The familial Alzheimer's disease APPV717I mutation alters APP processing and Tau expression in iPSC-derived neurons CR Muratore, HC Rice, P Srikanth, DG Callahan, T Shin, LNP Benjamin, ... Human molecular genetics 23 (13), 3523-3536, 2014 | 435 | 2014 |
Insulin receptor associates with promoters genome-wide and regulates gene expression ML Hancock, RC Meyer, M Mistry, RS Khetani, A Wagschal, T Shin, ... Cell 177 (3), 722-736. e22, 2019 | 161 | 2019 |
Sodium channel SCN3A (NaV1. 3) regulation of human cerebral cortical folding and oral motor development RS Smith, CJ Kenny, V Ganesh, A Jang, R Borges-Monroy, JN Partlow, ... Neuron 99 (5), 905-913. e7, 2018 | 157 | 2018 |
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions KM Girskis, AB Stergachis, EM DeGennaro, RN Doan, X Qian, ... Neuron 109 (20), 3239-3251. e7, 2021 | 132 | 2021 |
Cell-type dependent Alzheimer's disease phenotypes: probing the biology of selective neuronal vulnerability CR Muratore, C Zhou, M Liao, MA Fernandez, WM Taylor, ... Stem cell reports 9 (6), 1868-1884, 2017 | 92 | 2017 |
Rates and patterns of clonal oncogenic mutations in the normal human brain J Ganz, EA Maury, B Becerra, S Bizzotto, RN Doan, CJ Kenny, T Shin, ... Cancer discovery 12 (1), 172-185, 2022 | 38 | 2022 |
Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder R Borges-Monroy, C Chu, C Dias, J Choi, S Lee, Y Gao, T Shin, PJ Park, ... Mobile DNA 12, 1-15, 2021 | 28 | 2021 |
Evolutionary changes in transcriptional regulation: insights into human behavior and neurological conditions RN Doan, T Shin, CA Walsh Annual Review of Neuroscience 41 (1), 185-206, 2018 | 20 | 2018 |
TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system SK Akula, JH Marciano, Y Lim, D Exposito-Alonso, NK Hylton, GH Hwang, ... Proceedings of the National Academy of Sciences 120 (4), e2209964120, 2023 | 15 | 2023 |
Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder risk T Shin, JHT Song, M Kosicki, C Kenny, SG Beck, L Kelley, I Antony, ... Cell Genomics 4 (8), 2024 | 10 | 2024 |
Whole-genome analysis of de novo and polymorphic retrotransposon insertions in Autism Spectrum Disorder R Borges-Monroy, C Chu, C Dias, J Choi, S Lee, Y Gao, T Shin, PJ Park, ... bioRxiv, 2021.01. 29.428895, 2021 | 3 | 2021 |
Somatic Mosaicism in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Reveals Widespread Degeneration from Focal Mutations Z Zhou, J Kim, AY Huang, M Nolan, J Park, R Doan, T Shin, MB Miller, ... Biorxiv, 2023 | 1 | 2023 |
Intersecting evolutionary and medical genetics to understand human brain development and disease T Shin Harvard University, 2022 | | 2022 |
Abnormal Social and Cognitive Behavior is associated with Inherited Noncoding Mutations in Human Accelerated Regions (HARs) RN Doan, T Shin, B Bae, B Cubelos, C Chang, AA Hossain, S Al-Saad, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 841-842, 2019 | | 2019 |