Literature DB >> 24434855

The genetics of cognitive epigenetics.

Tjitske Kleefstra1, Annette Schenck1, Jamie M Kramer1, Hans van Bokhoven2.   

Abstract

Cognitive disorders (CDs) are a heterogeneous group of disorders for which the genetic foundations are rapidly being uncovered. The large number of CD-associated gene mutations presents an opportunity to identify common mechanisms of disease as well as molecular processes that are of key importance to human cognition. Given the disproportionately high number of epigenetic genes associated with CD, epigenetic regulation of gene transcription is emerging as a process of major importance in cognition. The cognate protein products of these genes often co-operate in shared protein complexes or pathways, which is reflected in similarities between the neurodevelopmental phenotypes corresponding to these mutant genes. Here we provide an overview of the genes associated with CDs, and highlight some of the epigenetic regulatory complexes involving multiple CD genes. Such common gene networks may provide a handle for designing therapeutic interventions applicable to a number of cognitive disorders with variable genetic etiology. Crown
Copyright © 2014. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Chromatin; Cognitive disorder; Epigenetic; Genetic; Intellectual disability; Mutation

Mesh:

Substances:

Year:  2014        PMID: 24434855     DOI: 10.1016/j.neuropharm.2013.12.025

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  24 in total

1.  Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.

Authors:  Josefine S Witteveen; Marjolein H Willemsen; Thaís C D Dombroski; Nick H M van Bakel; Willy M Nillesen; Josephus A van Hulten; Eric J R Jansen; Dave Verkaik; Hermine E Veenstra-Knol; Conny M A van Ravenswaaij-Arts; Jolien S Klein Wassink-Ruiter; Marie Vincent; Albert David; Cedric Le Caignec; Jolanda Schieving; Christian Gilissen; Nicola Foulds; Patrick Rump; Tim Strom; Kirsten Cremer; Alexander M Zink; Hartmut Engels; Sonja A de Munnik; Jasper E Visser; Han G Brunner; Gerard J M Martens; Rolph Pfundt; Tjitske Kleefstra; Sharon M Kolk
Journal:  Nat Genet       Date:  2016-07-11       Impact factor: 38.330

2.  Dopaminergic gene methylation is associated with cognitive performance in a childhood monozygotic twin study.

Authors:  Candace R Lewis; Adrienne Henderson-Smith; Reagan S Breitenstein; Hayley A Sowards; Ignazio S Piras; Matthew J Huentelman; Leah D Doane; Kathryn Lemery-Chalfant
Journal:  Epigenetics       Date:  2019-03-16       Impact factor: 4.528

Review 3.  Epigenetic Etiology of Intellectual Disability.

Authors:  Shigeki Iwase; Nathalie G Bérubé; Zhaolan Zhou; Nael Nadif Kasri; Elena Battaglioli; Marilyn Scandaglia; Angel Barco
Journal:  J Neurosci       Date:  2017-11-08       Impact factor: 6.167

Review 4.  Epigenetic mechanisms underlying nervous system diseases.

Authors:  Irfan A Qureshi; Mark F Mehler
Journal:  Handb Clin Neurol       Date:  2018

5.  Forebrain neurogenesis: From embryo to adult.

Authors:  Daniel Dennis; David Picketts; Ruth S Slack; Carol Schuurmans
Journal:  Trends Dev Biol       Date:  2016-01-01

6.  Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.

Authors:  Alma Kuechler; Alexander M Zink; Thomas Wieland; Hermann-Josef Lüdecke; Kirsten Cremer; Leonardo Salviati; Pamela Magini; Kimia Najafi; Christiane Zweier; Johanna Christina Czeschik; Stefan Aretz; Sabine Endele; Federica Tamburrino; Claudia Pinato; Maurizio Clementi; Jasmin Gundlach; Carina Maylahn; Laura Mazzanti; Eva Wohlleber; Thomas Schwarzmayr; Roxana Kariminejad; Avner Schlessinger; Dagmar Wieczorek; Tim M Strom; Gaia Novarino; Hartmut Engels
Journal:  Eur J Hum Genet       Date:  2014-08-20       Impact factor: 4.246

7.  DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental Disorders.

Authors:  Michelle T Siu; Sarah J Goodman; Isaac Yellan; Darci T Butcher; Maryam Jangjoo; Daria Grafodatskaya; Rageen Rajendram; Youliang Lou; Rujun Zhang; Chunhua Zhao; Rob Nicolson; Stelios Georgiades; Peter Szatmari; Stephen W Scherer; Wendy Roberts; Evdokia Anagnostou; Rosanna Weksberg
Journal:  J Autism Dev Disord       Date:  2021-01-04

Review 8.  Epigenetic Mistakes in Neurodevelopmental Disorders.

Authors:  Giuseppina Mastrototaro; Mattia Zaghi; Alessandro Sessa
Journal:  J Mol Neurosci       Date:  2017-03-02       Impact factor: 3.444

Review 9.  ODLURO syndrome: personal experience and review of the literature.

Authors:  Renata Conforti; Silvia Iovine; Gabriella Santangelo; Raffaella Capasso; Mario Cirillo; Mario Fratta; Ferdinando Caranci
Journal:  Radiol Med       Date:  2020-07-20       Impact factor: 3.469

10.  Loss of Kdm5c Causes Spurious Transcription and Prevents the Fine-Tuning of Activity-Regulated Enhancers in Neurons.

Authors:  Marilyn Scandaglia; Jose P Lopez-Atalaya; Alejandro Medrano-Fernandez; Maria T Lopez-Cascales; Beatriz Del Blanco; Michal Lipinski; Eva Benito; Roman Olivares; Shigeki Iwase; Yang Shi; Angel Barco
Journal:  Cell Rep       Date:  2017-10-03       Impact factor: 9.423

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