Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 1715 Records) |
| Query Trace: Autism[original query] |
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| HLA-A, -B, -C and -DRB1 Association with Autism Spectrum Disorder Risk: A Sex-Related Analysis in Italian ASD Children and Their Siblings. International journal of molecular sciences 2024 9 25 (18): . Franca Rosa Guerini, Elisabetta Bolognesi, Martina Maria Mensi, Michela Zanette, Cristina Agliardi, Milena Zanzottera, Matteo Chiappedi, Silvia Annunziata, Francisco García-García, Anna Cavallini, Mario Cleri |
| Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank. NPJ genomic medicine 2024 9 9 (1): 43. Thomas J Dinneen, Fiana Ní Ghrálaigh, Cathal Ormond, Elizabeth A Heron, George Kirov, Lorna M Lopez, Louise Gallagh |
| Association of air pollutants with psychiatric disorders: a two-sample Mendelian randomization. Ecotoxicology and environmental safety 2024 9 285 117105. Yuan-Yuan Ma, Qiong-Yan Li, An-Yu Shi, Jiang-Li Li, Yan-Jiang Wang, Xin |
| Associations between maternal gestational diabetes mellitus and offspring cerebral palsy: a two-sample Mendelian randomization study. Translational pediatrics 2024 12 13 (11): 1923-1932. Honghao Peng, Yun Shu, Siyu Lu, Qiongli Fan, Yuping Zhang, Li Ming, Zhifeng |
| Unveiling genetic insights: Array-CGH and WES discoveries in a cohort of 122 children with essential autism spectrum disorder. BMC genomics 2024 12 25 (1): 1186. Paola Granata, Alessandra Zito, Dario Cocciadiferro, Antonio Novelli, Chiara Pessina, Tommaso Mazza, Matteo Ferri, Paolo Piccinelli, Chiara Luoni, Cristiano Termine, Mauro Fasano, Rosario Casalo |
| Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder. Genetics in medicine : official journal of the American College of Medical Genetics 2024 12 101348. Nour Elkhateeb, Renarta Crookes, Michael Spiller, Lisa Pavinato, Flavia Palermo, Alfredo Brusco, Michael Parker, Soo-Mi Park, Ariana Costa Mendes, Jorge M Saraiva, Trine Bjørg Hammer, Lusine Nazaryan-Petersen, Tahsin Stefan Barakat, Martina Wilke, Elizabeth Bhoj, Rebecca C Ahrens-Nicklas, Dong Li, Tomoki Nomakuchi, Eva H Brilstra, David Hunt, Diana Johnson, Sahar Mansour, Kathryn Oprych, Sarju G Mehta, Konrad Platzer, Franziska Schnabel, Henriette Kiep, Helene Faust, Gillian Prinzing, Kimberly Wiltrout, Jessica A Radley, Alvaro H Serrano Russi, Isis Atallah, Belinda Campos-Xavier, David J Amor, Angela Morgan, Christina Fagerberg, Ulla A Andersen, Charlotte B Andersen, Emilia K Bijlsma, Lynne M Bird, Sureni V Mullegama, Andrew Green, Bertrand Isidor, Benjamin Cogné, Janna Kenny, Sally A Lynch, Shauna Quin, Karen Low, Theresia Herget, Fanny Kortüm, Rebecca J Levy, Jennifer L Morrison, Patricia G Wheeler, Tara Chandra Narumanch, Kristina Peron, Nicole Matthews, Jillian Uhlman, Lauren Bell, Lewis Pang, Ingrid Scurr, Rebecca S Belles, Bonnie Anne Salbert, Gerald Bradley Schaefer, Sarah Green, Andrea Ros, Agustí Rodríguez-Palmero, Tanja Višnjar, Karin Writzl, Pradeep C Vasudevan, Meena Balasubramani |
| Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology. NPJ genomic medicine 2024 12 9 (1): 67. Simone Montalbano, Morten Dybdahl Krebs, Anders Rosengren, Morteza Vaez, Kajsa-Lotta Georgii Hellberg, Preben B Mortensen, Anders D Børglum, Daniel H Geschwind, , Armin Raznahan, Wesley K Thompson, Dorte Helenius, Thomas Werge, Andrés Ingas |
| Association of CHD8 Gene Polymorphic Variants with the Clinical Phenotype of Autism Spectrum Disorder. Journal of clinical medicine 2024 12 13 (23): . Tomasz Iwanicki, Joanna Iwanicka, Anna Balcerzyk-Mati?, Alicja Jarosz, Tomasz Nowak, Ewa Emich-Widera, Beata Kazek, Agnieszka Kapinos-Gorczyca, Maciej Kapinos, Katarzyna Gawron, Aleksandra Augu?ciak-Duma, Wirginia Likus, Pawe? Niemi |
| Short report on a distinct electroencephalogram endophenotype for MTHFR gene variation co-occurring in autism spectrum disorder. Autism : the international journal of research and practice 2024 12 13623613241305721. Uchenna Ezedinma, Evan Jones, Alexander Ring, Spencer Miller, Andrew Ladhams, Shauna Fjaagesund, Terri Downer, Gary Campbell, Florin Opres |
| Impact of working memory training on brain network plasticity and genetic associations: insights from individual differences. Cerebral cortex (New York, N.Y. : 1991) 2024 12 34 (12): . Hang Wu, Xiongying Chen, Yinlong Li, Wan Zhao, Bofan Zhang, Caiying Luo, Xinyue Zhang, Jing Shi, Qiumei Zhang, Gao Li, Jun |
| Adverse food reactions and alterations in nutritional status in children with autism spectrum disorders: results of the NAFRA project. Italian journal of pediatrics 2024 11 50 (1): 228. Serena Coppola, Rita Nocerino, Franca Oglio, Paola Golia, Maria Candida Falco, Maria Pia Riccio, Laura Carucci, Teresa Rea, Silvio Simeone, Raffaele Garotti, Nadia Marani, Carmela Bravaccio, Roberto Berni Cana |
| Investigation of chromosomal anomalies and copy number variations in children diagnosed with autism spectrum disorder by array CGH method. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2024 11 . Fethiye K?l?çaslan, Özlem Öz, Mehmet Burak Mut |
| High penetrance and phenotypic landscape of methylenetetrahydrofolate reductase c.665 C>T polymorphism in the absence of folate fortification. Clinical nutrition ESPEN 2024 11 65 126-133. Srilatha Kadali, Ananthaneni Radhika, Yadam Reddy Kanaka Durga Devi, Jagadeesh Babu Sreemanthula, Gopi Palakonda, Tajamul Hussain, Shaik Mohammad Naush |
| Autism, Electrical Status Epilepticus in Sleep, and a Likely Pathogenic SEMA6B Variant. Pediatrics 2024 11 . Ahmed Ibrahim, David Jacks |
| A sexually dimorphic signature of activity-dependent BDNF signaling on the intrinsic excitability of pyramidal neurons in the prefrontal cortex. Frontiers in cellular neuroscience 2024 11 18 1496930. Kaijie Ma, Daoqi Zhang, Kylee McDaniel, Maria Webb, Samuel S Newton, Francis S Lee, Luye Q |
| Mitochondrial related Mendelian randomization identifies causal associations between metabolic disorders and childhood neurodevelopmental disorders. Medicine 2024 11 103 (46): e40481. Chenyan Hu, Junjun Li, Pengfei Heng, Jianrong L |
| Impact of gene polymorphisms involved in the vitamin D metabolic pathway on the susceptibility to and severity of autism spectrum disorder. Scientific reports 2024 11 14 (1): 28333. Chanarong Saechua, Tewarit Sarachana, Weerasak Chonchaiya, Pon Trairatvorakul, Wasana Yuwattana, Chayanit Poolcharoen, Montira Sangritdech, Thanit Saeliw, Marlieke Lisanne van Erp, Siriporn Sangsuthum, Natthakul Akarapredee, Sayanit Tipnoppanon, Rattanaporn Sukprasong, Patompong Satapornpong, Chalirmporn Atasilp, Chonlaphat Sukasem, Natchaya Vanwo |
| Individuals with SATB2-associated syndrome have impaired vitamin and energy metabolism pathways. Metabolic brain disease 2024 11 40 (1): 3. Roberto Collu, Yuri A Zarate, Weiming Xia, Jennifer L Fi |
| Negative effect of treatment with mGluR5 negative allosteric modulator AFQ056 on blood biomarkers in young individuals with Fragile X syndrome. SAGE open medicine 2024 11 12 20503121241282401. Dragana Protic, Elizabeth Breeze, Guadalupe Mendoza, Marwa Zafarullah, Leonard Abbeduto, Randi Hagerman, Christopher Coffey, Merit Cudkowicz, Blythe Durbin-Johnson, Paul Ashwood, Elizabeth Berry-Kravis, Craig A Erickson, Robin Filipink, Andrea Gropman, Lenora Lehwald, Angela Maxwell-Horn, Stephanie Morris, Amanda Palladino Bennett, Lisa Prock, Amy Talboy, Nicole Tartaglia, Jeremy Veenstra-VanderWeele, Flora Tasso |
| Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay. Molecular psychiatry 2024 10 . Senwei Tan, Qiumeng Zhang, Rui Zhan, Si Luo, Yaoling Han, Bin Yu, Candace Muss, Veronique Pingault, Sandrine Marlin, Andrée Delahaye, Sophia Peters, Claudia Perne, Martina Kreiß, Nino Spataro, Juan Pablo Trujillo-Quintero, Caroline Racine, Frederic Tran-Mau-Them, Chanika Phornphutkul, Aaron D Besterman, Julian Martinez, Xiuxia Wang, Xiaoyu Tian, Siddharth Srivastava, David K Urion, Jill A Madden, Hind Al Saif, Michelle M Morrow, Amber Begtrup, Xing Li, Sarah Jurgensmeyer, Peter Leahy, Shimin Zhou, Faxiang Li, Zhengmao Hu, Jieqiong Tan, Kun Xia, Hui G |
| Genetic Variations and Serum Levels of Leptin and Ghrelin in Autism Spectrum Disorder. Psychiatry and clinical psychopharmacology 2024 10 34 (3): 221-228. Özlem Nehir Yazici, Nilfer ?ahin, Çilem Özdemir, Ercan Saruhan, Hatice Topal, Tarkan Yaz?c?, Özge Dombayc?, Gülsüm Demirkan Ba?kaya, Tuba Edgün |
| A burden of rare copy number variants in obsessive-compulsive disorder. Molecular psychiatry 2024 10 . Matthew W Halvorsen, Elles de Schipper, Julia Bäckman, Nora I Strom, Kristen Hagen, , Kerstin Lindblad-Toh, Elinor K Karlsson, Nancy L Pedersen, John Wallert, Cynthia M Bulik, Bengt Fundín, Mikael Landén, Gerd Kvale, Bjarne Hansen, Jan Haavik, Manuel Mattheisen, Christian Rück, David Mataix-Cols, James J Crowl |
| Triplication of the PCDH19 Gene as a Novel Disease Mechanism Leading to Epileptic Encephalopathy Resembling Loss-of-Function Pathogenic Variants. Genes 2024 10 15 (10): . Alba Gabaldón-Albero, Patricia Smeyers, Sara Hernández-Muela, Mónica Roselló, Carmen Orellana, Sandra Monfort, Silvestre Oltra, Francisco Martín |
| Identification of immune traits associated with neurodevelopmental disorders by two-sample Mendelian randomization analysis. BMC psychiatry 2024 10 24 (1): 728. Jing Chen, Zhaopeng Han, Zhuiyue Wang, Lifei Chen, Shuxia Wang, Wenbo Yao, Zheng X |
| BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations. European journal of human genetics : EJHG 2024 10 . Angela Peron, Felice D'Arco, Kimberly A Aldinger, Constance Smith-Hicks, Christiane Zweier, Gyri A Gradek, Kimberley Bradbury, Andrea Accogli, Erica F Andersen, Ping Yee Billie Au, Roberta Battini, Daniah Beleford, Lynne M Bird, Arjan Bouman, Ange-Line Bruel, Øyvind Løvold Busk, Philippe M Campeau, Valeria Capra, Colleen Carlston, Jenny Carmichael, Anna Chassevent, Jill Clayton-Smith, Michael J Bamshad, Dawn L Earl, Laurence Faivre, Christophe Philippe, Patrick Ferreira, Luitgard Graul-Neumann, Mary J Green, Darrah Haffner, Parthiv Haldipur, Suhair Hanna, Gunnar Houge, Wendy D Jones, Cornelia Kraus, Birgit Elisabeth Kristiansen, James Lespinasse, Karen J Low, Sally Ann Lynch, Sofia Maia, Rong Mao, Ruta Kalinauskiene, Catherine Melver, Kimberly McDonald, Tara Montgomery, Manuela Morleo, Constance Motter, Amanda S Openshaw, Janice Cox Palumbos, Aditi Shah Parikh, Yezmin Perilla-Young, Cynthia M Powell, Richard Person, Megha Desai, Juliette Piard, Rolph Pfundt, Marcello Scala, Margaux Serey-Gaut, Deborah Shears, Anne Slavotinek, Mohnish Suri, Claire Turner, Tatiana Tvrdik, Karin Weiss, Ingrid M Wentzensen, Marcella Zollino, Tzung-Chien Hsieh, , , , Bert B A de Vries, Francois Guillemot, William B Dobyns, David Viskochil, Cristina Di |
| TAOK2 Drives Opposing Cilia Length Deficits in 16p11.2 Deletion and Duplication Carriers. bioRxiv : the preprint server for biology 2024 10 . Amy Ferreccio, Sujin Byeon, Moira Cornell, Juan Oses-Prieto, Aditi Deshpande, Lauren A Weiss, Alma Burlingame, Smita Yad |
| Combined Exposure to Folate and Lead during Pregnancy and Autistic-Like Behaviors among Canadian Children from the MIREC Pregnancy and Birth Cohort. Environmental health perspectives 2024 10 132 (10): 107003. Joshua D Alampi, Bruce P Lanphear, Amanda J MacFarlane, Youssef Oulhote, Joseph M Braun, Gina Muckle, Tye E Arbuckle, Jillian Ashley-Martin, Janice M Y Hu, Aimin Chen, Lawrence C McCandle |
| Evaluating the Joint Effects of Recurrent Copy Number Variants and Polygenic Scores on the Risk of Psychiatric Disorders in the iPSYCH2015 Case-Cohort Sample. medRxiv : the preprint server for health sciences 2024 10 . Morteza Vaez, Simone Montalbano, Ryan Waples, Morten Dybdahl Krebs, Kajsa-Lotta Georgii Hellberg, Jesper Gådin, Jonas Bybjerg-Grauholm, Preben B Mortensen, Anders D Børglum, Merete Nordentoft, Daniel H Geschwind, Dorte Helenius, Thomas Werge, Andrew J Schork, Andrés Ingas |
| R150S mutation in the human oxytocin receptor: Gain-of-function effects and implication in autism spectrum disorder. Peptides 2024 10 182 171301. Xiaoxi Liu, Stanislav Cherepanov, Mehdi Abouzari, Amila Zuko, Shu Yang, Jamasb Sayadi, Xiaoyuan Jia, Chikashi Terao, Tsukasa Sasaki, Shigeru Yokoya |
| Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman. International journal of molecular sciences 2025 1 25 (24): . Vijay Gupta, Afif Ben-Mahmoud, Ahmed B Idris, Jouke-Jan Hottenga, Wesal Habbab, Abeer Alsayegh, Hyung-Goo Kim, Watfa Al-Mamari, Lawrence W Stant |
- Page last reviewed:Feb 1, 2024
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