Literature DB >> 29696803

X-linked intellectual disability update 2017.

Giovanni Neri1,2, Charles E Schwartz1, Herbert A Lubs1, Roger E Stevenson1.   

Abstract

The X-chromosome comprises only about 5% of the human genome but accounts for about 15% of the genes currently known to be associated with intellectual disability. The early progress in identifying the X-linked intellectual disability (XLID)-associated genes through linkage analysis and candidate gene sequencing has been accelerated with the use of high-throughput technologies. In the 10 years since the last update, the number of genes associated with XLID has increased by 96% from 72 to 141 and duplications of all 141 XLID genes have been described, primarily through the application of high-resolution microarrays and next generation sequencing. The progress in identifying genetic and genomic alterations associated with XLID has not been matched with insights that improve the clinician's ability to form differential diagnoses, that bring into view the possibility of curative therapies for patients, or that inform scientists of the impact of the genetic alterations on cell organization and function.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  X-chromosome; XLID; genes; intellectual disability; syndrome

Mesh:

Substances:

Year:  2018        PMID: 29696803      PMCID: PMC6049830          DOI: 10.1002/ajmg.a.38710

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  43 in total

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Journal:  Hum Mol Genet       Date:  2015-10-06       Impact factor: 6.150

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Journal:  Hum Genet       Date:  2013-12-11       Impact factor: 4.132

Review 5.  The 3D Genome as Moderator of Chromosomal Communication.

Authors:  Job Dekker; Leonid Mirny
Journal:  Cell       Date:  2016-03-10       Impact factor: 41.582

6.  Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28.

Authors:  Michael J Friez; Julie R Jones; Katie Clarkson; Herbert Lubs; Dianne Abuelo; Jo-Ann Blaymore Bier; Shashidhar Pai; Richard Simensen; Charles Williams; Philip F Giampietro; Charles E Schwartz; Roger E Stevenson
Journal:  Pediatrics       Date:  2006-11-06       Impact factor: 7.124

Review 7.  Xp11.22 Microduplications Including HUWE1: Case Report and Literature Review.

Authors:  Sonia Orivoli; Elena Pavlidis; Gaetano Cantalupo; Marianna Pezzella; Federico Zara; Livia Garavelli; Francesco Pisani; Benedetta Piccolo
Journal:  Neuropediatrics       Date:  2015-11-20       Impact factor: 1.947

Review 8.  Duplication of the short arm of the X chromosome in mother and daughter.

Authors:  C M Tuck-Muller; J E Martinez; D A Batista; W G Kearns; W Wertelecki
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

9.  Two independent modes of chromatin organization revealed by cohesin removal.

Authors:  Wibke Schwarzer; Nezar Abdennur; Anton Goloborodko; Aleksandra Pekowska; Geoffrey Fudenberg; Yann Loe-Mie; Nuno A Fonseca; Wolfgang Huber; Christian H Haering; Leonid Mirny; Francois Spitz
Journal:  Nature       Date:  2017-09-27       Impact factor: 49.962

10.  Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.

Authors:  Korinna Kochinke; Christiane Zweier; Bonnie Nijhof; Michaela Fenckova; Pavel Cizek; Frank Honti; Shivakumar Keerthikumar; Merel A W Oortveld; Tjitske Kleefstra; Jamie M Kramer; Caleb Webber; Martijn A Huynen; Annette Schenck
Journal:  Am J Hum Genet       Date:  2016-01-07       Impact factor: 11.025

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  38 in total

1.  Understanding the Landscape of X-linked Variants Causing Intellectual Disability in Females Through Extreme X Chromosome Inactivation Skewing.

Authors:  Evelyn Quintanilha Vianna; Rafael Mina Piergiorge; Andressa Pereira Gonçalves; Jussara Mendonça Dos Santos; Veluma Calassara; Carla Rosenberg; Ana Cristina Victorino Krepischi; Raquel Tavares Boy da Silva; Suely Rodrigues Dos Santos; Márcia Gonçalves Ribeiro; Filipe Brum Machado; Enrique Medina-Acosta; Márcia Mattos Gonçalves Pimentel; Cíntia Barros Santos-Rebouças
Journal:  Mol Neurobiol       Date:  2020-06-20       Impact factor: 5.590

2.  Defective DNA Polymerase α-Primase Leads to X-Linked Intellectual Disability Associated with Severe Growth Retardation, Microcephaly, and Hypogonadism.

Authors:  Hilde Van Esch; Rita Colnaghi; Kathleen Freson; Petro Starokadomskyy; Andreas Zankl; Liesbeth Backx; Iga Abramowicz; Emily Outwin; Luis Rohena; Claire Faulkner; Gary M Leong; Ruth A Newbury-Ecob; Rachel C Challis; Katrin Õunap; Jacques Jaeken; Eve Seuntjens; Koen Devriendt; Ezra Burstein; Karen J Low; Mark O'Driscoll
Journal:  Am J Hum Genet       Date:  2019-04-18       Impact factor: 11.025

3.  Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.

Authors:  Jiyong Wang; Aidin Foroutan; Ellen Richardson; Steven A Skinner; Jack Reilly; Jennifer Kerkhof; Cynthia J Curry; Patrick S Tarpey; Stephen P Robertson; Isabelle Maystadt; Boris Keren; Joanne W Dixon; Cindy Skinner; Rachel Stapleton; Lyse Ruaud; Evren Gumus; Phillis Lakeman; Mariëlle Alders; Matthew L Tedder; Charles E Schwartz; Michael J Friez; Bekim Sadikovic; Roger E Stevenson
Journal:  Eur J Hum Genet       Date:  2022-01-07       Impact factor: 4.246

Review 4.  Gene-based therapeutics for rare genetic neurodevelopmental psychiatric disorders.

Authors:  Beverly L Davidson; Guangping Gao; Elizabeth Berry-Kravis; Allison M Bradbury; Carsten Bönnemann; Joseph D Buxbaum; Gavin R Corcoran; Steven J Gray; Heather Gray-Edwards; Robin J Kleiman; Adam J Shaywitz; Dan Wang; Huda Y Zoghbi; Terence R Flotte; Sitra Tauscher-Wisniewski; Cynthia J Tifft; Mustafa Sahin
Journal:  Mol Ther       Date:  2022-05-17       Impact factor: 12.910

5.  SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.

Authors:  Salima El Chehadeh; Kyung Ah Han; Dongwook Kim; Gyubin Jang; Somayeh Bakhtiari; Dongseok Lim; Hee Young Kim; Jinhu Kim; Hyeonho Kim; Julia Wynn; Wendy K Chung; Giuseppina Vitiello; Ioana Cutcutache; Matthew Page; Jozef Gecz; Kelly Harper; Ah-Reum Han; Ho Min Kim; Marja Wessels; Allan Bayat; Alberto Fernández Jaén; Angelo Selicorni; Silvia Maitz; Arjan P M de Brouwer; Anneke Vulto-van Silfhout; Martin Armstrong; Joseph Symonds; Sébastien Küry; Bertrand Isidor; Benjamin Cogné; Mathilde Nizon; Claire Feger; Jean Muller; Erin Torti; Dorothy K Grange; Marjolaine Willems; Michael C Kruer; Jaewon Ko; Amélie Piton; Ji Won Um
Journal:  Nat Commun       Date:  2022-07-15       Impact factor: 17.694

6.  Resting-State Functional Connectivity and Psychopathology in Klinefelter Syndrome (47, XXY).

Authors:  Ethan T Whitman; Siyuan Liu; Erin Torres; Allysa Warling; Kathleen Wilson; Ajay Nadig; Cassidy McDermott; Liv S Clasen; Jonathan D Blumenthal; François M Lalonde; Stephen J Gotts; Alex Martin; Armin Raznahan
Journal:  Cereb Cortex       Date:  2021-07-29       Impact factor: 5.357

7.  Shared Neurodevelopmental Perturbations Can Lead to Intellectual Disability in Individuals with Distinct Rare Chromosome Duplications.

Authors:  Thiago Corrêa; Cíntia B Santos-Rebouças; Maytza Mayndra; Albert Schinzel; Mariluce Riegel
Journal:  Genes (Basel)       Date:  2021-04-23       Impact factor: 4.096

Review 8.  X-factors in human disease: impact of gene content and dosage regulation.

Authors:  He Fang; Xinxian Deng; Christine M Disteche
Journal:  Hum Mol Genet       Date:  2021-10-01       Impact factor: 5.121

Review 9.  The Ubiquitin System: a Regulatory Hub for Intellectual Disability and Autism Spectrum Disorder.

Authors:  Stephen A Wood; Michael Piper; Maria A Kasherman; Susitha Premarathne; Thomas H J Burne
Journal:  Mol Neurobiol       Date:  2020-01-23       Impact factor: 5.590

Review 10.  X-chromosome regulation and sex differences in brain anatomy.

Authors:  Armin Raznahan; Christine M Disteche
Journal:  Neurosci Biobehav Rev       Date:  2020-11-07       Impact factor: 8.989

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