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PLoS Genetics, ISSN 1553-7390, 04/2007, Volume 3, Issue 4, pp. 0538 - 0543
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2011, Volume 43, Issue 1, pp. 43 - 47
Journal Article
Journal Article
by Fisher, Sheila A and Regueiro, Miguel D and Anderson, Carl A and Prescott, Natalie J and Mathew, Christopher G and Rutgeerts, Paul and Parkes, Miles and Steinhart, A Hillary and Drummond, Hazel and Bitton, Alain and Georges, Michel and Gut, Ivo and Jewell, Derek and Barrett, Jeffrey C and Daly, Mark J and Dewit, Olivier and Bumpstead, Suzannah and Hansoul, Sarah and Hugot, Jean-Pierre and Barmada, M Michael and Xavier, Ramnik J and Libioulle, Cécile and Tremelling, Mark and Laukens, Debby and Datta, Lisa Wu and Kistner, Emily O and Onnie, Clive M and Griffiths, Anne M and Franchimont, Denis and Lathrop, Mark and Nimmo, Elaine and Green, Todd and Mansfield, John and Zelenika, Diana and Deloukas, Panos and Taylor, Kent D and Ahmad, Tariq and de Vos, Martine and Van Gossum, André and Duerr, Richard H and Silverberg, Mark S and Nicolae, Dan L and Rotter, Jerome I and Schumm, L Philip and Cardon, Lon R and Ghori, Jilur and Heath, Simon and Dassopoulos, Themistocles and Vermeire, Severine and Sandor, Cynthia and Satsangi, Jack and Marchini, Jonathan and Gwilliam, Rhian and Louis, Edouard and Rioux, John D and Mni, Myriam and Belaiche, Jacques and Targan, Stephan R and Brant, Steven R and Murtha, Michael T and Cho, Judy H and Wellcome Trust Case Control and NIDDK IBD Genetics Consortium and Belgian-French IBD Consortium and Wellcome Trust Case Control Consortium and the NIDDK IBD Genetics Consortium and the Belgian-French IBD Consortium and the Wellcome Trust Case Control Consortium
Nature Genetics, ISSN 1061-4036, 08/2008, Volume 40, Issue 8, pp. 955 - 962
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 11, pp. e13795 - e13795
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2009, Volume 41, Issue 12, pp. 1335 - 1340
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2009, Volume 4, Issue 9, pp. e7154 - e7154
Background and Aims: The familial Mediterranean fever (FMF) gene (MEFV) encodes pyrin, a major regulator of the inflammasome platform controlling caspase-1... 
FLIP-FLOP | CONTRIBUTE | INFLAMMATORY-BOWEL-DISEASE | CASPASE-1 | INTERACTS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | MUTATIONS | EXPRESSION | GENOME-WIDE ASSOCIATION | PYRIN | Crohn Disease - genetics | Genetic Predisposition to Disease | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Colitis, Ulcerative - genetics | Familial Mediterranean Fever - genetics | Child, Preschool | Caspase 1 - metabolism | Male | Pyrin | Genetic Variation | Epistasis, Genetic | Interleukin-1beta - metabolism | Adolescent | Inflammatory Bowel Diseases - genetics | Aged, 80 and over | Adult | Cytoskeletal Proteins - metabolism | Female | Aged | Enzyme Activation | Child | Cohort Studies | Genes | Genetic research | Disease susceptibility | Genetic aspects | Familial Mediterranean fever | Colitis | Gene expression | Risk factors | Genetic screening | Haplotypes | Animal models | Inflammatory bowel diseases | DNA polymerase | Pathogenesis | Mucosa | Risk | Single-nucleotide polymorphism | Caspase-1 | Jews | Intestine | Rodents | Gastroenterology | Colon | Medical research | Cytokines | Cryopyrin | Research & development--R&D | Health risks | Caspase | Inflammation | Genetic diversity | IL-1β | Fever | Crohns disease | Medicine | Inflammatory bowel disease | Polymerase chain reaction | Crohn's Disease | Hospitals | Pyrin protein | Genotyping | Gene frequency | Alleles | Mutation | Ulcerative colitis | Index Medicus | Research & development | R&D
Journal Article
ACTA CLINICA BELGICA, ISSN 1784-3286, 2016, Volume 71, Issue S1, pp. 7 - 7
  To study the clinical phenotype, the genetics and therapeutic responses in a series of 35 consecutive patients with hypogonadotropic hypogonadism and... 
MEDICINE, GENERAL & INTERNAL | Genotype & phenotype | Genetics | Mutation | Patients
Conference Proceeding
Nature genetics, ISSN 1061-4036, 1/2009, Volume 41, Issue 1, pp. 71 - 76
We used a candidate gene approach to identify a set of SNPs, located in a predicted regulatory region on chromosome 1q44 downstream of NLRP3 (previously known... 
Journal Article