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Author
María Martínez
also known as John Hardy, M M Martinez, M Martinez
University Health Network · Universidad de Los Andes · University of Toronto · University of Washington
About this author
Works
252
Cited by
23,078
h-index
60
i10
148
ORCID ↗
Top papers
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, et al.
·
2019
·
The Lancet Neurology
↗ 2,501
OA
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Mike A. Nalls, 23andMe, GenePD, et al.
·
2014
·
Nature Genetics
↗ 1,956
OA
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Michael A Nalls, Michael A. Nalls, Vincent Plagnol, et al.
·
2011
·
The Lancet
↗ 917
OA
Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum
Dominique Campion, Cécile Dumanchin, Didier Hannequin, et al.
·
1999
·
The American Journal of Human Genetics
↗ 787
OA
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database
Christina M. Lill, Johannes T. Roehr, Matthew B. McQueen, et al.
·
2012
·
PLoS Genetics
↗ 543
OA
Genome-Wide Scan for Autism Susceptibility Genes
Anne Philippe, María Martínez, M Guilloud-Bataille, et al.
·
1999
·
Human Molecular Genetics
↗ 476
New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study
François Cornélis, Sabine Fauré, María Martínez, et al.
·
1998
·
Proceedings of the National Academy of Sciences
↗ 470
OA
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Suzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
·
2016
·
The American Journal of Human Genetics
↗ 440
OA
Intermittent Fasting and Human Metabolic Health
Ruth E. Patterson, Gail A. Laughlin, Andrea Z. LaCroix, et al.
·
2015
·
Journal of the Academy of Nutrition and Dietetics
↗ 390
OA
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich, et al.
·
2014
·
Proceedings of the National Academy of Sciences
↗ 365
OA
No Significant Association of 14 Candidate Genes With Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics
Alan R. Sanders, Jubao Duan, Douglas F. Levinson, et al.
·
2008
·
American Journal of Psychiatry
↗ 348
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease
Suzanne Lesage, Mathieu Anheim, Christel Condroyer, et al.
·
2010
·
Human Molecular Genetics
↗ 287
OA