Henry Oppermann
11PUBLICATIONS
46CO-AUTHORS
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Publications (11)
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|Mar 25, 2024
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly.Charlotte Herbst, Viktoria Bothe, Meret Wegler
|Aug 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.Henry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss
|May 15, 2023
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals.Henrike L Sczakiel, Max Zhao, Brigitte Wollert-Wulf
|Feb 09, 2023
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.Afshin Saffari, Tracy Lau, Homa Tajsharghi
|May 28, 2022
Viability of Glioblastoma Cells and Fibroblasts in the Presence of Imidazole-Containing Compounds.Elisabeth Christiane Seidel, Claudia Birkemeyer, Rainer Baran-Schmidt
|Apr 23, 2022
The Relation of Surgical Procedures and Diagnosis Groups to Unplanned Readmission in Spinal Neurosurgery: A Retrospective Single Center Study.Caroline Sander, Henry Oppermann, Ulf Nestler
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Frequent Collaborators
4 joint publications
Claudia Birkemeyer
4 joint publications
Frank Gaunitz
3 joint publications
Konrad Platzer
2 joint publications
Johannes R Lemke
1 joint publications
Ulf Nestler
1 joint publications
Michael Karl Fehrenbach
1 joint publications
Tim Wende
1 joint publications
Tracy Lau
1 joint publications
Stephanie Efthymiou
1 joint publications
Whalen Sandra
