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SVETLANA YATSENKO, MD
MD
Clinical Cytogenetics Physician
NPI: 1265293484Individual
Specialties, Licenses & Credentials
Clinical Cytogenetics PhysicianPrimary
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
MTO02403605(CA)
Molecular Genetic Pathology (Medical Genetics) Physician
Medical Genetics — Molecular Genetic Pathology
Code: 207SM0001X
MTO02403605(CA)
Research & Publications (20)
Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)].
PMID 15211662·Am J Med Genet A·2004
5-case
Identification of critical regions for clinical features of distal 10q deletion syndrome.
PMID 19558528·Clin Genet·2009
5-case
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.
PMID 19324990·J Mol Diagn·2009
8-other
Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.
PMID 19293338·Hum Mol Genet·2009
8-other
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
PMID 18663743·Am J Med Genet A·2008
8-other
Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement.
PMID 18655707·Mol Cytogenet·2008
8-other
De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
PMID 18203189·Am J Med Genet A·2008
5-case
Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
PMID 17849500·Prenat Diagn·2007
5-case
Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome.
PMID 17675367·Hum Mol Genet·2007
7-preclinical
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.
PMID 17457615·Hum Genet·2007
5-case
Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndrome.
PMID 17431898·Am J Med Genet A·2007
5-case
Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
PMID 17389918·PLoS One·2007
8-other
Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.
PMID 17357070·Am J Hum Genet·2007
4-observational
AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12.
PMID 17284672·Genome Res·2007
8-other
Isolation and characterization of mouse-human microcell hybrid cell clones permissive for infectious HIV particle release.
PMID 17270231·Virology·2007
7-preclinical
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia.
PMID 17204049·Clin Genet·2007
5-case
Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations.
PMID 16791615·Hum Genet·2006
8-other
Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
PMID 16470732·Am J Med Genet A·2006
5-case
Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype.
PMID 16278888·Am J Med Genet A·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 300 PASTEUR DR
STANFORD, CA 94305 - Phone
- (650) 723-4000
Quick Facts
- NPI
- 1265293484
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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