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Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany

Nature communications, 2020-11, Vol.11 (1), p.5829-5829, Article 5829

2020

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Familial occurrence of systemic mast cell activation disease

PloS one, 2013-09, Vol.8 (9), p.e76241-e76241

2013

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A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

Nature genetics, 2015-12, Vol.47 (12), p.1443-1448

2015

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Breakthroughs in the genetics of orofacial clefting

Trends in molecular medicine, 2011-12, Vol.17 (12), p.725-733

2011

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

American journal of human genetics, 2016-08, Vol.99 (2), p.337-351

2016

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Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells

Cell stem cell, 2012-04, Vol.10 (4), p.473-479

2012

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Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

The Journal of clinical investigation, 2015-08, Vol.125 (8), p.3132-3146

2015

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Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

American journal of human genetics, 2011-06, Vol.88 (6), p.788-795

2011

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Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness

PloS one, 2021-09, Vol.16 (9), p.e0256846-e0256846

2021

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Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

Nature genetics, 2017-05, Vol.49 (5), p.789-794

2017

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Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations

Nature communications, 2017-08, Vol.8 (1), p.266-10, Article 266

2017

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High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

Neuron (Cambridge, Mass.), 2011-12, Vol.72 (6), p.951-963

2011

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Nature genetics, 2008-03, Vol.40 (3), p.329-334

2008

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Hypomorphic Mutations in PGAP2, Encoding a GPI-Anchor-Remodeling Protein, Cause Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2013-04, Vol.92 (4), p.575-583

2013

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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Nature genetics, 2011-12, Vol.43 (12), p.1224-1227

2011

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Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only

Human molecular genetics, 2017-02, Vol.26 (4), p.829-842

2017

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genome-wide association study of alcohol dependence

Proceedings of the National Academy of Sciences - PNAS, 2010-03, Vol.107 (11), p.5082-5087

2010

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Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study

PloS one, 2019-11, Vol.14 (11), p.e0225521-e0225521

2019

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A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study

PloS one, 2019-08, Vol.14 (8), p.e0221252

2019

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Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III

American journal of human genetics, 2006-12, Vol.79 (6), p.1098-1104

2006

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Dihydropyrimidine Dehydrogenase Testing prior to Treatment with 5-Fluorouracil, Capecitabine, and Tegafur: A Consensus Paper

Oncology research and treatment, 2020-11, Vol.43 (11), p.628-636

2020

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Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy

Nature communications, 2017-10, Vol.8 (1), p.1056-10, Article 1056

2017

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Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification-Results of the Heinz Nixdorf Recall study

PloS one, 2020-05, Vol.15 (5), p.e0232735

2020

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Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy

PLoS genetics, 2015-03, Vol.11 (3), p.e1005024-e1005024

2015

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Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families

Journal of medical genetics, 2013-11, Vol.50 (11), p.760-764

2013

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Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany

Familial occurrence of systemic mast cell activation disease

A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

Breakthroughs in the genetics of orofacial clefting

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Hypomorphic Mutations in PGAP2, Encoding a GPI-Anchor-Remodeling Protein, Cause Autosomal-Recessive Intellectual Disability

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only

genome-wide association study of alcohol dependence

Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study

A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study

Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III

Dihydropyrimidine Dehydrogenase Testing prior to Treatment with 5-Fluorouracil, Capecitabine, and Tegafur: A Consensus Paper

Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy

Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification-Results of the Heinz Nixdorf Recall study

Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy

Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families

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