K. Hoff

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

M. Hurles, A. McCallion, A. Franco‐Cereceda, 2019, Nature Genetics.

Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.

Gabriele Gillessen-Kaesbach, Dagmar Wieczorek, Na Zhu, 2014, American journal of human genetics.

Rare variants in NR2F2 cause congenital heart defects in humans.

Marc Gewillig, Matthew E Hurles, Reiner Siebert, 2014, American journal of human genetics.

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

Tomas W. Fitzgerald, G. J. Swaminathan, J. Danesh, 2016, Nature Genetics.

DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs

R. Siebert, O. Ammerpohl, H. Kramer, 2019, Clinical Epigenetics.

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

R. Siebert, J. Coselli, K. Devriendt, 2020, bioRxiv.

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

G. J. Swaminathan, M. Hurles, R. Siebert, 2016, American journal of human genetics.

Title 1 Distinct genetic architectures for syndromic and nonsyndromic congenital 2 heart defects identified by exome sequencing 3

Tomas W. Fitzgerald, G. J. Swaminathan, J. Danesh, 2016 .