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Yvonne Wallis

Observed names: Wallis, Y, Wallis, Yvonne, Y Wallis, Y. Wallis, Yvonne L Wallis, Yvonne L. Wallis
Observed institutions: University of Insubria, North Bristol NHS Trust, St Bartholomew's Hospital, Manchester Academic Health Science Centre, Great Ormond Street Hospital, Maastricht University Medical Centre, Southmead Hospital, Southampton General Hospital, Bristol Royal Hospital for Children, Northwick Park Hospital, Cambridge University Hospitals NHS Foundation Trust, University of Manchester, London School of Hygiene & Tropical Medicine, Birmingham Women's Hospital, Birmingham Children's Hospital, Heartlands Hospital, Birmingham Women’s and Children’s NHS Foundation Trust, University College London, University of Birmingham, Icahn School of Medicine at Mount Sinai
ORCID: 0000-0002-5079-967X
Observed ORCID: 0000-0002-5079-967X
OpenAlex ID: A5050261696
The Wnt Antagonist sFRP1 in Colorectal Tumorigenesis
2004 · Germaine M. Caldwell, Carolyn Jones, et al. · Cancer Research · 280
Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD
2018 · Katrina A Andrews, David B Ascher, et al. · Journal of Medical Genetics · 255
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Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition
1999 · Yvonne L Wallis, Dion G Morton, et al. · Journal of Medical Genetics · 192
Population Testing for Cancer Predisposing BRCA1/BRCA2 Mutations in the Ashkenazi-Jewish Community: A Randomized Controlled Trial
2014 · Ranjit Manchanda, Kelly Loggenberg, et al. · JNCI Journal of the National Cancer Institute · 184
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Cost-effectiveness of Population Screening for BRCA Mutations in Ashkenazi Jewish Women Compared With Family History–Based Testing
2014 · Ranjit Manchanda, Rosa Legood, et al. · JNCI Journal of the National Cancer Institute · 173
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A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma
2013 · Eleanor Rattenberry, Lindsey Vialard, et al. · The Journal of Clinical Endocrinology & Metabolism · 102
Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected Individuals
2019 · Claire Forde, Derek H.K. Lim, et al. · European Urology Oncology · 94
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Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44
2017 · Lauren M. Watson, Elizabeth Bamber, et al. · The American Journal of Human Genetics · 85
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Multiplex PCR and Next Generation Sequencing for the Non-Invasive Detection of Bladder Cancer
2016 · Douglas G. Ward, Laura Baxter, et al. · PLoS ONE · 84
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p16 expression in Barrett's esophagus and esophageal adenocarcinoma: association with genetic and epigenetic alterations
2004 · Laura J. Hardie, S. Jane Darnton, et al. · Cancer Letters · 78
Randomised trial of population‐based BRCA testing in Ashkenazi Jews: long‐term outcomes
2019 · R Manchanda, M Burnell, et al. · BJOG An International Journal of Obstetrics & Gynaecology · 68
Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia
2016 · S R Cardoso, G Ryan, et al. · Leukemia · 68
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New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies
2018 · DDD Study, Fabiola Ceroni, et al. · Human Genetics · 54
Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations
2016 · Ranjit Manchanda, Matthew Burnell, et al. · Journal of Medical Genetics · 54
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An unusually severe phenotype for familial adenomatous polyposis
1997 · D M Eccles, P W Lunt, et al. · Archives of Disease in Childhood · 51
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Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review
2017 · Ruth T Casey, Anne Y Warren, et al. · The Journal of Clinical Endocrinology & Metabolism · 45
Bile Acids Reduce the Apoptosis-Inducing Effects of Sodium Butyrate on Human Colon Adenoma (AA/C1) Cells: Implications for Colon Carcinogenesis
2000 · Lorna McMillan, Stephen Butcher, et al. · Biochemical and Biophysical Research Communications · 43
Attitude towards and factors affecting uptake of population‐based BRCA testing in the Ashkenazi Jewish population: a cohort study
2019 · R Manchanda, M Burnell, et al. · BJOG An International Journal of Obstetrics & Gynaecology · 36
Germline ESR2 mutation predisposes to medullary thyroid carcinoma and causes up-regulation of RET expression
2016 · Joel Smith, Martin L. Read, et al. · Human Molecular Genetics · 34
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Population Study of Ovarian Cancer Risk Prediction for Targeted Screening and Prevention
2020 · Faiza Gaba, Oleg Blyuss, et al. · Cancers · 32
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A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia
2018 · Ben Johnson, Rachel Doak, et al. · Research and Practice in Thrombosis and Haemostasis · 31
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Automated DNA Sequencing
2010 · Yvonne Wallis, Natalie Morrell · Methods in molecular biology · 30
Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group
2018 · Sarah M. Nielsen, Diana M. Eccles, et al. · JCO Precision Oncology · 28
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British Gynaecological Cancer Society/British Association of Gynaecological Pathology consensus for germline and tumor testing for BRCA1/2 variants in ovarian cancer in the United Kingdom
2021 · Sudha Sundar, Ranjit Manchanda, et al. · International Journal of Gynecological Cancer · 27
Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing
2016 · Helen Byers, Yvonne Wallis, et al. · European Journal of Human Genetics · 26
Works count: 71
Citation count: 2,332
H-index: 25
I10-index: 33
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