Benjamin D. Solomon - Concepedia

Author

Benjamin D. Solomon

National Human Genome Research Institute ORCID

Also Known As

B D Solomon, B. Solomon, B.D. Solomon, Benjamin D Solomon, Benjamin D. Solomon, Benjamin Solomon, Benjamin D. Solomon, Hardisty, Emily E., John E. Niederhuber, Lilianna Solnica-Krezel

214

Publications

9.4K

Citations

H-Index

155

Concepts

All Affiliations

National Human Genome Research Institute National Institutes of Health Inova Health System Inova Children's Hospital Howard Hughes Medical Institute

About

Benjamin D. Solomon is an author at National Human Genome Research Institute specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	41	2.7K
2	Engineering	3	3	58
3	Health Sciences	3	3	67
4	Arts	1	1	11
5	Language Studies	1	1	131

Benjamin D. Solomon

Publications

5.7K

Citations

H-Index

Page 1

	Year	Citations
Somatic Mutations in <i>UBA1</i> and Severe Adult-Onset Autoinflammatory Disease David B. Beck, Marcela A. Ferrada, Keith A. Sikora, New England Journal of Medicine	2020	1.1K
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries Michael E. Talkowski, Jill A. Rosenfeld, Ian Blumenthal, Cell Developmental AnomalyConfer RiskDevelopmental BiologyMendelian DisorderGenetic Disorder	2012	586
Parent-of-origin-specific signatures of de novo mutations Jakob M. Goldmann, Wendy S.W. Wong, Michele Pinelli, Nature Genetics Somatic VariantGeneticsMolecular GeneticsParent-of-origin-specific SignaturesDisease Gene Identification	2016	359
New observations on maternal age effect on germline de novo mutations Wendy S.W. Wong, Benjamin D. Solomon, Dale L. Bodian, Nature Communications	2016	217
MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer Maegan E. Roberts, Sarah A. Jackson, Lisa R. Susswein, Genetics in Medicine	2018	168
Clinical Genomic Database Benjamin D. Solomon, Anh‐Dao Nguyen, Kelly Bear, Proceedings of the National Academy of Sciences	2013	147
Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates Dale L. Bodian, Elisabeth Klein, Ramaswamy K. Iyer, Genetics in Medicine	2015	133
Analysis of large-language model versus human performance for genetics questions Dat Duong, Benjamin D. Solomon European Journal of Human Genetics Natural LanguageComputational LinguisticsLanguage TestingLarge Language ModelLanguage Science	2023	131
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association Pawaree Saisawat, Stefan Kohl, Alina C. Hilger, Kidney International BiologyGenetic DisorderNatural SciencesGeneticsVacterl Association	2013	127
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by <i>EP300</i> mutations Patricia Fergelot, Martine van Belzen, Julien Van‐Gils, American Journal of Medical Genetics Part A	2016	122

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