Works matching AU Nembhard, Wendy N.

Results: 78
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    State-wide random seroprevalence survey of SARS-CoV-2 past infection in a southern US State, 2020.

    Published in:
    PLoS ONE, 2022, v. 17, n. 4, p. 1, doi. 10.1371/journal.pone.0267322
    By:
    • Cardenas, Victor M.;
    • Kennedy, Joshua L.;
    • Williams, Mark;
    • Nembhard, Wendy N.;
    • Zohoori, Namvar;
    • Du, Ruofei;
    • Jin, Jing;
    • Boothe, Danielle;
    • Fischbach, Lori A.;
    • Kirkpatrick, Catherine;
    • Modi, Zeel;
    • Caid, Katherine;
    • Owens, Shana;
    • Forrest, J. Craig;
    • James, Laura;
    • Boehme, Karl W.;
    • Olgaard, Ericka;
    • Gardner, Stephanie F.;
    • Amick III, Benjamin C.
    Publication type:
    Article
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    Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants.

    Published in:
    American Journal of Medical Genetics. Part A, 2023, v. 191, n. 6, p. 1546, doi. 10.1002/ajmg.a.63185
    By:
    • Sok, Pagna;
    • Sabo, Aniko;
    • Almli, Lynn M.;
    • Jenkins, Mary M.;
    • Nembhard, Wendy N.;
    • Agopian, A. J.;
    • Bamshad, Michael J.;
    • Blue, Elizabeth E.;
    • Brody, Lawrence C.;
    • Brown, Austin L.;
    • Browne, Marilyn L.;
    • Canfield, Mark A.;
    • Carmichael, Suzan L.;
    • Chong, Jessica X.;
    • Dugan‐Perez, Shannon;
    • Feldkamp, Marcia L.;
    • Finnell, Richard H.;
    • Gibbs, Richard A.;
    • Kay, Denise M.;
    • Lei, Yunping
    Publication type:
    Article
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    Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000–2017: A report from the National Birth Defects Prevention Network.

    Published in:
    American Journal of Medical Genetics. Part A, 2023, v. 191, n. 5, p. 1339, doi. 10.1002/ajmg.a.63181
    By:
    • Martin‐Giacalone, Bailey A.;
    • Lin, Angela E.;
    • Rasmussen, Sonja A.;
    • Kirby, Russell S.;
    • Nestoridi, Eirini;
    • Liberman, Rebecca F.;
    • Agopian, A. J.;
    • Carey, John C.;
    • Cragan, Janet D.;
    • Forestieri, Nina;
    • Leedom, Vinita;
    • Boyce, Aubree;
    • Nembhard, Wendy N.;
    • Piccardi, Monika;
    • Sandidge, Theresa;
    • Shan, Xiaoyi;
    • Shumate, Charles J.;
    • Stallings, Erin B.;
    • Stevenson, Roger;
    • Lupo, Philip J.
    Publication type:
    Article
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    Maternal Exposure to Disinfection By-Products and Risk of Hypospadias in the National Birth Defects Prevention Study (2000–2005).

    Published in:
    International Journal of Environmental Research & Public Health, 2020, v. 17, n. 24, p. 9564, doi. 10.3390/ijerph17249564
    By:
    • Zaganjor, Ibrahim;
    • Luben, Thomas J.;
    • Desrosiers, Tania A.;
    • Keil, Alexander P.;
    • Engel, Lawrence S.;
    • Michalski, Adrian M.;
    • Carmichael, Suzan L.;
    • Nembhard, Wendy N.;
    • Shaw, Gary M.;
    • Reefhuis, Jennita;
    • Yazdy, Mahsa M.;
    • Langlois, Peter H.;
    • Feldkamp, Marcia L.;
    • Romitti, Paul A.;
    • Olshan, Andrew F.
    Publication type:
    Article
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    Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012.

    Published in:
    2019
    By:
    • Bakker, Marian K.;
    • Kancherla, Vijaya;
    • Canfield, Mark A.;
    • Bermejo‐Sanchez, Eva;
    • Cragan, Janet D.;
    • Dastgiri, Saeed;
    • De Walle, Hermien E. K.;
    • Feldkamp, Marcia L.;
    • Groisman, Boris;
    • Gatt, Miriam;
    • Hurtado‐Villa, Paula;
    • Kallen, Karin;
    • Landau, Daniella;
    • Lelong, Nathalie;
    • Lopez Camelo, Jorge S.;
    • Martínez, Laura;
    • Morgan, Margery;
    • Mutchinick, Osvaldo M.;
    • Nembhard, Wendy N.;
    • Pierini, Anna
    Publication type:
    journal article
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    Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.

    Published in:
    Birth Defects Research, 2019, v. 111, n. 20, p. 1618, doi. 10.1002/bdr2.1554
    By:
    • Jenkins, Mary M.;
    • Almli, Lynn M.;
    • Pangilinan, Faith;
    • Chong, Jessica X.;
    • Blue, Elizabeth E.;
    • Shapira, Stuart K.;
    • White, Janson;
    • McGoldrick, Daniel;
    • Smith, Joshua D.;
    • Mullikin, James C.;
    • Bean, Christopher J.;
    • Nembhard, Wendy N.;
    • Lou, Xiang‐Yang;
    • Shaw, Gary M.;
    • Romitti, Paul A.;
    • Keppler‐Noreuil, Kim;
    • Yazdy, Mahsa M.;
    • Kay, Denise M.;
    • Carter, Tonia C.;
    • Olshan, Andrew F.
    Publication type:
    Article
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    Population‐based birth defects data in the United States, 2012–2016: A focus on abdominal wall defects.

    Published in:
    Birth Defects Research, 2019, v. 111, n. 18, p. 1436, doi. 10.1002/bdr2.1607
    By:
    • Stallings, Erin B.;
    • Isenburg, Jennifer L.;
    • Short, Tyiesha D.;
    • Heinke, Dominique;
    • Kirby, Russell S.;
    • Romitti, Paul A.;
    • Canfield, Mark A.;
    • O'Leary, Leslie A.;
    • Liberman, Rebecca F.;
    • Forestieri, Nina E.;
    • Nembhard, Wendy N.;
    • Sandidge, Theresa;
    • Nestoridi, Eirini;
    • Salemi, Jason L.;
    • Nance, Amy E.;
    • Duckett, Kirstan;
    • Ramirez, Glenda M.;
    • Shan, Xiaoyi;
    • Shi, Jing;
    • Lupo, Philip J.
    Publication type:
    Article
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    The role of genetic variation in DGKK on moderate and severe hypospadias.

    Published in:
    Birth Defects Research, 2019, v. 111, n. 13, p. 932, doi. 10.1002/bdr2.1522
    By:
    • Richard, Melissa A.;
    • Sok, Pagna;
    • Canon, Stephen;
    • Brown, Austin L.;
    • Peckham‐Gregory, Erin C.;
    • Nembhard, Wendy N.;
    • Carmichael, Suzan L.;
    • Ehli, Erik A.;
    • Kallsen, Noah A.;
    • Peyton, Shanna A.;
    • Davies, Gareth E.;
    • Patel, Ashay;
    • Zamilpa, Ismael;
    • Wyatt, Richard A.;
    • Hobbs, Charlotte A.;
    • Scheurer, Michael E.;
    • Lupo, Philip J.
    Publication type:
    Article
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    Population‐based birth defects data in the United States, 2011–2015: A focus on eye and ear defects.

    Published in:
    Birth Defects Research, 2018, v. 110, n. 19, p. 1478, doi. 10.1002/bdr2.1413
    By:
    • Stallings, Erin B.;
    • Isenburg, Jennifer L.;
    • Mai, Cara T.;
    • Liberman, Rebecca F.;
    • Moore, Cynthia A.;
    • Canfield, Mark A.;
    • Salemi, Jason L.;
    • Kirby, Russell S.;
    • Short, Tyiesha D.;
    • Nembhard, Wendy N.;
    • Forestieri, Nina E.;
    • Heinke, Dominique;
    • Alverson, C. J.;
    • Romitti, Paul A.;
    • Huynh, My‐Phuong;
    • Denson, Lindsay E.;
    • Judson, Emily M.;
    • Lupo, Philip J.
    Publication type:
    Article
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    Birth defect survival for hispanic subgroups.

    Published in:
    Birth Defects Research, 2018, v. 110, n. 4, p. 352, doi. 10.1002/bdr2.1157
    By:
    • Lopez, Keila N.;
    • Nembhard, Wendy N.;
    • Wang, Ying;
    • Liu, Gang;
    • Kucik, James E.;
    • Copeland, Glenn;
    • Gilboa, Suzanne M.;
    • Kirby, Russell S.;
    • Canfield, Mark
    Publication type:
    Article
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    Population-based birth defects data in the United States, 2010-2014: A focus on gastrointestinal defects.

    Published in:
    Birth Defects Research, 2017, v. 109, n. 18, p. 1504, doi. 10.1002/bdr2.1145
    By:
    • Lupo, Philip J.;
    • Isenburg, Jennifer L.;
    • Salemi, Jason L.;
    • Mai, Cara T.;
    • Liberman, Rebecca F.;
    • Canfield, Mark A.;
    • Copeland, Glenn;
    • Haight, Sarah;
    • Harpavat, Sanjiv;
    • Hoyt, Adrienne T.;
    • Moore, Cynthia A.;
    • Nembhard, Wendy N.;
    • Nguyen, Hoang N.;
    • Rutkowski, Rachel E.;
    • Steele, Amy;
    • Alverson, C.J.;
    • Stallings, Erin B.;
    • Kirby, Russell S.
    Publication type:
    Article
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    Temporal Variations in Seroprevalence of Severe Acute Respiratory Syndrome Coronavirus 2 Infections by Race and Ethnicity in Arkansas.

    Published in:
    Open Forum Infectious Diseases, 2022, v. 9, n. 5, p. 1, doi. 10.1093/ofid/ofac154
    By:
    • Kennedy, Joshua L;
    • Forrest, J Craig;
    • Young, Sean G;
    • Amick, Benjamin;
    • Williams, Mark;
    • James, Laura;
    • Snowden, Jessica;
    • Cardenas, Victor M;
    • Boothe, Danielle;
    • Kirkpatrick, Catherine;
    • Modi, Zeel;
    • Caid, Katherine;
    • Owens, Shana;
    • Kouassi, Marianne;
    • Mann, Ryan;
    • Putt, Claire;
    • Irish-Clardy, Katherine;
    • Macechko, Michael;
    • Brimberry, Ronald K;
    • Nembhard, Wendy N
    Publication type:
    Article
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    A longitudinal study of SARS-CoV-2 antibody seroprevalence and mitigation behaviors among college students at an Arkansas University.

    Published in:
    Journal of American College Health, 2025, v. 73, n. 1, p. 331, doi. 10.1080/07448481.2023.2217456
    By:
    • Allen, Jaimi L.;
    • Amick III., Benjamin C.;
    • Williams, Mark L.;
    • Kennedy, Joshua L.;
    • Boehme, Karl W.;
    • Forrest, J. Craig;
    • Primack, Brian;
    • Sides, Erica Ashley;
    • Nembhard, Wendy N.;
    • Gardner, Stephanie F.;
    • Snowden, Jessica N.;
    • James, Laura P.;
    • Olgaard, Ericka;
    • Gandy, Jay
    Publication type:
    Article
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    Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 8, p. 2376, doi. 10.1002/ajmg.a.62874
    By:
    • Li, Jingjing;
    • Yang, Wei;
    • Wang, Yuejun Jessie;
    • Ma, Chen;
    • Curry, Cynthia J.;
    • McGoldrick, Daniel;
    • Nickerson, Deborah A.;
    • Chong, Jessica X.;
    • Blue, Elizabeth E.;
    • Mullikin, James C.;
    • Reefhuis, Jennita;
    • Nembhard, Wendy N.;
    • Romitti, Paul A.;
    • Werler, Martha M.;
    • Browne, Marilyn L.;
    • Olshan, Andrew F.;
    • Finnell, Richard H.;
    • Feldkamp, Marcia L.;
    • Pangilinan, Faith;
    • Almli, Lynn M.
    Publication type:
    Article
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    A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 8, p. 2303, doi. 10.1002/ajmg.a.62759
    By:
    • Rashkin, Sara R.;
    • Cleves, Mario;
    • Shaw, Gary M.;
    • Nembhard, Wendy N.;
    • Nestoridi, Eirini;
    • Jenkins, Mary M.;
    • Romitti, Paul A.;
    • Lou, Xiang‐Yang;
    • Browne, Marilyn L.;
    • Mitchell, Laura E.;
    • Olshan, Andrew F.;
    • Lomangino, Kevin;
    • Bhattacharyya, Sudeepa;
    • Witte, John S.;
    • Hobbs, Charlotte A.
    Publication type:
    Article
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    Trisomy 13 and 18—Prevalence and mortality—A multi‐registry population based analysis.

    Published in:
    American Journal of Medical Genetics. Part A, 2019, v. 179, n. 12, p. 2382, doi. 10.1002/ajmg.a.61365
    By:
    • Goel, Nitin;
    • Morris, Joan K.;
    • Tucker, David;
    • Walle, Hermien E. K.;
    • Bakker, Marian K.;
    • Kancherla, Vijaya;
    • Marengo, Lisa;
    • Canfield, Mark A.;
    • Kallen, Karin;
    • Lelong, Nathalie;
    • Camelo, Jorge L.;
    • Stallings, Erin B.;
    • Jones, Abbey M.;
    • Nance, Amy;
    • Huynh, My‐Phuong;
    • Martínez‐Fernández, Maria‐Luisa;
    • Sipek, Antonin;
    • Pierini, Anna;
    • Nembhard, Wendy N.;
    • Goetz, Dorit
    Publication type:
    Article
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    Altered mechanisms of genital development identified through integration of DNA methylation and genomic measures in hypospadias.

    Published in:
    Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-69725-1
    By:
    • Richard, Melissa A.;
    • Sok, Pagna;
    • Canon, Stephen;
    • Nembhard, Wendy N.;
    • Brown, Austin L.;
    • Peckham-Gregory, Erin C.;
    • Ton, Minh;
    • Ehli, Erik A.;
    • Kallsen, Noah A.;
    • Peyton, Shanna A.;
    • Davies, Gareth E.;
    • Patel, Ashay;
    • Zamilpa, Ismael;
    • Hobbs, Charlotte A.;
    • Scheurer, Michael E.;
    • Lupo, Philip J.
    Publication type:
    Article
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