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C. Meldrum · SciRah

Researcher profile · Semantic Scholar

C. Meldrum

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C. Meldrum — researcher profile on SciRah

h-index: 28
Works: 74
Citations: 3,872

Most-cited papers

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.
K. Alsop, S. Fereday, C. Meldrum, A. deFazio +10 more
2012Journal of Clinical Oncology1,170 citations Open access
Semantic Scholar
Next-generation sequencing for cancer diagnostics: a practical perspective.
C. Meldrum, M. Doyle, R. Tothill
2011Clinical biochemist reviews395 citations
Semantic Scholar
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
G. Froyen, M. Corbett, J. Vandewalle, Irma Jarvela +30 more
2008American Journal of Human Genetics232 citations Open access
Semantic Scholar
Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.
R. Scott, M. McPhillips, C. Meldrum, P. Fitzgerald +5 more
2001American Journal of Human Genetics203 citations Open access
Semantic Scholar
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.
S. Anderson, K. Bloom, D. U. Vallera, J. Rueschoff +9 more
2012Archives of Pathology & Laboratory Medicine153 citations Open access
Semantic Scholar
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
W. Schmiegel, R. Scott, Susan Dooley, W. Lewis +33 more
2017Molecular Oncology145 citations Open access
Semantic Scholar
Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer
M. Wong-Brown, C. Meldrum, Jane E. Carpenter, C. Clarke +5 more
2015Breast Cancer Research and Treatment127 citations
Semantic Scholar
Phenotype-genotype correlations in a series of wolfram syndrome families.
C. Smith, P. Crock, Bruce R. King, C. Meldrum +1 more
2004Diabetes Care103 citations Open access
Semantic Scholar
Direct integrin αvβ6-ERK binding: implications for tumour growth
N. Ahmed, J. Niu, D. Dorahy, Xinhua Gu +6 more
2002Oncogene91 citations
Semantic Scholar
Integrin-mediated signalling of gelatinase B secretion in colon cancer cells.
J. Niu, Xinhua Gu, J. Turton, C. Meldrum +2 more
1998Biochemical and Biophysical Research Communications - BBRC90 citations
Semantic Scholar
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.
A. Bournazos, L. Riley, Shobhana Bommireddipalli, L. Adès +212 more
2021Genetics in Medicine85 citations Open access
Semantic Scholar
The αvβ6 integrin induces gelatinase B secretion in colon cancer cells
M. Agrez, Xinhua Gu, J. Turton, C. Meldrum +3 more
199970 citations Open access
Semantic Scholar
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update
Li-Jia Huang, M. Vanstone, T. Hartley, M. Osmond +49 more
2015Human Mutation62 citations Open access
Semantic Scholar
Direct integrin alphavbeta6-ERK binding: implications for tumour growth.
N. Ahmed, J. Niu, D. Dorahy, Xinhua Gu +6 more
2002Oncogene56 citations
Semantic Scholar
Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c‐KIT
R. Foster, E. Byrnes, C. Meldrum, R. Griffith +7 more
2008British Journal of Dermatology55 citations
Semantic Scholar
The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis.
J. Attia, A. Thakkinstian, Yang Wang, L. Lincz +6 more
2007Journal of Stroke & Cerebrovascular Diseases49 citations
Semantic Scholar
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
Bente A. Talseth, C. Meldrum, J. Suchy, G. Kurzawski +2 more
2007International Journal of Cancer48 citations Open access
Semantic Scholar
Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations
Carla F. Kairupan, C. Meldrum, R. Crooks, E. Milward +8 more
2005International Journal of Cancer46 citations Open access
Semantic Scholar
BRCA2 mutations in a population‐based series of patients with ocular melanoma
R. Scott, C. Vajdic, B. Armstrong, C. Ainsworth +3 more
2002International Journal of Cancer46 citations
Semantic Scholar
Aurora‐A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
Bente A. Talseth, Katie A. Ashton, C. Meldrum, J. Suchy +3 more
2008International Journal of Cancer42 citations Open access
Semantic Scholar
An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects.
A. Rao, Sheridan O'Donnell, N. Bain, C. Meldrum +2 more
2014European Journal of Medical Genetics41 citations
Semantic Scholar
Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53
Bente A. Talseth, C. Meldrum, J. Suchy, G. Kurzawski +2 more
2006International Journal of Cancer41 citations Open access
Semantic Scholar
Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity
R. Scott, C. Meldrum, R. Crooks, A. Spigelman +4 more
2001Gut41 citations Open access
Semantic Scholar
Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer
R. Ward, C. Meldrum, Rachael Williams, E. Mokany +6 more
2002Journal of Cancer Research and Clinical Oncology38 citations Open access
Semantic Scholar
Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data.
S. Easteal, R. Arkell, Renzo F. Balboa, S. Bellingham +37 more
2020American Journal of Human Genetics31 citations Open access
Semantic Scholar
MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
S. Reeves, C. Meldrum, Claire Groombridge, A. Spigelman +5 more
2009European Journal of Human Genetics30 citations Open access
Semantic Scholar
IGF1 is a modifier of disease risk in hereditary non‐polyposis colorectal cancer
S. Reeves, Dominique Rich, C. Meldrum, K. Colyvas +4 more
2008International Journal of Cancer30 citations Open access
Semantic Scholar
Whole genome amplification and its impact on CGH array profiles
Bente A. Talseth-Palmer, N. Bowden, A. Hill, C. Meldrum +1 more
2008BMC Research Notes28 citations Open access
Semantic Scholar
Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients
B. Talseth, C. Meldrum, J. Suchy, G. Kurzawski +2 more
2006Cancer Epidemiology, Biomarkers and Prevention28 citations Open access
Semantic Scholar
The alpha v beta 6 integrin induces gelatinase B secretion in colon cancer cells.
M. Agrez, X. Gu, J. Turton, C. Meldrum +3 more
1999International Journal of Cancer28 citations
Semantic Scholar
DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome.
S. Reeves, C. Meldrum, Claire Groombridge, A. Spigelman +4 more
2012Cancer Epidemiology26 citations Open access
Semantic Scholar
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
Bente A. Talseth-Palmer, E. Holliday, T. Evans, M. McEvoy +6 more
2013BMC Medical Genomics25 citations Open access
Semantic Scholar
Oral abstracts
Elizabeth Tracey, S. Gupta, D. Kaminski, P. Troke +17 more
2015Pneumonia22 citations Open access
Semantic Scholar
Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer
B. Talseth, C. Meldrum, J. Suchy, G. Kurzawski +2 more
2007Scandinavian Journal of Gastroenterology20 citations
Semantic Scholar
Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients
Katie A. Ashton, C. Meldrum, M. McPhillips, Carla F. Kairupan +1 more
2005Hereditary Cancer in Clinical Practice17 citations Open access
Semantic Scholar
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients
Bente A. Talseth-Palmer, J. Wijnen, Eva K Andreassen, Daniel Barker +8 more
2013Hereditary Cancer in Clinical Practice15 citations Open access
Semantic Scholar
Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients.
Jin-Yun Chen, Mala Pande, Yu-Jing Huang, Chong-Juan Wei +8 more
2013Carcinogenesis13 citations Open access
Semantic Scholar
Can a familial gastrointestinal tumour syndrome be allelic with Waardenburg syndrome?
R. Vilain, T. Dudding, S. Braye, Claire Groombridge +5 more
2011Clinical Genetics13 citations
Semantic Scholar
The -149C>T SNP within the DeltaDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer.
S. Reeves, D. Mossman, C. Meldrum, G. Kurzawski +3 more
2008Cancer Letters13 citations
Semantic Scholar
A Pathway to Precision Medicine for Aboriginal Australians: A Study Protocol
Yeu-yao Cheng, Jack S. Nunn, J. Skinner, B. Rambaldini +11 more
2021Methods and Protocols12 citations Open access
Semantic Scholar
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
Bente A. Talseth-Palmer, N. Bowden, C. Meldrum, J. Nicholl +7 more
2009Cytogenetic and Genome Research10 citations
Semantic Scholar
A fibroblast elongation factor purified from colon carcinoma cells shares sequence identity with TIMP-1.
M. Agrez, C. Meldrum, Alistair T. R. Sim, R. Aebersold +3 more
1995Biochemical and Biophysical Research Communications - BBRC10 citations
Semantic Scholar
Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions.
B. Kamien, M. Digilio, A. Novelli, Sheridan O'Donnell +5 more
2015European Journal of Medical Genetics9 citations
Semantic Scholar
Narrowing the Diagnostic Gap: Genomes, Episignatures, Long-Read Sequencing and Health Economic Analyses in an Exome-Negative Intellectual Disability Cohort
Kerith-Rae Dias, R. Shrestha, Deborah Schofield, Carey-Anne Evans +61 more
2024Genetics in Medicine7 citations Open access
Semantic Scholar
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
M. Wong-Brown, M. McPhillips, M. Gleeson, A. Spigelman +3 more
2016Hereditary Cancer in Clinical Practice7 citations Open access
Semantic Scholar
AmpliVar: Mutation Detection in High‐Throughput Sequence from Amplicon‐Based Libraries
A. Hsu, O. Kondrashova, S. Lunke, Clare J. Love +7 more
2015Human Mutation7 citations Open access
Semantic Scholar
Re: IGF-1 gene polymorphism and risk for hereditary nonpolyposis colorectal cancer.
S. Reeves, C. Meldrum, R. Scott
2006Journal of the National Cancer Institute7 citations
Semantic Scholar
Somatic‐gonadal mosaicism causing Sotos syndrome
B. Kamien, T. Dadd, M. Buckman, A. Ronan +4 more
2016American Journal of Medical Genetics. Part A5 citations
Semantic Scholar
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
Bente A. Talseth-Palmer, E. Holliday, T. Evans, M. McEvoy +6 more
2013BMC Medical Genomics4 citations Open access
Semantic Scholar
Are sense-antisense peptide interactions between HIV-1 (gp120), CD4, and the proto oncogene product p56lck important?
Richard A. Brown, C. Meldrum, S. Cousins
1992Medical Hypotheses4 citations
Semantic Scholar

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R. Scott — researcher profile on SciRah
A. Spigelman×11
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J. Lubiński×9
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M. Agrez — researcher profile on SciRah

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Bente A. Talseth-Palmer — researcher profile on SciRah

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