Postgenomic technologies: hunting the genes for common disorders

Por Mathew, Christopher
Publicado em 2001

Updates in the Management of Diabetic Macular Edema

Por Mathew, Christopher, Yunirakasiwi, Anastasia, Sanjay, Srinivasan
Publicado no J Diabetes Res (2015)

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)

Artificial Intelligence and its future potential in lung cancer screening

Por Joy Mathew, Christopher, David, Ashwini Maria, Joy Mathew, Chris Mariya
Publicado no EXCLI J (2020)

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

A Review of the Impact of Bariatric Surgery in Women With Polycystic Ovary Syndrome

Por Lee, Robert, Joy Mathew, Christopher, Jose, Merin Tresa, Elshaikh, Abeer O, Shah, Lisa, Cancarevic, Ivan
Publicado no Cureus (2020)

Do Menopause and Aging Affect the Onset and Progression of Rheumatoid Arthritis and Systemic Lupus Erythematosus?

Por Shah, Lisa, Elshaikh, Abeer O, Lee, Robert, Joy Mathew, Christopher, Jose, Merin Tresa, Cancarevic, Ivan
Publicado no Cureus (2020)

Is Hyperthyroidism a Possible Etiology of Early Onset Dementia?

Por Joy Mathew, Christopher, Jose, Merin Tresa, Elshaikh, Abeer O, Shah, Lisa, Lee, Robert, Cancarevic, Ivan
Publicado no Cureus (2020)

Influence of Vitamin K on Bone Mineral Density and Osteoporosis

Por Elshaikh, Abeer O, Shah, Lisa, Joy Mathew, Christopher, Lee, Robert, Jose, Merin Tresa, Cancarevic, Ivan
Publicado no Cureus (2020)

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

Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease

Por Polley, Shamik, Prescott, Natalie, Nimmo, Elaine, Veal, Colin, Vind, Ida, Munkholm, Pia, Fode, Peder, Mansfield, John, Skyt Andersen, Paal, Satsangi, Jack, G Mathew, Christopher, Hollox, Edward J
Publicado no Eur J Hum Genet (2016)

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