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Irene Ambrosetti, Laura Bernardini, Marzia Pollazzon, Maria Grazia Giuffrida, Valentina Guida, Francesca Peluso, Maria Chiara Baroni, Valeria Polizzi, Manuela Napoli, Simonetta Rosato, Gabriele Trimarchi, Chiara Gelmini, Stefano Giuseppe Caraffi, Anita Wischmeijer, Daniele Frattini, Antonio Novelli & Livia Garavelli. (2023) Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes. Genes 14:8, pages 1526.
Crossref
Crossref
Se Jin Jeon, Edson Luck Gonzales, Darine Froy N. Mabunga, Schley T. Valencia, Do Gyeong Kim, Yujeong Kim, Keremkleroo Jym L. Adil, Dongpil Shin, Donghyun Park & Chan Young Shin. (2018) Sex-specific Behavioral Features of Rodent Models of Autism Spectrum Disorder. Experimental Neurobiology 27:5, pages 321-343.
Crossref
Crossref
Marcella Vacca, Floriana Della Ragione, Francesco Scalabrì & Maurizio D'Esposito. (2016) X inactivation and reactivation in X-linked diseases. Seminars in Cell & Developmental Biology 56, pages 78-87.
Crossref
Crossref
Shikshya Shrestha & Steven M. Offer. (2016) Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy. Medical Epigenetics 4:1, pages 1-19.
Crossref
Crossref
Layla Hall & Elizabeth Kelley. (2013) The contribution of epigenetics to understanding genetic factors in autism. Autism 18:8, pages 872-881.
Crossref
Crossref
Vichithra Liyanage, Jessica Jarmasz, Nanditha Murugeshan, Marc Del Bigio, Mojgan Rastegar & James Davie. (2014) DNA Modifications: Function and Applications in Normal and Disease States. Biology 3:4, pages 670-723.
Crossref
Crossref
Anke Hoffmann, Guillaume Daniel, Udo Schmidt-Edelkraut & Dietmar Spengler. (2014) Roles of imprinted genes in neural stem cells. Epigenomics 6:5, pages 515-532.
Crossref
Crossref
Nicolas Brucato, Lynn E. DeLisi, Simon E. Fisher & Clyde Francks. (2014)
Hypomethylation of the paternally inherited
LRRTM1
promoter linked to schizophrenia
. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165:7, pages 555-563.
Crossref
Crossref
Jill D. Jacobson, Kathryn A. Ellerbeck, Kelsie A. Kelly, Kandace K. Fleming, T. Rene Jamison, Charles W. Coffey, Catherine M. Smith, R. Matthew Reese & Scott A. Sands. (2014) Evidence for alterations in stimulatory G proteins and oxytocin levels in children with autism. Psychoneuroendocrinology 40, pages 159-169.
Crossref
Crossref
Adrian Zhubi, Edwin H. Cook, Alessandro Guidotti & Dennis R. Grayson. 2014. Epigenetics. Epigenetics
203
244
.
Maartje C. Brink, Diewertje G. E. Piebes, Marloes L. de Groote, Martijn S. Luijsterburg, Corella S. Casas-Delucchi, Roel van Driel, Marianne G. Rots, M. Cristina Cardoso & Pernette J. Verschure. (2013) A Role for MeCP2 in Switching Gene Activity via Chromatin Unfolding and HP1γ Displacement. PLoS ONE 8:7, pages e69347.
Crossref
Crossref
Jorge Castro, Nikolaos Mellios & Mriganka Sur. (2013) Mechanisms and therapeutic challenges in autism spectrum disorders. Current Opinion in Neurology 26:2, pages 154-159.
Crossref
Crossref
A.M. Persico. 2013. Neural Circuit Development and Function in the Brain. Neural Circuit Development and Function in the Brain
651
694
.
Fiorella Gurrieri & Eugenio Sangiorgi. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.
Tessa Taylor Rivet & Johnny L. Matson. (2011) Review of gender differences in core symptomatology in autism spectrum disorders. Research in Autism Spectrum Disorders 5:3, pages 957-976.
Crossref
Crossref
Tamara B. Franklin & Isabelle M. Mansuy. (2011) The involvement of epigenetic defects in mental retardation. Neurobiology of Learning and Memory 96:1, pages 61-67.
Crossref
Crossref
Isaac N. Pessah. 2011. Developmental Neurotoxicology Research. Developmental Neurotoxicology Research
435
437
.
Patrick O. McGowan, Michael J. Meaney & Moshe Szyf. 2011. Handbook of Behavior, Food and Nutrition. Handbook of Behavior, Food and Nutrition
17
31
.
Kristin D Kernohan & Nathalie G Bérubé. (2010) Genetic and epigenetic dysregulation of imprinted genes in the brain. Epigenomics 2:6, pages 743-763.
Crossref
Crossref
B. Horsthemke. (2010) Genomisches Imprinting und ImprintingfehlerGenomic imprinting and imprinting defects. medizinische genetik 22:4, pages 385-391.
Crossref
Crossref
Bernhard Horsthemke. (2010) Mechanisms of imprint dysregulation. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 154C:3, pages 321-328.
Crossref
Crossref
Hans van Bokhoven & Jamie M. Kramer. (2010) Disruption of the epigenetic code: An emerging mechanism in mental retardation. Neurobiology of Disease 39:1, pages 3-12.
Crossref
Crossref
Patrick O. McGowan & Moshe Szyf. (2010) The epigenetics of social adversity in early life: Implications for mental health outcomes. Neurobiology of Disease 39:1, pages 66-72.
Crossref
Crossref
Melissa D. Cunningham, Judith A. Kassis & Karl Pfeifer. (2010) Chromatin Modifiers, Cognitive Disorders, and Imprinted Genes. Developmental Cell 18:2, pages 169-170.
Crossref
Crossref
Irva Hertz-Picciotto, Peter G. Green, Lora Delwiche, Robin Hansen, Cheryl Walker & Isaac N. Pessah. (2010) Blood Mercury Concentrations in CHARGE Study Children with and without Autism. Environmental Health Perspectives 118:1, pages 161-166.
Crossref
Crossref
Hala Harony & Shlomo Wagner. (2010) The Contribution of Oxytocin and Vasopressin to Mammalian Social Behavior: Potential Role in Autism Spectrum Disorder. Neurosignals 18:2, pages 82-97.
Crossref
Crossref
Bianca De Filippis, Laura Ricceri & Giovanni Laviola. 2010. Transgenic and Mutant Tools to Model Brain Disorders. Transgenic and Mutant Tools to Model Brain Disorders
151
178
.
Lilach M. Friedman & Karen B. Avraham. (2009) MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness. Mammalian Genome 20:9-10, pages 581-603.
Crossref
Crossref
Alexander H. JoynerCooper Roddey J.Cinnamon S. BlossTrygve E. Bakken, Lars M. Rimol, Ingrid Melle, Ingrid Agartz, Srdjan Djurovic, Eric J. TopolNicholas J. SchorkOle A. Andreassen & Anders M. Dale. (2009) A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations. Proceedings of the National Academy of Sciences 106:36, pages 15483-15488.
Crossref
Crossref
Geneviève P. Delcuve, Mojgan Rastegar & James R. Davie. (2009) Epigenetic control. Journal of Cellular Physiology 219:2, pages 243-250.
Crossref
Crossref
KE Szulwach, P Jin & RS Alisch. (2009) Noncoding RNAs in mental retardation. Clinical Genetics 75:3, pages 209-219.
Crossref
Crossref
Jennifer Marlowe, Soon-Siong Teo, Salah-Dine Chibout, François Pognan & Jonathan Moggs. 2009. Molecular, Clinical and Environmental Toxicology. Molecular, Clinical and Environmental Toxicology
259
288
.
C. S. Loat, S. Curran, C. M. Lewis, J. Duvall, D. Geschwind, P. Bolton & I. W. Craig. (2008) Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism. Genes, Brain and Behavior 7:7, pages 754-760.
Crossref
Crossref
Aleksey G. Kazantsev & Leslie M. Thompson. (2008) Therapeutic application of histone deacetylase inhibitors for central nervous system disorders. Nature Reviews Drug Discovery 7:10, pages 854-868.
Crossref
Crossref
Patrick O. McGowan, Michael J. Meaney & Moshe Szyf. (2008) Diet and the epigenetic (re)programming of phenotypic differences in behavior. Brain Research 1237, pages 12-24.
Crossref
Crossref
Laura Ricceri, Bianca De Filippis & Giovanni Laviola. (2008) Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches. Behavioural Pharmacology 19:5-6, pages 501-517.
Crossref
Crossref
Maria E Johnson & Jeffrey L Rausch. 2008. Asperger's Disorder. Asperger's Disorder
171
204
.
Bernard Crespi. (2008) Genomic imprinting in the development and evolution of psychotic spectrum conditions. Biological Reviews.
Crossref
Crossref
Moshe Szyf, Patrick McGowan & Michael J. Meaney. (2007) The social environment and the epigenome. Environmental and Molecular Mutagenesis 49:1, pages 46-60.
Crossref
Crossref