Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies-Reference-Cited by-同舟云学术

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

Published:2019-11-15 Issue:11 Volume:15 Page:e1008490
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Schlafly Andrew,Pfeiffer Ruth M.^ORCID,Nagore Eduardo^ORCID,Puig Susana,Calista Donato,Ghiorzo Paola^ORCID,Menin Chiara^ORCID,Fargnoli Maria Concetta^ORCID,Peris Ketty,Song Lei,Zhang Tongwu,Shi Jianxin,Landi Maria Teresa,Sampson Joshua Neil

Funder

Fondo de Investigaciones Sanitarias

Fundació La Marató

European Commission

Fundación Científica Asociación Española Contra el Cáncer

European Academy of Dermatology and Venereology

Italian Ministry of Health

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference23 articles.

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2. Online Mendelian Inheritance in Man, OMIM McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD) [12/12/2018]. Available from: https://omim.org/.

3. Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations;AV Khera;Nat Genet,2018

4. Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations;M Potrony;Jama Dermatol,2016

5. Reevaluation of SNP heritability in complex human traits;D Speed;Nat Genet,2017

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