A survey of genetic and epigenetic variation affecting human gene expression
Tomi Pastinen(Children's Mercy Hospital), Thomas J. Hudson(Ontario Institute for Cancer Research), Amélie Villeneuve(McGill University and Génome Québec Innovation Centre), Anna K. Naumova(McGill University Health Centre), Bing Ge(McGill University and Génome Québec Innovation Centre), Daniel Sinnett(Centre Hospitalier Universitaire Sainte-Justine), Helena Brändström(Uppsala University), Alya’a Sammak(McGill University and Génome Québec Innovation Centre), Tiffany Gaudin(McGill University and Génome Québec Innovation Centre), Damian Labuda(Centre Hospitalier Universitaire Sainte-Justine), Karine J. Lavergne(McGill University and Génome Québec Innovation Centre), Eef Harmsen(McGill University and Génome Québec Innovation Centre), Scott Gurd(McGill University and Génome Québec Innovation Centre), Marie‐Claude Vohl(Erasmus MC), Allon Beck(McGill University and Génome Québec Innovation Centre), Kenneth Morgan(University of London), Jade Kingsley(McGill University and Génome Québec Innovation Centre), Robert Sladek(McGill University and Génome Québec Innovation Centre), Andrei Verner(Montreal General Hospital), Patricia Lepage(Département Génétique Animale)
Cited by 264
Related Papers
Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome
|Science|1998|2.2k
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
|Nature Genetics|2000|1.8k
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
|Nature Genetics|1999|1.7k