Benedikt Reiz

Ratzeburger Allee 160
Luebeck, SH 23538, Germany

Last Updated: 09/26/2026

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Found 15 publications

Analysis of candidate genes for cleft lip ± cleft palate using murine single-cell expression data.

Analysis of candidate genes for cleft lip ± cleft palate using murine single-cell expression data.

Journal: Frontiers in cell and developmental biology

Published: November 07, 2022

Alveolar macrophages in early stage COPD show functional deviations with properties of impaired immune activation.

Alveolar macrophages in early stage COPD show functional deviations with properties of impaired immune activation.

Journal: Frontiers in immunology

Published: April 10, 2022

Human variation in population-wide gene expression data predicts gene perturbation phenotype.

Human variation in population-wide gene expression data predicts gene perturbation phenotype.

Journal: iScience

Published: March 02, 2022

A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A.

A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A.

Journal: Scientific reports

Published: January 31, 2018

A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors.

A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors.

Journal: Scientific reports

Published: March 16, 2017

Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression.

Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression.

Journal: Human molecular genetics

Published: March 02, 2017

New NR5A1 mutations and phenotypic variations of gonadal dysgenesis.

New NR5A1 mutations and phenotypic variations of gonadal dysgenesis.

Journal: PloS one

Published: January 17, 2017

Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.

Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.

Journal: Human genetics

Published: November 16, 2016

Novel Insights into 46,XY Disorders of Sex Development due to NR5A1 Gene Mutation.

Novel Insights into 46,XY Disorders of Sex Development due to NR5A1 Gene Mutation.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: September 30, 2015

Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.

Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: May 05, 2015

46,XY Gonadal Dysgenesis due to a Homozygous Mutation in Desert Hedgehog (DHH) Identified by Exome Sequencing.

46,XY Gonadal Dysgenesis due to a Homozygous Mutation in Desert Hedgehog (DHH) Identified by Exome Sequencing.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 01, 2015

Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.

Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.

Journal: European journal of human genetics : EJHG

Published: December 17, 2014

Showing 1-12 of 15

Last Updated: 09/26/2026