Zobrazeno 1 - 10
of 100
pro vyhledávání: '"A J, Agopian"'
Autor:
Philip J Lupo, Natalie P Archer, Rachel D Harris, Lisa K Marengo, Jeremy M Schraw, Adrienne T Hoyt, Susan Tanksley, Rachel Lee, Margaret Drummond-Borg, Debra Freedenberg, Priya B Shetty, A J Agopian, Charles Shumate, Sonja A Rasmussen, Peter H Langlois, Mark A Canfield
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0304238 (2024)
BackgroundEmerging evidence suggests newborn screening analytes may yield insights into the etiologies of birth defects, yet no effort has evaluated associations between a range of newborn screening analytes and birth defects.MethodsThis population-b
Externí odkaz:
https://doaj.org/article/d266256bfa9c4df689b541added34df9
Autor:
Thanh T. Hoang, Paulo Henrique Manso, Sharon Edman, Laura Mercer-Rosa, Laura E. Mitchell, Anshuman Sewda, Michael D. Swartz, Mark A. Fogel, A. J. Agopian, Elizabeth Goldmuntz
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 21, Iss 1, Pp 1-10 (2019)
Abstract Background Studies suggest that right ventricular (RV) fibrosis is associated with RV remodeling and long-term outcomes in patients with tetralogy of Fallot (TOF). Pre-operative hypoxia may increase expression of hypoxia inducible factor-1-a
Externí odkaz:
https://doaj.org/article/332f7a2ac8004734b36b89f90eb6cda8
Autor:
Bailey A. Martin‐Giacalone, Angela E. Lin, Sonja A. Rasmussen, Russell S. Kirby, Eirini Nestoridi, Rebecca F. Liberman, A. J. Agopian, John C. Carey, Janet D. Cragan, Nina Forestieri, Vinita Leedom, Aubree Boyce, Wendy N. Nembhard, Monika Piccardi, Theresa Sandidge, Xiaoyi Shan, Charles J. Shumate, Erin B. Stallings, Roger Stevenson, Philip J. Lupo
Publikováno v:
American Journal of Medical Genetics Part A. 191:1339-1349
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e10d5c980b841187a5cee8b2c3dc2553
https://doi.org/10.1002/ajmg.a.63181
https://doi.org/10.1002/ajmg.a.63181
Autor:
Cristina E. Trevino, Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler, H. Richard Johnston, Benjamin L. Rambo-Martin, Jai Oberoi, Kenneth J. Dooley, George T. Capone, Roger H. Reeves, Heather J. Cordell, Bernard D. Keavney, A. J. Agopian, Elizabeth Goldmuntz, Peter J. Gruber, James E. O’Brien, Douglas C. Bittel, Lalita Wadhwa, Clifford L. Cua, Ivan P. Moskowitz, Jennifer G. Mulle, Michael P. Epstein, Stephanie L. Sherman, Michael E. Zwick
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-2 (2021)
Externí odkaz:
https://doaj.org/article/4260a1524f6a4efb8f6fb3dd37c1c861
Autor:
Anshuman Sewda, A J Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E Morrow, Fadi Musfee, Deanne Taylor, Laura E Mitchell, Pediatric Cardiac Genomics Consortium
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0234357 (2020)
Congenital heart defects (CHDs) affect approximately 1% of newborns. Epidemiological studies have identified several genetically-mediated maternal phenotypes (e.g., pregestational diabetes, chronic hypertension) that are associated with the risk of C
Externí odkaz:
https://doaj.org/article/1b8dfd9772464e2784ed2899545c8c23
Autor:
Jeremy M. Schraw, J. P. Woodhouse, Renata H. Benjamin, Charles J. Shumate, Joanne Nguyen, Mark A. Canfield, A. J. Agopian, Philip J. Lupo
Publikováno v:
Birth Defects Research. 115:67-78
Few risk factors have been identified for nonsyndromic anotia/microtia (A/M).We obtained data on cases and a reference population of all livebirths in Texas for 1999-2014 from the Texas Birth Defects Registry (TBDR) and Texas vital records. We estima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01af77be95eb7b6844c434edd27f7987
https://doi.org/10.1002/bdr2.2130
https://doi.org/10.1002/bdr2.2130
Autor:
Justin Swanson, Charlie Shumate, A. J. Agopian, Laura E. Mitchell, Mark A. Canfield, Jason L. Salemi
Publikováno v:
Birth Defects Research. 114:895-905
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da730645849c958edec380fceeda5756
https://doi.org/10.1002/bdr2.2077
https://doi.org/10.1002/bdr2.2077
Autor:
Thanh T. Hoang, Yunping Lei, Laura E. Mitchell, Shreela V. Sharma, Michael D. Swartz, D. Kim Waller, Richard H. Finnell, Renata H. Benjamin, Marilyn L. Browne, Mark A. Canfield, Philip J. Lupo, Paige McKenzie, Gary M. Shaw, A. J. Agopian, The National Birth Defects Prevention Study
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background We examined the association between the maternal genotype for celiac disease‐associated variants and risk of neural tube defects (NTDs). Methods We conducted a case–control study, using data from the National Birth Defects Pre
Externí odkaz:
https://doaj.org/article/a190edf53def43389ea6c9963de122f8
Autor:
Anshuman Sewda, A J Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E Morrow, Deanne Taylor, Laura E Mitchell, Pediatric Cardiac Genomics Consortium
Publikováno v:
PLoS ONE, Vol 14, Iss 7, p e0219926 (2019)
Conotruncal heart defects (CTDs) are among the most common and severe groups of congenital heart defects. Despite evidence of an inherited genetic contribution to CTDs, little is known about the specific genes that contribute to the development of CT
Externí odkaz:
https://doaj.org/article/3151f7ca816e4d1980ccf5483f189e16
Autor:
Michelle Kaplinski, Deanne Taylor, Laura E Mitchell, Dorothy A Hammond, Elizabeth Goldmuntz, A J Agopian, Pediatric Cardiac Genomics Consortium
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0216477 (2019)
BackgroundMaternal hypertension, type 2 diabetes (T2D) and obesity are associated with an increased risk of having offspring with conotruncal heart defects (CTDs). Prior studies have identified sets of single nucleotide polymorphisms (SNPs) that are
Externí odkaz:
https://doaj.org/article/ed5c8184fa864b248da846fa8d5c8e85