Helge Martens

Years Active: 2020-2022
Publications (10 Years): 3

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

Publications

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)
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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