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Christina Fagerberg
Researcher at Odense University Hospital
Publications - 73
Citations - 2015
Christina Fagerberg is an academic researcher from Odense University Hospital. The author has contributed to research in topics: Medicine & Exome sequencing. The author has an hindex of 18, co-authored 64 publications receiving 1536 citations. Previous affiliations of Christina Fagerberg include University of Southern Denmark.
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Journal ArticleDOI
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey,Elliott H. Sherr,Noam D. Beckmann,Ellen Hanson,Anne M. Maillard,Loyse Hippolyte,Aurélien Macé,Carina Ferrari,Zoltán Kutalik,Joris Andrieux,Elizabeth Aylward,Mandy Barker,Raphael Bernier,Sonia Bouquillon,Philippe Conus,Bruno Delobel,W. Andrew Faucett,Robin P. Goin-Kochel,Ellen Grant,Louise Harewood,Jill V. Hunter,Sébastien Lebon,David H. Ledbetter,Christa Lese Martin,Katrin Männik,Danielle Martinet,Pratik Mukherjee,Melissa B. Ramocki,Sarah J. Spence,Kyle J. Steinman,Jennifer Tjernage,John E. Spiro,Alexandre Reymond,Jacques S. Beckmann,Wendy K. Chung,Sébastien Jacquemont,Marie-Claude Addor,Benoit Arveiler,Marco Belfiore,Frédérique Béna,Laura Bernardini,Patricia Blanchet,Dominique Bonneau,Odile Boute,Patrick Callier,Dominique Campion,Jean Chiesa,Marie Pierre Cordier,Jean Marie Cuisset,Albert David,Nicole de Leeuw,Bert B.A. de Vries,Gérard Didelot,Martine Doco-Fenzy,Bénédicte Duban Bedu,Christèle Dubourg,Sophie Dupuis-Girod,Christina Fagerberg,Laurence Faivre,Florence Fellmann,Bridget A. Fernandez,Richard I. Fisher,Elisabeth Flori,Alice Goldenberg,Delphine Héron,Muriel Holder,Juliane Hoyer,Bertrand Isidor,Sylvie Jaillard,Philippe Jonveaux,Sylvie Joriot,Hubert Journel,R. Frank Kooy,Cédric Le Caignec,Bruno Leheup,Marie Pierre Lemaitre,Suzanne M E Lewis,Valérie Malan,Michèle Mathieu-Dramard,Andres Metspalu,Fanny Morice-Picard,Mafalda Mucciolo,Eve Õiglane-Shlik,Katrin Õunap,Laurent Pasquier,Florence Petit,Anne Philippe,Ghislaine Plessis,Fabienne Prieur,Jacques Puechberty,Evica Rajcan-Separovic,Anita Rauch,Alessandra Renieri,Claudine Rieubland,Caroline Rooryck,Katharina Magdalena Rötzer,Mariken Ruiter,Damien Sanlaville,Stéphanie Selmoni,Yiping Shen,Vanessa Siffredi,Jacques Thonney,Louis Vallée,Ellen van Binsbergen,Nathalie Van der Aa,Mieke M. van Haelst,Jacqueline Vigneron,Catherine Vincent-Delorme,Disciglio Vittoria,Anneke T. Vulto-van Silfhout,Robert M. Witwicki,Simon A. Zwolinski,Alexandra Bowe,Arthur L. Beaudet,Christie M. Brewton,Zili Chu,Allison G. Dempsey,Yolanda L. Evans,Silvia Garza,Stephen M. Kanne,Anna L. Laakman,Morgan W. Lasala,Ashlie Llorens,Gabriela Marzano,Timothy J. Moss,Kerri P. Nowell,Monica Proud,Qixuan Chen,Roger Vaughan,Jeffrey I. Berman,Lisa Blaskey,Katherine Hines,Sudha Kilaru Kessler,Sarah Y. Khan,Saba Qasmieh,Audrey Lynn Bibb,Andrea M. Paal,Patricia Z. Page,Bethanny Smith-Packard,Randy L. Buckner,Jordan Burko,Alyss Lian Cavanagh,Bettina Cerban,Anne V. Snow,Lee Anne Green Snyder,Rebecca Mc Nally Keehn,David T. Miller,Fiona Miller,Jennifer Olson,Christina Triantafallou,Nicole Visyak,Constance Atwell,Marta Benedetti,Gerald D. Fischbach,Marion Greenup,Alan Packer,Polina Bukshpun,Maxwell Cheong,Corby L. Dale,Sarah E. Gobuty,Leighton B. Hinkley,Rita J. Jeremy,Hana Lee,Tracy Luks,Elysa J. Marco,Alastair J. Martin,Kathleen E. McGovern,Srikantan S. Nagarajan,Julia P. Owen,Brianna M. Paul,Nicholas J. Pojman,Tuhin K. Sinha,Vivek Swarnakar,Mari Wakahiro,Hanalore Alupay,Benjamin Aaronson,Sean Ackerman,Katy Ankenman,Jenna Elgin,Jennifer Gerdts,Kelly Johnson,Beau Reilly,Dennis Shaw,Arianne Stevens,Tracey Ward,Julia Wenegrat,Timothy P.L. Roberts +186 more
TL;DR: The 16p11.2 deletion impacts in a quantitative and independent manner FSIQ, behaviour and body mass index, possibly through direct influences on neural circuitry, and these features are clinically significant and reproducible.
Journal ArticleDOI
International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency.
Teresa Caballero,Henriette Farkas,Laurence Bouillet,Tom Bowen,Anne Gompel,Christina Fagerberg,Janne Bjökander,Konrad Bork,Anette Bygum,Marco Cicardi,Caterina De Carolis,Michael M. Frank,J. Gooi,Hilary Longhurst,Inmaculada Martinez-Saguer,Erik Waage Nielsen,Krystina Obtulowitz,Roberto Perricone,N. Prior +18 more
TL;DR: In this article, the management of gynecologic/obstetric events in female patients with hereditary angioedema caused by C1 inhibitor deficiency (HAE-C1-INH) was discussed.
Journal ArticleDOI
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Anath C. Lionel,Kristiina Tammimies,Kristiina Tammimies,Andrea K. Vaags,Jill A. Rosenfeld,Joo Wook Ahn,Daniele Merico,Abdul Noor,Cassandra K. Runke,Vamsee Pillalamarri,Melissa T. Carter,Matthew J. Gazzellone,Bhooma Thiruvahindrapuram,Christina Fagerberg,Lone W. Laulund,Giovanna Pellecchia,Sylvia Lamoureux,Charu Deshpande,Jill Clayton-Smith,Ann C White,Susan Leather,John Trounce,H. Melanie Bedford,Eli Hatchwell,Peggy S. Eis,Ryan K. C. Yuen,Susan Walker,Mohammed Uddin,Michael T. Geraghty,Michael T. Geraghty,Sarah M. Nikkel,Sarah M. Nikkel,Eva M Tomiak,Bridget A. Fernandez,Noam Soreni,Jennifer Crosbie,Paul D. Arnold,Russell Schachar,Wendy Roberts,Andrew D. Paterson,Joyce So,Peter Szatmari,Christina Chrysler,Marc Woodbury-Smith,R. Brian Lowry,Lonnie Zwaigenbaum,Divya Mandyam,John Wei,Jeffrey R. MacDonald,Jennifer L. Howe,Thomas Nalpathamkalam,Zhuozhi Wang,Daniel Tolson,David S Cobb,Timothy Wilks,Mark J Sorensen,Patricia I. Bader,Yu An,Bai-Lin Wu,Bai-Lin Wu,Bai-Lin Wu,Sebastiano A. Musumeci,Corrado Romano,Diana Postorivo,Anna Maria Nardone,Matteo Della Monica,Gioacchino Scarano,Leonardo Zoccante,Francesca Novara,Orsetta Zuffardi,Roberto Ciccone,Vincenzo Antona,Massimo Carella,Leopoldo Zelante,Pietro Cavalli,Carlo Poggiani,Ugo Cavallari,Bob Argiropoulos,Bob Argiropoulos,Bob Argiropoulos,Judy Chernos,Judy Chernos,Judy Chernos,Charlotte Brasch-Andersen,Marsha Speevak,Marco Fichera,Caroline Mackie Ogilvie,Yiping Shen,Yiping Shen,Yiping Shen,Jennelle C. Hodge,Michael E. Talkowski,Dimitri J. Stavropoulos,Christian R. Marshall,Stephen W. Scherer +94 more
TL;DR: The 3'-terminal ASTN2 deletions were significantly enriched compared with controls in males with NDDs, but not in females, and new light is shed on the role of the astrotactins in psychopathology and their interplay in human neurodevelopment.
Journal ArticleDOI
Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease
F. Buket Basmanav,Ana-Maria Oprisoreanu,Sandra M. Pasternack,Holger Thiele,Günter Fritz,Jörg Wenzel,Leopold Größer,Maria Wehner,Sabrina Wolf,Christina Fagerberg,Anette Bygum,Janine Altmüller,Arno Rütten,Laurent Parmentier,Laila El Shabrawi-Caelen,Christian Hafner,Peter Nürnberg,Roland Kruse,Susanne Schoch,Sandra Hanneken,Regina C. Betz +20 more
TL;DR: Interestingly, both POGLUT1 and POFUT1 are essential regulators of Notch activity, and the results emphasize the important role of the Notch pathway in pigmentation and keratinocyte morphology.
Journal Article
Phenotype and 244k array-CGH characterization of chromosome 13q deletions: An update of the phenotypic map
M Stefanova,R Stoeva,Anne-Marie Bisgaard,B Dimitrov,Gabriele Gillessen-Kaesbach,Jean-Pierre Fryns,Hanne Rose,L Grozdanova,Ivan Ivanov,K. Keymolen,Christina Fagerberg,Lisbeth Tranebjærg,Flemming Skovby,Maria Kirchhoff +13 more
TL;DR: Liss et al. as mentioned in this paper used Agilent oligonucleotide-based array-CGH to determine the exact breakpoints in 14 patients with partial deletions of this region.