The Relationship Between Environmental Exposure and Genetic Architecture of the 2q33 Locus With Esophageal Cancer in South Africa

por Matejcic, Marco, Mathew, Christopher G., Parker, M. Iqbal
Publicado no Front Genet (2019)

High Frequency of Large Intragenic Deletions in the Fanconi Anemia Group A Gene

por Morgan, Neil V., Tipping, Alex J., Joenje, Hans, Mathew, Christopher G.
Publicado em 1999

Cancer incidence in relatives of British Fanconi Anaemia patients

por Tischkowitz, Marc, Easton, Douglas F, Ball, Jan, Hodgson, Shirley V, Mathew, Christopher G
Publicado em 2008

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

por Matejcic, Marco, Li, DongPing, Prescott, Natalie J., Lewis, Cathryn M., Mathew, Christopher G., Parker, M. Iqbal
Publicado em 2011

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

por Bye, Hannah, Prescott, Natalie J., Matejcic, Marco, Rose, Elizabeth, Lewis, Cathryn M., Parker, M.Iqbal, Mathew, Christopher G.
Publicado em 2011

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

por Mathew, Christopher G, Bettis, Alison A, Chu, Brian K, English, Mike, Ottesen, Eric A, Bradley, Mark H, Turner, Hugo C
Publicado no Clin Infect Dis (2020)

Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression

por Rosenstiel, Philip, Huse, Klaus, Franke, Andre, Hampe, Jochen, Reichwald, Kathrin, Platzer, Cornelia, Roberts, Roland G, Mathew, Christopher G, Platzer, Matthias, Schreiber, Stefan
Publicado em 2007

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

por Bye, Hannah, Prescott, Natalie J., Lewis, Cathryn M., Matejcic, Marco, Moodley, Loven, Robertson, Barbara, van Rensburg, Christo, Parker, M.Iqbal, Mathew, Christopher G.
Publicado em 2012

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

por 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.
Publicado em 2010

Searching for Genotype-Phenotype Structure: Using Hierarchical Log-Linear Models in Crohn Disease

por Chapman, Juliet M., Onnie, Clive M., Prescott, Natalie J., Fisher, Sheila A., Mansfield, John C., Mathew, Christopher G., Lewis, Cathryn M., Verzilli, Claudio J., Whittaker, John C.
Publicado em 2009

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

por Saadati, Hamid Reza, Wittig, Michael, Helbig, Ingo, Häsler, Robert, Anderson, Carl A., Mathew, Christopher G., Kupcinskas, Limas, Parkes, Miles, Karlsen, Tom Hemming, Rosenstiel, Philip, Schreiber, Stefan, Franke, Andre
Publicado no BMC Med Genet (2016)

Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A

por Joenje, Hans, Levitus, Marieke, Waisfisz, Quinten, D’Andrea, Alan, Garcia-Higuera, Irene, Pearson, Tommy, van Berkel, Carola G. M., Rooimans, Martin A., Morgan, Neil, Mathew, Christopher G., Arwert, Fré
Publicado em 2000

Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study

por Boua, Palwende Romuald, Brandenburg, Jean-Tristan, Choudhury, Ananyo, Hazelhurst, Scott, Sengupta, Dhriti, Agongo, Godfred, Nonterah, Engelbert A., Oduro, Abraham R., Tinto, Halidou, Mathew, Christopher G., Sorgho, Hermann, Ramsay, Michèle
Publicado no Front Genet (2020)

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

por Whitwell, Sophia CL, 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
Publicado em 2011

Genetic Evidence for Interaction of the 5q31 Cytokine Locus and the CARD15 Gene in Crohn Disease

por Mirza, Muddassar M., Fisher, Sheila A., King, Kathy, Cuthbert, Andrew P., Hampe, Jochen, Sanderson, Jeremy, Mansfield, John, Donaldson, Peter, Macpherson, Andrew J. S., Forbes, Alastair, Schreiber, Stefan, Lewis, Cathryn M., Mathew, Christopher G.
Publicado em 2003

A Human Orthologue of Archaeal DNA Repair Protein Hef is Defective in Fanconi Anemia Complementation Group M

por Meetei, Amom Ruhikanta, Medhurst, Annette L., Ling, Chen, Xue, Yutong, Singh, Thiyam Ramsing, Bier, Patrick, Steltenpool, Jurgen, Stone, Stacie, Dokal, Inderjeet, Mathew, Christopher G., Hoatlin, Maureen, Joenje, Hans, de Winter, Johan P., Wang, Weidong
Publicado em 2005

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p

por Hampe, Jochen, Frenzel, Henning, Mirza, Muddassar M., Croucher, Peter J. P., Cuthbert, Andrew, Mascheretti, Silvia, Huse, Klaus, Platzer, Matthias, Bridger, Stephen, Meyer, Birgit, Nürnberg, Peter, Stokkers, Pieter, Krawczak, Michael, Mathew, Christopher G., Curran, Mark, Schreiber, Stefan
Publicado em 2002

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

por 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, Babb de Villiers, Chantal, Parker, M Iqbal, Mathew, Christopher G
Publicado no Carcinogenesis (2019)

Effect of communicating DNA based risk assessments for Crohn’s disease on smoking cessation: randomised controlled trial

por Hollands, Gareth J, Whitwell, Sophia C L, Parker, Richard A, Prescott, Natalie J, Forbes, Alastair, Sanderson, Jeremy, Mathew, Christopher G, Lewis, Cathryn M, Watts, Sally, Sutton, Stephen, Armstrong, David, Kinmonth, Ann Louise, Prevost, A Toby, Marteau, Theresa M
Publicado em 2012

Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn’s disease

por Elliott, Timothy R., Rayment, Neil B., Hudspith, Barry N., Hands, Rebecca E., Taylor, Kirstin, Parkes, Gareth C., Prescott, Natalie J., Petrovska, Liljana, Hermon-Taylor, John, Brostoff, Jonathan, Boussioutas, Alex, Mathew, Christopher G., Bustin, Stephen A., Sanderson, Jeremy D.
Publicado no BMC Gastroenterol (2015)