Works by Murray, Jeffrey C.

Results: 163
    1

    Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs.

    Published in:
    2020
    By:
    • Chen, Jing;
    • Bacelis, Jonas;
    • Sole-Navais, Pol;
    • Srivastava, Amit;
    • Juodakis, Julius;
    • Rouse, Amy;
    • Hallman, Mikko;
    • Teramo, Kari;
    • Melbye, Mads;
    • Feenstra, Bjarke;
    • Freathy, Rachel M.;
    • Smith, George Davey;
    • Lawlor, Deborah A.;
    • Murray, Jeffrey C.;
    • Williams, Scott M.;
    • Jacobsson, Bo;
    • Muglia, Louis J.;
    • Zhang, Ge
    Publication type:
    journal article
    2

    Shared genetic risk between major orofacial cleft phenotypes in an African population.

    Published in:
    Genetic Epidemiology, 2024, v. 48, n. 6, p. 258, doi. 10.1002/gepi.22564
    By:
    • Alade, Azeez;
    • Peter, Tabitha;
    • Busch, Tamara;
    • Awotoye, Waheed;
    • Anand, Deepti;
    • Abimbola, Oladayo;
    • Aladenika, Emmanuel;
    • Olujitan, Mojisola;
    • Rysavy, Oscar;
    • Nguyen, Phuong Fawng;
    • Naicker, Thirona;
    • Mossey, Peter A.;
    • Gowans, Lord J. J.;
    • Eshete, Mekonen A.;
    • Adeyemo, Wasiu L.;
    • Zeng, Erliang;
    • Van Otterloo, Eric;
    • O'Rorke, Michael;
    • Adeyemo, Adebowale;
    • Murray, Jeffrey C.
    Publication type:
    Article
    3

    Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes.

    Published in:
    Genetic Epidemiology, 2022, v. 46, n. 3, p. 182, doi. 10.1002/gepi.22447
    By:
    • Mukhopadhyay, Nandita;
    • Feingold, Eleanor;
    • Moreno‐Uribe, Lina;
    • Wehby, George;
    • Valencia‐Ramirez, Luz Consuelo;
    • Restrepo Muñeton, Claudia P.;
    • 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.
    Publication type:
    Article
    4

    FAT4 identified as a potential modifier of orofacial cleft laterality.

    Published in:
    Genetic Epidemiology, 2021, v. 45, n. 7, p. 721, doi. 10.1002/gepi.22420
    By:
    • Curtis, Sarah W.;
    • Chang, Daniel;
    • Sun, Miranda R.;
    • Epstein, Michael P.;
    • Murray, Jeffrey C.;
    • Feingold, Eleanor;
    • Beaty, Terri H.;
    • Weinberg, Seth M.;
    • Marazita, Mary L.;
    • Lipinski, Robert J.;
    • Carlson, Jenna C.;
    • Leslie, Elizabeth J.
    Publication type:
    Article
    5

    A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals.

    Published in:
    Genetic Epidemiology, 2019, v. 43, n. 6, p. 704, doi. 10.1002/gepi.22214
    By:
    • Carlson, Jenna C.;
    • Anand, Deepti;
    • Butali, Azeez;
    • Buxo, Carmen J.;
    • Christensen, Kaare;
    • Deleyiannis, Frederic;
    • Hecht, Jacqueline T.;
    • Moreno, Lina M.;
    • Orioli, Ieda M.;
    • Padilla, Carmencita;
    • Shaffer, John R.;
    • Vieira, Alexandre R.;
    • Wehby, George L.;
    • Weinberg, Seth M.;
    • Murray, Jeffrey C.;
    • Beaty, Terri H.;
    • Saadi, Irfan;
    • Lachke, Salil A.;
    • Marazita, Mary L.;
    • Feingold, Eleanor
    Publication type:
    Article
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    Genome‐wide interaction studies identify sex‐specific risk alleles for nonsyndromic orofacial clefts.

    Published in:
    Genetic Epidemiology, 2018, v. 42, n. 7, p. 664, doi. 10.1002/gepi.22158
    By:
    • 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 J.
    Publication type:
    Article
    8
    9

    Whole exome association of rare deletions in multiplex oral cleft families.

    Published in:
    Genetic Epidemiology, 2017, v. 41, n. 1, p. 61, doi. 10.1002/gepi.22010
    By:
    • Fu, Jack;
    • Beaty, Terri H.;
    • Scott, Alan F.;
    • Hetmanski, Jacqueline;
    • Parker, Margaret M.;
    • Wilson, Joan E. Bailey;
    • Marazita, Mary L.;
    • Mangold, Elisabeth;
    • Albacha‐Hejazi, Hasan;
    • Murray, Jeffrey C.;
    • Bureau, Alexandre;
    • Carey, Jacob;
    • Cristiano, Stephen;
    • Ruczinski, Ingo;
    • Scharpf, Robert B.
    Publication type:
    Article
    10

    Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip With/Without Cleft Palate Between Asians and Europeans.

    Published in:
    Genetic Epidemiology, 2012, v. 36, n. 4, p. 392, doi. 10.1002/gepi.21633
    By:
    • Murray, Tanda;
    • Taub, Margaret A.;
    • Ruczinski, Ingo;
    • Scott, Alan F.;
    • Hetmanski, Jacqueline B.;
    • Schwender, Holger;
    • Patel, Poorav;
    • Zhang, Tian Xiao;
    • Munger, Ronald G.;
    • Wilcox, Allen J.;
    • Ye, Xiaoqian;
    • Wang, Hong;
    • Wu, Tao;
    • Wu-Chou, Yah Huei;
    • Shi, Bing;
    • Jee, Sun Ha;
    • Chong, Samuel;
    • Yeow, Vincent;
    • Murray, Jeffrey C.;
    • Marazita, Mary L.
    Publication type:
    Article
    11

    Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate.

    Published in:
    Genetic Epidemiology, 2011, v. 35, n. 6, p. 469, doi. 10.1002/gepi.20595
    By:
    • Beaty, Terri H.;
    • Ruczinski, Ingo;
    • Murray, Jeffrey C.;
    • Marazita, Mary L.;
    • Munger, Ronald G.;
    • Hetmanski, Jacqueline B.;
    • Murray, Tanda;
    • Redett, Richard J.;
    • Fallin, M. Daniele;
    • Liang, Kung Yee;
    • Wu, Tao;
    • Patel, Poorav J.;
    • Jin, Sheng-Chih;
    • Zhang, Tian Xiao;
    • Schwender, Holger;
    • Wu-Chou, Yah Huei;
    • Chen, Philip K.;
    • Chong, Samuel S.;
    • Cheah, Felicia;
    • Yeow, Vincent
    Publication type:
    Article
    12

    Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study.

    Published in:
    Genetic Epidemiology, 2009, v. 33, n. 3, p. 247, doi. 10.1002/gepi.20376
    By:
    • Boyles, Abee L.;
    • Wilcox, Allen J.;
    • Taylor, Jack A.;
    • Shi, Min;
    • Weinberg, Clarice R.;
    • Meyer, Klaus;
    • Fredriksen, Åse;
    • Ueland, Per Magne;
    • Johansen, Anne Marte W.;
    • Drevon, Christian A.;
    • Jugessur, Astanand;
    • Trung, Truc Nguyen;
    • Gjessing, Håkon K.;
    • Vollset, Stein Emil;
    • Murray, Jeffrey C.;
    • Christensen, Kaare;
    • Lie, Rolv T.
    Publication type:
    Article
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    Noninvasive Whole-Genome Sequencing of a Human Fetus.

    Published in:
    Science Translational Medicine, 2012, v. 4, n. 137, p. 1, doi. 10.1126/scitranslmed.3004323
    By:
    • Kitzman, Jacob O.;
    • Snyder, Matthew W.;
    • Ventura, Mario;
    • Lewis, Alexandra P.;
    • Ruolan Qiu;
    • Simmons, LaVone E.;
    • Gammill, Hilary S.;
    • Rubens, Craig E.;
    • Santillan, Donna A.;
    • Murray, Jeffrey C.;
    • Tabor, Holly K.;
    • Bamshad, Michael J.;
    • Eichler, Evan E.;
    • Shendure, Jay
    Publication type:
    Article
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    High Dosage Folic Acid Supplementation, Oral Cleft Recurrence and Fetal Growth.

    Published in:
    International Journal of Environmental Research & Public Health, 2013, v. 10, n. 2, p. 590, doi. 10.3390/ijerph10020590
    By:
    • Wehby, George L.;
    • Félix, Têmis Maria;
    • Goco, Norman;
    • Richieri-Costa, Antonio;
    • Chakraborty, Hrishikesh;
    • Souza, Josiane;
    • Pereira, Rui;
    • Padovani, Carla;
    • Moretti-Ferreira, Danilo;
    • Murray, Jeffrey C.
    Publication type:
    Article
    21
    22

    Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 7, p. 1, doi. 10.1371/journal.pgen.1007394
    By:
    • Huusko, Johanna M.;
    • Karjalainen, Minna K.;
    • Graham, Britney E.;
    • Zhang, Ge;
    • Farrow, Emily G.;
    • Miller, Neil A.;
    • Jacobsson, Bo;
    • Eidem, Haley R.;
    • Murray, Jeffrey C.;
    • Bedell, Bruce;
    • Breheny, Patrick;
    • Brown, Noah W.;
    • Bødker, Frans L.;
    • Litterman, Nadia K.;
    • Jiang, Pan-Pan;
    • Russell, Laura;
    • Hinds, David A.;
    • Hu, Youna;
    • null, null;
    • Rokas, Antonis
    Publication type:
    Article
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    PITX2 and FOXC1 spectrum of mutations in ocular syndromes.

    Published in:
    European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1224, doi. 10.1038/ejhg.2012.80
    By:
    • Reis, Linda M;
    • Tyler, Rebecca C;
    • Volkmann Kloss, Bethany A;
    • Schilter, Kala F;
    • Levin, Alex V;
    • Lowry, R Brian;
    • Zwijnenburg, Petra J G;
    • Stroh, Eliza;
    • Broeckel, Ulrich;
    • Murray, Jeffrey C;
    • Semina, Elena V
    Publication type:
    Article
    26

    The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 6, p. 774, doi. 10.1038/ejhg.2008.245
    By:
    • Choi, Sun J.;
    • Marazita, Mary L.;
    • Hart, P. Suzanne;
    • Sulima, Pawel P.;
    • Field, L. Leigh;
    • McHenry, Toby Goldstein;
    • Govil, Manika;
    • Cooper, Margaret E.;
    • Letra, Ariadne;
    • Menezes, Renato;
    • Narayanan, Somnya;
    • Mansilla, Maria Adela;
    • Granjeiro, José M.;
    • Vieira, Alexandre R.;
    • Lidral, Andrew C.;
    • Murray, Jeffrey C.;
    • Hart, Thomas C.
    Publication type:
    Article
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    Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

    Published in:
    2010
    By:
    • Beaty, Terri H;
    • Murray, Jeffrey C;
    • Marazita, Mary L;
    • Munger, Ronald G;
    • Hetmanski, Ingo Ruczinski Jacqueline B;
    • Liang, Kung Yee;
    • Wu, Tao;
    • Murray, Tanda;
    • Fallin, M Daniele;
    • Redett, Richard A;
    • Raymond, Gerald;
    • Schwender, Holger;
    • Jin, Shin C;
    • Cooper, Margaret E;
    • Dunnwald, Martine;
    • Mansilla, Maria A;
    • Leslie, Elizabeth;
    • Bullard, Stephen;
    • Lidral, Andrew C;
    • Moreno, Lina M
    Publication type:
    Correction Notice
    33

    A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

    Published in:
    Nature Genetics, 2010, v. 42, n. 6, p. 525, doi. 10.1038/ng.580
    By:
    • Beaty, Terri H.;
    • Murray, Jeffrey C.;
    • Marazita, Mary L.;
    • Munger, Ronald G.;
    • Ruczinski, Ingo;
    • Hetmanski, Jacqueline B.;
    • Kung Yee Liang;
    • Wu, Tao;
    • Murray, Tanda;
    • Fallin, M. Daniele;
    • Redett, Richard A.;
    • Raymond, Gerald;
    • Schwender, Holger;
    • Jin, Sheng Chih;
    • Cooper, Margaret E.;
    • Dunnwald, Martine;
    • Mansilla, Maria A.;
    • Leslie, Elizabeth;
    • Bullard, Stephen;
    • Lidral, Andrew C.
    Publication type:
    Article
    34
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    Time for T.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 107, doi. 10.1038/ng1001-107
    By:
    • Murray, Jeffrey C.
    Publication type:
    Article
    37

    Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease.

    Published in:
    Nature Genetics, 2000, v. 26, n. 1, p. 19, doi. 10.1038/79128
    By:
    • Kinoshita, Akira;
    • Saito, Takashi;
    • Tomita, Hiro-aki;
    • Makita, Yoshio;
    • Yoshida, Kunihiro;
    • Ghadami, Mohsen;
    • Yamada, Koki;
    • Kondo, Shinji;
    • Ikegawa, Shiro;
    • Nishimura, Gen;
    • Fukushima, Yoshimitsu;
    • Nakagomi, Tadashi;
    • Saito, Haruki;
    • Sugimoto, Takeo;
    • Kamegaya, Makoto;
    • Hisa, Kenji;
    • Murray, Jeffrey C.;
    • Taniguchi, Naoyuki;
    • Niikawa, Norio
    Publication type:
    Article
    38
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    Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005059
    By:
    • Wolf, Zena T.;
    • Brand, Harrison A.;
    • Shaffer, John R.;
    • Leslie, Elizabeth J.;
    • Arzi, Boaz;
    • Willet, Cali E.;
    • Cox, Timothy C.;
    • McHenry, Toby;
    • Narayan, Nicole;
    • Feingold, Eleanor;
    • Wang, Xioajing;
    • Sliskovic, Saundra;
    • Karmi, Nili;
    • Safra, Noa;
    • Sanchez, Carla;
    • Deleyiannis, Frederic W. B.;
    • Murray, Jeffrey C.;
    • Wade, Claire M.;
    • Marazita, Mary L.;
    • Bannasch, Danika L.
    Publication type:
    Article
    40
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    Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth.

    Published in:
    PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002275
    By:
    • Geller, Frank;
    • Feenstra, Bjarke;
    • Zhang, Hao;
    • Shaffer, John R.;
    • Hansen, Thomas;
    • Esserlind, Ann-Louise;
    • Boyd, Heather A.;
    • Nohr, Ellen A.;
    • Timpson, Nicholas J.;
    • Fatemifar, Ghazaleh;
    • Paternoster, Lavinia;
    • Evans, David M.;
    • Weyant, Robert J.;
    • Levy, Steven M.;
    • Lathrop, Mark;
    • Smith, George Davey;
    • Murray, Jeffrey C.;
    • Olesen, Jes;
    • Werge, Thomas;
    • Marazita, Mary L.
    Publication type:
    Article
    42
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    Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate.

    Published in:
    PLoS Genetics, 2005, v. 1, n. 6, p. e64, doi. 10.1371/journal.pgen.0010064
    By:
    • Vieira, Alexandre R.;
    • Avila, Joseph R.;
    • Daack-Hirsch, Sandra;
    • Dragan, Ecaterina;
    • Félix, Têmis M.;
    • Rahimov, Fedik;
    • Harrington, Jill;
    • Schultz, Rebecca R.;
    • Watanabe, Yoriko;
    • Johnson, Marla;
    • Fang, Jennifer;
    • O'Brien, Sarah E.;
    • Orioli, Iêda M.;
    • Castilla, Eduardo E.;
    • FitzPatrick, David R.;
    • Jiang, Rulang;
    • Marazita, Mary L.;
    • Murray, Jeffrey C.
    Publication type:
    Article
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    Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results.

    Published in:
    Human Heredity, 2009, v. 68, n. 3, p. 151, doi. 10.1159/000224636
    By:
    • Marazita, Mary L.;
    • Lidral, Andrew C.;
    • Murray, Jeffrey C.;
    • Field, L.Leigh;
    • Maher, Brion S.;
    • Goldstein McHenry, Toby;
    • Cooper, Margaret E.;
    • Govil, Manika;
    • Daack-Hirsch, Sandra;
    • Riley, Bridget;
    • Jugessur, Astanand;
    • Felix, Temis;
    • Morene, Lina;
    • Mansilla, M.Adela;
    • Vieira, Alexandre R.;
    • Doheny, Kim;
    • Pugh, Elizabeth;
    • Valencia-Ramirez, Consuelo;
    • Arcos-Burgos, Mauricio
    Publication type:
    Article
    50