HuGE Literature Finder
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Records 1-100
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Getting to the Cores of Autism.
Cell 2019 Sep 178 (6): 1287-1298. Iakoucheva Lilia M, Muotri Alysson R, Sebat Jonath |
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The interaction between OXTR rs2268493 and perceived maternal care is associated with amygdala-dorsolateral prefrontal effective connectivity during explicit emotion processing.
European archives of psychiatry and clinical neuroscience 2019 Aug . Antonucci Linda A, Pergola Giulio, Passiatore Roberta, Taurisano Paolo, Quarto Tiziana, Dispoto Eleonora, Rampino Antonio, Bertolino Alessandro, Cassibba Rosalinda, Blasi Giusep |
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Cerebellar lesions as potential predictors of neurobehavioural phenotype in tuberous sclerosis complex.
Developmental medicine and child neurology 2019 Jul . Toldo Irene, Bugin Samuela, Perissinotto Egle, Pelizza Maria Federica, Vignoli Aglaia, Parazzini Cecilia, Canevini Maria Paola, Nosadini Margherita, Sartori Stefano, Manara Ren |
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Psychiatric Polygenic Risk Scores as Predictor for Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in a Clinical Child and Adolescent Sample.
Behavior genetics 2019 Jul . Jansen Arija G, Dieleman Gwen C, Jansen Philip R, Verhulst Frank C, Posthuma Danielle, Polderman Tinca J |
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eNeuro 2019 Jun . Trent Simon, Hall Jeremy, Connelly William M, Errington Adam |
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Associations between autistic-like traits and polymorphisms in NFKBIL1.
Acta neuropsychiatrica 2019 Jun 1-10. Strenn Nina, Hovey Daniel, Jonsson Lina, Anckarsäter Henrik, Lundström Sebastian, Lichtenstein Paul, Ekman Agne |
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Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population.
BMC psychiatry 2019 May 19 (1): 159. Wang Ziqi, Zhang Tian, Liu Jing, Wang Han, Lu Tianlan, Jia Meixiang, Zhang Dai, Wang Lifang, Li J |
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Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
The lancet. Psychiatry 2019 May . Chawner Samuel J R A, Owen Michael J, Holmans Peter, Raymond F Lucy, Skuse David, Hall Jeremy, van den Bree Marianne B |
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Polymorphisms of Ionotropic Glutamate Receptor-Related Genes and the Risk of Autism Spectrum Disorder in a Chinese Population.
Psychiatry investigation 2019 May 16 (5): 379-385. Xie Xinyan, Hou Fang, Li Li, Chen Yanlin, Liu Lingfei, Luo Xiu, Gu Huaiting, Li Xin, Zhang Jiajia, Gong Jianhua, Song Ranr |
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Variations in Genes Related to Sleep Patterns in Children With Autism Spectrum Disorder.
Biological research for nursing 2019 May 21 (3): 335-342. Johansson Ann E E, Dorman Janice S, Chasens Eileen R, Feeley Christine A, Devlin Bern |
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Association of Rare Copy Number Variants With Risk of Depression.
JAMA psychiatry 2019 Apr . Kendall Kimberley Marie, Rees Elliott, Bracher-Smith Matthew, Legge Sophie, Riglin Lucy, Zammit Stanley, O'Donovan Michael Conlon, Owen Michael John, Jones Ian, Kirov George, Walters James Tynan Rh |
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Association Study of Sequence Variants in Voltage-gated Ca2+ Channel Subunit Alpha-1C and Autism Spectrum Disorders.
Reports of biochemistry & molecular biology 2019 Apr 8 (1): 56-62. Sayad Arezou, Ghafouri-Fard Soudeh, Noroozi Rezvan, Omrani Mir Davood, Ganji Maziar, Dastmalchi Romina, Glassy Mark, Taheri Mohamm |
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Cumulative Risk of the Oxytocin Receptor Gene Interacts with Prenatal Exposure to Oxytocin Receptor Antagonist to Predict Children's Social Communication Development.
Autism research : official journal of the International Society for Autism Research 2019 Apr . Friedlander Edwa, Yirmiya Nurit, Laiba Efrat, Harel-Gadassi Ayelet, Yaari Maya, Feldstein Ohad, Mankuta David, Israel Salom |
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Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders.
European journal of human genetics : EJHG 2019 Apr . Nudel Ron, Benros Michael E, Krebs Morten Dybdahl, Allesøe Rosa Lundbye, Lemvigh Camilla Koldbæk, Bybjerg-Grauholm Jonas, Børglum Anders D, Daly Mark J, Nordentoft Merete, Mors Ole, Hougaard David M, Mortensen Preben Bo, Buil Alfonso, Werge Thomas, Rasmussen Simon, Thompson Wesley |
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Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Biological psychiatry 2019 Apr 85 (7): 563-572. Silva Ana I, Ulfarsson Magnus O, Stefansson Hreinn, Gustafsson Omar, Walters G Bragi, Linden David E J, Wilkinson Lawrence S, Drakesmith Mark, Owen Michael J, Hall Jeremy, Stefansson Ka |
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Study of C677T variant of methylene tetrahydrofolate reductase gene in autistic spectrum disorder Egyptian children.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019 Apr . Ismail Samira, Senna Azza Abo, Behiry Eman G, Ashaat Engy A, Zaki Maha S, Ashaat Neveen A, Salah Dina |
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Auditory evoked response delays in children with 47,XYY syndrome.
Neuroreport 2019 Mar . Bloy Luke, Ku Matthew, Edgar J Christopher, Miller Judith S, Blaskey Lisa, Ross Judith, Roberts Timothy P |
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CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
European journal of medical genetics 2019 Mar . Repnikova Elena A, Lyalin Dmitry A, McDonald Kimberly, Astbury Caroline, Hansen-Kiss Emily, Cooley Linda D, Pfau Ruthann, Herman Gail E, Pyatt Robert E, Hickey Scott |
Common-variant associations with fragile X syndrome.
Molecular psychiatry 2019 Mar 24 (3): 338-344. Crowley James J, Szatkiewicz Jin, Kähler Anna K, Giusti-Rodriguez Paola, Ancalade NaEshia, Booker Jessica K, Carr Jennifer L, Crawford Greg E, Losh Molly, Stockmeier Craig A, Taylor Annette K, Piven Joseph, Sullivan Patrick |
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Genetic variation of UBE3A is associated with schizotypy in a population of typical individuals.
Psychiatry research 2019 Mar 275 94-99. Salminen Iiro, Read Silven, Hurd Pete, Crespi Berna |
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Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
Biological psychiatry 2019 Mar . Zhang Xianglong, Abdellaoui Abdel, Rucker James, de Jong Simone, Potash James B, Weissman Myrna M, Shi Jianxin, Knowles James A, Pato Carlos, Pato Michele, Sobell Janet, Smit Johannes H, Hottenga Jouke-Jan, de Geus Eco J C, Lewis Cathryn M, Buttenschøn Henriette N, Craddock Nick, Jones Ian, Jones Lisa, McGuffin Peter, Mors Ole, Owen Michael J, Preisig Martin, Rietschel Marcella, Rice John P, Rivera Margarita, Uher Rudolf, Gejman Pablo V, Sanders Alan R, Boomsma Dorret, Penninx Brenda W J H, Breen Gerome, Levinson Douglas |
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Identification of common genetic risk variants for autism spectrum disorder.
Nature genetics 2019 Mar 51 (3): 431-444. Grove Jakob, Ripke Stephan, Als Thomas D, Mattheisen Manuel, Walters Raymond K, Won Hyejung, Pallesen Jonatan, Agerbo Esben, Andreassen Ole A, Anney Richard, Awashti Swapnil, Belliveau Rich, Bettella Francesco, Buxbaum Joseph D, Bybjerg-Grauholm Jonas, Bækvad-Hansen Marie, Cerrato Felecia, Chambert Kimberly, Christensen Jane H, Churchhouse Claire, Dellenvall Karin, Demontis Ditte, De Rubeis Silvia, Devlin Bernie, Djurovic Srdjan, Dumont Ashley L, Goldstein Jacqueline I, Hansen Christine S, Hauberg Mads Engel, Hollegaard Mads V, Hope Sigrun, Howrigan Daniel P, Huang Hailiang, Hultman Christina M, Klei Lambertus, Maller Julian, Martin Joanna, Martin Alicia R, Moran Jennifer L, Nyegaard Mette, Nærland Terje, Palmer Duncan S, Palotie Aarno, Pedersen Carsten Bøcker, Pedersen Marianne Giørtz, dPoterba Timothy, Poulsen Jesper Buchhave, Pourcain Beate St, Qvist Per, Rehnström Karola, Reichenberg Abraham, Reichert Jennifer, Robinson Elise B, Roeder Kathryn, Roussos Panos, Saemundsen Evald, Sandin Sven, Satterstrom F Kyle, Davey Smith George, Stefansson Hreinn, Steinberg Stacy, Stevens Christine R, Sullivan Patrick F, Turley Patrick, Walters G Bragi, Xu Xinyi, , , , , Stefansson Kari, Geschwind Daniel H, Nordentoft Merete, Hougaard David M, Werge Thomas, Mors Ole, Mortensen Preben Bo, Neale Benjamin M, Daly Mark J, Børglum Anders |
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Interaction of glutathione S-transferase polymorphisms and tobacco smoking during pregnancy in susceptibility to autism spectrum disorders.
Scientific reports 2019 Mar 9 (1): 3206. Mandic-Maravic Vanja, Coric Vesna, Mitkovic-Voncina Marija, Djordjevic Miroslav, Savic-Radojevic Ana, Ercegovac Marko, Matic Marija, Simic Tatjana, Lecic-Tosevski Dusica, Toskovic Oliver, Pekmezovic Tatjana, Pljesa-Ercegovac Marija, Pejovic-Milovancevic Mili |
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Neurexin 3 transmembrane and soluble isoform expression and splicing haplotype are associated with neuron inflammasome and Alzheimer's disease.
Alzheimer's research & therapy 2019 Mar 11 (1): 28. Hishimoto Akitoyo, Pletnikova Olga, Lang Doyle Lu, Troncoso Juan C, Egan Josephine M, Liu Qing-Ro |
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Screening for rare epigenetic variations in autism and schizophrenia.
Human mutation 2019 Mar . Garg Paras, Sharp Andrew |
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Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort.
The British journal of psychiatry : the journal of mental science 2019 Feb 1-7. Underwood Jack F G, Kendall Kimberley M, Berrett Jennifer, Lewis Catrin, Anney Richard, van den Bree Marianne B M, Hall Jere |
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Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.
The British journal of psychiatry : the journal of mental science 2019 Feb 1-8. Kendall Kimberley M, Bracher-Smith Matthew, Fitzpatrick Harry, Lynham Amy, Rees Elliott, Escott-Price Valentina, Owen Michael J, O'Donovan Michael C, Walters James T R, Kirov Geor |
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Genetic association of DNMT variants can play a critical role in defining the methylation patterns in autism.
IUBMB life 2019 Feb . Alex Ann Mary, Saradalekshmi Korammannil R, Shilen Neena, Suresh Poovathinal A, Banerjee Moin |
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Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.
Human mutation 2019 Feb . Zhou Wei-Zhen, Zhang Jie, Li Ziyi, Lin Xiaojing, Li Jiarui, Wang Sheng, Yang Changhong, Wu Qixi, Ye Adam Yongxin, Wang Meng, Wang Dandan, Pu Tad Zhengzhang, Wu Yu-Yu, Wei Lipi |
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A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
Translational psychiatry 2019 Jan 9 (1): 31. Zhang Linna, Qin Yue, Gong Xiaohong, Peng Rui, Cai Chunquan, Zheng Yufang, Du Yasong, Wang Hongy |
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Association between CNTNAP2 polymorphisms and autism: A family-based study in the chinese han population and a meta-analysis combined with GWAS data of psychiatric genomics consortium.
Autism research : official journal of the International Society for Autism Research 2019 Jan . Zhang Tian, Zhang Jishui, Wang Ziqi, Jia Meixiang, Lu Tianlan, Wang Han, Yue Weihua, Zhang Dai, Li Jun, Wang Lifa |
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Autistic traits and components of the folate metabolic system: an explorative analysis in the eastern Indian ASD subjects
Nutritional neuroscience 2019 Jan 1-8. Saha Sharmistha, Saha Tanusree, Sinha Swagata, Rajamma Usha, Mukhopadhyay Kanch |
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Common Polygenic Variations for Psychiatric Disorders and Cognition in Relation to Brain Morphology in the General Pediatric Population.
Journal of the American Academy of Child and Adolescent Psychiatry 2019 Jan . Alemany Silvia, Jansen Philip R, Muetzel Ryan L, Marques Natália, El Marroun Hanan, Jaddoe Vincent W V, Polderman Tinca J C, Tiemeier Henning, Posthuma Danielle, White Ton |
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Genome-wide association study and identification of chromosomal enhancer maps in multiple brain regions related to autism spectrum disorder.
Autism research : official journal of the International Society for Autism Research 2019 Jan 12 (1): 26-32. Zhang Lu, Liu Li, Wen Yan, Ma Mei, Cheng Shiqiang, Yang Jian, Li Ping, Cheng Bolun, Du Yanan, Liang Xiao, Zhao Yan, Ding Miao, Guo Xiong, Zhang Fe |
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SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
Autism research : official journal of the International Society for Autism Research 2019 Jan . Qiu Shuang, Li Yan, Bai Ye, Shi Jikang, Cui Heran, Gu Yulu, Ren Yaxuan, Zhao Qian, Zhang Kaixin, Lu Meihan, Wang Yihan, Li Yong, Zhong Weijing, Zhu Xiaojuan, Liu Yunkai, Cheng Yi, Qiao Yichun, Liu Yaw |
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Analysis of the SNP rs3747333 and rs3747334 in NLGN4X gene in autism spectrum disorder: a meta-analysis.
Annals of general psychiatry 2019 18 6. Sun Hongli, Yang Ying, Zhang Liyu, Wu Haibin, Zhang Huifang, Li H |
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Association Between 5-HTTLPR Polymorphism and the Risk of Autism: A Meta-Analysis Based on Case-Control Studies.
Frontiers in psychiatry 2019 10 51. Wang Hongbing, Yin Fangna, Gao Junwei, Fan Xiaota |
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Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
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Dysregulated Ca
Frontiers in synaptic neuroscience 2019 11 2. Danesi Claudia, Keinänen Kari, Castrén Maija |
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Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter trafficking.
Human molecular genetics 2019 04 28 (7): 1153-1161. Gabriele Stefano, Canali Marco, Lintas Carla, Sacco Roberto, Tirindelli Maria Cristina, Ricciardello Arianna, Persico Antonio |
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Genetic variation associated with chromosomal aberration frequency: A genome-wide association study.
Environmental and molecular mutagenesis 2019 01 60 (1): 17-28. Niazi Yasmeen, Thomsen Hauke, Smolkova Bozena, Vodickova Ludmila, Vodenkova Sona, Kroupa Michal, Vymetalkova Veronika, Kazimirova Alena, Barancokova Magdalena, Volkovova Katarina, Staruchova Marta, Hoffmann Per, Nöthen Markus M, Dušinská Maria, Musak Ludovit, Vodicka Pavel, Hemminki Kari, Försti As |
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Genetics of response to cognitive behavior therapy in adults with major depression: a preliminary report.
Molecular psychiatry 2019 04 24 (4): 484-490. Andersson Evelyn, Crowley James J, Lindefors Nils, Ljótsson Brjánn, Hedman-Lagerlöf Erik, Boberg Julia, El Alaoui Samir, Karlsson Robert, Lu Yi, Mattheisen Manuel, Kähler Anna K, Svanborg Cecilia, Mataix-Cols David, Mattsson Simon, Forsell Erik, Kaldo Viktor, Schalling Martin, Lavebratt Catharina, Sullivan Patrick F, Rück Christi |
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MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism.
PeerJ 2019 6 e6183. Capkova Pavlina, Srovnal Josef, Capkova Zuzana, Staffova Katerina, Becvarova Vera, Trkova Marie, Adamova Katerina, Santava Alena, Curtisova Vaclava, Hajduch Marian, Prochazka Mart |
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No Association between the rs1799836 Polymorphism of the Monoamine Oxidase B Gene and the Risk of Autism Spectrum Disorders in the Kazakhstani Population.
Disease markers 2019 2019 2846394. Perfilyeva Anastassiya V, Bespalova Kira B, Skvortsova Liliya A, Surdeanu Assel, Garshin Aleksandr A, Perfilyeva Yuliya V, Khamdiyeva Ozada Kh, Bekmanov Bakhytzhan O, Djansugurova Leyla |
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Outgroup Machine Learning Approach Identifies Single Nucleotide Variants in Noncoding DNA Associated with Autism Spectrum Disorder.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2019 24 260-271. Varma Maya, Paskov Kelley Marie, Jung Jae-Yoon, Sierra Chrisman Brianna, Stockham Nate Tyler, Washington Peter Yigitcan, Wall Dennis Pa |
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The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children.
Frontiers in neurology 2019 10 505. Long Shasha, Zhou Hao, Li Shuang, Wang Tianqi, Ma Yu, Li Chunpei, Zhou Yuanfeng, Zhou Shuizhen, Wu Bingbing, Wang |
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The Drosophila Gene
Frontiers in genetics 2019 10 574. Hope Kevin A, Flatten Daniel, Cavitch Peter, May Ben, Sutcliffe James S, O'Donnell Janis, Reiter Lawrence |
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The oxytocin receptor gene predicts brain activity during an emotion recognition task in autism.
Molecular autism 2019 10 12. Uzefovsky Florina, Bethlehem Richard A I, Shamay-Tsoory Simone, Ruigrok Amber, Holt Rosemary, Spencer Michael, Chura Lindsay, Warrier Varun, Chakrabarti Bhismadev, Bullmore Ed, Suckling John, Floris Dorothea, Baron-Cohen Sim |
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No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children.
Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2018 Nov 16 (4): 415-421. Bozdogan Sevcan Tug, Kutuk Meryem Ozlem, Tufan Evren, Altintas Zuhal, Temel Gülhan Orekici, Toros Fevzi |
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The 5-HTTLPR polymorphism of the serotonin transporter gene and child's sex moderate the relationship between disaster-related prenatal maternal stress and autism spectrum disorder traits: The QF2011 Queensland flood study.
Development and psychopathology 2018 Nov 1-15. Laplante David P, Simcock Gabrielle, Cao-Lei Lei, Mouallem Maya, Elgbeili Guillaume, Brunet Alain, Cobham Vanessa, Kildea Sue, King Suzan |
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Association study between inwardly rectifying potassium channels 2.1 and 4.1 and autism spectrum disorders.
Life sciences 2018 Oct . Sun Caihong, Zou Mingyang, Li Ling, Li Dexin, Ma Yongjuan, Xia Wei, Wu Lijie, Ren Hu |
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Autism & Gluten: The Proof By Regression!
Pediatric neurology briefs 2018 Sep 32 9. Rahmoune Hakim, Boutrid Na |
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Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Nature 2018 Sep . Niemi Mari E K, Martin Hilary C, Rice Daniel L, Gallone Giuseppe, Gordon Scott, Kelemen Martin, McAloney Kerrie, McRae Jeremy, Radford Elizabeth J, Yu Sui, Gecz Jozef, Martin Nicholas G, Wright Caroline F, Fitzpatrick David R, Firth Helen V, Hurles Matthew E, Barrett Jeffrey |
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Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Cell reports 2018 Sep 24 (11): 2838-2856. Kushima Itaru, Aleksic Branko, Nakatochi Masahiro, Shimamura Teppei, Okada Takashi, Uno Yota, Morikawa Mako, Ishizuka Kanako, Shiino Tomoko, Kimura Hiroki, Arioka Yuko, Yoshimi Akira, Takasaki Yuto, Yu Yanjie, Nakamura Yukako, Yamamoto Maeri, Iidaka Tetsuya, Iritani Shuji, Inada Toshiya, Ogawa Nanayo, Shishido Emiko, Torii Youta, Kawano Naoko, Omura Yutaka, Yoshikawa Toru, Uchiyama Tokio, Yamamoto Toshimichi, Ikeda Masashi, Hashimoto Ryota, Yamamori Hidenaga, Yasuda Yuka, Someya Toshiyuki, Watanabe Yuichiro, Egawa Jun, Nunokawa Ayako, Itokawa Masanari, Arai Makoto, Miyashita Mitsuhiro, Kobori Akiko, Suzuki Michio, Takahashi Tsutomu, Usami Masahide, Kodaira Masaki, Watanabe Kyota, Sasaki Tsukasa, Kuwabara Hitoshi, Tochigi Mamoru, Nishimura Fumichika, Yamasue Hidenori, Eriguchi Yosuke, Benner Seico, Kojima Masaki, Yassin Walid, Munesue Toshio, Yokoyama Shigeru, Kimura Ryo, Funabiki Yasuko, Kosaka Hirotaka, Ishitobi Makoto, Ohmori Tetsuro, Numata Shusuke, Yoshikawa Takeo, Toyota Tomoko, Yamakawa Kazuhiro, Suzuki Toshimitsu, Inoue Yushi, Nakaoka Kentaro, Goto Yu-Ichi, Inagaki Masumi, Hashimoto Naoki, Kusumi Ichiro, Son Shuraku, Murai Toshiya, Ikegame Tempei, Okada Naohiro, Kasai Kiyoto, Kunimoto Shohko, Mori Daisuke, Iwata Nakao, Ozaki Nor |
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De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Cell reports 2018 Sep 24 (13): 3441-3454.e12. Wang Sheng, Mandell Jeffrey D, Kumar Yogesh, Sun Nawei, Morris Montana T, Arbelaez Juan, Nasello Cara, Dong Shan, Duhn Clif, Zhao Xin, Yang Zhiyu, Padmanabhuni Shanmukha S, Yu Dongmei, King Robert A, Dietrich Andrea, Khalifa Najah, Dahl Niklas, Huang Alden Y, Neale Benjamin M, Coppola Giovanni, Mathews Carol A, Scharf Jeremiah M, , , , Fernandez Thomas V, Buxbaum Joseph D, De Rubeis Silvia, Grice Dorothy E, Xing Jinchuan, Heiman Gary A, Tischfield Jay A, Paschou Peristera, Willsey A Jeremy, State Matthew |
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FADS1-FADS2 and ELOVL2 gene polymorphisms in susceptibility to autism spectrum disorders in Chinese children.
BMC psychiatry 2018 Sep 18 (1): 283. Sun Caihong, Zou Mingyang, Wang Xuelai, Xia Wei, Ma Yongjuan, Liang Shuang, Hao Yanqiu, Wu Lijie, Fu Songb |
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NBEA: developmental disease gene with early generalized epilepsy phenotypes.
Annals of neurology 2018 Sep . Mulhern Maureen S, Stumpel Constance, Stong Nicholas, Brunner Han G, Bier Louise, Lippa Natalie, Riviello James, Rouhl Rob P W, Kempers Marlies, Pfundt Rolph, Stegmann Alexander P A, Kukolich Mary K, Telegrafi Aida, Lehman Anna, , Lopez-Rangel Elena, Houcinat Nada, Barth Magalie, den Hollander Nicolette, Hoffer Mariette Jv, Weckhuysen Sarah, , Roovers Jolien, Djemie Tania, Barca Diana, Ceulemans Berten, Craiu Dana, Lemke Johannes R, Korff Christian, Mefford Heather C, Meyers Candace T, Siegler Zsuzsanna, Hiatt Susan M, Cooper Gregory M, Martina Bebin E, Snijders-Blok Lot, Veenstra-Knol Hermine E, Baugh Evan H, Brilstra E H, Volker-Touw Catharina M L, van Binsbergen Ellen, Revah-Politi Anya, Pereira Elaine, McBrian Danielle, Pacault Mathilde, Isidor Bertrand, Le Caignec Cedric, Gilbert-Dussardier Brigitte, Bilan Frederic, Heinzen Erin L, Goldstein David B, Stevens Servi J C, Sands Tristan |
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A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.
Asian journal of psychiatry 2018 Aug 37 121-129. Devasenapathy Subhashree, Midha Rashi, Naskar Teesta, Mehta Anuradha, Prajapati Bharat, Ummekulsum Mariam, Sagar Rajesh, Singh Nandini C, Sinha Subra |
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Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population.
Translational psychiatry 2018 Aug 8 (1): 152. Wang Linyan, Li Jun, Shuang Mei, Lu Tianlan, Wang Ziqi, Zhang Tian, Yue Weihua, Jia Meixiang, Ruan Yanyan, Liu Jing, Wu Zhiliu, Zhang Dai, Wang Lifa |
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Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.
Molecular psychiatry 2018 Aug . Erlangsen Annette, Appadurai Vivek, Wang Yunpeng, Turecki Gustavo, Mors Ole, Werge Thomas, Mortensen Preben B, Starnawska Anna, Børglum Anders D, Schork Andrew, Nudel Ron, Bækvad-Hansen Marie, Bybjerg-Grauholm Jonas, Hougaard David M, Thompson Wesley K, Nordentoft Merete, Agerbo Esb |
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Levels of peripheral Neuregulin 1 are increased in non-medicated autism spectrum disorder patients.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2018 Aug . Esnafoglu Erm |
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Polygenic Scores for Neuropsychiatric Traits and White Matter Microstructure in the Pediatric Population.
Biological psychiatry. Cognitive neuroscience and neuroimaging 2018 Aug . Jansen Philip R, Muetzel Ryan L, Polderman Tinca J C, Jaddoe Vincent W, Verhulst Frank C, van der Lugt Aad, Tiemeier Henning, Posthuma Danielle, White Ton |
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Meta-analysis of GABRB3 Gene Polymorphisms and Susceptibility to Autism Spectrum Disorder.
Journal of molecular neuroscience : MN 2018 Jul . Noroozi Rezvan, Taheri Mohammad, Ghafouri-Fard Soudeh, Bidel Zeinab, Omrani Mir Davood, Moghaddam Ali Sanjari, Sarabi Parisa, Jarahi Alireza Mosa |
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Relationships between substance abuse/dependence and psychiatric disorders based on polygenic scores.
Genes, brain, and behavior 2018 Jul e12504. Gurriarán Xaquín, Rodríguez-López Julio, Flórez Gerardo, Pereiro César, Fernández José Manuel, Fariñas Emilio, Estévez Valentín, , Arrojo Manuel, Costas Javi |
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Adults with Autism and Adults with Depression Show Similar Attentional Biases to Social-Affective Images.
Journal of autism and developmental disorders 2018 Jun . Unruh Kathryn E, Bodfish James W, Gotham Katherine |
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Evidence for Association Between OXTR Gene and ASD Clinical Phenotypes.
Journal of molecular neuroscience : MN 2018 Jun . de Oliveira Pereira Ribeiro Lucas, Vargas-Pinilla Pedro, Kappel Djenifer B, Longo Danae, Ranzan Josiane, Becker Michele Michelin, Dos Santos Riesgo Rudimar, Schuler-Faccini Lavinia, Roman Tatiana, Schuch Jaqueline Bohr |
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Genetic association between SHANK2 polymorphisms and susceptibility to autism spectrum disorder.
IUBMB life 2018 Jun . Bai Ye, Qiu Shuang, Li Yan, Li Yong, Zhong Weijing, Shi Meijuan, Zhu Xiaojuan, Jiang Huiyi, Yu Yaqin, Cheng Yi, Liu Yaw |
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Genome wide analysis of rare copy number variations in alcohol abuse or dependence.
Journal of psychiatric research 2018 Jun 103 212-218. Rodríguez-López Julio, Flórez Gerardo, Blanco Vanessa, Pereiro César, Fernández José Manuel, Fariñas Emilio, Estévez Valentín, Gómez-Trigo Jesús, Gurriarán Xaquín, Calvo Raquel, Sáiz Pilar, , Vázquez Fernando Lino, Arrojo Manuel, Costas Javi |
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Increased expression of BDNF mRNA in the frontal cortex of autistic patients.
Behavioural brain research 2018 Jun . Maussion Gilles, Moalic Jean-Marie, Simonneau Michel, Gorwood Philip, Ramoz Nicol |
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Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHD.
Journal of developmental and physical disabilities 2018 Jun 30 (3): 355-371. Barrie Elizabeth S, Pinsonneault Julia K, Sadee Wolfgang, Hollway Jill A, Handen Benjamin L, Smith Tristram, Arnold L Eugene, Butter Eric, Hansen-Kiss Emily, Herman Gail E, Aman Michael |
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UGT1A1 polymorphisms associated with prolactin response in risperidone-treated children and adolescents with autism spectrum disorder.
The pharmacogenomics journal 2018 Jun . Hongkaew Yaowaluck, Medhasi Sadeep, Pasomsub Ekawat, Ngamsamut Nattawat, Puangpetch Apichaya, Vanwong Natchaya, Chamnanphon Monpat, Limsila Penkhae, Suthisisang Chuthamanee, Wilffert Bob, Sukasem Chonlaph |
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HLA-class II haplotypes and Autism Spectrum Disorders.
Scientific reports 2018 May 8 (1): 7639. Bennabi Meriem, Gaman Alexandru, Delorme Richard, Boukouaci Wahid, Manier Céline, Scheid Isabelle, Si Mohammed Nassima, Bengoufa Djaouida, Charron Dominique, Krishnamoorthy Rajagopal, Leboyer Marion, Tamouza Ry |
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Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD).
Journal of molecular neuroscience : MN 2018 May . Mahdavi Manijeh, Kheirollahi Majid, Riahi Roya, Khorvash Fariborz, Khorrami Mehdi, Mirsafaie Mary |
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Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.
The British journal of psychiatry : the journal of mental science 2018 May 212 (5): 287-294. Thygesen Johan H, Wolfe Kate, McQuillin Andrew, Viñas-Jornet Marina, Baena Neus, Brison Nathalie, D'Haenens Greet, Esteba-Castillo Susanna, Gabau Elisabeth, Ribas-Vidal Núria, Ruiz Anna, Vermeesch Joris, Weyts Eddy, Novell Ramon, Buggenhout Griet Van, Strydom André, Bass Nick, Guitart Miriam, Vogels Anni |
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Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.
Behavioural brain research 2018 May . Wang Geng-Fu, Ye Sheng, Gao Lei, Han Yu, Guo Xuan, Dong Xiao-Peng, Su Yuan-Yuan, Zhang X |
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An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder.
Molecular psychiatry 2018 Apr . Williams Sarah M, An Joon Yong, Edson Janette, Watts Michelle, Murigneux Valentine, Whitehouse Andrew J O, Jackson Colin J, Bellgrove Mark A, Cristino Alexandre S, Claudianos Charl |
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Association of copy number variation across the genome with neuropsychiatric traits in the general population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 Apr . Guyatt Anna L, Stergiakouli Evie, Martin Joanna, Walters James, O'Donovan Michael, Owen Michael, Thapar Anita, Kirov George, Rodriguez Santiago, Rai Dheeraj, Zammit Stan, Gaunt Tom |
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The role of genetic variation of human metabolism for BMI, mental traits and mental disorders.
Molecular metabolism 2018 Apr . Hebebrand Johannes, Peters Triinu, Schijven Dick, Hebebrand Moritz, Grasemann Corinna, Winkler Thomas W, Heid Iris M, Antel Jochen, Föcker Manuel, Tegeler Lisa, Brauner Lena, Adan Roger A H, Luykx Jurjen J, Correll Christoph U, König Inke R, Hinney Anke, Libuda La |
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Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder.
Clinica chimica acta; international journal of clinical chemistry 2018 Apr 479 144-147. Li Shi-Jun, Yu Shan-Shan, Luo Hong-Yu, Li Xin, Rao Bin, Wang Yi, Li Zhen-Zhen, Liu Gang, Zou Li-Ping, Zhang Ji-Shui, Feng Chen, Liu Jing, Liu Jian-Wei, Hu Nan, Chen Xiao-Qiao, Yu Sheng-Yuan, Li Ke, He Mian-Wang, Yu Xin-Guang, Wang Jun, Guo Sheng-Li, Chen Zhi-Ye, Zhang Lei, Ma L |
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An Investigation of
Psychiatry investigation 2018 Mar 15 (3): 300-305. Kara Tayfun, Akaltun Ismail, Cakmakoglu Bedia, Kaya Ilyas, Zoroglu Sal |
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Association between single nucleotide polymorphisms in estrogen receptor 1/2 genes and symptomatic severity of autism spectrum disorder.
Research in developmental disabilities 2018 Mar . Doi Hirokazu, Fujisawa Takashi X, Iwanaga Ryoichiro, Matsuzaki Junko, Kawasaki Chisato, Tochigi Mamoru, Sasaki Tsukasa, Kato Nobumasa, Shinohara Kazuyu |
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Association Study Between Metallothionein-3 Protein Polymorphisms and Autism.
Neurotoxicity research 2018 Mar . Yu MingXia, Cao Tao, Yu Dan, Huang Fushe |
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Copy number variation in fetal alcohol spectrum disorder.
Biochemistry and cell biology = Biochimie et biologie cellulaire 2018 Mar 1-6. Zarrei Mehdi, Hicks Geoffrey G, Reynolds James N, Thiruvahindrapuram Bhooma, Engchuan Worrawat, Pind Molly, Lamoureux Sylvia, Wei John, Wang Zhouzhi, Marshall Christian R, Wintle Richard F, Chudley Albert E, Scherer Stephen |
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Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.
Translational psychiatry 2018 Mar 8 (1): 35. Warrier Varun, Toro Roberto, Chakrabarti Bhismadev, , Børglum Anders D, Grove Jakob, , Hinds David A, Bourgeron Thomas, Baron-Cohen Sim |
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Association between SHANK3 polymorphisms and susceptibility to autism spectrum disorder.
Gene 2018 Feb . Qiu Shuang, Li Yan, Li Yong, Zhong Weijing, Shi Meijuan, Zhao Qian, Zhang Kaixin, Wang Yihan, Lu Meihan, Zhu Xiaojuan, Jiang Huiyi, Yu Yaqin, Cheng Yi, Liu Yaw |
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Genetic contribution to 'theory of mind' in adolescence.
Scientific reports 2018 Feb 8 (1): 3465. Warrier Varun, Baron-Cohen Sim |
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Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion.
Behavioral and brain functions : BBF 2018 Feb 14 (1): 4. Varga Noémi Ágnes, Pentelényi Klára, Balicza Péter, Gézsi András, Reményi Viktória, Hársfalvi Vivien, Bencsik Renáta, Illés Anett, Prekop Csilla, Molnár Mária Jud |
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Association Study of Polymorphisms in Genes Relevant to Vitamin B12 and Folate Metabolism with Childhood Autism Spectrum Disorder in a Han Chinese Population.
Medical science monitor : international medical journal of experimental and clinical research 2018 Jan 24 370-376. Zhang Zengyu, Yu Lianfang, Li Sufang, Liu J |
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Pharmacogenetics of Risperidone-Induced Insulin Resistance in Children and Adolescents with Autism Spectrum Disorder.
Basic & clinical pharmacology & toxicology 2018 Jan . Sukasem Chonlaphat, Vanwong Natchaya, Srisawasdi Pornpen, Ngamsamut Nattawat, Nuntamool Nopphadol, Hongkaew Yaowaluck, Puangpetch Apichaya, Chamkrachangpada Bhunnada, Limsila Penkh |
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The oxytocin receptor gene polymorphism -rs237902- is associated with the severity of autism spectrum disorder: A pilot study.
Asian journal of psychiatry 2018 Jan . Ocako?lu Fevzi Tuna, Köse Sezen, Özbaran Burcu, Onay Hüsey |
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Association of HLA alleles with autism.
Neuropsychiatric disease and treatment 2018 14 3259-3265. Sayad Arezou, Akbari Mohammad Taghi, Noroozi Rezvan, Omrani Mir Davood, Inoko Hidetoshi, Taheri Mohammad, Ghafouri-Fard Soud |
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Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development.
Molecular psychiatry 2018 03 23 (3): 747-758. Dang T, Duan W Y, Yu B, Tong D L, Cheng C, Zhang Y F, Wu W, Ye K, Zhang W X, Wu M, Wu B B, An Y, Qiu Z L, Wu B |
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Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
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Genetic and clinical evidence of mitochondrial dysfunction in autism spectrum disorder and intellectual disability.
Human molecular genetics 2018 03 27 (5): 891-900. Valiente-Pallejà Alba, Torrell Helena, Muntané Gerard, Cortés Maria J, Martínez-Leal Rafael, Abasolo Nerea, Alonso Yolanda, Vilella Elisabet, Martorell Lourd |
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Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder.
Frontiers in genetics 2018 9 594. Du Xiujuan, Gao Xueren, Liu Xin, Shen Lixiao, Wang Kai, Fan Yanjie, Sun Yu, Luo Xiaomei, Liu Huili, Wang Lili, Wang Yu, Gong Zhuwen, Wang Jianguo, Yu Yongguo, Li F |
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Heritable genotype contrast mining reveals novel gene associations specific to autism subgroups.
Journal of biomedical informatics 2018 01 77 50-61. Spencer Matt, Takahashi Nicole, Chakraborty Sounak, Miles Judith, Shyu Chi-R |
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Neurexin gene family variants as risk factors for autism spectrum disorder.
Autism research : official journal of the International Society for Autism Research 2018 01 11 (1): 37-43. Wang Jia, Gong Jianhua, Li Li, Chen Yanlin, Liu Lingfei, Gu HuaiTing, Luo Xiu, Hou Fang, Zhang Jiajia, Song Ranr |
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Neuropsychiatric disease-associated genetic variants of the dopamine transporter display heterogeneous molecular phenotypes.
The Journal of biological chemistry 2018 05 293 (19): 7250-7262. Herborg Freja, Andreassen Thorvald F, Berlin Frida, Loland Claus J, Gether Ulr |
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Polymorphisms in Vitamin D Receptor Genes in Association with Childhood Autism Spectrum Disorder.
Disease markers 2018 2018 7862892. Zhang Zengyu, Li Sufang, Yu Lianfang, Liu J |
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Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.
Translational psychiatry 2018 01 8 (1): 12. Yu Yanjie, Lin Yingni, Takasaki Yuto, Wang Chenyao, Kimura Hiroki, Xing Jingrui, Ishizuka Kanako, Toyama Miho, Kushima Itaru, Mori Daisuke, Arioka Yuko, Uno Yota, Shiino Tomoko, Nakamura Yukako, Okada Takashi, Morikawa Mako, Ikeda Masashi, Iwata Nakao, Okahisa Yuko, Takaki Manabu, Sakamoto Shinji, Someya Toshiyuki, Egawa Jun, Usami Masahide, Kodaira Masaki, Yoshimi Akira, Oya-Ito Tomoko, Aleksic Branko, Ohno Kinji, Ozaki Nor |
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