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Tabea Nöthe-Menchen

Observed names: T Nöthe-Menchen, T. Noethe-Menchen, T. Nöthe-Menchen
ORCID: 0000-0002-0571-6767
Observed ORCID: 0000-0002-0571-6767
OpenAlex ID: A5042055686
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry
2019 · Julia Wallmeier, Diana Frank, et al. · The American Journal of Human Genetics · 214
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Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects
2018 · Niki T. Loges, Dinu Antony, et al. · The American Journal of Human Genetics · 144
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CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module
2020 · Gerard W. Dougherty, Katsutoshi Mizuno, et al. · Nature Communications · 88
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Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility
2021 · Isabella Aprea, Johanna Raidt, et al. · PLoS Genetics · 86
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Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility
2018 · Asaf Ta-Shma, Rim Hjeij, et al. · PLoS Genetics · 81
Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype–phenotype correlations
2024 · Johanna Raidt, Sarah Riepenhausen, et al. · European Respiratory Journal · 73
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Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms
2018 · Inga M. Höben, Rim Hjeij, et al. · The American Journal of Human Genetics · 71
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Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system
2021 · Isabella Aprea, Tabea Nöthe-Menchen, et al. · Molecular Human Reproduction · 69
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Randomization of Left-Right Asymmetry and Congenital Heart Defects
2019 · Tabea Nöthe-Menchen, Julia Wallmeier, et al. · Circulation Genomic and Precision Medicine · 53
Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility
2023 · I. Aprea, A. Wilken, et al. · Frontiers in Genetics · 35
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis
2024 · Gerard W Dougherty, Lawrence E Ostrowski, et al. · American Journal of Respiratory and Critical Care Medicine · 14
Pathogenic variants in CLXN encoding the outer dynein arm docking–associated calcium-binding protein calaxin cause primary ciliary dyskinesia
2023 · Rim Hjeij, Isabella Aprea, et al. · Genetics in Medicine · 13
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miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary Disassembly
2022 · Merit Wildung, Christian Herr, et al. · International Journal of Molecular Sciences · 7
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The international primary ciliary dyskinesia (PCD) registry reports genotype/phenotype-correlations
2021 · Johanna Raidt, Petra Pennekamp, et al. · 3
Rezessiv vererbter Mangel an sekretorischem WFDC2 (HE4) verursacht Nasenpolypen und Bronchiektasen
2025 · G W Dougherty, T Nöthe-Menchen, et al. · Klinische Pädiatrie
The international registry for primary ciliary dyskinesia reveals regional variation of genotypes and significant genotype-phenotype correlations
2024 · Johanna Raidt, Sarah Riepenhausen, et al.
Late Breaking Abstract - Recessively inherited deficiency of secreted WFDC2 (HE4) causes nasal polyposis and bronchiectasis
2024 · Gerard Dougherty, Lawrence E Ostrowski, et al.
Genetische und diagnostische Charakterisierung einer großen israelischen PCD-Kohorte – Notwendigkeit der geografischen Anpassungen der aktuellen diagnostischen Leitlinien?
2023 · Johanna Raidt, Niki T. Loges, et al. · Klinische Pädiatrie
Primary Ciliary Dyskinesia Genotypes Vary Markedly Across 19 Countries and Identify Significant Genotype-Phenotype Correlations
2023 · Johanna Raidt, Sarah Riepenhausen, et al. · SSRN Electronic Journal
Recessive DNAH9 Loss-of-Function Mutations Cause Absence of ODAs Type 2 and Only Subtle Respiratory Ciliary Beating Defects
2019 · H. Omran, I.M. Hoeben, et al.
Works count: 20
Citation count: 951
H-index: 12
I10-index: 12
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