Helge Martens
Overview
Explore the profile of Helge Martens including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
98
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0
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Recent Articles
1.
Hartelt T, Martens H
Front Psychol
. 2024 Nov;
15:1450947.
PMID: 39502150
Self-regulatory and metacognitive instruction regarding student conceptions can help students become metacognitively (or more specifically, metaconceptually) aware of their conceptions and self-regulate their intuitive conceptions in scientific contexts when they...
2.
Brunkhorst M, Brunkhorst L, Martens H, Papizh S, Besouw M, Grasemann C, et al.
Kidney Int
. 2024 Oct;
107(1):116-129.
PMID: 39461557
Pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter 2a and 2c are rare causes of phosphate wasting. Since data on presentation and outcomes are scarce, we collected clinical, biochemical...
3.
Kesdiren E, Martens H, Brand F, Werfel L, Wedekind L, Trowe M, et al.
Eur J Hum Genet
. 2024 Oct;
33(1):44-55.
PMID: 39420202
Around 180 genes have been associated with congenital anomalies of the kidney and urinary tract (CAKUT) in mice, and represent promising novel candidate genes for human CAKUT. In whole-exome sequencing...
4.
Werfel L, Martens H, Hennies I, Gjerstad A, Frode K, Altarescu G, et al.
Kidney Int Rep
. 2023 Nov;
8(11):2439-2457.
PMID: 38025229
Introduction: Congenital anomalies of the kidney and urinary tract (CAKUT) are the predominant cause of chronic kidney disease (CKD) and the need for kidney replacement therapy (KRT) in children. Although...
5.
Christians A, Kesdiren E, Hennies I, Hofmann A, Trowe M, Brand F, et al.
Hum Genet
. 2022 Sep;
142(1):73-88.
PMID: 36066768
Most patients with congenital anomalies of the kidney and urinary tract (CAKUT) remain genetically unexplained. In search of novel genes associated with CAKUT in humans, we applied whole-exome sequencing in...
6.
Osmanovic A, Gogol I, Martens H, Widjaja M, Muller K, Schreiber-Katz O, et al.
Genes (Basel)
. 2022 Jan;
13(1).
PMID: 35052424
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by progressive upper and lower motor neuron (LMN) loss. As ALS and other neurodegenerative diseases share genetic risk factors, we...
7.
Forster A, Brand F, Banan R, Huneburg R, Weber C, Ewert W, et al.
Acta Neuropathol
. 2021 Apr;
142(1):191-210.
PMID: 33929593
The genetic basis of brain tumor development is poorly understood. Here, leukocyte DNA of 21 patients from 15 families with ≥ 2 glioma cases each was analyzed by whole-genome or...
8.
Martens H, Hennies I, Getwan M, Christians A, Weiss A, Brand F, et al.
Eur J Hum Genet
. 2020 Aug;
28(12):1681-1693.
PMID: 32737436
Although over 50 genes are known to cause renal malformation if mutated, the underlying genetic basis, most easily identified in syndromic cases, remains unsolved in most patients. In search of...
9.
Christians A, Weiss A, Martens H, Klopf M, Hennies I, Haffner D, et al.
Hum Mol Genet
. 2020 Mar;
29(7):1192-1204.
PMID: 32179912
Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of end-stage kidney disease in children. While the genetic aberrations underlying CAKUT pathogenesis are increasingly being...
10.
Beyer U, Brand F, Martens H, Weder J, Christians A, Elyan N, et al.
Acta Neuropathol
. 2017 Oct;
134(6):905-922.
PMID: 29030706
In search of novel germline alterations predisposing to tumors, in particular to gliomas, we studied a family with two brothers affected by anaplastic gliomas, and their father and paternal great-uncle...