Integrative genetic and transcriptomic analysis identifies candidate genes and compounds for Fragile X syndrome and autism spectrum disorder
Wen Zhang, Jingqi Yan, Michael DeGiorgio
bioRxiv · Oct 6, 2026 · PreprintBioinformatics
Author
Icahn School of Medicine at Mount Sinai
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
13 papers
Recent·Most cited
Wen Zhang, Jingqi Yan, Michael DeGiorgio
bioRxiv · Oct 6, 2026 · PreprintBioinformatics
Wei Guo, Wen Zhang, Lili Yang, Trine Zachariasen, Xuanji Li, Jakob Stokholm, Min Dai, Jonathan Thorsen, Søren Johannes Sørensen, Urvish Trivedi
The paper analyzes the evolutionary history and microbial interactions of Bifidobacterium longum subspecies in infants, finding that subspecies distribution is shaped by ecological factors and cross-feeding rather than host-specific factors.
bioRxiv · Jul 13, 2026 · PreprintMicrobiology
Siyuan Tong, Wen Zhang, Shiliang Ji
This paper develops a multi-modal deep learning framework to identify Class I HDAC inhibitors as broad-spectrum anti-cancer agents by integrating chemical and transcriptomic data.
bioRxiv · Apr 29, 2026 · PreprintBioinformatics
Yu Tian, Ziwu Wang, Feihong Yang, Wen Zhang, Jialin Li, Lin Yang, Tao Fu, Wenhui Zheng, Zhejun Xu, Tong Ma, Yan You, Xiaosu Li, Jiangang Song, Yunli Xie, Zhengang Yang, Zhuangzhi Zhang
This study shows that Olig1/2 knockout in gliogenesis shifts glial precursor cells to produce non-proliferative interneurons instead of oligodendrocyte precursors, and identifies dorsal cortical GPCs as origin of H3.3G34R/V-mutant tumors.
Nature Communications · Nov 5, 2025Peer-reviewedNeuroscience
Xiulai Li, Xin Li, Wen Zhang, Wei Wu
MACGA predicts lncRNA-disease associations using a graph attention network with multi-scale adaptive convolution, outperforming existing methods in cross-validation and validated by case studies.
bioRxiv · Jul 14, 2025 · PreprintBioinformatics
Rprot-Vec is a deep learning model that rapidly calculates protein structural similarity and detects homology using only sequences, achieving 65.3% accuracy in homologous protein prediction.
BMC Bioinformatics · Jul 10, 2025Peer-reviewedBioinformatics
Zhengkun Lin, Jianquan He, Hui Huang, Xiaomei Lin, Heqing Chen, Wen Zhang, Jian‐Min Chen
This study generates an Fzd8-knockout mouse model using CRISPR/Cas9 to investigate its role in bone development and homeostasis, finding altered osteoclast and osteoblast activity and potential links to osteoporosis.
bioRxiv · Jan 19, 2025 · PreprintBioengineering
Xi Zha, Zhuolei Jiao, Shuaishuai Li, Xiao-Yao Liu, Xing-Yu Li, Yi-Zhuo Sun, Xiao‐Jing Ding, Meng-Tong Gao, Shu-Chen Gao, Ai-Xiao Chen, Jun-Kai Lin, Wen Zhang, Xuan-Zi Cao, Yanli Zhang, Rong-Rong Yang, , Xiao-Hong Xu
The paper identifies a hypothalamic circuit involving Calb1+ neurons and Pomc+ neurons that coordinates β-endorphin release with ejaculation in male mice.
bioRxiv · Sep 18, 2024 · PreprintNeuroscience
Jaroslav M. Bendl, Mads E. Hauberg, Kiran Girdhar, Eunju Im, James M. Vicari, Samir Rahman, Michael B. Fernando, Kayla G. Townsley, Pengfei Dong, Ruth Misir, Steven P. Kleopoulos, Sarah M. Reach, Pasha Apontes, Biao Zeng, Wen Zhang, , Panos Roussos
This study maps chromatin accessibility in Alzheimer's disease using ATAC-seq, identifying regulatory changes and 3D genomic alterations linked to disease.
Nature Neuroscience · Sep 28, 2022Peer-reviewedNeuroscience
Pengfei Dong, Gabriel E. Hoffman, Pasha Apontes, Jaroslav M. Bendl, Samir Rahman, Michael B. Fernando, Biao Zeng, James M. Vicari, Wen Zhang, Kiran Girdhar, Kayla G. Townsley, Ruth Misir, Andrew J. Chess, Attila Gulyás-Kovács, Bibi S. Kassim, , Panos Roussos
The paper identifies population-level variation in enhancer expression in the human brain and links enhancer eQTL to schizophrenia heritability.
Nature Genetics · Sep 26, 2022Peer-reviewedNeuroscience
Penelope H. Benchek, Robert P. Igo, Heather A. Voss-Hoynes, Yvonne E. Wren, Gabrielle J. Miller, Barbara J. Truitt, Wen Zhang, Michael D. Osterman, Lisa A. Freebairn, Jessica Tag, H. Gerry Taylor, E. Ricky Chan, Panos Roussos, Barbara Ann Lewis, Catherine M. Stein, Sudha K. Iyengar
This study identifies 18 significant genetic loci associated with speech sound disorders through GWAS and finds polygenic risk scores linked to clinical severity.
npj Genomic Medicine · Jul 27, 2021Peer-reviewedGenetic & Genomic Medicine
Lide Han, Xuefang Zhao, Mary Lauren Benton, Thanneer Malai Perumal, Ryan L. Collins, Gabriel E. Hoffman, Jessica Johnson, Laura Gail Sloofman, Harold Z. Wang, Matthew R. Stone, Schahram Akbarian, Jaroslav M. Bendl, Michael S. Breen, Kristen Brennand, Leanne Brown, , Michael E. Talkowski
The paper functionally annotates rare structural variants in the human brain by integrating SV calling with RNA-seq data to assess their regulatory effects and prioritize pathogenic deletions.
Nature Communications · Jun 12, 2020Peer-reviewedGenomics
Yan-Xiang Ni, Wen-Qian Xue, Nan Zhou, Wing-Ho Yung, Rao-Zhou Lin, Richard Yi-Tsun Kao, Zhi-Gang Duan, Xu-Ming Tang, Meng-Fei Liu, Wen Zhang, Shuang Qi, Xi-Bin Lu, Jian-jiang Hu, Sookja Chung, You-Qiang Song, Jian-Dong Huang
This study shows Kif5b interacts with clathrin heavy chain and facilitates CCV uncoating, linking anterograde transport to clathrin-mediated endocytosis.
bioRxiv · Mar 18, 2018 · PreprintCell Biology