About: Alisa M. Goldstein

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American genetic epidemiologist

Attributes	Values
rdf:type	Item
field of work	wds:Q91400899-3a177b16-4884-2b9f-ca28-a65d6c406f3d wds:Q91400899-db178a1b-4ae0-5fdd-2689-e6bd3bd09730
field of work	genetic epidemiology cancer epidemiology
description	wetenschapper (nl) дослідник (uk) American genetic epidemiologist (en)
rdfs:label	Alisa M Goldstein (nl) Alisa M. Goldstein (en) Alisa M. Goldstein (es)
skos:prefLabel	Alisa M Goldstein (nl) Alisa M. Goldstein (en) Alisa M. Goldstein (es)
name	Alisa M Goldstein (nl) Alisa M. Goldstein (en) Alisa M. Goldstein (es)
Scopus author ID	wds:Q91400899-cb07d48e-475c-b687-3699-49818ad5ebe3
Scopus author ID	7403063085
given name	wds:Q91400899-9d1ee9dc-4a84-6556-1328-3598df7c3ca2 wds:Q91400899-ec6decfa-4552-a0da-49b1-6006f5924f31
given name	Miriam Alisa
image	wds:Q91400899-2ddea2b0-419d-e03d-c737-735745402e35
instance of	wds:Q91400899-D9FBFB97-E54E-404D-8749-B44031C0A67C
image
instance of	Homo sapiens
doctoral advisor	wds:Q91400899-0211f15b-4ea4-7c81-987b-7fc0f7f9b1be
Google Knowledge Graph ID	wds:Q91400899-AFB38102-DC2A-4CC2-9D07-03DB830055DC
Google Knowledge Graph ID	http://g.co/kg/g/11fj56p4_l
doctoral advisor	Robert W. Haile
Google Knowledge Graph ID	/g/11fj56p4_l
Semantic Scholar author ID	wds:Q91400899-860ef6ca-438d-f2d6-b68a-a3ef0739aea4
Semantic Scholar author ID	3154489
skos:altLabel	A. M Goldstein (en) Alisa Goldstein (en) Alisa M Goldstein (en) Alisa Miriam Goldstein (en)
occupation	wds:Q91400899-53F9580F-44C3-47B4-8685-51FAEC4CECD0
sex or gender	wds:Q91400899-ED025A18-4EE8-419F-846B-4E9DF607034E
country of citizenship	wds:Q91400899-2c461165-4e35-613a-8fcc-f37e567efe64
educated at	wds:Q91400899-930260a8-4367-5efd-9475-86b04803bc9c
family name	wds:Q91400899-7d34edbf-4ec3-7c80-97cc-23c1cfc9a86a
occupation	epidemiologist
sex or gender	female organism
country of citizenship	United States of America
educated at	University of California, Los Angeles
family name	Goldstein
ORCID iD	wds:Q91400899-3AE7BFDB-7B0E-4885-9C05-22563D6932D4
ORCID iD	https://orcid.org/0000-0002-7538-3582
ORCID iD	0000-0002-7538-3582
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q91400899 Alisa M. Goldstein
is author of	Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types The effect on melanoma risk of genes previously associated with telomere length Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma A variant in FTO shows association with melanoma risk not due to BMI Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33 Genome-wide association study identifies three new melanoma susceptibility loci Genome-wide association study identifies three loci associated with melanoma risk Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations Comprehensive evaluation of allele frequency differences of MC1R variants across populations. Common sequence variants on 20q11.22 confer melanoma susceptibility Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 Geographical variation in the penetrance of CDKN2A mutations for melanoma Common genetic variants in the 9p21 region and their associations with multiple tumours Heterogeneity of risk for melanoma and pancreatic and digestive malignancies Telomere length and the risk of cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations On the interplay of telomeres, nevi and the risk of melanoma A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma Detectable clonal mosaicism and its relationship to aging and cancer High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL Characterization of large structural genetic mosaicism in human autosome CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF. A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours Nucleotide diversity and population differentiation of the melanocortin 1 receptor gene, MC1R. Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma-prone families with/without CDKN2A mutations A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies Pediatric melanoma in melanoma-prone families Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families Cutaneous phenotype andMC1R variants as modifying factors for the development of melanoma inCDKN2A G101W mutation carriers from 4 countries Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility Germline variation at CDKN2A and associations with nevus phenotypes among members of melanoma families. Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

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