Sonja W. Scholz

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Andrew SingletonNational Institute on AgingAdresse e-mail validée de mail.nih.gov
J Raphael GibbsLaboratory of Neurogenetics, NIA, NIHAdresse e-mail validée de mail.nih.gov
Dena G. HernandezNational Institutes of Health, National Institute on AgingAdresse e-mail validée de mail.nih.gov
Bryan TraynorLaboratory of Neurogenetics, National Institute on AgingAdresse e-mail validée de mail.nih.gov
Javier Simón-SánchezHertie Institute for Clinical Brain Research (HIH)Adresse e-mail validée de dzne.de
Mike A. NallsFounder/consultant with Data Tecnica International + Data science lead at NIH’s Center for AlzheimerAdresse e-mail validée de mail.nih.gov
Adriano Chio'Professor of Neurology, 'Rita Levi Montalcini' Department of Neuroscience, University of TurinAdresse e-mail validée de unito.it
Juan TroncosoProfessor of Pathology, Johns Hopkins University School of MedicineAdresse e-mail validée de jhmi.edu
Mark CooksonLaboratory of Neurogenetics, National Institute on Aging, National Institutes of HealthAdresse e-mail validée de mail.nih.gov
Michael S. OkunDistinguished Professor of Neurology, Director, Norman Fixel Institute for Neurological DiseasesAdresse e-mail validée de neurology.ufl.edu
Gregor K. WenningChair Division of Clinical Neurobiology, Medical University of InnsbruckAdresse e-mail validée de i-med.ac.at
Owen A. RossMayo ClinicAdresse e-mail validée de mayo.edu
Rimona WeilUCLAdresse e-mail validée de ucl.ac.uk
Huw R MorrisUCL Queen Square Institute of NeurologyAdresse e-mail validée de ucl.ac.uk
Justin KwanStaff Clinician, National Institutes of HealthAdresse e-mail validée de nih.gov
Howard J FederoffDistinguished Professor of neurology, retired
John HardyAdresse e-mail validée de ion.ucl.ac.uk
Mina RytenUniversity College London

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Sonja W. Scholz

National Institute of Neurological Disorders and Stroke

Adresse e-mail validée de nih.gov - Page d'accueil

Genomics Cognitive Neurology Movement Disorders Neurodegeneration


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ... Neuron 72 (2), 257-268, 2011	4905	2011
Genome-wide association study reveals genetic risk underlying Parkinson's disease J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308-1312, 2009	2244	2009
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019	1836	2019
Exome sequencing reveals VCP mutations as a cause of familial ALS JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ... Neuron 68 (5), 857-864, 2010	1479	2010
Genotype, haplotype and copy-number variation in worldwide human populations M Jakobsson, SW Scholz, P Scheet, JR Gibbs, JM VanLiere, HC Fung, ... Nature 451 (7181), 998-1003, 2008	1033	2008
Challenges in the diagnosis of Parkinson's disease E Tolosa, A Garrido, SW Scholz, W Poewe The Lancet Neurology 20 (5), 385-397, 2021	997	2021
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1268-1283. e6, 2018	648	2018
A genome-wide association study identifies protein quantitative trait loci (pQTLs) D Melzer, JR Perry, D Hernandez, AM Corsi, K Stevens, I Rafferty, ... PLoS Genet 4 (5), e1000072, 2008	571	2008
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data HC Fung, S Scholz, M Matarin, J Simón-Sánchez, D Hernandez, A Britton, ... The Lancet Neurology 5 (11), 911-916, 2006	473	2006
SNCA variants are associated with increased risk for multiple system atrophy SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ... Annals of neurology 65 (5), 610-614, 2009	329	2009
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans J Van de Leemput, J Chandran, MA Knight, LA Holtzclaw, S Scholz, ... PLoS Genet 3 (6), e108, 2007	328	2007
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study H Laaksovirta, T Peuralinna, JC Schymick, SW Scholz, SL Lai, ... The Lancet Neurology 9 (10), 978-985, 2010	321	2010
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R von Coelln, ... Movement Disorders 34 (6), 866-875, 2019	315	2019
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals J Simon-Sanchez, S Scholz, HC Fung, M Matarin, D Hernandez, JR Gibbs, ... Human molecular genetics 16 (1), 1-14, 2006	286	2006
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ... Nature genetics 53 (3), 294-303, 2021	277	2021
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data JC Schymick, SW Scholz, HC Fung, A Britton, S Arepalli, JR Gibbs, ... The Lancet Neurology 6 (4), 322-328, 2007	268	2007
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA S Camargos, S Scholz, J Simón-Sánchez, C Paisán-Ruiz, P Lewis, ... The Lancet Neurology 7 (3), 207-215, 2008	264	2008
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study R Guerreiro, OA Ross, C Kun-Rodrigues, DG Hernandez, T Orme, ... The Lancet Neurology 17 (1), 64-74, 2018	262	2018
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release M Matarín, WM Brown, S Scholz, J Simón-Sánchez, HC Fung, ... The Lancet Neurology 6 (5), 414-420, 2007	253	2007
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia C Blauwendraat, X Reed, L Krohn, K Heilbron, S Bandres-Ciga, M Tan, ... Brain 143 (1), 234-248, 2020	211	2020

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