Lehrstuhl für Humangenetik


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

Deletion 7q31.2q31.31 segregating in a family with speech and language deficiencies (2020) Rieger M, Krumbiegel M, Reuter M, Schützenberger A, Reis A, Zweier C Conference contribution A case of autosomal recessive spinocerebellar ataxia type 18 with a novel mutation in GRID2 (2020) Hetzelt K, Kraus C, Kusnik S, Thiel C, Ekici AB, Reis A, Zweier C Conference contribution Enriched environment ameliorates adult hippocampal neurogenesis deficits in Tcf4 haploinsufficient mice (2020) Braun K, Häberle B, Wittmann MT, Lie DC Journal article Loss of PHF6 leads to aberrant development of human neuron-like cells (2020) Fliedner A, Gregor A, Ferrazzi F, Ekici AB, Sticht H, Zweier C Journal article Unique signatures of stress-induced senescent human astrocytes (2020) Simmnacher K, Krach F, Schneider Y, Alecu JE, Mautner L, Klein P, Roybon L, et al. Journal article Author Correction: A monocyte gene expression signature in the early clinical course of Parkinson’s disease (Scientific Reports, (2018), 8, 1, (10757), 10.1038/s41598-018-28986-7) (2020) Schlachetzki J, Prots I, Tao J, Chun HB, Saijo K, Gosselin D, Winner B, et al. Journal article, Erratum Intracellular A53T Mutant α-Synuclein Impairs Adult Hippocampal Newborn Neuron Integration (2020) Regensburger M, Stemick J, Masliah E, Kohl Z, Winner B Journal article PERIPHERAL PULSE MEASUREMENTS FOR THE DETECTION OF SILENT ATRIAL FIBRILLATION: RESULTS FROM THE PROSPECTIVE, CONTROLLED TRIAL "KNOW YOUR PULSE POST STROKE" (2020) Kallmünzer B, Macha K, Wang R, Siedler G, Stoll S, Marsch A, Gerner S, et al. Conference contribution MANAGEMENT OF INSUFFICIENT FUNCTIONAL ANTITHROMBOTIC ACTIVITY DURING TREATMENT WITH DIRECT ORAL ANTICOAGULANTS FOR STROKE PREVENTION (2020) Macha K, Stoll S, Siedler G, Volbers B, Strasser E, Schwab S, Kallmünzer B Conference contribution Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND) (2020) Vera G, Sorlin A, Delplancq G, Lecoquierre F, Brasseur-Daudruy M, Petit F, Smol T, et al. Journal article