| | Title | Authors / Editors | Date |
|
unige:8607 |
Mendelian disorders and multifactorial traits: the big divide or one for all? |
Antonarakis, Stylianos; Chakravarti, Aravinda; Cohen, J. C.; Hardy, John |
2010 |
|
unige:37956 |
SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia |
Marelli, Cecilia; van de Leemput, Joyce; Johnson, Janel O; Tison, Francois; ... Brice, Alexis |
2011 |
|
unige:45211 |
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies |
Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W |
2011 |
|
unige:45200 |
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities |
Mittag, Florian; Büchel, Finja; Saad, Mohamad; Jahn, Andreas; ... Sharma, Manu |
2012 |
|
unige:33603 |
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism |
Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe |
2013 |
|
unige:45249 |
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease |
Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; ... Morris, Huw R |
2013 |
|
unige:146847 |
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates |
Ling, Helen; Gelpi, Ellen; Davey, Karen; Jaunmuktane, Zane; ... Revesz, Tamas |
2020 |
Hardy, John
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