A
Alisa M. Goldstein
Researcher at National Institutes of Health
Publications - 309
Citations - 24663
Alisa M. Goldstein is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Cancer & Population. The author has an hindex of 72, co-authored 297 publications receiving 22773 citations. Previous affiliations of Alisa M. Goldstein include United States Department of Health and Human Services.
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Journal ArticleDOI
Family history of gallstones and the risk of biliary tract cancer and gallstones: a population-based study in Shanghai, China.
Ann W. Hsing,Yan Bai,Gabriella Andreotti,Asif Rashid,Jie Deng,Jinbo Chen,Jinbo Chen,Alisa M. Goldstein,Tian Quan Han,Ming Chang Shen,Joseph F. Fraumeni,Yu-Tang Gao +11 more
TL;DR: This large population‐based study not only supports the role of gallstones in biliary carcinogenesis but also suggests that the underlying genetic or lifestyle determinants of stones within families contribute to the risk of biliary tract cancer.
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Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population.
Nan Hu,Mark J. Roth,Mihael Polymeropolous,Ze-Zhong Tang,Michael R. Emmert-Buck,Quan-Hong Wang,Alisa M. Goldstein,Shou-Shan Feng,Sanford M. Dawsey,Ti Ding,Zhengping Zhuang,Xiao-You Han,Thomas Ried,Carol Giffen,Philip R. Taylor +14 more
TL;DR: The very high frequency LOH regions identified here may point to major susceptibility genes, including potential tumor suppressor genes and inherited gene loci, which will assist in understanding the molecular events involved in esophageal carcinogenesis and may help in the development of markers for genetic susceptibility testing and screening for the early detection of this cancer.
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A genome-wide search for loci contributing to smoking and alcoholism.
TL;DR: The number of loci identified using EVRNVR suggests that a threshold‐based phenotype may better identify loci affecting smoking history, and some of these regions may represent loci increasing vulnerability to both smoking and alcoholism.
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Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer
Ruta Sahasrabudhe,Paul Lott,Mabel Bohorquez,Ted Toal,Ana P. Estrada,John J. Suarez,Alejandro Brea-Fernández,José Cameselle-Teijeiro,Carla M. A. Pinto,Irma Ramos,Alejandra Mantilla,Rodrigo Prieto,Alejandro H. Corvalan,Enrique Norero,Carolina Alvarez,Teresa Tapia,Pilar Carvallo,Luz María González,Alicia Cock-Rada,Angela R. Solano,Florencia Neffa,Adriana Della Valle,Christopher Yau,Gabriela Soares,Alexander D. Borowsky,Nan Hu,Li Ji He,Xiao You Han,Magdalena Echeverry,John Suarez,Gilbert Mateus,María Mercedes Bravo,Fernando Bolaños,Alejandro Vélez,Javier Torres,Luis G. Carvajal-Carmona,Philip R. Taylor,Alisa M. Goldstein,Clara Ruiz-Ponte,Manuel R. Teixeira,Luis Guillermo Carvajal-Carmona +40 more
TL;DR: In this paper, the authors identify genetic variants that affect risk for gastric cancer, and perform whole-exome sequence analysis to identify mutations in genes that regulate homologous DNA recombination.
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Molecular Characterization of the Human Stomach Microbiota in Gastric Cancer Patients.
Guoqin Yu,Javier Torres,Nan Hu,Rafael Medrano-Guzmán,Roberto Herrera-Goepfert,Michael S. Humphrys,Lemin Wang,Chaoyu Wang,Ti Ding,Jacques Ravel,Philip R. Taylor,Christian C. Abnet,Alisa M. Goldstein +12 more
TL;DR: It was showed that Hp is the dominant member of the non-malignant gastric tissue microbiota in many gastric cancer patients, and taxonomic and derived functional profiles of gastric microbiota were distinct from those found in other body sites and had higher inter-subject dissimilarity.