Katharina Wassilew

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

Anne-Karin Arndt, Sebastian Schäfer, Jörg‐Detlef Drenckhahn et al. · The American Journal of Human Genetics · 2013 · 208 citations · Full text

Cardiomyopathy, Genetics, Pathology +5

Human cardiac extracellular matrix supports myocardial lineage commitment of pluripotent stem cells†

Barbara Oberwallner, A Brodarac, Petra Anić et al. · European Journal of Cardio-Thoracic Surgery · 2014 · 61 citations · Full text

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

Marcel Grunert, C. Dorn, Markus Schueler et al. · Human Molecular Genetics · 2014 · 53 citations · Full text

Tof Cases, Genetics, Disease Gene Identification +16

ISHLT consensus document on lung transplantation in patients with connective tissue disease: Part I: Epidemiology, assessment of extrapulmonary conditions, candidate evaluation, selection criteria, and pathology statements

M. Crespo, Erika D. Lease, Amparó Solé et al. · The Journal of Heart and Lung Transplantation · 2021 · 37 citations

Ishlt Consensus Document, Heartlung Transplant, Medicine +4

Peri-operative chemotherapy in the management of resectable colorectal cancer pulmonary metastases

Eliza A. Hawkes, George Ladas, David Cunningham et al. · BMC Cancer · 2012 · 28 citations · Full text