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LISHIANA SHAFFER, MD
MD
Obstetrics & Gynecology Physician
NPI: 1497827158IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
MD153333(OR)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
MEDICAL COLLEGE OF PENNSYLVANIA
Class of 2001
Research & Publications (20)
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
PMID 18646242·Prenat Diagn·2008
4-observational
The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future.
PMID 17910076·Am J Med Genet C Semin Med Genet·2007
6-review
Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis.
PMID 17290441·Am J Med Genet C Semin Med Genet·2007
6-review
Microarray analysis for constitutional cytogenetic abnormalities.
PMID 17873655·Genet Med·2007
6-review
Medical applications of array CGH and the transformation of clinical cytogenetics.
PMID 17124414·Cytogenet Genome Res·2006
6-review
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.
PMID 16860135·J Pediatr·2006
8-other
Diagnosis of microdeletion syndromes by fluorescence in situ hybridization (FISH).
PMID 18428311·Curr Protoc Hum Genet·2001
6-review
Molecular mechanisms for constitutional chromosomal rearrangements in humans.
PMID 11092830·Annu Rev Genet·2000
6-review
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies.
PMID 19597142·Proc Natl Acad Sci U S A·2009
8-other
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
PMID 19193630·Hum Mol Genet·2009
8-other
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH.
PMID 19365269·Genet Med·2009
8-other
Development and validation of an assay for iodide in serum using ion chromatography with pulsed amperometric detection.
PMID 19259884·Inhal Toxicol·2009
4-observational
Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.
PMID 19271239·Hum Genet·2009
8-other
aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy.
PMID 19353629·Am J Med Genet A·2009
8-other
Incidental findings in the cervical spine at CT for trauma evaluation.
PMID 19234270·AJR Am J Roentgenol·2009
8-other
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report.
PMID 19664229·Mol Cytogenet·2009
8-other
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.
PMID 19668335·PLoS One·2009
8-other
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
PMID 19500772·Am J Hum Genet·2009
8-other
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
- 364 SE 8TH AVE STE 205
HILLSBORO, OR 97123 - Phone
- (503) 681-4145
Quick Facts
- NPI
- 1497827158
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 25
- Publications
- 20
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