Physician

Pediatrics

Dr. Kathleen E. Wiley, MD

Kathleen Wiley practices Pediatrics. She researched medicine at Eastern Virginia Medical School. Kathleen Wiley is a published doctor and has 50 publications published. The lastest was: 'Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associa...'

Publications

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associa...
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).
Germline mutations in HOXB13 and prostate-cancer risk.
Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk.
Large-scale fine mapping of the HNF1B locus and prostate cancer risk.
Inherited genetic variant predisposes to aggressive but not indolent prostate cancer.
Identification of a new prostate cancer susceptibility locus on chromosome 8q24.
Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.
Prostate cancer risk associated loci in African Americans.
Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11.
Two independent prostate cancer risk-associated Loci at 11q13.
A novel prostate cancer susceptibility locus at 19q13.
Sequence variants at 22q13 are associated with prostate cancer risk.
Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12.
Association of prostate cancer risk variants with clinicopathologic characteristics of the disease.
Cumulative effect of five genetic variants on prostate cancer risk in multiple study populations.
Association between sequence variants at 17q12 and 17q24.3 and prostate cancer risk in European and African Americans.
Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients.
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.
Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP.
Multiple myeloma and treatment-related thromboembolism: oncology nurses' role in prevention, assessment, and diagnosis.
Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans.
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
Germline ATBF1 mutations and prostate cancer risk.
A germline DNA polymorphism enhances alternative splicing of the KLF6 tumor suppressor gene and is associated with increased prostate cancer risk.
Mutational analysis of PINX1 in hereditary prostate cancer.
Combined genome-wide scan for prostate cancer susceptibility genes.
Familial aggregation of bothersome benign prostatic hyperplasia symptoms.
Common sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk.
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk.
Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk.
Discovery of recently adopted orphan receptors for apelin, urotensin II, and ghrelin identified using novel radioligands and functional role in the human cardiovascula...
Linkage and association of CYP17 gene in hereditary and sporadic prostate cancer.
Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families.
Polymorphisms in the CYP1B1 gene are associated with increased risk of prostate cancer.
Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci.
Germline mutations in the ribonuclease L gene in families showing linkage with HPC1.
Association of CASP8 D302H polymorphism with reduced risk of aggressive prostate carcinoma.
Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer.
Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23.
Linkage of prostate cancer susceptibility loci to chromosome 1.
Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer.
Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect.
A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics.
Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics.
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics.
Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses.
Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.

Schools

Eastern Virginia Medical School
Children39s Hospital Of The King39s Daughters

Doctors Specialties

Pediatrics

Accepted Insurances

Education

Eastern Virginia Medical School

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