Works matching AU Murray, Jeffrey C.

Results: 163

Prenatal care effectiveness and utilization in Brazil.
Published in:
Health Policy & Planning, 2009, v. 24, n. 3, p. 175, doi. 10.1093/heapol/czp005
By:
- George L Wehby;
- Jeffrey C Murray;
- Eduardo E Castilla;
- Jorge S Lopez-Camelo;
- Robert L Ohsfeldt
Publication type:
Article
Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants.
Published in:
2016
By:
- Sampath, Venkatesh;
- Helbling, Daniel;
- Menden, Heather;
- Dimmock, David;
- Mulrooney, Neil P.;
- Murray, Jeffrey C.;
- Dagle, John M.;
- Garland, Jeffery S.
Publication type:
journal article
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.
Published in:
Birth Defects Research, 2017, v. 109, p. 1030, doi. 10.1002/bdr2.23605
By:
- Carlson, Jenna C.;
- Taub, Margaret A.;
- Feingold, Eleanor;
- Beaty, Terri H.;
- Murray, Jeffrey C.;
- Marazita, Mary L.;
- Leslie, Elizabeth J.
Publication type:
Article
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.
Published in:
Birth Defects Research, 2017, v. 109, n. 13, p. 1030, doi. 10.1002/bdr2.23605
By:
- Carlson, Jenna C.;
- Taub, Margaret A.;
- Feingold, Eleanor;
- Beaty, Terri H.;
- Murray, Jeffrey C.;
- Marazita, Mary L.;
- Leslie, Elizabeth J.
Publication type:
Article
Genome-wide study of gene-by-sex interactions identifies risks for cleft palate.
Published in:
Human Genetics, 2024, v. 143, n. 11, p. 1341, doi. 10.1007/s00439-024-02704-y
By:
- Robinson, Kelsey;
- Parrish, Randy;
- Adeyemo, Wasiu Lanre;
- Beaty, Terri H.;
- Butali, Azeez;
- Buxó, Carmen J.;
- Gowans, Lord J. J.;
- Hecht, Jacqueline T.;
- Moreno Uribe, Lina;
- Murray, Jeffrey C.;
- Shaw, Gary M.;
- Weinberg, Seth M.;
- Brand, Harrison;
- Marazita, Mary L.;
- Cutler, David J.;
- Epstein, Michael P.;
- Yang, Jingjing;
- Leslie, Elizabeth J.
Publication type:
Article
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Published in:
Human Genetics, 2023, v. 142, n. 10, p. 1531, doi. 10.1007/s00439-023-02596-4
By:
- Curtis, Sarah W.;
- Carlson, Jenna C.;
- Beaty, Terri H.;
- Murray, Jeffrey C.;
- Weinberg, Seth M.;
- Marazita, Mary L.;
- Cotney, Justin L.;
- Cutler, David J.;
- Epstein, Michael P.;
- Leslie, Elizabeth J.
Publication type:
Article
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.
Published in:
Human Genetics, 2020, v. 139, n. 2, p. 215, doi. 10.1007/s00439-019-02099-1
By:
- Mukhopadhyay, Nandita;
- Bishop, Madison;
- Mortillo, Michael;
- Chopra, Pankaj;
- Hetmanski, Jacqueline B.;
- Taub, Margaret A.;
- Moreno, Lina M.;
- Valencia-Ramirez, Luz Consuelo;
- Restrepo, Claudia;
- Wehby, George L.;
- Hecht, Jacqueline T.;
- Deleyiannis, Frederic;
- Butali, Azeez;
- Weinberg, Seth M.;
- Beaty, Terri H.;
- Murray, Jeffrey C.;
- Leslie, Elizabeth J.;
- Feingold, Eleanor;
- Marazita, Mary L.
Publication type:
Article
Racial Gaps in Child Health Insurance Coverage in Four South American Countries: The Role of Wealth, Human Capital, and Other Household Characteristics.
Published in:
Health Services Research, 2011, v. 46, n. 6pt2, p. 2119, doi. 10.1111/j.1475-6773.2010.01225.x
By:
- Wehby, George L.;
- Murray, Jeffrey C.;
- McCarthy, Ann Marie;
- Castilla, Eduardo E.
Publication type:
Article
Plasma Lipids, Genetic Variants Near APOA1, and the Risk of Infantile Hypertrophic Pyloric Stenosis.
Published in:
JAMA: Journal of the American Medical Association, 2013, v. 310, n. 7, p. 714, doi. 10.1001/jama.2013.242978
By:
- Feenstra, Bjarke;
- Geller, Frank;
- Carstensen, Lisbeth;
- Romitti, Paul A.;
- Körberg, Izabella Baranowska;
- Bedell, Bruce;
- Krogh, Camilla;
- Fan, Ruzong;
- Svenningsson, Anna;
- Caggana, Michele;
- Nordenskjöld, Agneta;
- Mills, James L.;
- Murray, Jeffrey C.;
- Melbye, Mads
Publication type:
Article
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Published in:
American Journal of Medical Genetics. Part A, 2023, v. 191, n. 10, p. 2558, doi. 10.1002/ajmg.a.63336
By:
- Diaz Perez, Kimberly K.;
- Chung, Sydney;
- Head, S. Taylor;
- Epstein, Michael P.;
- Hecht, Jacqueline T.;
- Wehby, George L.;
- Weinberg, Seth M.;
- Murray, Jeffrey C.;
- Marazita, Mary L.;
- Leslie, Elizabeth J.
Publication type:
Article
Association of low‐frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
Published in:
American Journal of Medical Genetics. Part A, 2019, v. 179, n. 3, p. 467, doi. 10.1002/ajmg.a.61002
By:
- Shaffer, John R.;
- LeClair, Jessica;
- Carlson, Jenna C.;
- Feingold, Eleanor;
- Buxó, Carmen J.;
- Christensen, Kaare;
- Deleyiannis, Frederic W. B.;
- Field, L. Leigh;
- Hecht, Jacqueline T.;
- Moreno, Lina;
- Orioli, Ieda M.;
- Padilla, Carmencita;
- Vieira, Alexandre R.;
- Wehby, George L.;
- Murray, Jeffrey C.;
- Weinberg, Seth M.;
- Marazita, Mary L.;
- Leslie, Elizabeth J.
Publication type:
Article
Genetic Variants and the Cortisol Response in Children: An Exploratory Study.
Published in:
Biological Research for Nursing, 2019, v. 21, n. 2, p. 157, doi. 10.1177/1099800419826315
By:
- Ersig, Anne L.;
- Schutte, Debra L.;
- Standley, Jennifer;
- Leslie, Elizabeth J.;
- Zimmerman, Bridget;
- Hanrahan, Kirsten;
- Murray, Jeffrey C.;
- McCarthy, Ann Marie
Publication type:
Article
Relationship of Genetic Variants With Procedural Pain, Anxiety, and Distress in Children.
Published in:
Biological Research for Nursing, 2017, v. 19, n. 3, p. 339, doi. 10.1177/1099800417692878
By:
- Ersig, Anne L.;
- Schutte, Debra L.;
- Standley, Jennifer;
- Leslie, Elizabeth;
- Zimmerman, Bridget;
- Kleiber, Charmaine;
- Hanrahan, Kirsten;
- Murray, Jeffrey C.;
- McCarthy, Ann Marie
Publication type:
Article
A phase 2 study of valproic acid and radiation, followed by maintenance valproic acid and bevacizumab in children with newly diagnosed diffuse intrinsic pontine glioma or high-grade glioma.
Published in:
2020
By:
- Su, Jack Meng‐Fen;
- Murray, Jeffrey C.;
- McNall‐Knapp, Rene Y.;
- Bowers, Daniel C.;
- Shah, Shafqat;
- Adesina, Adekunle M.;
- Paulino, Arnold C.;
- Jo, Eunji;
- Mo, Qianxing;
- Baxter, Patricia A.;
- Blaney, Susan M.;
- Su, Jack Meng-Fen;
- McNall-Knapp, Rene Y
Publication type:
journal article
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Published in:
2018
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;
- Rokas, Antonis;
- Teramo, Kari
Publication type:
Correction Notice
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
Co‐occurrence of orofacial clefts and clubfoot phenotypes in a sub‐Saharan African cohort: Whole‐exome sequencing implicates multiple syndromes and genes.
Published in:
Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1655
By:
- Gowans, Lord J. J.;
- Al Dhaheri, Noura;
- Li, Mary;
- Busch, Tamara;
- Obiri‐Yeboah, Solomon;
- Oti, Alexander A.;
- Sabbah, Daniel K.;
- Arthur, Fareed K. N.;
- Awotoye, Waheed O.;
- Alade, Azeez A.;
- Twumasi, Peter;
- Agbenorku, Pius;
- Plange‐Rhule, Gyikua;
- Naicker, Thirona;
- Donkor, Peter;
- Murray, Jeffrey C.;
- Sobreira, Nara L. M.;
- Butali, Azeez
Publication type:
Article
Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 929, doi. 10.1515/jpem-2013-0366
By:
- Ryckman, Kelli K.;
- Spracklen, Cassandra N.;
- Dagle, John M.;
- Murray, Jeffrey C.
Publication type:
Article
Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 3/4, p. 301, doi. 10.1515/jpem-2011-0456
By:
- Ryckman, Kelli K.;
- Cook, Daniel E.;
- Berberich, Stanton L.;
- Shchelochkov, Oleg A.;
- Berends, Susan K.;
- Busch, Tamara;
- Dagle, John M.;
- Murray, Jeffrey C.
Publication type:
Article
The Impact of Household Investments on Early Child Neurodevelopment and on Racial and Socioeconomic Developmental Gaps: Evidence from South America.
Published in:
Forum for Health Economics & Policy, 2011, v. 14, n. 1, p. 1, doi. 10.2202/1558-9544.1237
By:
- Wehby, George L.;
- McCarthy, Ann Marie;
- Castilla, Eduardo;
- Murray, Jeffrey C.
Publication type:
Article
Medulloblastoma in a toddler with Gorlin syndrome.
Published in:
Baylor University Medical Center Proceedings, 2018, v. 31, n. 2, p. 216, doi. 10.1080/08998280.2018.1435111
By:
- Al-Rahawan, Mohamad G.;
- Trevino, Sorleen;
- Jacob, Roy;
- Murray, Jeffrey C.;
- Al-Rahawan, Mohamad M.
Publication type:
Article
Abdominal obesity, liver fat, and muscle composition in survivors of childhood acute lymphoblastic leukemia.
Published in:
2007
By:
- Janiszewski, Peter M;
- Oeffinger, Kevin C;
- Church, Timothy S;
- Dunn, Andrea L;
- Eshelman, Debra A;
- Victor, Ronald G;
- Brooks, Sandra;
- Turoff, Alicia J;
- Sinclair, Erin;
- Murray, Jeffrey C;
- Bashore, Lisa;
- Ross, Robert
Publication type:
journal article
Saving Lives at Birth; development of a retrospective theory of change, impact framework and prioritised metrics.
Published in:
2018
By:
- Lalli, Marek;
- Ruysen, Harriet;
- Blencowe, Hannah;
- Yee, Kristen;
- Clune, Karen;
- DeSilva, Mary;
- Leffler, Marissa;
- Hillman, Emily;
- El-Noush, Haitham;
- Mulligan, Jo;
- Murray, Jeffrey C.;
- Silver, Karlee;
- Lawn, Joy E.
Publication type:
journal article
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.
Published in:
Human Mutation, 2001, v. 18, n. 5, p. 422, doi. 10.1002/humu.1213
By:
- Watanabe, Yoriko;
- Murray, Jeffrey C.;
- Bjork, Bryan C.;
- Bird, Christine P.;
- Chiang, P.-W.;
- Gregory, Simon G.;
- Kurnit, David M.;
- Schutte, Brian C.
Publication type:
Article
Detection of de novo copy number deletions from targeted sequencing of trios.
Published in:
Bioinformatics, 2019, v. 35, n. 4, p. 571, doi. 10.1093/bioinformatics/bty677
By:
- Fu, Jack M;
- Ruczinski, Ingo;
- Leslie, Elizabeth J;
- Scott, Alan F;
- Murray, Jeffrey C;
- Marazita, Mary L;
- Beaty, Terri H;
- Scharpf, Robert B
Publication type:
Article
Cleft lip and palate: understanding genetic and environmental influences.
Published in:
2011
By:
- Dixon, Michael J.;
- Marazita, Mary L.;
- Beaty, Terri H.;
- Murray, Jeffrey C.
Publication type:
journal article
Dermatoglyphic Fingerprint Heterogeneity Among Individuals with Nonsyndromic Cleft Lip With or Without Cleft Palate and Their Unaffected Relatives in China and the Philippines.
Published in:
Human Biology, 2005, v. 77, n. 2, p. 257, doi. 10.1353/hub.2005.0042
By:
- Scott, Nicole M.;
- Weinberg, Seth M.;
- Neiswanger, Katherine;
- Brandon, Carla A.;
- Daack-Hirsch, Sandra;
- Murray, Jeffrey C.;
- You-e Liu;
- Marazita, Mary L.
Publication type:
Article
Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans.
Published in:
Genetics, 2018, v. 208, n. 1, p. 283, doi. 10.1534/genetics.117.300535
By:
- Lansdon, Lisa A.;
- Darbro, Benjamin W.;
- Petrin, Aline L.;
- Hulstrand, Alissa M.;
- Standley, Jennifer M.;
- Brouillette, Rachel B.;
- Long, Abby;
- Mansilla, M. Adela;
- Cornell, Robert A.;
- Murray, Jeffrey C.;
- Houston, Douglas W.;
- Manak, J. Robert
Publication type:
Article
Novel IRF6 mutations in Japanese patients with Van der Woude Syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.
Published in:
Journal of Human Genetics, 2003, v. 48, n. 12, p. 622, doi. 10.1007/s10038-003-0089-0
By:
- Kayano, Shuji;
- Kure, Shigeo;
- Suzuki, Yoichi;
- Kanno, Kiyoshi;
- Aoki, Yoko;
- Kondo, Shinji;
- Schutte, Brian C.;
- Murray, Jeffrey C.;
- Yamada, Atsushi;
- Matsubara, Yoichi
Publication type:
Article
CDH1 Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer.
Published in:
Genes, 2020, v. 11, n. 4, p. 1, doi. 10.3390/genes11040391
By:
- Selvanathan, Arthavan;
- Nixon, Cheng Yee;
- Ying Zhu;
- Scietti, Luigi;
- Forneris, Federico;
- Uribe, Lina M. Moreno;
- Lidral, Andrew C.;
- Jezewski, Peter A.;
- Mulliken, John B.;
- Murray, Jeffrey C.;
- Buckley, Michael F.;
- Cox, Timothy C.;
- Roscioli, Tony
Publication type:
Article
Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data.
Published in:
Journal of Management & Public Policy, 2012, p. 241
By:
- Jugessur, Astanand;
- Gjessing, Håkon K.;
- Wilcox, Allen J.;
- Nguyen, Truc Trung;
- Nilsen, Roy M.;
- Murray, Jeffrey C.;
- Lie, Rolv T.
Publication type:
Article
Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data.
Published in:
Norsk Epidemiologi, 2012, v. 21, n. 2, p. 241, doi. 10.5324/nje.v21i2.1500
By:
- Jugessur, Astanand;
- Gjessing, Håkon K.;
- Wilcox, Allen J.;
- Nguyen, Truc Trung;
- Nilsen, Roy M.;
- Murray, Jeffrey C.;
- Lie, Rolv T.
Publication type:
Article
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.
Published in:
Muscle & Nerve, 1995, v. 18, n. S13, p. S14, doi. 10.1002/mus.880181305
By:
- Wijmenga, Cisca;
- Dauwerse, Hans G.;
- Padberg, George W.;
- Meyer, Nicolle;
- Murray, Jeffrey C.;
- Mills, Kate;
- van Ommen, Gertjan B.;
- Hofker, Marten H.;
- Frants, Rune R.
Publication type:
Article
Mouse myodystrophy ( myd) mutation: Refined mapping in an interval flanked by homology with distal human 4q.
Published in:
Muscle & Nerve, 1995, v. 18, n. S13, p. S98, doi. 10.1002/mus.880181318
By:
- Mathews, Katherine D.;
- Mills, Kathleen A.;
- Bailey, Holly L.;
- Schelper, Robert L.;
- Murray, Jeffrey C.
Publication type:
Article
Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13.
Published in:
1989
By:
- Bell, Graeme I.;
- Murray, Jeffrey C.;
- Nakamura, Yusuke;
- Kayano, Toshiaki;
- Eddy, Roger L.;
- Yao-Shan Fan;
- Byers, Mary G.;
- Shows, Thomas B.;
- Bell, G I;
- Murray, J C;
- Nakamura, Y;
- Kayano, T;
- Eddy, R L;
- Fan, Y S;
- Byers, M G;
- Shows, T B
Publication type:
journal article
Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149].
Published in:
BMC Pediatrics, 2006, v. 6, p. 9, doi. 10.1186/1471-2431-6-9
By:
- Wehby, George L.;
- Castilla, Eduardo E.;
- Goco, Norman;
- Rittler, Monica;
- Cosentino, Viviana;
- Javois, Lorette;
- McCarthy, Ann Marie;
- Bobashev, Georgiy;
- Litavecz, Stephen;
- Mariona, Alejandra;
- Dutra, Graca;
- López-Camelo, Jorge S.;
- Orioli, Iêda M.;
- Murray, Jeffrey C.
Publication type:
Article
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
Published in:
PLoS Genetics, 2021, v. 17, n. 7, p. 1, doi. 10.1371/journal.pgen.1009584
By:
- 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 H.
Publication type:
Article
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
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
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
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
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
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Published in:
Genetic Epidemiology, 2019, v. 43, n. 1, p. 37, doi. 10.1002/gepi.22155
By:
- Bureau, Alexandre;
- Begum, Ferdouse;
- Taub, Margaret A.;
- Hetmanski, Jacqueline B.;
- Parker, Margaret M.;
- Albacha‐Hejazi, Hasan;
- Scott, Alan F.;
- Murray, Jeffrey C.;
- Marazita, Mary L.;
- Bailey‐Wilson, Joan E.;
- Beaty, Terri H.;
- Ruczinski, Ingo
Publication type:
Article
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
Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.
Published in:
Genetic Epidemiology, 2017, v. 41, n. 3, p. 244, doi. 10.1002/gepi.22023
By:
- Xiao, Yanzi;
- Taub, Margaret A.;
- Ruczinski, Ingo;
- Begum, Ferdouse;
- Hetmanski, Jacqueline B.;
- Schwender, Holger;
- Leslie, Elizabeth J.;
- Koboldt, Daniel C.;
- Murray, Jeffrey C.;
- Marazita, Mary L.;
- Beaty, Terri H.
Publication type:
Article
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
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
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
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
Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: Assessing gene-environment interactions in case-parent triads.
Published in:
Genetic Epidemiology, 2003, v. 25, n. 4, p. 367, doi. 10.1002/gepi.10268
By:
- Astanand Jugessur;
- Rolv T. Lie;
- Allen J. Wilcox;
- Jeffrey C. Murray;
- Jack A. Taylor;
- Ola D. Saugstad;
- Hallvard A. Vindenes;
- Frank E. Åbyholm
Publication type:
Article