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DONNA LOHMANN, M.D.
M.D.
Psychiatry Physician
NPI: 1790838886Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
MD00035778(WA)
Research & Publications (20)
Microcephaly, microtia, preauricular tags, choanal atresia and developmental delay in three unrelated patients: a mandibulofacial dysostosis distinct from Treacher Collins syndrome.
PMID 19334086·Am J Med Genet A·2009
5-case
Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma.
PMID 18509746·Fam Cancer·2009
5-case
Meningioma 40 years after radiation therapy for retinoblastoma: genetic and phenotypic analysis, and minireview of literature.
PMID 18666063·Zentralbl Neurochir·2008
5-case
Patterns of missplicing caused by RB1 gene mutations in patients with retinoblastoma and association with phenotypic expression.
PMID 18181215·Hum Mutat·2008
8-other
Neurotrophin receptor expression in human primary retinoblastomas and retinoblastoma cell lines.
PMID 17973327·Pediatr Blood Cancer·2008
8-other
Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma.
PMID 17210724·Cancer Res·2007
8-other
A rapid hemodynamic monitor of acute ischemia during cardiac procedures: changes in relaxation via a continuous left ventricular pressure-derivative loop.
PMID 16488437·J Surg Res·2006
7-preclinical
Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome 3.
PMID 16750193·Exp Eye Res·2006
6-review
Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
PMID 15763650·Eur J Cancer·2005
8-other
Minimal region of deletion on chromosomal arm 3p25.1-p25.2 in uveal melanoma.
PMID 16288058·Cancer Res·2005
8-other
Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression.
PMID 16127685·Hum Mutat·2005
8-other
Gains and overexpression identify DEK and E2F3 as targets of chromosome 6p gains in retinoblastoma.
PMID 16007192·Oncogene·2005
8-other
Loss of heterozygosity of 1p in uveal melanomas with monosomy 3.
PMID 15849744·Int J Cancer·2005
8-other
Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization.
PMID 15834944·Genes Chromosomes Cancer·2005
4-observational
Genomic gains on chromosome 1q in retinoblastoma: consequences on gene expression and association with clinical manifestation.
PMID 15825178·Int J Cancer·2005
8-other
Retinoblastoma: revisiting the model prototype of inherited cancer.
PMID 15264269·Am J Med Genet C Semin Med Genet·2004
6-review
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B element.
PMID 15591264·J Med Genet·2004
8-other
A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus.
PMID 15353561·Nucleic Acids Res·2004
8-other
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
PMID 15340364·Eur J Hum Genet·2004
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
- 3417 EVANSTON AVE N, 306
SEATTLE, WA 98103 - Phone
- (206) 445-4952
Quick Facts
- NPI
- 1790838886
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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