C. Meldrum

发表

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

R. Scott, A. Spigelman, J. Attia, 2013, BMC Medical Genomics.

Direct integrin αvβ6-ERK binding: implications for tumour growth

I. Macreadie, C. Meldrum, M. Baker, 2002, Oncogene.

CD36 forms covalently associated dimers and multimers in platelets and transfected COS-7 cells.

C. Meldrum, G. Burns, R. Thorne, 1997, Biochemical and biophysical research communications.

Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer

R. Scott, A. Spigelman, C. Meldrum, 2002, Journal of Cancer Research and Clinical Oncology.

Direct integrin alphavbeta6-ERK binding: implications for tumour growth.

I. Macreadie, C. Meldrum, M. Baker, 2002, Oncogene.

AmpliVar: Mutation Detection in High‐Throughput Sequence from Amplicon‐Based Libraries

G. Taylor, C. Meldrum, O. Kondrashova, 2015, Human mutation.

Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations

R. Scott, A. Spigelman, J. Kirk, 2005, International journal of cancer.

Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data.

Shivashankar H. Nagaraj, Kylie Gwynne, S. Easteal, 2020, American journal of human genetics.

Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer

R. Scott, J. Lubiński, C. Meldrum, 2007, Scandinavian journal of gastroenterology.

BRCA2 mutations in a population‐based series of patients with ocular melanoma

J. Aitken, C. Meldrum, B. Armstrong, 2002, International journal of cancer.

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients

R. Scott, A. Spigelman, B. Talseth-Palmer, 2013, Hereditary cancer in clinical practice.

When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans

R. Scott, A. Spigelman, C. Meldrum, 2016, Hereditary Cancer in Clinical Practice.

cDNA analysis of the BRCA1 unclassified variant c.5194‐12G>A

C. Meldrum, M. Wong-Brown, M. McPhillips, 2013, Clinical genetics.

Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients

R. Scott, J. Lubiński, C. Meldrum, 2006, Cancer Epidemiology Biomarkers & Prevention.

Can a familial gastrointestinal tumour syndrome be allelic with Waardenburg syndrome?

L. Ashman, C. Meldrum, S. Ackland, 2011, Clinical genetics.

Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c‐KIT

L. Ashman, C. Meldrum, G. Varigos, 2008, The British journal of dermatology.

Biochemical isolation of a membrane microdomain from resting platelets highly enriched in the plasma membrane glycoprotein CD36.

C. Meldrum, G. Burns, D. Dorahy, 1996, The Biochemical journal.

Hereditary Cancer in Clinical Practice 2006; 4(2) pp. 94-102 The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria

R. Scott, J. Lubiński, C. Meldrum, 2006 .

Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions.

R. Scott, M. Digilio, C. Meldrum, 2015, European journal of medical genetics.

Hereditary non‐polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations

A. Spigelman, C. Meldrum, E. Thompson, 2004, Clinical genetics.

A Comparison Between Denaturing Gradient Gel Electrophoresis and Denaturing High Performance Liquid Chromatography in Detecting Mutations in Genes Associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC) and the Identification of 9 New Mutations Previously Unidentified by DGGE

R. Scott, C. Meldrum, M. Agrez, 2003, Hereditary Cancer in Clinical Practice.

The αvβ6 integrin induces gelatinase B secretion in colon cancer cells

C. Meldrum, J. Niu, X. Gu, 1999 .

IGF1 is a modifier of disease risk in hereditary non‐polyposis colorectal cancer

R. Scott, J. Lubiński, C. Meldrum, 2008, International journal of cancer.

A Pathway to Precision Medicine for Aboriginal Australians: A Study Protocol

M. Dinger, C. Meldrum, A. Brown, 2021, Methods and protocols.

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Peter Marynen, Rodney Scott, Patrick S Tarpey, 2008, American journal of human genetics.

An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.

C. Meldrum, S. O’Donnell, Anupam Rao, 2014, European journal of medical genetics.

Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients

R. Scott, C. Meldrum, K. Ashton, 2005, Hereditary cancer in clinical practice.

The alpha v beta 6 integrin induces gelatinase B secretion in colon cancer cells.

C. Meldrum, J. Niu, X. Gu, 1999, International journal of cancer.

Somatic‐gonadal mosaicism causing Sotos syndrome

R. Scott, C. Meldrum, B. Kamien, 2016, American journal of medical genetics. Part A.

Integrin-mediated signalling of gelatinase B secretion in colon cancer cells.

C. Meldrum, J. Niu, X. Gu, 1998, Biochemical and biophysical research communications.

MDM2 SNP309 T>G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients

R. Scott, J. Lubiński, C. Meldrum, 2007, International journal of cancer.

Aurora‐A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

R. Scott, J. Lubiński, C. Meldrum, 2008, International journal of cancer.

Missense Mutations in Cancer Predisposing Genes: Can We Make Sense of Them?

R. Scott, C. Meldrum, Rodney J Scott, 2005, Hereditary cancer in clinical practice.

The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis.

R. Scott, J. Attia, C. Levi, 2007, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome.

R. Scott, J. Lubiński, A. Spigelman, 2012, Cancer epidemiology.

Next-generation sequencing for cancer diagnostics: a practical perspective.

Richard W Tothill, Cliff Meldrum, Maria A Doyle, 2011, The Clinical biochemist. Reviews.

BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group.

J. George, S. Fox, S. Fereday, 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Are sense-antisense peptide interactions between HIV-1 (gp120), CD4, and the proto oncogene product p56lck important?

C. Meldrum, R. Brown, S. Cousins, 1992, Medical Hypotheses.

Blood‐based detection of RAS mutations to guide anti‐EGFR therapy in colorectal cancer patients: concordance of results from circulating tumor DNA and tissue‐based RAS testing

S. Fox, H. Friess, R. Scott, 2017, Molecular oncology.

Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer

Jane E. Carpenter, R. Scott, C. Clarke, 2015, Breast Cancer Research and Treatment.

A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology

E. Haan, B. Talseth-Palmer, C. Meldrum, 2009, Cytogenetic and Genome Research.

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.

R. Scott, A. Spigelman, J. Kirk, 2001, American journal of human genetics.

Clinicopathological and molecular aspects of foregut gastrointestinal stromal tumours

J. Samra, A. Gill, C. Meldrum, 2014, ANZ journal of surgery.

Germline Missense Changes in the APC Gene and Their Relationship to Disease

R. Scott, A. Spigelman, J. Attia, 2004, Hereditary cancer in clinical practice.

Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity

R. Scott, J. Kirk, C. Meldrum, 2001, Gut.

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.

Robert J. Weatheritt, Stephanie L. White, N. Brown, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Whole genome amplification and its impact on CGH array profiles

R. Scott, B. Talseth-Palmer, C. Meldrum, 2008, BMC Research Notes.

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update

E. Zackai, J. Allanson, F. Quintero-Rivera, 2016, Human mutation.

Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53

J. Lubiński, C. Meldrum, Janina Suchy, 2006, International journal of cancer.

Multisite analytic performance studies of a real-time polymerase chain reaction assay for the detection of BRAF V600E mutations in formalin-fixed, paraffin-embedded tissue specimens of malignant melanoma.

K. Bloom, C. Meldrum, M. Dugan, 2012, Archives of pathology & laboratory medicine.

R. Scott, C. Amos, I. Gorlov, 2013, Carcinogenesis.

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

R. Scott, A. Spigelman, J. Attia, 2013, BMC Medical Genomics.

The -149C>T SNP within the DeltaDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer.

J. Lubiński, C. Meldrum, Janina Suchy, 2008, Cancer letters.

Phenotype-genotype correlations in a series of wolfram syndrome families.

Rodney J Scott, Cliff J Meldrum, Casey J A Smith, 2004, Diabetes care.

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

J. Lubiński, A. Spigelman, P. McElduff, 2009, European Journal of Human Genetics.

Congenital late onset thrombotic thrombocytopenic purpura: a diagnostic challenge.

C. Meldrum, A. Enjeti, K. Chapman, 2015, Pathology.

Re: IGF-1 gene polymorphism and risk for hereditary nonpolyposis colorectal cancer.

R. Scott, C. Meldrum, S. Reeves, 2006, Journal of the National Cancer Institute.

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients

R. Scott, A. Spigelman, B. Talseth-Palmer, 2013, Hereditary cancer in clinical practice.

Deletion Mutations in an Australian Series of HNPCC Patients

Rodney J Scott, Mary McPhillips, Cliff J Meldrum, 2005, Hereditary cancer in clinical practice.

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz–Jeghers syndrome patients

C. Meldrum, D. Mowat, M. McPhillips, 2002, Clinical genetics.