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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Cellular models and therapeutic perspectives in hypertrophic cardiomyopathyGökhan Yigit, Bernd WollnikAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Hallermann-Streiff syndrome: A missing molecular link for a highly recognizable syndromeJulia Schmidt, Bernd WollnikSeminars in Cell & Developmental Biology|December 22, 2015
Altered FGF signalling in congenital craniofacial and skeletal disordersShahida Moosa, Bernd WollnikFrontiers in Molecular Neuroscience|August 21, 2018
Mutational Landscapes and Phenotypic Spectrum of SWI/SNF-Related Intellectual Disability DisordersNina Bögershausen, Bernd WollnikMedizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 10, 2025
Understanding inherited cardiomyopathies: clinical aspects and genetic determinantsGökhan Yigit, Silke Kaulfuß, Bernd WollnikDeutsche Medizinische Wochenschrift (1946)|April 29, 2017
[Genetic diagnostics for cardiomyopathies]Frauke Czepluch, Bernd Wollnik, Gerd HasenfußClinical Genetics|August 30, 2020
Premature aging disorders: A clinical and genetic compendiumFranziska Schnabel, Uwe Kornak, Bernd WollnikESC Heart Failure|February 20, 2018
Genetic determinants of heart failure: facts and numbersFrauke S Czepluch, Bernd Wollnik, Gerd HasenfußEuropean Journal of Medical Genetics|September 1, 2023
B3GALT6-linkeropathy: Three illustrative patients spanning the disease spectrumKimberly Christine Coetzer, Jost Dieckerhoff, Bernd Wollnik, et al.Clinical Genetics|June 7, 2022
Progressive frontal intraosseous lipoma: Detection of the mosaic AKT1 variant discloses Proteus syndromeJulia Schmidt, Felix Bremmer, Knut Brockmann, et al.Pageof 17