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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2002 2
2003 4
2004 6
2005 8
2006 2
2007 14
2008 20
2009 30
2010 39
2011 36
2012 34
2013 47
2014 57
2015 34
2016 39
2017 37
2018 35
2019 30
2020 33
2021 36
2022 34
2023 27
2024 27
2025 21
2026 17

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579 results

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Page 1
Enduring autism-like phenotypes and deregulated hypothalamic prosocial peptides after early-life exposure to indoor flame retardants in male C57BL/6 mice.
Kozlova EV, Gonzalez GM, Denys ME, Bishay AE, Gutierrez R, Reid J, Krum JM, Lampel G, Luvsanravdan N, Rabbani KM, Tu J, Campoy L, Anchondo LM, Luna CN, Olomi DS, Monarrez E, Carrillo V, Tran JD, Platt D, Korde Y, Chinthirla BD, Blaibel M, Kim S, Chompre G, Phillips AL, Stapleton HM, Henkelmann B, Schramm KW, Curras-Collazo MC. Kozlova EV, et al. J Neuroendocrinol. 2026 Aug;38(8):e70237. doi: 10.1111/jne.70237. J Neuroendocrinol. 2026. PMID: 42552960 Free PMC article.
PBDEs have been implicated as risk factors for autism spectrum disorder (ASD), which is characterized by abnormal psychosocial functioning and is commonly comorbid with cognitive deficits and sensory abnormalities. ...DE-71-exposed adult F1 male offspring displayed …
PBDEs have been implicated as risk factors for autism spectrum disorder (ASD), which is characterized by abnormal psychosocial …
Incidental Detection of Acute Leukemia During Genetic Evaluation of Neurodevelopmental Disorder in a Pediatric Clinic: A Case Report.
Jones SG. Jones SG. Case Rep Pediatr. 2026 Jul 15;2026:1527918. doi: 10.1155/crpe/1527918. eCollection 2026. Case Rep Pediatr. 2026. PMID: 42466354 Free PMC article.
Neurologic imaging was unremarkable, but clinical features consistent with autism spectrum disorder were noted. As part of standard-of-care ASD evaluation, SNP chromosomal microarray (CMA) on peripheral blood revealed a hypodiploid genome ( 35 chromosomes), s …
Neurologic imaging was unremarkable, but clinical features consistent with autism spectrum disorder were noted. As part of sta …
Genomic basis of developmental defects of enamel and sex-specific effects.
Shrestha P, Graff M, Gu Y, Wang Y, Ahn HS, Nguyen KN, Khanna A, Avery CL, Highland HM, Ginnis J, Simancas-Pallares MA, Ferreira Zandoná AG, Alotaibi RN, Lin DY, Preisser JS, Slade GD, Marazita ML, North KE, Divaris K. Shrestha P, et al. medRxiv [Preprint]. 2026 Jul 10:2026.07.06.26355672. doi: 10.64898/2026.07.06.26355672. medRxiv. 2026. PMID: 42465942 Free PMC article. Preprint.
We investigated four DDE phenotypes (demarcated opacities, diffuse opacities, hypoplastic defects, and a combined DDE trait) leveraging main-effect models, joint gene-sex interaction testing (2df), and sex-stratified analyses. SNP-based heritability for the combined DDE tr …
We investigated four DDE phenotypes (demarcated opacities, diffuse opacities, hypoplastic defects, and a combined DDE trait) leveraging main …
Genome-wide association study and polygenic risk score analysis for bipolar disorder in the Korean population.
Choi MJ, Kim Y, Lee HJ, Joo EJ, Ahn YM, Myung W, Kim SH, Lee BD, Ha TH, Kim SJ, Chung YC, Kim SW, Cho EY, Bin Lee D, Huang H, Ha K, Hong KS, Won HH, Baek JH. Choi MJ, et al. Asian J Psychiatr. 2026 Aug;122:105034. doi: 10.1016/j.ajp.2026.105034. Epub 2026 Jun 1. Asian J Psychiatr. 2026. PMID: 42229218 Free article.
This study aimed to identify common genetic variants associated with bipolar disorder (BD) in the Korean population and to evaluate the predictive performance of polygenic risk scores (PRSs) derived from other population data. ...We identified one genome-wide significant l …
This study aimed to identify common genetic variants associated with bipolar disorder (BD) in the Korean population and to evaluate t …
Biomarker Variants of Dopamine Receptor Genes Influence the Binding Interaction Between Dopamine Receptor and Risperidone.
Almandil NB, AbdulAzeez S, Gomaa MS, Ibrahim AM, John SJ, Prathas S, Dhas TS, Borgio JF. Almandil NB, et al. Drug Des Devel Ther. 2026 Apr 23;20:587705. doi: 10.2147/DDDT.S587705. eCollection 2026. Drug Des Devel Ther. 2026. PMID: 42052100 Free PMC article.
INTRODUCTION: Risperidone is atypical antipsychotic medication commonly used to control behavioral symptoms in children with autism and widely considered a first-line treatment for acute and maintenance treatment of schizophrenia and bipolar mania. ...In-silico tools such …
INTRODUCTION: Risperidone is atypical antipsychotic medication commonly used to control behavioral symptoms in children with autism a …
Association Between miR-146a rs2910164 Polymorphism and Tuberculosis Susceptibility: A Comprehensive Meta-Analysis.
Alikhani MY, Khoobbakht F, Khazaei S, Etesamifard T, Kazemi S. Alikhani MY, et al. Int J Mol Cell Med. 2025 Jul 28;14(4):1084-1098. doi: 10.22088/IJMCM.BUMS.14.4.1084. eCollection 2025. Int J Mol Cell Med. 2025. PMID: 42016032 Free PMC article.
This meta-analysis was therefore conducted to systematically assess the relationship between this specific single nucleotide polymorphism (SNP) and the risk of developing tuberculosis. A systematic literature search was performed utilizing the electronic databases PubMed, …
This meta-analysis was therefore conducted to systematically assess the relationship between this specific single nucleotide polymorphism ( …
Convergent genetic pathways linking neuropsychiatric and ocular disorders in children.
Pan M, Zhou W, Qu HQ, Xiu Z, Sun R, Hakonarson H, Li J, Shi X. Pan M, et al. J Child Psychol Psychiatry. 2026 Sep;67(9):1460-1475. doi: 10.1111/jcpp.70151. Epub 2026 Apr 7. J Child Psychol Psychiatry. 2026. PMID: 41947537 Free PMC article.
An in-house independent cohort (2,726 attention deficit hyperactivity disorder (ADHD) cases and 16,299 controls) was also assessed to confirm the disease relationships. ...Finally, we explored their underlying biological pathways by SNP- and Gene-based enrichment an …
An in-house independent cohort (2,726 attention deficit hyperactivity disorder (ADHD) cases and 16,299 controls) was also assessed to …
Symptom-specific genetics reveal heterogeneity within major depressive disorder.
Goula AA, Huider F, Hottenga JJ, Pasman JA, Bot M, Rietman ML, 't Hart LM, Rutters F, Blom MT, Rhebergen D, Visser M, Hartman CA, Oldehinkel AJ, de Geus EJC, Franke B, Picavet HSJ, Verschuren WMM, van Loo HM, Boomsma DΙ, Penninx BWJH, Milaneschi Y. Goula AA, et al. medRxiv [Preprint]. 2026 Mar 25:2026.03.24.26349158. doi: 10.64898/2026.03.24.26349158. medRxiv. 2026. PMID: 41929285 Free PMC article. Preprint.
BACKGROUND: Major Depressive Disorder (MDD) is clinically and biologically heterogeneous. Here, we leveraged the genetics of individual depressive symptoms to dissect the disorder's underlying heterogeneity. ...RESULTS: All symptoms demonstrated substantial SNP …
BACKGROUND: Major Depressive Disorder (MDD) is clinically and biologically heterogeneous. Here, we leveraged the genetics of individu …
A key gene modulating oxytocin efficacy in autism: genome-wide discovery and verification in randomized controlled trials datasets.
Kuwabara H, Kojima M, Benner S, Otowa T, Watanabe T, Kuroda M, Owada K, Yassin W, Hamada J, Kano Y, Uno Y, Kushima I, Mori D, Arioka Y, Munesue T, Kasai K, Higashida H, Abe O, Takao H, Wakuda T, Kameno Y, Inoue J, Harada T, Yamauchi A, Ogawa N, Honda N, Kikuchi S, Seto M, Tomita H, Miyoshi N, Matsumoto M, Kawaguchi Y, Kanai K, Ikeda M, Nakamura I, Isomura S, Hirano Y, Onitsuka T, Takahashi N, Nakashima M, Saitsu H, Kondo K, Ikeda M, Iwata N, Shimada M, Sasaki T, Takei N, Ozaki N, Kosaka H, Okada T, Yamasue H. Kuwabara H, et al. Mol Psychiatry. 2026 Aug;31(8):4475-4482. doi: 10.1038/s41380-026-03562-y. Epub 2026 Mar 28. Mol Psychiatry. 2026. PMID: 41904269 Clinical Trial.
Previous studies suggest that oxytocin has therapeutic potential for modulating core symptoms of autism spectrum disorder (ASD), although findings have been inconsistent. The unknown mechanisms underlying oxytocin's effects and the substantial individual variability …
Previous studies suggest that oxytocin has therapeutic potential for modulating core symptoms of autism spectrum disorder (ASD …
Outlook on ACADSB variants shaping metabolomic patterns and clinical outcomes - experience from a Central European country.
Bandura A, Chandoga J, Vengríni J, Juhosová M, Vavrová A, Gregová E, Lysinová M, Mydlová Z, Brennerová K, Šaligová J, Maceková D, Böhmer D. Bandura A, et al. Clin Biochem. 2026 Mar;142:111105. doi: 10.1016/j.clinbiochem.2026.111105. Epub 2026 Feb 19. Clin Biochem. 2026. PMID: 41722717 Free article.
Over the available follow-up period, no episodes of metabolic decompensation were observed; two patients remained clinically well, and one patient had autism spectrum disorder. Free carnitine concentrations were within the reference range in all probands. ...
Over the available follow-up period, no episodes of metabolic decompensation were observed; two patients remained clinically well, and one p …
579 results