Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

ChroMoS: an integrated web tool for SNP classification, prioritization and functional interpretation

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Cancer statistics, 2013

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Ral GTPases in tumorigenesis: Emerging from the shadows

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HLA and disease: guilt by association

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Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population

(2013) Dennis E K Tan et al.   NATURE GENETICS

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

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Adaptor Proteins Intersectin 1 and 2 Bind Similar Proline-Rich Ligands but Are Differentially Recognized by SH2 Domain-Containing Proteins

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Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies

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Invited Commentary: More Surprises From a Gene Desert

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A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11

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The genetic landscape of mutations in Burkitt lymphoma

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Proteomic analysis of HIV-1 Nef cellular binding partners reveals a role for exocyst complex proteins in mediating enhancement of intercellular nanotube formation

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Estimating Missing Heritability for Disease from Genome-wide Association Studies

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Genome-wide association study identifies new prostate cancer susceptibility loci

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Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility

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Analysis of the coding genome of diffuse large B-cell lymphoma

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GWAS of Follicular Lymphoma Reveals Allelic Heterogeneity at 6p21.32 and Suggests Shared Genetic Susceptibility with Diffuse Large B-cell Lymphoma

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Tumor Necrosis Factor (TNF) and Lymphotoxin-  (LTA) Polymorphisms and Risk of Non-Hodgkin Lymphoma in the InterLymph Consortium

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Human leukocyte antigen class I and II alleles in non-Hodgkin lymphoma etiology

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Sec5 and Exo84 Foster Oncogenic Ras-Mediated Tumorigenesis

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A map of human genome variation from population-scale sequencing

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

(2010) Dalemari Crowther-Swanepoel et al.   NATURE GENETICS

A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)

(2010) Victor Enciso-Mora et al.   NATURE GENETICS

Common SNPs explain a large proportion of the heritability for human height

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Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32

(2010) Lucia Conde et al.   NATURE GENETICS

Polymorphic Cis- and Trans-Regulation of Human Gene Expression

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MYC gene rearrangements are associated with a poor prognosis in diffuse large B-cell lymphoma patients treated with R-CHOP chemotherapy

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Highly increased familial risks for specific lymphoma subtypes

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Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma

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Common Gene Variants in the Tumor Necrosis Factor (TNF) and TNF Receptor Superfamilies and NF-kB Transcription Factors and Non-Hodgkin Lymphoma Risk

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A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

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

(2008) Maria Chiara Di Bernardo et al.   NATURE GENETICS