Moneef Shoukier - Georg-August-Universitat Gottingen

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论文共 52 篇作者统计合作学者相似作者

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De Novo Heterozygous Missense Variants in CELSR1 As Cause of Fetal Pleural Effusions and Progressive Fetal Hydrops

Maayke A. de Koning, Paula A. Pimienta Ramirez,Monique C. Haak,Xiao Han, Martina H. A. Ruiterkamp-Versteeg,Nicole de Leeuw,Ulrich A. Schatz,Moneef Shoukier,Esther Rieger-Fackeldey,Javier U. Ortiz,Sjoerd G. van Duinen,Willemijn M. Klein,Ruben S. G. M. Witlox,Richard H. Finnell,Gijs W. E. Santen,Yunping Lei,Manon Suerink

JOURNAL OF MEDICAL GENETICSno. 6 (2024): 549-552

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Prenatal Diagnosis of Fryns Syndrome Through Identification of Two Novel Splice Variants in the PIGN Gene—A Case Series

Aruna Marchetto, Susanne Leidescher, Theresia van Hoi, Niklas Hirschberger, Florian Vogel,Siegmund Koehler,Ivonne Alexandra Bedei,Roland Axt-Fliedner,Moneef Shoukier,Corinna Keil

LIFE-BASELno. 5 (2024)

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Dysregulation of FLVCR1a-dependent Mitochondrial Calcium Handling in Neural Progenitors Causes Congenital Hydrocephalus

Francesca Bertino,Dibyanti Mukherjee,Massimo Bonora, Christoph Bagowski,Jeannette Nardelli, Livia Metani, Diletta Isabella Zanin Venturini,Diego Chianese,Nicolas Santander,Iris Chiara Salaroglio,Andreas Hentschel,Elisa Quarta,Tullio Genova,Arpana Arjun Mckinney,Anna Lucia Allocco,Veronica Fiorito,Sara Petrillo,Giorgia Ammirata,Francesco De Giorgio,Evan Dennis,Garrett Allington, Felicitas Maier,Moneef Shoukier,Karl-Philipp Gloning,Luca Munaron,Federico Mussano,Ettore Salsano,Davide Pareyson, Maja di Rocco,Fiorella Altruda, Georgia Panagiotakos,Kristopher T. Kahle,Pierre Gressens,Chiara Riganti,Paolo P. Pinton,Andreas Roos,Thomas Arnold,Emanuela Tolosano,Deborah Chiabrando

Cell Reports Medicineno. 7 (2024): 101647-101647

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Supplementary Figure Legends 1-7 from Pathways of Proliferation and Antiapoptosis Driven in Breast Cancer Stem Cells by Stem Cell Protein Piwil2

Jae Ho Lee,Cornelia Jung,Parisa Javadian-Elyaderani,Stefan Schweyer,Dorothea Schütte,Moneef Shoukier,Feridoun Karimi-Busheri,Michael Weinfeld,Aghdass Rasouli-Nia,Jan G. Hengstler,Alejandra Mantilla,Hamid Reza Soleimanpour-Lichaei,Wolfgang Engel,Craig N. Robson,Karim Nayernia

crossref（2023）

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BCORL1 variant in two male fetuses with multiple ultrasonographic abnormalities

Rebecca Gembicki,Jan Weichert,Moneef Shoukier,Inga Nagel,Malte Spielmann,Irina Huening

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 242-243

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Cfdna Mit Verdacht Auf XXX Bei Einem Weiblichen Feten Mit Zytogenetisch Diagnostizierter Pentasomie X

Ivonne Bedei, Katrin Fröbius,Moneef Shoukier,A Wolter,J. Schenk,Katharina Schoner

Ultraschall in der Medizin (2023)

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Supplementary Table 2 from Pathways of Proliferation and Antiapoptosis Driven in Breast Cancer Stem Cells by Stem Cell Protein Piwil2

crossref（2023）

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MMIHS Und ACTG2-Mutation: Pränatale Diagnostik Und Prognose

Anne Janke, Niklas Hirschberger,Cornelia Daumer-Haas,Moneef Shoukier,Karl-Philipp Gloning

Ultraschall in der Medizin - European Journal of Ultrasound 46 Dreiländertreffen der DEGUM in Zusammenarbeit mit ÖGUM &amp SGUM (2023)

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Identification of a new frameshift deletion in the PTRHD1 gene in two affected children with juvenile-onset parkinsonism and intellectual disability

Aruna Marchetto, Felicitas Maier,Moneef Shoukier,Sabine Minderer,Karl-Philipp Gloning

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 169-169

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Supplementary Table 1 from Pathways of Proliferation and Antiapoptosis Driven in Breast Cancer Stem Cells by Stem Cell Protein Piwil2

crossref（2023）

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