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Gloria Ribas

Researcher at University of Valencia

Publications -  96
Citations -  7010

Gloria Ribas is an academic researcher from University of Valencia. The author has contributed to research in topics: Breast cancer & Single-nucleotide polymorphism. The author has an hindex of 32, co-authored 94 publications receiving 6673 citations. Previous affiliations of Gloria Ribas include Autonomous University of Barcelona & Hospital General Universitario Gregorio Marañón.

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Genome-wide association study identifies novel breast cancer susceptibility loci

Douglas F. Easton, +109 more
- 28 Jun 2007 - 
TL;DR: To identify further susceptibility alleles, a two-stage genome-wide association study in 4,398 breast cancer cases and 4,316 controls was conducted, followed by a third stage in which 30 single nucleotide polymorphisms were tested for confirmation.
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A common coding variant in CASP8 is associated with breast cancer risk

Angela Cox, +84 more
- 11 Feb 2007 - 
TL;DR: It is demonstrated that common breast cancer susceptibility alleles with small effects on risk can be identified, given sufficiently powerful studies, as well as the need for further studies to confirm putative genetic associations with breast cancer.
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Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Sergey Nejentsev, +221 more
- 06 Dec 2007 - 
TL;DR: In this article, the major histocompatibility complex (MHC) on chromosome 6 is associated with susceptibility to more common diseases than any other region of the human genome, including almost all disorders classified as autoimmune.
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Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

Shahana Ahmed, +144 more
- 29 Mar 2009 - 
TL;DR: Strong evidence is found for additional susceptibility loci on 3p and 17q and potential causative genes include SLC4A7 and NEK10 on3p and COX11 on 17q.
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Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics

Montserrat Garcia-Closas, +112 more
- 25 Apr 2008 - 
TL;DR: The findings show that common genetic variants influence the pathological subtype of breast cancer and provide further support for the hypothesis that ER-positive and ER-negative disease are biologically distinct.