Ruthild G Weber

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Venues

Journal of neurology

Acta neuropathologica

European journal of human genetics : EJHG

Acta neuropathologica communications

This page only lists publications with an associated author ORCID identifier.

Publications

Christine A M Weber, Nicole Krönke, Valery Volk, Bernd Auber, Alisa Förster, Detlef Trost, Robert Geffers, Majid Esmaeilzadeh, Michael Lalk, Arya Nabavi, Amir Samii, Joachim K Krauss, Friedrich Feuerhake, Christian Hartmann, Bettina Wiese, Frank Brand, Ruthild G Weber
Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families. Acta neuropathologica communications 11 (1) (2023)
Alma Osmanovic, Alisa Förster, Maylin Widjaja, Bernd Auber, Anibh M Das, Anne Christians, Frank Brand, Susanne Petri, Ruthild G Weber
A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics. Journal of neurology 269 (9) (2022)
Anne Christians, Esra Kesdiren, Imke Hennies, Alejandro Hofmann, Mark-Oliver Trowe, Frank Brand, Helge Martens, Ann Christin Gjerstad, Zoran Gucev, Matthias Zirngibl, Robert Geffers, Tomáš Seeman, Heiko Billing, Anna Bjerre, Velibor Tasic, Andreas Kispert, Benno Ure, Dieter Haffner, Jens Dingemann, Ruthild G Weber
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2. Human genetics (2022)
Alma Osmanovic, Isabel Gogol, Helge Martens, Maylin Widjaja, Kathrin Müller, Olivia Schreiber-Katz, Friedrich Feuerhake, Claus-Dieter Langhans, Gunnar Schmidt, Peter M Andersen, Albert C Ludolph, Jochen H Weishaupt, Frank Brand, Susanne Petri, Ruthild G Weber
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients. Genes 13 (1) (2021)
Alisa Förster, Frank Brand, Rouzbeh Banan, Robert Hüneburg, Christine A M Weber, Wiebke Ewert, Jessica Kronenberg, Christopher Previti, Natalie Elyan, Ulrike Beyer, Helge Martens, Bujung Hong, Jan H Bräsen, Andreas Erbersdobler, Joachim K Krauss, Martin Stangel, Amir Samii, Stephan Wolf, Matthias Preller, Stefan Aretz, Bettina Wiese, Christian Hartmann, Ruthild G Weber
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin. Acta neuropathologica 142 (1) (2021)
Helge Martens, Imke Hennies, Maike Getwan, Anne Christians, Anna-Carina Weiss, Frank Brand, Ann Christin Gjerstad, Arne Christians, Zoran Gucev, Robert Geffers, Tomáš Seeman, Andreas Kispert, Velibor Tasic, Anna Bjerre, Soeren S Lienkamp, Dieter Haffner, Ruthild G Weber
Rare heterozygous GDF6 variants in patients with renal anomalies. European journal of human genetics : EJHG 28 (12) (2020)

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Publication Activity (10 Years)

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Top Venues

Ruthild G Weber