Mohamad saad
Mohamad saad
Senior Scientist, Qatar Computing Research Institute, Hamad Bin Khalifa University, Qatar.
E-mailová adresa ověřena na: - Domovská stránka
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
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
International Parkinson Disease Genomics Consortium
The Lancet 377 (9766), 641-649, 2011
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
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
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
Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis
Y Allanore, M Saad, P Dieudé, J Avouac, JHW Distler, P Amouyel, ...
PLoS genetics 7 (7), e1002091, 2011
Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Human molecular genetics 21 (22), 4996-5009, 2012
A two-stage meta-analysis identifies several new loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium (IPDGC), ...
PLoS genetics 7 (6), e1002142, 2011
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population
M Saad, S Lesage, A Saint-Pierre, JC Corvol, D Zelenika, JC Lambert, ...
Human molecular genetics 20 (3), 615-627, 2011
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
P Holmans, V Moskvina, L Jones, M Sharma, ...
Human molecular genetics 22 (5), 1039-1049, 2013
Germline genetic contribution to the immune landscape of cancer
RW Sayaman, M Saad, V Thorsson, D Hu, W Hendrickx, J Roelands, ...
Immunity 54 (2), 367-386. e8, 2021
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
IE Jansen, H Ye, S Heetveld, MC Lechler, H Michels, RI Seinstra, ...
Genome biology 18, 1-26, 2017
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
MA Nalls, J Bras, DG Hernandez, MF Keller, E Majounie, AE Renton, ...
Neurobiology of aging 36 (3), 1605. e7-1605. e12, 2015
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk
V Moskvina, D Harold, GC Russo, A Vedernikov, M Sharma, M Saad, ...
JAMA neurology 70 (10), 1268-1276, 2013
Genetic comorbidities in Parkinson's disease
MA Nalls, M Saad, AJ Noyce, MF Keller, A Schrag, JP Bestwick, ...
Human molecular genetics 23 (3), 831-841, 2014
Oncogenic states dictate the prognostic and predictive connotations of intratumoral immune response
J Roelands, W Hendrickx, G Zoppoli, R Mall, M Saad, K Halliwill, ...
Journal for immunotherapy of cancer 8 (1), 2020
Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities
F Mittag, F Büchel, M Saad, A Jahn, C Schulte, Z Bochdanovits, ...
Human mutation 33 (12), 1708-1718, 2012
Parkinson’s Study Group (PSG) Parkinson’s Research: The Organized GENetics Initiative (PROGENI); 23andMe
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
GenePD 46 (9), 989-93, 2014
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
S Klebe, JL Golmard, MA Nalls, M Saad, AB Singleton, JM Bras, J Hardy, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (6), 666-673, 2013
International Parkinson's Disease Genomics Consortium (IPDGC)
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics …, 2014
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Články 1–20