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American Journal of Obstetrics and Gynecology|June 23, 2020
Advancing human health in the decade ahead: pregnancy as a key window for discovery: A Burroughs Wellcome Fund Pregnancy Think TankYoel Sadovsky, Sam Mesiano, Graham J Burton, et al.
Human Molecular Genetics|January 21, 2014
An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effectsWalid D Fakhouri, Fedik Rahimov, Catia Attanasio, et al.
Neuro-Oncology Advances|January 6, 2022
Reevaluating surgery and re-irradiation for locally recurrent pediatric ependymoma-a multi-institutional studyDavid Y Mak, Normand Laperriere, Vijay Ramaswamy, et al.
Pediatric Cardiology|May 31, 2012
Outcome of extremely preterm infants (<1,000 g) with congenital heart defects from the National Institute of Child Health and Human Development Neonatal Research NetworkAthina Pappas, Seetha Shankaran, Nellie I Hansen, et al.
Plos Genetics|December 6, 2005
Medical sequencing of candidate genes for nonsyndromic cleft lip and palateAlexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, et al.
Genetic Epidemiology|December 3, 2008
Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association studyAbee L Boyles, Allen J Wilcox, Jack A Taylor, et al.
European Journal of Human Genetics : EJHG|December 19, 2008
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/PSun J Choi, Mary L Marazita, P Suzanne Hart, et al.
The Journal of Nutrition|October 2, 2015
Short Maternal Stature Increases Risk of Small-for-Gestational-Age and Preterm Births in Low- and Middle-Income Countries: Individual Participant Data Meta-Analysis and Population Attributable FractionNaoko Kozuki, Joanne Katz, Anne C C Lee, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Expanding the genetic and phenotypic spectrum of popliteal pterygium disordersElizabeth J Leslie, James O'Sullivan, Michael L Cunningham, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex familiesEmily R Holzinger, Qing Li, Margaret M Parker, et al.
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