Search Results - "Engchuan W"

Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion.

Authors: Cheng M Yin Y Engchuan W et al.

Corporate Authors: Cheng M Yin Y Engchuan W et al.

Source: Molecular psychiatry [Mol Psychiatry] 2026 Apr 15. Date of Electronic Publication: 2026 Apr 15.

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

An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.

Authors: Bradley CA Ko SY Tian M et al.

Source: Nature [Nature] 2026 Jul; Vol. 655 (8122), pp. 418-428. Date of Electronic Publication: 2026 May 13.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE

Diverse short tandem repeat sequences influence gene regulation in human populations.

Authors: Mitina A Engchuan W Trost B et al.

Source: Genome biology [Genome Biol] 2025 Sep 12; Vol. 26 (1), pp. 279. Date of Electronic Publication: 2025 Sep 12.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 100960660 Publication Model: Electronic Cited Medium: Internet ISSN: 1474-760X (Electronic) Linking ISSN: 14747596 NLM ISO Abbreviation: Genome Biol Subsets: MEDLINE

DPSO‐Q: A Reinforcement Learning–Enhanced Swarm Algorithm for Solving the Traveling Salesman Problem.

Authors: Kappagantula, Sivayazi Sangubotla, Rohit Varenya, Vippagunta Vidhu Sri et al.

Source: International Journal of Intelligent Systems; 8/24/2025, Vol. 2025, p1-27, 27p

Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.

Authors: Kumar K Kazem S Huguet G et al.

Source: Research square [Res Sq] 2025 Nov 28. Date of Electronic Publication: 2025 Nov 28.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101768035 Publication Model: Electronic Cited Medium: Internet ISSN: 2693-5015 (Electronic) Linking ISSN: 26935015 NLM ISO Abbreviation: Res Sq Subsets: PubMed not MEDLINE

Determinants of pleiotropy and monotonic gene dosage responses across human traits.

Authors: Kazem S Kumar K Huguet G et al.

Source: Research square [Res Sq] 2025 Nov 19. Date of Electronic Publication: 2025 Nov 19.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101768035 Publication Model: Electronic Cited Medium: Internet ISSN: 2693-5015 (Electronic) Linking ISSN: 26935015 NLM ISO Abbreviation: Res Sq Subsets: PubMed not MEDLINE

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Authors: Gillentine, Madelyn A. Wang, Tianyun Hoekzema, Kendra et al.

Source: Genome Medicine. 5/31/2021, Vol. 13 Issue 1, p1-26. 26p.

Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review.

Authors: Baris, Savas Dogan, Mustafa Terali, Kerem et al.

Source: International Journal of Molecular Sciences. Jan2026, Vol. 27 Issue 2, p575. 15p.

Summarizing Recent Developments on Autism Spectrum Disorder Detection and Classification Through Machine Learning and Deep Learning Techniques.

Authors: Ahmed, Masroor Hussain, Sadam Ali, Farman et al.

Source: Applied Sciences (2076-3417); Jul2025, Vol. 15 Issue 14, p8056, 40p

Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants.

Authors: Haque, Bushra Cheerie, David Pan, Amy et al.

Source: PLoS Genetics. 1/6/2025, Vol. 21 Issue 1, p1-21. 21p.

Autism Spectrum Disorder: Integrating Genetic and Environmental Risk.

Authors: Kamijo, Satoshi Miwa, Hideki Ikeda, Kazutaka

Source: Cells (2073-4409). Jun2026, Vol. 15 Issue 11, p985. 37p.

Autism Information Progression and the Impact of Misinformation on Autism Knowledge, Awareness and Stigmatization.

Authors: Madali, Nayana Pampapura Hawamdeh, Suliman

Source: Behavioral Sciences (2076-328X). May2026, Vol. 16 Issue 5, p660. 26p.

Unveiled SOX2 disorder in a child initially diagnosed as cerebral palsy.

Authors: Rim, Hanee Kim, Jaewon Kim, Myungshin et al.

Source: Egyptian Journal of Medical Human Genetics. 10/23/2025, Vol. 26 Issue 1, p1-6. 6p.

Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India.

Authors: Shah, Jhanvi Mondal, Debasrija Jain, Deepika et al.

Source: BMC Medical Genomics. 8/20/2025, Vol. 18 Issue 1, p1-12. 12p.

Screening, identification, and experimental validation of SUMOylation biomarkers in Parkinson's disease.

Authors: Wei, Yifo Zhang, Xinning Zuo, Rui et al.

Source: Hereditas. 8/8/2025, Vol. 162 Issue 1, p1-20. 20p.

Urban Built Environment as a Predictor for Coronary Heart Disease—A Cross-Sectional Study Based on Machine Learning.

Authors: Jiang, Dan Guo, Fei Zhang, Ziteng et al.

Source: Buildings (2075-5309); Dec2024, Vol. 14 Issue 12, p4024, 20p

Harmonizing two measures of adaptive functioning using computational approaches: prediction of vineland adaptive behavior scales II (VABS-II) from the adaptive behavior assessment system II (ABAS-II) scores.

Authors: Smith, Corinna Lautarescu, Alexandra Charman, Tony et al.

Source: Molecular Autism. 12/3/2024, Vol. 15 Issue 1, p1-11. 11p.

Gene dosage architecture across complex traits.

Authors: Kazem S Kumar K Jean-Louis M et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2025 Feb 26. Date of Electronic Publication: 2025 Feb 26.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencing.

Authors: Suresh, Abhilash Morton, Sarah U. Quiat, Daniel et al.

Source: BMC Medical Genomics. 7/25/2025, Vol. 18 Issue 1, p1-9. 9p.

Insights into the genetic landscape of cerebral palsy.

Authors: Wang, Yangong Zhu, Changlian Xing, Qinghe

Source: Clinical & Translational Medicine. Jul2025, Vol. 15 Issue 7, p1-4. 4p.