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Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene

PLoS genetics, 2016-03, Vol.12 (3), p.e1005914-e1005914

2016

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Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis

The lancet oncology, 2016-10, Vol.17 (10), p.1363-1373

2016

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Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data

PloS one, 2019-12, Vol.14 (12), p.e0227072-e0227072

2019

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Innovationsunterstützung im BfArM – Erfahrungen aus den Beratungen zu digitalen Gesundheitsanwendungen (DiGA)

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2021, Vol.64 (10), p.1241-1248

2021

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Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

Nature communications, 2019-09, Vol.10 (1), p.4219-10, Article 4219

2019

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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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Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies

Cancer epidemiology, biomarkers & prevention, 2020-02, Vol.29 (2), p.427-433

2020

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Detection of head-to-tail DNA sequences of human bocavirus in clinical samples

PloS one, 2011-05, Vol.6 (5), p.e19457-e19457

2011

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No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study

Clinical gastroenterology and hepatology, 2019-10, Vol.17 (11), p.2227-2235.e1

2019

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A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization

Nature communications, 2021-01, Vol.12 (1), p.246-246, Article 246

2021

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eQTL Set-Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma

Cancer epidemiology, biomarkers & prevention, 2022-09, Vol.31 (9), p.1735-1745

2022

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Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population

Birth defects research. A Clinical and molecular teratology, 2016-02, Vol.106 (2), p.81-87

2016

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Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.822-830

2014

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Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate

Birth defects research. A Clinical and molecular teratology, 2016-09, Vol.106 (9), p.767-772

2016

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Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen

Birth defects research. A Clinical and molecular teratology, 2014-04, Vol.100 (4), p.307-313

2014

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Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

American journal of human genetics, 2014-12, Vol.95 (6), p.698-707

2014

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Author Correction: Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

Nature communications, 2019-12, Vol.10 (1), p.5617-1, Article 5617

2019

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Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population

Birth defects research. A Clinical and molecular teratology, 2014-01, Vol.100 (1), p.43-47

2014

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Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample

American journal of medical genetics. Part A, 2013-10, Vol.161A (10), p.2545-2549

2013

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Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety

Psychiatric genetics, 2017-06, Vol.27 (3), p.96-102

2017

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Genetic estimators of DNA methylation provide insights into the molecular basis of polygenic traits

Translational psychiatry, 2018-01, Vol.8 (1), p.31-13, Article 31

2018

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Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene

Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis

Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

Innovationsunterstützung im BfArM – Erfahrungen aus den Beratungen zu digitalen Gesundheitsanwendungen (DiGA)

Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

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

Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies

Detection of head-to-tail DNA sequences of human bocavirus in clinical samples

No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study

Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis

A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization

eQTL Set-Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma

Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population

Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate

Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen

Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

Author Correction: Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population

Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample

Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety

Genetic estimators of DNA methylation provide insights into the molecular basis of polygenic traits

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