Tabea Nöthe-Menchen - Department of General Pediatrics, University Hospital Münster

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论文共 18 篇作者统计合作学者相似作者

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Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

Gerard W. Dougherty,Lawrence E. Ostrowski,Tabea Noethe-Menchen,Johanna Raidt, Andre Schramm,Heike Olbrich,Weining Yin,Patrick R. Sears,Hong Dang,Amanda J. Smith, Achim G. Beule,Rim Hjeij,Niels Rutjes,Eric G. Haarman,Saskia M. Maas,Thomas W. Ferkol,Peadar G. Noone,Kenneth N. Olivier,Diana C. Bracht,Pascal Barbry,Laure-Emmanuelle Zaragosi, Morgane Fierville,Sabine Kliesch,Kai Wohlgemuth, Julia Koenig, Sebastian George,Niki T. Loges,Agathe Ceppe,Matthew R. Markovetz,Hong Luo,Ting Guo,Hoda Rizk,Tarek Eldesoky, Katrin Dahlke,Karsten Boldt,Marius Ueffing,David B. Hill,Yuan-Ping Pang,Michael R. Knowles,Maimoona A. Zariwala,Heymut Omran

AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEno. 1 (2024): 63-76

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Analyses of 1,236 Genotyped Primary Ciliary Dyskinesia Individuals Identify Regional Clusters of Distinct DNA Variants and Significant Genotype-Phenotype Correlations

Johanna Raidt,Sarah Riepenhausen,Petra Pennekamp, Heike Olbrich,Israel Amirav, Rodrigo Athanázio,Micha Aviram,Juan E. Balinotti, O. Baron,Sebastian Bode,Mieke Boon,Melissa Borrelli, S.B. Carr,Suzanne Crowley,Eleonora Dehlink, Sandra Diepenhorst,Peter Ďurdík,Bernd Dworniczak,Nagehan Emiralioğlu,Ela Erdem Eralp,Rossella Fonnesu,Serena Gracci,Jörg Große-Onnebrink, Karolina Gwozdziewicz,Eric G. Haarman, C.R. Hansen,Claire Hogg,Mathias Geldermann Holgersen,Eitan Kerem, Rebecca Körner,Karsten Kötz,Panayiotis Kouis, Michael R. Loebinger,Natalie Lorent,Jane S. Lucas,Debora Maj, Marcus Mall,June K. Marthin,Vendula Martinů,Henryk Mazurek,Hannah M. Mitchison,Tabea Nöthe-Menchen,U. Özçelik,Massimo Pifferi,Andrzej Pogorzelski,Felix C. Ringshausen,Jobst Roehmel,Sandra Rovira‐Amigo,Nisreen Rumman,Anne Schlegtendal, Amelia Shoemark,Synne Sperstad Kennelly,Ben O. Staar,Sivagurunathan Sutharsan,Simon Thomas,Nicola Ullmann,Julian Varghese,Sandra von Hardenberg,Woolf T. Walker,Martin Wetzke, Michał Witt,Panayiotis Yiallouros,Anna Zschocke,Ewa Ziętkiewicz,Kim G. Nielsen,Heymut Omran

European respiratory journal/The European respiratory journalpp.2301769-2301769, (2024)

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Analyses of 1,236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations

Johanna Raidt,Sarah Riepenhausen,Petra Pennekamp,Heike Olbrich,Israel Amirav,Rodrigo A Athanazio,Micha Aviram,Juan E Balinotti,Ophir Bar-On, Sebastian Fn Bode,Mieke Boon,Melissa Borrelli,Siobhan B Carr,Suzanne Crowley,Eleonora Dehlink, Sandra Diepenhorst,Peter Durdik,Bernd Dworniczak,Nagehan Emiralioğlu,Ela Erdem,Rossella Fonnesu,Serena Gracci,Jörg Große-Onnebrink, Karolina Gwozdziewicz,Eric G Haarman,Christine R Hansen,Claire Hogg,Mathias G Holgersen,Eitan Kerem,Robert W Körner,Karsten Kötz,Panayiotis Kouis,Michael R Loebinger,Natalie Lorent,Jane S Lucas,Debora Maj,Marcus A Mall,June K Marthin,Vendula Martinu,Henryk Mazurek,Hannah M Mitchison,Tabea Nöthe-Menchen,Ugur Özçelik,Massimo Pifferi,Andrzej Pogorzelski,Felix C Ringshausen,Jobst F Roehmel,Sandra Rovira-Amigo,Nisreen Rumman,Anne Schlegtendal,Amelia Shoemark,Synne Sperstad Kennelly,Ben O Staar,Sivagurunathan Sutharsan,Simon Thomas,Nicola Ullmann,Julian Varghese,Sandra von Hardenberg,Woolf T Walker,Martin Wetzke,Michal Witt,Panayiotis Yiallouros,Anna Zschocke,Ewa Ziętkiewicz,Kim G Nielsen,Heymut Omran

The European respiratory journal (2024)

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Primary Ciliary Dyskinesia Genotypes Vary Markedly Across 19 Countries and Identify Significant Genotype-Phenotype Correlations

Johanna Raidt,Sarah Riepenhausen,Petra Pennekamp, Heike Olbrich, Israel Amirav, Rodrigo A. Athanazio, Juan E. Balinotti,Ophir Bar-On, Sebastian Bode,Mieke Boon, Melissa Borrelli,Siobhán B. Carr, Suzanne Crowley, Eleonora Dehlink, Peter Durdik,Bernd Dworniczak,Nagehan Emiralioğlu,Ela Erdem, Rossella Fonnesu,Serena Gracci,Jörg Große-Onnebrink, Karolina Gwozdziewicz,Eric G. Haarman, Christine R. Hansen,Claire Hogg, Mathias Geldermann Holgersen,Eitan Kerem, Robert W. Körner, Karsten Kötz,Panayiotis Kouis, Michael Loebinger, N Lorent,Jane Lucas, Debora Maj,Marcus A. Mall, June K. Marthin, Vendula Martinu,Henryk Mazurek,Hannah M. Mitchison,Tabea Nöthe-Menchen, Ugur Özçelik,Massimo Pifferi,Andrzej Pogorzelski,Felix Ringshausen,Jobst Roehmel,Sandra Rovira-Amigo,Nisreen Rumman,Anne Schlegtendal, Amelia Shoemark, Synne Sperstad Kennelly, Ben O. Staar,Sivagurunathan Sutharsan, N. Simon Thomas,Nicola Ullmann,Julian Varghese,Sandra von Hardenberg, Woolf T. Walker, Martin Wetzke, Michal Witt,Panayiotis K. Yiallouros, Anna Zschocke,Ewa Ziętkiewicz,Kim G. Nielsen,Heymut Omran

crossref（2023）

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Genetische Und Diagnostische Charakterisierung Einer Großen Israelischen PCD-Kohorte – Notwendigkeit Der Geografischen Anpassungen Der Aktuellen Diagnostischen Leitlinien

Johanna Raidt,Niki T. Loges,Israel Amirav,Sarah Sandmann,Henrike Krenz,Revital Abitbul,Moran Lavie, Huda Mussafi,Avigdor Mandelberg, Alexander Wolter,Gerard W. Dougherty,Tabea Nöthe-Menchen,Julia Wallmeier,Sandra Cindric,Claudius Werner,Petra Pennekamp,Bernd Dworniczak,Miriam Schmidts,Heike Olbrich,Martin Dugas,Heymut Omran

Klinische Pädiatrie 44 Jahrestagung der Gesellschaft für Pädiatrische Pneumologie (2023)

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Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia

Rim Hjeij,Isabella Aprea,Marco Poeta,Tabea Noethe-Menchen,Diana Bracht,Johanna Raidt, Barbara I. Honecker,Gerard W. Dougherty,Heike Olbrich,Oliver Schwartz,Ulrike Keller,Harald Nuesse,Karin E. M. Diderich,Christian Vogelberg,Francesca Santamaria,Heymut Omran

Genetics in medicine : official journal of the American College of Medical Genetics（2023）

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Pathogenic gene variants in CCDC39 , CCDC40 , RSPH1 , RSPH9 , HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility

I Aprea, A Wilken,C Krallmann,T Nöthe-Menchen,H Olbrich,N T Loges,G W Dougherty,D Bracht,C Brenker,S Kliesch,T Strünker,F Tüttelmann,J Raidt,H Omran

Front Genet（2023）

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Genetic and diagnostic Characterization of a large Israeli PCD Cohort - Need for geographic Adjustments of current diagnostic Guidelines

Raidt Johanna,Loges T. Niki,Amirav Israel,Sandmann Sarah,Krenz Henrike,Abitbul Revital,Lavie Moran, Mussafi Huda,Mandelberg Avigdor, Wolter Alexander,Dougherty W. Gerard,Noethe-Menchen Tabea,Wallmeier Julia,Cindric Sandra,Werner Claudius,Pennekamp Petra,Dworniczak Bernd,Schmidts Miriam,Olbrich Heike,Dugas Martin,Omran Heymut

KLINISCHE PADIATRIEno. 02 (2023): 123-123

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Motility Of Efferent Duct Cilia Aids Passage Of Sperm Cells Through The Male Reproductive System

I Aprea,T Nöthe-Menchen,G W Dougherty,J Raidt,N T Loges, T Kaiser,J Wallmeier,H Olbrich,T Strünker,S Kliesch,P Pennekamp,H Omran

MOLECULAR HUMAN REPRODUCTION（2021）

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