Mark R. Morris

Germline SDHB Mutations and Familial Renal Cell Carcinoma

Christopher J. Ricketts, Emma R. Woodward, Pip Killick et al. · JNCI Journal of the National Cancer Institute · 2008 · 339 citations · Full text

Life Sciences, Genetics, Oncology +17

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

Dewi Astuti, Mark R. Morris, Wendy N. Cooper et al. · Nature Genetics · 2012 · 252 citations

Life Sciences, Genetics, Molecular Genetics +16

Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

Neil V. Morgan, Mark R. Morris, Hakan Cangül et al. · PLoS Genetics · 2010 · 225 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinoma

Mark R. Morris, Christopher J. Ricketts, Dean Gentle et al. · Oncogene · 2010 · 197 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Identification of candidate tumour suppressor genes frequently methylated in renal cell carcinoma

Mark R. Morris, Christopher J. Ricketts, Dean Gentle et al. · Oncogene · 2010 · 173 citations · Full text

Medicine, Genetics, Molecular Genetics +14