Seth Ian Berger, MD

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

George Washington University School Of Medicine And Health Sciences - Washington DC
Rank: Assistant Professor
Years: 2018-present

None Reported

SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly.
Congenit Anom
58(1):29-32.
Date: 08 2017

Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype.
Hum Mutat
38(12):1774-1785
Date: 12 2017

Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects.
J Med Genet
54(12):825-829
Date: 12 2017

Low-level parental mosaicism affects the recurrence risk of holoprosencephaly.
Genet Med.
21(4):1015-1020
Date: 09 2018

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.
Hum Mutat.
39(10):1416-1427.
Date: 10 2018

A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly
Am J Hum Genet
104(5):990-993
Date: 05 2019

Cohesin complex-associated holoprosencephaly
Brain
142(9):2631-2643
Date: 09 2019

MAP1B related syndrome: Case presentation and review of literature
Am J Med Genet A
179(9):1703-1708
Date: 09 2019

Nonimmune hydrops fetalis and congenital disorders of glycosylation: A systematic literature review
J Inherit Metab Dis.
43(2):223-233.
Date: 03 2020

Defining the clinical phenotype of Saul-Wilson syndrome
Genet Med.
22(5):857-866
Date: 05 2020