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
Genome-wide association study in esophageal cancer using GeneChip mapping 10K array.
Nan Hu,Chaoyu Wang,Ying Hu,Howard H. Yang,Carol Giffen,Ze Zhong Tang,Xiao Yu Han,Alisa M. Goldstein,Michael R. Emmert-Buck,Kenneth H. Buetow,Philip R. Taylor,Maxwell P. Lee +11 more
TL;DR: The feasibility of the Affymetrix 10K SNP array in genome-wide association studies of common cancers and identified new candidate loci to study in ESCC are shown.
Journal ArticleDOI
Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants
Hanne E. Puntervoll,Xiaohong R. Yang,Hildegunn Hoøberg Vetti,Ingeborg M. Bachmann,Ingeborg M. Bachmann,Marie-Françoise Avril,M. Benfodda,Caterina Catricalà,Stéphane Dalle,Anne Benedicte Duval-Modeste,Paola Ghiorzo,Paola Grammatico,Mark Harland,Nicholas K. Hayward,Hui Han Hu,Thomas Jouary,Tanguy Martin-Denavit,Aija Ozola,Jane M. Palmer,Lorenza Pastorino,Dace Pjanova,Nadem Soufir,Solrun J. Steine,Alexander J. Stratigos,Luc Thomas,Julie Tinat,Hensin Tsao,Ruta Veinalde,Margaret A. Tucker,Brigitte Bressac-de Paillerets,Julia Newton-Bishop,Alisa M. Goldstein,Lars A. Akslen,Lars A. Akslen,Anders Molven,Anders Molven +35 more
TL;DR: This study shows that families with CDK4 germline mutations cannot be distinguished phenotypically from CDKN2A melanoma families, which are characterised by early onset of disease, increased occurrence of clinically atypical nevi, and development of MPM.
Journal ArticleDOI
Family history of cancer and risk for esophageal and gastric cancer in Shanxi, China
TL;DR: These data provide strong evidence that shared susceptibility is involved in esophageal carcinogenesis and also suggest a role in prognosis.
Journal ArticleDOI
Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.
Deborah J. Marsh,Patricia L. M. Dahia,Valérie Coulon,Zimu Zheng,Françoise Dorion-Bonnet,Katherine M. Call,Randall Little,Albert Y. Lin,Rosalind A. Eeles,Alisa M. Goldstein,Shirley Hodgson,Anne Louise Richardson,Bruce G. Robinson,Bruce G. Robinson,H. Christian Weber,Michel Longy,Charis Eng,Charis Eng +17 more
TL;DR: The LOH identified in samples from individuals with CD and the suggestion of allelic loss and reduced transcription in hamartomas from a CD patient provide evidence that PTEN/MMAC1 functions as a tumor suppressor in CD.
Journal ArticleDOI
Familial Eosinophilia Maps to the Cytokine Gene Cluster on Human Chromosomal Region 5q31-q33
John D. Rioux,Valerie Stone,Mark J. Daly,Michele Cargill,Todd Green,Huy Nguyen,Thomas B. Nutman,Peter A. Zimmerman,Margaret A. Tucker,Thomas J. Hudson,Alisa M. Goldstein,Eric S. Lander,Albert Lin +12 more
TL;DR: No functional sequence polymorphisms were found within the promoter, the exons, or the introns of any of these genes or within the IL-3/GM-CSF enhancer, suggesting that the primary defect in FE is not caused by a mutation in any one ofThese genes but, rather, is caused by another gene in the area.