Christopher G. Mathew

53.5k total citations · 3 hit papers
246 papers, 14.2k citations indexed

About

Christopher G. Mathew is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Christopher G. Mathew has authored 246 papers receiving a total of 14.2k indexed citations (citations by other indexed papers that have themselves been cited), including 109 papers in Genetics, 105 papers in Molecular Biology and 38 papers in Epidemiology. Recurrent topics in Christopher G. Mathew's work include DNA Repair Mechanisms (51 papers), Inflammatory Bowel Disease (50 papers) and BRCA gene mutations in cancer (19 papers). Christopher G. Mathew is often cited by papers focused on DNA Repair Mechanisms (51 papers), Inflammatory Bowel Disease (50 papers) and BRCA gene mutations in cancer (19 papers). Christopher G. Mathew collaborates with scholars based in United Kingdom, United States and South Africa. Christopher G. Mathew's co-authors include Hans Joenje, Cathryn M. Lewis, Alastair Forbes, Jochen Hampe, Stefan Schreiber, Sheila Fisher, Martin Bobrow, Muddassar M. Mirza, John Edward Lennard-Jones and Johan P. de Winter and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Christopher G. Mathew

237 papers receiving 13.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

2001 837 citations Jochen Hampe, Andrew Cuthbert et al. profile →
Mapping of a susceptibility locus for Crohn's disease on chromosome 16

1996 727 citations Christopher G. Mathew et al. profile →
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

2002 523 citations Andrew Cuthbert, Sheila Fisher et al. profile →

Peers

Countries citing papers authored by Christopher G. Mathew

Since Specialization

Citations

This map shows the geographic impact of Christopher G. Mathew's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christopher G. Mathew with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher G. Mathew more than expected).

Fields of papers citing papers by Christopher G. Mathew

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher G. Mathew. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christopher G. Mathew. The network helps show where Christopher G. Mathew may publish in the future.

Co-authorship network of co-authors of Christopher G. Mathew

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher G. Mathew. A scholar is included among the top collaborators of Christopher G. Mathew based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Christopher G. Mathew. Christopher G. Mathew is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genome-wide association study identifies common variants associated with breast cancer in South African Black women 2025 ·Nature Communications ·(unknown), Wenlong Carl Chen, Chantal Babb de Villiers, Sang Hyuck Lee, Charles Curtis, Robert Newton, Tim Waterboer, Freddy Sitas, Debbie Bradshaw, Mazvita Muchengeti, Elvira Singh, Cathryn M. Lewis, Michèle Ramsay, Christopher G. Mathew, Jean‐Tristan Brandenburg	1
2	Prevalence and Reclassification of Genetic Variants in South African Populations with Breast Cancer 2024 ·Genes Chromosomes and Cancer ·(unknown), Jean‐Tristan Brandenburg, (unknown), Wenlong Carl Chen, Michael Urban, Christopher G. Mathew	1
3	Kaposi sarcoma‐associated herpesvirus, HIV‐1 and Kaposi sarcoma risk in black South Africans diagnosed with cancer during antiretroviral treatment rollout 2023 ·International Journal of Cancer ·(unknown), Mazvita Muchengeti, Debbie Bradshaw, Wenlong Carl Chen, (unknown), Chantal Babb de Villiers, Cathryn M. Lewis, Noemi Bender, Christopher G. Mathew, Robert Newton, Tim Waterboer, Elvira Singh, Freddy Sitas	4
4	Thirteen cancers associated with HIV infection in a Black South African cancer patient population (1995‐2016) 2022 ·International Journal of Cancer ·(unknown), Elvira Singh, Wenlong Carl Chen, Debbie Bradshaw, Chantal Babb de Villiers, Robert Newton, Tim Waterboer, Christopher G. Mathew, Freddy Sitas	11
5	Usefulness of high‐risk HPV early oncoprotein (E6 and E7) serological markers in the detection of cervical cancer: A systematic review and meta‐analysis 2022 ·Journal of Medical Virology ·(unknown), Elvira Singh, Debbie Bradshaw, (unknown), Wenlong Carl Chen, (unknown), Abram Bunya Kamiza, Chantal Babb de Villiers, Mazvita Muchengeti, Christopher G. Mathew, Robert Newton, Noemi Bender, Tim Waterboer, Freddy Sitas	16
6	Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans 2022 ·Nature Communications ·Palwendé Romuald Boua, Jean‐Tristan Brandenburg, Ananyo Choudhury, Hermann Sorgho, Engelbert A. Nonterah, Godfred Agongo, Gershim Asiki, Lisa K. Micklesfield, Solomon Choma, F. Xavier Gómez‐Olivé, Scott Hazelhurst, Halidou Tinto, Nigel J. Crowther, Christopher G. Mathew, Michèle Ramsay, (unknown)	13
7	Johannesburg Cancer Study (JCS): contribution to knowledge and opportunities arising from 20 years of data collection in an African setting 2020 ·Cancer Epidemiology ·Wenlong Carl Chen, Elvira Singh, Mazvita Muchengeti, Debbie Bradshaw, Christopher G. Mathew, Chantal Babb de Villiers, Cathryn M. Lewis, Tim Waterboer, Robert Newton, Freddy Sitas	15
8	Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis 2017 ·Journal of Crohn s and Colitis ·Alexandros Onoufriadis, Kristina L. Stone, (unknown), (unknown), (unknown), Katrina M. de Lange, Kirstin M. Taylor, Jeffrey C. Barrett, Richard Pollok, Bu Hayee, John Mansfield, Jeremy Sanderson, Michael A. Simpson, Christopher G. Mathew, Natalie J. Prescott	15
9	"Left-sided" Chilaiditi sign? A large gastric perforation with secondary pancreatitis. 2014 ·PubMed ·(unknown), (unknown), Gianpiero Gravante, (unknown), (unknown), Christopher G. Mathew	1
10	Autophagy gene polymorphisms influence the interaction of E coli and macrophages in Crohn's disease 2011 ·Gut ·Tim Elliott, Natalie J. Prescott, B N Hudspith, Neil B. Rayment, John Hermon-Taylor, Jonathan Brostoff, Christopher G. Mathew, Jeremy Sanderson	1
11	The pharmacogenetics of folate and purine metabolic pathways in methotrexate therapy of inflammatory bowel disease. 2007 ·Gut ·Bijay Baburajan, M Arenas, Natalie J. Prescott, K Herrlinger, (unknown), Mark Tremelling, Miles Parkes, (unknown), Christopher G. Mathew, Anthony M. Marinaki, Jeremy Sanderson	1
12	Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia 2003 ·European Journal of Human Genetics ·Marc Tischkowitz, Najim Ameziane, Quinten Waisfisz, Peter de Winter, R. J. C. Harris, Reinhard Stöger, Shirley Hodgson, Christopher G. Mathew, Hans Joenje	7
13	Efficient candidate gene study design for association studies in complex diseases 2002 ·Genetic Epidemiology ·Sheila Fisher, Anne Marie Moody, Christopher G. Mathew, Cathryn M. Lewis	1
14	Evidence for a NOD2 -independent susceptibility locus for inflammatory bowel disease on chromosome 16p 2001 ·Proceedings of the National Academy of Sciences ·Jochen Hampe, H Frenzel, Muddassar M. Mirza, Peter J.P. Croucher, Andrew Cuthbert, Silvia Mascheretti, Klaus Huse, Matthias Platzer, Stephen Bridger, Birgit Meyer, Peter Nürnberg, Pieter Stokkers, Michael Krawczak, Christopher G. Mathew, (unknown), Stefan Schreiber	82
15	Mutation analysis of the Fanconi Anaemia group A, C, E, F and G genes in sporadic acute myeloid leukaemia 2001 ·Journal of Medical Genetics ·Marc Tischkowitz, Neil V. Morgan, S V Hodgson, Carey-Anne Eddy, Sarah E. Ball, Stephen E. Langabeer, Igor Vořechovský, David Grimwade, Christopher G. Mathew	0
16	Molecular genetic analysis of Fanconi anaemia in Black South Africans. 2001 ·The American Journal of Human Genetics ·(unknown), (unknown), Linda Wainwright, Jason C. Poole, Christopher G. Mathew	1
17	Corneodesmosin (S) gene association with psoriasis vulgaris 2000 ·Journal of Investigative Dermatology ·(unknown), M H Allen, Cathryn M. Lewis, Scott Fisher, Colin Veal, G. Rowley, Christopher G. Mathew, Richard C. Trembath, Juliet N. Barker, Robert Vaughan	2
18	Exclusion of four candidate kidney disease loci by linkage analysis in familial juvenile hyperuricaemic nephropathy [FJHN] 1999 ·Cellular & Molecular Biology Letters ·(unknown), Anthony M. Marinaki, Margaret Town, Fernando Moro, H. Anne Simmonds, J. S. Cameron, J. A. Duley, Christopher G. Mathew	2
19	Dystrophin Point Mutation Screening Using a Multiplexed Protein Truncation Test 1997 ·Genetic Testing ·Neil V. Whittock, Roland G. Roberts, Christopher G. Mathew, Stephen Abbs	23
20	Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I. 1986 ·Journal of Medical Genetics ·Gillian A. Wallis, Peter Beighton, C. D. Boyd, Christopher G. Mathew	20

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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