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Henry Oppermann

11PUBLICATIONS

46CO-AUTHORS

Cellular nervous systemEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesBiologically active moleculesFood properties (incl. characteristics and health benefits)

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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

Frequent Collaborators

4 joint publications

Claudia Birkemeyer

4 joint publications

Frank Gaunitz

3 joint publications

Konrad Platzer

2 joint publications

Johannes R Lemke

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