Works matching DE "GENETICS of autism"

Results: 463

Dosage effects of human ribosomal genes (rDNA) in health and disease.

Published in:

Chromosome Research, 2019, v. 27, n. 1/2, p. 5, doi. 10.1007/s10577-018-9587-y

By:

Porokhovnik, L. N.;
Lyapunova, N. A.

Publication type:

Article

Hypermethylation of the enolase gene ( ENO2) in autism.

Published in:

European Journal of Pediatrics, 2014, v. 173, n. 9, p. 1233, doi. 10.1007/s00431-014-2311-9

By:

Wang, Yu;
Fang, Yudan;
Zhang, Fengling;
Xu, Miao;
Zhang, Jingzhi;
Yan, Jingbin;
Ju, Weina;
Brown, W.;
Zhong, Nanbert

Publication type:

Article

Shared Immune and Nutrient Metabolism Pathways Between Autism Spectrum Disorder and Celiac Disease: An In Silico Approach.

Published in:

Nutrients, 2025, v. 17, n. 9, p. 1439, doi. 10.3390/nu17091439

By:

Sykioti, Panagiota;
Zis, Panagiotis;
Hadjikonstanti, Despina;
Hadjivassiliou, Marios;
Vavougios, George D.

Publication type:

Article

Knowledge on Care of Autistic Child among the Mother's Attending Protibondhi Foundation, Dhaka.

Published in:

Bangladesh Journal of Medical Science, 2015, v. 14, n. 2, p. 179, doi. 10.3329/bjms.v14i2.21563

By:

Parvin, M. N.;
Haque, M. M.;
Bhuiyan, M. R.;
Haqe, M.;
Saha, P. K.;
Islam, A. S. M. M.

Publication type:

Article

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 422, doi. 10.1038/sj.ejhg.5201785

By:

Castermans, Dries;
Vermeesch, Joris R.;
Fryns, Jean-Pierre;
Steyaert, Jean G.;
Van de Ven, Wim J. M.;
Creemers, John W M;
Devriendt, Koen

Publication type:

Article

Autism spectrum disorder today: not only genetics.

Published in:

Türk Pediatri Arşivi, 2019, v. 54, n. 2, p. 137, doi. 10.14744/TurkPediatriArs.2019.98216

By:

Posar, Annio;
Visconti, Paola

Publication type:

Article

Investigation of Pogz Gene Variants in Non-Syndromic Autism Spectrum Disorder.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2024, v. 61, n. 3, p. 208, doi. 10.29399/npa.28625

By:

Tozkır, Jülide;
Yıldırım, Gökberk;
Demir, Selma;
Palabıyık, Orkide;
Görker, Işık;
Gürkan, Hakan

Publication type:

Article

Association Study between DUF1220 Copy Number and Severity of Social Impairment in Sex-balanced Simplex Cases of Autism.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2023, v. 60, n. 1, p. 43, doi. 10.29399/npa.28020

By:

EFTEKHAR, Mohammad;
PANAHI, Yasin;
ESKANDARI, Mohammad Reza;
PEDRAM, Mehrdad

Publication type:

Article

Autism Spectrum Disorder as an Initial Diagnosis in Adults.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2020, v. 57, n. 1, p. 1, doi. 10.29399/npa.25050

By:

ATBAŞOĞLU, E. Cem

Publication type:

Article

Could acupuncture have a role in the treatment of autism spectrum disorder via modulation of BDNF expression and activation?

Published in:

2014

By:

Li-Ya Li;
Nan Jiang;
Yue Zhao

Publication type:

Journal Article

Genetics of Autism Spectrum Disorder: An Update.

Published in:

Psychiatric Annals, 2019, v. 49, n. 3, p. 109, doi. 10.3928/00485713-20190212-01

By:

Malik, Salma;
Khan, Yasser Saeed;
Sah, Robert;
Elzamzamy, Khalid;
Nazeer, Ahsan

Publication type:

Article

Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.

Published in:

BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-34

By:

Campbell, Malcolm G.;
Kohane, Isaac S.;
Sek Won Kong

Publication type:

Article

Mutation screening of melatonin-related genes in patients with autism spectrum disorders.

Published in:

BMC Medical Genomics, 2010, v. 3, p. 10, doi. 10.1186/1755-8794-3-10

By:

Jonsson, Lina;
Ljunggren, Elin;
Bremer, Anna;
Pedersen, Christin;
Landén, Mikael;
Thuresson, Kent;
Giacobini, MaiBritt;
Melke, Jonas

Publication type:

Article

The Role of Molecular Karyotyping in the Genetic Etiology of Autism.

Published in:

Turk Psikiyatri Dergisi, 2017, v. 28, n. 3, p. 1, doi. 10.5080/u18239

By:

ÖZBARAN, Burcu;
AKGÜN, Bilçağ;
KAÇAMAK, Duygu;
KÖSE, Sezen;
KAVASOĞLU, Ayşenur;
ONAY, Hüseyin

Publication type:

Article

Genetic insights beginning to divide autism diagnosis.

Published in:

Nature Medicine, 2011, v. 17, n. 4, p. 398, doi. 10.1038/nm0411-398a

By:

Heger, Monica

Publication type:

Article

Excess of rare, inherited truncating mutations in autism.

Published in:

Nature Genetics, 2015, v. 47, n. 6, p. 582, doi. 10.1038/ng.3303

By:

Krumm, Niklas;
Turner, Tychele N;
Baker, Carl;
Vives, Laura;
Mohajeri, Kiana;
Witherspoon, Kali;
Coe, Bradley P;
Stessman, Holly A;
Raja, Archana;
Eichler, Evan E;
He, Zong-Xiao;
Leal, Suzanne M;
Bernier, Raphael

Publication type:

Article

Genetic diagnosis of autism spectrum disorders: The opportunity and challenge in the genomics era.

Published in:

Critical Reviews in Clinical Laboratory Sciences, 2014, v. 51, n. 5, p. 249, doi. 10.3109/10408363.2014.910747

By:

Jiang, Yong-Hui;
Wang, Yi;
Xiu, Xu;
Choy, Kwong Wai;
Pursley, Amber Nolen;
Cheung, Sau W.

Publication type:

Article

Genes found linked to autism and intellectual disability.

Published in:: Medical Journal of Australia, 2017, v. 206, n. 4, p. 148, doi. 10.1038/ng.3792
Publication type:: Article

News.

Published in:: Medical Journal of Australia, 2017, v. 206, n. 4, p. 146
Publication type:: Article

A Case with a Ring Chromosome 13 in a Cohort of 203 Children with Non-Syndromic Autism and Review of the Cytogenetic Literature.

Published in:

Cytogenetic & Genome Research, 2014, v. 144, n. 1, p. 1, doi. 10.1159/000365909

By:

Charalsawadi, Chariyawan;
Maisrikhaw, Worathai;
Praphanphoj, Verayuth;
Wirojanan, Juthamas;
Hansakunachai, Tippawan;
Roongpraiwan, Rawiwan;
Sombuntham, Tasnawat;
Ruangdaraganon, Nichara;
Limprasert, Pornprot

Publication type:

Article

Methylation and Expression Analyses of the 7q Autism Susceptibility Locus Genes MEST, COPG2, and TSGA14 in Human and Anthropoid Primate Cortices.

Published in:

Cytogenetic & Genome Research, 2012, v. 136, n. 4, p. 278, doi. 10.1159/000337298

By:

Schneider, E.;
Mayer, S.;
El Hajj, N.;
Jensen, L.R.;
Kuss, A.W.;
Zischler, H.;
Kondova, I.;
Bontrop, R.E.;
Navarro, B.;
Fuchs, E.;
Zechner, U.;
Haaf, T.

Publication type:

Article

Genetik und Tiermodelle von Autismusspektrumstörungen.

Published in:

Der Nervenarzt, 2011, v. 82, n. 5, p. 553, doi. 10.1007/s00115-010-3241-z

By:

Klauck, S. M.;
Poustka, L.;
Chiocchetti, A.

Publication type:

Article

Social and non-social autism symptoms and trait domains are genetically dissociable.

Published in:

Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0558-4

By:

Warrier, Varun;
Toro, Roberto;
Won, Hyejung;
Leblond, Claire S.;
Cliquet, Freddy;
Delorme, Richard;
De Witte, Ward;
Bralten, Janita;
Chakrabarti, Bhismadev;
Børglum, Anders D.;
Grove, Jakob;
Poelmans, Geert;
Hinds, David A.;
Bourgeron, Thomas;
Baron-Cohen, Simon

Publication type:

Article

A Genetic Multimutation Model of Autism Spectrum Disorder Fits Disparate Twin Concordance Data from the USA and Canada.

Published in:

International Scholarly Research Notices, 2015, p. 1, doi. 10.1155/2015/519828

By:

Kramer, Ivan;
Lipkin, Paul H.;
Marvin, Alison R.;
Law, Paul A.

Publication type:

Article

A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorder.

Published in:

Journal of the Peripheral Nervous System, 2017, v. 22, n. 4, p. 460, doi. 10.1111/jns.12235

By:

Tomaselli, Pedro J.;
Rossor, Alexander M.;
Horga, Alejandro;
Laura, Matilde;
Blake, Julian C.;
Houlden, Henry;
Reilly, Mary M.

Publication type:

Article

Cytogenetic, Molecular-Cytogenetic, and Clinical-Genealogical Studies of the Mothers of Children with Autism: A Search for Familial Genetic Markers for Autistic Disorders.

Published in:

Neuroscience & Behavioral Physiology, 2010, v. 40, n. 7, p. 745, doi. 10.1007/s11055-010-9321-5

By:

Vorsanova, S. G.;
Voinova, V. Yu.;
Yurov, I. Yu.;
Kurinnaya, O. S.;
Demidova, I. A.;
Yurov, Yu. B.

Publication type:

Article

Using Sibling Designs to Understand Neurodevelopmental Disorders: From Genes and Environments to Prevention Programming.

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/672784

By:

Wade, Mark;
Prime, Heather;
Madigan, Sheri

Publication type:

Article

Clinical Characteristics of Autism Spectrum Disorder in Israel: Impact of Ethnic and Social Diversities.

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/962093

By:

Mahajnah, Muhammad;
Sharkia, Rajech;
Shalabe, Haitham;
Terkel-Dawer, Ruth;
Akawi, Ashraf;
Zelnik, Nathanel

Publication type:

Article

Behavioural, developmental and psychological characteristics in children with germline PTEN mutations: a carer report study.

Published in:

Journal of Intellectual Disability Research, 2024, v. 68, n. 8, p. 916, doi. 10.1111/jir.13130

By:

Cummings, K.;
Dias, R. P.;
Hart, R.;
Welham, A.

Publication type:

Article

Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.

Published in:

Journal of Intellectual Disability Research, 2017, v. 61, n. 6, p. 568, doi. 10.1111/jir.12382

By:

Butler, M. G.

Publication type:

Article

CYP1A2 polymorphisms in slow melatonin metabolisers: a possible relationship with autism spectrum disorder?

Published in:

Journal of Intellectual Disability Research, 2013, v. 57, n. 11, p. 993, doi. 10.1111/j.1365-2788.2012.01595.x

By:

Braam, W.;
Keijzer, H.;
Struijker Boudier, H.;
Didden, R.;
Smits, M.;
Curfs, L.

Publication type:

Article

Keynote Abstracts.

Published in:: Journal of Intellectual Disability Research, 2013, v. 57, n. 9, p. 796, doi. 10.1111/jir.12072
Publication type:: Article

Early identification of autism in fragile X syndrome: a review.

Published in:

Journal of Intellectual Disability Research, 2013, v. 57, n. 9, p. 803, doi. 10.1111/j.1365-2788.2012.01609.x

By:

McCary, L. M.;
Roberts, J. E.

Publication type:

Article

Recognition of facial emotion and affective prosody in children with ASD (+ADHD) and their unaffected siblings.

Published in:

European Child & Adolescent Psychiatry, 2014, v. 23, n. 5, p. 257, doi. 10.1007/s00787-013-0446-2

By:

Oerlemans, Anoek;
Meer, Jolanda;
Steijn, Daphne;
Ruiter, Saskia;
Bruijn, Yvette;
Sonneville, Leo;
Buitelaar, Jan;
Rommelse, Nanda

Publication type:

Article

A case report of two male siblings with autism and duplication of Xq13-q21, a region including three genes predisposing for autism.

Published in:

European Child & Adolescent Psychiatry, 2014, v. 23, n. 5, p. 329, doi. 10.1007/s00787-013-0455-1

By:

Wentz, Elisabet;
Vujic, Mihailo;
Kärrstedt, Ewa-Lotta;
Erlandsson, Anna;
Gillberg, Christopher

Publication type:

Article

Association of autism with polyomavirus infection in postmortem brains.

Published in:

Journal of NeuroVirology, 2010, v. 16, n. 2, p. 141, doi. 10.3109/13550281003685839

By:

Lintas, Carla;
Altieri, Laura;
Lombardi, Federica;
Sacco, Roberto;
Persico, Antonio M.

Publication type:

Article

Triggers for Autism: Genetic and Environmental Factors.

Published in:

Journal of Central Nervous System Disease, 2012, v. 4, n. 3, p. 1, doi. 10.4137/JCNSD.S9058

By:

Matsuzaki, Hideo;
Iwata, Keiko;
Manabe, Takayuki;
Mori, Norio

Publication type:

Article

Genetic Studies of Autism: From the 1970's into the Millennium.

Published in:

Journal of Abnormal Child Psychology, 2000, v. 28, n. 1, p. 3, doi. 10.1023/A:1005113900068

By:

Rutter, Michael

Publication type:

Article

NEUROPSYCHIATRY: Recognizing and Treating Comorbid Psychiatric Disorders in People With Autism.

Published in:

Psychiatric Times, 2019, v. 36, n. 8, p. 14

By:

Collins, Heidi C.;
Siegel, Matthew S.

Publication type:

Article

Research Points to Shared Environmental Factors for Autism and ASD.

Published in:

Psychiatric Times, 2012, v. 29, n. 3, p. 1

By:

Kaplan, Arline

Publication type:

Article

Autism and Schizophrenia.

Published in:

Psychiatric Times, 2011, v. 28, n. 3, p. 34

By:

Dvir, Yael;
Frazier, Jean A.

Publication type:

Article

Protein Interaction Networks Reveal Novel Autism Risk Genes within GWAS Statistical Noise.

Published in:

PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0112399

By:

Correia, Catarina;
Oliveira, Guiomar;
Vicente, Astrid M.

Publication type:

Article

A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease.

Published in:

PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111462

By:

Zheng, Xiaojing;
Demirci, F. Yesim;
Barmada, M. Michael;
Richardson, Gale A.;
Lopez, Oscar L.;
Sweet, Robert A.;
Kamboh, M. Ilyas;
Feingold, Eleanor

Publication type:

Article

A Genome-Wide Survey of Transgenerational Genetic Effects in Autism.

Published in:

PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0076978

By:

Tsang, Kathryn M.;
Croen, Lisa A.;
Torres, Anthony R.;
Kharrazi, Martin;
Delorenze, Gerald N.;
Windham, Gayle C.;
Yoshida, Cathleen K.;
Zerbo, Ousseny;
Weiss, Lauren A.

Publication type:

Article

Brain-Derived Neurotrophic Factor Role in Autism Remains Elusive: A Flashback on the Route That Has Brought Us Here.

Published in:

Acta Medica Iranica, 2017, v. 55, n. 12, p. 733

By:

Rahmani, Farzaneh;
Rezaei, Nima

Publication type:

Article

Exploring links between genotypes, phenotypes, and clinical predictors of response to early intensive behavioral intervention in autism spectrum disorder.

Published in:

Frontiers in Human Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnhum.2013.00567

By:

Eapen, Valsamma;
rnčec, Rudi Č;
Walter, Amelia

Publication type:

Article

Evidence for Dysregulation of Axonal Growth and Guidance in the Etiology of ASD.

Published in:

Frontiers in Human Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnhum.2013.00671

By:

McFadden, Kathryn;
Minshew, Nancy

Publication type:

Article

Genome-wide association study of autistic-like traits in a general population study of young adults.

Published in:

Frontiers in Human Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnhum.2013.00658

By:

Jones, Rachel Maree;
Abraham, Lawrence;
Cadby, Gemma;
Melton, Phillip;
Moses, Eric;
Whitehouse, Andrew

Publication type:

Article

Cerberus, an Access Control Scheme for Enforcing Least Privilege in Patient Cohort Study Platforms.

Published in:

Journal of Medical Systems, 2018, v. 42, n. 1, p. 1, doi. 10.1007/s10916-017-0844-y

By:

Parrend, Pierre;
Mazzucotelli, Timothée;
Colin, Florent;
Collet, Pierre;
Mandel, Jean-Louis

Publication type:

Article

Autism cornered: network analyses reveal mechanisms of autism spectrum disorders.

Published in:

Molecular Systems Biology, 2014, v. 10, n. 12, p. 1, doi. 10.15252/msb.20145937

By:

Auffray, Charles

Publication type:

Article