16S gut community of the Cameron County Hispanic Cohort

by Ross, Matthew C, Muzny, Donna M, McCormick, Joseph B, Gibbs, Richard A, Fisher-Hoch, Susan P, Petrosino, Joseph F
Published 2015

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders

by Schaaf, Christian P., Sabo, Aniko, Sakai, Yasunari, Crosby, Jacy, Muzny, Donna, Hawes, Alicia, Lewis, Lora, Akbar, Humeira, Varghese, Robin, Boerwinkle, Eric, Gibbs, Richard A., Zoghbi, Huda Y.
Published 2011

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities

by Bainbridge, Matthew N, Wang, Min, Wu, Yuanqing, Newsham, Irene, Muzny, Donna M, Jefferies, John L, Albert, Thomas J, Burgess, Daniel L, Gibbs, Richard A
Published 2011

Genetic diversity in India and the inference of Eurasian population expansion

by Xing, Jinchuan, Watkins, W Scott, Hu, Ya, Huff, Chad D, Sabo, Aniko, Muzny, Donna M, Bamshad, Michael J, Gibbs, Richard A, Jorde, Lynn B, Yu, Fuli
Published 2010

Complete Genome Sequence of Elephant Endotheliotropic Herpesvirus 1A

by Ling, Paul D., Reid, Jeffrey G., Qin, Xiang, Muzny, Donna M., Gibbs, Richard, Petrosino, Joseph, Peng, RongSheng, Zong, Jian-Chao, Heaggans, Sarah Y., Hayward, Gary S.
Published 2013

Whole Genome Sequence of Treponema pallidum ssp. pallidum, Strain Mexico A, Suggests Recombination between Yaws and Syphilis Strains

by Pětrošová, Helena, Zobaníková, Marie, Čejková, Darina, Mikalová, Lenka, Pospíšilová, Petra, Strouhal, Michal, Chen, Lei, Qin, Xiang, Muzny, Donna M., Weinstock, George M., Šmajs, David
Published 2012

Mind the Gap: Upgrading Genomes with Pacific Biosciences RS Long-Read Sequencing Technology

by English, Adam C., Richards, Stephen, Han, Yi, Wang, Min, Vee, Vanesa, Qu, Jiaxin, Qin, Xiang, Muzny, Donna M., Reid, Jeffrey G., Worley, Kim C., Gibbs, Richard A.
Published 2012

Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull’s Eye Maculopathy

by Collison, Frederick T., Xie, Yajing (Angela), Gambin, Tomasz, Jhangiani, Shalini, Muzny, Donna, Gibbs, Richard, Lupski, James R., Fishman, Gerald A., Allikmets, Rando
Published 2015

Loss-of-function variants influence the human serum metabolome

by Yu, Bing, Li, Alexander H., Metcalf, Ginger A., Muzny, Donna M., Morrison, Alanna C., White, Simon, Mosley, Thomas H., Gibbs, Richard A., Boerwinkle, Eric
Published 2016

Draft genome sequences and description of Lactobacillus rhamnosus strains L31, L34, and L35

by Boonma, Prapaporn, Spinler, Jennifer K., Qin, Xiang, Jittaprasatsin, Chutima, Muzny, Donna M., Doddapaneni, Harsha, Gibbs, Richard, Petrosino, Joe, Tumwasorn, Somying, Versalovic, James
Published 2014

The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes

by Challis, Danny, Antunes, Lilian, Garrison, Erik, Banks, Eric, Evani, Uday S, Muzny, Donna, Poplin, Ryan, Gibbs, Richard A, Marth, Gabor, Yu, Fuli
Published 2015

Complete Genome Sequence of Treponema paraluiscuniculi, Strain Cuniculi A: The Loss of Infectivity to Humans Is Associated with Genome Decay

by Šmajs, David, Zobaníková, Marie, Strouhal, Michal, Čejková, Darina, Dugan-Rocha, Shannon, Pospíšilová, Petra, Norris, Steven J., Albert, Tom, Qin, Xiang, Hallsworth-Pepin, Kym, Buhay, Christian, Muzny, Donna M., Chen, Lei, Gibbs, Richard A., Weinstock, George M.
Published 2011

Whole Genome Sequences of Three Treponema pallidum ssp. pertenue Strains: Yaws and Syphilis Treponemes Differ in Less than 0.2% of the Genome Sequence

by Čejková, Darina, Zobaníková, Marie, Chen, Lei, Pospíšilová, Petra, Strouhal, Michal, Qin, Xiang, Mikalová, Lenka, Norris, Steven J., Muzny, Donna M., Gibbs, Richard A., Fulton, Lucinda L., Sodergren, Erica, Weinstock, George M., Šmajs, David
Published 2012

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

by Bainbridge, Matthew N, Hu, Hao, Muzny, Donna M, Musante, Luciana, Lupski, James R, Graham, Brett H, Chen, Wei, Gripp, Karen W, Jenny, Kim, Wienker, Thomas F, Yang, Yaping, Sutton, V Reid, Gibbs, Richard A, Ropers, H Hilger
Published 2013

Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy

by Lupski, James R, Gonzaga-Jauregui, Claudia, Yang, Yaping, Bainbridge, Matthew N, Jhangiani, Shalini, Buhay, Christian J, Kovar, Christie L, Wang, Min, Hawes, Alicia C, Reid, Jeffrey G, Eng, Christine, Muzny, Donna M, Gibbs, Richard A
Published 2013

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

by Reid, Jeffrey G, Carroll, Andrew, Veeraraghavan, Narayanan, Dahdouli, Mahmoud, Sundquist, Andreas, English, Adam, Bainbridge, Matthew, White, Simon, Salerno, William, Buhay, Christian, Yu, Fuli, Muzny, Donna, Daly, Richard, Duyk, Geoff, Gibbs, Richard A, Boerwinkle, Eric
Published 2014

Whole Genome Sequence-Based Analysis of a Model Complex Trait, High Density Lipoprotein Cholesterol

by Morrison, Alanna C., Voorman, Arend, Johnson, Andrew D., Liu, Xiaoming, Yu, Jin, Li, Alexander, Muzny, Donna, Yu, Fuli, Rice, Kenneth, Zhu, Chengsong, Bis, Joshua, Heiss, Gerardo, O’Donnell, Christopher J., Psaty, Bruce M., Cupples, L. Adrienne, Gibbs, Richard, Boerwinkle, Eric
Published 2013

Structural variation and missense mutation in SBDS associated with Shwachman-Diamond syndrome

by Carvalho, Claudia M B, Zuccherato, Luciana W, Williams, Christopher L, Neill, Nicholas J, Murdock, David R, Bainbridge, Matthew, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Ip, Wan, Guillerman, Robert Paul, Lupski, James R, Bertuch, Alison A
Published 2014

Structure and function of the healthy pre-adolescent pediatric gut microbiome

by Hollister, Emily B., Riehle, Kevin, Luna, Ruth Ann, Weidler, Erica M., Rubio-Gonzales, Michelle, Mistretta, Toni-Ann, Raza, Sabeen, Doddapaneni, Harsha V., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Petrosino, Joseph F., Shulman, Robert J., Versalovic, James
Published 2015

Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome

by Polfus, Linda M., Boerwinkle, Eric, Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Grove, Megan, Shete, Sanjay, Wallace, Stephanie, Milewicz, Dianna, Hanchard, Neil, Lupski, James R., Hashmi, Syed Shahrukh, Gupta-Malhotra, Monesha
Published 2016