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JAMES LEEK, M.D.
M.D.
Interventional Pain Medicine Physician
NPI: 1528042033Individual
Specialties, Licenses & Credentials
Anesthesiology Physician
Anesthesiology
Code: 207L00000X
37777-020(WI)
Interventional Pain Medicine PhysicianPrimary
Pain Medicine — Interventional Pain Medicine
Code: 208VP0014X
37777-20(WI)
Research & Publications (20)
The tspair package for finding top scoring pair classifiers in R.
PMID 19276151·Bioinformatics·2009
8-other
A general framework for multiple testing dependence.
PMID 19033188·Proc Natl Acad Sci U S A·2008
8-other
Haematopoietic repopulating activity in human cord blood CD133+ quiescent cells.
PMID 18997827·Bone Marrow Transplant·2009
7-preclinical
The optimal discovery procedure for large-scale significance testing, with applications to comparative microarray experiments.
PMID 16928955·Biostatistics·2007
4-observational
Capturing heterogeneity in gene expression studies by surrogate variable analysis.
PMID 17907809·PLoS Genet·2007
8-other
On the design and analysis of gene expression studies in human populations.
PMID 17597765·Nat Genet·2007
4-observational
Antisense c-myc fragments induce normal differentiation cycles in HL-60 cells.
PMID 16403010·Eur J Clin Invest·2006
8-other
Phenotypic changes associated with DYNACTIN-2 (DCTN2) over expression characterise SJSA-1 osteosarcoma cells.
PMID 16369996·Mol Carcinog·2006
8-other
EDGE: extraction and analysis of differential gene expression.
PMID 16357033·Bioinformatics·2006
8-other
Significance analysis of time course microarray experiments.
PMID 16141318·Proc Natl Acad Sci U S A·2005
8-other
Marker gene transfer into human haemopoietic cells using a herpesvirus saimiri-based vector.
PMID 15616605·Gene Ther·2005
8-other
PRELI (protein of relevant evolutionary and lymphoid interest) is located within an evolutionarily conserved gene cluster on chromosome 5q34-q35 and encodes a novel mitochondrial protein.
PMID 14640972·Biochem J·2004
7-preclinical
Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders.
PMID 15571623·BMC Neurol·2004
5-case
Identification of SATB2 as the cleft palate gene on 2q32-q33.
PMID 12915443·Hum Mol Genet·2003
4-observational
Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis.
PMID 12660032·Cancer Genet Cytogenet·2003
8-other
Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse development.
PMID 14516659·Mech Dev·2002
7-preclinical
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease.
PMID 12161614·J Med Genet·2002
8-other
BCL10 in malignant lymphomas--an evaluation using fluorescence in situ hybridization.
PMID 11748643·J Pathol·2002
8-other
Genetic events during the transformation of a tamoxifen-sensitive human breast cancer cell line into a drug-resistant clone.
PMID 11675139·Cancer Genet Cytogenet·2001
8-other
A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?
PMID 11494964·J Med Genet·2001
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 550 W HWY 50
SALIDA, CO 81201 - Phone
- (719) 530-2000
Quick Facts
- NPI
- 1528042033
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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