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Translational Psychiatry|July 5, 2025
Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disordersLydia M Federmann, Lisa Sindermann, Sabrina Primus, et al.Neurological Research|March 7, 2022
SPG11: clinical and genetic features of seven Czech patients and literature reviewKristyna Doleckova, Jan Roth, Julia Stellmachova, et al.Parkinsonism & Related Disorders|October 2, 2022
ACTB gene mutation in combined Dystonia-Deafness syndrome with parkinsonism: Expanding the phenotype and highlighting the long-term GPi DBS outcomeGiulia Straccia, Chiara Reale, Massimo Castellani, et al.Sleep Medicine|April 30, 2022
ExomeChip-based rare variant association study in restless legs syndromeErik Tilch, Barbara Schormair, Chen Zhao, et al.Pharmaceutics|January 21, 2023
Identification of Autophagy as a Functional Target Suitable for the Pharmacological Treatment of Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN) In VitroEnrica Zanuttigh, Kevork Derderian, Miriam A Güra, et al.Clinical Epigenetics|February 16, 2024
Epigenome-wide association study of dietary fatty acid intakeJulia Lange de Luna, Aayah Nounu, Sonja Neumeyer, et al.Frontiers in Neurology|April 15, 2026
Beyond SGCE: expanding the clinical and molecular spectrum of KCTD17- and KCNN2-related myoclonus-dystoniaMagdalena Krygier, Emilia J Sitek, Magdalena Chylińska, et al.Neurogenetics|January 15, 2008
Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13David Kemlink, Giuseppe Plazzi, Roberto Vetrugno, et al.Journal of Medical Genetics|May 17, 2011
MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal diseaseBarbara Schormair, Jens Plag, Maria Kaffe, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2007
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndromeJuliane Winkelmann, Peter Lichtner, Barbara Schormair, et al.Pageof 33