Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study.

by Dorthe Almind Pedersen, George L Wehby, Jeffrey C Murray, Kaare Christensen
Published 2016-01-01

Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP51 protein structure.

by Monika Lewińska, Urska Zelenko, Franci Merzel, Simona Golic Grdadolnik, Jeffrey C Murray, Damjana Rozman
Published 2013-01-01

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development.

by Kathryn L Mueller, Jeffrey C Murray, Jacob J Michaelson, Morten H Christiansen, Sheena Reilly, J Bruce Tomblin
Published 2016-01-01

X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia.

by Astanand Jugessur, Øivind Skare, Rolv T Lie, Allen J Wilcox, Kaare Christensen, Lene Christiansen, Truc Trung Nguyen, Jeffrey C Murray, Håkon K Gjessing
Published 2012-01-01

Genome-Wide Analysis of DNA Methylation in Human Amnion

by Jinsil Kim, Mitchell M. Pitlick, Paul J. Christine, Amanda R. Schaefer, Cesar Saleme, Belén Comas, Viviana Cosentino, Enrique Gadow, Jeffrey C. Murray
Published 2013-01-01

High Dosage Folic Acid Supplementation, Oral Cleft Recurrence and Fetal Growth

by Carla Padovani, Danilo Moretti-Ferreira, Rui Pereira, Josiane Souza, Hrishikesh Chakraborty, Antonio Richieri-Costa, Têmis Maria Félix, Norman Goco, Jeffrey C. Murray, George L. Wehby
Published 2013-02-01

Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios.

by Øystein A Haaland, Astanand Jugessur, Miriam Gjerdevik, Julia Romanowska, Min Shi, Terri H Beaty, Mary L Marazita, Jeffrey C Murray, Allen J Wilcox, Rolv T Lie, Håkon K Gjessing
Published 2017-01-01

Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.

by Debashree Ray, Sowmya Venkataraghavan, Wanying Zhang, Elizabeth J Leslie, Jacqueline B Hetmanski, Seth M Weinberg, Jeffrey C Murray, Mary L Marazita, Ingo Ruczinski, Margaret A Taub, Terri H Beaty
Published 2021-07-01

Saving Lives at Birth; development of a retrospective theory of change, impact framework and prioritised metrics

by Marek Lalli, Harriet Ruysen, Hannah Blencowe, Kristen Yee, Karen Clune, Mary DeSilva, Marissa Leffler, Emily Hillman, Haitham El-Noush, Jo Mulligan, Jeffrey C. Murray, Karlee Silver, Joy E. Lawn
Published 2018-01-01

A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence.

by Zena T Wolf, Elizabeth J Leslie, Boaz Arzi, Kartika Jayashankar, Nili Karmi, Zhonglin Jia, Douglas J Rowland, Amy Young, Noa Safra, Saundra Sliskovic, Jeffrey C Murray, Claire M Wade, Danika L Bannasch
Published 2014-04-01

<i>CDH1</i> Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer

by Arthavan Selvanathan, Cheng Yee Nixon, Ying Zhu, Luigi Scietti, Federico Forneris, Lina M. Moreno Uribe, Andrew C. Lidral, Peter A. Jezewski, John B. Mulliken, Jeffrey C. Murray, Michael F. Buckley, Timothy C. Cox, Tony Roscioli
Published 2020-04-01

Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.

by Ritva Haataja, Minna K Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Marja Ojaniemi, Teppo Varilo, Bimal P Chaudhari, Jevon Plunkett, Jeffrey C Murray, Steven A McCarroll, Leena Peltonen, Louis J Muglia, Aarno Palotie, Mikko Hallman
Published 2011-02-01

Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth

by Johanna M. Huusko, Heli Tiensuu, Antti M. Haapalainen, Anu Pasanen, Pinja Tissarinen, Minna K. Karjalainen, Ge Zhang, Kaare Christensen, Kelli K. Ryckman, Bo Jacobsson, Jeffrey C. Murray, Stephen F. Kingsmore, Mikko Hallman, Louis J. Muglia, Mika Rämet
Published 2021-08-01

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting.

by Adam P Ross, M Adela Mansilla, Youngshik Choe, Simon Helminski, Richard Sturm, Roy L Maute, Scott R May, Kamil K Hozyasz, Piotr Wójcicki, Adrianna Mostowska, Beth Davidson, Iannis E Adamopoulos, Samuel J Pleasure, Jeffrey C Murray, Konstantinos S Zarbalis
Published 2013-01-01

A solution pathway for preterm birth: accelerating a priority research agenda

by Eve M Lackritz, Christopher B Wilson, Alan E Guttmacher, Jennifer L Howse, Cyril M Engmann, Craig E Rubens, Elizabeth M Mason, Louis J Muglia, Michael G Gravett, Robert L Goldenberg, Jeffrey C Murray, Catherine Y Spong, Joe Leigh Simpson
Published 2013-12-01

Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight

by Xiaojing eZheng, Xiaojing eZheng, Eleanor eFeingold, Eleanor eFeingold, Kelli K Ryckman, John R Shaffer, Heather A Boyd, Bjarke eFeenstra, Mads eMelbye, Mary L Marazita, Jeffrey C Murray, Karen eT.Cuenco, Karen eT.Cuenco
Published 2013-10-01

X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study.

by Solveig Myking, Heather A Boyd, Ronny Myhre, Bjarke Feenstra, Astanand Jugessur, Aase S Devold Pay, Ingrid H G Ostensen, Nils-Halvdan Morken, Tamara Busch, Kelli K Ryckman, Frank Geller, Per Magnus, Håkon K Gjessing, Mads Melbye, Bo Jacobsson, Jeffrey C Murray
Published 2013-01-01

The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip

by Sarah W. Curtis, Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein, David J. Cutler, Jeffrey C. Murray, Eleanor Feingold, Terri H. Beaty, Peter Claes, Seth M. Weinberg, Mary L. Marazita, Jenna C. Carlson, Elizabeth J. Leslie
Published 2021-04-01

Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype...

by Jing Chen, Jonas Bacelis, Pol Sole-Navais, Amit Srivastava, Julius Juodakis, Amy Rouse, Mikko Hallman, Kari Teramo, Mads Melbye, Bjarke Feenstra, Rachel M Freathy, George Davey Smith, Deborah A Lawlor, Jeffrey C Murray, Scott M Williams, Bo Jacobsson, Louis J Muglia, Ge Zhang
Published 2020-08-01

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.

by Alexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, Ecaterina Dragan, Têmis M Félix, Fedik Rahimov, Jill Harrington, Rebecca R Schultz, Yoriko Watanabe, Marla Johnson, Jennifer Fang, Sarah E O'Brien, Iêda M Orioli, Eduardo E Castilla, David R Fitzpatrick, Rulang Jiang, Mary L Marazita, Jeffrey C Murray
Published 2005-12-01