HuGE Literature Finder
Records 1-30
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Association Analysis of ANRIL Polymorphisms and Haplotypes with Autism Spectrum Disorders.
Journal of molecular neuroscience : MN 2020 Jul . Safa Amin, Noroozi Rezvan, Taheri Mohammad, Ghafouri-Fard Soud |
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Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes.
Translational psychiatry 2020 Jul 10 (1): 258. González-Peñas Javier, Costas Javier Costas, García-Alcón Alicia, Penzol María José, Rodríguez Julio, Rodríguez-Fontenla Cristina, Alonso-González Aitana, Fernández-Prieto Montse, Carracedo Ángel, Arango Celso, Parellada Ma |
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Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Translational psychiatry 2020 Jul 10 (1): 215. Yousaf Afsheen, Waltes Regina, Haslinger Denise, Klauck Sabine M, Duketis Eftichia, Sachse Michael, Voran Anette, Biscaldi Monica, Schulte-Rüther Martin, Cichon Sven, Nöthen Markus, Ackermann Jörg, Koch Ina, Freitag Christine M, Chiocchetti Andreas |
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Right Posterior Insula and Putamen Volume Mediate the Effect of Oxytocin Receptor Polygenic Risk for Autism Spectrum Disorders on Reward Dependence in Healthy Adults.
Cerebral cortex (New York, N.Y. : 1991) 2020 Jul . Wang Junping, Zhang Peng, Li Wei, Wen Qin, Liu Feng, Xu Jiayuan, Xu Qiang, Zhu Dan, Ye Zhaoxiang, Yu Chunsh |
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Polymorphism of interleukin-1ß and interleukin-1 receptor antagonist genes in children with autism spectrum disorders.
Progress in neuro-psychopharmacology & biological psychiatry 2020 Jun 109999. Saad Khaled, Abdallah Alam-Eldin M, Abdel-Rahman Ahmed A, Al-Atram Abdulrahman A, Abdel-Raheem Yasser F, Gad Eman Fathallah, Abo-Elela Mohamed Gamil M, Elserogy Yasser M, Elhoufey Amira, Nigm Dalia A, Nagiub Abdelsalam Eman M, Alruwaili Thamer A |
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Assessment of haptoglobin alleles in autism spectrum disorders.
Scientific reports 2020 May 10 (1): 7758. Cupaioli Francesca Anna, Mosca Ettore, Magri Chiara, Gennarelli Massimo, Moscatelli Marco, Raggi Maria Elisabetta, Landini Martina, Galluccio Nadia, Villa Laura, Bonfanti Arianna, Renieri Alessandra, Fallerini Chiara, Minelli Alessandra, Marabotti Anna, Milanesi Luciano, Fasano Alessio, Mezzelani Alessand |
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Biases in arginine codon usage correlate with genetic disease risk.
Genetics in medicine : official journal of the American College of Medical Genetics 2020 May . Schulze Katharina V, Hanchard Neil A, Wangler Michael |
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Family-based association study identifies SNAP25 as a susceptibility gene for autism in the Han Chinese population.
Progress in neuro-psychopharmacology & biological psychiatry 2020 May 109985. Wang Ziqi, Li Jun, Zhang Tian, Lu Tianlan, Wang Han, Jia Meixiang, Liu Jing, Xiong Jun, Zhang Dai, Wang Lifa |
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Genetic stratification of depression in UK Biobank.
Translational psychiatry 2020 May 10 (1): 163. Howard David M, Folkersen Lasse, Coleman Jonathan R I, Adams Mark J, Glanville Kylie, Werge Thomas, Hagenaars Saskia P, Han Buhm, Porteous David, Campbell Archie, Clarke Toni-Kim, Breen Gerome, Sullivan Patrick F, Wray Naomi R, Lewis Cathryn M, McIntosh Andrew |
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Association study between genetic variants in vitamin D metabolism related genes and childhood autism spectrum disorder.
Metabolic brain disease 2020 Apr . Yu Hong, Zhang Zengyu, Liu Jun, Hu Pingfang, Liu Zh |
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Comment on "Association Between DCC Polymorphisms and Susceptibility to Autism Spectrum Disorder".
Journal of autism and developmental disorders 2020 Apr . Meisami Amirhose |
Genetic Contributions to Maternal and Neonatal Vitamin D Levels.
Genetics 2020 Apr 214 (4): 1091-1102. Traglia Michela, Windham Gayle C, Pearl Michelle, Poon Victor, Eyles Darryl, Jones Karen L, Lyall Kristen, Kharrazi Martin, Croen Lisa A, Weiss Lauren |
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Association Between DCC Polymorphisms and Susceptibility to Autism Spectrum Disorder.
Journal of autism and developmental disorders 2020 Mar . Li Yan, Qiu Shuang, Zhong Weijing, Li Yong, Liu Yunkai, Cheng Yi, Liu Yaw |
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Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity.
Translational psychiatry 2020 Mar 10 (1): 82. Hernandez Leanna M, Lawrence Katherine E, Padgaonkar N Tanya, Inada Marisa, Hoekstra Jackson N, Lowe Jennifer K, Eilbott Jeffrey, Jack Allison, Aylward Elizabeth, Gaab Nadine, Van Horn John D, Bernier Raphael A, McPartland James C, Webb Sara J, Pelphrey Kevin A, Green Shulamite A, Geschwind Daniel H, Bookheimer Susan Y, Dapretto Mirella, |
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Vitamin D polygenic score is associated with neuroticism and the general psychopathology factor.
Progress in neuro-psychopharmacology & biological psychiatry 2020 Mar 100 109912. Avinun Reut, Romer Adrienne L, Israel Salom |
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An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
Scientific reports 2020 Feb 10 (1): 3198. Bacchelli Elena, Cameli Cinzia, Viggiano Marta, Igliozzi Roberta, Mancini Alice, Tancredi Raffaella, Battaglia Agatino, Maestrini Ele |
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Vitamin D Receptor Polymorphisms Associated with Autism Spectrum Disorder.
Autism research : official journal of the International Society for Autism Research 2020 Feb . Guerini Franca Rosa, Bolognesi Elisabetta, Chiappedi Matteo, Mensi Maria Martina, Fumagalli Oscar, Rogantini Chiara, Zanzottera Milena, Ghezzo Alessandro, Zanette Michela, Agliardi Cristina, Costa Andrea Saul, Sotgiu Stefano, Carta Alessandra, Al Daghri Nasser, Clerici Mar |
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Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.
Translational psychiatry 2020 Feb 10 (1): 57. Forstner Andreas J, Fischer Sascha B, Schenk Lorena M, Strohmaier Jana, Maaser-Hecker Anna, Reinbold Céline S, Sivalingam Sugirthan, Hecker Julian, Streit Fabian, Degenhardt Franziska, Witt Stephanie H, Schumacher Johannes, Thiele Holger, Nürnberg Peter, Guzman-Parra José, Orozco Diaz Guillermo, Auburger Georg, Albus Margot, Borrmann-Hassenbach Margitta, González Maria José, Gil Flores Susana, Cabaleiro Fabeiro Francisco J, Del Río Noriega Francisco, Perez Perez Fermin, Haro González Jesus, Rivas Fabio, Mayoral Fermin, Bauer Michael, Pfennig Andrea, Reif Andreas, Herms Stefan, Hoffmann Per, Pirooznia Mehdi, Goes Fernando S, Rietschel Marcella, Nöthen Markus M, Cichon Sv |
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AVPR1A variation is linked to gray matter covariation in the social brain network of chimpanzees.
Genes, brain, and behavior 2020 Jan e12631. Mulholland Michele M, Navabpour Shaghayegh V, Mareno Mary C, Schapiro Steven J, Young Larry J, Hopkins William |
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Common variant of CNTNAP2 gene modulate the social performances and functional connectivity of posterior right temporoparietal junction.
Social cognitive and affective neuroscience 2020 Jan . Bai Tongjian, Zhang Long, Xie Xiaohui, Xiao Guixian, Huang Wanling, Li Dandan, Zu Meidan, Wei Lin, Zuo Xianbo, Gong-Jun J I, Hu Panpan, Zhu Chunyan, Qiu Bensheng, Tian Yanghua, Wang K |
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Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations.
JAMA network open 2020 Jan 3 (1): e1920415. Yehia Lamis, Seyfi Marilyn, Niestroj Lisa-Marie, Padmanabhan Roshan, Ni Ying, Frazier Thomas W, Lal Dennis, Eng Char |
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Environmental exposure pathway analysis of trace elements and autism risk in Pakistani children population.
The Science of the total environment 2020 Jan 712 136471. Nabgha-E-Amen , Eqani Syed Ali Musstjab Akber Shah, Khuram Faiza, Alamdar Ambreen, Tahir Ayesha, Shah Syed Tahir Abbas, Nasir Arshan, Javed Sundus, Bibi Nazia, Hussain Alamdar, Rasheed Hifza, Shen Heqi |
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
Cell 2020 Jan . Satterstrom F Kyle, Kosmicki Jack A, Wang Jiebiao, Breen Michael S, De Rubeis Silvia, An Joon-Yong, Peng Minshi, Collins Ryan, Grove Jakob, Klei Lambertus, Stevens Christine, Reichert Jennifer, Mulhern Maureen S, Artomov Mykyta, Gerges Sherif, Sheppard Brooke, Xu Xinyi, Bhaduri Aparna, Norman Utku, Brand Harrison, Schwartz Grace, Nguyen Rachel, Guerrero Elizabeth E, Dias Caroline, , , Betancur Catalina, Cook Edwin H, Gallagher Louise, Gill Michael, Sutcliffe James S, Thurm Audrey, Zwick Michael E, Børglum Anders D, State Matthew W, Cicek A Ercument, Talkowski Michael E, Cutler David J, Devlin Bernie, Sanders Stephan J, Roeder Kathryn, Daly Mark J, Buxbaum Joseph |
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Polygenetic Risk Scores for Major Psychiatric Disorders Among Schizophrenia Patients, Their First-Degree Relatives and Healthy Subjects.
The international journal of neuropsychopharmacology 2020 Jan . Ohi Kazutaka, Nishizawa Daisuke, Shimada Takamitsu, Kataoka Yuzuru, Hasegawa Junko, Shioiri Toshiki, Kawasaki Yasuhiro, Hashimoto Ryota, Ikeda Kazuta |
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The Correlation Between Vitamin D Receptor (VDR) Gene Polymorphisms and Autism: A Meta-analysis.
Journal of molecular neuroscience : MN 2020 Jan . Yang Hongchang, Wu Xuepi |
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The Prevalence of Insomnia and the Link between Iron Metabolism Genes Polymorphisms,
International journal of environmental research and public health 2020 Jan 17 (2): . Skonieczna-Zydecka Karolina, Jamiol-Milc Dominika, Borecki Krzysztof, Stachowska Ewa, Zabielska Paulina, Kaminska Magdalena, Karakiewicz Bea |
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The rs594445 in MOCOS gene is associated with risk of autism spectrum disorder.
Metabolic brain disease 2020 Jan . Taheri Mohammad, Noroozi Rezvan, Aghaei Kamyar, Omrani Mir Davood, Ghafouri-Fard Soud |
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Molecular Biomarkers Predictive of Sertraline Treatment Response in Young Children With Autism Spectrum Disorder.
Frontiers in genetics 2020 11 308. Alolaby Reem Rafik, Jiraanont Poonnada, Durbin-Johnson Blythe, Jasoliya Mittal, Tang Hiu-Tung, Hagerman Randi, Tassone Flo |
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Preliminary Evidence That CD38 Moderates the Association of Neuroticism on Amygdala-Subgenual Cingulate Connectivity.
Frontiers in neuroscience 2020 14 11. Tabak Benjamin A, Young Katherine S, Torre Jared B, Way Baldwin M, Burklund Lisa J, Eisenberger Naomi I, Lieberman Matthew D, Craske Michelle |
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The role of 5-HTTLPR in autism spectrum disorder: New evidence and a meta-analysis of this polymorphism in Latin American population with psychiatric disorders.
PloS one 2020 15 (7): e0235512. Nuñez-Rios D L, Chaskel R, Lopez A, Galeano L, Lattig M |
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Damaging coding variants within kainate receptor channel genes are enriched in individuals with schizophrenia, autism and intellectual disabilities.
Scientific reports 2019 Dec 9 (1): 19215. Koromina Maria, Flitton Miles, Blockley Alix, Mellor Ian R, Knight Helen |
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
Cell 2019 Dec 179 (7): 1469-1482.e11. , |
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High-resolution chromosomal microarray analysis for copy-number variations in high-functioning autism reveals large aberration typical for intellectual disability.
Journal of neural transmission (Vienna, Austria : 1996) 2019 Dec . Werling Anna Maria, Grünblatt Edna, Oneda Beatrice, Bobrowski Elise, Gundelfinger Ronnie, Taurines Regina, Romanos Marcel, Rauch Anita, Walitza Susan |
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Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study.
Journal of neural transmission (Vienna, Austria : 1996) 2019 Dec 126 (12): 1679-1693. Waltes Regina, Freitag Christine M, Herlt Timo, Lempp Thomas, Seitz Christiane, Palmason Haukur, Meyer Jobst, Chiocchetti Andreas |
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Sex-dependent effects of Cacna1c haploinsufficiency on behavioral inhibition evoked by conspecific alarm signals in rats.
Progress in neuro-psychopharmacology & biological psychiatry 2019 Dec 109849. Wöhr Markus, Willadsen Maria, Kisko Theresa M, Schwarting Rainer K W, Fendt Mark |
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Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Cortex; a journal devoted to the study of the nervous system and behavior 2019 Nov 124 137-153. Carrion-Castillo Amaia, Pepe Antonietta, Kong Xiang-Zhen, Fisher Simon E, Mazoyer Bernard, Tzourio-Mazoyer Nathalie, Crivello Fabrice, Francks Cly |
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Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
Autism research : official journal of the International Society for Autism Research 2019 Nov . da Silva Montenegro Eduarda Morgana, Costa Claudia Samogy, Campos Gabriele, Scliar Marília, de Almeida Tatiana Ferreira, Zachi Elaine Cristina, Silva Isabela Maya Wahys, Chan Ada J S, Zarrei Mehdi, Lourenço Naila C V, Yamamoto Guilherme Lopes, Scherer Stephen, Passos-Bueno Maria Ri |
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Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
Clinical genetics 2019 Nov . Wu Huidan, Li Honghui, Bai Ting, Han Lin, Ou Jianjun, Xun Guanglei, Zhang Yu, Wang Yazhe, Duan Guiqin, Zhao Ningxia, Chen Biyuan, Du Xiaogang, Yao Meiling, Zou Xiaobing, Zhao Jingping, Hu Zhengmao, Eichler Evan E, Guo Hui, Xia K |
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A common variant in OXTR rs53576 impacts topological patterns of brain functional networks.
European child & adolescent psychiatry 2019 Oct . Wang Junping, Zhang Yan, Zhu Dan, Yang Zonghe, Liu Feng, Qin Wen, Zhu Jiajia, Liu Bing, Jiang Tianzi, Yu Chunsh |
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Association between vitamin D receptor gene FokI and TaqI variants with autism spectrum disorder predisposition in Iranian population.
Gene 2019 Oct 144133. Mobasheri Leila, Moossavi Seyedeh Zahra, Esmaeili Aliakbar, Mohammadoo-Khorasani Milad, Sarab Gholamreza Ana |
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De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
Biological psychiatry 2019 Oct . Cappi Carolina, Oliphant Melody E, Péter Zsanett, Zai Gwyneth, Conceição do Rosário Maria, Sullivan Catherine A W, Gupta Abha R, Hoffman Ellen J, Virdee Manmeet, Olfson Emily, Abdallah Sarah B, Willsey A Jeremy, Shavitt Roseli G, Miguel Euripedes C, Kennedy James L, Richter Margaret A, Fernandez Thomas |
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Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.
Mutagenesis 2019 Oct . 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, Dusinska Maria, Musak Ludovit, Vodicka Pavel, Hemminki Kari, Försti As |
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Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.
Cell 2019 Oct 179 (3): 750-771.e22. Walker Rebecca L, Ramaswami Gokul, Hartl Christopher, Mancuso Nicholas, Gandal Michael J, de la Torre-Ubieta Luis, Pasaniuc Bogdan, Stein Jason L, Geschwind Daniel |
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.
Nature communications 2019 Oct 10 (1): 4897. Oetjens M T, Kelly M A, Sturm A C, Martin C L, Ledbetter D |
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Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis.
The European respiratory journal 2019 Oct . Zhu Zhaozhong, Zhu Xi, Liu Cong-Lin, Shi Huwenbo, Shen Sipeng, Yang Yunqi, Hasegawa Kohei, Camargo Carlos A, Liang Limi |
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The rs12826786 in HOTAIR lncRNA Is Associated with Risk of Autism Spectrum Disorder.
Journal of molecular neuroscience : MN 2019 Oct . Safari Mohammadreza, Noroozi Rezvan, Taheri Mohammad, Ghafouri-Fard Soud |
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Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits.
JAMA psychiatry 2019 Sep . Legge Sophie E, Jones Hannah J, Kendall Kimberley M, Pardiñas Antonio F, Menzies Georgina, Bracher-Smith Matthew, Escott-Price Valentina, Rees Elliott, Davis Katrina A S, Hotopf Matthew, Savage Jeanne E, Posthuma Danielle, Holmans Peter, Kirov George, Owen Michael J, O'Donovan Michael C, Zammit Stanley, Walters James T |
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Association of MTHFR 677C>T and 1298A>C polymorphisms with susceptibility to autism: A systematic review and meta-analysis.
Asian journal of psychiatry 2019 Sep 46 54-61. Sadeghiyeh Tahereh, Dastgheib Seyed Alireza, Mirzaee-Khoramabadi Khadijeh, Morovati-Sharifabad Majid, Akbarian-Bafghi Mohammad Javad, Poursharif Zahra, Mirjalili Seyed Reza, Neamatzadeh Hosse |
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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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Towards Identifying Genetic Biomarkers for Gastrointestinal Dysfunction in Autism.
Journal of autism and developmental disorders 2019 Sep . Shindler A E, Hill-Yardin E L, Petrovski S, Bishop N, Franks A |
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Phenome-wide Burden of Copy-Number Variation in the UK Biobank.
American journal of human genetics 2019 Aug 105 (2): 373-383. Aguirre Matthew, Rivas Manuel A, Priest Jam |
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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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Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes.
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2019 Jul . Chen Jingchun, Loukola Anu, Gillespie Nathan A, Peterson Roseann, Jia Peilin, Riley Brien, Maes Hermine, Dick Daniella M, Kendler Kenneth S, Damaj M Imad, Miles Michael F, Zhao Zhongming, Li Ming D, Vink Jacqueline M, Minica Camelia C, Willemsen Gonneke, Boomsma Dorret I, Qaiser Beenish, Madden Pamela A F, Korhonen Tellervo, Jousilahti Pekka, Hällfors Jenni, Gelernter Joel, Kranzler Henry R, Sherva Richard, Farrer Lindsay, Maher Brion, Vanyukov Michael, Taylor Michelle, Ware Jenifer J, Munafò Marcus R, Lutz Sharon M, Hokanson John E, Gu Fangyi, Landi Maria T, Caporaso Neil E, Hancock Dana B, Gaddis Nathan C, Baker Timothy B, Bierut Laura J, Johnson Eric O, Chenoweth Meghan, Lerman Caryn, Tyndale Rachel, Kaprio Jaakko, Chen Xiangni |
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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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Polygenic Risk Scores for Developmental Disorders, Neuromotor Functioning During Infancy, and Autistic Traits in Childhood.
Biological psychiatry 2019 Jun . Serdarevic Fadila, Tiemeier Henning, Jansen Philip R, Alemany Silvia, Xerxa Yllza, Neumann Alexander, Robinson Elise, Hillegers Manon H J, Verhulst Frank C, Ghassabian Akhg |
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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 |
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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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