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VIVIANNE BEYER, M.D.

M.D.

Dermatology Physician

NPI: 1619110038IndividualAccepts Medicare

Specialties, Licenses & Credentials

Dermatology PhysicianPrimary

Dermatology

Code: 207N00000X

036.132245(IL)

CMS Specialties

PrimaryDERMATOLOGY

Education

INDIANA UNIVERSITY SCHOOL OF MEDICINE

Class of 2009

Research & Publications (13)

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.
PMID 19582487·Neurogenetics·2010
5-case
Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype.
PMID 19250383·Clin Genet·2009
5-case
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.
PMID 19028668·Hum Mol Genet·2009
8-other
pp32/PHAPI determines the apoptosis response of non-small-cell lung cancer.
PMID 17962813·Cell Death Differ·2008
7-preclinical
Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemia.
PMID 18940469·Cancer Genet Cytogenet·2008
8-other
Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
PMID 18564498·Genet Couns·2008
5-case
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis.
PMID 18160797·Cytogenet Genome Res·2007
5-case
Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases.
PMID 15993266·Cancer Genet Cytogenet·2005
6-review
Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
PMID 15193439·Cancer Genet Cytogenet·2004
4-observational
Determination of cutoff values to detect small aneuploid clones by interphase fluorescence in situ hybridization: the Poisson model is a more appropriate approach. Should single-cell trisomy 8 be considered a clonal defect?
PMID 14623458·Cancer Genet Cytogenet·2003
8-other
Patient with Kabuki syndrome and acute leukemia.
PMID 12949977·Am J Med Genet A·2003
5-case
[Fluorescent in situ hybridization (FISH), cytogenetic analytical complement for the diagnosis of malignant blood diseases].
PMID 10911742·Rev Med Suisse Romande·2000
8-other
Autologous transplantation of in vivo purged PBSC in CML: comparison of FISH, cytogenetics, and PCR detection of Philadelphia chromosome in leukapheresis products.
PMID 10700858·Cancer Genet Cytogenet·2000
4-observational

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

4.8(1410)
Address
1025 S 6TH ST
SPRINGFIELD, IL 62703
4.8
(1410)
See full reviews

Location

Springfield Clinic Main Campus West

1025 S 6TH ST, SPRINGFIELD, IL
4.8(217) 528-7541

Quick Facts

NPI
1619110038
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
17
Publications
13

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