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Refining genetic associations in multiple sclerosis

Authors :
Åslaug R. Lorentzen
Bertram Müller-Myhsok
David R. Booth
Jonathan L. Haines
Françoise Clerget-Darpoux
Anne Spurkland
David A. Hafler
P. Villoslada
Bertrand Fontaine
Graeme J. Stewart
An Goris
Stephen Sawcer
Virpi M. Leppä
Tania Mihalova
Daniela Galimberti
Alastair Compston
Xavier Montalban
Margaret A. Pericak-Vance
Hanne F. Harbo
Antje Kroner
Colin M. Graham
A. Oturai
Janna Saarela
Sandra D'Alfonso
A Ivinson
Paola Naldi
Stephen L. Hauser
Tomas Olsson
C M van Duijn
Manuel Comabella
R Q Hintzen
Rita Dobosi
Ingrid Kockum
John D. Rioux
Amie Walton
J. Hoksenberg
P. L. De Jager
L. F. Barcellos
Francesco Cucca
Bénédicte Dubois
Maria Ban
Mark J. Daly
Koen Vandenbroeck
Helle Bach Søndergaard
Laura Bergamaschi
Peter Rieckmann
Neil Robertson
Elisabeth Gulowsen Celius
David Sexton
Robert Heard
Florian Holsboer
Finn Sellebjerg
Marie-Claude Babron
Frank Weber
Leena Peltonen
Stanley Hawkins
Jacob L. McCauley
Isabelle Cournu-Rebeix
J. Hillert
Maria Giovanna Marrosu
Marco Salvetti
A. Palotie
Gillian Ingram
Franca Rosa Guerini
Clive Hawkins
Source :
Lancet Neurology
Publisher :
Elsevier Ltd.

Abstract

Genome-wide association studies involve several hundred thousand markers and, even when quality control is scrupulous, are invariably confounded by residual uncorrected errors that can falsely inflate the apparent difference between cases and controls (so-called genomic inflation). As a consequence such studies inevitably generate false positives alongside genuine associations. By use of Bayesian logic and empirical data, the Wellcome Trust Case Control Consortium suggested that association studies in complex disease should involve at least 2000 cases and 2000 controls, at which level they predicted that p values of less than 5×10 −7 would more commonly signify true positives than false positives.

Details

Language :
English
ISSN :
14744422
Issue :
7
Database :
OpenAIRE
Journal :
The Lancet Neurology
Accession number :
edsair.doi.dedup.....85a0090ff68a759d68a5d75caa169640
Full Text :
https://doi.org/10.1016/S1474-4422(08)70122-4