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D. Bodian · SciRah

Researcher profile · Semantic Scholar

D. Bodian

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D. Bodian — researcher profile on SciRah

h-index: 30
Works: 63
Citations: 4,408

Most-cited papers

cell type–specific gene expression differences in complex tissues
S. Shen-Orr, R. Tibshirani, P. Khatri, D. Bodian +6 more
2010Nature Methods520 citations Open access
Semantic Scholar
Molecular docking using shape descriptors
Brian K. Shoichet, I. D. Kuntz, D. Bodian
1992422 citations
Semantic Scholar
Identification of a family of cAMP response element-binding protein coactivators by genome-scale functional analysis in mammalian cells
V. Iourgenko, Wenjun Zhang, C. Mickanin, Ira Daly +17 more
2003Proceedings of the National Academy of Sciences of the United States of America381 citations Open access
Semantic Scholar
Parent-of-origin-specific signatures of de novo mutations
J. Goldmann, Wendy S. W. Wong, M. Pinelli, T. Farrah +11 more
2016Nature Genetics308 citations
Semantic Scholar
Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population.
D. Beck, D. Bodian, Vandan Shah, U. Mirshahi +14 more
2023Journal of the American Medical Association (JAMA)216 citations Open access
Semantic Scholar
New observations on maternal age effect on germline de novo mutations
Wendy S. W. Wong, B. Solomon, D. Bodian, Prachi Kothiyal +7 more
2016Nature Communications208 citations Open access
Semantic Scholar
Whole Genome Sequencing of a Healthy Aging Cohort
Galina A. Erikson, D. Bodian, M. Rueda, Bhuvan Molparia +7 more
2016Cell203 citations Open access
Semantic Scholar
Inhibition of the fusion-inducing conformational change of influenza hemagglutinin by benzoquinones and hydroquinones.
D. Bodian, R. Yamasaki, R. Buswell, J. Stearns +2 more
1993Biochemistry185 citations
Semantic Scholar
Mutations in NOTCH1 cause Adams-Oliver syndrome.
Anna-Barbara Stittrich, A. Lehman, D. Bodian, J. Ashworth +15 more
2014American Journal of Human Genetics184 citations Open access
Semantic Scholar
Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates
B. Solomon, D. Bodian, A. Khromykh, R. Hastak +13 more
2015Genetics in Medicine139 citations Open access
Semantic Scholar
Crystal structure of the extracellular region of the human cell adhesion molecule CD2 at 2.5 A resolution.
D. Bodian, E. Jones, K. Harlos, D. I. Stuart +1 more
1994Structure137 citations Open access
Semantic Scholar
Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships
D. Bodian, T. Chan, A. Poon, U. Schwarze +4 more
2008Human Molecular Genetics126 citations Open access
Semantic Scholar
Intermonomer disulfide bonds impair the fusion activity of influenza virus hemagglutinin
G. Kemble, D. Bodian, J. K. Rose, I. Wilson +1 more
1992Journal of Virology109 citations Open access
Semantic Scholar
Mutational Analysis of the Active Site and Antibody Epitopes of the Complement-inhibitory Glycoprotein, CD59
D. Bodian, Simon J. Davis, B. Morgan, Neil K. Rushmere
1997Journal of Experimental Medicine100 citations Open access
Semantic Scholar
Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing
D. Bodian, Justine N. McCutcheon, Prachi Kothiyal, Kathi Huddleston +3 more
2014PLoS ONE98 citations Open access
Semantic Scholar
Predicting the clinical lethality of osteogenesis imperfecta from collagen glycine mutations.
D. Bodian, B. Madhan, B. Brodsky, Teri E. Klein
2008Biochemistry79 citations Open access
Semantic Scholar
A Splice Variant of β-Secretase Deficient in the Amyloidogenic Processing of the Amyloid Precursor Protein*
U. Bodendorf, Frauke Fischer, D. Bodian, G. Multhaup +1 more
2001Journal of Biological Chemistry74 citations Open access
Semantic Scholar
Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence
J. Goldmann, V. Seplyarskiy, Wendy S. W. Wong, T. Vilboux +7 more
2018Nature Genetics72 citations Open access
Semantic Scholar
Genomic and molecular characterization of preterm birth
T. Knijnenburg, J. Vockley, N. Chambwe, D. Gibbs +27 more
2019Proceedings of the National Academy of Sciences of the United States of America68 citations Open access
Semantic Scholar
Ligand Binding by the Immunoglobulin Superfamily Recognition Molecule CD2 Is Glycosylation-independent (*)
Simon J. Davis, Elizabeth A. Davies, A. N. Barclay, S. Daenke +6 more
1995Journal of Biological Chemistry65 citations Open access
Semantic Scholar
GENE-CENTRIC ANALYSIS OF PREECLAMPSIA IDENTIFIES MATERNAL ASSOCIATION AT PLEKHG1
K. J. Gray, V. Kovacheva, H. Mirzakhani, A. Bjonnes +19 more
2018HYPERTENSION55 citations Open access
Semantic Scholar
Development of comprehensive functional genomic screens to identify novel mediators of osteoarthritis.
Sherif Daouti, Brian Jude Latario, S. Nagulapalli, Frank P. Buxton +8 more
2005Osteoarthritis and Cartilage51 citations Open access
Semantic Scholar
Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
A. Deaton, M. Parker, L. D. Ward, A. Flynn-Carroll +89 more
2021Scientific Reports43 citations Open access
Semantic Scholar
Leveraging population‐based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project
M. Kelly, J. Leader, K. Wain, D. Bodian +4 more
2021American Journal of Medical Genetics. Part C, Seminars in Medical Genetics42 citations
Semantic Scholar
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth
Nadav Rappoport, J. Toung, D. Hadley, R. Wong +30 more
2018Scientific Reports41 citations Open access
Semantic Scholar
Expanding the phenotypic spectrum in EP300‐related Rubinstein–Taybi syndrome
B. Solomon, D. Bodian, A. Khromykh, Gabriela Gomez Mora +5 more
2015American Journal of Medical Genetics. Part A39 citations
Semantic Scholar
Identification of residues in CD6 which are critical for ligand binding.
D. Bodian, J. Skonier, Michael A. Bowen, Michael Neubauer +3 more
1997Biochemistry39 citations
Semantic Scholar
Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn
A. Pavey, D. Bodian, T. Vilboux, A. Khromykh +8 more
2017Genetics in Medicine35 citations Open access
Semantic Scholar
Genetic Variants That Presdispose to DNA Double-strand Breaks in Lymphocytes from a Subset of Patients With Familial Colorectal Carcinomas
S. Arora, Hong Yan, Iltaeg Cho, Hua-Ying Fan +14 more
2015Gastroenterology33 citations Open access
Semantic Scholar
Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone
Michael E. Dunn, A. Kithcart, Jee Hae Kim, A. Ho +188 more
2024Nature31 citations Open access
Semantic Scholar
Expression cloning of an equine T-lymphocyte glycoprotein CD2 cDNA. Structure-based analysis of conserved sequence elements.
Angela S. Tavernor, J. Kydd, D. Bodian, E. Jones +3 more
1994European Journal of Biochemistry27 citations
Semantic Scholar
MOLECULAR DYNAMICS SIMULATIONS OF THE FULL TRIPLE HELICAL REGION OF COLLAGEN TYPE I PROVIDE AN ATOMIC SCALE VIEW OF THE PROTEIN’S REGIONAL HETEROGENEITY
D. Bodian, Randall J. Radmer, S. Holbert, Teri E. Klein
2011Pacific Symposium on Biocomputing24 citations Open access
Semantic Scholar
Identification of copy number variants in whole-genome data using Reference Coverage Profiles
Gwênlyn Glusman, Alissa L. Severson, V. Dhankani, Max Robinson +11 more
2015Frontiers in Genetics23 citations Open access
Semantic Scholar
Mutational analysis of the CD6 ligand binding domain.
J. Skonier, D. Bodian, J. Emswiler, Michael A. Bowen +2 more
1997Protein Engineering22 citations
Semantic Scholar
Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy
D. Bodian, T. Vilboux, Suchitra K. Hourigan, Callie Jenevein +5 more
2017Cold Spring Harbor molecular case studies19 citations Open access
Semantic Scholar
Diagnosis of an imprinted-gene syndrome by a novel bioinformatics analysis of whole-genome sequences from a family trio
D. Bodian, B. Solomon, A. Khromykh, D. Thach +6 more
2014Molecular Genetics & Genomic Medicine18 citations Open access
Semantic Scholar
Pitfalls of clinical exome and gene panel testing: alternative transcripts
D. Bodian, Prachi Kothiyal, N. Hauser
2018Genetics in Medicine17 citations Open access
Semantic Scholar
Experience with genomic sequencing in pediatric patients with congenital cardiac defects in a large community hospital
N. Hauser, B. Solomon, T. Vilboux, A. Khromykh +2 more
2018Molecular Genetics & Genomic Medicine17 citations Open access
Semantic Scholar
Tools for annotation and comparison of structural variation
F. Sedlazeck, Andi Dhroso, D. Bodian, J. Paschall +2 more
2017F1000Research16 citations Open access
Semantic Scholar
Systematic evaluation of underlying defects in DNA repair as an approach to case-only assessment of familial prostate cancer
E. Nicolas, S. Arora, Yan Zhou, I. Serebriiskii +11 more
2015OncoTarget16 citations Open access
Semantic Scholar
COLdb, a database linking genetic data to molecular function in fibrillar collagens
D. Bodian, Teri E. Klein
2009Human Mutation16 citations Open access
Semantic Scholar
Analysis of the structure and interactions of CD2.
Simon J. Davis, E. Jones, D. Bodian, A. Barclay +1 more
1993Biochemical Society Transactions16 citations
Semantic Scholar
Mutation in an alternative transcript of CDKL5 in a boy with early-onset seizures
D. Bodian, John M. Schreiber, T. Vilboux, A. Khromykh +1 more
2018Cold Spring Harbor molecular case studies12 citations Open access
Semantic Scholar
Moving Beyond Clinical Risk Scores with a Mobile App for the Genomic Risk of Coronary Artery Disease
E. Muse, Nathan E. Wineinger, Brian Schrader, Bhuvan Molparia +4 more
2017bioRxiv11 citations Open access
Semantic Scholar
Genotype-first analysis of a generally healthy population cohort supports genetic testing for diagnosis of hereditary angioedema of unknown cause
D. Bodian, T. Vilboux, N. Hauser
2019Allergy, Asthma & Clinical Immunology10 citations Open access
Semantic Scholar
Diagnosis of D-Bifunctional Protein Deficiency through Whole-Genome Sequencing: Implications for Cost-Effective Care
A. Khromykh, B. Solomon, D. Bodian, Eyby Leon +6 more
2015Molecular Syndromology9 citations Open access
Semantic Scholar
Mendelian Inconsistent Signatures from 1314 Ancestrally Diverse Family Trios Distinguish Biological Variation from Sequencing Error
Prachi Kothiyal, Wendy S. W. Wong, D. Bodian, J. Niederhuber
2019J. Comput. Biol.7 citations Open access
Semantic Scholar
Author Correction: Parent-of-origin-specific signatures of de novo mutations
J. Goldmann, Wendy S. W. Wong, M. Pinelli, T. Farrah +11 more
2018Nature Genetics7 citations Open access
Semantic Scholar
Mutational analysis of the CD 6 ligand binding domain
J. Skonier, D. Bodian, J. Emswiler, M. A. Bowen +2 more
19976 citations
Semantic Scholar
Germline de novo mutation clusters arise during oocyte aging in genomic regions with increased double-strand break incidence
J. Goldmann, V. Seplyarskiy, Wendy S. W. Wong, T. Vilboux +6 more
2017bioRxiv4 citations Open access
Semantic Scholar

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