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BRYAN ZOLL, MD, MBA
MD, MBA
Gastroenterology Physician
NPI: 1437619350IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
292423(MA)
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
1015406(MA)
CMS Specialties
PrimaryGASTROENTEROLOGY
Education
TEMPLE UNIVERSITY SCHOOL OF MEDICINE
Class of 2019
Research & Publications (20)
First non-mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter --> q22.1::q22.1 --> pter) is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q- syndrome.
PMID 15103719·Am J Med Genet A·2004
5-case
Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.
PMID 12497637·Hum Mutat·2003
8-other
Modulation of cell surface markers on NK-like T lymphocytes by using IL-2, IL-7 or IL-12 in vitro stimulation.
PMID 10975999·Cytokine·2000
8-other
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.
PMID 19284615·Mol Cytogenet·2009
8-other
Impairment of gastric acid secretion and increase of embryonic lethality in Foxq1-deficient mice.
PMID 18544931·Cytogenet Genome Res·2008
7-preclinical
Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay.
PMID 17431920·Am J Med Genet A·2007
8-other
Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.
PMID 16506277·Prenat Diagn·2006
5-case
Manifestations of hereditary hemorrhagic telangiectasia in children and adolescents.
PMID 15976991·Eur Arch Otorhinolaryngol·2006
8-other
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
PMID 16007665·Am J Med Genet A·2005
5-case
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
PMID 15340364·Eur J Hum Genet·2004
8-other
Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations.
PMID 15054834·Am J Med Genet A·2004
8-other
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].
PMID 12884434·Am J Med Genet A·2003
5-case
Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.
PMID 12746416·J Med Genet·2003
5-case
A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.
PMID 12725591·Genet Couns·2003
5-case
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis.
PMID 12584434·Cytogenet Genome Res·2002
5-case
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution.
PMID 12161600·J Med Genet·2002
8-other
Isolation and characterization of the human forkhead gene FOXQ1.
PMID 11747606·DNA Cell Biol·2001
7-preclinical
Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26).
PMID 11471178·Am J Med Genet·2001
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 330 BROOKLINE AVE
BOSTON, MA 02215 - Phone
- (610) 999-2757
Quick Facts
- NPI
- 1437619350
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 7
- Publications
- 20
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