Ruthild G Weber

7PUBLICATIONS
13CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Predictive and prognostic markersCancer geneticsNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (7)

|Oct 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

Esra Kesdiren, Helge Martens, Frank Brand

|Nov 22, 2023
Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families.

Christine A M Weber, Nicole Krönke, Valery Volk

|Sep 06, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2.

Anne Christians, Esra Kesdiren, Imke Hennies

|May 03, 2022
A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.

Alma Osmanovic, Alisa Förster, Maylin Widjaja

|Jan 21, 2022
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients.

Alma Osmanovic, Isabel Gogol, Helge Martens

|Apr 30, 2021
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin.

Alisa Förster, Frank Brand, Rouzbeh Banan

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Frequent Collaborators

4 joint publications

Helge Martens

4 joint publications

Frank Brand

2 joint publications

Velibor Tasic

2 joint publications

Dieter Haffner