Jochen Hampe
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Jochen Hampe's Degrees
- Bachelors Computer Science University of Hamburg
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(Suggest an Edit or Addition)Jochen Hampe's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 (2007) (1868)
- Reduction in diversity of the colonic mucosa associated bacterial microflora in patients with active inflammatory bowel disease (2004) (1141)
- Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations (2001) (1126)
- The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. (2002) (704)
- Activation of nuclear factor κB in inflammatory bowel disease (1998) (684)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
- Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 (2008) (629)
- Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 (2008) (629)
- Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer (2008) (599)
- Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer (2008) (599)
- A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 (2008) (578)
- A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 (2008) (578)
- Obesity accelerates epigenetic aging of human liver (2014) (557)
- Genetic variation in DLG5 is associated with inflammatory bowel disease (2004) (499)
- Sarcoidosis is associated with a truncating splice site mutation in BTNL2 (2005) (441)
- Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study (2002) (405)
- A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. (1999) (388)
- DNA methylation analysis in nonalcoholic fatty liver disease suggests distinct disease-specific and remodeling signatures after bariatric surgery. (2013) (384)
- A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis (2015) (376)
- A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis (2015) (376)
- Single base‐pair substitutions in exon–intron junctions of human genes: nature, distribution, and consequences for mRNA splicing (2007) (354)
- Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study. (2015) (347)
- Genetics of Crohn disease, an archetypal inflammatory barrier disease (2005) (343)
- Detection of Diverse Bacterial Signatures in Atherosclerotic Lesions of Patients With Coronary Heart Disease (2006) (336)
- Genome-wide association analysis in primary sclerosing cholangitis. (2010) (323)
- A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease (2007) (317)
- A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease (2007) (317)
- A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5. (2007) (306)
- Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in caucasians (2010) (291)
- Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in caucasians (2010) (291)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (279)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (279)
- Effect of Lactobacillus gasseri PA 16/8, Bifidobacterium longum SP 07/3, B. bifidum MF 20/5 on common cold episodes: a double blind, randomized, controlled trial. (2005) (256)
- Tumour necrosis factor α and interleukin 1β in relapse of Crohn's disease (1999) (249)
- Linkage of inflammatory bowel disease to human chromosome 6p. (1999) (245)
- Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations (2003) (239)
- Dissection of the Inflammatory Bowel Disease Transcriptome Using Genome-Wide cDNA Microarrays (2005) (236)
- Increased proteasome subunit protein expression and proteasome activity in colon cancer relate to an enhanced activation of nuclear factor E2-related factor 2 (Nrf2) (2009) (214)
- Probiotic bacteria reduced duration and severity but not the incidence of common cold episodes in a double blind, randomized, controlled trial. (2006) (214)
- Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. (2005) (211)
- Hepatitis B virus–induced lipid alterations contribute to natural killer T cell–dependent protective immunity (2012) (205)
- The ascending pathophysiology of cholestatic liver disease (2017) (205)
- Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting (2012) (201)
- Activation of signal transducer and activator of transcription (STAT) 1 in human chronic inflammatory bowel disease (2002) (198)
- A novel lumen-apposing metal stent for endoscopic ultrasound-guided drainage of pancreatic fluid collections: a prospective cohort study (2014) (197)
- Widespread occurrence of alternative splicing at NAGNAG acceptors contributes to proteome plasticity (2004) (191)
- Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16. (1998) (180)
- IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis. (2003) (173)
- Pathophysiology and Management of Alcoholic Liver Disease: Update 2016 (2017) (164)
- Comparison of Gene Expression Patterns Between Mouse Models of Nonalcoholic Fatty Liver Disease and Liver Tissues From Patients. (2016) (161)
- Endoscopic endoluminal vacuum therapy is superior to other regimens in managing anastomotic leakage after esophagectomy: a comparative retrospective study (2013) (159)
- 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. (2002) (151)
- Pharmacogenetic investigation of the TNF/TNF-receptor system in patients with chronic active Crohn's disease treated with infliximab (2002) (150)
- 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 Flora (2004) (141)
- Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene (2007) (139)
- Vedolizumab provides clinical benefit over 1 year in patients with active inflammatory bowel disease – a prospective multicenter observational study (2016) (137)
- SNP-Based Analysis of Genetic Substructure in the German Population (2006) (137)
- Non-invasive stratification of hepatocellular carcinoma risk in non-alcoholic fatty liver using polygenic risk scores (2020) (133)
- Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals (2012) (133)
- Drainage of esophageal leakage using endoscopic vacuum therapy: a prospective pilot study. (2010) (132)
- Genetic determinants of alcoholic liver disease (2011) (131)
- Evaluation of AGR2 and AGR3 as candidate genes for inflammatory bowel disease (2006) (131)
- In vitro alterations of intestinal bacterial microbiota in fecal samples during storage. (2004) (125)
- The genetics of alcohol dependence and alcohol-related liver disease. (2017) (122)
- A short isoform of NOD2/CARD15, NOD2-S, is an endogenous inhibitor of NOD2/receptor-interacting protein kinase 2-induced signaling pathways. (2006) (120)
- Influence of polymorphisms in the NOD1/CARD4 and NOD2/CARD15 genes on the clinical outcome of Helicobacter pylori infection (2006) (119)
- Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease. (2003) (114)
- An integrated system for high throughput TaqManTM based SNP genotyping (2001) (109)
- Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p (2001) (108)
- Patterns of linkage disequilibrium in the MHC region on human chromosome 6p (2004) (107)
- IL-6 blockade by monoclonal antibodies inhibits apolipoprotein (a) expression and lipoprotein (a) synthesis in humans[S] (2015) (103)
- Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition. (2010) (102)
- Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition. (2010) (102)
- Novel Common Genetic Susceptibility Loci for Colorectal Cancer (2018) (102)
- Postdiagnosis body mass index and risk of mortality in colorectal cancer survivors: a prospective study and meta-analysis (2014) (99)
- Predictors of gallstone composition in 1025 symptomatic gallstones from Northern Germany (2006) (97)
- Predictors of gallstone composition in 1025 symptomatic gallstones from Northern Germany (2006) (97)
- Heterozygous carriage of the alpha1-antitrypsin Pi*Z variant increases the risk to develop liver cirrhosis (2018) (93)
- CARD15 gene mutations in sarcoidosis (2003) (93)
- Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. (2008) (93)
- Heterozygous carriage of the alpha1-antitrypsin Pi*Z variant increases the risk to develop liver cirrhosis (2018) (93)
- Tumour necrosis factor alpha and interleukin 1beta in relapse of Crohn's disease. (1999) (92)
- [S2k Guideline non-alcoholic fatty liver disease]. (2015) (92)
- Polymorphism in IgG Fc receptor gene FCGR3A and response to infliximab in Crohn's disease: a subanalysis of the ACCENT I study (2006) (90)
- Distinct DNA methylation patterns in cirrhotic liver and hepatocellular carcinoma (2012) (86)
- Epithelial calcineurin controls microbiota-dependent intestinal tumor development (2016) (85)
- Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease (2000) (84)
- Lack of association between the C3435T MDR1 gene polymorphism and inflammatory bowel disease in two independent Northern European populations. (2003) (83)
- Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus (2013) (82)
- Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus (2013) (82)
- Entropy-based SNP selection for genetic association studies (2003) (81)
- Sirtuin 1 (SIRT1) sequence variation is not associated with exceptional human longevity (2006) (81)
- Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11 q 23 and replicates risk loci at 8 q 24 and 18 q 21 (2009) (80)
- Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11 q 23 and replicates risk loci at 8 q 24 and 18 q 21 (2009) (80)
- Genetic variants in PNPLA3 and TM6SF2 predispose to the development of hepatocellular carcinoma in individuals with alcohol‐related cirrhosis (2018) (79)
- Genetic variants in PNPLA3 and TM6SF2 predispose to the development of hepatocellular carcinoma in individuals with alcohol‐related cirrhosis (2018) (79)
- Cumulative Burden of Colorectal Cancer-Associated Genetic Variants is More Strongly Associated With Early-onset vs Late-onset Cancer. (2019) (78)
- Cumulative Burden of Colorectal Cancer-Associated Genetic Variants is More Strongly Associated With Early-onset vs Late-onset Cancer. (2019) (78)
- Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis (2020) (76)
- Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk. (2020) (74)
- Endoscopic endoluminal vacuum therapy in esophageal perforation. (2014) (72)
- Association of inflammatory bowel disease with indicators for childhood antigen and infection exposure (2003) (72)
- Different HLA class II associations in ulcerative colitis patients with and without primary sclerosing cholangitis (2007) (67)
- Association study of a functional Toll-like receptor 4 polymorphism with susceptibility to gastric mucosa-associated lymphoid tissue lymphoma (2005) (67)
- Shared heritability and functional enrichment across six solid cancers (2018) (67)
- Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses (2019) (66)
- Genetic Variation in HSD17B13 Reduces the Risk of Developing Cirrhosis and Hepatocellular Carcinoma in Alcohol Misusers (2020) (65)
- Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies. (2016) (65)
- Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies. (2016) (65)
- Genetic Variation in HSD17B13 Reduces the Risk of Developing Cirrhosis and Hepatocellular Carcinoma in Alcohol Misusers (2020) (65)
- Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms (2019) (64)
- Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms (2019) (64)
- TLR-3 polymorphism is an independent prognostic marker for stage II colorectal cancer. (2011) (64)
- TLR-3 polymorphism is an independent prognostic marker for stage II colorectal cancer. (2011) (64)
- Lean Patients with Non-Alcoholic Fatty Liver Disease Have a Severe Histological Phenotype Similar to Obese Patients (2018) (64)
- Lean Patients with Non-Alcoholic Fatty Liver Disease Have a Severe Histological Phenotype Similar to Obese Patients (2018) (64)
- Lack of association of SPINK5 polymorphisms with nonsyndromic atopic dermatitis in the population of Northern Germany (2005) (63)
- Genetic variants in the NOD2/CARD15 gene are associated with early mortality in sepsis patients (2007) (63)
- Lifestyle factors and health-related quality of life in colorectal cancer survivors (2013) (61)
- Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing. (2006) (60)
- Increased intestinal permeability and tight junction disruption by altered expression and localization of occludin in a murine graft versus host disease model (2011) (60)
- Genetic Polymorphisms Associated With Inflammatory Bowel Disease Do Not Confer Risk for Primary Sclerosing Cholangitis (2007) (60)
- Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. (2010) (59)
- Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. (2010) (59)
- Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease (2006) (58)
- Epigenomic map of human liver reveals principles of zonated morphogenic and metabolic control (2018) (58)
- Association of genetic polymorphisms in ESR2, HSD17B1, ABCB1, and SHBG genes with colorectal cancer risk. (2011) (57)
- Transmembrane 6 superfamily member 2 gene E167K variant impacts on steatosis and liver damage in chronic hepatitis C patients (2015) (57)
- Association of genetic polymorphisms in ESR2, HSD17B1, ABCB1, and SHBG genes with colorectal cancer risk. (2011) (57)
- Glucagon cell hyperplasia and neoplasia with and without glucagon receptor mutations. (2015) (55)
- Health-related quality of life in long-term survivors of colorectal cancer and its association with all-cause mortality: a German cohort study (2018) (55)
- Terminal part of thoracic duct: high-resolution US imaging. (2009) (55)
- Anti-TNF-α antibodies improve intestinal barrier function in Crohn's disease. (2012) (55)
- Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6 (2002) (55)
- Adipocyte-Specific Hypoxia-Inducible Factor 2α Deficiency Exacerbates Obesity-Induced Brown Adipose Tissue Dysfunction and Metabolic Dysregulation (2015) (55)
- Glucagon cell hyperplasia and neoplasia with and without glucagon receptor mutations. (2015) (55)
- Loss of hepatic Mboat7 leads to liver fibrosis (2020) (54)
- Loss of hepatic Mboat7 leads to liver fibrosis (2020) (54)
- InSNP: A tool for automated detection and visualization of SNPs and InDels (2005) (53)
- A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer (2012) (52)
- A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer (2012) (52)
- Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations (2006) (51)
- Functional TLR5 genetic variants affect human colorectal cancer survival. (2013) (50)
- rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis (2020) (50)
- Genetic investigation of DNA‐repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer (2007) (50)
- COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (50)
- Genetic investigation of DNA‐repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer (2007) (50)
- rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis (2020) (50)
- Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case‐control sample (2009) (50)
- COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (50)
- Study of C-C chemokine receptor 2 alleles in sarcoidosis, with emphasis on family-based analysis. (2005) (50)
- Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case‐control sample (2009) (50)
- Adiposity, metabolites, and colorectal cancer risk: Mendelian randomization study (2020) (49)
- Association of NOD 2 ( CARD 15 ) genotype with clinical course of Crohn ’ s disease : a cohort study (49)
- Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis. (2014) (48)
- Increased Hepatic PDGF-AA Signaling Mediates Liver Insulin Resistance in Obesity-Associated Type 2 Diabetes (2017) (48)
- Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis. (2014) (48)
- The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's disease. (2011) (47)
- Disease-Associated miRNA-mRNA Networks in Oral Lichen Planus (2013) (46)
- Distinct, alcohol-modulated effects of PNPLA3 genotype on progression of chronic hepatitis C. (2011) (46)
- Distinct, alcohol-modulated effects of PNPLA3 genotype on progression of chronic hepatitis C. (2011) (46)
- SNPSplicer: systematic analysis of SNP‐dependent splicing in genotyped cDNAs (2006) (45)
- Study of Toll‐like receptor gene loci in sarcoidosis (2008) (44)
- A Mechanistic, Model-Based Approach to Safety Assessment in Clinical Development (2012) (43)
- Technology-specific error signatures in the 1000 Genomes Project data (2011) (42)
- Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer (2009) (42)
- Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer (2009) (42)
- Open Surgical versus Minimal Invasive Necrosectomy of the Pancreas—A Retrospective Multicenter Analysis of the German Pancreatitis Study Group (2016) (41)
- Genetic Variants in Matrix Metalloproteinase Genes Are Associated With Development of Gastric Ulcer in H. Pylori Infection (2006) (41)
- Postdiagnostic Mediterranean and Healthy Nordic Dietary Patterns Are Inversely Associated with All-Cause Mortality in Long-Term Colorectal Cancer Survivors. (2017) (40)
- Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease (2000) (40)
- Genome-wide investigation of gene–environment interactions in colorectal cancer (2013) (39)
- Shotgun lipidomics-based characterization of the landscape of lipid metabolism in colorectal cancer. (2019) (38)
- Anticipation in inflammatory bowel disease: a phenomenon caused by an accumulation of confounders. (1998) (38)
- Histologic improvement of NAFLD in patients with obesity after bariatric surgery based on standardized NAS (NAFLD activity score). (2018) (37)
- Immune mechanisms linking metabolic injury to inflammation and fibrosis in fatty liver disease - novel insights into cellular communication circuits. (2022) (37)
- 3D spatially-resolved geometrical and functional models of human liver tissue reveal new aspects of NAFLD progression (2019) (37)
- Activation of signal‐transducer and activator of transcription 1 (STAT1) in pouchitis (2001) (36)
- Clip closure versus endoscopic suturing versus thoracoscopic repair of an iatrogenic esophageal perforation: a randomized, comparative, long-term survival study in a porcine model (with videos). (2010) (35)
- Efficacy of Endoscopic Dilation of Gastroduodenal Crohn’s Disease Strictures: A Systematic Review and Meta-Analysis of Individual Patient Data (2018) (34)
- The interferon-Á gene as a positional and functional candidate gene for inflammatory bowel disease (1998) (34)
- Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. (2020) (33)
- Genetic variants in the CCR gene cluster and spontaneous viral elimination in hepatitis C‐infected patients (2004) (33)
- Endoscopic ultrasound-guided biliary drainage using a lumen-apposing self-expanding metal stent: a case series (2015) (33)
- High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases. (2003) (33)
- Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. (2020) (33)
- Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression (2007) (32)
- The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene. (1997) (32)
- Definition of polymorphisms and haplotypes in the interleukin-12B gene: association with IL-12 production but not with Crohn's disease (2004) (32)
- Elevated Levels of Endocannabinoids in Chronic Hepatitis C May Modulate Cellular Immune Response and Hepatic Stellate Cell Activation (2015) (32)
- GENOMIZER: an integrated analysis system for genome‐wide association data (2006) (29)
- Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry (2019) (28)
- Dynamics of epigenetic age following hematopoietic stem cell transplantation (2017) (28)
- Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (28)
- EUS-guided drainage in the management of postoperative pancreatic leaks and fistulas (with video). (2019) (28)
- Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. (2014) (28)
- Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer (2015) (28)
- Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry (2019) (28)
- Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. (2014) (28)
- Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer (2015) (28)
- Systematic evaluation of the effect of common SNPs on pre‐mRNA splicing (2009) (27)
- Candidate gene association study of type 2 diabetes in a nested case-control study of the EPIC-Potsdam cohort - role of fat assimilation. (2007) (27)
- Genetic Variants of the Copy Number Polymorphic β-Defensin Locus Are Associated with Sporadic Prostate Cancer (2008) (27)
- Prognostic relevance of gastric cancer staging by endoscopic ultrasound (2013) (27)
- Association between functional FABP2 promoter haplotype and type 2 diabetes. (2006) (27)
- Postdiagnostic physical activity, sleep duration, and TV watching and all-cause mortality among long-term colorectal cancer survivors: a prospective cohort study (2017) (26)
- Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses (2020) (26)
- A functional promotor polymorphism of TNF-alpha is associated with primary gastric B-Cell lymphoma. (2005) (26)
- SETDB1 is required for intestinal epithelial differentiation and the prevention of intestinal inflammation (2020) (26)
- Association Study of TRPC4 as a Candidate Gene for Generalized Epilepsy with Photosensitivity (2010) (26)
- No association between the TUCAN (CARD8) Cys10Stop mutation and inflammatory bowel disease in a large retrospective German and a clinically well-characterized Norwegian sample. (2007) (25)
- A case-only study of gene-environment interaction between genetic susceptibility variants in NOD2 and cigarette smoking in Crohn's disease aetiology (2012) (25)
- Aberrant DNA methylation of ADAMTS16 in colorectal and other epithelial cancers (2018) (25)
- Aberrant DNA methylation of ADAMTS16 in colorectal and other epithelial cancers (2018) (25)
- Refinement of the MHC Risk Map in a Scandinavian Primary Sclerosing Cholangitis Population (2014) (24)
- Identifying novel susceptibility genes for colorectal cancer risk from a transcriptome-wide association study of 125,478 subjects. (2020) (24)
- Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility (2013) (24)
- CARD15 mutations in patients with plaque-type psoriasis and psoriatic arthritis: lack of association (2006) (24)
- Oral glutamine supplementation improves intestinal permeability dysfunction in a murine acute graft-vs.-host disease model. (2011) (24)
- Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility (2013) (24)
- Nonalcoholic fatty liver disease stratification by liver lipidomics (2021) (24)
- Identifying novel susceptibility genes for colorectal cancer risk from a transcriptome-wide association study of 125,478 subjects. (2020) (24)
- Nonalcoholic fatty liver disease stratification by liver lipidomics (2021) (24)
- Metabolomic tissue signature in human non‐alcoholic fatty liver disease identifies protective candidate metabolites (2015) (23)
- The L513S polymorphism in medium-chain acyl-CoA synthetase 2 (MACS2) is associated with risk factors of the metabolic syndrome in a Caucasian study population. (2006) (23)
- Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas (2017) (22)
- POPSIM: a general population simulation program (1998) (22)
- A Functional Promotor Polymorphism of TNF-α Is Associated with Primary Gastric B-Cell Lymphoma (2005) (22)
- Endoscopic ultrasound-guided drainage of pancreatic walled-off necrosis using 20-mm versus 15-mm lumen-apposing metal stents: an international, multicenter, case-matched study (2020) (22)
- Genetic architectures of proximal and distal colorectal cancer are partly distinct (2020) (21)
- Genetic architectures of proximal and distal colorectal cancer are partly distinct (2020) (21)
- A targeted analysis reveals relevant shifts in the methylation and transcription of genes responsible for bile acid homeostasis and drug metabolism in non-alcoholic fatty liver disease (2016) (21)
- The interferon-gamma gene as a positional and functional candidate gene for inflammatory bowel disease. (1998) (21)
- Statistical inference of allelic imbalance from transcriptome data (2011) (21)
- IL-1β and ADAM17 are central regulators of β-defensin expression in Candida esophagitis. (2011) (20)
- Haplotyping and copy number estimation of the highly polymorphic human beta-defensin locus on 8p23 by 454 amplicon sequencing (2010) (20)
- Known Risk Factors Do Not Explain Disparities in Gallstone Prevalence Between Denmark and Northeast Germany (2009) (20)
- Recurrence of gallstones after cholecystectomy is associated with ABCG5/8 genotype (2013) (20)
- Recurrence of gallstones after cholecystectomy is associated with ABCG5/8 genotype (2013) (20)
- Genetics of biliary lithiasis from an ethnic perspective. (2013) (20)
- TassDB2 - A comprehensive database of subtle alternative splicing events (2010) (20)
- New strategies for efficient typing of HLA class-II loci DQB1 and DRB1 by using Pyrosequencing. (2005) (20)
- Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer (2012) (19)
- Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer (2012) (19)
- Chronic portal vein thrombosis: transcapsular hepatic collateral vessels and communicating ectopic varices. (2010) (19)
- Mapping Genes for Polygenic Disorders: Considerations for Study Design in the Complex Trait of Inflammatory Bowel Disease (1999) (19)
- Polymorphisms in the 3′-untranslated region of the CDH1 gene are a risk factor for primary gastric diffuse large B-cell lymphoma (2011) (19)
- Mendelian Randomization of Circulating Polyunsaturated Fatty Acids and Colorectal Cancer Risk (2020) (18)
- ALCOHOL LIVER DISEASE (2013) (18)
- ALCOHOL LIVER DISEASE (2013) (18)
- Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis (2010) (18)
- PNPLA3 genetic variation in alcoholic steatosis and liver disease progression. (2015) (18)
- Use of a NOTES closure device for full-thickness suturing of a postoperative anastomotic esophageal leakage. (2010) (18)
- NAFLD is associated with methylation shifts with relevance for the expression of genes involved in lipoprotein particle composition. (2017) (17)
- Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease (2006) (17)
- Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease. (2006) (17)
- Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease (2006) (17)
- 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). (2002) (17)
- Solutions for biomedical grid computing - Case studies from the D-Grid project Services@MediGRID (2012) (17)
- Efficacy assessment of SNP sets for genome-wide disease association studies (2007) (17)
- Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease. (2006) (17)
- Long-term quality of life after endovac-therapy in anastomotic leakages after esophagectomy. (2018) (17)
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- Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer (2013) (16)
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- Association between the dietary inflammatory index and all‐cause mortality in colorectal cancer long‐term survivors (2018) (16)
- Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer (2013) (16)
- Antibiosis of Necrotizing Pancreatitis (2014) (16)
- Specific neurophysiological mechanisms underlie cognitive inflexibility in inflammatory bowel disease (2017) (15)
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- Helicobacter pylori infection in Africa and Europe: enigma of host genetics (2003) (15)
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- Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans (2019) (13)
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- Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans (2019) (13)
- Physiological state co-regulates thousands of mammalian mRNA splicing events at tandem splice sites and alternative exons (2014) (12)
- A TWO-STAGE GENOME-WIDE ASSOCIATION STUDY CONFIRMS PNPLA 3 AND IDENTIFIES TM 6 SF 2 AND MBOAT 7 AS RISK LOCI FOR ALCOHOL-RELATED CIRRHOSIS (2017) (12)
- Role of IL-10 promoter haplotypes in Helicobacter pylori associated gastric inflammation. (2005) (12)
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- Locking of 3' ends of single-stranded DNA templates for improved Pyrosequencing performance. (2004) (12)
- A TWO-STAGE GENOME-WIDE ASSOCIATION STUDY CONFIRMS PNPLA 3 AND IDENTIFIES TM 6 SF 2 AND MBOAT 7 AS RISK LOCI FOR ALCOHOL-RELATED CIRRHOSIS (2017) (12)
- Oligonucleotide fingerprinting as a means to identify and survey long-term cultured B cell hybridomas and T cell lines. (1992) (12)
- Pipeline for Large-Scale Microdroplet Bisulfite PCR-Based Sequencing Allows the Tracking of Hepitype Evolution in Tumors (2011) (12)
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- Mutation detection and physical mapping of the CD11 gene cluster in association with inflammatory bowel disease (2002) (11)
- The rs738409 G Allele in PNPLA3 Is Associated With a Reduced Risk of COVID-19 Mortality and Hospitalization (2021) (11)
- Mutual Zonated Interactions of Wnt and Hh Signaling Are Orchestrating the Metabolism of the Adult Liver in Mice and Human. (2019) (11)
- Endoscopic ultrasound criteria to predict the need for intervention in pancreatic necrosis (2012) (11)
- Constant Splice-Isoform Ratios in Human Lymphoblastoid Cells Support the Concept of a Splico-Stat (2011) (11)
- Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease (2021) (11)
- Translational learning from clinical studies predicts drug pharmacokinetics across patient populations (2017) (11)
- Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease. (2003) (11)
- Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation (2021) (11)
- The rs738409 G Allele in PNPLA3 Is Associated With a Reduced Risk of COVID-19 Mortality and Hospitalization (2021) (11)
- Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease (2021) (11)
- Does neoadjuvant treatment before oncologic esophagectomy affect the postoperative quality of life? A prospective, longitudinal outcome study. (2015) (11)
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- Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians (2019) (10)
- Zebrafish In-Vivo Screening for Compounds Amplifying Hematopoietic Stem and Progenitor Cells: - Preclinical Validation in Human CD34+ Stem and Progenitor Cells (2017) (10)
- SFRS10--a splicing factor gene reduced in human obesity? (2012) (10)
- Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis (2021) (10)
- Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis (2017) (10)
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- Salivary Gland Swelling in Wegener’s Granulomatosis: A Rare Cause of a Frequent Symptom (2010) (10)
- The MLH1 c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer: Genetic Association Study in 18,723 Individuals (2014) (9)
- Analysis of relative gene dosage and expression differences of the paralogs RABL2A and RABL2B by Pyrosequencing. (2010) (9)
- Combined effects of PNPLA3, TM6SF2 and HSD17B13 variants on severity of biopsy-proven non-alcoholic fatty liver disease (2021) (9)
- Performance of routine risk scores for predicting cirrhosis-related morbidity in the community. (2022) (9)
- Functional genomics in gastroenterology (2000) (9)
- Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis. (2014) (9)
- The MLH1 c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer: Genetic Association Study in 18,723 Individuals (2014) (9)
- Prevalence of a First-Degree Relative with Colorectal Cancer and Uptake of Screening Among Persons 40 to 54 Years Old. (2019) (9)
- Diagnosing Fatty Liver Disease: A Comparative Evaluation of Metabolic Markers, Phenotypes, Genotypes and Established Biomarkers (2013) (9)
- Genomics and inflammatory bowel disease (2000) (9)
- PSD3 downregulation confers protection against fatty liver disease (2022) (9)
- Flexible percutaneous endoscopic retroperitoneal necrosectomy as rescue therapy for pancreatic necroses beyond the reach of endoscopic ultrasonography: A case series (2017) (9)
- PSD3 downregulation confers protection against fatty liver disease (2022) (9)
- Microbiota-dependent activation of the myeloid calcineurin-NFAT pathway inhibits B7H3- and B7H4-dependent anti-tumor immunity in colorectal cancer. (2022) (9)
- Combined effects of PNPLA3, TM6SF2 and HSD17B13 variants on severity of biopsy-proven non-alcoholic fatty liver disease (2021) (9)
- Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis. (2014) (9)
- Sequencing errors or SNPs at splice-acceptor guanines in dbSNP? (2006) (9)
- 'Complicated' autosomal dominant familial spastic paraplegia is genetically distinct from 'pure' forms. (1997) (9)
- Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2022) (8)
- Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study (2022) (8)
- Correspondence: SEMA4A variation and risk of colorectal cancer (2016) (8)
- Comprehensive assessment of sequence variation within the copy number variable defensin cluster on 8p23 by target enriched in-depth 454 sequencing (2011) (8)
- Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study (2022) (8)
- Correspondence: SEMA4A variation and risk of colorectal cancer (2016) (8)
- B Lymphocyte Stimulator (BLyS) Is Expressed in Human Adipocytes In Vivo and Is Related to Obesity but Not to Insulin Resistance (2014) (8)
- Clostridium Difficile infections in patients with AML or MDS undergoing allogeneic hematopoietic stem cell transplantation identify high risk for adverse outcome (2019) (8)
- The PNPLA3 I148M variant promotes lipid-induced hepatocyte secretion of CXC chemokines establishing a tumorigenic milieu (2019) (7)
- Investigation of the Lith6 candidate genes APOBEC1 and PPARG in human gallstone disease (2007) (7)
- Genetic Variation at the Chromosome 16 Chemokine Gene Cluster: Development of a Strategy for Association Studies in Complex Disease (2003) (7)
- The PNPLA3 I148M variant promotes lipid-induced hepatocyte secretion of CXC chemokines establishing a tumorigenic milieu (2019) (7)
- Corrigendum: Sarcoidosis is associated with a truncating splice site mutation in the gene BTNL2 (2005) (7)
- Genetics and inflammatory bowel disease. (1999) (7)
- Investigation of the Lith6 candidate genes APOBEC1 and PPARG in human gallstone disease (2007) (7)
- UFMylation regulates translational homeostasis and cell cycle progression (2020) (7)
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- 4-O′-methylhonokiol protects from alcohol/carbon tetrachloride-induced liver injury in mice (2017) (6)
- Association of genetic polymorphisms in ESR 2 , HSD 17 B 1 , ABCB 1 , and SHBG genes with colorectal cancer risk (2011) (6)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (6)
- PS-177-HSD17B13 rs72613567 TA is associated with a reduced risk for developing hepatocellular carcinoma in patients with alcohol-related cirrhosis (2019) (6)
- The rs429358 Locus in Apolipoprotein E Is Associated With Hepatocellular Carcinoma in Patients With Cirrhosis (2021) (6)
- The rs429358 Locus in Apolipoprotein E Is Associated With Hepatocellular Carcinoma in Patients With Cirrhosis (2021) (6)
- Erratum: Pathophysiology and Management of Alcoholic Liver Disease: Update 2016 (2017) (6)
- Higher fetuin-A level is associated with coexistence of elevated alanine aminotransferase and the metabolic syndrome in the general population. (2013) (6)
- Nonelectrophoretic method for high-throughput HLA-DRB1 group genotyping. (2004) (6)
- Association of genetic polymorphisms in ESR 2 , HSD 17 B 1 , ABCB 1 , and SHBG genes with colorectal cancer risk (2011) (6)
- Heterozygous carriage of the alpha1-antitrypsin Z variant rs28929474 predisposes to the development of cirrhosis in the presence of alcohol misuse and non-alcohol-related fatty liver disease (2017) (6)
- PS-177-HSD17B13 rs72613567 TA is associated with a reduced risk for developing hepatocellular carcinoma in patients with alcohol-related cirrhosis (2019) (6)
- Utility of fiducial markers for target positioning in proton radiotherapy of oesophageal carcinoma. (2019) (6)
- Heterozygous carriage of the alpha1-antitrypsin Z variant rs28929474 predisposes to the development of cirrhosis in the presence of alcohol misuse and non-alcohol-related fatty liver disease (2017) (6)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (6)
- rs641738C>T near MBOAT7 promotes steatosis, NASH, fibrosis and hepatocellular carcinoma in non-alcoholic fatty liver disease: a meta-analysis (2020) (5)
- Menopausal hormone therapy and gallbladder disease: the Study of Health in Pomerania (SHIP) (2007) (5)
- Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) (2022) (5)
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- Genetics in gastrointestinal disease: how much can we learn from molecular analysis? (1999) (5)
- Detecting drug resistance in pancreatic cancer organoids guides optimized chemotherapy treatment (2022) (5)
- rs641738C>T near MBOAT7 promotes steatosis, NASH, fibrosis and hepatocellular carcinoma in non-alcoholic fatty liver disease: a meta-analysis (2020) (5)
- The RNA binding protein human antigen R is a gatekeeper of liver homeostasis (2021) (5)
- Eso-Sponge® for anastomotic leakage after oesophageal resection or perforation: outcomes from a national, prospective multicentre registry (2022) (5)
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- Detectability and structural stability of a liquid fiducial marker in fresh ex vivo pancreas tumour resection specimens on CT and 3T MRI (2019) (4)
- Publisher Correction: Shared heritability and functional enrichment across six solid cancers (2019) (4)
- Investigation of cholangiocarcinoma associated NKG2D polymorphisms in colorectal carcinoma (2008) (4)
- Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis (2021) (4)
- Investigation of cholangiocarcinoma associated NKG2D polymorphisms in colorectal carcinoma (2008) (4)
- Pharmacogenetic association between the TNF receptor 2 genotype and response to infliximab treatment in Crohn disease (2001) (4)
- 50 A Genome-Wide Scan Identifies TM4SF4 (Intestine and Liver Tetraspan Membrane Protein 4) as a Susceptibility Locus for Gallstone Disease (2010) (4)
- Reproducibility of preoperative endoscopic injection of botulinum toxin into the sphincter of Oddi to prevent postoperative pancreatic fistula (2018) (4)
- Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis (2021) (4)
- 50 A Genome-Wide Scan Identifies TM4SF4 (Intestine and Liver Tetraspan Membrane Protein 4) as a Susceptibility Locus for Gallstone Disease (2010) (4)
- Cell atlas of the regenerating human liver after portal vein embolization (2021) (4)
- EUS-guided stent removal in buried lumen-apposing metal stent syndrome: a case series (2019) (4)
- Characterization of Tissue Transglutaminase as a Potential Biomarker for Tissue Response toward Biomaterials. (2019) (4)
- S1850 Metabolomic Analysis of Breath Air and Tongue Swabs Using Gas Chromatography/Mass Spectrometry Identifies Novel Metabolic Markers of Hepatic Encephalopathy (2009) (3)
- Wet-tip versus dry-tip regimes of osmotically driven fluid flow (2019) (3)
- Evolutionary Distance Predicts Recurrence After Liver Transplantation in Multifocal Hepatocellular Carcinoma (2018) (3)
- Deskription der medizinischen Versorgung von jüngeren Patienten ( <65 Jahre) mit kolorektalem Karzinom in Schleswig-Holstein und Abgleich der Bereiche Diagnostik und Therapie mit der aktuellen S3-Leitlinie (2007) (3)
- rs641738C>T near MBOAT7 is positively associated with liver fat, ALT, and histological severity of NAFLD: a meta-analysis (2019) (3)
- Post-diagnostic reliance on plant-compared with animal-based foods and all-cause mortality in omnivorous long-term colorectal cancer survivors. (2021) (3)
- Genome-Wide Association Studies Herald a New Era of Rapid Discoveries in Inflammatory Bowel Disease Research (2007) (3)
- Life-Threatening Chronic Enteritis Due to Colonization of the Small Bowel With (2005) (3)
- Metabolomic tissue signature in human non-alcoholic fatty liver disease identifies protective candidate metabolites (2013) (3)
- Plasma Levels of K18 Fragments Do Not Correlate with Alcoholic Liver Fibrosis (2018) (3)
- SGCaller: a program to call and review genotypes measured by sequencing. (2005) (3)
- OWE-016 Genetic variants in PNPLA3 and TM6SF2 predispose to hepatocellular carcinoma in patients with alcohol-related cirrhosis (2018) (3)
- S1850 Metabolomic Analysis of Breath Air and Tongue Swabs Using Gas Chromatography/Mass Spectrometry Identifies Novel Metabolic Markers of Hepatic Encephalopathy (2009) (3)
- Copy number variants in lipid metabolism genes are associated with gallstones disease in men (2019) (3)
- rs641738C>T near MBOAT7 is positively associated with liver fat, ALT, and histological severity of NAFLD: a meta-analysis (2019) (3)
- OWE-016 Genetic variants in PNPLA3 and TM6SF2 predispose to hepatocellular carcinoma in patients with alcohol-related cirrhosis (2018) (3)
- Copy number variants in lipid metabolism genes are associated with gallstones disease in men (2019) (3)
- Evolutionary Distance Predicts Recurrence After Liver Transplantation in Multifocal Hepatocellular Carcinoma (2018) (3)
- [Description of the medical care of younger patients (<65 years) with colorectal cancer in Schleswig-Holstein--are diagnostics and therapy compliant with the actual S3-guidelines?]. (2007) (2)
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- Sequence variation in the CARD15 (NOD2) gene and susceptibity to Crohn's disease (2003) (2)
- Metabolic Signature of Electrosurgical Liver Dissection (2013) (2)
- Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis (2020) (2)
- Treatment of Complicated Anal Fistula by an Endofistular Polyurethane-Sponge Vacuum Therapy: A Pilot Study (2018) (2)
- Risk Factor Prevalence and Their Relative Influence on Fatty Liver and Gallstone Disease: A Cross-Ethnic Study Comparing Two High-Risk Populations from Chile and Northeast Germany (2016) (2)
- Increased heritability of gallstone disease in early onset cases (2008) (2)
- The NOD2 genotype and the clinical course of Crohns disease. (2002) (2)
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- Postdiagnosis body mass index and risk of mortality in colorectal cancer survivors: a prospective study and meta-analysis (2014) (2)
- Oligonucleotide DNA fingerprinting: results of a multi-center study on reliability and validity. (1993) (2)
- Genetic variation of PNPLA3 and TM6SF2 associate with hepatocellular carcinoma in patients with alcohol-related cirrhosis (2017) (2)
- Correction: Genetic Variants in PNPLA3 and TM6SF2 Predispose to the Development of Hepatocellular Carcinoma in Individuals With Alcohol-Related Cirrhosis (2018) (2)
- Corrigendum: Widespread occurrence of alternative splicing at NAGNAG acceptors contributes to proteome plasticity (2005) (2)
- Nonalcoholic fatty liver disease strati fi cation by liver lipidomics (2021) (2)
- Increased heritability of gallstone disease in early onset cases (2008) (2)
- Genetic variation of PNPLA3 and TM6SF2 associate with hepatocellular carcinoma in patients with alcohol-related cirrhosis (2017) (2)
- Response to Li and Hopper. (2021) (2)
- Risk Factor Prevalence and Their Relative Influence on Fatty Liver and Gallstone Disease: A Cross-Ethnic Study Comparing Two High-Risk Populations from Chile and Northeast Germany (2016) (2)
- Physical activity and risks of breast and colorectal cancer: A Mendelian randomization analysis (2019) (2)
- Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (1)
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- 592 Evaluation of Genome-Wide Loci of Iron Metabolism in Hereditary Hemochromatosis Identifies Pcsk7 as a Predictor of Liver Cirrhosis (2012) (1)
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- Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in people with hereditary haemochromatosis (2020) (1)
- 134 EVALUATION OF GENOME-WIDE LOCI OF IRON METABOLISM IN HEREDITARY HEMOCHROMATOSIS IDENTIFIES PCSK7 AS A PREDICTOR OF LIVER CIRRHOSIS (2012) (1)
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- Digitalisierung in der Gastroenterologie (2019) (1)
- Macroscopic, Histologic and Clinical Assessment of Acute GVHD of the Upper Gastrointestinal Tract within 6 Weeks after Allogeneic Hematopoietic Cell Transplantation (2022) (1)
- A TWO-STAGE GENOME-WIDE ASSOCIATION STUDY IDENTIFIES TM6SF2 AND MBOAT7 AS RISK LOCI FOR ALCOHOL-RELATED CIRRHOSIS (2015) (1)
- A TWO-STAGE GENOME-WIDE ASSOCIATION STUDY IDENTIFIES TM6SF2 AND MBOAT7 AS RISK LOCI FOR ALCOHOL-RELATED CIRRHOSIS (2015) (1)
- [Digital Health Innovation in Gastroenterology]. (2019) (1)
- Reply to: “Modulation of the effect of PNPLA3 I148M mutation on steatosis and liver damage by alcohol intake in patients with chronic hepatitis C” (2011) (1)
- Common variants in ABCG8 and TRAF3 genes confer risk for gallstone disease and gallbladder cancer in admixed Latinos with Mapuche Native American ancestry (2018) (1)
- Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer (2018) (1)
- Temperature profile and residual heat of monopolar laparoscopic and endoscopic dissection instruments (2021) (1)
- Carriage of HSD17B13 rs72613567TA is associated with a reduced risk for developing hepatocellular carcinoma in patients with alcohol-related cirrhosis (2019) (1)
- Common variants in ABCG8 and TRAF3 genes confer risk for gallstone disease and gallbladder cancer in admixed Latinos with Mapuche Native American ancestry (2018) (1)
- A Mechanistic, Model-Based Approach to Safety Assessment in Clinical Development (2013) (1)
- Menopausal hormone therapy is not associated with gallbladder disease. Results from a population-based study (2007) (1)
- Digital single-operator pancreatoscopy for the treatment of symptomatic pancreatic duct stones: a prospective multicenter cohort trial (2022) (1)
- Genetic predictors of spontaneous viral elimination or chronic liver disease in hepatitis C infection (2001) (1)
- Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (1)
- 683o: Closure of Anastomotic Leakage and Iatrogenic Perforation With Endoscopic Suturing: An Ongoing Pilot Study in Patients (2010) (1)
- Randomised, double-blind, placebo-controlled trial of oral budesonide for prophylaxis of acute intestinal graft-versus-host disease after allogeneic stem cell transplantation (PROGAST) (2014) (1)
- Tu1519 Staging of Gastric Cancer by Endoscopic Ultrasound As a Selection Criterion for Neoadjuvant Chemotherapy (2012) (1)
- S2k-Leitlinie nicht alkoholische Fettlebererkrankungen (2015) (1)
- P326 Efficacy of vedolizumab on patient-reported outcomes in ulcerative colitis patients: results from a prospective German observational study. (2017) (1)
- A non-synonymous SNP in an autophagy-related gene is associated with Chron's disease. (2007) (1)
- Carriage of HSD17B13 rs72613567TA is associated with a reduced risk for developing hepatocellular carcinoma in patients with alcohol-related cirrhosis (2019) (1)
- Sinnvolle genetische Untersuchungen in der Gastroenterologie (2018) (1)
- Whole genome sequence of Mapuche-Huilliche Native Americans (2018) (1)
- 592 Evaluation of Genome-Wide Loci of Iron Metabolism in Hereditary Hemochromatosis Identifies Pcsk7 as a Predictor of Liver Cirrhosis (2012) (1)
- Su1571 Placement of a Fully Covered Metal Stent (AXIOS) for EUS-Guided Drainage of Peripancreactic Fluid Collections; a Prospective European Cohort Study (2013) (1)
- Alteration of Composition and Diversity of the Mucosa-associated Fungal Microflora in Patients With IBD (2006) (1)
- Whole genome sequence of Mapuche-Huilliche Native Americans (2018) (1)
- Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis (2020) (1)
- 134 EVALUATION OF GENOME-WIDE LOCI OF IRON METABOLISM IN HEREDITARY HEMOCHROMATOSIS IDENTIFIES PCSK7 AS A PREDICTOR OF LIVER CIRRHOSIS (2012) (1)
- No association between HLA-DRB1 and helicobacter pylori related diseases found (2000) (1)
- High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis (2023) (1)
- The PRV-1 gene expression in essential thrombocythemia (2004) (1)
- 128th Congress of the German Society of Surgery (2011) (1)
- Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in people with hereditary haemochromatosis (2020) (1)
- Genomweite Untersuchung identifiziert den hepatischen Cholesterol Transporter ABCG8 als Suszeptibilitäts-Faktor für das humane Gallensteinleiden (2008) (0)
- SAT-330-Whole metabolome profiling identifies the combination of an eicosanoid, a bile acid and an androgen as a highly accurate marker of liver fibrosis in patients with non-alcoholic fatty liver disease (2019) (0)
- Evaluation of SNPs in TNF (C-857T) and MDR1 (C3435T) as susceptibility factors for IBD. (2004) (0)
- Does genetic variation within the SLC22A4 and SLC22A5 (OCTN1 and 2) genes fully describe the contribution of the IBD5 locus to the risk of Crohn's disease? (2005) (0)
- Health-related quality of life in long-term survivors of colorectal cancer and its association with all-cause mortality: a German cohort study (2018) (0)
- Severe histological liver phenotype of lean subjects with non-alcoholic fatty liver disease (2017) (0)
- Analysis of single nucleotide polymorphisms in the NRAMP2 gene, for association with inflammatory bowel disease (2000) (0)
- Biomarkers for differentiating between non-alcoholic steatohepatitis (NASH) and non-alcoholic fatty liver disease (NAFLD) (2015) (0)
- Representation of human non-alcoholic fatty liver disease in murine models (2015) (0)
- Phenotype-genotype correlation and genetic epidemiology of epilepsy, febrile seizures and neonatal seizures in a defined nothern German region – “popgen-epilepsy“ (2005) (0)
- Inflammatory Bowel Disease: on the importance of NOD2 and sex (2001) (0)
- Comparative analysis of metabolic signature from malignant melanoma and uninvolved skin. (2015) (0)
- A new familial inflammatory syndrome of aortic valve sclerosis, chronic orral ulceration, terminal ileitis and corneal opacities (1998) (0)
- Variants APOE (rs429358) and TM6SF2 (rs187429064) confer risk to hepatocellular carcinoma (2021) (0)
- Genome-wide analysis of 944,133 individuals provides insights into the etiology of hemorrhoidal disease (2020) (0)
- Identification of an IBD associated haplotype on BACs A-249810 and 504N19 on proximal chromosome 16p (2001) (0)
- Serum metabolic signatures in patients with overt hepatic encephalopathy. (2017) (0)
- B lymphocyte stimulator (BLyS) is a novel adipokine in humans in vivo being related to obesity but not to insulin resistance (2013) (0)
- ASIC — LIVER , PANCREAS , AND BILIARY RACT enome-Wide Association Analysis in Primary Sclerosing Cholangitis (0)
- Thoracic pain and pericardial effusion in a patient with chronic pancreatitis. (2020) (0)
- A novel hyperplasia-neoplasia sequence in pancreatic endocrine tumors: Glucagon cell adenomatosis (2014) (0)
- Erratum to “CFTR Expression Analysis for Subtyping of Human Pancreatic Cancer Organoids” (2019) (0)
- Investigation of HLA-DPA1 associations with IBD in European, South-African and South Korean populations (2000) (0)
- Explorer COGENT ( COlorectal cancer GENeTics ) : an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2017) (0)
- A targeted analysis reveals relevant shifts in the methylation and transcription of genes responsible for bile acid homeostasis and drug metabolism in non-alcoholic fatty liver disease (2016) (0)
- Discovering the genomic basis of morphological and physiological differences between mammalian species with Forward Genomics (2016) (0)
- Localization, Management, Resource Consumption and Outcome of Major Gastrointestinal Bleeding in Patients with Direct Oral Anticoagulants, Vka and Antiplatelet Therapy (2016) (0)
- BASIC—LIVER, PANCREAS, AND BILIARY TRACT Genome-Wide Association Analysis in Primary Sclerosing Cholangitis (2010) (0)
- DNA methylation signatures in non-alcoholic fatty liver disease reveal disease-specific signatures and molecular remodelling drivers after weight loss in non-alcoholic fatty liver disease (2013) (0)
- The emerging realm of morphogens in the adult liver of mice and human – a deep insight into distribution, interaction and regulation (2018) (0)
- Edinburgh Research Explorer COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer role (2009) (0)
- Gene expression profiling in normal, ulceralive colitis (UC) and Crohn's disease (CO) samples using high density cDNA arrays (2001) (0)
- A transcript-based search for inflammatory bowel disease susceptibility genes on chromosome 16 (2001) (0)
- Genetic variant PNPLA3 I148M accelerates fat accumulation in livers of mice with ASH/NASH via damping of PPAR alpha and PPAR gamma signalling pathways (2020) (0)
- Cell Metabolism Letters SFRS 10 — A Splicing Factor Gene Reduced in Human Obesity ? (2012) (0)
- Translational learning from clinical studies predicts drug pharmacokinetics across patient populations (2017) (0)
- The functional (cid:1) 374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn’s disease (2011) (0)
- [Genetics and the environment. Has the picture become clearer?]. (2002) (0)
- Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
- high density mapping of pericentromeric chromosome 12 in inflammatory bowel disease (2000) (0)
- 403 Regulation of Human β-Defensin Expression by a Disintegrin and Metalloprotease Family of Membrane Glycoproteins (ADAM) in Candida Esophagitis (2010) (0)
- Increased Intestinal Permeability and Disturbance of Tight-Junctions in an Acute Graft Versus Host Disease Model in Mice (2011) (0)
- Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (0)
- Fatty acid binding protein 2 promoter polymorphism is associated with insulin sensitivity after a mixed meal in the metabolic intervention cohort Kiel (2004) (0)
- Genetic polymorphisms as predictors of chronic liver disease in hepatitis C infection (2001) (0)
- Tu1375 A CASE-MATCHED STUDY ON EUS-GUIDED DRAINAGE OF WALLED-OFF NECROSIS USING 20MM VS 15MM LUMEN APPOSING METAL STENTS: IS BIGGER BETTER? (2019) (0)
- Tu1837 - Efficacy, Safety and Long-Term Outcome of Endoscopic Dilation Therapy for Crohn's Disease Strictures of the Upper Gastrointestinal Tract - An International Multicenter Cohort Study Including 99 Patients and 129 Dilation Procedures (2018) (0)
- Loss of zonation in end stage liver disease revealed by in situ omics (2019) (0)
- Haplotype structure analysis in the HLA region and implications for association mapping in inflammatory bowel disease (2003) (0)
- Erratum: COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (British Journal of Cancer 102 (447-454) DOI: 10.1038/sj.bjc.6605338)) (2010) (0)
- The HSF1-CPT1a Pathway Is Differentially Regulated in NAFLD Progression (2022) (0)
- Testing IBD candidate loci on chromosome 12: The interferon gamma gene (1998) (0)
- Lifestyle factors and health-related quality of life in colorectal cancer survivors (2013) (0)
- Alteration of composition and diversity of the mucosa-associated fungal microflora in patients with inflammatory bowel disease (2005) (0)
- [Fecal microbiota transplantation: when and for whom?]. (2014) (0)
- Is there a Benefit from Rescue-Allocated Organs for HCCPatients Staged outside the Milan Criteria? (2016) (0)
- TITLE: Mendelian randomization of circulating polyunsaturated fatty acids and colorectal cancer risk (2020) (0)
- Mendelian randomization study of age at menarche and age at 1 menopause and the risk of colorectal cancer (2018) (0)
- Analysis of candidate genes within the chromosome 16 region associated with susceptibility to IBD (2001) (0)
- 742 Hepatitis B Virus Infection Leads to Alterations in the Repertoire of Self Lipid Antigens Presented by Hepatocytes and is Associated With Direct and Indirect Activation of Natural Killer T Cells (2012) (0)
- Endofistula Vacuum Therapy as an Innovative Treatment for Transsphincteric Anal Fistula: Results of a Preclinical Trial (2022) (0)
- Polymorphisms in the ICAM-1 gene but not in the CD11 cluster are disease modifying factors in inflammatory bowel disease (2001) (0)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
- 760 – Mutations in X-Linked Inhibitor of Apoptosis Protein Promote Susceptibility to Microbiota-Induced Intestinal Inflammation (2019) (0)
- Exploring the causal role of the human gut microbiome in colorectal cancer: Application of Mendelian randomization (2022) (0)
- Contribution of genetic variants at CARD15 and the chromosome 5q31 locus to Crohn's disease (2002) (0)
- Postdiagnostic physical activity, sleep duration, and TV watching and all-cause mortality among long-term colorectal cancer survivors: a prospective cohort study (2017) (0)
- SEMA 4 A variation and risk of colorectal cancer (2016) (0)
- Title COGENT ( COlorectal cancer GENeTics ) : An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (0)
- Cumulative impact of 10 common genetic variants on colorectal cancer risk in 42,333 individuals from eight populations (2013) (0)
- The TNF-857C/T polymorphism is associated with early onset, smoking and arthritic complications in inflammatory bowel disease and acts independently of CARD15 (2003) (0)
- Confirmation of IBD5 in a German population and exploration of genotype-phenotype interactions (2003) (0)
- COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2010) (0)
- [Practical Genetic Testing in Gastroenterology]. (2018) (0)
- Flexible Percutaneous Retroperitoneal Necrosectomy for Pancreatic Necrosis Beyond the Reach of EUS: A Case Series (2016) (0)
- 1012 – Genome-Wide Association Analysis of Diverticular Disease Points Towards Neuromuscular, Connective Tissue and Epithelial Pathomechanisms (2019) (0)
- BASIC AND TRANSLATIONAL—BILIARY Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies (2016) (0)
- XIAP Regulates Paneth Cell Homeostasis and the Susceptibility to Microbial Triggers of Intestinal Inflammation (2020) (0)
- ' s response to reviews Predictors of gallstone composition in 1025 symptomatic gallstones from Northern Germany Title : (2006) (0)
- Two-Dimensional DNA Fingerprinting (1999) (0)
- A Framework To Assess Technology-Specific Error Signatures In Next-Generation Sequencing, With An Application To The 1000 Genomes Project Data (2012) (0)
- Edinburgh Research Explorer The MLH1 c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer (2018) (0)
- Association of BMI and promotor polymorphisms of the ghrelin gene (2003) (0)
- T1240 Context-Dependent Splicing of Two Novel 5 Prime Untranslated Exons Contributes to the Complex Regulation of NOD2 Protein Expression in Intestinal Inflammation (2008) (0)
- S1828 High Prevalence and Bleeding Risk of Unusual Transcapsular Portal Vein (PV) Collaterals in Chronic Pv Thrombosis After Liver Transplantation, Pancreaticobiliary Surgery or Severe Pancreatitis (2009) (0)
- 1255 REGULATION OF PATATINE-LIKE PHOSPOLIPASE DOMAIN-CONTAINING PROTEIN-3 (PNPLA3) EXPRESSION BY FATTY ACIDS AND ALCOHOL IN VITRO AND IN VIVO (2012) (0)
- T2094 Investigation of the Colorectal Cancer Susceptibility Region On Chromosome 8q24.21 in a Large German Patient Sample (2008) (0)
- COGENT cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. (2009) (0)
- J HEPAT-S16-01356 The Genetics of Alcohol Dependence and Alcohol-related Liver Disease (2018) (0)
- T1280 A Combined Analysis of Genome-Wide Scans for Sarcoidosis and Crohn Disease Identifies a Common Susceptibility Locus (2008) (0)
- Fine mapping of the 5q31 risk haplotype in Crohn's disease (2004) (0)
- Direct endoscopy and diagnosis of adenocarcinoma following metal stent-based drainage of a pancreatic cyst (2018) (0)
- Genetic analysis of inflammatory bowel disease in a large european patient population supports linkage to human chromosomes 12 and 16 (1998) (0)
- Edinburgh Research Explorer SEMA4A variation and risk of colorectal cancer (2018) (0)
- PO-0954: Fiducial markers and daily kV imaging improve patient setup during proton RT of esophageal cancer (2018) (0)
- 619 – Myeloid Calcineurin in the Control of Immune Checkpoint Inhibition in Intestinal Tumor Development (2019) (0)
- genetic susceptibility variants in NOD 2 and cigarette smoking in Crohn ' s disease aetiology (2012) (0)
- Su1431 SAFETY AND EFFICACY OF THE NEW 20 MM LUMEN APPOSING METAL STENT (LAMS) FOR ENDOSCOPIC TREATMENT OF PANCREATIC AND PERIPANCREATIC FLUID COLLECTIOS: A LARGE, INTERNATIONAL, MULTICENTER STUDY (2018) (0)
- 1331 “HEALTHY LIVER” IN MORBIDLY OBESE: TRANSITION TO NASH IN THE CONTEXT OF INSULIN RESISTANCE AS PREREQUISITE FOR HEPATIC STEATOSIS REQUIRES ADDITIONAL TRIGGERS (2012) (0)
- DOP044 Efficacy, safety and long-term outcome of endoscopic dilation therapy for Crohn’s disease strictures of the upper gastrointestinal tract: an international multicentre cohort study including 99 patients with 129 dilation procedures (2018) (0)
- Tu1041 “Healthy Liver” in Morbidly Obese: Transition to NASH in the Context of Insulin Resistance as Prerequisite for Hepatic Steatosis Requires Additional Triggers (2012) (0)
- CpG Methylation Analysis from Targeted Sequencing of Bisulfite Converted DNA (2010) (0)
- CHAPTER 4 DEFINITION OF POLYMORPHISMS AND HAPLOTYPES IN THE INTERLEUKIN-12 B GENE : ASSOCIATION WITH IL-12 PRODUCTION BUT NOT WITH CROHN ’ S DISEASE (2011) (0)
- Changes of the Steatosis Hepatis and Diabetes Mellitus after Laparoscopic Sleevegastrectomy: Prospective Follow Up Study About Reduction of Comorbidities and Histological Liver Findings in Obese Patients (2011) (0)
- Genome-wide investigation of gene–environment interactions in colorectal cancer (2012) (0)
- High density CDNA arrays for the characterisation of mucosal gene expression in inflammatory bowel disease (2000) (0)
- Paternity Testing by Oligonucleotide DNA Fingerprinting: A Multi-Center Study Proving Reliability and Validity (1994) (0)
- Analysis of single nucleotide polymorphisms in the IL12p35 gene: A putative association with ulcerative colitis (2001) (0)
- Association Analysis and Mutation Screening of Candidate Genes for Photosensitivity in the Chromosomal Region 13q31 (2009) (0)
- Variants in TM6SF2, PNPLA3 and PCSK7 are risk factors for the development of cirrhosis in people with genetic haemochromatosis (2019) (0)
- Severe histological liver phenotype of lean subjects with non-alcoholic fatty liver disease (2017) (0)
- Variants APOE (rs429358) and TM6SF2 (rs187429064) confer risk to hepatocellular carcinoma (2021) (0)
- Genome-wide analysis of 944,133 individuals provides insights into the etiology of hemorrhoidal disease (2020) (0)
- Explorer COGENT ( COlorectal cancer GENeTics ) : an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2017) (0)
- Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans (2019) (0)
- The rs72613567:TA polymorphism in HSD17B13 is associated with survival benefit after development of hepatocellular carcinoma (2023) (0)
- Edinburgh Research Explorer COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer role (2009) (0)
- Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry (2019) (0)
- Genetic Variation of SAMM50 Is Not an Independent Risk Factor for Alcoholic Hepatocellular Carcinoma in Caucasian Patients (2022) (0)
- Erratum: COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (British Journal of Cancer 102 (447-454) DOI: 10.1038/sj.bjc.6605338)) (2010) (0)
- and SHBG genes with colorectal cancer risk 2 (2011) (0)
- Understanding the role of Mboat7 in liver disease (2021) (0)
- SEMA 4 A variation and risk of colorectal cancer (2016) (0)
- Title COGENT ( COlorectal cancer GENeTics ) : An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (0)
- Cumulative impact of 10 common genetic variants on colorectal cancer risk in 42,333 individuals from eight populations (2013) (0)
- COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2010) (0)
- 1012 – Genome-Wide Association Analysis of Diverticular Disease Points Towards Neuromuscular, Connective Tissue and Epithelial Pathomechanisms (2019) (0)
- Copy number variants in lipid metabolism genes are associated with gallstones disease in men (2019) (0)
- BASIC AND TRANSLATIONAL—BILIARY Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies (2016) (0)
- Genetically determined expression of lipoprotein lipase is linked to hepatocellular carcinoma in alcohol-associated cirrhosis (2023) (0)
- Edinburgh Research Explorer The MLH1 c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer (2018) (0)
- 1255 REGULATION OF PATATINE-LIKE PHOSPOLIPASE DOMAIN-CONTAINING PROTEIN-3 (PNPLA3) EXPRESSION BY FATTY ACIDS AND ALCOHOL IN VITRO AND IN VIVO (2012) (0)
- T2094 Investigation of the Colorectal Cancer Susceptibility Region On Chromosome 8q24.21 in a Large German Patient Sample (2008) (0)
- COGENT cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. (2009) (0)
- Edinburgh Research Explorer SEMA4A variation and risk of colorectal cancer (2018) (0)
- Variants APOE (rs429358) and TM6SF2 (rs187429064) modify the risk of hepatocellular carcinoma (2022) (0)
- Aberrant DNA methylation of ADAMTS16 in colorectal and other epithelial cancers (2018) (0)
- B7H3- und B7H4-vermittelte Checkpoint-Inhibition in der intestinalen Tumorentwicklung (2019) (0)
- Neue Erkenntnisse zur Rolle der Mikrobiota im kolorektalen Karzinom (2016) (0)
- Bestätigung und Feinkartierung der Risikoregion für das kolorektale Karzinom auf 8q24.21 in einer großen deutschen Patientenkohorte (2008) (0)
- Kongresskalender (2007) (0)
- Deutsches ESD-Register – aktueller Stand (2018) (0)
- 3D Rekonstruktion und quantitative räumliche Analyse der nicht-alkoholischen Fettlebererkrankung (NAFLD) (2017) (0)
- Differenzialdiagnostik und Therapie des akuten Abdomens (2016) (0)
- Myeloides Calcineurin fördert die intestinale Tumorentwicklung durch STAT3-abhängige epitheliale Expression von Immun-Checkpoint-Inhibitoren (2018) (0)
- Rolle des Transkriptionsfaktors Nrf2 bei der proteasomalen Genexpression und erhöhter Proteasomaktivität im kolorektalen Karzinom (2009) (0)
- Retrospektive multizentrische Analyse der Erfolgs- und Komplikationsraten selbstexpandierender Metallstents in der endoskopischen Versorgung peripankreatischer Flüssigkeitsverhalte (2018) (0)
- Verschluss von Nahtinsuffizienzen und iatrogenen Perforationen am oberen Gastrointestinaltrakt mittels endoskopischer Naht am Menschen (2010) (0)
- TM6SF2 rs58542926 und PCSK7 rs236918 sind genetische Risikoloci einer Leberzirrhose bei hereditärer Hämochromatose (2017) (0)
- Langzeitanalyse zur Endospongetherapie von Anastomoseninsuffizienzen nach kolorektalen Resektionen (2013) (0)
- Diagnostik der Leberfibrose bei nicht-alkoholischer Fettlebererkrankung mittels Composite Score aus einem Eicosanoid, einer Gallensäure und einem Androgen (2018) (0)
- CED – Von der Genetik zum Krankheitsverständnis (2007) (0)
- Komplikationsprofil und Langzeitverlauf nach Drainage von Pankreasnekrosen und Pseudozysten mittels LAMS (Lumen-apposing metal stent) (2017) (0)
- Künstliche Intelligenz in der Viszeralmedizin – „brave new world“ oder digitaler Horror? (2021) (0)
- In-situ Omics Analyse zeigt Zonierungsverlust in der Leberzirrhose (2019) (0)
- Vedolizumab in der Therapie chronisch-entzündlicher Darmerkrankungen: Klinische Wirksamkeit und Sicherheit nach 12 Monaten (2016) (0)
- Transkapsuläre Kollateralen und ektope Varizen bei chronischer Pfortaderthrombose–Vorkommen und klinische Bedeutung (2011) (0)
- Identifizierung assoziierter Genvarianten des IL12-Signalwegs bei primär biliärer Zirrhose (2010) (0)
- Intestinal-epitheliales Calcineurin in der Mikrobiota-abhängigen Regulation des kolorektalen Karzinoms (2016) (0)
- Genetik und Genomik in der Gastroenterologie (2017) (0)
- Pilotstudie zu metabolomischen Signaturen elektrochirurgischer Leberpräparation (2011) (0)
- Polymorphe Varianten im PNPLA3- und TM6SF2-Gen sind mit dem Hepatozellulären Karzinom bei alkoholischer Leberzirrhose assoziiert (2017) (0)
- Untersuchung der murinen LITH1 Kandidatengene ABCB11 AND LXRA beim humanen Gallensteinleiden (2006) (0)
- Die endoskopische endoluminale Vakuum (EndoVAC) Therapie ist anderen Therapiemodalitäten bei der Behandlung von Anastomoseninsuffizienzen nach Ösophagusresektion überlegen – eine vergleichende retrospektive Analyse (2014) (0)
- Spezialgebiete: Leberpathologie Pankreaspathologie Molekularpathologie (2013) (0)
- CD1 d als Regulator des Lipidmetabolismus in der nicht-alkoholischen Fettlebererkrankung (2019) (0)
- Vorkommen und Blutungsrisko von transkapsulären mesentericoportalen Kollateralen bei chronischer Pfortaderthrombose (2009) (0)
- EUS gesteuerte Drainage im Vergleich zur Behandlung postoperativer Pankreasfisteln (2018) (0)
- Heterozygote Träger der Alpha1-Antitrypsin-Variante PiZ neigen zur Entwicklung einer Leberfibrose (2017) (0)
- Mutationen im Gen des X-linked inhibitor of apoptosis protein (XIAP) führen zu Suszeptibilität gegenüber Mikrobiota-induzierter intestinaler Entzündung (2018) (0)
- Pilotstudie zur Behandlung komplexer Analfisteln durch eine endofistuläre Polyurethanschwamm Vakuumtherapie (2018) (0)
- Die Sleevegastrektomie: Verlaufsuntersuchung der Komorbiditäten, Stoffwechselveränderungen und Lebensqualität Vorstellung einer Prospektive Studie eines universitären Adipositaszentrum (2010) (0)
- Genetik der Fettlebererkrankung (2013) (0)
- Genomweite Analyse identifiziert TM4SF4 (intestine and liver tetraspan membrane protein 4) als Risikogen für das Gallensteinleiden (2010) (0)
- Der Verlust von intestinal epithelialem SETDB1 führt zu fehlender Repression endogener Retroviren, Genotoxizität und intestinaler Entzündung (2020) (0)
- Metabolomische Analysen von Atemluft mittels Gas-Chromatografie/Massenspectrometrie identifiert Metaboliten als neue Marker für hepatische Enzephalopathie (2009) (0)
- Digitalisierung in der Gastroenterologie (2019) (0)
- Das Eso-Sponge Register: Prospektive multizentrische Untersuchung der endoluminalen Vakuumtherapie am oberen Gastrointestinaltrakt (2019) (0)
- Loci einer genomweiten Metaanalyse von Serum-Bilirubinwerten sind mit dem Gallensteinrisiko und der Gallensteinzusammensetzung assoziiert (2011) (0)
- Interleukin-1β (IL-1β) und „a disintegrin and metalloprotease“ 17 (ADAM17) sind zentrale Regulatoren der β-defensin Expression im Rahmen einer Candida Ösophagitis (2010) (0)
- Effektivität, Sicherheit und Langzeitergebnis endoskopischer Ballondilatationen von Morbus Crohn-bedingten Stenosen des oberen Gastrointestinaltraktes – eine internationale Multicenter Kohortenstudie mit 99 Patienten und 165 Dilatationen (2018) (0)
- Die Calcineurin-abhängige Regulation der zytotoxischen T-Zell-Antwort in der intestinalen Tumorentwicklung (2019) (0)
- Hepatocyte-derived calcineurin regulates the development of hepatocellular carcinoma independent of hepatic steatohepatitis (2019) (0)
- Wnt/β-Catenin and Hh signaling in the adult liver – an insight into distribution, interaction and regulation (2019) (0)
- The RNA binding protein HuR is a master regulator of hepatic-lipid homeostasis (2019) (0)
- The rs72613567:TA polymorphism in HSD17B13 is associated with survival benefit after development of hepatocellular carcinoma (2023) (0)
- Capacitive Proximity Sensor for Non-Contact Endoscope Localization (2022) (0)
- German guideline diverticular disease/diverticulitis (2022) (0)
- The Pnpla3 Variant I148M Reveals Protective Effects Towards Hepatocellular Carcinoma in Mice via Restoration of Omega-3 Polyunsaturated Fats. (2022) (0)
- Validation of a genetic-enhanced risk prediction model for colorectal cancer in a large community-based cohort. (2023) (0)
- Shared heritability and functional enrichment across six solid cancers (2019) (0)
- Correction: Digital single-operator pancreatoscopy for the treatment of symptomatic pancreatic duct stones: a prospective multicenter cohort trial (2022) (0)
- Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer (2023) (0)
- German guideline diverticular disease/diverticulitis (2022) (0)
- Specific neurophysiological mechanisms underlie cognitive inflexibility in inflammatory bowel disease (2017) (0)
- Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2023) (0)
- Whole metabolome profiling identifies the combination of an eicosanoid, a bile acid and an androgen as a highly accurate marker of liver fibrosis in patients with non-alcoholic fatty liver disease (2019) (0)
- P787 Subcutaneous infliximab in IBD patients with previous immunogenic failure of intravenous infliximab (2023) (0)
- Variants APOE (rs429358) and TM6SF2 (rs187429064) modify the risk of hepatocellular carcinoma (2022) (0)
- Aberrant DNA methylation of ADAMTS16 in colorectal and other epithelial cancers (2018) (0)
- The Gut Dysmotility Questionnaire for Parkinson's disease: Insights into development and pretest studies (2023) (0)
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What Schools Are Affiliated With Jochen Hampe?
Jochen Hampe is affiliated with the following schools:
