Absence of Significant Linkage between Phonological Coding Dyslexia and Chromosome 6p23-21.3, as Determined by Use of Quantitative-Trait Methods: Confirmation of Qualitative Analys...

Por Petryshen, Tracey L., Kaplan, Bonnie J., Liu, Ming Fu, Field, L. Leigh
Publicado em 2000

Absence of Age Effect on Meiotic Recombination between Human X and Y Chromosomes

Por Shi, Qinghua, Spriggs, Elizabeth, Field, L. Leigh, Rademaker, Alfred, Ko, Evelyn, Barclay, Leona, Martin, Renée H.
Publicado em 2002

Genome Scan for Loci Involved in Cleft Lip With or Without Cleft Palate, in Chinese Multiplex Families

Por Marazita, Mary L., Field, L. Leigh, Cooper, Margaret E., Tobias, Rose, Maher, Brion S., Peanchitlertkajorn, Supakit, Liu, You-e
Publicado em 2002

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

Por 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
Publicado em 2009

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 Res...

Por 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
Publicado em 2009

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate

Por Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Buxó, Carmen J., Castilla, Eduardo E., 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., Feingold, Eleanor, Weinberg, Seth M., Murray, Jeffrey C., Marazita, Mary L.
Publicado no Am J Med Genet A (2017)

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

Por Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Butali, Azeez, Buxó, Carmen J., Castilla, Eduardo E., Christensen, Kaare, Deleyiannis, Fred W.-B., Field, L. Leigh, 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 L.
Publicado no Hum Genet (2017)

Whole Exome Sequencing of Distant Relatives in Multiplex Families Implicates Rare Variants in Candidate Genes for Oral Clefts

Por Bureau, Alexandre, Parker, Margaret M., Ruczinski, Ingo, Taub, Margaret A., Marazita, Mary L., Murray, Jeffrey C., Mangold, Elisabeth, Noethen, Markus M., Ludwig, Kirsten U., Hetmanski, Jacqueline B., Bailey-Wilson, Joan E., Cropp, Cheryl D., Li, Qing, Szymczak, Silke, Albacha-Hejazi, Hasan, Alqosayer, Khalid, Field, L. Leigh, Wu-Chou, Yah-Huei, Doheny, Kimberly F., Ling, Hua, Scott, Alan F., Beaty, Terri H.
Publicado em 2014

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

Por Carlson, Jenna C., Standley, Jennifer, Petrin, Aline, Shaffer, John R., Butali, Azeez, Buxo, Carmen J., Castilla, Eduardo, Christensen, Kaare, Deleyiannis, Frederic W-D, Hecht, Jacqueline T., Field, L. Leigh, Garidkhuu, Ariuntuul, Moreno Uribe, Lina M., Nagato, Natsume, Orioli, Ieda M., Padilla, Carmencita, Poletta, Fernando, Suzuki, Satoshi, Vieira, Alexandre R., Wehby, George L., Weinberg, Seth M., Beaty, Terri H., Feingold, Eleanor, Murray, Jeffrey C., Marazita, Mary L., Leslie, Elizabeth J.
Publicado no Genet Epidemiol (2017)

Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35

Por Marazita, Mary L., Murray, Jeffrey C., Lidral, Andrew C., Arcos-Burgos, Mauricio, Cooper, Margaret E., Goldstein, Toby, Maher, Brion S., Daack-Hirsch, Sandra, Schultz, Rebecca, Mansilla, M. Adela, Field, L. Leigh, Liu, You-e, Prescott, Natalie, Malcolm, Sue, Winter, Robin, Ray, Ajit, Moreno, Lina, Valencia, Consuelo, Neiswanger, Katherine, Wyszynski, Diego F., Bailey-Wilson, Joan E., Albacha-Hejazi, Hasan, Beaty, Terri H., McIntosh, Iain, Hetmanski, Jacqueline B., Tunçbilek, Gökhan, Edwards, Matthew, Harkin, Louise, Scott, Rodney, Roddick, Laurence G.
Publicado em 2004

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

Por Beaty, Terri H, Murray, Jeffrey C, Marazita, Mary L, Munger, Ronald G, Ruczinski, Ingo, Hetmanski, 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, Menezes, Renato, Vieira, Alexandre R, Petrin, Aline, Wilcox, Allen J, Lie, Rolv T, Jabs, Ethylin W, Wu-Chou, Yah Huei, Chen, Philip K, Wang, Hong, Ye, Xiaoqian, Huang, Shangzhi, Yeow, Vincent, Chong, Samuel S, Jee, Sun Ha, Shi, Bing, Christensen, Kaare, Kimberly, Doheny, Pugh Elizabeth, W, Hua, Ling, Castilla Eduardo, E, Czeizel, Andrew E, Ma, Lian, Field, L Leigh, Brody, Lawrence, Pangilinan, Faith, Mills, James L, Molloy, Anne M, Kirke, Peadar N, Scott, John M, Arcos-Burgos, Mauricio, Scott, Alan F
Publicado em 2010

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13

Por Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Czeizel, Andrew E., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria, C., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Abate, Fikre, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Murray, Jeffrey C., Marazita, Mary L.
Publicado no Hum Mol Genet (2016)

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

Por Leslie, Elizabeth J., Liu, Huan, Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Standley, Jennifer, Czeizel, Andrew E., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria C., Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Deribew, Milliard, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Cornell, Robert A., Murray, Jeffrey C., Marazita, Mary L.
Publicado no Am J Hum Genet (2016)