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CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Mar 22, 2023. (Total: 4244 publications since 2011)
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Records 1-13 (of 13 Records)
Query Trace: all>>Mary M Jenkins[CDC Author]
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Jingjing Li, Wei Yang, Yuejun Jessie Wang, Chen Ma, Cynthia J Curry, Daniel McGoldrick, Deborah A Nickerson, Jessica X Chong, Elizabeth E Blue, James C Mullikin, Jennita Reefhuis, Wendy N Nembhard, Paul A Romitti, Martha M Werler, Marilyn L Browne, Andrew F Olshan, Richard H Finnell, Marcia L Feldkamp, Faith Pangilinan, Lynn M Almli, Mike J Bamshad, Lawrence C Brody, Mary M Jenkins, Gary M Shaw, ,
American journal of medical genetics. Part A 2022
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
Sara R Rashkin, Mario Cleves, Gary M Shaw, Wendy N Nembhard, Eirini Nestoridi, Mary M Jenkins, Paul A Romitti, Xiang-Yang Lou, Marilyn L Browne, Laura E Mitchell, Andrew F Olshan, Kevin Lomangino, Sudeepa Bhattacharyya, John S Witte, Charlotte A Hobbs, and
American journal of medical genetics. Part A 2022
Exome sequencing identifies variants in infants with sacral agenesis.
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, John Lane, Denise M Kay, Kristin M Conway, Charlotte Hobbs, Gary M Shaw, Jennita Reefhuis, Mary M Jenkins, Lynn M Almli, Cynthia Moore, Martha Werler, Marilyn L Browne, Chris Cunniff, Andrew F Olshan, Faith Pangilinan, Lawrence C Brody, Robert J Sicko, Richard H Finnell, Michael J Bamshad, Daniel McGoldrick, Deborah A Nickerson, James C Mullikin, Paul A Romitti, James L Mills, and
Birth defects research 2022
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children.
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, John Lane, Denise M Kay, Kristin M Conway, Gary M Shaw, Jennita Reefhuis, Mary M Jenkins, Lynn M Almli, Andrew F Olshan, Faith Pangilinan, Lawrence C Brody, Robert J Sicko, Charlotte A Hobbs, Mike Bamshad, Daniel McGoldrick, Deborah A Nickerson, Richard H Finnell, James Mullikin, Paul A Romitti, James L Mills, and
American journal of medical genetics. Part A 2021
Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.
Jenil Patel, Emine Bircan, Xinyu Tang, Mohammed Orloff, Charlotte A Hobbs, Marilyn L Browne, Lorenzo D Botto, Richard H Finnell, Mary M Jenkins, Andrew Olshan, Paul A Romitti, Gary M Shaw, Martha M Werler, Jingyun Li, Wendy N Nembhard, and
PLoS genetics 2021 17(3) e1009413
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Cristina M Justice, Araceli Cuellar, Krithi Bala, Jeremy A Sabourin, Michael L Cunningham, Karen Crawford, Julie M Phipps, Yan Zhou, Deirdre Cilliers, Jo C Byren, David Johnson, Steven A Wall, Jenny E V Morton, Peter Noons, Elizabeth Sweeney, Astrid Weber, Katie E M Rees, Louise C Wilson, Emil Simeonov, Radka Kaneva, Nadezhda Yaneva, Kiril Georgiev, Assen Bussarsky, Craig Senders, Marike Zwienenberg, James Boggan, Tony Roscioli, Gianpiero Tamburrini, Marta Barba, Kristin Conway, Val C Sheffield, Lawrence Brody, James L Mills, Denise Kay, Robert J Sicko, Peter H Langlois, Rachel K Tittle, Lorenzo D Botto, Mary M Jenkins, Janine M Lasalle, Wanda Lattanzi, Andrew O M Wilkie, Alexander F Wilson, Paul A Romitti, Simeon A Boyadjiev, and
Human genetics 2020 Apr
Genome-wide association studies of structural birth defects: A review and commentary.
Philip J Lupo, Laura E Mitchell, and Mary M Jenkins
Birth defects research 2019 Oct
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.
Mary M Jenkins, Lynn M Almli, Faith Pangilinan, Jessica X Chong, Elizabeth E Blue, Stuart K Shapira, Janson White, Daniel McGoldrick, Joshua D Smith, James C Mullikin, Christopher J Bean, Wendy N Nembhard, Xiang-Yang Lou, Gary M Shaw, Paul A Romitti, Kim Keppler-Noreuil, Mahsa M Yazdy, Denise M Kay, Tonia C Carter, Andrew F Olshan, Kristin J Moore, Nanette Nascone-Yoder, Richard H Finnell, Philip J Lupo, Marcia L Feldkamp, , Deborah A Nickerson, Michael J Bamshad, Lawrence C Brody, Jennita Reefhuis,
Birth defects research 2019 Jul
Impact of sample collection participation on the validity of estimated measures of association in the National Birth Defects Prevention Study when assessing gene-environment interactions.
Mary M Jenkins, Jennita Reefhuis, Amy H Herring, and Margaret A Honein
Genetic epidemiology 2017 Dec 41(8) 834-843
Challenges in Studying Modifiable Risk Factors for Birth Defects.
Sarah C Tinker, Suzanne Gilboa, Jennita Reefhuis, Mary M Jenkins, Marcy Schaeffer, and Cynthia A Moore
Curr Epidemiol Rep 2015 Mar 2(1) 23-30
Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.
Mary M Jenkins, Jennita Reefhuis, Margaret L Gallagher, Jennifer G Mulle, Thomas J Hoffmann, Deborah A Koontz, Cynthia Sturchio, Sonja A Rasmussen, John S Witte, Patricia Richter, Margaret A Honein, and
Am. J. Med. Genet. A 2014 Jun 164A(6) 1454-63
Qualitative assessment of study materials and communication strategies used in studies that include DNA collection.
Mary M Jenkins, Erika Reed-Gross, Wanda D Barfield, Christine E Prue, Margaret L Gallagher, Sonja A Rasmussen, and Margaret A Honein
Am. J. Med. Genet. A 2011 Nov 155A(11) 2721-31
Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects.
Margaret L Gallagher, Cynthia Sturchio, Ashley Smith, Deborah Koontz, Mary M Jenkins, Margaret A Honein, and Sonja A Rasmussen
Birth Defects Res. Part A Clin. Mol. Teratol. 2011 Jul 91(7) 642-8
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