Search Results - "Tsetsos F"

Deciphering cell type-specific causal genetic effects on brain imaging-derived phenotypes and disorders with single-cell Mendelian randomization.

Authors: Yang, Anyi Zhao, Xingzhong Zhao, Xing-Ming et al.

Source: PLoS Computational Biology. 6/17/2026, Vol. 22 Issue 6, p1-32. 32p.

A single-cell spatiotemporal transcriptomic atlas of mouse prefrontal cortex maps dynamics of intratelencephalic neurons during postnatal development.

Authors: Zheng, Hu Yan, Keji Gou, Xiaojuan et al.

Source: PLoS Biology. 1/12/2026, Vol. 24 Issue 1, p1-24. 24p.

Is Ecopipam an effective treatment for Tourette syndrome? A systematic review and meta-analysis with GRADE assessment.

Authors: Darwish, Mohamed Khalafalla Nasser, Mohamed Mohammed, Hazem E. et al.

Source: Egyptian Journal of Neurology, Psychiatry & Neurosurgery. 1/6/2026, Vol. 62 Issue 1, p1-12. 12p.

Challenging current diagnostic and classification criteria for primary tic disorders.

Authors: Nilles, Christelle Martino, Davide Fletcher, Julian et al.

Source: European Child & Adolescent Psychiatry. Dec2025, Vol. 34 Issue 12, p3883-3890. 8p.

The Role of Mitochondrial DNA Copy Number in Neurodevelopmental Disorders: A Bidirectional Two-Sample Mendelian Randomization Study.

Authors: Qiu, Xinhui Song, Huilu Wu, Chenyang et al.

Source: Psychology Research & Behavior Management. Nov2025, Vol. 18, p2323-2332. 10p.

A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron Excitability.

Authors: Nasello, Cara Yilmaz, G. Duygu Poppi, Lauren A. et al.

Source: International Journal of Molecular Sciences. Nov2025, Vol. 26 Issue 21, p10307. 29p.

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A Tourette Syndrome/ADHD-like Phenotype Results from Postnatal Disruption of CB 1 and CB 2 Receptor Signalling.

Authors: Gorberg, Victoria Harpaz, Tamar Shamir, Emilya Natali et al.

Source: International Journal of Molecular Sciences. Jul2025, Vol. 26 Issue 13, p6052. 24p.

Identifying potential drug targets for tourette syndrome: a Mendelian randomization study based on druggable genes.

Authors: Zhou, Shilin Li, Lixin

Source: Italian Journal of Pediatrics. 6/9/2025, Vol. 51 Issue 1, p1-7. 7p.

MCP‐1 Is Elevated in the Cerebral Fluid of Children With Tourette Syndrome: Case Series and Literature Review.

Authors: Zhongling, Ke Mengxin, Chen Yuxian, Huang et al.

Source: Brain & Behavior. Jun2025, Vol. 15 Issue 6, p1-6. 6p.

SOX7: Autism associated gene identified by analysis of multi-Omics data.

Authors: Gonzales, Samantha Zhao, Jane Zizhen Choi, Na Young et al.

Source: PLoS ONE. 5/15/2025, Vol. 20 Issue 5, p1-19. 19p.

A novel classification framework for genome-wide association study of whole brain MRI images using deep learning.

Authors: Yu, Shaojun Wu, Junjie Shao, Yumeng et al.

Source: PLoS Computational Biology. 10/15/2024, Vol. 20 Issue 10, p1-24. 24p.

Transcriptome analysis of possible genetic-level defects in the use of large-sized Chinese mitten crab (Eriocheir sinensis) parents for breeding.

Authors: Xuan, Fujun Hu, Jinghao Gao, Lei et al.

Source: Invertebrate Reproduction & Development. Mar2026, Vol. 70 Issue 1, p57-73. 17p.

Cytokine expression profiles in children and adolescents with tic disorders.

Authors: Kutuk, Meryem Ozlem Tufan, Ali Evren Kilicaslan, Fethiye et al.

Source: Scientific Reports. 7/2/2024, Vol. 14 Issue 1, p1-9. 9p.

Transcriptomics Reveals the Differences in mRNA Expression Patterns in Yak Uterus of Follicular, Luteal, and Pregnant Phases.

Authors: Beng, Shaohui Lan, Daoliang Li, Yueyue et al.

Source: Animals (2076-2615). Mar2025, Vol. 15 Issue 6, p837. 18p.

Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease.

Authors: Roumeliotis A Roumeliotis S Tsetsos F et al.

Source: Oxidative medicine and cellular longevity [Oxid Med Cell Longev] 2021 Sep 02; Vol. 2021, pp. 2531062. Date of Electronic Publication: 2021 Sep 02 (Print Publication: 2021).

Publication Type: Journal Article

Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101479826 Publication Model: eCollection Cited Medium: Internet ISSN: 1942-0994 (Electronic) Linking ISSN: 19420994 NLM ISO Abbreviation: Oxid Med Cell Longev Subsets: MEDLINE

Combined family-based association and linkage analyses in families affected by attention-deficit hyperactivity disorder.

Authors: Justice CM Ahn K Jung B et al.

Source: Human genetics [Hum Genet] 2026 Jun 22; Vol. 145 (1). Date of Electronic Publication: 2026 Jun 22.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

A genetic atlas of relationships between circulating metabolites and liability to psychiatric conditions.

Authors: Kiltschewskij DJ Reay WR Cairns MJ

Source: Molecular psychiatry [Mol Psychiatry] 2026 Jun; Vol. 31 (6), pp. 3345-3359. Date of Electronic Publication: 2026 Feb 06.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

Computational Identification of Blood–Brain Barrier-Permeant Microbiome Metabolites with Binding Affinity to Neurotransmitter Receptors in Neurodevelopmental Disorders.

Authors: Buendia-Corona, Ricardo E. Velasco Dey, María Fernanda Valencia Robles, Lisset et al.

Source: Molecules. Jan2026, Vol. 31 Issue 2, p366. 23p.

In the genetics of the beholder: gene-environment interplay for internalising and externalising behaviours using polygenic scores and adolescent perceptions of parenting.

Authors: Rainy, Nisa R. Meaburn, Emma Oliver, Bonamy R. et al.

Source: European Child & Adolescent Psychiatry. Dec2025, Vol. 34 Issue 12, p4009-4022. 14p.