Christina Fenger - Danish Epilepsy Centre Filadelfia

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论文共 13 篇作者统计合作学者相似作者

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Elisa Musto, Vivian W. Y. Liao,Katrine M. Johannesen,Christina D. Fenger,Damien Lederer,Kavitha Kothur, Katrina Fisk,Bruce Bennetts,Pascal Vrielynck, Delphine Delaby,Berten Ceulemans,Sarah Weckhuysen,Peter Sparber,Arjan Bouman, Simone Ardern-Holmes,Christopher Troedson, Domenica I. Battaglia, Himanshu Goel,Timothy Feyma, Somayeh Bakhtiari, Linda Tjoa,Martin Boxill, Nina Demina,Olga Shchagina, Elena Dadali, Michael Kruer,Gaetano Cantalupo,Ilaria Contaldo, Tilman Polster,Bertrand Isidor,Stefania M. Bova,Walid Fazeli, Leen Wouters,Maria J. Miranda,Francesca Darra, Elisa Pede,Diana Le Duc,Rami Abou Jamra,Sebastien Kury,Jacopo Proietti, Niamh Mcsweeney, Elly Brokamp, Peter Ian Andrews, Marie Gouray Garcia, Mary Chebib,Rikke S. Moller, Philip K. Ahring,Elena Gardella

ANNALS OF NEUROLOGY（2024）

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Ritscher-Schinzel Syndrome: Broadening the Phenotype in Prenatal and Adulthood

Sabrina Nery,Nuno Maia,Ana Maria Fortuna,Joana Damasio, Elizabeth Coale, Mary Willisi,Paula Jorge,Anne F. Hojte,Christina Duhring Fenger,Rikke Steensbjerre Moeller,Allan Bayat

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 538-538

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X-linked Creatine Transporter Deficiency (SLC6A8): an Underdiagnosed Disease in Females with Intellectual Disability

Malene Mejdahl Nielsen,Esben Thade Petersen,Christina Duhring Fenger,Mette Cathrine Orngreen,Hartwig R. Siebner,Vincent Oltman Boer,Michal Povazan,Allan Lund,Sabine Gronborg,Trine Bjorg Hammer

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 427-428

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Epilepsy As a Novel Phenotype of BPTF-related Disorders

Alessandro Ferretti, Margherita Furlan,Kevin E. Glinton,Christina D. Fenger,Felix Boschann,Louise Amlie-Wolf,Shimriet Zeidler,Raffaella Moretti,Corinna Stoltenburg,Daniel C. Tarquinio,Francesca Furia,Pasquale Parisi,Guido Rubboli,Orrin Devinsky,Cyril Mignot,Karen W. Gripp,Rikke S. Moller,Yaping Yang,Pawel Stankiewicz,Elena Gardella

PEDIATRIC NEUROLOGY (2024): 17-25

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Intrafamilial Variability in SLC6A1-related Neurodevelopmental Disorders

Benedetta Kassabian,Christina Duhring Fenger,Marjolaine Willems,Angel Aledo-Serrano,Tarja Linnankivi,Pamela Pojomovsky McDonnell,Laina Lusk, Birgit Susanne Jepsen,Michael Bayat,Anja Kattentidt, Anna Abuli Vidal,Gabriel Valero-Lopez,Helena Alarcon-Martinez,Kimberly Goodspeed,Marjon van Slegtenhorst,Tahsin Stefan Barakat,Rikke S. Moller,Katrine M. Johannesen,Guido Rubboli

Frontiers in neuroscience (2023)

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Intrafamilial variability in SLC6A1-related neurodevelopmental disorders (vol 17, 1219262, 2023)

Benedetta Kassabian,Christina Duhring Fenger,Marjolaine Willems,Angel Aledo-Serrano,Tarja Linnankivi,Pamela Pojomovsky Mcdonnell,Laina Lusk, Birgit Susanne Jepsen,Michael Bayat,Anja A. Kattentidt-Mouravieva, Anna Abuli Vidal,Gabriel Valero-Lopez,Helena Alarcon-Martinez,Kimberly Goodspeed,Marjon van Slegtenhorst,Tahsin Stefan Barakat,Rikke S. Moller,Katrine M. Johannesen,Guido Rubboli

FRONTIERS IN NEUROSCIENCE (2023)

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An O-GlcNAc Transferase Pathogenic Variant Linked to Intellectual Disability Affects Pluripotent Stem Cell Self-Renewal

Michaela Omelkova,Christina Duhring Fenger,Marta Murray,Trine Bjorg Hammer,Veronica M. Pravata,Sergio Galan Bartuai,Ignacy Czajewski,Allan Bayat,Andrew T. Ferenbach,Marios P. Stavridis,Daan M. F. van Aalten

DISEASE MODELS & MECHANISMSno. 6 (2023)

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Ploidy-stratified Single Cardiomyocyte Transcriptomics Map Zinc Finger E-Box Binding Homeobox 1 to Underly Cardiomyocyte Proliferation Before Birth

Sara Thornby Bak,Eva Bang Harvald,Ditte Gry Ellman,Sabrina Bech Mathiesen, Ting Chen,Shu Fang,Kristian Skriver Andersen,Christina Dühring Fenger,Mark Burton,Mads Thomassen,Ditte Caroline Andersen

Basic Research in Cardiology（2023）

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X-linked Creatine Transporter (SLC6A8) Deficiency in Females: Difficult to Recognize, but a Potentially Treatable Disease

Malene Mejdahl Nielsen,Esben Thade Petersen,Christina Dühring Fenger,Mette Cathrine Ørngreen,Hartwig Roman Siebner,Vincent Oltman Boer,Michal Považan,Allan Lund,Sabine Weller Grønborg,Trine Bjørg Hammer

Molecular genetics and metabolismno. 3 (2023): 107694-107694

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An O-GlcNAc transferase pathogenic variant that affects pluripotent stem cell self-renewal

Michaela Omelková,Christina Dühring Fenger,Marta Murray,Trine Bjørg Hammer,Veronica M. Pravata,Sergio Galan Bartual,Ignacy Czajewski,Allan Bayat,Andrew T. Ferenbach,Marios P. Stavridis,Daan M. F. van Aalten

biorxiv（2023）

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