FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Christopher Mathew

Research Profile

Disorders

Physiology

Chemicals & Drugs

Co-author Network

Publications

TOP 3
Hannah Bye; Cathryn M Lewis; Marco Matejcic; Loven Moodley; M Iqbal Parker; Natalie J Prescott; Christo van Rensburg; Barbara Robertson; Christopher G Mathew
Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.
Jane L Benjamin; Alastair Forbes; Ailsa L Hart; Charlotte R H Hedin; Michael A Kamm; Stella C Knight; Andreas Koutsoumpas; JO Lindsay; Christopher G Mathew; Neil E McCarthy; Siew C Ng; Pedro Pessoa-Lopes; Natalie J Prescott; Jeremy Sanderson; Andrew J Stagg; Kevin Whelan
Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota.
David Ellinghaus; Eva Ellinghaus; Tõnu Esko; Gonçalo R Abecasis; Vito Annese; Tobias Balschun; Jonathan N Barker; Majid Belouchi; Sophie Debrus; James T Elder; Christian Gieger; Michael Kabesch; Külli Kingo; Sulev Kõks; Christopher G Mathew; Andres Metspalu; Rajan P Nair; Susanna Nikolaus; Michael Nothnagel; Orazio Palmieri; John V Raelson; Stefan Schreiber; Philip E Stuart; Trilokraj Tejasvi; Richard C Trembath; Michael Weichenthal; Stephan Weidinger; Sarah L West; H-Erich Wichmann; Andre Franke
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Christopher Mathew (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Hannah Bye; Cathryn M Lewis; Marco Matejcic; Loven Moodley; M Iqbal Parker; Natalie J Prescott; Christo van Rensburg; Barbara Robertson; Christopher G Mathew
Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.
Carcinogenesis 2012;33(11):2155-61.
2012: Jane L Benjamin; Alastair Forbes; Ailsa L Hart; Charlotte R H Hedin; Michael A Kamm; Stella C Knight; Andreas Koutsoumpas; JO Lindsay; Christopher G Mathew; Neil E McCarthy; Siew C Ng; Pedro Pessoa-Lopes; Natalie J Prescott; Jeremy Sanderson; Andrew J Stagg; Kevin Whelan
Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota.
Inflammatory bowel diseases 2012;18(6):1092-100.
2012: David Ellinghaus; Eva Ellinghaus; Tõnu Esko; Gonçalo R Abecasis; Vito Annese; Tobias Balschun; Jonathan N Barker; Majid Belouchi; Sophie Debrus; James T Elder; Christian Gieger; Michael Kabesch; Külli Kingo; Sulev Kõks; Christopher G Mathew; Andres Metspalu; Rajan P Nair; Susanna Nikolaus; Michael Nothnagel; Orazio Palmieri; John V Raelson; Stefan Schreiber; Philip E Stuart; Trilokraj Tejasvi; Richard C Trembath; Michael Weichenthal; Stephan Weidinger; Sarah L West; H-Erich Wichmann; Andre Franke
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
American journal of human genetics 2012;90(4):636-47.
2012: Gareth J Hollands; Ann Louise Kinmonth; Cathryn M Lewis; David Armstrong; Alastair Forbes; Christopher G Mathew; Richard A Parker; Natalie J Prescott; A Toby Prevost; Jeremy Sanderson; Stephen Sutton; Sally Watts; Sophia C L Whitwell; Theresa M Marteau
Effect of communicating DNA based risk assessments for Crohn's disease on smoking cessation: randomised controlled trial.
BMJ (Clinical research ed.) 2012;345():e4708.
2011: Hannah Bye; Cathryn M Lewis; Marco Matejcic; M Iqbal Parker; Natalie J Prescott; Elizabeth Rose; Christopher G Mathew
Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa.
Carcinogenesis 2011;32(12):1855-61.
2011: Sophia C L Whitwell; Christopher G Mathew; Cathryn M Lewis; Alastair Forbes; Sally Watts; Jeremy Sanderson; Gareth J Hollands; A Toby Prevost; David Armstrong; Ann Louise Kinmonth; Stephen Sutton; Theresa M Marteau
Trial Protocol: Communicating DNA-based risk assessments for Crohn's disease: a randomised controlled trial assessing impact upon stopping smoking.
BMC public health 2011;11():44.
2010: Alfons Meindl; Heide Hellebrand; Constanze Wiek; Verena Erven; Barbara Wappenschmidt; Dieter Niederacher; Marcel Freund; Peter Lichtner; Linda Hartmann; Heiner Schaal; Juliane Ramser; Ellen Honisch; Christian Kubisch; Hans E Wichmann; Karin Kast; Helmut Deissler; Christoph Engel; Bertram Müller-Myhsok; Kornelia Neveling; Marion Kiechle; Christopher G Mathew; Detlev Schindler; Rita K Schmutzler; Helmut Hanenberg
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Nature genetics 2010;42(5):410-4.
2010: Fiona Vaz; Helmut Hanenberg; Beatrice Schuster; Karen Barker; Constanze Wiek; Verena Erven; Kornelia Neveling; Daniela Endt; Ian Kesterton; Flavia Autore; Franca Fraternali; Marcel Freund; Linda Hartmann; David Grimwade; Roland Roberts; Heiner Schaal; Shehla Mohammed; Nazneen Rahman; Detlev Schindler; Christopher G Mathew
Mutation of the RAD51C gene in a Fanconi anemia-like disorder.
Nature genetics 2010;42(5):406-9.
2010: Natalie Prescott; Katherine M Dominy; Michiaki Kubo; Cathryn M Lewis; Sheila A Fisher; Richard Redon; Ni Huang; Barbara E Stranger; Katarzyna Blaszczyk; Barry Hudspith; Gareth Parkes; Naoya Hosono; Keiko Yamazaki; Clive M Onnie; Alastair Forbes; Emmanouil T Dermitzakis; Yusuke Nakamura; John C Mansfield; Jeremy Sanderson; Matthew E Hurles; Roland Roberts; Christopher G Mathew
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
Human molecular genetics 2010;19(9):1828-39.
2010: Andre Franke; Tobias Balschun; Christian Sina; David Ellinghaus; Robert Häsler; Gabriele Mayr; Mario Albrecht; Michael Wittig; Eva Buchert; Susanna Nikolaus; Christian Gieger; H-Erich Wichmann; Jurgita Sventoraityte; Limas Kupcinskas; Clive M Onnie; Maria Gazouli; Nicholas P Anagnou; David Strachan; Wendy L McArdle; Christopher G Mathew; Paul Rutgeerts; Séverine Vermeire; Morten H Vatn; Michael Krawczak; Philip Rosenstiel; Tom H Karlsen; Stefan Schreiber
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).
Nature genetics 2010;42(4):292-4.
2009: Juliet M Chapman; Clive M Onnie; Natalie Prescott; Sheila A Fisher; John C Mansfield; Christopher G Mathew; Cathryn M Lewis; Claudio J Verzilli; John C Whittaker
Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease.
American journal of human genetics 2009;84(2):178-87.
2008: Andre Franke; Tobias Balschun; Tom H Karlsen; Jurgita Sventoraityte; Susanna Nikolaus; Gabriele Mayr; Francisco S Domingues; Mario Albrecht; Michael Nothnagel; David Ellinghaus; Christian Sina; Clive M Onnie; Rinse Weersma; Pieter C F Stokkers; Cisca Wijmenga; Maria Gazouli; David Strachan; Wendy L McArdle; Séverine Vermeire; Paul Rutgeerts; Philip Rosenstiel; Michael Krawczak; Morten Vatn; Christopher G Mathew; Stefan Schreiber
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.
Nature genetics 2008;40(11):1319-23.
2008: James B Wilson; K Yamamoto; A S Marriott; Shobbir Hussain; P Sung; Maureen Hoatlin; Christopher G Mathew; M Takata; Larry H Thompson; G M Kupfer; Nigel Jones
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.
Oncogene 2008;27(26):3641-52.
2008: Richard Bagnall; Roland Roberts; Muddassar M Mirza; Toshihiko Torigoe; Natalie Prescott; Christopher G Mathew
Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.
European journal of human genetics : EJHG 2008;16(5):619-25.
2008: Clive M Onnie; Sheila A Fisher; Natalie Prescott; Muddassar M Mirza; Peter Green; Jeremy Sanderson; Alastair Forbes; Cathryn M Lewis; Christopher G Mathew
Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.
European journal of gastroenterology & hepatology 2008;20(1):37-45.
2007: Cathryn M Lewis; S C L Whitwell; Alastair Forbes; Jeremy Sanderson; Christopher G Mathew; Theresa M Marteau
Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn disease.
Journal of medical genetics 2007;44(11):689-94.
2007: Kathy King; Richard Bagnall; Sheila A Fisher; Faisal Sheikh; Andrew P Cuthbert; Sipin Tan; Nicholas I Mundy; Philip Rosenstiel; Stefan Schreiber; Christopher G Mathew; Roland Roberts
Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.
Genomics 2007;90(4):493-501.
2007: Sheila A Fisher; Muddassar M Mirza; Clive M Onnie; Dianne Soars; Cathryn M Lewis; Natalie Prescott; Christopher G Mathew; Jeremy Sanderson; Alastair Forbes; Catherine Todhunter; Peter Donaldson; John Mansfield
Combined evidence from three large British Association studies rejects TUCAN/CARD8 as an IBD susceptibility gene.
Gastroenterology 2007;132(5):2078-80.
2007: Natalie Prescott; Sheila A Fisher; Andre Franke; Jochen Hampe; Clive M Onnie; Dianne Soars; Richard Bagnall; Muddassar M Mirza; Jeremy Sanderson; Alastair Forbes; John C Mansfield; Cathryn M Lewis; Stefan Schreiber; Christopher G Mathew
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
Gastroenterology 2007;132(5):1665-71.
2007: Mark Tremelling; Fraser Cummings; Sheila A Fisher; John Mansfield; Rhian Gwilliam; Andrew Keniry; Elaine R Nimmo; Hazel E Drummond; Clive M Onnie; Natalie Prescott; Jeremy Sanderson; Francesca Bredin; Carlo Berzuini; Alastair Forbes; Cathryn M Lewis; Lon Cardon; Panos Deloukas; Derek Jewell; Christopher G Mathew; Miles Parkes; Jack Satsangi
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease.
Gastroenterology 2007;132(5):1657-64.
2007: Alexandra V Pearce; Sheila A Fisher; Natalie Prescott; Clive M Onnie; Reenal Pattni; Peter Green; Alastair Forbes; John Mansfield; Jeremy Sanderson; Stefan Schreiber; Cathryn M Lewis; Christopher G Mathew
Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.
International journal of colorectal disease 2007;22(4):419-24.
2007: Sarah Reid; Detlev Schindler; Helmut Hanenberg; Karen Barker; Sandra Hanks; Reinhard Kalb; Kornelia Neveling; Patrick Kelly; Sheila Seal; Marcel Freund; Melanie Wurm; Sat Dev Batish; Francis P Lach; Sevgi Yetgin; Heidemarie Neitzel; Hany Ariffin; Marc Tischkowitz; Christopher G Mathew; Arleen D Auerbach; Nazneen Rahman
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
Nature genetics 2007;39(2):162-4.
2007: Jochen Hampe; Andre Franke; Philip Rosenstiel; Andreas Till; Markus Teuber; Klaus Huse; Mario Albrecht; Gabriele Mayr; Francisco M De La Vega; Jason Briggs; Simone Günther; Natalie Prescott; Clive M Onnie; Robert Häsler; Bence Sipos; Ulrich R Fölsch; Thomas Lengauer; Matthias Platzer; Christopher G Mathew; Michael Krawczak; Stefan Schreiber
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Nature genetics 2007;39(2):207-11.
2007: Andre Franke; Jochen Hampe; Philip Rosenstiel; Christian Becker; Florian Wagner; Robert Häsler; Randall Little; Klaus Huse; Andreas Ruether; Tobias Balschun; Michael Wittig; Abdou ElSharawy; Gabriele Mayr; Mario Albrecht; Natalie Prescott; Clive M Onnie; Hélène Fournier; Tim P Keith; Uwe Radelof; Matthias Platzer; Christopher G Mathew; Monika Stoll; Michael Krawczak; Peter Nürnberg; Stefan Schreiber
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
PloS one 2007;2(8):e691.
2007: Josephine C Dorsman; Marieke Levitus; Davy A P Rockx; Martin A Rooimans; Anneke B Oostra; Anneke Haitjema; Sietske T Bakker; Jûrgen Steltenpool; Dezsö Schuler; Sheila Mohan; Detlev Schindler; Fré Arwert; Gerard Pals; Christopher G Mathew; Quinten Waisfisz; Johan P de Winter; Hans Joenje
Identification of the Fanconi anemia complementation group I gene, FANCI.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2007;29(3):211-8.
2006: Ad van Bodegraven; Christine R Curley; Karen A Hunt; Alienke J Monsuur; Ronald K Linskens; Clive M Onnie; J B A Crusius; Vito Annese; Anna Latiano; Mark S Silverberg; Alain Bitton; Sheila A Fisher; A Hillary Steinhart; Alastair Forbes; Jeremy Sanderson; Natalie Prescott; David P Strachan; Raymond J Playford; Christopher G Mathew; Cisca Wijmenga; Mark J Daly; John D Rioux; David A van Heel
Genetic variation in myosin IXB is associated with ulcerative colitis.
Gastroenterology 2006;131(6):1768-74.
2006: Erin P Reid; Alastair Forbes; Jeremy Sanderson; Christopher G Mathew; Cathryn Lewis; Theresa M Marteau
Recruiting first-degree relatives for prevention research: a comparison of clinician and proband-led methods of contact in Crohn's disease.
European journal of human genetics : EJHG 2006;14(12):1263-8.
2006: Sheila A Fisher; Jochen Hampe; Clive M Onnie; Mark J Daly; Christine R Curley; Shaun Purcell; Jeremy Sanderson; John Mansfield; Vito Annese; Alastair Forbes; Cathryn M Lewis; Stefan Schreiber; John D Rioux; Christopher G Mathew
Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
Human mutation 2006;27(8):778-85.
2006: David A van Heel; Karen A Hunt; Kathy King; Subrata Ghosh; Simon M Gabe; Christopher G Mathew; Alastair Forbes; Raymond J Playford
Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's disease.
Inflammatory bowel diseases 2006;12(7):598-605.
2006: Clive M Onnie; Sheila A Fisher; Kathy King; Muddassar M Mirza; Roland Roberts; Alastair Forbes; Jeremy Sanderson; Cathryn M Lewis; Christopher G Mathew
Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.
Genes and immunity 2006;7(5):359-65.
2006: Shobbir Hussain; James B Wilson; Eric Blom; Larry H Thompson; Patrick Sung; Susan M Gordon; Gary M Kupfer; Hans Joenje; Christopher G Mathew; Nigel Jones
Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2.
DNA repair 2006;5(5):629-40.
2006: Clive M Onnie; Sheila A Fisher; Reenal Pattni; Jeremy Sanderson; Alastair Forbes; Cathryn M Lewis; Christopher G Mathew
Associations of allelic variants of the multidrug resistance gene (ABCB1 or MDR1) and inflammatory bowel disease and their effects on disease behavior: a case-control and meta-analysis study.
Inflammatory bowel diseases 2006;12(4):263-71.
2006: Kathy King; Mohammed F Sheikh; Andrew P Cuthbert; Sheila A Fisher; Clive M Onnie; Muddassar M Mirza; Reenal Pattni; Jeremy Sanderson; Alastair Forbes; John Mansfield; Cathryn M Lewis; Roland Roberts; Christopher G Mathew
Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.
Human mutation 2006;27(1):44-54.
2006: Weiyue Zheng; Philip Rosenstiel; Klaus Huse; Christian Sina; Ruta Valentonyte; Nancy Mah; Lutz Zeitlmann; Johannes Grosse; N Ruf; Peter Nürnberg; Christine M Costello; Clive M Onnie; Christopher G Mathew; Matthias Platzer; Stefan Schreiber; Jochen Hampe
Evaluation of AGR2 and AGR3 as candidate genes for inflammatory bowel disease.
Genes and immunity 2006;7(1):11-8.
2005: David A van Heel; Subrata Ghosh; Karen A Hunt; Christopher G Mathew; Alastair Forbes; Derek P Jewell; Raymond J Playford
Synergy between TLR9 and NOD2 innate immune responses is lost in genetic Crohn's disease.
Gut 2005;54(11):1553-7.
2005: Natalie Prescott; Sheila A Fisher; Clive M Onnie; Reenal Pattni; Sophia Steer; Jeremy Sanderson; Alastair Forbes; Cathryn M Lewis; Christopher G Mathew
A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British population.
Tissue antigens 2005;66(4):318-20.
2005: Marieke Levitus; Quinten Waisfisz; Barbara C Godthelp; Yne de Vries; Shobbir Hussain; Wouter W Wiegant; Elhaam Elghalbzouri-Maghrani; Jûrgen Steltenpool; Martin A Rooimans; Gerard Pals; Fré Arwert; Christopher G Mathew; Malgorzata Z Zdzienicka; Kevin Hiom; Johan P de Winter; Hans Joenje
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Nature genetics 2005;37(9):934-5.
2005: Amom Ruhikanta Meetei; Annette L Medhurst; Chen Ling; Yutong Xue; Thiyam Ramsing Singh; Patrick Bier; Jûrgen Steltenpool; Stacie Stone; Inderjeet Dokal; Christopher G Mathew; Maureen Hoatlin; Hans Joenje; Johan P de Winter; Weidong Wang
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
Nature genetics 2005;37(9):958-63.
2005: M M Mirza; S A Fisher; Clive M Onnie; C M Lewis; Christopher G Mathew; J Sanderson; Alastair Forbes
No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohort.
Gut 2005;54(8):1205-6.
2005: Mark J Daly; Alexandra V Pearce; Lisa Farwell; Sheila A Fisher; Anna Latiano; Natalie Prescott; Alastair Forbes; John Mansfield; Jeremy Sanderson; Diane Langelier; Albert Cohen; Alain Bitton; Gary Wild; Cathryn M Lewis; Vito Annese; Christopher G Mathew; John D Rioux
Association of DLG5 R30Q variant with inflammatory bowel disease.
European journal of human genetics : EJHG 2005;13(7):835-9.
2005: David A van Heel; Subrata Ghosh; Matt Butler; Karen A Hunt; Anna M C Lundberg; Tariq Ahmad; Dermot P B McGovern; Clive M Onnie; Kenichi Negoro; Sue Goldthorpe; Brian M J Foxwell; Christopher G Mathew; Alastair Forbes; Derek P Jewell; Raymond J Playford
Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease.
Lancet 2005;365(9473):1794-6.
2005: Neil V Morgan; Fahmida Essop; Ilja Demuth; T J L de Ravel; Stander Jansen; Marc Tischkowitz; Cathryn M Lewis; Linda Wainwright; Janet Poole; Hans Joenje; Martin Digweed; Amanda Krause; Christopher G Mathew
A common Fanconi anemia mutation in black populations of sub-Saharan Africa.
Blood 2005;105(9):3542-4.
2005: Helen V New; Catherine M Cale; Marc Tischkowitz; A Jones; P Telfer; Paul Veys; Alan D D'Andrea; Christopher G Mathew; Ian Hann
Nijmegen breakage syndrome diagnosed as Fanconi anaemia.
Pediatric blood & cancer 2005;44(5):494-9.
2005: Elsa Callén; José A Casado; Marc Tischkowitz; Juan A. Bueren; Amadeu Creus; Ricard Marcos; Angeles Dasí; Jesús Estella; Arturo Muñoz; Juan J Ortega; Johan P de Winter; Hans Joenje; Detlev Schindler; Helmut Hanenberg; Shirley V Hodgson; Christopher G Mathew; Jordi Surrallés
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain.
Blood 2005;105(5):1946-9.
2004: Shobbir Hussain; James B Wilson; Annette L Medhurst; James Hejna; Emily Witt; Sahana Ananth; Adelina Davies; Jean-Yves Masson; Robb Moses; Stephen C West; Johan P de Winter; Alan Ashworth; Nigel Jones; Christopher G Mathew
Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways.
Human molecular genetics 2004;13(12):1241-8.
2004: Monika Stoll; Brit Corneliussen; Christine M Costello; Georg H Waetzig; Bjorn Mellgard; W Andreas Koch; Philip Rosenstiel; Mario Albrecht; Peter J P Croucher; Dirk Seegert; Susanna Nikolaus; Jochen Hampe; Thomas Lengauer; Stefan Pierrou; Ulrich R Foelsch; Christopher G Mathew; Maria Lagerstrom-Fermer; Stefan Schreiber
Genetic variation in DLG5 is associated with inflammatory bowel disease.
Nature genetics 2004;36(5):476-80.
2004: Marieke Levitus; Martin A Rooimans; Jûrgen Steltenpool; Nicolle F C Cool; Anneke B Oostra; Christopher G Mathew; Maureen Hoatlin; Quinten Waisfisz; Fré Arwert; Johan P de Winter; Hans Joenje
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.
Blood 2004;103(7):2498-503.
2004: Marc Tischkowitz; Neil V Morgan; David Grimwade; C Eddy; S Ball; I Vorechovsky; Stephen E Langabeer; Reinhard Stöger; Shirley V Hodgson; Christopher G Mathew
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia.
Leukemia 2004;18(3):420-5.
2004: Elsa Callén; Marc Tischkowitz; Amadeu Creus; Ricard Marcos; Juan A. Bueren; José A Casado; Christopher G Mathew; Jordi Surrallés
Quantitative PCR analysis reveals a high incidence of large intragenic deletions in the FANCA gene in Spanish Fanconi anemia patients.
Cytogenetic and genome research 2004;104(1-4):341-5.
2003: Martyn C Byng; John C Whittaker; Andrew P Cuthbert; Christopher G Mathew; Cathryn M Lewis
SNP subset selection for genetic association studies.
Annals of human genetics 2003;67(Pt 6):543-56.
2003: Marc Tischkowitz; Najim Ameziane; Quinten Waisfisz; Johan P de Winter; Richard Harris; Toshiyasu Taniguchi; Alan D D'Andrea; Shirley V Hodgson; Christopher G Mathew; Hans Joenje
Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia.
British journal of haematology 2003;123(3):469-71.
2003: Sarah H Shaw; Jochen Hampe; Raymond White; Christopher G Mathew; Mark E Curran; Stefan Schreiber
Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci.
Human genetics 2003;113(6):514-21.
2003: Tanja Reuter; Annette L Medhurst; Quinten Waisfisz; Yu Zhi; Sabine Herterich; Holger Hoehn; Hans J Gross; Hans Joenje; Maureen Hoatlin; Christopher G Mathew; Pia A J Huber
Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport.
Experimental cell research 2003;289(2):211-21.
2003: Shobbir Hussain; Emily Witt; Pia A J Huber; Annette L Medhurst; Alan Ashworth; Christopher G Mathew
Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
Human molecular genetics 2003;12(19):2503-10.
2003: Sheila A Fisher; A Moody; Muddassar M Mirza; Andrew P Cuthbert; Jochen Hampe; A Macpherson; Jeremy Sanderson; Alastair Forbes; John Mansfield; Stefan Schreiber; Cathryn M Lewis; Christopher G Mathew
Genetic variation at the chromosome 16 chemokine gene cluster: development of a strategy for association studies in complex disease.
Annals of human genetics 2003;67(Pt 5):377-90.
2003: M William Lensch; Marc Tischkowitz; Tracy A Christianson; Carol A Reifsteck; S Ashley Speckhart; Petra Jakobs; Michael O'Dwyer; Susan B Olson; Michelle M Le Beau; Shirley V Hodgson; Christopher G Mathew; Richard A Larson; Grover C Bagby
Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia.
Blood 2003;102(1):7-16.
2003: Kathy King; A Moody; Sheila A Fisher; Muddassar M Mirza; Andrew P Cuthbert; Jochen Hampe; A Sutherland-Craggs; Jeremy Sanderson; Andrew J S Macpherson; Alastair Forbes; John Mansfield; Stefan Schreiber; Cathryn M Lewis; Christopher G Mathew
Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 2003;30(3):187-90.
2003: Toshiyasu Taniguchi; Marc Tischkowitz; Najim Ameziane; Shirley V Hodgson; Christopher G Mathew; Hans Joenje; Samuel C Mok; Alan D D'Andrea
Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors.
Nature medicine 2003;9(5):568-74.
2003: Muddassar M Mirza; Sheila A Fisher; Kathy King; Andrew P Cuthbert; Jochen Hampe; Jeremy Sanderson; John Mansfield; Peter Donaldson; Andrew J S Macpherson; Alastair Forbes; Stefan Schreiber; Cathryn M Lewis; Christopher G Mathew
Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.
American journal of human genetics 2003;72(4):1018-22.
2003: Sophia Steer; Sheila A Fisher; Mark Fife; A Cuthbert; J Newton; Paul Wordsworth; Cathryn M Lewis; Christopher G Mathew; Jerry S Lanchbury
Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15.
Rheumatology (Oxford, England) 2003;42(2):304-7.
2002: Koji Nakanishi; Toshiyasu Taniguchi; Velvizhi Ranganathan; Helen V New; Lisa A Moreau; Maria Stotsky; Christopher G Mathew; Michael B Kastan; David Weaver; Alan D D'Andrea
Interaction of FANCD2 and NBS1 in the DNA damage response.
Nature cell biology 2002;4(12):913-20.
2002: Sheila A Fisher; Jochen Hampe; Andrew J S Macpherson; Alastair Forbes; John E Lennard-Jones; Stefan Schreiber; Mark E Curran; Christopher G Mathew; Cathryn M Lewis
Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6.
European journal of human genetics : EJHG 2002;10(4):259-65.
2002: Andrew P Cuthbert; Sheila A Fisher; Muddassar M Mirza; Kathy King; Jochen Hampe; Peter J P Croucher; Silvia Mascheretti; Jeremy Sanderson; Alastair Forbes; John Mansfield; Stefan Schreiber; Cathryn M Lewis; Christopher G Mathew
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.
Gastroenterology 2002;122(4):867-74.
2002: Jochen Hampe; Henning Frenzel; Muddassar M Mirza; Peter J P Croucher; Andrew P Cuthbert; Silvia Mascheretti; Klaus Huse; Matthias Platzer; Stephen Bridger; Birgit Meyer; Peter Nürnberg; Pieter C F Stokkers; Michael Krawczak; Christopher G Mathew; Mark Curran; Stefan Schreiber
Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(1):321-6.
2001: G Daniels; R Pettigrew; Alan R Thornhill; Stephen Abbs; Alison Lashwood; F O'Mahony; Christopher G Mathew; Alan H Handyside; Peter Braude
Six unaffected livebirths following preimplantation diagnosis for spinal muscular atrophy.
Molecular human reproduction 2001;7(10):995-1000.
2001: Jochen Hampe; Andrew P Cuthbert; Peter J P Croucher; Muddassar M Mirza; Silvia Mascheretti; S Fisher; Henning Frenzel; Kathy King; A Hasselmeyer; Andrew J S Macpherson; Stephen Bridger; SJ Van Deventer; Alastair Forbes; Susanna Nikolaus; John E Lennard-Jones; Ulrich R Foelsch; Michael Krawczak; C Lewis; Stefan Schreiber; Christopher G Mathew
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.
Lancet 2001;357(9272):1925-8.
2001: Alex J Tipping; T Pearson; Neil V Morgan; Robert Alan Gibson; L P Kuyt; C Havenga; Eliane Gluckman; Hans Joenje; T J L de Ravel; Stander Jansen; Christopher G Mathew
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(10):5734-9.
2001: Annette L Medhurst; Pia A J Huber; Quinten Waisfisz; Johan P de Winter; Christopher G Mathew
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway.
Human molecular genetics 2001;10(4):423-9.
2001: Anne-Marie Cleton-Jansen; David F Callen; Ram Seshadri; S Goldup; B Mccallum; Joanna Crawford; Jason A Powell; C Settasatian; Hetty M van Beerendonk; Elna W Moerland; Vincent T H B M Smit; W H Harris; R Millis; Neil V Morgan; D Barnes; Christopher G Mathew; Cees J Cornelisse
Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions.
Cancer research 2001;61(3):1171-7.
2001: Jochen Hampe; Nicholas J Lynch; S Daniels; Stephen Bridger; Andrew J S Macpherson; Pieter C F Stokkers; Alastair Forbes; John E Lennard-Jones; Christopher G Mathew; Mark E Curran; Stefan Schreiber
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease.
Gut 2001;48(2):191-7.
2001: H Hanson; Christopher G Mathew; Zoe Docherty; Caroline Mackie Ogilvie
Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach.
Cytogenetics and cell genetics 2001;93(3-4):203-6.
2000: L Faivre; Philippe Guardiola; C Lewis; Inderjeet Dokal; Wolfram Ebell; Adriana Zatterale; Cigdem Altay; Janet Poole; David Stones; Mei Lan Kwee; M van Weel-Sipman; C Havenga; N Morgan; Johan P de Winter; Martin Digweed; Anna Savoia; J Pronk; T J L de Ravel; Stander Jansen; Hans Joenje; Eliane Gluckman; Christopher G Mathew
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
Blood 2000;96(13):4064-70.
2000: Ilja Demuth; M Wlodarski; Alex J Tipping; Neil V Morgan; Johan P de Winter; M Thiel; S Gräsl; Detlev Schindler; Alan D D'Andrea; Cigdem Altay; H Kayserili; Adriana Zatterale; Jürgen Kunze; Wolfram Ebell; Christopher G Mathew; Hans Joenje; Karl Sperling; Martin Digweed
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
European journal of human genetics : EJHG 2000;8(11):861-8.
2000: Johan P de Winter; France Léveillé; Carola G M van Berkel; Martin A Rooimans; Laura van der Weel; Jûrgen Steltenpool; Ilja Demuth; Neil V Morgan; Noa Alon; Lucine Bosnoyan-Collins; J Lightfoot; P A J Leegwater; Quinten Waisfisz; K Komatsu; Fré Arwert; Jan C Pronk; Christopher G Mathew; Martin Digweed; Manuel Buchwald; Hans Joenje
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
American journal of human genetics 2000;67(5):1306-8.
2000: D Ellis; J Greenman; Shirley Hodgson; S McCall; Fiona Lalloo; J Cameron; Louise Izatt; G Scott; C Jacobs; S Watts; W Chorley; C Perrett; K Macdermot; S Mohammed; G Evans; Christopher G Mathew
Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history.
Journal of medical genetics 2000;37(10):792-4.
2000: Hans Joenje; Marieke Levitus; Quinten Waisfisz; Alan D D'Andrea; Irene Garcia-Higuera; T Pearson; Carola G M van Berkel; Martin A Rooimans; N Morgan; Christopher G Mathew; Fré Arwert
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.
American journal of human genetics 2000;67(3):759-62.
2000: Pia A J Huber; Annette L Medhurst; H Youssoufian; Christopher G Mathew
Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis.
Biochemical and biophysical research communications 2000;268(1):73-7.
2000: MG Olavesen; Jochen Hampe; Muddassar M Mirza; Robert Saiz; Cathryn M Lewis; Stephen Bridger; D Teare; D F Easton; T Herrmann; G Scott; J Hirst; Jeremy Sanderson; Shirley V Hodgson; J Lee; A MacPherson; Stefan Schreiber; John E Lennard-Jones; Mark E Curran; Christopher G Mathew
Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease.
Immunogenetics 2000;51(1):1-7.
2000: Johan P de Winter; Martin A Rooimans; Laura van der Weel; Carola G M van Berkel; Noa Alon; Lucine Bosnoyan-Collins; Jan de Groot; Yu Zhi; Quinten Waisfisz; Jan C Pronk; Fré Arwert; Christopher G Mathew; Rik J Scheper; Maureen Hoatlin; Manuel Buchwald; Hans Joenje
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.
Nature genetics 2000;24(1):15-6.
1999: Jochen Hampe; Sarah H Shaw; Robert Saiz; N Leysens; Annette Lantermann; Silvia Mascheretti; Nicholas J Lynch; Andrew J S Macpherson; Stephen Bridger; SJ Van Deventer; Pieter C F Stokkers; P Morin; Muddassar M Mirza; Alastair Forbes; John E Lennard-Jones; Christopher G Mathew; Mark E Curran; Stefan Schreiber
Linkage of inflammatory bowel disease to human chromosome 6p.
American journal of human genetics 1999;65(6):1647-55.
1999: Louise Izatt; J Greenman; Shirley Hodgson; D Ellis; S Watts; G Scott; C Jacobs; R Liebmann; Marketa Zvelebil; Christopher G Mathew; Ellen Solomon
Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer.
Genes, chromosomes & cancer 1999;26(4):286-94.
1999: Neil V Morgan; Alex J Tipping; Hans Joenje; Christopher G Mathew
High frequency of large intragenic deletions in the Fanconi anemia group A gene.
American journal of human genetics 1999;65(5):1330-41.
1999: Neil Whittock; G H S Ashton; R Mohammedi; Jemima E Mellerio; Christopher G Mathew; Stephen Abbs; Robin A J Eady; John A McGrath
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.
The Journal of investigative dermatology 1999;113(4):673-86.
1999: Quinten Waisfisz; Neil V Morgan; Maria Savino; Johan P de Winter; Carola G M van Berkel; Maureen Hoatlin; L Ianzano; Robert Alan Gibson; Fré Arwert; Anna Savoia; Christopher G Mathew; Jan C Pronk; Hans Joenje
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
Nature genetics 1999;22(4):379-83.
1999: Quinten Waisfisz; Kathrin Saar; Neil V Morgan; Cigdem Altay; P A J Leegwater; Johan P de Winter; K Komatsu; G R Evans; Rolf-Dieter Wegner; A Reis; Hans Joenje; Fré Arwert; Christopher G Mathew; Jan C Pronk; Martin Digweed
The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.
American journal of human genetics 1999;64(5):1400-5.
1999: Gary M Kupfer; D Naf; Irene Garcia-Higuera; J Wasik; A Cheng; Takayuki Yamashita; Alex J Tipping; N Morgan; Christopher G Mathew; Alan D D'Andrea
A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation.
Experimental hematology 1999;27(4):587-93.
1999: Anne-Marie Cleton-Jansen; Elna W Moerland; Jan C Pronk; Carola G M van Berkel; S Apostolou; Joanna Crawford; Anna Savoia; Arleen D Auerbach; Christopher G Mathew; David F Callen; Cees J Cornelisse
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3.
British journal of cancer 1999;79(7-8):1049-52.
1999: Jochen Hampe; Stefan Schreiber; Sarah H Shaw; K F Lau; Stephen Bridger; Andrew J S Macpherson; LR Cardon; H Sakul; T J Harris; AJ Buckler; J Hall; Pieter C F Stokkers; SJ Van Deventer; Peter Nürnberg; Muddassar M Mirza; J C Lee; John E Lennard-Jones; Christopher G Mathew; Mark E Curran
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.
American journal of human genetics 1999;64(3):808-16.
1999: Joanna Crawford; L Ianzano; Maria Savino; Scott A Whitmore; Anne-Marie Cleton-Jansen; C Settasatian; Maria D'Apolito; Ram Seshadri; Jan C Pronk; Arleen D Auerbach; Peter C Verlander; Christopher G Mathew; Alex J Tipping; Norman A Doggett; Leopoldo Zelante; David F Callen; Anna Savoia
The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer.
Genomics 1999;56(1):90-7.
1999: Aurélie Catteau; Chun-Fang Xu; Melissa A Brown; Shirley Hodgson; J Greenman; Christopher G Mathew; Alison M Dunning; Ellen Solomon
Identification of a C/G polymorphism in the promoter region of the BRCA1 gene and its use as a marker for rapid detection of promoter deletions.
British journal of cancer 1999;79(5-6):759-63.
1999: M J MacLeod; J E Taylor; P W Lunt; Christopher G Mathew; Stephanie Robb
Prenatal onset spinal muscular atrophy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1999;3(2):65-72.
1998: Mark E Curran; K F Lau; Jochen Hampe; Stefan Schreiber; Stephen Bridger; Andrew J S Macpherson; LR Cardon; H Sakul; T J Harris; Pieter C F Stokkers; SJ Van Deventer; Muddassar M Mirza; Andreas Raedler; Wolfgang Kruis; U Meckler; D Theuer; T Herrmann; P Gionchetti; J Lee; Christopher G Mathew; John E Lennard-Jones
Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16.
Gastroenterology 1998;115(5):1066-71.
1998: Scott A Whitmore; C Settasatian; Joanna Crawford; Karen M Lower; B McCallum; Ram Seshadri; Cees J Cornelisse; Elna W Moerland; Anne-Marie Cleton-Jansen; Alex J Tipping; Christopher G Mathew; M Savnio; Anna Savoia; Peter C Verlander; Arleen D Auerbach; Carola G M van Berkel; Jan C Pronk; Norman A Doggett; David F Callen
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer.
Genomics 1998;52(3):325-31.
1998: J E Taylor; N H Thomas; Cathryn M Lewis; Stephen Abbs; N R Rodrigues; K E Davies; Christopher G Mathew
Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.
European journal of human genetics : EJHG 1998;6(5):467-74.
1998: Scott A Whitmore; Joanna Crawford; S Apostolou; Helen Eyre; Elizabeth Baker; Karen M Lower; C Settasatian; S Goldup; Ram Seshadri; Robert Alan Gibson; Christopher G Mathew; Anne-Marie Cleton-Jansen; Anna Savoia; Jan C Pronk; Arleen D Auerbach; Norman A Doggett; Grant R Sutherland; David F Callen
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.
Genomics 1998;50(1):1-8.
1998: Muddassar M Mirza; J Lee; D Teare; J P Hugot; P Laurent-Puig; J F Colombel; Shirley V Hodgson; G Thomas; D F Easton; John E Lennard-Jones; Christopher G Mathew
Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitis.
Journal of medical genetics 1998;35(3):218-21.
1998: J Greenman; S Mohammed; D Ellis; S Watts; G Scott; Louise Izatt; D Barnes; Ellen Solomon; Shirley Hodgson; Christopher G Mathew
Identification of missense and truncating mutations in the BRCA1 gene in sporadic and familial breast and ovarian cancer.
Genes, chromosomes & cancer 1998;21(3):244-9.
1998: Jochen Hampe; B Hermann; Stephen Bridger; Andrew J S Macpherson; Christopher G Mathew; Stefan Schreiber
The interferon-gamma gene as a positional and functional candidate gene for inflammatory bowel disease.
International journal of colorectal disease 1998;13(5-6):260-3.
1998: J R Lo Ten Foe; Frank A E Kruyt; M B Zweekhorst; Gerard Pals; Robert Alan Gibson; Christopher G Mathew; Hans Joenje; Fré Arwert
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstream.
Human mutation 1998;Suppl 1():S25-7.
1997: J R Lo Ten Foe; Mei Lan Kwee; Martin A Rooimans; Anneke B Oostra; A J Veerman; M van Weel; R M Pauli; N T Shahidi; Inderjeet Dokal; I Roberts; Cigdem Altay; Eliane Gluckman; Robert Alan Gibson; Christopher G Mathew; Fré Arwert; Hans Joenje
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.
European journal of human genetics : EJHG 1997;5(3):137-48.
1997: L Ianzano; Maria D'Apolito; Marta Centra; Maria Savino; Orna Levran; Arleen D Auerbach; Anne-Marie Cleton-Jansen; Norman A Doggett; Jan C Pronk; Alex J Tipping; Robert Alan Gibson; Christopher G Mathew; Scott A Whitmore; S Apostolou; David F Callen; Leopoldo Zelante; Anna Savoia
The genomic organization of the Fanconi anemia group A (FAA) gene.
Genomics 1997;41(3):309-14.
1997: Neil Whittock; Roland Roberts; Christopher G Mathew; Stephen Abbs
Dystrophin point mutation screening using a multiplexed protein truncation test.
Genetic testing 1997;1(2):115-23.
1997: Angela Barnicoat; Q Wang; J Turk; E Green; Christopher G Mathew; G Flynn; V Buckle; M Hirst; K Davies; Martin Bobrow
Clinical, cytogenetic, and molecular analysis of three families with FRAXE.
Journal of medical genetics 1997;34(1):13-7.
1996: H Iwase; J M Greenman; DM Barnes; Shirley Hodgson; LG Bobrow; Christopher G Mathew
Sequence variants of the estrogen receptor (ER) gene found in breast cancer patients with ER negative and progesterone receptor positive tumors.
Cancer letters 1996;108(2):179-84.
1996: S C Yau; Martin Bobrow; Christopher G Mathew; Stephen Abbs
Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.
Journal of medical genetics 1996;33(7):550-8.
1996: I Naom; J Lee; D Ford; S J Bowman; J S Lanchbury; I Haris; Shirley V Hodgson; D Easton; J Lennard-Jones; Christopher G Mathew
Analysis of the contribution of HLA genes to genetic predisposition in inflammatory bowel disease.
American journal of human genetics 1996;59(1):226-33.
1996: Inderjeet Dokal; Andrew Chase; Neil V Morgan; S Coulthard; G Hall; Christopher G Mathew; I Roberts
Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.
British journal of haematology 1996;93(4):813-6.
1996: Robert Alan Gibson; Neil V Morgan; L H Goldstein; I C Pearson; I P Kesterton; N J Foot; S Jansen; C Havenga; T Pearson; T J de Ravel; R J Cohn; I M Marques; Inderjeet Dokal; I Roberts; Judith Marsh; S Ball; R D Milner; J C Llerena; E Samochatova; S P Mohan; P Vasudevan; F Birjandi; A Hajianpour; M Murer-Orlando; Christopher G Mathew
Novel mutations and polymorphisms in the Fanconi anemia group C gene.
Human mutation 1996;8(2):140-8.
1995: C P Bennett; Angela Barnicoat; F Cotter; Q Wang; Christopher G Mathew
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.
Journal of medical genetics 1995;32(9):757-8.
1995: H Iwase; J M Greenman; DM Barnes; LG Bobrow; Shirley Hodgson; Christopher G Mathew
Loss of heterozygosity of the oestrogen receptor gene in breast cancer.
British journal of cancer 1995;71(3):448-50.
1995: Q Wang; E Green; Martin Bobrow; Christopher G Mathew
A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci.
Journal of medical genetics 1995;32(3):170-3.
1994: Barbara Pertl; S C Yau; Jon K Sherlock; Angela F Davies; Christopher G Mathew; Matteo Adinolfi
Rapid molecular method for prenatal detection of Down's syndrome.
Lancet 1994;343(8907):1197-8.
1994: Peter C Verlander; J D Lin; M U Udono; Q Zhang; R A Gibson; Christopher G Mathew; Arleen D Auerbach
Mutation analysis of the Fanconi anemia gene FACC.
American journal of human genetics 1994;54(4):595-601.
1993: C Holding; D Bentley; Roland Roberts; Martin Bobrow; Christopher G Mathew
Development and validation of laboratory procedures for preimplantation diagnosis of Duchenne muscular dystrophy.
Journal of medical genetics 1993;30(11):903-9.
1993: Q Wang; E Green; Angela Barnicoat; D Garrett; M Mullarkey; Martin Bobrow; Christopher G Mathew
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndrome.
Lancet 1993;342(8878):1025-6.
1993: M Murer-Orlando; J C Llerena; F Birjandi; Robert Alan Gibson; Christopher G Mathew
FACC gene mutations and early prenatal diagnosis of Fanconi's anaemia.
Lancet 1993;342(8872):686.
1993: Robert Alan Gibson; Anna Savoia; Manuel Buchwald; Christopher G Mathew
EcoRI RFLP in the Fanconi anaemia complementation group C gene (FACC).
Human molecular genetics 1993;2(9):1509.
1993: Robert Alan Gibson; A Hajianpour; M Murer-Orlando; Manuel Buchwald; Christopher G Mathew
A nonsense mutation and exon skipping in the Fanconi anaemia group C gene.
Human molecular genetics 1993;2(6):797-9.
1993: S C Yau; Roland Roberts; Martin Bobrow; Christopher G Mathew
Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.
Lancet 1993;341(8840):273-5.
1993: Robert Alan Gibson; Manuel Buchwald; Roland Roberts; Christopher G Mathew
Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR.
Human molecular genetics 1993;2(1):35-8.
1993: R D Milner; K A Khallouf; R Gibson; A Hajianpour; Christopher G Mathew
A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype.
Archives of disease in childhood 1993;68(1):101-3.
1992: A M Differ; Martin Bobrow; Christopher G Mathew
A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.
Human genetics 1992;89(6):689.
1992: R J Daniels; G K Suthers; Karen E Morrison; N H Thomas; M J Francis; Christopher G Mathew; S Loughlin; A Heiberg; D Wood; Victor Dubowitz
Prenatal prediction of spinal muscular atrophy.
Journal of medical genetics 1992;29(3):165-70.
1991: S C Yau; Roland Roberts; David R Bentley; Christopher G Mathew; Martin Bobrow
A MseI polymorphism in exon 48 of the dystrophin gene.
Nucleic acids research 1991;19(20):5803.
1991: Stephen Abbs; S C Yau; S Clark; Christopher G Mathew; Martin Bobrow
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
Journal of medical genetics 1991;28(5):304-11.
1990: A Harris; F Beards; Christopher G Mathew
Mutation analysis at the cystic fibrosis locus in the British population.
Human genetics 1990;85(4):408-9.
1990: Stephen Abbs; Roland Roberts; Christopher G Mathew; David R Bentley; Martin Bobrow
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.
Genomics 1990;7(4):602-6.