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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 15, 2019
Germline GPR161 Mutations Predispose to Pediatric MedulloblastomaMatthias Begemann, Sebastian M Waszak, Giles W Robinson, et al.
Neuroprotection|October 15, 2024
Tolerability and first hints for potential efficacy of motor-cognitive training under inspiratory hypoxia in health and neuropsychiatric disorders: A translational viewpointSvea-Solveig Mennen, Maren Franta, Martin Begemann, et al.
Frontiers in Immunology|January 2, 2023
Dissecting CD8+ T cell pathology of severe SARS-CoV-2 infection by single-cell immunoprofilingFelix Schreibing, Monica T Hannani, Hyojin Kim, et al.
Annals of Neurology|April 12, 2019
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonismAna Westenberger, Charles Jourdan Reyes, Gerard Saranza, et al.
Molecular Psychiatry|February 11, 2018
Uncoupling the widespread occurrence of anti-NMDAR1 autoantibodies from neuropsychiatric disease in a novel autoimmune modelHong Pan, Bárbara Oliveira, Gesine Saher, et al.
Brain : a Journal of Neurology|June 6, 2018
Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain developmentMichael S Nahorski, Sateesh Maddirevula, Ryosuke Ishimura, et al.
Blood|February 27, 2026
MDM4 HAPLOINSUFFICIENCY LEADS TO P53-MEDIATED BONE MARROW FAILURERicha Sharma, Senthil Velan Bhoopalan, Robert Meyer, et al.
European Journal of Human Genetics : EJHG|October 29, 2015
Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counselingThomas Eggermann, Frédéric Brioude, Silvia Russo, et al.
Archives of General Psychiatry|September 8, 2010
Modification of cognitive performance in schizophrenia by complexin 2 gene polymorphismsMartin Begemann, Sabrina Grube, Sergi Papiol, et al.
European Journal of Human Genetics : EJHG|December 16, 2018
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number studySorina M Papuc, Lucia Abela, Katharina Steindl, et al.
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