Works matching AU Mathew, Christopher G

Results: 61

Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.

Published in:

Human Mutation, 2006, v. 27, n. 8, p. 778, doi. 10.1002/humu.20358

By:

Fisher, Sheila A.;
Hampe, Jochen;
Onnie, Clive M.;
Daly, Mark J.;
Curley, Christine;
Purcell, Shaun;
Sanderson, Jeremy;
Mansfield, John;
Annese, Vito;
Forbes, Alastair;
Lewis, Cathryn M.;
Schreiber, Stefan;
Rioux, John D.;
Mathew, Christopher G.

Publication type:

Article

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

Published in:

Human Mutation, 2006, v. 27, n. 1, p. 44, doi. 10.1002/humu.20264

By:

King, Kathy;
Sheikh, Mohammed F.;
Cuthbert, Andrew P.;
Fisher, Sheila A.;
Onnie, Clive M.;
Mirza, Muddassar M.;
Pattni, Reenal C.;
Sanderson, Jeremy;
Forbes, Alastair;
Mansfield, John;
Lewis, Cathryn M.;
Roberts, Roland G.;
Mathew, Christopher G.

Publication type:

Article

Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 5, p. 619, doi. 10.1038/sj.ejhg.5201996

By:

Bagnall, Richard D.;
Roberts, Roland G.;
Mirza, Muddassar M.;
Torigoe, Toshihiko;
Prescott, Natalie J.;
Mathew, Christopher G.

Publication type:

Article

Recruiting first-degree relatives for prevention research: a comparison of clinician and proband-led methods of contact in Crohn's disease.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 12, p. 1263, doi. 10.1038/sj.ejhg.5201699

By:

Reid, Erin P.;
Forbes, Alastair;
Sanderson, Jeremy;
Mathew, Christopher G.;
Lewis, Cathryn;
Marteau, Theresa M.

Publication type:

Article

Association of DLG5 R30Q variant with inflammatory bowel disease.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 835, doi. 10.1038/sj.ejhg.5201403

By:

Daly, Mark J.;
Pearce, Alexandra V.;
Farwell, Lisa;
Fisher, Sheila A.;
Latiano, Anna;
Prescott, Natalie J.;
Forbes, Alastair;
Mansfield, John;
Sanderson, Jeremy;
Langelier, Diane;
Cohen, Albert;
Bitton, Alain;
Wild, Gary;
Lewis, Cathryn M.;
Annese, Vito;
Mathew, Christopher G.;
Rioux, John D.

Publication type:

Article

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 259, doi. 10.1038/sj.ejhg.5200792

By:

Fisher, Sheila A.;
Hampe, Jochen;
Macpherson, Andrew J.S.;
Forbes, Alastair;
Lennard-Jones, John E.;
Schreiber, Stefan;
Curran, Mark E.;
Mathew, Christopher G.;
Lewis, Cathryn M.

Publication type:

Article

Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 11, p. 861, doi. 10.1038/sj.ejhg.5200552

By:

Demuth, Ilja;
Wlodarski, Marcin;
Tipping, Alex J;
Morgan, Neil V;
de Winter, Johan P;
Thiel, Michaela;
Gräsl, Sonja;
Schindler, Detlev;
D'Andrea, Alan D;
Altay, Cigdem;
Kayserili, Hülya;
Zatterale, Adriana;
Kunze, Jürgen;
Ebell, Wolfram;
Mathew, Christopher G;
Joenje, Hans;
Sperling, Karl;
Digweed, Martin

Publication type:

Article

Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.

Published in:

European Journal of Human Genetics, 1998, v. 6, n. 5, p. 467, doi. 10.1038/sj.ejhg.5200210

By:

Taylor, Joanne E;
Thomas, Neil H;
Lewis, Cathryn M;
Abbs, Stephen J;
Rodrigues, Nanda R;
Davies, Kay E;
Mathew, Christopher G

Publication type:

Article

Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer.

Published in:

PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0188911

By:

Traylor, Matthew;
Walker, Jemma L.;
Corrigan, Adele A.;
Hernandez, Monica A.;
Newhouse, Stephen J.;
Folarin, Amos A.;
Patel, Hamel;
Ross, Paul J.;
Sanderson, Jeremy D.;
Spicer, James;
Prescott, Natalie J.;
Mathew, Christopher G.;
Marinaki, Anthony M.;
Lewis, Cathryn M.

Publication type:

Article

Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors.

Published in:

Nature Medicine, 2003, v. 9, n. 5, p. 568, doi. 10.1038/nm852

By:

Taniguchi, Toshiyasu;
Tischkowitz, Marc;
Ameziane, Najim;
Hodgson, Shirley V.;
Mathew, Christopher G.;
Joenje, Hans;
Mok, Samuel C.;
D'Andrea, Alan D.

Publication type:

Article

Bayesian refinement of association signals for 14 loci in 3 common diseases.

Published in:

Nature Genetics, 2012, v. 44, n. 12, p. 1294, doi. 10.1038/ng.2435

By:

Maller, Julian B;
McVean, Gilean;
Byrnes, Jake;
Vukcevic, Damjan;
Palin, Kimmo;
Su, Zhan;
Howson, Joanna M M;
Auton, Adam;
Myers, Simon;
Morris, Andrew;
Pirinen, Matti;
Brown, Matthew A;
Burton, Paul R;
Caulfield, Mark J;
Compston, Alastair;
Farrall, Martin;
Hall, Alistair S;
Hattersley, Andrew T;
Hill, Adrian V S;
Mathew, Christopher G

Publication type:

Article

Mutation of the RAD51C gene in a Fanconi anemia–like disorder.

Published in:

Nature Genetics, 2010, v. 42, n. 5, p. 406, doi. 10.1038/ng.570

By:

Vaz, Fiona;
Hanenberg, Helmut;
Schuster, Beatrice;
Barker, Karen;
Wiek, Constanze;
Erven, Verena;
Neveling, Kornelia;
Endt, Daniela;
Kesterton, Ian;
Autore, Flavia;
Fraternali, Franca;
Freund, Marcel;
Hartmann, Linda;
Grimwade, David;
Roberts, Roland G.;
Schaal, Heiner;
Mohammed, Shehla;
Rahman, Nazneen;
Schindler, Detlev;
Mathew, Christopher G.

Publication type:

Article

Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).

Published in:

Nature Genetics, 2010, v. 42, n. 4, p. 292, doi. 10.1038/ng.553

By:

Franke, Andre;
Balschun, Tobias;
Sina, Christian;
Ellinghaus, David;
Häsler, Robert;
Mayr, Gabriele;
Albrecht, Mario;
Wittig, Michael;
Buchert, Eva;
Nikolaus, Susanna;
Gieger, Christian;
Wichmann, H. Erich;
Sventoraityte, Jurgita;
Kupcinskas, Limas;
Onnie, Clive M.;
Gazouli, Maria;
Anagnou, Nicholas P.;
Strachan, David;
McArdle, Wendy L.;
Mathew, Christopher G.

Publication type:

Article

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.

Published in:

Nature Genetics, 2007, v. 39, n. 2, p. 162, doi. 10.1038/ng1947

By:

Reid, Sarah;
Schindler, Detlev;
Hanenberg, Helmut;
Barker, Karen;
Hanks, Sandra;
Kalb, Reinhard;
Neveling, Kornelia;
Kelly, Patrick;
Seal, Sheila;
Freund, Marcel;
Wurm, Melanie;
Batish, Sat Dev;
Lach, Francis P.;
Yetgin, Sevgi;
Neitzel, Heidemarie;
Ariffin, Hany;
Tischkowitz, Marc;
Mathew, Christopher G.;
Auerbach, Arleen D.;
Rahman, Nazneen

Publication type:

Article

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.

Published in:

Nature Genetics, 2007, v. 39, n. 2, p. 207, doi. 10.1038/ng1954

By:

Hampe, Jochen;
Franke, Andre;
Rosenstiel, Philip;
Till, Andreas;
Teuber, Markus;
Huse, Klaus;
Albrecht, Mario;
Mayr, Gabriele;
De La Vega, Francisco M.;
Briggs, Jason;
Günther, Simone;
Prescott, Natalie J.;
Onnie, Clive M.;
Häsler, Robert;
Sipos, Bence;
Fölsch, Ulrich R.;
Lengauer, Thomas;
Platzer, Matthias;
Mathew, Christopher G.;
Krawczak, Michael

Publication type:

Article

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.

Published in:

2005

By:

Levitus, Marieke;
Waisfisz, Quinten;
Godthelp, Barbara C.;
Vries, Yne de;
Hussain, Shobbir;
Wiegant, Wouter W.;
Elghalbzouri-Maghrani, Elhaam;
Steltenpool, Jûrgen;
Rooimans, Martin A.;
Pals, Gerard;
Arwert, Fré;
Mathew, Christopher G.;
Zdzienicka, Małgorzata Z.;
Hiom, Kevin;
de Winter, Johan P.;
Joenje, Hans

Publication type:

Letter

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

Published in:

2005

By:

Meetei, Amom Ruhikanta;
Medhurst, Annette L.;
Chen Ling;
Yutong Xue;
Singh, Thiyam Ramsing;
Bier, Patrick;
Steltenpool, Jurgen;
Stone, Stacie;
Dokal, Inderjeet;
Mathew, Christopher G.;
Hoatlin, Maureen;
Joenje, Hans;
de Winter, Johan P.;
Weidong Wang

Publication type:

Letter

Genetic variation in DLG5 is associated with inflammatory bowel disease.

Published in:

Nature Genetics, 2004, v. 36, n. 5, p. 476, doi. 10.1038/ng1345

By:

Stoll, Monika;
Corneliussen, Brit;
Costello, Christine M;
Waetzig, Georg H;
Mellgard, Bjorn;
Koch, W Andreas;
Rosenstiel, Philip;
Albrecht, Mario;
Croucher, Peter J P;
Seegert, Dirk;
Nikolaus, Susanna;
Hampe, Jochen;
Lengauer, Thomas;
Pierrou, Stefan;
Foelsch, Ulrich R;
Mathew, Christopher G;
Lagerstrom-Fermer, Maria;
Schreiber, Stefan

Publication type:

Article

The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.

Published in:

Nature Genetics, 2000, v. 24, n. 1, p. 15, doi. 10.1038/71626

By:

de Winter, Johan P.;
Rooimans, Martin A.;
van der Weel, Laura;
van Berkel, Carola G.M.;
Alon, Noa;
Bosnoyan-Collins, Lucine;
de Groot, Jan;
Zhi, Yu;
Waisfisz, Quinten;
Pronk, Jan C.;
Arwert, Fré;
Mathew, Christopher G.;
Scheper, Rik J.;
Hoatlin, Maureen E.;
Buchwald, Manuel;
Joenje, Hans

Publication type:

Article

Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 379, doi. 10.1038/11956

By:

Waisfisz, Quinten;
Morgan, Neil V.;
Savino, Maria;
de Winter, Johan P.;
van Berkel, Carola G.M.;
Hoatlin, Maureen E.;
Ianzano, Leonarda;
Gibson, Rachel A.;
Arwert, Fre;
Savoia, Anna;
Mathew, Christopher G.;
Pronk, Jan C.;
Joenje, Hans

Publication type:

Article

Cancer incidence in relatives of British Fanconi Anaemia patients.

Published in:

BMC Cancer, 2008, v. 8, p. 1, doi. 10.1186/1471-2407-8-257

By:

Tischkowitz, Marc;
Easton, Douglas F.;
Ball, Jan;
Hodgson, Shirley V.;
Mathew, Christopher G.

Publication type:

Article

Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.

Published in:

Carcinogenesis, 2019, v. 40, n. 4, p. 513, doi. 10.1093/carcin/bgz026

By:

Chen, Wenlong C;
Bye, Hannah;
Matejcic, Marco;
Amar, Ariella;
Govender, Dhiren;
Khew, Yee Wen;
Beynon, Victoria;
Kerr, Robyn;
Singh, Elvira;
Prescott, Natalie J;
Lewis, Cathryn M;
Villiers, Chantal Babb de;
Parker, M Iqbal;
Mathew, Christopher G

Publication type:

Article

Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.

Published in:

Carcinogenesis, 2012, v. 33, n. 11, p. 2155, doi. 10.1093/carcin/bgs262

By:

Bye, Hannah;
Prescott, Natalie J.;
Lewis, Cathryn M.;
Matejcic, Marco;
Moodley, Loven;
Robertson, Barbara;
Rensburg, Christo van;
Parker, M.Iqbal;
Mathew, Christopher G.

Publication type:

Article

Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa.

Published in:

Carcinogenesis, 2011, v. 32, n. 12, p. 1855, doi. 10.1093/carcin/bgr211

By:

Bye, Hannah;
Prescott, Natalie J.;
Matejcic, Marco;
Rose, Elizabeth;
Lewis, Cathryn M.;
Parker, M.Iqbal;
Mathew, Christopher G.

Publication type:

Article

Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28276-x

By:

Boua, Palwende Romuald;
Brandenburg, Jean-Tristan;
Choudhury, Ananyo;
Sorgho, Hermann;
Nonterah, Engelbert A.;
Agongo, Godfred;
Asiki, Gershim;
Micklesfield, Lisa;
Choma, Solomon;
Gómez-Olivé, Francesc Xavier;
Hazelhurst, Scott;
Tinto, Halidou;
Crowther, Nigel J.;
Mathew, Christopher G.;
Ramsay, Michèle;
AWI-Gen Study;
the H3Africa Consortium

Publication type:

Article

Association of a Deletion of GSTT2B with an Altered Risk of Oesophageal Squamous Cell Carcinoma in a South African Population: A Case-Control Study.

Published in:

PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029366

By:

Matejcic, Marco;
Li, DongPing;
Prescott, Natalie J.;
Lewis, Cathryn M.;
Mathew, Christopher G.;
Parker, M. Iqbal

Publication type:

Article

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34349-8

By:

Grange, Laura J.;
Reynolds, John J.;
Ullah, Farid;
Isidor, Bertrand;
Shearer, Robert F.;
Latypova, Xenia;
Baxley, Ryan M.;
Oliver, Antony W.;
Ganesh, Anil;
Cooke, Sophie L.;
Jhujh, Satpal S.;
McNee, Gavin S.;
Hollingworth, Robert;
Higgs, Martin R.;
Natsume, Toyoaki;
Khan, Tahir;
Martos-Moreno, Gabriel Á.;
Chupp, Sharon;
Mathew, Christopher G.;
Parry, David

Publication type:

Article

Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci.

Published in:

Human Genetics, 2003, v. 113, n. 6, p. 514, doi. 10.1007/s00439-003-1020-7

By:

Shaw, Sarah H.;
Hampe, Jochen;
White, Ray;
Mathew, Christopher G.;
Curran, Mark E.;
Schreiber, Stefan

Publication type:

Article

Esophageal Cancer Genomics in Africa: Recommendations for Future Research.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.864575

By:

Simba, Hannah;
Tromp, Gerard;
Sewram, Vikash;
Mathew, Christopher G;
Chen, Wenlong C.;
Kuivaniemi, Helena

Publication type:

Article

Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway.

Published in:

Human Molecular Genetics, 2001, v. 10, n. 4, p. 423, doi. 10.1093/hmg/10.4.423

By:

Medhurst, Annette L.;
Huber, Pia A.J.;
Waisfisz, Quinten;
deWinter, Johan P.;
Mathew, Christopher G.

Publication type:

Article

A nonsense mutation and exon skipping in the Fanconi anaemia group C gene.

Published in:

Human Molecular Genetics, 1993, v. 2, n. 6, p. 797

By:

Gibson, Rachel A.;
Hajianpour, Atieh;
Murer-Orlando, Manuela;
Buchwald, Manuel;
Mathew, Christopher G.

Publication type:

Article

Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR.

Published in:

Human Molecular Genetics, 1993, v. 2, n. 1, p. 35

By:

Gibson, Rachel A.;
Buchwald, Manuel;
Roberts, Roland G.;
Mathew, Christopher G.

Publication type:

Article

Comparative Mutation Detection Screening of the Type VII Collagen Gene (COL7A1) Using the Protein Truncation Test, Fluorescent Chemical Cleavage of Mismatch, and Conformation Sensitive Gel Electrophoresis.

Published in:

Journal of Investigative Dermatology, 1999, v. 113, n. 4, p. 673, doi. 10.1046/j.1523-1747.1999.00732.x

By:

Whittock, Neil V.;
Ashton, Gabrielle H. S.;
Mohammedi, Rafik;
Mellerio, Jemima E.;
Mathew, Christopher G.;
Abbs, Stephen J.;
Eady, Robin A. J.;
McGrath, John A.

Publication type:

Article

Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease.

Published in:

Immunogenetics, 2000, v. 51, n. 1, p. 1, doi. 10.1007/s002510050001

By:

Olavesen, Mark G.;
Hampe, Jochen;
Mirza, Muddassar M.;
Saiz, Robert.;
Lewis, Cathryn M.;
Bridger, Stephen;
Teare, Dawn;
Easton, Douglas F.;
Herrmann, Torsten;
Scott, Gillian;
Hirst, Jo;
Sanderson, Jeremy;
Hodgson, Shirley V.;
Lee, John;
MacPherson, Andrew;
Schreiber, Stefan;
Lennard-Jones, John E.;
Curran, Mark E.;
Mathew, Christopher G.

Publication type:

Article

New links to the pathogenesis of Crohn disease provided by genome-wide association scans.

Published in:

Nature Reviews Genetics, 2008, v. 9, n. 1, p. 9, doi. 10.1038/nrg2203

By:

Mathew, Christopher G.

Publication type:

Article

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 24, p. 4930, doi. 10.1093/hmg/ddq411

By:

Aldhous, Marian C.;
Abu Bakar, Suhaili;
Prescott, Natalie J.;
Palla, Raquel;
Soo, Kimberley;
Mansfield, John C.;
Mathew, Christopher G.;
Satsangi, Jack;
Armour, John A.L.

Publication type:

Article

Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 12, p. 1241, doi. 10.1093/hmg/ddh135

By:

Hussain, Shobbir;
Wilson, James B.;
Medhurst, Annette L.;
Hejna, James;
Witt, Emily;
Ananth, Sahana;
Davies, Adelina;
Masson, Jean-Yves;
Moses, Robb;
West, Stephen C.;
de Winter, Johan P.;
Ashworth, Alan;
Jones, Nigel J.;
Mathew, Christopher G.

Publication type:

Article

Genetics of inflammatory bowel disease: progress and prospects.

Published in:

Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R161

By:

Mathew, Christopher G.;
Lewis, Cathryn M.

Publication type:

Article

Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2503, doi. 10.1093/hmg/ddg266

By:

Hussain, Shobbir;
Witt, Emily;
Huber, Pia A.J.;
Medhurst, Annette L.;
Ashworth, Alan;
Mathew, Christopher G.

Publication type:

Article

Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.

Published in:

Journal of Crohn's & Colitis, 2018, v. 12, n. 3, p. 321, doi. 10.1093/ecco-jcc/jjx157

By:

Onoufriadis, Alexandros;
Stone, Kristina;
Katsiamides, Antreas;
Amar, Ariella;
Omar, Yasmin;
de Lange, Katrina M.;
Taylor, Kirstin;
Barrett, Jeffrey C.;
Pollok, Richard;
Hayee, Bu'Hussain;
Mansfield, John C.;
Sanderson, Jeremy D.;
Simpson, Michael A.;
Mathew, Christopher G.;
Prescott, Natalie J.

Publication type:

Article

HPV types 16/18 L1 E6 and E7 proteins seropositivity and cervical cancer risk in HIV-positive and HIV-negative black South African women.

Published in:

Infectious Agents & Cancer, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13027-022-00418-2

By:

Singini, Mwiza Gideon;
Singh, Elvira;
Bradshaw, Debbie;
Chen, Wenlong Carl;
Motlhale, Melitah;
Kamiza, Abram Bunya;
de Villiers, Chantal Babb;
Muchengeti, Mazvita;
Mathew, Christopher G.;
Newton, Robert;
Bender, Noemi;
Waterboer, Tim;
Sitas, Freddy

Publication type:

Article

Prevalence and Reclassification of Genetic Variants in South African Populations with Breast Cancer.

Published in:

Genes, Chromosomes & Cancer, 2024, v. 63, n. 9, p. 1, doi. 10.1002/gcc.23275

By:

Osler, Tabitha S.;
Brandenburg, Jean‐Tristan;
Schoeman, Mardelle;
Chen, Wenlong Carl;
Urban, Michael F.;
Mathew, Christopher G.

Publication type:

Article

Kaposi sarcoma‐associated herpesvirus, HIV‐1 and Kaposi sarcoma risk in black South Africans diagnosed with cancer during antiretroviral treatment rollout.

Published in:

International Journal of Cancer, 2023, v. 152, n. 10, p. 2081, doi. 10.1002/ijc.34454

By:

Motlhale, Melitah;
Muchengeti, Mazvita;
Bradshaw, Debbie;
Chen, Wenlong Carl;
Singini, Mwiza Gideon;
de Villiers, Chantal Babb;
Lewis, Cathryn M.;
Bender, Noemi;
Mathew, Christopher G.;
Newton, Robert;
Waterboer, Tim;
Singh, Elvira;
Sitas, Freddy

Publication type:

Article

Thirteen cancers associated with HIV infection in a Black South African cancer patient population (1995‐2016).

Published in:

International Journal of Cancer, 2023, v. 152, n. 2, p. 183, doi. 10.1002/ijc.34236

By:

Sengayi‐Muchengeti, Mazvita;
Singh, Elvira;
Chen, Wenlong Carl;
Bradshaw, Debbie;
de Villiers, Chantal Babb;
Newton, Robert;
Waterboer, Tim;
Mathew, Christopher G;
Sitas, Freddy

Publication type:

Article

Genome-wide association study identifies common variants associated with breast cancer in South African Black women.

Published in:

Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-58789-0

By:

Hayat, Mahtaab;
Chen, Wenlong C.;
Babb de Villiers, Chantal;
Hyuck Lee, Sang;
Curtis, Charles;
Newton, Rob;
Waterboer, Tim;
Sitas, Freddy;
Bradshaw, Debbie;
Muchengeti, Mazvita;
Singh, Elvira;
Lewis, Cathryn M.;
Ramsay, Michele;
Mathew, Christopher G.;
Brandenburg, Jean-Tristan

Publication type:

Article

FGFR2 genetic variants in women with breast cancer.

Published in:

Molecular Medicine Reports, 2023, v. 28, n. 6, p. N.PAG, doi. 10.3892/mmr.2023.13113

By:

Dix-Peek, Thérèse;
Dickens, Caroline;
Augustine, Tanya N.;
Phakathi, Boitumelo P.;
Van Den Berg, Eunice J.;
Joffe, Maureen;
Ayeni, Oluwatosin A.;
Cubasch, Herbert;
Nietz, Sarah;
Mathew, Christopher G.;
Hayat, Mahtaab;
Neugut, Alfred I.;
Jacobson, Judith S.;
Ruff, Paul;
Duarte, Raquel A.B.

Publication type:

Article

Usefulness of high‐risk HPV early oncoprotein (E6 and E7) serological markers in the detection of cervical cancer: A systematic review and meta‐analysis.

Published in:

Journal of Medical Virology, 2023, v. 95, n. 1, p. 1, doi. 10.1002/jmv.27900

By:

Singini, Mwiza Gideon;
Singh, Elvira;
Bradshaw, Debbie;
Ramaliba, Thendo;
Chen, Wenlong Carl;
Motlhale, Melitah;
Kamiza, Abram Bunya;
Babb de Villiers, Chantal;
Muchengeti, Mazvita;
Mathew, Christopher G.;
Newton, Robert;
Bender, Noemi;
Waterboer, Tim;
Sitas, Freddy

Publication type:

Article

Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.

Published in:

International Journal of Colorectal Disease, 2007, v. 22, n. 4, p. 419, doi. 10.1007/s00384-006-0151-4

By:

Pearce, Alexandra V.;
Fisher, Sheila A.;
Prescott, Natalie J.;
Onnie, Clive M.;
Pattni, Reenal;
Green, Peter;
Forbes, Alastair;
Mansfield, John;
Sanderson, Jeremy;
Schreiber, Stefan;
Lewis, Cathryn M.;
Mathew, Christopher G.

Publication type:

Article

The Health and Economic Burdens of Lymphatic Filariasis Prior to Mass Drug Administration Programs.

Published in:

Clinical Infectious Diseases, 2020, v. 70, n. 12, p. 2561, doi. 10.1093/cid/ciz671

By:

Mathew, Christopher G;
Bettis, Alison A;
Chu, Brian K;
English, Mike;
Ottesen, Eric A;
Bradley, Mark H;
Turner, Hugo C

Publication type:

Article

Trial Protocol: Communicating DNA-based risk assessments for Crohn's disease: a randomised controlled trial assessing impact upon stopping smoking.

Published in:

BMC Public Health, 2011, v. 11, n. 1, p. 44, doi. 10.1186/1471-2458-11-44

By:

Whitwell, Sophia C. L.;
Mathew, Christopher G.;
Lewis, Cathryn M.;
Forbes, Alastair;
Watts, Sally;
Sanderson, Jeremy;
Hollands, Gareth J.;
Prevost, A. Toby;
Armstrong, David;
Kinmonth, Ann Louise;
Sutton, Stephen;
Marteau, Theresa M.

Publication type:

Article