C. Dorn

发表

Outlier-Based Identification of Copy Number Variations Using Targeted Resequencing in a Small Cohort of Patients with Tetralogy of Fallot

Vikas Bansal, Marcel Grunert, Roland Hetzer, 2014, PloS one.

Application of high-throughput sequencing for studying genomic variations in congenital heart disease.

S. Sperling, Marcel Grunert, C. Dorn, 2014, Briefings in functional genomics.

Response of Patient-Derived Non-Small Cell Lung Cancer Xenografts to Classical and Targeted Therapies Is Not Related to Multidrug Resistance Markers

I. Fichtner, J. Rolff, C. Dorn, 2009, Journal of Oncology.

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.

Wei Chen, I. Dunkel, S. Sperling, 2016, Cardiovascular research.

Chemoresistance in non-small-cell lung cancer: can multidrug resistance markers predict the response of xenograft lung cancer models to chemotherapy?

I. Fichtner, J. Rolff, G. Leschber, 2011, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Human Genetics of Tetralogy of Fallot and Double Outlet Right Ventricle

A. Perrot, C. Dorn, S. Rickert-Sperling, 2016 .

Muscle-relevant genes marked by stable H3K4me2/3 profiles and enriched MyoD binding during myogenic differentiation

V. Bansal, Barbora Malecova, Wei Chen, 2017, PloS one.

Cardiac Transcription Factors and Regulatory Networks.

Marcel Grunert, C. Dorn, S. Rickert-Sperling, 2024, Advances in experimental medicine and biology.

Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.

R. Hetzer, B. Timmermann, M. Schueler, 2014, Human molecular genetics.

Technologies to study genetics and molecular pathways

A. Dopazo, E. Lara-Pezzi, A. Gatto, 2016 .

Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.

R. Hetzer, B. Timmermann, M. Schueler, 2014, Human molecular genetics.