1-4 of 4
Gabrielle S. Sellick
Close
Sort by
Journal Articles

Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis

Gabrielle S. Sellick, Rachel Wade, Susan Richards, David G. Oscier, Daniel Catovsky, Richard S. Houlston
Journal: Blood
Blood (2008) 111 (3): 1625–1633.
https://doi.org/10.1182/blood-2007-08-110130
Published: 2008
Includes: Supplemental data
Journal Articles

A high-density SNP genome-wide linkage search of 206 families identifies susceptibility loci for chronic lymphocytic leukemia

Gabrielle S. Sellick, Lynn R. Goldin, Ruth W. Wild, Susan L. Slager, Laura Ressenti, Sara S. Strom, Martin J. S. Dyer, Francesca R. Mauro, Gerald E. Marti, Stephen Fuller, Matthew Lyttelton, Thomas J. Kipps, Michael J. Keating, Timothy G. Call, Daniel Catovsky, Neil Caporaso, Richard S. Houlston
Journal: Blood
Blood (2007) 110 (9): 3326–3333.
https://doi.org/10.1182/blood-2007-05-091561
Published: 2007
Journal Articles

Variants in the ATM - BRCA2-CHEK2 axis predispose to chronic lymphocytic leukemia

Matthew F. Rudd, Gabrielle S. Sellick, Emily L. Webb, Daniel Catovsky, Richard S. Houlston
Journal: Blood
Blood (2006) 108 (2): 638–644.
https://doi.org/10.1182/blood-2005-12-5022
Published: 2006
Includes: Supplemental data
Journal Articles

Genomewide Linkage Analysis of Chronic Lymphocytic Leukemia by Use of a High-Density Single Nucleotide Polymorphism Assay Containing 11,555 Markers.

Gabrielle S. Sellick, PhD, Ruth Allinson, Estella Matutes, MD, Martin Yuille, PhD, Daniel Catovsky, MD, Richard S. Houlston, MD, PhD
Journal: Blood
Blood (2004) 104 (11): 1904.
https://doi.org/10.1182/blood.V104.11.1904.1904
Published: 2004