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David Ellinghaus

Name	David Ellinghaus
Ort	Kiel (Wirkungsort) Deutschland
Akademischer Grad bzw. Titel	Prof. Dr. rer. nat.
Beziehung	Christian-Albrechts-Universität zu Kiel. Institut für Klinische Molekularbiologie
Quelle	UnivIS Kiel
Datensatztyp	Person
GND-Nummer	1120024528
Datensatz-ID	1120024528
Beteiligt an alle anzeigen Corrigendum: Sex differences in the genetics of sarcoidosis across European and African ancestry populations Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group Genetic and transcriptomic cross-disease studies for inflammatory bowel disease and comorbid conditions HLA-DPA102:01~B101:01 is a risk haplotype for primary sclerosing cholangitis mediating activation of NKp44+ NK cells Mendelian randomisation shows diverticular disease and irritable bowel syndrome increase the risk of haemorrhoidal disease Sex differences in the genetics of sarcoidosis across European and African ancestry populations Sex differences in the genetics of sarcoidosis across European and African ancestry populations DNA methyltransferase 3A controls intestinal epithelial barrier function and regeneration in the colon Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota How genetic risk contributes to autoimmune liver disease Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease Customized workflow development and omics data integration concepts in systems medicine Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level Current software for genotype imputation

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David Ellinghaus

Corrigendum: Sex differences in the genetics of sarcoidosis across European and African ancestry populations

Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group

Genetic and transcriptomic cross-disease studies for inflammatory bowel disease and comorbid conditions

HLA-DPA1*02:01~B1*01:01 is a risk haplotype for primary sclerosing cholangitis mediating activation of NKp44+ NK cells

Mendelian randomisation shows diverticular disease and irritable bowel syndrome increase the risk of haemorrhoidal disease

Sex differences in the genetics of sarcoidosis across European and African ancestry populations

Sex differences in the genetics of sarcoidosis across European and African ancestry populations

DNA methyltransferase 3A controls intestinal epithelial barrier function and regeneration in the colon

Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota

How genetic risk contributes to autoimmune liver disease

Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease

Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease

Customized workflow development and omics data integration concepts in systems medicine

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine.

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci

Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level

Current software for genotype imputation

HLA-DPA102:01~B101:01 is a risk haplotype for primary sclerosing cholangitis mediating activation of NKp44+ NK cells