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Martha Linet
Institutions:
National Institutes of Health,
University of Eastern Finland,
National Cancer Institute,
Division of Cancer Epidemiology and Genetics
Observed institutions:
National Institutes of Health,
University of Eastern Finland,
Chinese Center For Disease Control and Prevention,
National Cancer Institute,
Division of Cancer Epidemiology and Genetics
OpenAlex ID:
A5070086359
Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma
2012
·
Yanhong Liu
, Beatrice S. Melin
, et al.
·
Human Genetics
·
21
PDF
Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women
2025
·
Peh Joo Ho
, Christine Kim Yan Loo
, et al.
·
Cancers
PDF
Overlap of high-risk individuals across family history, genetic & non-genetic breast cancer risk models: Analysis of 180,398 women from European & Asian ancestries
2025
·
Peh Joo Ho
, Christine Kim Yan Loo
, et al.
·
medRxiv
神経膠芽腫:サブタイプのゲノムワイド関連解析から,神経膠芽腫と膠芽腫以外の神経膠腫との遺伝性発症リスクの差異が明らかになる
2017
·
Melin Beatrice S
, Andersson Ulrika
, et al.
·
Nature Genetics
Illumina® - based multiplexed genotyping indicates a role for altered DNA repair and genomic maintenance in susceptibility to benzene toxicity
2006
·
Qing Lan
, Martyn T. Smith
, et al.
·
Cancer Research
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Works count:
5
Citation count:
21
H-index:
1
I10-index:
1
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