No observed association for mitochondrial SNPs with preterm delivery and related outcomes
Brandon W. Alleman(University of Iowa), Jeffrey C. Murray(University of Iowa), Kim Doheny(Johns Hopkins University), Per Magnus(Norwegian Institute of Public Health), Ferdouse Begum, Heather A. Boyd(Statens Serum Institut), Bjarke Feenstra(Statens Serum Institut), David R. Crosslin(Tulane University), Solveig Myking(Norwegian Institute of Public Health), Aase Serine Devold Pay(Norwegian Institute of Public Health), Ronny Myhre(Norwegian Institute of Public Health), John R. Shaffer(University of Pittsburgh), Frank Geller(Statens Serum Institut), Eleanor Feingold(University of Pittsburgh), Mary L. Marazita(University of Pittsburgh), Kelli K. Ryckman(University of Iowa), Nils‐Halvdan Morken(Haukeland University Hospital), Bo Jacobsson(Sahlgrenska University Hospital), Qi Zhang(University of Washington), Mads Melbye(University of Copenhagen), Elizabeth Pugh(University of North Carolina at Chapel Hill), Ingrid H. G. Østensen(Norwegian Institute of Public Health)
Cited by 24
Related Papers
A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants
|Science|2007|2.8k
Defining the role of common variation in the genomic and biological architecture of adult human height
|Nature Genetics|2014|2.1k
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
|Nature Biotechnology|2013|1.1k
Genome partitioning of genetic variation for complex traits using common SNPs
|Nature Genetics|2011|966