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KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)), 2005-08, Vol.67 Suppl 1, p.S26

2005

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ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome

Leukemia, 2013-01, Vol.27 (1), p.82-91

2013

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Schizophrenia shows a unique metabolomics signature in plasma

Translational psychiatry, 2012-08, Vol.2 (8), p.e149-e149

2012

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Increased efficacy of omalizumab in atopic dermatitis patients with wild‐type filaggrin status and higher serum levels of phosphatidylcholines

Allergy (Copenhagen), 2014-01, Vol.69 (1), p.132-135

2014

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Autoantibodies to zinc transporter 8 and SLC30A8 genotype stratify type 1 diabetes risk

Diabetologia, 2009-09, Vol.52 (9), p.1881-1888

2009

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Diagnosis of monogenic liver diseases in childhood by next‐generation sequencing

Clinical genetics, 2018-03, Vol.93 (3), p.665-670

2018

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Synergistic Expression of Histone Deacetylase 9 and Matrix Metalloproteinase 12 in M4 Macrophages in Advanced Carotid Plaques

European journal of vascular and endovascular surgery, 2017-05, Vol.53 (5), p.632-640

2017

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A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1

Journal of lipid research, 2010-01, Vol.51 (1), p.182-191

2010

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Schizophrenia shows a unique metabolomics signature in plasma

Translational psychiatry, 2012-08, Vol.2 (8), p.e149-e149

2012

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Fine‐mapping of IgE‐associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project data

Allergy (Copenhagen), 2014-08, Vol.69 (8), p.1077-1084

2014

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Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

Neurology, 2011-11, Vol.77 (20), p.1853

2011

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Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma

Allergy (Copenhagen), 2013-05, Vol.68 (5), p.629-636

2013

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Increased amino acids levels and the risk of developing of hypertriglyceridemia in a 7-year follow-up

Journal of endocrinological investigation, 2014-04, Vol.37 (4), p.369-374

2014

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Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma

Clinical genetics, 2018-07, Vol.94 (1), p.185-186

2018

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Early post-discharge mortality in CAP: frequency, risk factors and a prediction tool

European journal of clinical microbiology & infectious diseases, 2022-04, Vol.41 (4), p.621-630

2022

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Chemokines as risk factors for type 2 diabetes : results from the MONICA/KORA Augsburg study, 1984-2002

Diabetologia, 2006-05, Vol.49 (5), p.921-929

2006

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Pathogen spectrum of community acquired pneumonia in people living with HIV (PLWH) in the German CAPNETZ-Cohort

Infection, 2024-02, Vol.52 (1), p.129-137

2024

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Smokers with COPD Show a Shift in Energy and Nitrogen Metabolism at Rest and During Exercise

International journal of chronic obstructive pulmonary disease, 2020-01, Vol.15, p.1-13

2020

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Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities

Allergy (Copenhagen), 2011-07, Vol.66 (7), p.893-902

2011

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Shift in bacterial etiology from the CAPNETZ cohort in patients with community-acquired pneumonia: data over more than a decade

Infection, 2021-06, Vol.49 (3), p.533-537

2021

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Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact

Allergy (Copenhagen), 2015-10, Vol.70 (10), p.1288-1299

2015

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Evaluation of a multiplex PCR screening approach to identify community-acquired bacterial co-infections in COVID-19: a multicenter prospective cohort study of the German competence network of community-acquired pneumonia (CAPNETZ)

Infection, 2021-12, Vol.49 (6), p.1299-1306

2021

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Genetic variants of the FADS gene cluster are associated with erythrocyte membrane LC PUFA levels in patients with mild cognitive impairment

The Journal of nutrition, health & aging, 2016-06, Vol.20 (6), p.611-620

2016

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Single nucleotide polymorphisms in Wnt signaling and cell death pathway genes and susceptibility to colorectal cancer

Carcinogenesis (New York), 2010-08, Vol.31 (8), p.1381-1386

2010

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KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome

Schizophrenia shows a unique metabolomics signature in plasma

Increased efficacy of omalizumab in atopic dermatitis patients with wild‐type filaggrin status and higher serum levels of phosphatidylcholines

Autoantibodies to zinc transporter 8 and SLC30A8 genotype stratify type 1 diabetes risk

Diagnosis of monogenic liver diseases in childhood by next‐generation sequencing

Synergistic Expression of Histone Deacetylase 9 and Matrix Metalloproteinase 12 in M4 Macrophages in Advanced Carotid Plaques

A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1

Schizophrenia shows a unique metabolomics signature in plasma

Fine‐mapping of IgE‐associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project data

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma

Long-term health sequelae and quality of life at least 6 months after infection with SARS-CoV-2: design and rationale of the COVIDOM-study as part of the NAPKON population-based cohort platform (POP)

Increased amino acids levels and the risk of developing of hypertriglyceridemia in a 7-year follow-up

Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma

Early post-discharge mortality in CAP: frequency, risk factors and a prediction tool

Chemokines as risk factors for type 2 diabetes : results from the MONICA/KORA Augsburg study, 1984-2002

Pathogen spectrum of community acquired pneumonia in people living with HIV (PLWH) in the German CAPNETZ-Cohort

Smokers with COPD Show a Shift in Energy and Nitrogen Metabolism at Rest and During Exercise

Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities

Shift in bacterial etiology from the CAPNETZ cohort in patients with community-acquired pneumonia: data over more than a decade

Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact

Evaluation of a multiplex PCR screening approach to identify community-acquired bacterial co-infections in COVID-19: a multicenter prospective cohort study of the German competence network of community-acquired pneumonia (CAPNETZ)

Genetic variants of the FADS gene cluster are associated with erythrocyte membrane LC PUFA levels in patients with mild cognitive impairment

Single nucleotide polymorphisms in Wnt signaling and cell death pathway genes and susceptibility to colorectal cancer

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