Benjamin D Solomon


Ontology type: schema:Person     


Person Info

NAME

Benjamin D

SURNAME

Solomon

Publications in SciGraph latest 50 shown

  • 2019-04 Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis in FAMILIAL CANCER
  • 2019-01-12 Mother−child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers in GENES & IMMUNITY
  • 2019-01 Response to ten Broeke et al. in GENETICS IN MEDICINE
  • 2018-12-19 Response to Evans et al. in GENETICS IN MEDICINE
  • 2018-11 Author Correction: Parent-of-origin-specific signatures of de novo mutations in NATURE GENETICS
  • 2018-11 Utility of Expedited Hereditary Cancer Testing in the Surgical Management of Patients with a New Breast Cancer Diagnosis in ANNALS OF SURGICAL ONCOLOGY
  • 2018-10 MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer in GENETICS IN MEDICINE
  • 2018-04 Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence in NATURE GENETICS
  • 2017-12 Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn in GENETICS IN MEDICINE
  • 2016-08 Parent-of-origin-specific signatures of de novo mutations in NATURE GENETICS
  • 2016-03 Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates in GENETICS IN MEDICINE
  • 2016-01-19 New observations on maternal age effect on germline de novo mutations in NATURE COMMUNICATIONS
  • 2014-06 Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association in KIDNEY INTERNATIONAL
  • 2013-05 Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease in MOLECULAR PSYCHIATRY
  • 2012-09 Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses in CHILD'S NERVOUS SYSTEM
  • 2012-07 Inheritance of the VATER/VACTERL association in PEDIATRIC SURGERY INTERNATIONAL
  • 2012-06 A common genetic network underlies substance use disorders and disruptive or externalizing disorders in HUMAN GENETICS
  • 2012-02 Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH in HUMAN GENETICS
  • 2011-12 VACTERL/VATER Association in ORPHANET JOURNAL OF RARE DISEASES
  • 2011-12 Genetic–environmental interaction in a unique case of Muenke syndrome with intracranial hypertension in CHILD'S NERVOUS SYSTEM
  • 2011-06 Holoprosencephaly: A guide to diagnosis and clinical management in INDIAN PEDIATRICS
  • 2010-06 Evidence for inheritance in patients with VACTERL association in HUMAN GENETICS
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