C. Clark

发表

Ascertainment of myotonic dystrophy through cataract by selective screening.

N. Haites, P. Turnpenny, J. Dean, 1995, Journal of medical genetics.

Intelligence quotient profile in myotonic dystrophy, intergenerational deficit, and correlation with CTG amplification.

P. Turnpenny, K. Kelly, C. Clark, 1994, Journal of medical genetics.

Length and somatic mosaicism of CAG and GGN repeats in the androgen receptor gene and the risk of prostate cancer in men with benign prostatic hyperplasia

H. McLeod, N. Haites, G. Murray, 2004, Annals of Saudi medicine.

Continuing the sequence? Towards an economic evaluation of whole genome sequencing for the diagnosis of rare diseases in Scotland

M. Ryan, Z. Miedzybrodzka, R. McGowan, 2021, Journal of Community Genetics.

Interactions between anti-EGFR therapies and cytotoxic chemotherapy in oesophageal squamous cell carcinoma: why clinical trials might have failed and how they could succeed

Z. Miedzybrodzka, G. Murray, R. Petty, 2020, Cancer Chemotherapy and Pharmacology.

Improvement in the quality of molecular analysis of EGFR in non-small-cell lung cancer detected by three rounds of external quality assessment

R. Butler, Z. Deans, S. Parry, 2013, Journal of Clinical Pathology.

The Novel Virus Genotyping Tool (STAR) and its Use in Subtyping Human Immunodeficiency Virus Type-1 and Hepatitis B Viruses

Richard Myers, Paul Kellam, Catherine V. Gale, 2004, Spanish Bioinformatics Conference.

Genotyping Hepatitis B virus from whole- and sub-genomic fragments using position-specific scoring matrices in HBV STAR.

Paul Kellam, Richard Myers, Caroline Clark, 2006, The Journal of general virology.

Interactions between anti-EGFR therapies and cytotoxic chemotherapy in oesophageal squamous cell carcinoma: why clinical trials might have failed and how they could succeed

Z. Miedzybrodzka, G. Murray, R. Petty, 2020, Cancer Chemotherapy and Pharmacology.

Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2‐year‐old girl with familial adenomatous polyposis

N. Haites, M. Dunlop, J. Dean, 1996 .

Enhancement of Synthetic Lethality via Combinations of ABT-888, a PARP Inhibitor, and Carboplatin In Vitro and In Vivo Using BRCA1 and BRCA2 Isogenic Models

T. O'Connor, J. Weitzel, C. Clark, 2012, Molecular Cancer Therapeutics.

Preclinical Development Enhancement of Synthetic Lethality via Combinations of ABT-888 , a PARP Inhibitor , and Carboplatin In Vitro and In Vivo Using BRCA 1 and BRCA 2 Isogenic Models

T. O'Connor, J. Weitzel, C. Clark, 2012 .

Vitamin D receptor, HER-2 polymorphisms and risk of prostate cancer in men with benign prostate hyperplasia.

H. McLeod, N. Haites, G. Murray, 2004, Saudi medical journal.

HGVS Nomenclature in Practice: An Example from the United Kingdom National External Quality Assessment Scheme

Caroline Clark, J. T. Dunnen, J. Fairley, 2016, Human mutation.

Evidence for 28 genetic disorders discovered by combining healthcare and research data

Patrick J. Short, M. Hurles, L. Vissers, 2020, Nature.

The contribution of X-linked coding variation to severe developmental disorders

M. Hurles, R. Sandford, D. Baralle, 2020, Nature Communications.

Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: results from the ETOP Lungscape Project

A. Warth, A. Marchetti, L. Bubendorf, 2018, Annals of oncology : official journal of the European Society for Medical Oncology.

Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing

Sancha Martin, E. Tobias, A. Biankin, 2022, European Journal of Human Genetics.

Gefitinib and EGFR Gene Copy Number Aberrations in Esophageal Cancer.

Z. Miedzybrodzka, D. Ferry, G. Murray, 2017, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Combined linkage and association analysis of classical Hodgkin lymphoma

T. Cezard, R. Houlston, G. Murray, 2018, Oncotarget.

Estimation of the Mutation Frequencies in Charcot-Marie-Tooth Disease Type 1 and Hereditary Neuropathy with Liability to Pressure Palsies: A European Collaborative Study

X. Estivill, E. Mariman, N. Archidiacono, 1996, European journal of human genetics : EJHG.

Epidermal Growth Factor (EGFR) copy number aberrations in esophageal and gastro-esophageal junctional carcinoma

Z. Miedzybrodzka, D. Ferry, G. Murray, 2015, Molecular Cytogenetics.

Epidermal Growth Factor ( EGFR ) copy number aberrations in esophageal and gastroesophageal junctional carcinoma

Z. Miedzybrodzka, D. Ferry, G. Murray, 2015 .

Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies.

C. van Broeckhoven, N. Haites, V. Timmerman, 1999, Journal of the peripheral nervous system : JPNS.

Linkage in a family with X‐linked Charcot‐Marie‐Tooth disease

N. Haites, K. Kelly, C. Clark, 1989, Clinical genetics.

CYP3A4 and VDR gene polymorphisms and the risk of prostate cancer in men with benign prostate hyperplasia

H. McLeod, N. Haites, G. Murray, 2003, British Journal of Cancer.

The C677T polymorphism in the methylenetetrahydrofolate reductase gene (MTHFR), maternal use of folic acid supplements, and risk of isolated clubfoot: A case-parent-triad analysis.

Z. Miedzybrodzka, N. Maffulli, L. Sharp, 2006, American journal of epidemiology.

Urinary bladder recurrences following ureteroscopic biopsies of upper tract urothelial cancers: a multi-centre observational study with genomic assessment for clonality

J. Bourdon, S. Bray, Sunjay Jain, 2022, Scottish medical journal.

CYP3A4 promoter variant is associated with prostate cancer risk in men with benign prostate hyperplasia.

H. McLeod, N. Haites, G. Murray, 2002, Oncology reports.

Gastric fundic gland polyps in south‐east Scotland: Absence of adenomatous polyposis coli gene mutations and a strikingly low prevalence of Helicobacter pylori infection

Subrata Ghosh, J. Coia, A. Shand, 2002, Journal of gastroenterology and hepatology.

CYP3A4 promoter variant in Saudi, Ghanaian and Scottish Caucasian populations.

H. McLeod, N. Haites, D. Ofori-Adjei, 2000, Pharmacogenetics.

Ascertainment ofmyotonic dystrophy through cataractbyselective screening

N. Haites, A. Kidd, K. Kelly, 2011 .

GASTRIC CARCINOMA: EXPERIMENTAL AND CLINICAL Gastric fundic gland polyps in south-east Scotland: Absence of adenomatous polyposis coli gene mutations and a strikingly low prevalence of Helicobacter pylori infection

Subrata Ghosh, J. Coia, A. Shand, 2002 .