Christina D Fenger - Northwestern University

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论文共 16 篇作者统计合作学者相似作者

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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

引用0浏览0WOS引用

The Severity of SLC1A2-Associated Neurodevelopmental Disorders Correlates with Transporter Dysfunction

Peter Kovermann,Allan Bayat,Christina D. Fenger, Lisette Leeuwen,Artem Sharkov,Artem Borovikov, Virginie Levrat,Gaetan Lesca,Laurence Perrin,Jonathan Levy, Christoph Fahlke, Rikke S. Møller,anders A. jensen

crossref（2024）

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A New Neurodevelopmental Disorder Linked to Heterozygous Variants in UNC79

Allan Bayat,Zhenjiang Liu,Sheng Luo,Christina D. Fenger,Anne F. Hojte,Bertrand Isidor,Benjamin Cogne,Austin Larson,Caterina Zanus,Flavio Faletra,Boris Keren,Luciana Musante,Isabelle Gourfikel-An,Charles Perrine, Caroline Demily, Gaeton Lesca,Weiping Liao,Dejian Ren

GENETICS IN MEDICINE（2023）

引用1浏览0WOS引用

Non-invasive preimplantation genetic testing for optimizing of IVF treatments

Sabrina Frrederiksen,Christina D. Fenger, Mads Fruensgaard,Steen B. Laursen,Hans Atli Dahl

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 587-587

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Neurodevelopmental and Epilepsy Phenotypes in Individuals with Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5

Hannah C Happ,Lynette G Sadleir,Matthew Zemel,Guillem de Valles-Ibáñez,Michael S Hildebrand,Allyn McConkie-Rosell,Marie McDonald,Halie May,Tristan Sands,Vimla Aggarwal,Christopher Elder,Timothy Feyma,Allan Bayat,Rikke S Møller,Christina D Fenger,Jens Erik Klint Nielsen,Anita N Datta,Kathleen M Gorman,Mary D King,Natalia D Linhares,Barbara K Burton,Andrea Paras,Sian Ellard,Julia Rankin,Anju Shukla,Purvi Majethia,Rory J Olson,Karthik Muthusamy,Lisa A Schimmenti,Keith Starnes,Lucie Sedláčková,Katalin Štěrbová,Markéta Vlčková,Petra Laššuthová,Alena Jahodová,Brenda E Porter,Nathalie Couque,Estelle Colin,Clément Prouteau,Corinne Collet,Thomas Smol,Roseline Caumes,Fleur Vansenne,Francesca Bisulli,Laura Licchetta,Richard Person,Erin Torti,Kirsty McWalter,Richard Webster,Elizabeth E Gerard,Gaetan Lesca,Pierre Szepetowski,Ingrid E Scheffer,Heather C Mefford,Gemma L Carvill

Neurology（2022）

引用2浏览0WOS引用

Genotype-phenotype Correlations in SCN8A-related Disorders Reveal Prognostic and Therapeutic Implications

Katrine M. Johannesen,Yuanyuan Liu,Mahmoud Koko,Cathrine E. Gjerulfsen,Lukas Sonnenberg,Julian Schubert,Christina D. Fenger,Ahmed Eltokhi,Maert Rannap,Nils A. Koch,Stephan Lauxmann,Johanna Krueger,Josua Kegele,Laura Canafoglia,Silvana Franceschetti,Thomas Mayer,Johannes Rebstock,Pia Zacher,Susanne Ruf,Michael Alber,Katalin Sterbova,Petra Lassuthova,Marketa Vlckova,Johannes R. Lemke, Konrad Platzer,Ilona Krey,Constanze Heine,Dagmar Wieczorek,Judith Kroell-Seger,Caroline Lund,Karl Martin Klein,P. Y. Billie Au,Jong M. Rho,Alice W. Ho,Silvia Masnada,Pierangelo Veggiotti,Lucio Giordano,Patrizia Accorsi,Christina E. Hoei-Hansen,Pasquale Striano,Federico Zara,Helene Verhelst,Judith S. Verhoeven, Hilde M. H. Braakman,Bert van der Zwaag,Aster V. E. Harder,Eva Brilstra,Manuela Pendziwiat,Sebastian Lebon,Maria Vaccarezza,Ngoc Minh Le,Jakob Christensen,Sabine Gronborg,Stephen W. Scherer,Jennifer Howe,Walid Fazeli,Katherine B. Howell,Richard Leventer,Chloe Stutterd,Sonja Walsh,Marion Gerard,Benedicte Gerard,Sara Matricardi,Claudia M. Bonardi,Stefano Sartori,Andrea Berger,Dorota Hoffman-Zacharska,Massimo Mastrangelo,Francesca Darra,Arve Vollo,M. Mahdi Motazacker,Phillis Lakeman,Mathilde Nizon,Cornelia Betzler,Cecilia Altuzarra,Roseline Caume,Agathe Roubertie,Philippe Gelisse,Carla Marini,Renzo Guerrini,Frederic Bilan, Daniel Tibussek,Margarete Koch-Hogrebe,M. Scott Perry,Shoji Ichikawa,Elena Dadali,Artem Sharkov,Irina Mishina,Mikhail Abramov,Ilya Kanivets,Sergey Korostelev,Sergey Kutsev,Karen E. Wain,Nancy Eisenhauer,Monisa Wagner,Juliann M. Savatt, Karen Muller-Schluter,Haim Bassan,Artem Borovikov,Marie-Cecile Nassogne,Anne Destree,An-Sofie Schoonjans,Marije Meuwissen,Marga Buzatu,Anna Jansen,Emmanuel Scalais,Siddharth Srivastava,Wen-Hann Tan,Heather E. Olson,Tobias Loddenkemper,Annapurna Poduri,Katherine L. Helbig,Ingo Helbig,Mark P. Fitzgerald,Ethan M. Goldberg,Timo Roser,Ingo Borggraefe,Tobias Brunger,Patrick May,Dennis Lal,Damien Lederer,Guido Rubboli, Henrike O. Heyne,Gaetan Lesca,Ulrike B. S. Hedrich,Jan Benda,Elena Gardella,Holger Lerche,Rikke S. Moller

Brain a journal of neurology（2022）

引用58浏览0WOS引用

Expanding the Pre- and Postnatal Phenotype of WASHC5 and CCDC22 -Related Ritscher-Schinzel Syndromes

Sabrina Neri,Nuno Maia,Ana M. Fortuna,Joana Damasio, Elizabeth Coale,Mary Willis,Paula Jorge,Anne F. Hojte,Christina D. Fenger,Rikke S. Moller,Allan Bayat

Social Science Research Network (2022)

引用3浏览0WOS引用

Expansion of the CCDC22 associated Ritscher-Schinzel/3C syndrome and review of the literature: Should the minimal diagnostic criteria be revised

Cathrine E Gjerulfsen,Rikke S Møller,Christina D Fenger,Trine B Hammer,Allan Bayat

European journal of medical genetics（2021）

引用10浏览0WOS引用

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