Richard S. Houlston

发表

Association Studies

Emily L. Webb, Richard S. Houlston, 2009, Statistics and Informatics in Molecular Cancer Research.

Algorithmic considerations when analysing capture Hi-C data

Richard S. Houlston, Linden Disney-Hogg, Ben Kinnersley, 2020, Wellcome open research.

Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic

Andriy Derkach, Ian Tomlinson, Lisa J. Strug, 2014, Bioinform..

SNPLINK: multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal

Emily L. Webb, Richard S. Houlston, Gabrielle S. Sellick, 2005, Bioinform..

visPIG - A Web Tool for Producing Multi-Region, Multi-Track, Multi-Scale Plots of Genetic Data

Gabriele Migliorini, Richard S. Houlston, Matthew Scales, 2014, PloS one.

Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma

Christopher I. Amos, Faith Davis, Sanjay Shete, 2012, Human Genetics.

Pleiotropic Associations of Risk Variants Identified for Other Cancers With Lung Cancer Risk: The PAGE and TRICL Consortia

Wei Chen, Dana C. Crawford, Ewa Deelman, 2014, Journal of the National Cancer Institute.

Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia

Daniel Sinnett, Csaba Szalai, Jasmine Healy, 2011, Haematologica.

The Predicted Impact of Coding Single Nucleotide Polymorphisms Database

Emily L. Webb, Richard S. Houlston, Gabrielle S. Sellick, 2005, Cancer Epidemiology Biomarkers & Prevention.

Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer

Steven Gallinger, Oliver Sieber, David J. Kerr, 2011, PLoS genetics.

Putative cis-regulatory drivers in colorectal cancer

Emmanouil T. Dermitzakis, Pedro G. Ferreira, Ian Tomlinson, 2014, Nature.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

William S. Bush, Bin Zhu, Angeline S. Andrew, 2017, Nature Genetics.

The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression

Emmanouil T. Dermitzakis, Jussi Taipale, Tianran Peng, 2017, Nature Communications.

Architecture of inherited susceptibility to common cancer

Olivia Fletcher, Richard S. Houlston, R. Houlston, 2010, Nature Reviews Cancer.

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer

Ian J. Deary, Archie Campbell, Sergi Castellví-Bel, 2015, Scientific Reports.

Common variation at 6 p 21 . 31 ( BAK 1 ) influences the risk of chronic lymphocytic leukemia *

Eran Halperin, Nicola J. Camp, Neil E. Caporaso, 2012 .

Low-Penetrance Susceptibility Variants in Familial Colorectal Cancer

Jukka-Pekka Mecklin, Richard S. Houlston, Lauri A. Aaltonen, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Allelic Variation at the 8q23.3 Colorectal Cancer Risk Locus Functions as a Cis-Acting Regulator of EIF3H

Miguel Manzanares, Yussanne Ma, Richard S. Houlston, 2010, PLoS genetics.

Genome-wide association study identiﬁes multiple susceptibility loci for glioma

Melissa Bondy, Markus M. Nöthen, Anthony Swerdlow, 2022 .