S. Mascheretti

发表

Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations

M. Vatn, J. Hampe, S. Schreiber, 2006, European Journal of Human Genetics.

Population genetic analyses provide insights on the introduction pathway and spread patterns of the North American forest pathogen Heterobasidion irregulare in Italy

M. Garbelotto, P. Gonthier, S. Mascheretti, 2013, Molecular ecology.

Reconstruction of the Sudden Oak Death epidemic in California through microsatellite analysis of the pathogen Phytophthora ramorum

M. Garbelotto, A. Vettraino, S. Prospero, 2008, Molecular ecology.

Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study

M. Vatn, J. Hampe, S. Schreiber, 2002, The Lancet.

Functional promotor polymorphism in RANTES gene does not influence the clinical course of Helicobacter pylori infection

S. Schreiber, S. Mascheretti, U. Fölsch, 2005, Journal of gastroenterology and hepatology.

The role of pharmacogenomics in the prediction of efficacy of anti-TNF therapy in patients with Crohn's disease.

S. Schreiber, S. Mascheretti, S. Schreiber, 2004, Pharmacogenomics.

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations

K. Huse, J. Hampe, M. Krawczak, 2003, European Journal of Human Genetics.

Response to infliximab treatment in Crohn's disease is not associated with mutations in the CARD15 (NOD2) gene: an analysis in 534 patients from two multicenter, prospective GCP-level trials.

J. Hampe, S. Nikolaus, S. Mascheretti, 2002, Pharmacogenetics.

Pharmacogenetics of inflammatory bowel disease.

S. Mascheretti, P. Croucher, S. Schreiber, 2004, Best practice & research. Clinical gastroenterology.

Transmission disequilibrium test of stromelysin-1 gene variation in relation to Crohn’s disease

S. Fisher, S. Ye, S. Mascheretti, 2004, Journal of Medical Genetics.

Lack of association between the C3435T MDR1 gene polymorphism and inflammatory bowel disease in two independent Northern European populations.

J. Hampe, S. Mascheretti, P. Croucher, 2003, Gastroenterology.

Mutation detection and physical mapping of the CD11 gene cluster in association with inflammatory bowel disease

K. Huse, R. Siebert, J. Hampe, 2002, Immunogenetics.

Association of NOD 2 ( CARD 15 ) genotype with clinical course of Crohn ’ s disease : a cohort study

M. Vatn, J. Hampe, M. Krawczak, 2022 .

Genetic variants in the CCR gene cluster and spontaneous viral elimination in hepatitis C‐infected patients

J. Hampe, P. Buggisch, S. Mascheretti, 2004, Clinical and experimental immunology.

Pharmacogenetic association between the TNF receptor 2 genotype and response to infliximab treatment in Crohn disease

J. Hampe, H. Herfarth, S. Mascheretti, 2001 .

Clinical efficacy of treatment with infliximab in a german multicenter, prospective, open-label trial in refractory crohn's disease

H. Lochs, C. Pohl, S. Mascheretti, 2000 .

Non-telomeric chromosome localization of (TTAGGG)n repeats in the genus Eulemur

Y. Rumpler, S. Garagna, E. Ronchetti, 1997, Chromosome Research.

Combining field observations and genetic data to reconstruct the invasion of Phytophthora ramorum in California

M. Garbelotto, S. Mascheretti, P. Croucher, 2013 .

Pharmacogenetics of inflammatory bowel disease$star;*1

S. Mascheretti, 2004 .

Mediterranean Europe as an area of endemism for small mammals rather than a source for northwards postglacial colonization

J. Searle, D. Bilton, S. Mascheretti, 1998, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Development and loss of the ability of mouse oolemma to fuse with spermatozoa

N. Marziliano, C. Redi, S. Mascheretti, 1994, Zygote.

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

S. Fisher, C. Lewis, C. Mathew, 2001, The Lancet.

Linkage of inflammatory bowel disease to human chromosome 6p.

N J Lynch, A. Forbes, C. Mathew, 1999, American journal of human genetics.

Genetic testing in Crohn disease: utility in individualizing patient management.

S. Mascheretti, S. Schreiber, 2005, American journal of pharmacogenomics : genomics-related research in drug development and clinical practice.

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

K. Huse, C. Mathew, J. Hampe, 2001, Proceedings of the National Academy of Sciences of the United States of America.

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Alastair Forbes, Christopher G Mathew, Jochen Hampe, 2002, Gastroenterology.

A northern glacial refugium for bank voles (Clethrionomys glareolus)

V. Deffontaine, J. Searle, S. Mascheretti, 2006, Proceedings of the National Academy of Sciences.

Combining field epidemiological information and genetic data to comprehensively reconstruct the invasion history and the microevolution of the sudden oak death agent Phytophthora ramorum (Stramenopila: Oomycetes) in California

M. Garbelotto, S. Mascheretti, P. Croucher, 2013, Biological Invasions.

Multiple nuclear pseudogenes of mitochondrial cytochrome b in Ctenomys (Caviomorpha, Rodentia) with either great similarity to or high divergence from the true mitochondrial sequence

J. Searle, S. Mascheretti, P. Mirol, 2000, Heredity.

Haplotype analysis of the CD11 gene cluster in patients with chronic Helicobacter pylori infection and gastric ulcer disease.

J. Hampe, H. Frenzel, S. Mascheretti, 2005, Tissue antigens.

An evaluation of a new series of fluorescent dUTPs for fluorescence in situ hybridization.

J. Wiegant, A. Raap, H. Tanke, 1996, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Pharmacogenetic investigation of the TNF/TNF-receptor system in patients with chronic active Crohn's disease treated with infliximab

J. Hampe, M. Krawczak, H. Herfarth, 2002, The Pharmacogenomics Journal.

Genetic epidemiology of the Sudden Oak Death pathogen Phytophthora ramorum in California

M. Garbelotto, S. Mascheretti, P. Croucher, 2009, Molecular ecology.

Phylogenetics of the speciose and chromosomally variable rodent genus Ctenomys (Ctenomyidae, Octodontoidea), based on mitochondrial cytochrome b sequences

J. Searle, S. Mascheretti, C. Bidau, 2000 .

Genetic Testing in Crohn Disease

S. Mascheretti, S. Schreiber, 2005 .

A First Generation Heterobasidion Hybrid Discovered in Larix lyalli in Montana.

M. Garbelotto, S. Mascheretti, S. Schechter, 2014, Plant disease.

Evaluation of TNF microsatellites and SNPS in a cohort of chronic active, therapy refractory Crohn's disease patients treated with anti TNF-alpha

J. Hampe, S. Mascheretti, W. Kruis, 2000 .

Genome composition in Venezuelan spiny-rats of the genus Proechimys(Rodentia, Echimyidae). I. Genome size, C-heterochromatin and repetitive DNAs in situ hybridization patterns.

N. Marziliano, C. Redi, S. Garagna, 1997, Cytogenetics and cell genetics.

The NOD2 genotype and the clinical course of Crohns disease.

C. Mathew, M. Vatn, J. Hampe, 2002 .