Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 1642 Records) |
Query Trace: Autism[original query] |
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Polygenic risk of mental disorders and subject-specific school grades. Biological psychiatry 2023 12 . Oskar Hougaard Jefsen, Katrine Holde, John J McGrath, Veera Manikandan Rajagopal, Clara Albiñana, Bjarni Jóhann Vilhjálmsson, Jakob Grove, Esben Agerbo, Zeynep Yilmaz, Oleguer Plana-Ripoll, Trine Munk-Olsen, Ditte Demontis, Anders Børglum, Ole Mors, Cynthia M Bulik, Preben Bo Mortensen, Liselotte Vogdrup Peters |
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD. Nature communications 2023 12 14 (1): 8077. Sheng Wang, Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo, Juan Arbelaez, Clif Duhn, , Vanessa H Bal, Kate Langley, Joanna Martin, Pieter J Hoekstra, Andrea Dietrich, Jinchuan Xing, Gary A Heiman, Jay A Tischfield, Thomas V Fernandez, Michael J Owen, Michael C O'Donovan, Anita Thapar, Matthew W State, A Jeremy Wills |
Genomic insights and advanced machine learning: characterizing autism spectrum disorder biomarkers and genetic interactions. Metabolic brain disease 2023 12 . Laila Dabab Nahas, Ankur Datta, Alsamman M Alsamman, Monica H Adly, Nader Al-Dewik, Karthik Sekaran, K Sasikumar, Kanika Verma, George Priya C Doss, Hatem Zay |
SNAP-25 Polymorphisms in Autism Spectrum Disorder: A Pilot Study towards a Possible Endophenotype. Pediatric reports 2023 12 15 (4): 766-773. Martina Maria Mensi, Franca Rosa Guerini, Michele Marchesi, Matteo Chiappedi, Elisabetta Bolognesi, Renato Borgat |
CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case report. Heliyon 2023 12 9 (12): e22987. Eleni Angelopoulou, Athina Theodosiou, Ioannis Papaevripidou, Angelos Alexandrou, Thomas Liehr, Yolanda Gyftodimou, Eunice G Stefanou, Carolina Sisma |
The Frequency of CYP2D6 and CYP3A4/5 Genotypes and The Impact of Their Allele Translation and Phenoconversion-Predicted Enzyme Activity on Risperidone Pharmacokinetics in Saudi Children with Autism. Biochemical genetics 2023 12 . Sireen Abdul Rahim Shilbayeh, Iman Sharaf Adeen, Ayman Shawqi Alhazmi, Samah Fathy Ibrahim, Fawwaz Abdul Razaq Al Enazi, Ezzeldeen Hasan Ghanem, Adel Mohammed Binduraih |
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). medRxiv : the preprint server for health sciences 2023 12 . Jessica H Hall, Samuel J R A Chawner, , Jeanne Wolstencroft, David Skuse, Peter Holmans, Michael J Owen, Marianne B M van den Br |
Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders. Gene 2023 12 897 148071. Nan Pang, Kuokuo Li, Senwei Tan, Meilin Chen, Fang He, Chen Chen, Lifen Yang, Ciliu Zhang, Xiaolu Deng, Li Yang, Leilei Mao, Guoli Wang, Haolin Duan, Xiaole Wang, Wen Zhang, Hui Guo, Jing Peng, Fei Yin, Kun X |
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability. medRxiv : the preprint server for health sciences 2023 12 . Zoe Schmilovich, Vincent-Raphaël Bourque, Elise Douard, Guillaume Huguet, Cécile Poulain, Jay P Ross, Paria Alipour, Charles-Étienne Castonguay, Nadine Younis, Martineau Jean-Louis, Zohra Saci, Zdenka Pausova, Tomas Paus, Gunter Schuman, David Porteous, Gail Davies, Paul Redmond, Sarah E Harris, Ian J Deary, Heather Whalley, Caroline Hayward, Patrick A Dion, Sébastien Jacquemont, Guy A Roule |
Mitochondrial DNA Haplogroup K Is Protective of Autism Spectrum Disorder Risk in Populations of European Ancestry. Journal of the American Academy of Child and Adolescent Psychiatry 2023 12 . Xiao Chang, Hui-Qi Qu, Yichuan Liu, Joseph T Glessner, Hakon Hakonars |
Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing. Frontiers in psychiatry 2023 11 14 1251884. Vijay Gupta, Afif Ben-Mahmoud, Bonsu Ku, Dinesh Velayutham, Zainab Jan, Abdi Yousef Aden, Ahmad Kubbar, Fouad Alshaban, Lawrence W Stanton, Puthen Veettil Jithesh, Lawrence C Layman, Hyung-Goo K |
Identification of Neurotransmission and Synaptic Biological Processes Disrupted in Autism Spectrum Disorder Using Interaction Networks and Community Detection Analysis. Biomedicines 2023 11 11 (11): . Joana Vilela, Hugo Martiniano, Ana Rita Marques, João Xavier Santos, Muhammad Asif, Célia Rasga, Guiomar Oliveira, Astrid Moura Vicen |
Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants. American journal of human genetics 2023 11 . Corrine Smolen, Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee, Laura Rohan, Emily Huber, Laila El Khattabi, Paolo Prontera, Jean-Hubert Caberg, Anke Van Dijck, Charles Schwartz, Laurence Faivre, Patrick Callier, Anne-Laure Mosca-Boidron, Mathilde Lefebvre, Kate Pope, Penny Snell, Paul J Lockhart, Lucia Castiglia, Ornella Galesi, Emanuela Avola, Teresa Mattina, Marco Fichera, Giuseppa Maria Luana Mandarà, Maria Grazia Bruccheri, Olivier Pichon, Cedric Le Caignec, Radka Stoeva, Silvestre Cuinat, Sandra Mercier, Claire Bénéteau, Sophie Blesson, Ashley Nordsletten, Dominique Martin-Coignard, Erik Sistermans, R Frank Kooy, David J Amor, Corrado Romano, Bertrand Isidor, Jane Juusola, Santhosh Giriraj |
Contribution of autosomal rare and de novo variants to sex differences in autism. medRxiv : the preprint server for health sciences 2024 5 . Mahmoud Koko, F Kyle Satterstrom, , , Varun Warrier, Hilary Mart |
The genetic landscape of autism spectrum disorder in the Middle Eastern population. Frontiers in genetics 2024 4 15 1363849. Yasser Al-Sarraj, Rowaida Z Taha, Eman Al-Dous, Dina Ahram, Somayyeh Abbasi, Eman Abuazab, Hibah Shaath, Wesal Habbab, Khaoula Errafii, Yosra Bejaoui, Maryam AlMotawa, Namat Khattab, Yasmin Abu Aqel, Karim E Shalaby, Amina Al-Ansari, Marios Kambouris, Adel Abouzohri, Iman Ghazal, Mohammed Tolfat, Fouad Alshaban, Hatem El-Shanti, Omar M E Albag |
Allele-Specific Regulation of the Candidate Autism Liability Gene RAI1 by the Enhancer Variant rs4925102 (C/G). Genes 2024 4 15 (4): . Xi Yuan, Li Chen, David Saff |
Genetic correlation and causal associations between psychiatric disorders and lung cancer risk. Journal of affective disorders 2024 4 356 647-656. Jiajun Shi, Wanqing Wen, Jirong Long, Eric R Gamazon, Ran Tao, Qiuyin C |
Exome-wide analysis implicates rare protein-altering variants in human handedness. Nature communications 2024 4 15 (1): 2632. Dick Schijven, Sourena Soheili-Nezhad, Simon E Fisher, Clyde Franc |
Shared Genetic Determinants of Schizophrenia and Autism Spectrum Disorder Implicate Opposite Risk Patterns: A Genome-Wide Analysis of Common Variants. Schizophrenia bulletin 2024 4 . Yu Chen, Wenqiang Li, Luxian Lv, Weihua Y |
Metabotropic glutamate receptor genetic variants and peripheral receptor expression affects trait scores of autistic probands. Scientific reports 2024 4 14 (1): 8558. Nilanjana Dutta, Mahasweta Chatterjee, Sharmistha Saha, Swagata Sinha, Kanchan Mukhopadhy |
Linked OXTR Variants Are Associated with Social Behavior Differences in Bonobos (Pan paniscus). bioRxiv : the preprint server for biology 2024 1 . Sara A Skiba, Alek Hansen, Ryan McCall, Azeeza Byers, Sarah Waldron, Amanda J Epping, Jared P Taglialatela, Martin L Huds |
Association of verbal and non-verbal theory of mind abilities with non-coding variants of OXTR in youth with autism spectrum disorder and typically developing individuals: a case-control study. BMC psychiatry 2024 1 24 (1): 30. Rana Ghamari, Mohammad Tahmaseb, Atiye Sarabi-Jamab, Seyed-Alireza Etesami, Azar Mohammadzadeh, Fatemeh Alizadeh, Mehdi Tehrani-Doo |
Epilepsy and psychiatric comorbidities: A bidirectional mendelian randomization study. Journal of affective disorders 2024 1 350 774-783. Hongyuan Chu, Bing Wang, Xinyu Zhao, Li |
Inferring the genetic effects of serum homocysteine and vitamin B levels on autism spectral disorder through Mendelian randomization. European journal of nutrition 2024 1 . Tianyu Jin, Wei Huang, Qiongyi Pang, Zitian He, Linran Yuan, Haojie Zhang, Dalin Xing, Shunyuan Guo, Tong Zha |
Association between psychiatric disorders and glioma risk: evidence from Mendelian randomization analysis. BMC cancer 2024 1 24 (1): 118. Wenzhuo Yang, Yu Han, Changjia He, Sheng Zhong, Fei Ren, Zhongping Chen, Yonggao Mou, Ke S |
A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder. Research square 2024 1 . Matthew Halvorsen, Elles de Schipper, Julia Boberg, Nora Strom, Kristen Hagen, Kerstin Lindblad-Toh, Elinor Karlsson, Nancy Pedersen, Cynthia Bulik, Bengt Fundín, Mikael Landén, Gerd Kvale, Bjarne Hansen, Jan Haavik, Manuel Mattheisen, Christian Rück, David Mataix-Cols, James Crowl |
Reanalysis of Trio Whole-Genome Sequencing Data Doubles the Yield in Autism Spectrum Disorder: De Novo Variants Present in Half. International journal of molecular sciences 2024 1 25 (2): . Omri Bar, Elizabeth Vahey, Mark Mintz, Richard E Frye, Richard G Bol |
Replication of previous autism-GWAS hits suggests the association between NAA1, SORCS3, and GSDME and autism in the Han Chinese population. Heliyon 2024 1 10 (1): e23677. Fen Lin, Jun Li, Ziqi Wang, Tian Zhang, Tianlan Lu, Miaomiao Jiang, Kang Yang, Meixiang Jia, Dai Zhang, Lifang Wa |
Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus. medRxiv : the preprint server for health sciences 2024 1 . Marcello Scala, Clarrisa A Bradley, Jennifer L Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum, Miriam S Reuter, Jeffrey R MacDonald, Sangyoon Y Ko, Paul W Frankland, Leslie Granger, George Anadiotis, Verdiana Pullano, Alfredo Brusco, Roberto Keller, Sarah Parisotto, Helio F Pedro, Laina Lusk, Pamela Pojomovsky McDonnell, Ingo Helbig, Sureni V Mullegama, , Emilie D Douine, Bianca E Russell, Stanley F Nelson, Federico Zara, Stephen W Scher |
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder. Computational and structural biotechnology journal 2024 1 21 3109-3123. Tao Wang, Liqiu Liu, Tianda Fan, Kun Xia, Zhongsheng S |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
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