Sabine Schröder

Identification of 27 Novel Variants in Genes COL4A3, COL4A4, and COL4A5 in Lithuanian Families With Alport Syndrome

A. Rolfs, A. Jankauskienė, A. Laurinavičius, 2022, Frontiers in Medicine.

Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome

A. Masood, A. Bertoli-Avella, R. Halwani, 2022, Frontiers in Genetics.

An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

A. Bertoli-Avella, L. Selim, H. Tomoum, 2022, European Journal of Human Genetics.

Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia

Thomas W. Mühleisen, T. Mühleisen, A. Schumann, 2022, Genes.

Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia

Thomas W. Mühleisen, T. Mühleisen, M. Nöthen, 2022, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Clinical Presentation and Genetic Heterogeneity Including Two Novel Variants in Sri Lankan Patients With Infantile Sandhoff Disease

E. Jasinge, Siddiqa Ozaal, Sabine Schröder, 2022, Child neurology open.