Research Topics
Genomes and Genes
Species | Ludmila Prokunina-OlssonSummaryAffiliation: National Institutes of Health Country: USA Publications
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Detail Information
Publications
Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2Ludmila Prokunina-Olsson
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, 8717 Grovemont Circle, Bethesda, MD 20892 4605, USA
Cancer Epidemiol Biomarkers Prev 19:1349-55. 2010..2, showed a promising association with PrCa overall (P=2.14x10(-6)), with a suggestion of stronger association with aggressive disease (P=1.2x10(-7))...
A variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virusLudmila Prokunina-Olsson
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, US National Institutes of Health, Bethesda, Maryland, USA
Nat Genet 45:164-71. 2013..Our findings provide new insights into the genetic regulation of HCV clearance and its clinical management...
No association between a candidate TCF7L2 variant and risk of breast or ovarian cancerEllen L Goode
Health Sciences Research, Mayo Clinic College of Medicine, Rochester, USA
BMC Cancer 9:312. 2009..No studies of ovarian cancer have been reported to date...
Evidence for neuroendocrine function of a unique splicing form of TCF7L2 in human brain, islets and gutL Prokunina-Olsson
Laboratory of Translational Genomics, National Cancer Institute, National Institutes of Health, 8717 Grovemont Circle, Bethesda, MD 20892 4605, USA
Diabetologia 53:712-6. 2010..The goal of this study was to further characterise this unique TCF7L2 splicing form in human tissues...
No effect of cancer-associated SNP rs6983267 in the 8q24 region on co-expression of MYC and TCF7L2 in normal colon tissueLudmila Prokunina-Olsson
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, 20892, MD, USA
Mol Cancer 8:96. 2009..These findings suggest that some splicing forms of TCF7L2 may be functionally important for regulation of MYC expression in colon tissue but this regulation is not directly dependent on rs6983267...
Alternative splicing of TCF7L2 gene in omental and subcutaneous adipose tissue and risk of type 2 diabetesLudmila Prokunina-Olsson
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America
PLoS ONE 4:e7231. 2009..We hypothesized that these genetic variants might increase the risk of T2D through regulation of alternative splicing or expression level of TCF7L2 in human adipose tissue...
Tissue-specific alternative splicing of TCF7L2Ludmila Prokunina-Olsson
Genome Technology Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA
Hum Mol Genet 18:3795-804. 2009..Alternative splicing of TCF7L2 in pancreatic islets warrants future studies. GenBank Accession Numbers: FJ010164-FJ010174...
Common genetic variants in the PSCA gene influence gene expression and bladder cancer riskYi Ping Fu
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA
Proc Natl Acad Sci U S A 109:4974-9. 2012....
NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutationsYi Ping Fu
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA
Mol Cancer 9:113. 2010..2 region as a novel genetic risk factor for breast cancer, and this association was stronger in patients with estrogen receptor (ER)+ versus ER- cancer...
Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancerWei Tang
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA
Hum Mol Genet 21:1918-30. 2012..1 protein. Our study shows an example of genetic and functional role of an uncommon protective genetic variant in a complex human disease, such as bladder cancer...
Fine mapping of 14q24.1 breast cancer susceptibility locusPhoebe Lee
Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA
Hum Genet 131:479-90. 2012..Therefore, we conclude that rs999737 is an optimal tag SNP for common variants in the 14q24.1 region and thus narrow the candidate variants that should be investigated in follow-up laboratory evaluation...
A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3Montserrat Garcia-Closas
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA
Hum Mol Genet 20:4282-9. 2011..Our findings suggest that genetic variation in SLC14A1 could provide new etiological insights into bladder carcinogenesis...
Genetic variant as a selection marker for anti-prostate stem cell antigen immunotherapy of bladder cancerIndu Kohaar
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, 8717 Grovemont Cir, Bethesda, MD 20892 4605, USA
J Natl Cancer Inst 105:69-73. 2013..Future clinical studies will be needed to validate PSCA as a therapeutic target for bladder cancer...
Detectable clonal mosaicism and its relationship to aging and cancerKevin B Jacobs
Division of Cancer Epidemiology and Genetics, National Cancer Institute NCI, Rockville, Maryland, USA
Nat Genet 44:651-8. 2012..4; P = 3.8 × 10(-11)). These findings underscore the time-dependent nature of somatic events in the etiology of cancer and potentially other late-onset diseases...
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)Gilles Thomas
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA
Nat Genet 41:579-84. 2009..1 (rs999737; P = 1.74 x 10(-7)) localizes to RAD51L1, a gene in the homologous recombination DNA repair pathway. We also confirmed associations with loci on chromosomes 2q35, 5p12, 5q11.2, 8q24, 10q26 and 16q12.1...
Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European backgroundIdan Menashe
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, United States of America
PLoS ONE 7:e29396. 2012..Identification of the aromatic amine metabolism pathway provides support for the ability of this approach to identify pathways with established relevance to bladder carcinogenesis...
IL28B rs12979860 genotype and spontaneous clearance of hepatitis C virus in a multi-ethnic cohort of injection drug users: evidence for a supra-additive associationFatma M Shebl
Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA
J Infect Dis 204:1843-7. 2011....
IL-29 is the dominant type III interferon produced by hepatocytes during acute hepatitis C virus infectionHeiyoung Park
Immunology Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health NIH, Department of Health and Human Services DHHS, Bethesda, MD 20892, USA
Hepatology 56:2060-70. 2012..CONCLUSION: Hepatocyte-derived type III IFNs contribute to ISG induction and antiviral activity, but are not the principal determinant of the outcome of HCV infection...
Splicing diversity of the human OCLN gene and its biological significance for hepatitis C virus entryIndu Kohaar
Laboratory of Translational Genomics, National Cancer Institute, National Institutes of Health, 8717 Grovemont Circle, Bethesda, MD 20892 4605, USA
J Virol 84:6987-94. 2010..Genetic factors crucial for regulation of OCLN expression and susceptibility to HCV infection remain to be elucidated...
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociNathaniel Rothman
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA
Nat Genet 42:978-84. 2010..Our findings on common variants associated with bladder cancer risk should provide new insights into the mechanisms of carcinogenesis...
Cancer sequencing gets a little more personalLudmila Prokunina-Olsson
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892 4605, USA
Sci Transl Med 2:20ps8. 2010..More validation and a reduction in cost are required for this approach to become common in clinics...
