Helge Martens
4PUBLICATIONS
11CO-AUTHORS
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Publications (4)
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|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
|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
|Jan 21, 2022
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients.Alma Osmanovic, Isabel Gogol, Helge Martens
|Aug 02, 2020
Rare heterozygous GDF6 variants in patients with renal anomalies.Helge Martens, Imke Hennies, Maike Getwan
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Frequent Collaborators
4 joint publications
Ruthild G Weber
2 joint publications
Velibor Tasic
2 joint publications
Dieter Haffner
2 joint publications
Frank Brand
1 joint publications
Alma Osmanovic
1 joint publications
Olivia Schreiber-Katz
1 joint publications
Friedrich Feuerhake
1 joint publications
Gunnar Schmidt
1 joint publications
Robert Geffers
1 joint publications
Laurent Fasano
