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LAWRENCE SHAFFER, M.D.
M.D.
Psychiatry Physician
NPI: 1629133285Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
19495(NE)
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
Microarray analysis for constitutional cytogenetic abnormalities.
PMID 17873655·Genet Med·2007
6-review
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.
PMID 17873649·Genet Med·2007
4-observational
Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis.
PMID 17290441·Am J Med Genet C Semin Med Genet·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
Risk estimates for uniparental disomy following prenatal detection of a nonhomologous Robertsonian translocation.
PMID 16491515·Prenat Diagn·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
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
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
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH.
PMID 19365269·Genet Med·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
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
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.
PMID 19668335·PLoS One·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
- Address
- 301 CENTENNIAL MALL S
LINCOLN, NE 68508 - Phone
- (402) 471-7795
Quick Facts
- NPI
- 1629133285
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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