H. Zouali

发表

Gene–environment interaction modulated by allelic heterogeneity in inflammatory diseases

J. Hugot, M. Chamaillard, D. Philpott, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus

M. Stoffel, P. Froguel, H. Zouali, 1992, Nature.

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Mourad Sahbatou, Pierre Laurent-Puig, Jean-Pierre Hugot, 2001, Nature.

Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.

M. Stoffel, P. Froguel, I. Weber, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus.

P. Froguel, H. Zouali, G. Velho, 1993, The New England journal of medicine.

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

J. Beckmann, J. Weissenbach, K. Clément, 1992, Nature.

Genetic analyses of glucose transporter genes in French non-insulin-dependent diabetic families.

P. Froguel, H. Zouali, S. Lesage, 1997, Diabetes & metabolism.

Insulin receptor substrate (IRS-1) gene polymorphisms in French NIDDM families

P. Froguel, H. Zouali, G. Velho, 1993, The Lancet.

Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the young.

M. Vaxillaire, H. Zouali, S. Lesage, 1993, The Journal of clinical investigation.

Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease

J. Belaiche, J. Hugot, M. Chamaillard, 2001, European Journal of Human Genetics.

Indication for genetic linkage of the phosphoenolpyruvate carboxykinase (PCK1) gene region on chromosome 20q to non-insulin-dependent diabetes mellitus.

P. Froguel, H. Zouali, A. Philippi, 1996, Diabetes & metabolism.

Nod2 protects the gut from spreading experimental colitis to small intestine.

J. Hugot, E. Ogier-Denis, H. Zouali, 2019, Journal of Crohn's & colitis.

Nod2 protects remote small intestinal sites in case of colonic inflammation

J. Hugot, E. Ogier-Denis, H. Zouali, 2019, bioRxiv.

NOD 2 / CARD 15 Does Not Influence Response to Infliximab in Crohn ' s Disease *

J. Belaiche, P. Rutgeerts, A. Gossum, 2009 .

NOD2/CARD15 does not influence response to infliximab in Crohn's disease.

J. Belaiche, P. Rutgeerts, J. Hugot, 2002, Gastroenterology.

RNA sequencing of chronic GVHD skin lesions defines shared and unique inflammatory pathways characterizing lichen planus and morphea

H. Zouali, M. Robin, A. Boland, 2022, Blood advances.

1.P.26 Prevalence of common lipoprotein lipase (LPL) gene mutation Ser447Stop is increased while prevalence of Asn291Ser mutation is decreased in centenarians

H. Zouali, G. Béréziat, P. Benlian, 1997 .

[Clinical and molecular consequences of microsatellite instability in human cancers].

H. Zouali, A. Duval, R. Hamelin, 2008, Bulletin du cancer.

Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the young

K. Clément, P. Froguel, H. Zouali, 1992, The Lancet.

Erratum: Human glucokinase gene: Isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin- dependent (type 2) diabetes mellitus (Proc. Natl. Acad. Sci. USA (August 15, 1992) 89 (7698-7702))

M. Stoffel, P. Froguel, I. Weber, 1992 .

RIP2 polymorphisms in inflammatory bowel diseases.

C. O'Morain, J. Hugot, H. Zouali, 2011, Inflammatory Bowel Diseases.

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

J. Beckmann, M. Permutt, M. Stoffel, 1993, The New England journal of medicine.

No evidence for an association between the -871 T/C promoter polymorphism in the B-cell-activating factor gene and primary Sjögren's syndrome

H. Zouali, X. Mariette, J. Gottenberg, 2006, Arthritis research & therapy.

CARD15 mutations in Blau syndrome

G. Thomas, J. Hugot, M. Chamaillard, 2001, Nature Genetics.

CARD4/NOD1 is not involved in inflammatory bowel disease

C. O'Morain, J. Belaiche, J. Hugot, 2003, Gut.

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

J. Beckmann, J. Weissenbach, K. Clément, 1992, Nature.

Operational tolerance after hematopoietic stem cell transplantation is characterized by distinct transcriptional, phenotypic, and metabolic signatures

Y. Saeys, R. Seurinck, H. Zouali, 2022, Science Translational Medicine.

Human Longevity and R506Q Factor V Gene Mutation

H. Zouali, I. Quéré, L. Faure-Delanef, 1997, Thrombosis and Haemostasis.

Association between mutations in the CARD15 (NOD2) gene and Crohn's disease in Israeli Jewish patients

H. Zouali, S. Olschwang, B. Avidan, 2003, American journal of medical genetics. Part A.

Clustering of Crohn's disease within affected sibships

J. Belaiche, J. Hugot, M. Chamaillard, 2003, European Journal of Human Genetics.

DISEASE CARD 4 / NOD 1 is not involved in inflammatory bowel disease

C. O'Morain, H. Zouali, S. Lesage, 2002 .

CARD 4 / NOD 1 is not involved in inflammatory bowel disease

C. O'Morain, H. Zouali, S. Lesage, 2002 .

Etiology of the inflammatory bowel diseases

J. Hugot, H. Zouali, S. Lesage, 1999, International Journal of Colorectal Disease.

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.

C. O'Morain, J. Belaiche, J. Hugot, 2002, American journal of human genetics.

CARD15/NOD2 Is Not a Predisposing Factor for Necrotizing Enterocolitis

J. Hugot, H. Zouali, J. Cézard, 2005, Digestive Diseases and Sciences.

CARD15/NOD2 Is Not a Predisposing Factor for Necrotizing Enterocolitis

J. Hugot, H. Zouali, J. Cézard, 2005, Digestive Diseases and Sciences.

Card15 gene overexpression in mononuclear and epithelial cells of the inflamed Crohn’s disease colon

J. Hugot, H. Zouali, F. Chareyre, 2003, Gut.

Lessons to be learned from the NOD2 gene in Crohn's disease

J. Hugot, H. Zouali, S. Lesage, 2003, European journal of gastroenterology & hepatology.

A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene.

J. Beckmann, P. Froguel, H. Zouali, 1997, Human molecular genetics.

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

T. Bourgeron, E. Génin, M. Gross, 2018, European Journal of Human Genetics.

Significant linkage to spondyloarthropathy on 9q31-34.

M. Dougados, G. Thomas, C. de Toma, 2004, Human molecular genetics.

Expression of a mutant HSP110 sensitizes colorectal cancer cells to chemotherapy and improves disease prognosis

C. Tournigand, H. Zouali, V. Penard-Lacronique, 2011, Nature Medicine.

Linkage Analysis and Molecular Scanning of Glucokinase Gene in NIDDM Families

J. Beckmann, P. Froguel, H. Zouali, 1993, Diabetes.

Genotype/Phenotype Analyses for 53 Crohn’s Disease Associated Genetic Polymorphisms

J. Hugot, H. Zouali, G. Thomas, 2012, PloS one.

CARD15/NOD2 analyses in spondylarthropathy.

J. Hugot, H. Zouali, S. Lesage, 2002, Arthritis and rheumatism.

CA repeat polymorphism in the glucose transporter GLUT 2 gene

P. Froguel, H. Zouali, F. Sun, 1991, Nucleic Acids Res..

Estimating the odds ratios of Crohn disease for the main CARD15/NOD2 mutations using a conditional maximum likelihood method in pedigrees collected via affected family members

J. Hugot, H. Zouali, L. Pascoe, 2007, European Journal of Human Genetics.

Date of birth in familial Crohn's disease suggests environmental factors

J. Belaiche, A. Gossum, J. Hugot, 1998 .

Genetic analyses of chromosome 12 loci in Crohn's disease

J. Belaiche, M. Chamaillard, H. Zouali, 2000, Gut.

No evidence for an association between the -871 T/C promoter polymorphism in the B-cell-activating factor gene and primary Sjögren's syndrome

H. Zouali, X. Mariette, J. Gottenberg, 2006, Arthritis Research & Therapy.

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

T. Bourgeron, E. Génin, M. Gross, 2018, European Journal of Human Genetics.