Molecules and Cells

Cited by CrossRef (17)

  1. Muhammad Kamran, Aodán Laighneach, Farhana Bibi, Gary Donohoe, Naveed Ahmed, Asim Ur Rehman, Derek W. Morris. Independent Associated SNPs at SORCS3 and Its Protein Interactors for Multiple Brain-Related Disorders and Traits. Genes 2023;14:482
    https://doi.org/10.3390/genes14020482
  2. Lan Liu, Jiamin Wang, Xijing Liu, Jing Wang, Lin Chen, Hongmei Zhu, Jingqun Mai, Ting Hu, Shanling Liu. Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis. Clinica Chimica Acta 2024;552:117671
    https://doi.org/10.1016/j.cca.2023.117671
  3. Fang Liu, Chen Liang, Zhengchang Li, Sen Zhao, Haiming Yuan, Ruen Yao, Zailong Qin, Shaofang Shangguan, Shujie Zhang, Li-Ping Zou, Qian Chen, Zhijie Gao, Suiwen Wen, Jing Peng, Fei Yin, Fei Chen, Xiaoxia Qiu, Jingsi Luo, Yingjun Xie, Dian Lu, Yu Zhang, Hua Xie, Guozhuang Li, Terry Jianguo Zhang, Pengfei Luan, Hongying Wang, Xiaodai Cui, Hailiang Huang, Ruize Liu, Xiaofang Sun, Chao Chen, Nan Wu, Jian Wang, Chunyu Liu, Yiping Shen, James F Gusella, Xiaoli Chen. Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment. 2023;146:3347
    https://doi.org/10.1093/brain/awad071
  4. Ramit Sharma, Aarti Tiwari, Saloni Rahi, Sidharth Mehan. Current Neuropharmacological Interventions in Autism: Potential Drug Targets from Pre-clinical and Clinical Findings. CPSP 2021;10:98
    https://doi.org/10.2174/1389203721999200820165117
  5. Xuqian Fang, Yuwen Zhang, Jialin Cai, Tingwei Lu, Junjie Hu, Fei Yuan, Peizhan Chen. Identification of novel candidate pathogenic genes in pituitary stalk interruption syndrome by whole‐exome sequencing. J Cellular Molecular Medi 2020;24:11703
    https://doi.org/10.1111/jcmm.15781
  6. Laura E. Egolf, Zalman Vaksman, Gonzalo Lopez, Jo Lynne Rokita, Apexa Modi, Patricia V. Basta, Hakon Hakonarson, Andrew F. Olshan, Sharon J. Diskin. Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma. The American Journal of Human Genetics 2019;105:658
    https://doi.org/10.1016/j.ajhg.2019.07.020
  7. Zhuoran Xu, Quan Li, Luigi Marchionni, Kai Wang. PhenoSV: interpretable phenotype-aware model for the prioritization of genes affected by structural variants. Nat Commun 2023;14
    https://doi.org/10.1038/s41467-023-43651-y
  8. Ibuki Ueoka, Hang Thi Nguyet Pham, Kinzo Matsumoto, Masamitsu Yamaguchi. Autism Spectrum Disorder-Related Syndromes: Modeling with Drosophila and Rodents. IJMS 2019;20:4071
    https://doi.org/10.3390/ijms20174071
  9. Maryam Rastegari, Najmeh Salehi, Fatemeh Zare-Mirakabad. Biomarker prediction in autism spectrum disorder using a network-based approach. BMC Med Genomics 2023;16
    https://doi.org/10.1186/s12920-023-01439-5
  10. Alessandra Suuberg. Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2. SSRN Journal 2018
    https://doi.org/10.2139/ssrn.3185741
  11. Jonathan C. Andrews, Michael F. Wangler, Shinya Yamamoto, Jennifer E. Posey. Encyclopedia of Behavioral Neuroscience, 2nd edition. 2018.
    https://doi.org/10.1016/B978-0-12-819641-0.00145-6
  12. Jian Jiao, Manxue Zhang, Pingyuan Yang, Yan Huang, Xiao Hu, Jia Cai, Chan Yang, Mingjing Situ, Hui Zhang, Lei Fu, Kuifang Guo, Yi Huang. Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample. J Mol Neurosci 2020;70:219
    https://doi.org/10.1007/s12031-019-01456-z
  13. Giovanni Messina, Yuri Prozzillo, Greta Bizzochi, Renè Massimiliano Marsano, Patrizio Dimitri. The Green Valley of Drosophila melanogaster Constitutive Heterochromatin: Protein-Coding Genes Involved in Cell Division Control. Cells 2022;11:3058
    https://doi.org/10.3390/cells11193058
  14. Anthony Wong, Anbo Zhou, Xiaolong Cao, Vaidhyanathan Mahaganapathy, Marco Azaro, Christine Gwin, Sherri Wilson, Steven Buyske, Christopher W. Bartlett, Judy F. Flax, Linda M. Brzustowicz, Jinchuan Xing. MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders. Genes 2022;13:1329
    https://doi.org/10.3390/genes13081329
  15. Sabah Nisar, Ajaz A. Bhat, Tariq Masoodi, Sheema Hashem, Sabah Akhtar, Tayyiba Akbar Ali, Sara Amjad, Sanjeev Chawla, Puneet Bagga, Michael P. Frenneaux, Ravinder Reddy, Khalid Fakhro, Mohammad Haris. Genetics of glutamate and its receptors in autism spectrum disorder. Mol Psychiatry 2022;27:2380
    https://doi.org/10.1038/s41380-022-01506-w
  16. Bradley P. Coe, Holly A. F. Stessman, Arvis Sulovari, Madeleine R. Geisheker, Trygve E. Bakken, Allison M. Lake, Joseph D. Dougherty, Ed S. Lein, Fereydoun Hormozdiari, Raphael A. Bernier, Evan E. Eichler. Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity. Nat Genet 2019;51:106
    https://doi.org/10.1038/s41588-018-0288-4
  17. Reem Al‐Jawahiri, Myles Jones, Elizabeth Milne. Atypical neural variability in carriers of 16p11.2 copy number variants. Autism Research 2019;12:1322
    https://doi.org/10.1002/aur.2166