Author details

Full Name

Christopher G Mathew

Affiliation

ORCID

Career Start Year

1979

Papers

269

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36727526	Kaposi sarcoma-associated herpesvirus, HIV-1 and Kaposi sarcoma risk in black South Africans diagnosed with cancer during antiretroviral treatment rollout.		2023
35641882	Usefulness of high-risk HPV early oncoprotein (E6 and E7) serological markers in the detection of cervical cancer: A systematic review and meta-analysis.	Journal of Medical Virology	2023
36054877	Thirteen cancers associated with HIV infection in a Black South African cancer patient population (1995-2016).	International Journal of Cancer	2023
37673066	Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations.	Am J Hum Genet	2023
34388042	Processing and Analysis of Tissue Samples from Esophageal Cancer Patients in an African Setting.	Biopreservation and Biobanking	2022
35504064	Epidemiology of Kaposi's sarcoma in sub-Saharan Africa.	Cancer Epidemiology	2022
36333305	Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.	Nat Commun	2022
35421713	Lifestyle factors associated with sex differences in Kaposi sarcoma incidence among adult black South Africans: A case-control study.	Cancer Epidemiology	2022
35401654	Esophageal Cancer Genomics in Africa: Recommendations for Future Research.	Front Genet	2022
35351184	HPV types 16/18 L1 E6 and E7 proteins seropositivity and cervical cancer risk in HIV-positive and HIV-negative black South African women.	Infectious Agents and Cancer	2022
34879064	Ranking lifestyle risk factors for cervical cancer among Black women: A case-control study from Johannesburg, South Africa.	PLoS ONE	2021
34623906	Genetic Susceptibility to Breast Cancer in Sub-Saharan African Populations.	JCO Global Oncology	2021
31343064	The Health and Economic Burdens of Lymphatic Filariasis Prior to Mass Drug Administration Programs.	Clinical Infectious Diseases	2020
32233050	Association of TP53 rs1042522 with cervical cancer in the sub-Saharan African population: a meta-analysis.	Tropical Medicine and International Health	2020
32169796	Johannesburg Cancer Study (JCS): contribution to knowledge and opportunities arising from 20 years of data collection in an African setting.	Cancer Epidemiology	2020
32562888	HLA-DRB1 alleles and cervical cancer: A meta-analysis of 36 case-control studies.	Cancer Epidemiology	2020
31202982	Genetic and Inflammatory Biomarkers Classify Small Intestine Inflammation in Asymptomatic First-degree Relatives of Patients With Crohn's Disease.	Clinical Gastroenterology and Hepatology	2020
30753320	Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.	Carcinogenesis	2019
32117412	Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study.	Frontiers in Genetics	2019
29211899	Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.	J Crohns Colitis	2018
30241229	The African Esophageal Cancer Consortium: A Call to Action.	J Glob Oncol	2018
29715290	Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer.	PLoS One	2018
29091079	NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.	Mucosal Immunol	2018
29298092	The Integrity and Yield of Genomic DNA Isolated from Whole Blood Following Long-Term Storage at -30Â°C.	Biopreservation and Biobanking	2018
28191891	Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism.	Nat Genet	2017
28911061	International cancer seminars: a focus on esophageal squamous cell carcinoma.	Ann Oncol	2017
28658209	Fine-mapping inflammatory bowel disease loci to single-variant resolution.	Nature	2017
28067908	Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.	Nat Genet	2017
28067910	Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.	Nat Genet	2017
27503255	A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.	Nat Commun	2016
27306066	Genetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis.	Inflammatory Bowel Diseases	2016
27236921	Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.	Am J Hum Genet	2016
27037036	Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.	BMC Med Genet	2016
26813944	Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease.	European Journal of Human Genetics	2016
26137941	Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease.	BMC Gastroenterol	2015
25671699	Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.	PLoS Genet	2015
25809337	Defective macrophage handling of Escherichia coli in Crohn's disease.	J Gastroenterol Hepatol	2015
25003214	The correlation between reading and mathematics ability at age twelve has a substantial genetic component.	Nat Commun	2014
23871474	A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.	Biol Psychiatry	2014
23698362	Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.	Nature	2013
22821403	Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4.	Hepatology	2013
23974872	Genome-wide association analysis identifies 13 new risk loci for schizophrenia.	Nat Genet	2013
23624108	Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.	Gastroenterology	2013
23291585	Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.	Nat Genet	2013
22102318	Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota.	Inflammatory Bowel Diseases	2012
22306652	Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.	Nat Genet	2012
22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Nat Genet	2012
22865593	Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.	Carcinogenesis	2012
22822007	Effect of communicating DNA based risk assessments for Crohn's disease on smoking cessation: randomised controlled trial.	BMJ, The	2012
22482804	Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.	Am J Hum Genet	2012