P. Croucher

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.

Identification of probable genotyping errors by consideration of haplotypes

K. Strauch, J. Hampe, S. Schreiber, 2006, European Journal of Human Genetics.

Genetic variation in DLG5 is associated with inflammatory bowel disease

Thomas Lengauer, Mario Albrecht, Philip Rosenstiel, 2004, Nature 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.

PopGen: Population-Based Recruitment of Patients and Controls for the Analysis of Complex Genotype-Phenotype Relationships

Michael Krawczak, Stefan Schreiber, S. Schreiber, 2006, Public Health Genomics.

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.

A Highly Sensitive and Quantitative Test Platform for Detection of NSCLC EGFR Mutations in Urine and Plasma

M. Erlander, H. Wakelee, L. Sequist, 2016, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Refinement of the MHC Risk Map in a Scandinavian Primary Sclerosing Cholangitis Population

T. Karlsen, K. Boberg, A. Bergquist, 2014, PloS one.

Sirtuin 1 (SIRT1) sequence variation is not associated with exceptional human longevity

J. Hampe, S. Schreiber, F. Flachsbart, 2006, Experimental Gerontology.

Polo-like kinase-1 Inhibitors and the Antiandrogen Abiraterone Synergistically Disrupt Mitosis and Kill Cancer Cells of Disparate Origin Independently of Androgen Receptor Signaling

M. Erlander, M. Yaffe, Jun Luo, 2022, bioRxiv.

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.

New sequencing technologies, the development of genomics tools, and their applications in evolutionary arachnology

R. Gillespie, P. Croucher, M. Brewer, 2014 .

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.

Genomic structure, chromosome mapping and expression analysis of the human AVIL gene, and its exclusion as a candidate for locus for inflammatory bowel disease at 12q13-14 (IBD2).

J. Hampe, Z. Tümer, N. Tommerup, 2002, Gene.

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

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

No association between microsomal triglyceride transfer protein (MTP) haplotype and longevity in humans

M. Krawczak, A. Nebel, S. Nikolaus, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Study of C-C chemokine receptor 2 alleles in sarcoidosis, with emphasis on family-based analysis.

J. Hampe, M. Schürmann, E. Schwinger, 2005, American journal of respiratory and critical care medicine.

The Met-196 → Arg Variation of Human Tumor Necrosis Factor Receptor 2 (TNFR2) Affects TNF-α-induced Apoptosis by Impaired NF-κB Signaling and Target Gene Expression*

P. Rosenstiel, P. Scheurich, A. Till, 2005, Journal of Biological Chemistry.

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

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

Species Differentiation on a Dynamic Landscape: Shifts in Metapopulation Genetic Structure Using the Chronology of the Hawaiian Archipelago

G. Roderick, R. Gillespie, A. G. Vandergast, 2012, Evolutionary Biology.

Innate Resistance and Phosphite Treatment Affect Both the Pathogen’s and Host’s Transcriptomes in the Tanoak-Phytophthora ramorum Pathosystem

T. Kasuga, M. Garbelotto, P. Croucher, 2021, Journal of fungi.

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.

Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis

Judy H. Cho, Nadezhda T. Doncheva, O. Andreassen, 2013, Nature Genetics.

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.

Population structure and dispersal in a patchy landscape: nuclear and mitochondrial markers reveal area effects in the spider Theridion californicum (Araneae: Theridiidae)

R. Gillespie, P. Croucher, G. Oxford, 2011 .

Linkage Disequilibrium

P. Croucher, 2008 .

A common haplotype of the annexin A5 (ANXA5) gene promoter is associated with recurrent pregnancy loss.

M. Krawczak, A. Nebel, V. Gerke, 2007, Human molecular genetics.

Many a slip: dissecting the causes of reproductive isolation in two species of Tegenaria spiders (Agelenidae)

P. Croucher, G. Oxford, 2014 .

Can Zipf's law be adapted to normalize microarrays?

Günther Deuschl, Stefan Schreiber, Timothy Lu, 2005, BMC Bioinformatics.

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.

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.

The islands' story: Genomics and adaptive radiation on remote islands

R. Gillespie, P. Croucher, 2009 .

Convergent evolution in the colour polymorphism of Selkirkiella spiders (Theridiidae) from the South American temperate rainforest

D. Lindberg, R. Gillespie, P. Croucher, 2016 .

The Met-196 -> Arg variation of human tumor necrosis factor receptor 2 (TNFR2) affects TNF-alpha-induced apoptosis by impaired NF-kappaB signaling and target gene expression.

P. Rosenstiel, P. Scheurich, A. Till, 2005, The Journal of biological chemistry.

A microsatellite analysis identifies global pathways of movement of Phytophthora cinnamomi and the likely sources of wildland infestations in California and Mexico.

M. Garbelotto, T. Osmundson, P. Croucher, 2019, Phytopathology.

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

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

Common coding polymorphisms in the ABCA1 gene and risk of early-onset coronary heart disease in northern Germany.

F. Flachsbart, A. Nebel, N. E. El Mokhtari, 2007, Atherosclerosis.

De novo characterization of the gene-rich transcriptomes of two color-polymorphic spiders, Theridion grallator and T. californicum (Araneae: Theridiidae), with special reference to pigment genes

R. Gillespie, C. Winchell, P. Croucher, 2013, BMC Genomics.

The NOD2 genotype and the clinical course of Crohns disease.

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

A Highly Sensitive and Quantitative Test Platform for Detection of NSCLC EGFR Mutations in Urine and Plasma

M. Erlander, H. Wakelee, L. Sequist, 2016, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Linkage Disequilibrium

P. Croucher, 2008 .