Literature DB >> 26240977

Haploinsufficiency of the MYT1L gene causes intellectual disability frequently associated with behavioral disorder.

Sonia Mayo1, Mónica Roselló1, Sandra Monfort1, Silvestre Oltra1, Carmen Orellana1, Francisco Martínez1.   

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Year:  2015        PMID: 26240977     DOI: 10.1038/gim.2015.86

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


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  2 in total

1.  Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes.

Authors:  Martine Doco-Fenzy; Camille Leroy; Anouck Schneider; Florence Petit; Marie-Ange Delrue; Joris Andrieux; Laurence Perrin-Sabourin; Emilie Landais; Azzedine Aboura; Jacques Puechberty; Manon Girard; Magali Tournaire; Elodie Sanchez; Caroline Rooryck; Agnès Ameil; Michel Goossens; Philippe Jonveaux; Geneviève Lefort; Laurence Taine; Dorothée Cailley; Dominique Gaillard; Bruno Leheup; Pierre Sarda; David Geneviève
Journal:  Eur J Hum Genet       Date:  2013-10-16       Impact factor: 4.246

2.  Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity.

Authors:  Nina De Rocker; Sarah Vergult; David Koolen; Eva Jacobs; Alexander Hoischen; Susan Zeesman; Birgitte Bang; Frédérique Béna; Nele Bockaert; Ernie M Bongers; Thomy de Ravel; Koenraad Devriendt; Sabrina Giglio; Laurence Faivre; Shelagh Joss; Saskia Maas; Nathalie Marle; Francesca Novara; Malgorzata J M Nowaczyk; Hilde Peeters; Abeltje Polstra; Filip Roelens; Carla Rosenberg; Julien Thevenon; Zeynep Tümer; Suzanne Vanhauwaert; Konstantinos Varvagiannis; Andy Willaert; Marjolein Willemsen; Marjolaine Willems; Orsetta Zuffardi; Paul Coucke; Frank Speleman; Evan E Eichler; Tjitske Kleefstra; Björn Menten
Journal:  Genet Med       Date:  2014-09-18       Impact factor: 8.822

  2 in total
  6 in total

1.  MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.

Authors:  Juliette Coursimault; Anne-Marie Guerrot; Michelle M Morrow; Catherine Schramm; Francisca Millan Zamora; Anita Shanmugham; Shuxi Liu; Fanggeng Zou; Frédéric Bilan; Gwenaël Le Guyader; Ange-Line Bruel; Anne-Sophie Denommé-Pichon; Laurence Faivre; Frédéric Tran Mau-Them; Marine Tessarech; Estelle Colin; Salima El Chehadeh; Bénédicte Gérard; Elise Schaefer; Benjamin Cogne; Bertrand Isidor; Mathilde Nizon; Diane Doummar; Stéphanie Valence; Delphine Héron; Boris Keren; Cyril Mignot; Charles Coutton; Françoise Devillard; Anne-Sophie Alaix; Jeanne Amiel; Laurence Colleaux; Arnold Munnich; Karine Poirier; Marlène Rio; Sophie Rondeau; Giulia Barcia; Bert Callewaert; Annelies Dheedene; Candy Kumps; Sarah Vergult; Björn Menten; Wendy K Chung; Rebecca Hernan; Austin Larson; Kelly Nori; Sarah Stewart; James Wheless; Christina Kresge; Beth A Pletcher; Roseline Caumes; Thomas Smol; Sabine Sigaudy; Christine Coubes; Margaret Helm; Rosemarie Smith; Jennifer Morrison; Patricia G Wheeler; Amy Kritzer; Guillaume Jouret; Alexandra Afenjar; Jean-François Deleuze; Robert Olaso; Anne Boland; Christine Poitou; Thierry Frebourg; Claude Houdayer; Pascale Saugier-Veber; Gaël Nicolas; François Lecoquierre
Journal:  Hum Genet       Date:  2021-11-08       Impact factor: 4.132

2.  Myt1l haploinsufficiency leads to obesity and multifaceted behavioral alterations in mice.

Authors:  Markus Wöhr; Wendy M Fong; Justyna A Janas; Moritz Mall; Christian Thome; Madhuri Vangipuram; Lingjun Meng; Thomas C Südhof; Marius Wernig
Journal:  Mol Autism       Date:  2022-05-10       Impact factor: 6.476

3.  MYT1L: A systematic review of genetic variation encompassing schizophrenia and autism.

Authors:  Patricia Mansfield; John N Constantino; Dustin Baldridge
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2020-04-08       Impact factor: 3.568

4.  Associations of the Intellectual Disability Gene MYT1L with Helix-Loop-Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval.

Authors:  Agnieszka Kepa; Lourdes Martinez Medina; Susanne Erk; Deepak P Srivastava; Alinda Fernandes; Roberto Toro; Sabine Lévi; Barbara Ruggeri; Cathy Fernandes; Franziska Degenhardt; Stephanie H Witt; Andreas Meyer-Lindenberg; Jean-Christophe Poncer; Jean-Luc Martinot; Marie-Laure Paillère Martinot; Christian P Müller; Andreas Heinz; Henrik Walter; Gunter Schumann; Sylvane Desrivières
Journal:  Neuropsychopharmacology       Date:  2017-05-04       Impact factor: 7.853

5.  Copy number variation in a hospital-based cohort of children with epilepsy.

Authors:  Danique R M Vlaskamp; Petra M C Callenbach; Patrick Rump; Lucia A A Giannini; Trijnie Dijkhuizen; Oebele F Brouwer; Conny M A van Ravenswaaij-Arts
Journal:  Epilepsia Open       Date:  2017-05-08

6.  Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.

Authors:  Elisabetta Tabolacci; Maria Grazia Pomponi; Laura Remondini; Roberta Pietrobono; Daniela Orteschi; Veronica Nobile; Cecilia Pucci; Elisa Musto; Marika Pane; Eugenio M Mercuri; Giovanni Neri; Maurizio Genuardi; Pietro Chiurazzi; Marcella Zollino
Journal:  Genes (Basel)       Date:  2021-11-27       Impact factor: 4.096

  6 in total

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