Publications:

Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs315122

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Dataset of GWAS-identified variants underlying venous thromboembolism susceptibility and linkage to cancer aggressiveness.

Data In Brief

Tavares, Valéria V; Pinto, Ricardo R; Assis, Joana J; Pereira, Deolinda D; Medeiros, Rui R

Publication Date: 2020-06

Variant appearance in text: rs315122

PubMed Link: 32258274

Variant Present in the following documents:

• Main text

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs315122

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.

Bmc Medical Genetics

Greliche, Nicolas N; Germain, Marine M; Lambert, Jean-Charles JC; Cohen, William W; Bertrand, Marion M; Dupuis, Anne-Marie AM; Letenneur, Luc L; Lathrop, Mark M; Amouyel, Philippe P; Morange, Pierre-Emmanuel PE; Trégouët, David-Alexandre DA

Publication Date: 2013-03-20

Variant appearance in text: rs315122

PubMed Link: 23509962

Variant Present in the following documents:

• Main text
• 1471-2350-14-36.pdf

View BVdb publication page