Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Birth defects[original query] |
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Genome-wide association study of maternal and inherited loci for conotruncal heart defects.
PloS one 2014 9 (5): e96057. Agopian A J, Mitchell Laura E, Glessner Joseph, Bhalla Angela D, Sewda Anshuman, Hakonarson Hakon, Goldmuntz Elizabe |
Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate.
PloS one 2014 9 (2): e88088. Wu Tao, Schwender Holger, Ruczinski Ingo, Murray Jeffrey C, Marazita Mary L, Munger Ronald G, Hetmanski Jacqueline B, Parker Margaret M, Wang Ping, Murray Tanda, Taub Margaret, Li Shuai, Redett Richard J, Fallin M Daniele, Liang Kung Yee, Wu-Chou Yah Huei, Chong Samuel S, Yeow Vincent, Ye Xiaoqian, Wang Hong, Huang Shangzhi, Jabs Ethylin W, Shi Bing, Wilcox Allen J, Jee Sun Ha, Scott Alan F, Beaty Terri |
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate.
Nature communications 2015 6 6414. Sun Yimin, Huang Yongqing, Yin Aihua, Pan Yongchu, Wang Yirui, Wang Cheng, Du Yong, Wang Meilin, Lan Feifei, Hu Zhibin, Wang Guoqing, Jiang Min, Ma Junqing, Zhang Xiaozhuang, Ma Hongxia, Ma Jian, Zhang Weibing, Huang Qun, Zhou Zhongwei, Ma Lan, Li Yadi, Jiang Hongbing, Xie Lan, Jiang Yuyang, Shi Bing, Cheng Jing, Shen Hongbing, Wang Lin, Yang Yinx |
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Human molecular genetics 2016 Mar . Hanchard Neil A, Swaminathan Shanker, Bucasas Kristine, Furthner Dieter, Fernbach Susan, Azamian Mahshid S, Wang Xueqing, Lewin Mark, Towbin Jeffrey A, D'Alessandro Lisa C A, Morris Shaine A, Dreyer William, Denfield Susan, Ayres Nancy A, Franklin Wayne J, Justino Henri, Lantin-Hermoso M Regina, Ocampo Elena C, Santos Alexia B, Parekh Dhaval, Moodie Douglas, Jeewa Aamir, Lawrence Emily, Allen Hugh D, Penny Daniel J, Fraser Charles D, Lupski James R, Popoola Mojisola, Wadhwa Lalita, Brook J David, Bu'Lock Frances A, Bhattacharya Shoumo, Lalani Seema R, Zender Gloria A, Fitzgerald-Butt Sara, Bowman Jessica, Corsmeier Don, White Peter, Lecerf Kelsey, Zapata Gladys, Hernandez Patricia, Goodship Judith A, Garg Vidu, Keavney Bernard D, Leal Suzanne M, Cordell Heather J, Belmont John W, McBride Kim |
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
Nature communications 2017 Feb 8 14364. Yu Yanqin, Zuo Xianbo, He Miao, Gao Jinping, Fu Yuchuan, Qin Chuanqi, Meng Liuyan, Wang Wenjun, Song Yaling, Cheng Yong, Zhou Fusheng, Chen Gang, Zheng Xiaodong, Wang Xinhuan, Liang Bo, Zhu Zhengwei, Fu Xiazhou, Sheng Yujun, Hao Jiebing, Liu Zhongyin, Yan Hansong, Mangold Elisabeth, Ruczinski Ingo, Liu Jianjun, Marazita Mary L, Ludwig Kerstin U, Beaty Terri H, Zhang Xuejun, Sun Liangdan, Bian Zhu |
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Human genetics 2017 Mar 136 (3): 275-286. Leslie Elizabeth J, Carlson Jenna C, Shaffer John R, Butali Azeez, Buxó Carmen J, Castilla Eduardo E, Christensen Kaare, Deleyiannis Fred W B, Leigh Field L, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Feingold Eleanor, Weinberg Seth M, Murray Jeffrey C, Beaty Terri H, Marazita Mary |
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
Human molecular genetics 2017 Feb 26 (4): 829-842. Ludwig Kerstin U, Böhmer Anne C, Bowes John, Nikolic Miloš, Ishorst Nina, Wyatt Niki, Hammond Nigel L, Gölz Lina, Thieme Frederic, Barth Sandra, Schuenke Hannah, Klamt Johanna, Spielmann Malte, Aldhorae Khalid, Rojas-Martinez Augusto, Nöthen Markus M, Rada-Iglesias Alvaro, Dixon Michael J, Knapp Michael, Mangold Elisabe |
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.
Genetic epidemiology 2018 10 42 (7): 664-672. Carlson Jenna C, Nidey Nichole L, Butali Azeez, Buxo Carmen J, Christensen Kaare, Deleyiannis Frederic W-D, Hecht Jacqueline T, Field L Leigh, Moreno-Uribe Lina M, Orioli Ieda M, Poletta Fernando A, Padilla Carmencita, Vieira Alexandre R, Weinberg Seth M, Wehby George L, Feingold Eleanor, Murray Jeffrey C, Marazita Mary L, Leslie Elizabeth |
A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.
PLoS genetics 2019 12 15 (12): e1008414. Chernus Jonathan M, Allen Emily G, Zeng Zhen, Hoffman Eva R, Hassold Terry J, Feingold Eleanor, Sherman Stephanie |
Secondary Genome-Wide Association Study Using Novel Analytical Strategies Disentangle Genetic Components of Cleft Lip and/or Cleft Palate in 1q32.2.
Genes 2020 Oct 11 (11): . Yang Yunju, Suzuki Akiko, Iwata Junichi, Jun G |
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.
Frontiers in cell and developmental biology 2021 4 9 621482. Mukhopadhyay Nandita, Feingold Eleanor, Moreno-Uribe Lina, Wehby George, Valencia-Ramirez Luz Consuelo, Muñeton Claudia P Restrepo, Padilla Carmencita, Deleyiannis Frederic, Christensen Kaare, Poletta Fernando A, Orioli Ieda M, Hecht Jacqueline T, Buxó Carmen J, Butali Azeez, Adeyemo Wasiu L, Vieira Alexandre R, Shaffer John R, Murray Jeffrey C, Weinberg Seth M, Leslie Elizabeth J, Marazita Mary |
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
American journal of medical genetics. Part A 2022 4 188 (8): 2303-2314. 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, |
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