Publications by authors named "Anne Christians"

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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, Lina Werfel, Lukas Wedekind, Anne Christians

Eur J Hum Genet· January 2025

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Diagnostic Yield and Benefits of Whole Exome Sequencing in CAKUT Patients Diagnosed in the First Thousand Days of Life.
Lina Werfel, Helge Martens, Imke Hennies, Ann Christin Gjerstad, Kerstin Fröde, Anne Christians

Kidney Int Rep· November 2023

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Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2.
Anne Christians, Esra Kesdiren, Imke Hennies, Alejandro Hofmann, Mark-Oliver Trowe

Hum Genet· January 2023

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A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.
Alma Osmanovic, Alisa Förster, Maylin Widjaja, Bernd Auber, Anibh M Das, Anne Christians

J Neurol· September 2022

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Rare heterozygous GDF6 variants in patients with renal anomalies.
Helge Martens, Imke Hennies, Maike Getwan, Anne Christians, Anna-Carina Weiss, Arne Christians

Eur J Hum Genet· December 2020

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SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.
Alma Osmanovic, Maylin Widjaja, Alisa Förster, Julia Weder, Mike P Wattjes, Anne Christians

J Neurol· September 2020

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Inflammation-like changes in the urothelium of Lifr-deficient mice and LIFR-haploinsufficient humans with urinary tract anomalies.
Anne Christians, Anna-Carina Weiss, Helge Martens, Maximilian Georg Klopf, Imke Hennies

Hum Mol Genet· May 2020

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FOCAD loss impacts microtubule assembly, G2/M progression and patient survival in astrocytic gliomas.
Frank Brand, Alisa Förster, Anne Christians, Martin Bucher, Carina M Thomé

Acta Neuropathol· January 2020

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