Benjamin Delgrosso Solomon, MD

Unless otherwise indicated, this information has been self-reported and has not been verified by the Board of Medicine.

None Reported

None Reported

VACTERL/VATER Association.
Orphanet J Rare Dis.
Volume: 16
Date: 08 2011

Personalized genomic medicine: lessons from the exome.
Mol Genet Metab.
Volume: 104
Date: 09 2011

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.
Cell
Volume: 149
Date: 04 2012

Incidental medical information in whole-exome sequencing.
Pediatrics
Volume: 129
Date: 06 2012

Applying Genomic Analysis to Newborn Screening.
Mol Syndromol
Volume: 3
Date: 08 2012

When to suspect a genetic syndrome.
Am Fam Physician
Volume: 86
Date: 11 2012

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease.
Mol Psychiatry.
Volume: 18
Date: 05 2013

Clinical genomic database.
Proc Natl Acad Sci U S A.
Volume: 110
Date: 06 2013

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.
Kidney Int.
[Epub ahead of print]
Date: 10 2013

An Approach to the Identification of Anomalies and Etiologies in Neonates with Identified or Suspected VACTERL (Vertebral Defects, Anal Atresia, Tracheo-Esophageal Fistula with Esophageal Atresia, Cardiac Anomalies, Renal Anomalies, and Limb Anomalies) As
J Pediatr
[Epub ahead of print]
Date: 12 2013