Benjamin Solomon
Benjamin Solomon
National Human Genome Research Institute
Verified email at - Homepage
Cited by
Cited by
A systematic review of antibody mediated immunity to coronaviruses: kinetics, correlates of protection, and association with severity
AT Huang, B Garcia-Carreras, MDT Hitchings, B Yang, LC Katzelnick, ...
Nature communications 11 (1), 4704, 2020
Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease
DB Beck, MA Ferrada, KA Sikora, AK Ombrello, JC Collins, W Pei, ...
New England Journal of Medicine 383 (27), 2628-2638, 2020
Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries
ME Talkowski, JA Rosenfeld, I Blumenthal, V Pillalamarri, C Chiang, ...
Cell 149 (3), 525-537, 2012
Vacterl/vater association
BD Solomon
Orphanet journal of rare diseases 6, 1-12, 2011
Parent-of-origin-specific signatures of de novo mutations
JM Goldmann, WSW Wong, M Pinelli, T Farrah, D Bodian, AB Stittrich, ...
Nature genetics 48 (8), 935-939, 2016
New observations on maternal age effect on germline de novo mutations
WSW Wong, BD Solomon, DL Bodian, P Kothiyal, G Eley, KC Huddleston, ...
Nature communications 7 (1), 10486, 2016
Strategic vision for improving human health at The Forefront of Genomics
ED Green, C Gunter, LG Biesecker, V Di Francesco, CL Easter, ...
Nature 586 (7831), 683-692, 2020
Mutations in NOTCH1 cause Adams-Oliver syndrome
AB Stittrich, A Lehman, DL Bodian, J Ashworth, Z Zong, H Li, P Lam, ...
The American Journal of Human Genetics 95 (3), 275-284, 2014
Analysis of genotype–phenotype correlations in human holoprosencephaly
BD Solomon, S Mercier, JI Vélez, DE Pineda‐Alvarez, A Wyllie, N Zhou, ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2010
M Muenke, B Solomon, S Odent
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2010
MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer
ME Roberts, SA Jackson, LR Susswein, N Zeinomar, X Ma, ML Marshall, ...
Genetics in Medicine 20 (10), 1167-1174, 2018
The clinical content of preconception care: women with chronic medical conditions
AL Dunlop, BW Jack, JN Bottalico, MC Lu, A James, CS Shellhaas, ...
American journal of obstetrics and gynecology 199 (6), S310-S327, 2008
Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates
DL Bodian, E Klein, RK Iyer, WSW Wong, P Kothiyal, D Stauffer, ...
Genetics in Medicine 18 (3), 221-230, 2016
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association
P Saisawat, S Kohl, AC Hilger, DY Hwang, HY Gee, GC Dworschak, ...
Kidney international 85 (6), 1310-1317, 2014
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
P Fergelot, M Van Belzen, J Van Gils, A Afenjar, CM Armour, B Arveiler, ...
American Journal of Medical Genetics Part A 170 (12), 3069-3082, 2016
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with …
BD Solomon, LA Baker, KA Bear, BK Cunningham, PF Giampietro, ...
The Journal of pediatrics 164 (3), 451-457. e1, 2014
Clinical genomic database
BD Solomon, AD Nguyen, KA Bear, TG Wolfsberg
Proceedings of the National Academy of Sciences 110 (24), 9851-9855, 2013
Analysis of component findings in 79 patients diagnosed with VACTERL association
BD Solomon, DE Pineda‐Alvarez, MS Raam, SM Bous, AA Keaton, ...
American Journal of Medical Genetics Part A 152 (9), 2236-2244, 2010
Clinical geneticists' views of VACTERL/VATER association
BD Solomon, KA Bear, V Kimonis, A de Klein, DA Scott, C Shaw‐Smith, ...
American Journal of Medical Genetics Part A 158 (12), 3087-3100, 2012
Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia
BD Solomon, DE Pineda‐Alvarez, JZ Balog, D Hadley, AL Gropman, ...
American Journal of Medical Genetics Part A 149 (11), 2543-2546, 2009
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