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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
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma (The American Journal of Human Genetics (2009) 85 (679-691))
Maria Teresa Landi,Nilanjan Chatterjee,Kai Yu,Lynn R. Goldin,Alisa M. Goldstein,Melissa Rotunno,Lisa Mirabello,Kevin B. Jacobs,William Wheeler,Meredith Yeager,Andrew W. Bergen,Qizhai Li,Dario Consonni,Angela Cecilia Pesatori,Sholom Wacholder,Michael J. Thun,Ryan Diver,Martin M. Oken,Jarmo Virtamo,Demetrius Albanes,Zhaoming Wang,Laurie Burdette,Kimberly F. Doheny,Elizabeth W. Pugh,Cathy C. Laurie,Paul Brennan,Rayjean J. Hung,Valerie Gaborieau,James McKay,Mark Lathrop,John R. McLaughlin,Ying Wang,Ming-Sound Tsao,Margaret R. Spitz,Yufei Wang,Hans E. Krokan,Lars J. Vatten,Frank Skorpen,Egil Arnesen,Simone Benhamou,Christine Bouchard,Andres Metspalu,Tõnu Vooder,Mari Nelis,Kristian Välk,John K. Field,Chu Chen,Gary E. Goodman,Patrick Sulem,Gudmar Thorleifsson,Thorunn Rafnar,Timothy Eisen,Wiebke Sauter,Albert Rosenberger,Heike Bickeböller,Angela Risch,Jenny Chang-Claude,H.-Erich Wichmann,Kari Stefansson,Richard S. Houlston,Christopher I. Amos,Joseph F. Fraumeni,Sharon A. Savage,Pier Alberto Bertazzi,Margaret A. Tucker,Stephen J. Chanock,Neil E. Caporaso +66 more
Journal ArticleDOI
Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes
TL;DR: There is no evidence to support CHD5 as a major melanoma susceptibility gene among the eight CMM/DN families screened.
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Effect of mutations in XPD(ERCC2) on pregnancy and prenatal development in mothers of patients with trichothiodystrophy or xeroderma pigmentosum
Deborah Tamura,Sikandar G. Khan,Melissa A. Merideth,John J. DiGiovanna,Margaret A. Tucker,Alisa M. Goldstein,Kyu-Seon Oh,Takahiro Ueda,Jennifer Boyle,Mansi Sarihan,Kenneth H. Kraemer +10 more
TL;DR: It is found that 94% of the TTD pregnancies had pre-term delivery, pre-eclampsia, hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome, prematurity or low birth weight, and none of the 17 XP pregnancies had these complications (P<0.001).
Journal ArticleDOI
Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma
Jianxin Shi,Weiyin Zhou,Bin Zhu,Paula L. Hyland,Hunter Bennett,Yanzi Xiao,Xijun Zhang,Laura Burke,Lei Song,Chih Hao Hsu,Chunhua Yan,Qing-Rong Chen,Daoud Meerzaman,Casey L. Dagnall,Laurie Burdette,Belynda Hicks,Neal D. Freedman,Stephen J. Chanock,Meredith Yeager,Margaret A. Tucker,Alisa M. Goldstein,Xiaohong R. Yang +21 more
TL;DR: The results suggest that rare cosegregating CNVs may influence melanoma susceptibility in some melanoma-prone families and genes found in this study warrant further evaluation in future genetic analyses of melanoma.
Journal ArticleDOI
Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms
Tongwu Zhang,Jiyeon Choi,Ramile Dilshat,Berglind Osk Einarsdottir,Michael A. Kovacs,Mai Xu,Michael Malasky,Salma Chowdhury,Kristine Jones,D. Timothy Bishop,Alisa M. Goldstein,Mark M. Iles,Maria Teresa Landi,Matthew Law,Matthew Law,Jianxin Shi,Eiríkur Steingrímsson,Kevin M. Brown +17 more
TL;DR: In this paper, the authors established an meQTL dataset by using primary melanocytes from 106 individuals and identified 1,497,502 significant cis-meQTLs, including DNA methylation QTLs.