Marc-Phillip Hitz

发表

Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative

Peter N. Robinson, M. Reijnders, J. Hehir-Kwa, 2019, Front. Genet..

Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease

S. Scherer, A. C. Lionel, C. Marshall, 2012, PLoS genetics.

Genetic regulation of heart valve development: Clinical implications

G. Andelfinger, Marc-Phillip Hitz, T. Brand, 2011 .

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

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

Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms

Masa Umicevic Mirkov, M. Hurles, R. Zwart, 2020, Genetics in Medicine.

Cardiology: Race for healthy hearts

G. Andelfinger, Marc-Phillip Hitz, M. Hitz, 2015, Nature.

Rare variants in NR2F2 cause congenital heart defects in humans.

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

Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes

T. Meitinger, Marc-Phillip Hitz, U. Bauer, 2022, European Journal of Human Genetics.

Fetal Cardiac Troponin Isoforms Rescue the Increased Ca2+ Sensitivity Produced by a Novel Double Deletion in Cardiac Troponin T Linked to Restrictive Cardiomyopathy

J. Potter, G. Andelfinger, Marc-Phillip Hitz, 2011, The Journal of Biological Chemistry.

Levosimendan for bridging in a pediatric patient with Alström syndrome awaiting heart-lung transplantation

A. Wessel, T. M. Yelbuz, Marc-Phillip Hitz, 2008, Clinical Research in Cardiology.

Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier

G. Andelfinger, Marc-Phillip Hitz, S. Yang, 2010, Cardiology in the Young.