Author

Richard Houghton

Observed name: Houghton, R

Institution: Wellcome Sanger Institute

Observed institutions: Scripps Research Institute, Wellcome Sanger Institute, Roche (United Kingdom), MRC Prion Unit, National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, University College London, Medical Research Council

ORCID: 0000-0002-6646-548X

Observed ORCID: 0000-0002-6646-548X

OpenAlex ID: A5081054223

Genome-wide Generation and Systematic Phenotyping of Knockout Mice Reveals New Roles for Many Genes

2013 · Jacqueline K. White, Anna-Karin Gerdin, et al. · Cell · 513

The mammalian gene function resource: the international knockout mouse consortium

2012 · Allan Bradley, Konstantinos Anastassiadis, et al. · Mammalian Genome · 312

A naturally occurring variant of the human prion protein completely prevents prion disease

2015 · Emmanuel A. Asante, Michelle Smidak, et al. · Nature · 199

Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project

2012 · Abdel Ayadi, Marie-Christine Birling, et al. · Mammalian Genome · 158

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

2015 · Martin Hrabě de Angelis, George Nicholson, et al. · Nature Genetics · 147

A resource of targeted mutant mouse lines for 5,061 genes

2021 · Marie-Christine Birling, Atsushi Yoshiki, et al. · Nature Genetics · 108

The Role of Sphingosine-1-Phosphate Transporter Spns2 in Immune System Function

2012 · Anastasia Nijnik, Simon Clare, et al. · The Journal of Immunology · 100

Dissociation of pathological and molecular phenotype of variant Creutzfeldt–Jakob disease in transgenic human prion protein 129 heterozygous mice

2006 · Emmanuel A. Asante, Jacqueline M. Linehan, et al. · Proceedings of the National Academy of Sciences · 84

Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource

2013 · Sanger Mouse Genetics Project, Edward Ryder, et al. · Mammalian Genome · 71

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins

2009 · Emmanuel A. Asante, Ian Gowland, et al. · Journal of General Virology · 67

Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase

2013 · Sanger Mouse Genetics Project, Edward Ryder, et al. · Transgenic Research · 47

Pattern of Cytokine Release in Patients with Chronic Lymphocytic Leukemia Treated with Obinutuzumab and Possible Relationship with Development of Infusion Related Reactions (IRR)

2014 · Ciara Louise Freeman, Franck Morschhauser, et al. · Blood · 11

Risk Factors Associated with the Development of Infusion-Related Reactions in Patients with Chronic Lymphocytic Leukaemia Treated with Anti-CD20 Monoclonal Antibodies: Analysis of the CLL11 Study Dataset

2014 · Ciara Louise Freeman, Mark Dixon, et al. · Blood · 10

Large‐scale mouse knockouts and phenotypes

2012 · Ramiro Ramírez‐Solis, Edward Ryder, et al. · WIREs Systems Biology and Medicine · 7

Genomic analysis of a novel spontaneous albino C57BL/6N mouse strain

2013 · Edward Ryder, Kim Wong, et al. · genesis · 2

Works count: 18

Citation count: 1,836

H-index: 11

I10-index: 13