| Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ... Cell 180 (3), 568-584. e23, 2020 | 2055 | 2020 |
| Integrative functional genomic analysis of human brain development and neuropsychiatric risks M Li, G Santpere, Y Imamura Kawasawa, OV Evgrafov, FO Gulden, ... Science 362 (6420), eaat7615, 2018 | 729 | 2018 |
| Rare coding variation provides insight into the genetic architecture and phenotypic context of autism JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ... Nature genetics 54 (9), 1320-1331, 2022 | 350 | 2022 |
| Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder J An, K Lin, L Zhu, DM Werling, S Dong, H Brand, HZ Wang, X Zhao, ... Science 362 (6420), 2018 | 312 | 2018 |
| An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. DM Werling, H Brand, JY An, MR Stone, L Zhu, JT Glessner, RL Collins, ... Nature Genetics 50, 727-736, 2018 | 292 | 2018 |
| Opposing effects on NaV1. 2 function underlie differences between SCN2A variants observed in individuals with autism spectrum disorder or infantile seizures R Ben-Shalom, CM Keeshen, KN Berrios, JY An, SJ Sanders, KJ Bender Biological psychiatry 82 (3), 224-232, 2017 | 277 | 2017 |
| Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system AS Cristino, SM Williams, Z Hawi, JY An, MA Bellgrove, CE Schwartz, ... Molecular psychiatry 19 (3), 294-301, 2014 | 246 | 2014 |
| Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome RL Collins, H Brand, CE Redin, C Hanscom, C Antolik, MR Stone, ... Genome biology 18, 1-21, 2017 | 205 | 2017 |
| Integrative multi-omics approaches in cancer research: from biological networks to clinical subtypes YJ Heo, C Hwa, GH Lee, JM Park, JY An Molecules and cells 44 (7), 433-443, 2021 | 141 | 2021 |
| Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex DM Werling, S Pochareddy, J Choi, JY An, B Sheppard, M Peng, Z Li, ... Cell reports 31 (1), 2020 | 128 | 2020 |
| Whole genome sequencing in psychiatric disorders: the WGSPD consortium SJ Sanders, BM Neale, H Huang, DM Werling, JY An, S Dong, ... Nature Neuroscience 20 (12), 1661, 2017 | 104 | 2017 |
| Genetic heterogeneity in autism: From single gene to a pathway perspective JY An, C Claudianos Neuroscience & Biobehavioral Reviews, 2016 | 84 | 2016 |
| An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder SM Williams, JY An, J Edson, M Watts, V Murigneux, AJO Whitehouse, ... Molecular psychiatry 24 (11), 1707-1719, 2019 | 81 | 2019 |
| Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders B Hu, H Won, W Mah, RB Park, B Kassim, K Spiess, A Kozlenkov, ... Nature communications 12 (1), 3968, 2021 | 78 | 2021 |
| Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach JY An, A Hunt, AJO Whitehouse, AS Cristino, C Claudianos, D Ravine, ... Translational psychiatry 4 (6), e394, 2014 | 76 | 2014 |
| Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies L Choi, JY An Neuroscience & Biobehavioral Reviews 128, 244-257, 2021 | 60 | 2021 |
| Revealing the brain's molecular architecture PsychENCODE Consortium* Science 362 (6420), 1262-1263, 2018 | 55 | 2018 |
| High-throughput characterization of the role of non-B DNA motifs on promoter function I Georgakopoulos-Soares, J Victorino, GE Parada, V Agarwal, J Zhao, ... Cell Genomics 2 (4), 2022 | 41 | 2022 |
| Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain L Liang, S Fazel Darbandi, S Pochareddy, FO Gulden, MC Gilson, ... Genome medicine 13, 1-14, 2021 | 39 | 2021 |
| Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies C Lowther, E Valkanas, JL Giordano, HZ Wang, BB Currall, K O’Keefe, ... The American Journal of Human Genetics 110 (9), 1454-1469, 2023 | 38* | 2023 |
Stephan J. SandersProfessor, Oxford and UCSFایمیل تأیید شده در ucsf.edu
