, Morris HR (2018)
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype
Ann Neurol, 84 (4), 485-496
DOI 10.1002/ana.25308, PubMed 30066433
Malek N, Weil RS, Bresner C, Lawton MA, Grosset KA, Tan M, Bajaj N, Barker RA, Burn DJ, Foltynie T, Hardy J, Wood NW, Ben-Shlomo Y, Williams NW, Grosset DG, Morris HR, PRoBaND clinical consortium (2018)
Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study
J Neurol Neurosurg Psychiatry, 89 (7), 702-709
DOI 10.1136/jnnp-2017-317348, PubMed 29378790
Johnston IN, Tan M, Cao J, Matsos A, Forrest DRL, Si E, Fardell JE, Hutchinson MR (2017)
Ibudilast reduces oxaliplatin-induced tactile allodynia and cognitive impairments in rats
Behav Brain Res, 334, 109-118
DOI 10.1016/j.bbr.2017.07.021, PubMed 28739131
Norman BP, Lubbe SJ, Tan M, Warren N, Morris HR (2017)
Early Onset Parkinson's Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report
BMC Neurol, 17 (1), 153
DOI 10.1186/s12883-017-0933-z, PubMed 28789629
