Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kannabiran Nandakumar"'
Autor:
Fergus J. Couch, Robert R. McWilliams, Gloria M. Petersen, Yean K. Lee, Bruce W. Eckloff, Kannabiran Nandakumar, Raymond M. Moore, William R. Bamlet, Steven N. Hart, Chunling Hu
Tables listing the mutations identified in the 96 patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42a5105dbb91b20df747d265a1e397bc
https://doi.org/10.1158/1055-9965.22438018
https://doi.org/10.1158/1055-9965.22438018
Autor:
Fergus J. Couch, Robert R. McWilliams, Gloria M. Petersen, Yean K. Lee, Bruce W. Eckloff, Kannabiran Nandakumar, Raymond M. Moore, William R. Bamlet, Steven N. Hart, Chunling Hu
The prevalence of germline pathogenic mutations in a comprehensive panel of cancer predisposition genes is not well-defined for patients with pancreatic ductal adenocarcinoma (PDAC). To estimate the frequency of mutations in a panel of 22 cancer pred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8cfc336f48b6449ea10827ad10bfbe
https://doi.org/10.1158/1055-9965.c.6516163
https://doi.org/10.1158/1055-9965.c.6516163
Autor:
Shulin Zhang, Kannabiran Nandakumar, Eric B. Durbin, Justine Pickarski, Megan L. Hutchcraft, Frederick R. Ueland, Jill M. Kolesar, Rachel W. Miller, Nan Lin
Publikováno v:
Gynecologic Oncology. 162:S112
Objectives: Approximately 18% of ovarian cancer and 5% of uterine cancer patients have underlying genetic predispositions. All women with ovarian cancer and young women with uterine cancer should receive germline genetic testing and counseling; howev
Autor:
Justine Pickarski, Thèrése Bocklage, Isaac Hands, Ming Poi, Elizabeth Belcher, Rachel L. Miller, Micheal Cavnar, Susanne M. Arnold, Marissa Schuh, Kannabiran Nandakumar, Mark Evers, Frederick R. Ueland, Jill M. Kolesar, Shulin Zhang, Eric B. Durbin, Jong Cheol Jeong
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 29:A001-A001
Background: Reduced access to treatment advances in rural populations contributes to increased cancer mortality. Rural Appalachian Kentucky is a geographically isolated population with a unique carcinogen exposure and a low frequency guideline-recomm
Autor:
Randall L. Woltjer, Li-San Wang, Jonathan L. Haines, Ishita Parikh, Julie A. Schneider, Paul K. Crane, Erin L. Abner, Craig Horbinski, Manasi Malik, Maria M. Corrada, Amanda Partch, KatieRose Richmire, Peter T. Nelson, Sarah E. Monsell, Gregory A. Jicha, Richard Mayeux, David H. Cribbs, Claudia H. Kawas, Bernard R. Wilfred, Kannabiran Nandakumar, David W. Fardo, Margaret A. Pericak-Vance, Leonard W. Poon, Steven Estus, Eric B. Larson, Richard J. Kryscio, Lindsay A. Farrer, Alexander J. Rajic, Thomas J. Montine, Otto Valladares, Wayne W. Poon, Wang-Xia Wang, Frederick A. Schmitt, Robert C. Green, Walter A. Kukull, Gerard D. Schellenberg, Marla Gearing, Linda J. Van Eldik, Mark L. Farman, Joshua A. Sonnen, Eseosa T. Ighodaro, Charles D. Smith, Stephen W. Scheff, Patricia L. Kramer, Janna H. Neltner, David A. Bennett
Publikováno v:
Nelson, PT; Estus, S; Abner, EL; Parikh, I; Malik, M; Neltner, JH; et al.(2014). ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Acta Neuropathologica, 127(6), 825-843. doi: 10.1007/s00401-014-1282-2. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/4fr967hw
Hippocampal sclerosis of aging (HS-Aging) is a high-morbidity brain disease in the elderly but risk factors are largely unknown. We report the first genome-wide association study (GWAS) with HS-Aging pathology as an endophenotype. In collaboration wi
Publikováno v:
BMC Systems Biology. 2010, Vol. 4, p162-173. 12p.
Autor:
Richard A. Gibbs, André G. Uitterlinden, Richard Gill, Jennifer A. Brody, Kannabiran Nandakumar, L. Adrienne Cupples, Ching-Ti Liu, Wen-Chi Chou, John A Robbins, Fernando Rivadeneira, Chia-Ho Cheng, Karol Estrada, Serkalem Demissie, Tamara B. Harris, Yi-Hsiang Hsu, Donna M. Muzny, Bruce M. Psaty, Yanhua Zhou, Vilmundur Gudnason, Guo Li, Jireh Santibanez, David Karasik, Douglas P. Kiel
Publikováno v:
Human Molecular Genetics, 25(23), 5234-5243. Oxford University Press
Human molecular genetics, vol 25, iss 23
Human molecular genetics, vol 25, iss 23
Background: Bone mineral density (BMD) is a heritable phenotype that predicts fracture risk. We performed fine-mapping by targeted sequencing at WLS, MEF2C, ARHGAP1/F2 and JAG1 loci prioritized by eQTL and bioinformatic approaches among 56 BMD loci f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04fa5753ebec91c8c27c4de9e26cf8df
https://pure.eur.nl/en/publications/e5fbf654-25b7-4816-abad-bcc62ad3dc35
https://pure.eur.nl/en/publications/e5fbf654-25b7-4816-abad-bcc62ad3dc35
Publikováno v:
IBMS BoneKEy. 8:112-122
Autor:
Raymond Moore, Kannabiran Nandakumar, Fergus J. Couch, Steven N. Hart, Bruce W. Eckloff, William R. Bamlet, Robert R. McWilliams, Yean Kit Lee, Chunling Hu, Gloria M. Petersen
The prevalence of germline pathogenic mutations in a comprehensive panel of cancer predisposition genes is not well-defined for patients with pancreatic ductal adenocarcinoma (PDAC). To estimate the frequency of mutations in a panel of 22 cancer pred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4caf702c9870dcea82ba998931f27827
https://europepmc.org/articles/PMC4754121/
https://europepmc.org/articles/PMC4754121/
Autor:
Shilpa Nagaraju, Giovanni Parmigiani, Kannabiran Nandakumar, Suresh Mathivanan, Goparani Mishra, Nandan P. Deshpande, Jörg Schultz, Akhilesh Pandey, Jun Zhong, Salil Sharma, Balamurugan Periaswamy, Tejal K. Gandhi, Stefan Pinkert, Joel S. Bader, Subburaman Mohan, Jef D. Boeke, L. Karthick, Rashmi Nayak, Malabika Sarker, K N Chandrika, Beiyi Shen
Publikováno v:
Nature Genetics. 38:285-293
We present the first analysis of the human proteome with regard to interactions between proteins. We also compare the human interactome with the available interaction datasets from yeast (Saccharomyces cerevisiae), worm (Caenorhabditis elegans) and f