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Results 1 to 25 of 43

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Genetic determinants of alcoholic liver diseaseSTICKEL, Felix; HAMPE, Jochen.Gut. 2012, Vol 61, Num 1, pp 150-159, issn 0017-5749, 10 p.Article

Entropy-based SNP selection for genetic association studiesHAMPE, Jochen; SCHREIBER, Stefan; KRAWCZAK, Michael et al.Human genetics. 2003, Vol 114, Num 1, pp 36-43, issn 0340-6717, 8 p.Article

Genetics of Crohn disease, an archetypal inflammatory barrier diseaseSCHREIBER, Stefan; ROSENSTIEL, Philip; ALBRECHT, Mario et al.Nature reviews. Genetics (Print). 2005, Vol 6, Num 5, pp 376-388, issn 1471-0056, 13 p.Article

Quantification of intestinal bacterial populations by real-time PCR with a universal primer set and minor groove binder probes: a global approach to the enteric floraOTT, Stephan J; MUSFELDT, Meike; ULLMANN, Uwe et al.Journal of clinical microbiology (Print). 2004, Vol 42, Num 6, pp 2566-2572, issn 0095-1137, 7 p.Article

Salivary Gland Swelling in Wegener's Granulomatosis: A Rare Cause of a Frequent SymptomGAS SLING, Volker; WILTFANG, Jörg; HAMPE, Jochen et al.Journal of rheumatology. 2010, Vol 37, Num 12, pp 2633-2636, issn 0315-162X, 4 p.Article

Genetic variants in matrix metalloproteinase genes are associated with development of gastric ulcer in H. Pylori infectionHELLMIG, Stephan; OTT, Stefan; ROSENSTIEL, Phillip et al.The American journal of gastroenterology. 2006, Vol 101, Num 1, pp 29-35, issn 0002-9270, 7 p.Article

SGCaller : a program to call and review genotypes measured by sequencingMANASTER, Carl; VALENTONYTE, Ruta; TEUBER, Markus et al.BioTechniques. 2005, Vol 38, Num 4, pp 544-546, issn 0736-6205, 2 p.Article

Known Risk Factors Do Not Explain Disparities in Gallstone Prevalence Between Denmark and Northeast GermanyFRIEDRICH, Nele; VÖLZKE, Henry; HAMPE, Jochen et al.The American journal of gastroenterology. 2009, Vol 104, Num 1, pp 89-95, issn 0002-9270, 7 p.Article

Distinct DNA methylation patterns in cirrhotic liver and hepatocellular carcinomaAMMERPOHL, Ole; PRATSCHKE, Johann; RÖCKEN, Christoph et al.International journal of cancer (Print). 2012, Vol 130, Num 6, pp 1319-1328, issn 0020-7136, 10 p.Article

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1HAMPE, Jochen; FRANKE, Andre; GÜNTHER, Simone et al.Nature genetics. 2007, Vol 39, Num 2, pp 207-211, issn 1061-4036, 5 p.Article

Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitisKARLSEN, Tom H; HAMPE, Jochen; WIENCKE, Kristine et al.The American journal of gastroenterology. 2007, Vol 102, Num 1, pp 115-121, issn 0002-9270, 7 p.Article

Study of C-C chemokine receptor 2 alleles in sarcoidosis, with emphasis on family-based analysisVALENTONYTE, Ruta; HAMPE, Jochen; CROUCHER, Peter J. P et al.American journal of respiratory and critical care medicine. 2005, Vol 171, Num 10, pp 1136-1141, issn 1073-449X, 6 p.Article

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populationsCROUCHER, Peter J. P; MASCHERETTI, Silvia; WON HO KIM et al.European journal of human genetics. 2003, Vol 11, Num 1, pp 6-16, issn 1018-4813, 11 p.Article

Chronic Portal Vein Thrombosis: Transcapsular Hepatic Collateral Vessels and Communicating Ectopic VaricesSEEGER, Marcus; GÜNTHER, Rainer; BRAUN, Felix et al.Radiology. 2010, Vol 257, Num 2, pp 568-578, issn 0033-8419, 11 p.Article

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibilityLASCORZ, Jesús; FÖRSTI, Asta; SCHULMANN, Karsten et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 9, pp 1612-1619, issn 0143-3334, 8 p.Article

Genome-wide association scan identifies a colorectal cancer susceptibility locus on llq23 and replicates risk loci at 8q24 and 18q21TENESA, Albert; FARRINGTON, Susan M; SEMPLE, Colin et al.Nature genetics. 2008, Vol 40, Num 5, pp 631-637, issn 1061-4036, 7 p.Article

Extreme heterogeneity in CARD15 and DLG5 crohn disease-associated polymorphisms between German and Norwegian populationsMEDICI, Valentina; MASCHERETTI, Silvia; SCHREIBER, Stefan et al.European journal of human genetics. 2006, Vol 14, Num 4, pp 459-468, issn 1018-4813, 10 p.Article

The L513S polymorphism in medium-chain acyl-CoA synthetase 2 (MACS2) is associated with risk factors of the metabolic syndrome in a Caucasian study populationLINDNER, Inka; RUBIN, Diana; HELWIG, Ulf et al.Molecular nutrition & food research (Print). 2006, Vol 50, Num 3, pp 270-274, issn 1613-4125, 5 p.Article

Probiotic bacteria reduced duration and severity but not the incidence of common cold episodes in a double blind, randomized, controlled trialDE VRESE, Michael; WINKLER, Petra; SCHREZENMEIR, Jürgen et al.Vaccine. 2006, Vol 24, Num 44-46, pp 6670-6674, issn 0264-410X, 5 p.Article

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaHILLMER, Axel M; HANNEKEN, Sandra; HEYN, Uwe et al.American journal of human genetics. 2005, Vol 77, Num 1, pp 140-148, issn 0002-9297, 9 p.Article

An integrated system for high throughput TaqMan based SNP genotypingHAMPE, Jochen; WOLLSTEIN, Andreas; LU, Timothy et al.Bioinformatics (Oxford. Print). 2001, Vol 17, Num 7, pp 654-655, issn 1367-4803Article

The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's diseaseDÄBRITZ, Jan; FRIEDRICHS, Frauke; FOELL, Dirk et al.American journal of physiology. Gastrointestinal and liver physiology. 2011, Vol 63, Num 5, issn 0193-1857, G823-G832Article

Genetic Variation in the PNPLA3 Gene Is Associated with Alcoholic Liver Injury in CaucasiansSTICKEL, Felix; BUCH, Stephan; GÜNTHER, Rainer et al.Hepatology (Baltimore, Md.). 2011, Vol 53, Num 1, pp 86-95, issn 0270-9139, 10 p.Article

Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case-control sampleSCHAFMAYER, Clemens; BUCH, Stephan; SIPOS, Bence et al.International journal of cancer (Print). 2009, Vol 124, Num 1, pp 75-80, issn 0020-7136, 6 p.Article

Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancerSCHAFMAYER, Clemens; BUCH, Stephan; KREMER, Bernd et al.International journal of cancer. 2007, Vol 121, Num 3, pp 555-558, issn 0020-7136, 4 p.Article

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