Victoria A. Murday

Southern General Hospital — United Kingdom

Medicine · Health Sciences

22h-index5.0kcitations38works0.02yr avg
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Research Topics

Genetic factors in colorectal cancer(14), Colorectal Cancer Screening and Detection(7), BRCA gene mutations in cancer(6), Genomic variations and chromosomal abnormalities(6), Cancer Genomics and Diagnostics(5)

Publications38 total

Screening for Genetic Susceptibility to Paediatric Tumours
2016
Abstract 3673: Molecular analysis of pheochromocytoma after <i>maternal</i> transmission of <i>SDHD</i> mutation elucidates mechanism of parent-of-origin effect.
Cancer Research·2012
Molecular Analysis of Pheochromocytoma after Maternal Transmission of SDHD Mutation Elucidates Mechanism of Parent-of-Origin Effect
The Journal of Clinical Endocrinology & Metabolism·2011· 61 citedOpen Access
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Nature Genetics·2011· 494 cited
Genetic Predisposition to Cancer: The Consequences of a Delayed Diagnosis of Gorlin Syndrome
Clinical Oncology·2005· 14 cited
Congress Calendar
Respiration·2004Open Access
Pulmonary Masses Presenting 11 Years after Abdominal Surgery
Respiration·2004· 5 cited
The cancer family clinic
2003
An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome
The American Journal of Human Genetics·2003· 107 citedOpen Access
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with <i>FOXC2</i> mutations or linkage to 16q24
Journal of Medical Genetics·2002· 283 citedOpen Access
Colonoscopy in asymptomatic individuals with a family history of colorectal cancer
Annals of Surgical Oncology·2002· 26 cited
Two Families with Blepharophimosis/Ptosis/Epicanthus Inversus Syndrome Have Mutations in the Putative Forkhead Transcription Factor <i>FOXL2</i>
Genetic Testing·2001· 25 cited
Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene?
Familial Cancer·2001· 12 cited
Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection
American Journal of Medical Genetics·2001· 117 cited
Colonoscopy in symptomatic patients with positive family history of colorectal cancer.
PubMed·2000· 11 cited
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2
Nature Genetics·2000· 303 cited
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
Human Genetics·2000· 28 cited
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
Human Genetics·2000· 6 cited
Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2
Journal of Medical Genetics·2000· 4 cited
Three novel mutations of the proto-oncogeneKIT cause human piebaldism
American Journal of Medical Genetics·2000· 20 cited
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Frequent Co-authors

D. Timothy Bishop(8), Richard S. Houlston(6), Rosalind A. Eeles(5), Walter F. Bodmer(4), E. Solomon(4), Charis Eng(4), Steve Jeffery(4), Anna Rajab(4), Christiane Fenske(4), E. Ternes-Pereira(4), P J Finan(4), S V Hodgson(3), Glen Brice(3), Peter Mortimer(3), Sahar Mansour(3), Ali R. Afzal(3), Michael A. Patton(3), Steven Jeffery(3), B. M. Stephenson(3), Denise Sheer(2)