David Allsup

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood et al. · The American Journal of Human Genetics · 2016 · 463 citations · Full text

Whole-genome Sequencing, Allelic Variant, Genetic Disorder +11

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia

Maria Chiara Di Bernardo, Dalemari Crowther-Swanepoel, Peter Broderick et al. · Nature Genetics · 2008 · 359 citations · Full text

Genome-wide Association Study, Disease Susceptibility, Chronic Lymphocytic Leukemia +11

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

Dalemari Crowther-Swanepoel, Peter Broderick, Maria Chiara Di Bernardo et al. · Nature Genetics · 2010 · 224 citations · Full text

Hematological Malignancy, Allelic Variant, Oncology +11

Alemtuzumab in Combination With Methylprednisolone Is a Highly Effective Induction Regimen for Patients With Chronic Lymphocytic Leukemia and Deletion of <i>TP53</i>: Final Results of the National Cancer Research Institute CLL206 Trial

Andrew R. Pettitt, Richard E. Jackson, Stacey Carruthers et al. · Journal of Clinical Oncology · 2012 · 164 citations

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

Benjamin C. Johnson, Gillian Lowe, Jane Wong Fütterer et al. · Haematologica · 2016 · 138 citations · Full text