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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 16, 2024. (Total: 231503Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Ovarian Neoplasms and DROSHA[original query]
MicroRNA processing and binding site polymorphisms are not replicated in the Ovarian Cancer Association Consortium.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Aug 20 (8): 1793-7.
Permuth-Wey Jennifer, Chen Zhihua, Tsai Ya-Yu, Lin Hui-Yi, Chen Y Ann, Barnholtz-Sloan Jill, Birrer Michael J, Chanock Stephen J, Cramer Daniel W, Cunningham Julie M, Fenstermacher David, Fridley Brooke L, Garcia-Closas Montserrat, Gayther Simon A, Gentry-Maharaj Aleksandra, Gonzalez-Bosquet Jesus, Iversen Edwin, Jim Heather, McLaughlin John, Menon Usha, Narod Steven A, Phelan Catherine M, Ramus Susan J, Risch Harvey, Song Honglin, Sutphen Rebecca, Terry Kathryn L, Tyrer Jonathan, Vierkant Robert A, Wentzensen Nicolas, Lancaster Johnathan M, Cheng Jin Q, Berchuck Andrew, Pharoah Paul D P, Schildkraut Joellen M, Goode Ellen L, Sellers Thomas A,
LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer.
Cancer research 2011 Jun 71 (11): 3896-903.
Permuth-Wey Jennifer, Kim Donghwa, Tsai Ya-Yu, Lin Hui-Yi, Chen Y Ann, Barnholtz-Sloan Jill, Birrer Michael J, Bloom Gregory, Chanock Stephen J, Chen Zhihua, Cramer Daniel W, Cunningham Julie M, Dagne Getachew, Ebbert-Syfrett Judith, Fenstermacher David, Fridley Brooke L, Garcia-Closas Montserrat, Gayther Simon A, Ge William, Gentry-Maharaj Aleksandra, Gonzalez-Bosquet Jesus, Goode Ellen L, Iversen Edwin, Jim Heather, Kong William, McLaughlin John, Menon Usha, Monteiro Alvaro N A, Narod Steven A, Pharoah Paul D P, Phelan Catherine M, Qu Xiaotao, Ramus Susan J, Risch Harvey, Schildkraut Joellen M, Song Honglin, Stockwell Heather, Sutphen Rebecca, Terry Kathryn L, Tyrer Jonathan, Vierkant Robert A, Wentzensen Nicolas, Lancaster Johnathan M, Cheng Jin Q, Sellers Thomas A,
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Human mutation 2020 Dec .
Felicio Paula S, Grasel Rebeca S, Campacci Natalia, de Paula Andre E, Galvão Henrique C R, Torrezan Giovana T, Sabato Cristina S, Fernandes Gabriela C, Souza Cristiano P, Michelli Rodrigo D, Andrade Carlos E, Barros Bruna Durães De Figueiredo, Matsushita Marcus M, Revil Timothée, Ragoussis Jiannis, Couch Fergus J, Hart Steven N, Reis Rui M, Melendez Matias E, Tonin Patricia N, Carraro Dirce M, Palmero Edenir
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