Follow
Maria Martinez Rande
Maria Martinez Rande
Inserm, IRSD U1220, Toulouse
Verified email at inserm.fr
Title
Cited by
Cited by
Year
Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial
HC Gerstein, HM Colhoun, GR Dagenais, R Diaz, M Lakshmanan, P Pais, ...
The Lancet 394 (10193), 121-130, 2019
21652019
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
19662014
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
14492019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13112018
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum
D Campion, C Dumanchin, D Hannequin, B Dubois, S Belliard, M Puel, ...
The American Journal of Human Genetics 65 (3), 664-670, 1999
10871999
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ...
PLoS genetics 8 (3), e1002548, 2012
6092012
New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study
F Cornélis, S Fauré, M Martinez, JF Prud’homme, P Fritz, C Dib, H Alves, ...
Proceedings of the National Academy of Sciences 95 (18), 10746-10750, 1998
6071998
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ...
Nature genetics 42 (3), 234-239, 2010
5782010
Genome-wide scan for autism susceptibility genes
A Philippe, M Martinez, M Guilloud-Bataille, C Gillberg, M Råstam, ...
Human molecular genetics 8 (5), 805-812, 1999
5681999
Genome-wide scan for autism susceptibility genes
A Philippe, M Martinez, M Guilloud-Bataille, C Gillberg, M Råstam, ...
Human molecular genetics 8 (5), 805-812, 1999
5681999
Dulaglutide and renal outcomes in type 2 diabetes: an exploratory analysis of the REWIND randomised, placebo-controlled trial
HC Gerstein, HM Colhoun, GR Dagenais, R Diaz, M Lakshmanan, P Pais, ...
The Lancet 394 (10193), 131-138, 2019
5172019
Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study
G Prucher, M Assenza, B Binda, M Biondi, G Brachini, P Bruzzaniti, ...
Anaesthesia 76 (6), 748-758, 2021
5162021
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics
AR Sanders, J Duan, DF Levinson, J Shi, D He, C Hou, GJ Burrell, ...
American Journal of Psychiatry 165 (4), 497-506, 2008
4802008
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
4012016
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
3812014
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
3632017
Mutations of the presenilin I gene in families with early-onset Alzheimer's disease
D Campion, JM Flaman, A Brice, D Hannequin, B Dubois, C Martin, ...
Human molecular genetics 4 (12), 2373-2377, 1995
3541995
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease
S Lesage, M Anheim, C Condroyer, P Pollak, F Durif, C Dupuits, F Viallet, ...
Human molecular genetics 20 (1), 202-210, 2011
3152011
Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees
Q Cao, M Martinez, J Zhang, AR Sanders, JA Badner, A Cravchik, ...
Genomics 43 (1), 1-8, 1997
2761997
Diseño de la investigación.[Apuntes en internet]. 2008.[citado 2010 sep. 13].[1 pantalla]
N Martínez, J Cabrero, M Martínez
Disponible en URL: http://perso. wanadoo. es/aniorte_nic …, 2008
2622008
The system can't perform the operation now. Try again later.
Articles 1–20