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B. Solomon · SciRah

Researcher profile · Semantic Scholar

B. Solomon

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B. Solomon — researcher profile on SciRah

h-index: 43
Works: 159
Citations: 7,867

Most-cited papers

Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease
D. Beck, M. Ferrada, K. Sikora, A. Ombrello +58 more
2020New England Journal of Medicine924 citations Open access
Semantic Scholar
A systematic review of antibody mediated immunity to coronaviruses: kinetics, correlates of protection, and association with severity
A. Huang, Bernardo García-Carreras, M. Hitchings, Bing-Yi Yang +13 more
2020Nature Communications725 citations Open access
Semantic Scholar
A systematic review of antibody mediated immunity to coronaviruses: antibody kinetics, correlates of protection, and association of antibody responses with severity of disease
A. Huang, Bernardo García-Carreras, M. Hitchings, Bing-Yi Yang +11 more
2020medRxiv321 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
Strategic vision for improving human health at The Forefront of Genomics
E. Green, C. Gunter, L. Biesecker, V. Di Francesco +26 more
2020Nature278 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
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
MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer
Maegan E. Roberts, S. A. Jackson, Lisa R. Susswein, Nur Zeinomar +10 more
2018Genetics in Medicine152 citations Open access
Semantic Scholar
Helicobacter species are potent drivers of colonic T cell responses in homeostasis and inflammation
Jiani N. Chai, Yang-Qing Peng, Sunaina Rengarajan, B. Solomon +14 more
2017Science immunology145 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
Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer
Kezhi Yan, J. Rousseau, K. Machol, L. Cross +28 more
2020Science Advances102 citations Open access
Semantic Scholar
Analysis of large-language model versus human performance for genetics questions
Dat Van Duong, B. Solomon
2023European Journal of Human Genetics85 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
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations.
J. Johnston, K. Lewis, David Ng, Larry N. Singh +16 more
2015American Journal of Human Genetics71 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
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.
C. Ferreira, Zhi-Jie Xia, A. Clément, David A. Parry +50 more
2018American Journal of Human Genetics67 citations Open access
Semantic Scholar
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly
K. Bear, B. Solomon, S. Antonini, I. J. Arnhold +14 more
2014Journal of Medical Genetics64 citations Open access
Semantic Scholar
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature
Marissa LoPresti, D. Beck, P. Duggal, D. Cummings +1 more
2020medRxiv63 citations Open access
Semantic Scholar
The etiology of VACTERL association: Current knowledge and hypotheses
B. Solomon
2018American Journal of Medical Genetics. Part C, Seminars in Medical Genetics59 citations
Semantic Scholar
Germline pathogenic variants identified in women with ovarian tumors.
Natalie J. Carter, M. Marshall, Lisa R. Susswein, K. Zorn +10 more
2018Gynecologic Oncology51 citations
Semantic Scholar
Management of Secondary Genomic Findings.
Alexander E. Katz, R. Nussbaum, B. Solomon, H. Rehm +2 more
2020American Journal of Human Genetics50 citations Open access
Semantic Scholar
Analysis of Renal Anomalies in VACTERL Association
Bridget K. Cunningham, A. Khromykh, Ariel F. Martinez, T. Carney +2 more
2014Birth defects research. Clinical and molecular teratology50 citations Open access
Semantic Scholar
Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience
Nader I. Al-Dewik, Howaida Mohd, Mariam Al-Mureikhi, R. Ali +13 more
2019American Journal of Medical Genetics. Part A49 citations Open access
Semantic Scholar
Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes
M. Malicdan, T. Vilboux, J. Stephen, D. Maglić +15 more
2015Journal of Medical Genetics48 citations Open access
Semantic Scholar
Antigen specific development of mucosal Foxp3+RORγt+ T cells from regulatory T cell precursors
B. Solomon, Chyi-Song Hsieh
2016Journal of Immunology46 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
Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings.
N. Agochukwu, B. Solomon, M. Muenke
2014International Journal of Pediatric Otorhinolaryngology36 citations
Semantic Scholar
The Ability to Rearrange Dual TCRs Enhances Positive Selection, Leading to Increased Allo- and Autoreactive T Cell Repertoires
Peggy P. Ni, B. Solomon, Chyi-Song Hsieh, P. Allen +1 more
2014Journal of Immunology36 citations Open access
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
Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis
E. Sutcliffe, Amanda Bartenbaker Thompson, A. Stettner, M. Marshall +6 more
2019Familial Cancer34 citations
Semantic Scholar
Human Germline Hedgehog Pathway Mutations Predispose to Fatty Liver
M. J. Guillen Sacoto, Ariel F. Martinez, Yu Abe, P. Kruszka +9 more
2017Journal of Hepatology29 citations Open access
Semantic Scholar
Incidentalomas in genomics and radiology.
B. Solomon
2014New England Journal of Medicine29 citations
Semantic Scholar
Perspectives on the future of dysmorphology
B. Solomon, M. Adam, C. Fong, K. Girisha +7 more
2022American Journal of Medical Genetics. Part A27 citations Open access
Semantic Scholar
Neural Networks for Classification and Image Generation of Aging in Genetic Syndromes
D. Duong, P. Hu, C. Tekendo-Ngongang, Suzanna E. Ledgister Hanchard +3 more
2021Frontiers in Genetics27 citations Open access
Semantic Scholar
Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling
E. Roessler, P. Hu, J. Marino, Sungkook Hong +14 more
2018Human Mutation25 citations Open access
Semantic Scholar
Clinical genetics and genomic medicine in Qatar
Nader I. Al-Dewik, Mariam Al-Mureikhi, Noora Shahbeck, R. Ali +10 more
2018Molecular Genetics & Genomic Medicine24 citations Open access
Semantic Scholar
Should all babies have their genome sequenced at birth?
L. Biesecker, E. Green, T. Manolio, B. Solomon +1 more
2021British medical journal20 citations Open access
Semantic Scholar
Increased risk of rheumatoid arthritis among mothers with children who carry DRB1 risk-associated alleles
Giovanna I. Cruz, X. Shao, Hong L. Quach, Kimberly A. Ho +10 more
2017Annals of the Rheumatic Diseases20 citations Open access
Semantic Scholar
Aberrant splicing induced by the most common EPG5 mutation in an individual with Vici syndrome.
Megan S. Kane, T. Vilboux, L. Wolfe, Paul R. Lee +5 more
2016Brain : a journal of neurology20 citations Open access
Semantic Scholar
Scoping review and classification of deep learning in medical genetics
Suzanna E. Ledgister Hanchard, Michelle Dwyer, Simon Liu, P. Hu +4 more
2022Genetics in Medicine19 citations Open access
Semantic Scholar
Neural network classifiers for images of genetic conditions with cutaneous manifestations
Dat Van Duong, R. Waikel, P. Hu, C. Tekendo-Ngongang +1 more
2021HGG advances19 citations Open access
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
Interference of nuclear mitochondrial DNA segments in mitochondrial DNA testing resembles biparental transmission of mitochondrial DNA in humans
Renkui Bai, H. Cui, J. Devaney, Katrina Allis +13 more
2021Genetics 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
Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes
C. Tekendo-Ngongang, Angela R. Grochowsky, B. Solomon, Sho T. Yano
2021Genes16 citations Open access
Semantic Scholar
Obstacles and opportunities for the future of genomic medicine
B. Solomon
2014Molecular Genetics & Genomic Medicine16 citations Open access
Semantic Scholar
The utility of exome sequencing for fetal pleural effusions
A. Jelin, N. Sobreira, Elizabeth Wohler, B. Solomon +8 more
2020Prenatal Diagnosis15 citations Open access
Semantic Scholar
A Child's HLA-DRB1 Genotype Increases Maternal Risk of Systemic Lupus Erythematosus
Giovanna I. Cruz, X. Shao, Hong L. Quach, Kimberly A. Ho +10 more
2016Journal of Autoimmunity15 citations Open access
Semantic Scholar
The Benefits of Whole-Genome Sequencing Now and in the Future
A. Khromykh, B. Solomon
2015Molecular Syndromology15 citations Open access
Semantic Scholar

Frequent co-authors

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J. Niederhuber×14
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J. Niederhuber — researcher profile on SciRah
D. Bodian×11
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D. Bodian — researcher profile on SciRah
A. Khromykh×9
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A. Khromykh — researcher profile on SciRah
J. Vockley×8
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J. Vockley — researcher profile on SciRah

Wendy S. W. Wong

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Wendy S. W. Wong — researcher profile on SciRah

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R. Iyer — researcher profile on SciRah

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T. Vilboux — researcher profile on SciRah

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Kathi Huddleston — researcher profile on SciRah

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R. Baveja — researcher profile on SciRah

C. Tekendo-Ngongang×5

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C. Tekendo-Ngongang — researcher profile on SciRah

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J. Mullikin — researcher profile on SciRah

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W. Gahl — researcher profile on SciRah