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论文共 19 篇作者统计合作学者相似作者

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Lessons from Two Series by Physicians and Caregivers' Self-Reported Data in DDX3X-related Disorders
Valentin Ruault,Pauline Burger, Johanna Gradels-Hauguel,Nathalie Ruiz,Rami Abou Jamra,Alexandra Afenjar,Yves Alembik,Jean-Luc Alessandri,Stephanie Arpin,Giulia Barcia,Sarka Bendova,Ange-Line Bruel,Perrine Charles,Nicolas Chatron,Maya Chopra,Solene Conrad,Valerie Cormier Daire,Auriane Cospain,Christine Coubes,Juliette Coursimault,Andree Delahaye-Duriez,Martine Doco,William Dufour,Benjamin Durand,Camille Engel,Laurence Faivre, Fanny Ferroul,Melanie Fradin, Helene Frenkiel,Carlo Fusco,Livia Garavelli,Aurore Garde,Benedicte Gerard,David Germanaud,Louise Goujon,Aurelie Gouronc,Emmanuelle Ginglinger,Alice Goldenberg,Miroslava Hancarova,Marketa Havlovicova,Delphine Heron,Bertrand Isidor,Nolwenn Jean Marcais,Boris Keren,Margarete Koch-Hogrebe,Paul Kuentz, Victoria Lamure,Anne-Sophie Lebre,Francois Lecoquierre,Natacha Lehman,Gaetan Lesca,Stanislas Lyonnet, Delphine Martin,Cyril Mignot,Teresa M. Neuhann,Gael Nicolas,Mathilde Nizon,Florence Petit,Christophe Philippe,Amelie Piton,Marzia Pollazzon,Darina Prchalova,Audrey Putoux,Marlene Rio,Sophie Rondeau,Massimiliano Rossi,Quentin Sabbagh,Pascale Saugier-Veber,Ariane Schmetz,Julie Steffann,Christel Thauvin-Robinet,Annick Toutain,Frederic Tran Mau Them,Gabriele Trimarchi,Marie Vincent,Marketa Vlckova,Dagmar Wieczorek,Marjolaine Willems,Kevin Yauy,Michaela Zelinova,Alban Ziegler,Boris Chaumette,Bekim Sadikovic,Jean-Louis Mandel,David Genevieve
MOLECULAR GENETICS & GENOMIC MEDICINE（2024）
引用0浏览0WOS引用
0
0
Expanded Phenotypic Spectrum of Neurodevelopmental and Neurodegenerative Disorder Bryant-Li-Bhoj Syndrome with 38 Additional Individuals
Dana E. Layo-Carris,Emily E. Lubin,Annabel K. Sangree,Kelly J. Clark,Emily L. Durham,Elizabeth M. Gonzalez, Sarina Smith,Rajesh Angireddy, Xiao Min Wang, Erin Weiss,Roberto Mendoza-Londono,Lucie Dupuis,Nadirah Damseh,Danita Velasco,Irene Valenzuela,Marta Codina-Sola,Catherine Ziats, Jaclyn Have,Katie Clarkson,Dora Steel,Manju Kurian,Katy Barwick, Diana Carrasco,Aditi I. Dagli,M. J. M. Nowaczyk,Miroslava Hancarova,Sarka Bendova,Darina Prchalova,Zdenek Sedlacek, Alica Baxova,Catherine Bearce Nowak,Jessica Douglas,Wendy K. Chung,Nicola Longo,Konrad Platzer,Chiara Kloeckner,Luisa Averdunk,Dagmar Wieczorek,Ilona Krey,Christiane Zweier,Andre Reis,Tugce Balci,Marleen Simon,Hester Y. Kroes,Antje Wiesener,Georgia Vasileiou,Nikolaos M. Marinakis,Danai Veltra,Christalena Sofocleous,Konstantina Kosma,Joanne Traeger Synodinos, Konstantinos A. Voudris,Marie-Laure Vuillaume,Paul Gueguen,Nicolas Derive,Estelle Colin, Clarisse Battault,Billie Au,Martin Delatycki,Mathew Wallis,Lyndon Gallacher,Fatma Majdoub,Noor Smal,Sarah Weckhuysen,An-Sofie Schoonjans,R. Frank Kooy,Marije Meuwissen,Benjamin T. Cocanougher,Kathryn Taylor,Carolyn E. Pizoli,Marie T. McDonald, Philip James,Elizabeth R. Roeder,Rebecca Littlejohn,Nicholas A. Borja,Willa Thorson, Kristine King,Radka Stoeva,Manon Suerink,Esther Nibbeling, Stephanie Baskin, Gwenael L. E. Guyader,Julie Kaplan,Candace Muss,Deanna Alexis Carere,Elizabeth J. K. Bhoj,Laura M. Bryant
EUROPEAN JOURNAL OF HUMAN GENETICS (2024)
引用0浏览0WOSNATURE引用
0
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Iqsec2-Related Encephalopathy In Males And Females: A Comparative Study Including 37 Novel Patients (Vol 21, Pg 837, 2019)
Cyril Mignot,Aoife C. Mcmahon,Claire Bar,Philippe M. Campeau,Claire Davidson,Julien Buratti,Caroline Nava,Marie-Line Jacquemont,Marilyn Tallot,Mathieu Milh,Patrick Edery,Pauline Marzin,Giulia Barcia,Christine Barnerias,Claude Besmond,Thierry Bienvenu,Ange-Line Bruel,Ledia Brunga,Berten Ceulemans,Christine Coubes,Ana G. Cristancho,Fiona Cunningham,Marie-Bertille Dehouck,Elizabeth J. Donner,Benedicte Duban-Bedu,Christele Dubourg,Elena Gardella,Julie Gauthier,David Genevieve,Stephanie Gobin-Limballe,Ethan M. Goldberg,Eveline Hagebeuk,Fadi F. Hamdan,Miroslava Hancarova,Laurence Hubert,Christine Ioos,Shoji Ichikawa,Sandra Janssens,Hubert Journel,Anna Kaminska,Boris Keren,Marije Koopmans,Caroline Lacoste,Petra Lassuthova,Damien Lederer,Daphne Lehalle,Dragan Marjanovic,Julia Metreau,Jacques L. Michaud,Kathryn Miller,Berge A. Minassian,Joannella Morales,Marie-Laure Moutard,Arnold Munnich,Xilma R. Ortiz-Gonzalez,Jean-Marc Pinard,Darina Prchalova,Audrey Putoux,Chloe Quelin,Alyssa R. Rosen,Joelle Roume,Elsa Rossignol,Marleen E. H. Simon,Thomas Smol,Natasha Shur,Ivan Shelihan,Katalin Sterbova,Emilie Vyhnalkova,Catheline Vilain,Julie Soblet,Guillaume Smits,Samuel P. Yang,Jasper J. Van Der Smagt,Peter M. Van Hasselt,Marjan Van Kempen,Sarah Weckhuysen,Ingo Helbig,Laurent Villard,Delphine Heron,Bobby Koeleman,Rikke S. Moller,Gaetan Lesca,Katherine L. Helbig,Rima Nabbout,Nienke E. Verbeek,Christel Depienne
GENETICS IN MEDICINE（2019）
引用1浏览0引用
1
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IQSEC2-related Encephalopathy in Males and Females: a Comparative Study Including 37 Novel Patients
Cyril Mignot,Aoife McMahon,Claire Bar, Philippe M. Campeau,Claire Davidson,Julien Buratti, Caroline Nava,Marie‐Line Jacquemont,Marilyn Tallot,Mathieu Milh,Patrick Edery,Pauline Marzin,Giulia Barcia,Christine Barnérias,Claude Besmond,Thierry Bienvenu, Ange-Line Bruel,Ledia Brunga,Berten Ceulemans,Christine Coubes, Ana G. Cristancho,Fiona Cunningham, Marie-Bertille Dehouck,Elizabeth Donner,Bénédicte Duban‐Bedu, Christèle Dubourg,Elena Gardella,Julie Gauthier,David Geneviève,Stéphanie Gobin-Limballe,Ethan Em Goldberg,Eveline Hagebeuk,Fadi F. Hamdan, Miroslava Hančárová,Laurence Hubert, Christine Ioos,Shoji Ichikawa,Sandra Janssens,Hubert Journel,Anna Kamińska,Boris Keren,Marije Koopmans,Caroline Lacoste, Petra Laššuthová,Damien Lederer,Daphné Lehalle,Dragan Marjanović,Julia Métreau,Jacques J.L. Michaud,Kathryn Miller,Berge Ba Minassian,Joannella Morales, Marie‐Laure Moutard,Arnold Münnich,Xilma R. Ortiz‐González,Jean-Marc Pinard,Darina Prchalová,Audrey Putoux,Chloé Quēlin,Alyssa Rosen, J. Roume,Elsa Rossignol, Marleen Simon,Thomas Smol, Natasha Shur, Ivan Shelihan,Katalin Štěrbová,Emílie Vyhnálková,Catheline Vilain,Julie Soblet,Guillaume Smits, Samuel P. Yang, J.J. Van Der Smagt,Peter M. van Hasselt,Marjan van Kempen,Sarah Weckhuysen,Ingo Helbig,Laurent Villard,Delphine Héron, Bobby Koeleman, Rikke S. Møller, Gaëtan Lesca, Katherine Kl Helbig,Rima Nabbout,Nienke Ne Verbeek, Christel Depienne
Genetics in medicineno. 4 (2019): 837-849
引用0浏览0引用
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Correction: IQSEC2-related Encephalopathy in Males and Females: a Comparative Study Including 37 Novel Patients
Cyril Mignot,Aoife C McMahon,Claire Bar,Philippe M Campeau,Claire Davidson,Julien Buratti,Caroline Nava,Marie-Line Jacquemont,Marilyn Tallot,Mathieu Milh,Patrick Edery,Pauline Marzin,Giulia Barcia,Christine Barnerias,Claude Besmond,Thierry Bienvenu,Ange-Line Bruel,Ledia Brunga,Berten Ceulemans,Christine Coubes,Ana G Cristancho,Fiona Cunningham,Marie-Bertille Dehouck,Elizabeth J Donner,Bénédicte Duban-Bedu,Christèle Dubourg,Elena Gardella,Julie Gauthier,David Geneviève,Stéphanie Gobin-Limballe,Ethan M Goldberg,Eveline Hagebeuk,Fadi F Hamdan,Miroslava Hančárová,Laurence Hubert,Christine Ioos,Shoji Ichikawa,Sandra Janssens,Hubert Journel,Anna Kaminska,Boris Keren,Marije Koopmans,Caroline Lacoste,Petra Laššuthová,Damien Lederer,Daphné Lehalle,Dragan Marjanovic,Julia Métreau,Jacques L Michaud,Kathryn Miller,Berge A Minassian,Joannella Morales,Marie-Laure Moutard,Arnold Munnich,Xilma R Ortiz-Gonzalez,Jean-Marc Pinard,Darina Prchalová,Audrey Putoux,Chloé Quelin,Alyssa R Rosen,Joelle Roume,Elsa Rossignol,Marleen E H Simon,Thomas Smol,Natasha Shur,Ivan Shelihan,Katalin Štěrbová,Emílie Vyhnálková,Catheline Vilain,Julie Soblet,Guillaume Smits,Samuel P Yang,Jasper J van der Smagt,Peter M van Hasselt,Marjan van Kempen,Sarah Weckhuysen,Ingo Helbig,Laurent Villard,Delphine Héron,Bobby Koeleman,Rikke S Møller,Gaetan Lesca,Katherine L Helbig,Rima Nabbout,Nienke E Verbeek,Christel Depienne
Genetics in medicine official journal of the American College of Medical Genetics（2019）
引用49浏览0WOS引用
49
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作者统计

#Papers: 20

#Citation: 324

H-Index: 10

G-Index: 14

Sociability: 6

Diversity: 2

Activity: 5

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