MOLECULAR DYNAMICS SIMULATIONS OF THE FULL TRIPLE HELICAL REGION OF COLLAGEN TYPE I PROVIDE AN ATOMIC SCALE VIEW OF THE PROTEIN’S REGIONAL HETEROGENEITY

Por BODIAN, DALE L., RADMER, RANDALL J., HOLBERT, SEAN, KLEIN, TERI E.
Publicado no Pac Symp Biocomput (2011)

Mutational Analysis of the Active Site and Antibody Epitopes of the Complement-inhibitory Glycoprotein, CD59

Por Bodian, Dale L., Davis, Simon J., Morgan, B. Paul, Rushmere, Neil K.
Publicado em 1997

Mutation in an alternative transcript of CDKL5 in a boy with early-onset seizures

Por Bodian, Dale L., Schreiber, John M., Vilboux, Thierry, Khromykh, Alina, Hauser, Natalie S.
Publicado no Cold Spring Harb Mol Case Stud (2018)

Experience with genomic sequencing in pediatric patients with congenital cardiac defects in a large community hospital

Por Hauser, Natalie S., Solomon, Benjamin D., Vilboux, Thierry, Khromykh, Alina, Baveja, Rajiv, Bodian, Dale L.
Publicado no Mol Genet Genomic Med (2018)

CD80 (B7-1) Binds Both CD28 and CTLA-4 with a Low Affinity and Very Fast Kinetics

Por van der Merwe, P.  Anton, Bodian, Dale L., Daenke, Susan, Linsley, Peter, Davis, Simon J.
Publicado em 1997

Tools for annotation and comparison of structural variation

Por Sedlazeck, Fritz J., Dhroso, Andi, Bodian, Dale L., Paschall, Justin, Hermes, Farrah, Zook, Justin M.
Publicado no F1000Res (2017)

Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships

Por Bodian, Dale L., Chan, Ting-Fung, Poon, Annie, Schwarze, Ulrike, Yang, Kathleen, Byers, Peter H., Kwok, Pui-Yan, Klein, Teri E.
Publicado em 2009

Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships

Por Bodian, Dale L., Chan, Ting-Fung, Poon, Annie, Schwarze, Ulrike, Yang, Kathleen, Byers, Peter H., Kwok, Pui-Yan, Klein, Teri E.
Publicado em 2009

Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing

Por Bodian, Dale L., McCutcheon, Justine N., Kothiyal, Prachi, Huddleston, Kathi C., Iyer, Ramaswamy K., Vockley, Joseph G., Niederhuber, John E.
Publicado em 2014

Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy

Por Bodian, Dale L., Vilboux, Thierry, Hourigan, Suchitra K., Jenevein, Callie L., Mani, Haresh, Kent, Kathleen C., Khromykh, Alina, Solomon, Benjamin D., Hauser, Natalie S.
Publicado no Cold Spring Harb Mol Case Stud (2017)

cell type–specific gene expression differences in complex tissues

Por Shen-Orr, Shai S, Tibshirani, Robert, Khatri, Purvesh, Bodian, Dale L, Staedtler, Frank, Perry, Nicholas M, Hastie, Trevor, Sarwal, Minnie M, Davis, Mark M, Butte, Atul J
Publicado em 2010

Diagnosis of an imprinted-gene syndrome by a novel bioinformatics analysis of whole-genome sequences from a family trio

Por Bodian, Dale L, Solomon, Benjamin D, Khromykh, Alina, Thach, Dzung C, Iyer, Ramaswamy K, Link, Kathleen, Baker, Robin L, Baveja, Rajiv, Vockley, Joseph G, Niederhuber, John E
Publicado no Mol Genet Genomic Med (2014)

Diagnosis of D-Bifunctional Protein Deficiency through Whole-Genome Sequencing: Implications for Cost-Effective Care

Por Khromykh, Alina, Solomon, Benjamin D., Bodian, Dale L., Leon, Eyby L., Iyer, Ramaswamy K., Baker, Robin L., Ascher, David P., Baveja, Rajiv, Vockley, Joseph G., Niederhuber, John E.
Publicado no Mol Syndromol (2015)

New observations on maternal age effect on germline de novo mutations

Por Wong, Wendy S. W., Solomon, Benjamin D., Bodian, Dale L., Kothiyal, Prachi, Eley, Greg, Huddleston, Kathi C., Baker, Robin, Thach, Dzung C., Iyer, Ramaswamy K., Vockley, Joseph G., Niederhuber, John E.
Publicado no Nat Commun (2016)

Whole Genome Sequencing of a Healthy Aging Cohort

Por Erikson, Galina A., Bodian, Dale L., Rueda, Manuel, Molparia, Bhuvan, Scott, Erick R., Scott-Van Zeeland, Ashley A., Topol, Sarah E., Wineinger, Nathan E., Niederhuber, John E., Topol, Eric J., Torkamani, Ali
Publicado no Cell (2016)

Identification of copy number variants in whole-genome data using Reference Coverage Profiles

Por Glusman, Gustavo, Severson, Alissa, Dhankani, Varsha, Robinson, Max, Farrah, Terry, Mauldin, Denise E., Stittrich, Anna B., Ament, Seth A., Roach, Jared C., Brunkow, Mary E., Bodian, Dale L., Vockley, Joseph G., Shmulevich, Ilya, Niederhuber, John E., Hood, Leroy
Publicado no Front Genet (2015)

Systematic evaluation of underlying defects in DNA repair as an approach to case-only assessment of familial prostate cancer

Por Nicolas, Emmanuelle, Arora, Sanjeevani, Zhou, Yan, Serebriiskii, Ilya G., Andrake, Mark D., Handorf, Elizabeth D., Bodian, Dale L., Vockley, Joseph G., Dunbrack, Roland L., Ross, Eric A., Egleston, Brian L., Hall, Michael J., Golemis, Erica A., Giri, Veda N., Daly, Mary B.
Publicado no Oncotarget (2015)

Genetic Variants That Presdispose to DNA Double-strand Breaks in Lymphocytes from a Subset of Patients With Familial Colorectal Carcinomas

Por Arora, Sanjeevani, Yan, Hong, Cho, Iltaeg, Fan, Hua-Ying, Luo, Biao, Gai, Xiaowu, Bodian, Dale L., Vockley, Joseph G., Zhou, Yan, Handorf, Elizabeth, Egleston, Brian L., Andrake, Mark, Nicolas, Emmanuelle, Serebriiskii, Ilya, Yen, Timothy J., Hall, Michael J., Golemis, Erica A., Enders, Greg H.
Publicado no Gastroenterology (2015)

Mutations in NOTCH1 Cause Adams-Oliver Syndrome

Por Stittrich, Anna-Barbara, Lehman, Anna, Bodian, Dale L., Ashworth, Justin, Zong, Zheyuan, Li, Hong, Lam, Patricia, Khromykh, Alina, Iyer, Ramaswamy K., Vockley, Joseph G., Baveja, Rajiv, Silva, Ermelinda Santos, Dixon, Joanne, Leon, Eyby L., Solomon, Benjamin D., Glusman, Gustavo, Niederhuber, John E., Roach, Jared C., Patel, Millan S.
Publicado em 2014

GENE-CENTRIC ANALYSIS OF PREECLAMPSIA IDENTIFIES MATERNAL ASSOCIATION AT PLEKHG1

Por Gray, Kathryn J., Kovacheva, Vesela P., Mirzakhani, Hooman, Bjonnes, Andrew C., Almoguera, Berta, DeWan, Andrew T., Triche, Elizabeth W., Saftlas, Audrey F., Hoh, Josephine, Bodian, Dale L., Klein, Elisabeth, Huddleston, Kathi C., Ingles, Sue Ann, Lockwood, Charles J., Hakonarson, Hakon, McElrath, Thomas F., Murray, Jeffrey C., Wilson, Melissa L., Norwitz, Errol R., Karumanchi, S. Ananth, Bateman, Brian T., Keating, Brendan J., Saxena, Richa
Publicado no Hypertension (2018)