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Exploring polygenic contributors to subgroups of comorbid conditions in autism spectrum disorder. Scientific reports 2022 Mar 12 (1): 3416. Klein Louis, D'Urso Shannon, Eapen Valsamma, Hwang Liang-Dar, Lin Ping |
Psychopathology in adults with copy number variants. Psychological medicine 2022 Feb 1-8. Adams Rachael L, Baird Alister, Smith Jacqueline, Williams Nigel, van den Bree Marianne B M, Linden David E J, Owen Michael J, Hall Jeremy, Linden Stefanie |
Systemic inflammatory regulators and 7 major psychiatric disorders: A two-sample Mendelian randomization study. Progress in neuro-psychopharmacology & biological psychiatry 2022 Feb 116 110534. Chen Xinzhen, Yao Ting, Cai Jinliang, Fu Xihang, Li Huiru, Wu Ji |
Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder. Genes, brain, and behavior 2022 Jan e12797. Waldron Sophie, Pass Rachel, Griesius Simonas, Mellor Jack R, Robinson Emma S J, Thomas Kerrie L, Wilkinson Lawrence S, Humby Trevor, Hall Jeremy, Dwyer Dominic |
Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder.
![]() Pharmaceuticals (Basel, Switzerland) 2022 Jan 15 (2): . Almandil Noor B, AlSulaiman Abdulla, Aldakeel Sumayh A, Alkuroud Deem N, Aljofi Halah Egal, Alzahrani Safah, Al-Mana Aishah, Alfuraih Asma A, Alabdali Majed, Alkhamis Fahd A, AbdulAzeez Sayed, Borgio J Franc |
Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy. Nature communications 2021 Nov 12 (1): 6534. Verhoef Ellen, Grove Jakob, Shapland Chin Yang, Demontis Ditte, Burgess Stephen, Rai Dheeraj, Børglum Anders D, St Pourcain Bea |
Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center. Journal of autism and developmental disorders 2021 Nov . Du Xiaoli, Glass Jennifer Elaine, Balow Stephanie, Dyer Lisa M, Rathbun Pamela A, Guan Qiaoning, Liu Jie, Wu Yaning, Dawson D Brian, Walters-Sen Lauren, Smolarek Teresa A, Zhang Wenyi |
How rare and common risk variation jointly affect liability for autism spectrum disorder. Molecular autism 2021 Oct 12 (1): 66. Klei Lambertus, McClain Lora Lee, Mahjani Behrang, Panayidou Klea, De Rubeis Silvia, Grahnat Anna-Carin Säll, Karlsson Gun, Lu Yangyi, Melhem Nadine, Xu Xinyi, Reichenberg Abraham, Sandin Sven, Hultman Christina M, Buxbaum Joseph D, Roeder Kathryn, Devlin Bern |
Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome medicine 2021 Oct 13 (1): 172. Vysotskiy Mikhail, Zhong Xue, Miller-Fleming Tyne W, Zhou Dan, , , , Cox Nancy J, Weiss Lauren |
Family-Based Cohort Association Study of PRKCB1, CBLN1 and KCNMB4 Gene Polymorphisms and Autism in Polish Population. Journal of autism and developmental disorders 2021 Sep . Iwanicki Tomasz, Balcerzyk Anna, Kazek Beata, Emich-Widera Ewa, Likus Wirginia, Iwanicka Joanna, Kapinos-Gorczyca Agnieszka, Kapinos Maciej, Jarosz Alicja, Grzeszczak W?adys?aw, Górczy?ska-Kosiorz Sylwia, Niemiec Paw |
Impact on the Risk and Severity of Childhood Onset Schizophrenia of Schizophrenia Risk Genetic Variants at the DRD2 and ZNF804A Loci. Child psychiatry and human development 2021 Sep . Alfimova Margarita V, Nikitina Svetlana G, Lezheiko Tatyana V, Simashkova Nataliya V, Golimbet Vera |
The contribution of platelets to peripheral BDNF elevation in children with autism spectrum disorder. Scientific reports 2021 Sep 11 (1): 18158. Farmer Cristan A, Thurm Audrey E, Honnekeri Bianca, Kim Paul, Swedo Susan E, Han Joan |
The influence of NRXN1 on systemizing and the brain structure in healthy adults. Brain imaging and behavior 2021 Sep . Shiota Yuka, Matsudaira Izumi, Takeuchi Hikaru, Ono Chiaki, Tomita Hiroaki, Kawashima Ryuta, Taki Yasuyu |
[Genetic testing and prenatal diagnosis for a family with 10q22.3q23.2 microdeletion]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 Aug 38 (8): 768-770. Zeng Li'na, Zhang Yan, Lin Li, Dong Xian, Li Lij |
Association and epistatic analysis of white matter related genes across the continuum schizophrenia and autism spectrum disorders: The joint effect of NRG1-ErbB genes. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2021 Aug 1-11. Prats C, Fatjó-Vilas M, Penzol M J, Kebir O, Pina-Camacho L, Demontis D, Crespo-Facorro B, Peralta V, González-Pinto A, Pomarol-Clotet E, Papiol S, Parellada M, Krebs M O, Fañanás |
Potential role for immune-related genes in autism spectrum disorders: Evidence from genome-wide association meta-analysis of autistic traits. Autism : the international journal of research and practice 2021 Aug 13623613211019547. Arenella Martina, Cadby Gemma, De Witte Ward, Jones Rachel M, Whitehouse Andrew Jo, Moses Eric K, Fornito Alex, Bellgrove Mark A, Hawi Ziarih, Johnson Beth, Tiego Jeggan, Buitelaar Jan K, Kiemeney Lambertus A, Poelmans Geert, Bralten Jani |
Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder. Journal of child psychology and psychiatry, and allied disciplines 2021 Jul . Peyre Hugo, Schoeler Tabea, Liu Chaoyu, Williams Camille Michèle, Hoertel Nicolas, Havdahl Alexandra, Pingault Jean-Baptis |
Dysfunction in Mitochondrial Electron Transport Chain Complex I, Pyruvate Dehydrogenase Activity, and Mutations in ND1 and ND4 Gene in Autism Spectrum Disorder Subjects from Tamil Nadu Population, India. Molecular neurobiology 2021 Jul . Mahalaxmi Iyer, Subramaniam Mohana Devi, Gopalakrishnan Abilash Valsala, Vellingiri Balachand |
Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.
![]() Communications biology 2021 Jul 4 (1): 908. Qu Hui-Qi, Qu Jingchun, Bradfield Jonathan, Marchand Luc, Glessner Joseph, Chang Xiao, March Michael, Li Jin, Connolly John J, Roizen Jeffrey D, Sleiman Patrick, Polychronakos Constantin, Hakonarson Hak |
Randomized clinical trial shows no substantial modulation of empathy-related neural activation by intranasal oxytocin in autism. Scientific reports 2021 Jul 11 (1): 15056. Mayer Annalina V, Wermter Anne-Kathrin, Stroth Sanna, Alter Peter, Haberhausen Michael, Stehr Thomas, Paulus Frieder M, Krach Sören, Kamp-Becker In |
Early social rearing, the V1A arginine vasopressin receptor genotype, and autistic traits in chimpanzees. Autism research : official journal of the International Society for Autism Research 2021 Jun . Weiss Alexander, Wilson Vanessa A D, Hopkins William |
GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders. Neuroscience bulletin 2021 Jun . Zheng Fengyun, Liu Guoyuan, Dang Ting, Chen Qiaowen, An Yu, Wu Meng, Kong Xiangxuan, Qiu Zilong, Wu Bai-L |
Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD.
![]() The American journal of psychiatry 2021 Jun appiajp202020121686. Brikell Isabell, Wimberley Theresa, Albiñana Clara, Pedersen Emil Michael, Vilhjálmsson Bjarni Jóhann, Agerbo Esben, Demontis Ditte, Børglum Anders D, Schork Andrew J, LaBianca Sonja, Werge Thomas, Mors Ole, Hougaard David M, Thapar Anita, Mortensen Preben Bo, Dalsgaard Sør |
Polygenic scores differentially predict developmental trajectories of subtypes of social withdrawal in childhood. Journal of child psychology and psychiatry, and allied disciplines 2021 Jun . Morneau-Vaillancourt Geneviève, Andlauer Till F M, Ouellet-Morin Isabelle, Paquin Stéphane, Brendgen Mara R, Vitaro Frank, Gouin Jean-Philippe, Séguin Jean R, Gagnon Éloi, Cheesman Rosa, Forget-Dubois Nadine, Rouleau Guy A, Turecki Gustavo, Tremblay Richard E, Côté Sylvana M, Dionne Ginette, Boivin Mich |
Sensory Reactivity Phenotype in Phelan-McDermid Syndrome Is Distinct from Idiopathic ASD. Genes 2021 Jun 12 (7): . Tavassoli Teresa, Layton Christina, Levy Tess, Rowe Mikaela, George-Jones Julia, Zweifach Jessica, Lurie Stacey, Buxbaum Joseph D, Kolevzon Alexander, Siper Paige |
[Association of polymorphic variants of DDC (AADC), AANAT and ASMT genes encoding enzymes for melatonin synthesis with the higher risk of neuropsychiatric disorders]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2021 121 (5): 151-157. Moskaleva P V, Shnayder N A, Nasyrova R |
Effects of eight neuropsychiatric copy number variants on human brain structure. Translational psychiatry 2021 07 11 (1): 399. Modenato Claudia, Kumar Kuldeep, Moreau Clara, Martin-Brevet Sandra, Huguet Guillaume, Schramm Catherine, Jean-Louis Martineau, Martin Charles-Olivier, Younis Nadine, Tamer Petra, Douard Elise, Thébault-Dagher Fanny, Côté Valérie, Charlebois Audrey-Rose, Deguire Florence, Maillard Anne M, Rodriguez-Herreros Borja, Pain Aurèlie, Richetin Sonia, , , Melie-Garcia Lester, Kushan Leila, Silva Ana I, van den Bree Marianne B M, Linden David E J, Owen Michael J, Hall Jeremy, Lippé Sarah, Chakravarty Mallar, Bzdok Danilo, Bearden Carrie E, Draganski Bogdan, Jacquemont Sébasti |
Identification of pleiotropy at the gene level between psychiatric disorders and related traits. Translational psychiatry 2021 07 11 (1): 410. Polushina Tatiana, Banerjee Niladri, Giddaluru Sudheer, Bettella Francesco, Espeseth Thomas, Lundervold Astri J, Djurovic Srdjan, Cichon Sven, Hoffmann Per, Nöthen Markus M, Steen Vidar M, Andreassen Ole A, Le Hellard Stéphan |
Pharmacogenomics Factors Influencing the Effect of Risperidone on Prolactin Levels in Thai Pediatric Patients With Autism Spectrum Disorder. Frontiers in pharmacology 2021 12 743494. Hongkaew Yaowaluck, Gaedigk Andrea, Wilffert Bob, Gaedigk Roger, Kittitharaphan Wiranpat, Ngamsamut Nattawat, Limsila Penkhae, Puangpetch Apichaya, Sukprasong Rattanaporn, Sukasem Chonlaph |
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. NPJ genomic medicine 2020 Oct 5 (1): 45. Li Danyang, Choque-Olsson Nora, Jiao Hong, Norgren Nina, Jonsson Ulf, Bölte Sven, Tammimies Kristii |
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- Page last updated:Jun 22, 2022
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