| Year |
Citation |
Score |
| 2024 |
Kim S, Lee J, Koh IG, Ji J, Kim HJ, Kim E, Park J, Park JE, An JY. An integrative single-cell atlas for exploring the cellular and temporal specificity of genes related to neurological disorders during human brain development. Experimental & Molecular Medicine. PMID 39363111 DOI: 10.1038/s12276-024-01328-6 |
0.405 |
|
| 2024 |
Kim SW, Lee H, Song DY, Lee GH, Ji J, Park JW, Han JH, Lee JW, Byun HJ, Son JH, Kim YR, Lee Y, Kim J, Jung A, Lee J, ... ... An JY, et al. Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism. Genome Medicine. 16: 114. PMID 39334436 DOI: 10.1186/s13073-024-01385-6 |
0.742 |
|
| 2024 |
Kim Y, Jeong M, Koh IG, Kim C, Lee H, Kim JH, Yurko R, Kim IB, Park J, Werling DM, Sanders SJ, An JY. CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. Briefings in Bioinformatics. 25. PMID 38966948 DOI: 10.1093/bib/bbae323 |
0.799 |
|
| 2024 |
Kissel LT, Pochareddy S, An JY, Sestan N, Sanders SJ, Wang X, Werling DM. Sex-Differential Gene Expression in Developing Human Cortex and Its Intersection With Autism Risk Pathways. Biological Psychiatry Global Open Science. 4: 100321. PMID 38957312 DOI: 10.1016/j.bpsgos.2024.100321 |
0.763 |
|
| 2024 |
Fazel Darbandi S, An JY, Lim K, Page NF, Liang L, Young DM, Ypsilanti AR, State MW, Nord AS, Sanders SJ, Rubenstein JLR. Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes. Cell Reports. 43: 114329. PMID 38850535 DOI: 10.1016/j.celrep.2024.114329 |
0.738 |
|
| 2024 |
Kim JH, Koh IG, Lee H, Lee GH, Song DY, Kim SW, Kim Y, Han JH, Bong G, Lee J, Byun H, Son JH, Kim YR, Lee Y, Kim JJ, ... ... An JY, et al. Short tandem repeat expansions in cortical layer-specific genes implicate in phenotypic severity and adaptability of autism spectrum disorder. Psychiatry and Clinical Neurosciences. PMID 38751214 DOI: 10.1111/pcn.13676 |
0.51 |
|
| 2024 |
Kim Y, Jeong M, Koh IG, Kim C, Lee H, Kim JH, Yurko R, Kim IB, Park J, Werling DM, Sanders SJ, An JY. CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. Medrxiv : the Preprint Server For Health Sciences. PMID 38699372 DOI: 10.1101/2024.04.15.24305828 |
0.805 |
|
| 2023 |
Lagunas T, Plassmeyer SP, Fischer AD, Friedman RZ, Rieger MA, Selmanovic D, Sarafinovska S, Sol YK, Kasper MJ, Fass SB, Aguilar Lucero AF, An JY, Sanders SJ, Cohen BA, Dougherty JD. A Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of non-coding elements in vivo. Communications Biology. 6: 1151. PMID 37953348 DOI: 10.1038/s42003-023-05483-w |
0.59 |
|
| 2023 |
Lowther C, Valkanas E, Giordano JL, Wang HZ, Currall BB, O'Keefe K, Pierce-Hoffman E, Kurtas NE, Whelan CW, Hao SP, Weisburd B, Jalili V, Fu J, Wong I, Collins RL, ... ... An JY, et al. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies. American Journal of Human Genetics. PMID 37595579 DOI: 10.1016/j.ajhg.2023.07.010 |
0.739 |
|
| 2023 |
Koesterich J, An JY, Inoue F, Sohota A, Ahituv N, Sanders SJ, Kreimer A. Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays. International Journal of Molecular Sciences. 24. PMID 36834916 DOI: 10.3390/ijms24043509 |
0.687 |
|
| 2022 |
Jang WE, Park JH, Park G, Bang G, Na CH, Kim JY, Kim KY, Kim KP, Shin CY, An JY, Lee YS, Kim MS. Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis. Molecular Psychiatry. PMID 36253443 DOI: 10.1038/s41380-022-01822-1 |
0.367 |
|
| 2022 |
Kim IB, Lee T, Lee J, Kim J, Lee S, Koh IG, Kim JH, An JY, Lee H, Kim WK, Ju YS, Cho Y, Yu SJ, Kim SA, Oh M, et al. Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder. Molecular Psychiatry. PMID 35840799 DOI: 10.1038/s41380-022-01697-2 |
0.363 |
|
| 2022 |
Georgakopoulos-Soares I, Victorino J, Parada GE, Agarwal V, Zhao J, Wong HY, Umar MI, Elor O, Muhwezi A, An JY, Sanders SJ, Kwok CK, Inoue F, Hemberg M, Ahituv N. High-throughput characterization of the role of non-B DNA motifs on promoter function. Cell Genomics. 2. PMID 35573091 DOI: 10.1016/j.xgen.2022.100111 |
0.543 |
|
| 2021 |
Liang L, Fazel Darbandi S, Pochareddy S, Gulden FO, Gilson MC, Sheppard BK, Sahagun A, An JY, Werling DM, Rubenstein JLR, Sestan N, Bender KJ, Sanders SJ. Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain. Genome Medicine. 13: 135. PMID 34425903 DOI: 10.1186/s13073-021-00949-0 |
0.747 |
|
| 2021 |
Choi L, An JY. Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies. Neuroscience and Biobehavioral Reviews. PMID 34166716 DOI: 10.1016/j.neubiorev.2021.06.028 |
0.523 |
|
| 2020 |
Genç Ö, An JY, Fetter RD, Kulik Y, Zunino G, Sanders SJ, Davis GW. Homeostatic plasticity fails at the intersection of autism-gene mutations and a novel class of common genetic modifiers. Elife. 9. PMID 32609087 DOI: 10.7554/Elife.55775 |
0.614 |
|
| 2020 |
Kim Y, An JY. Spatio-Temporal Roles of ASD-Associated Variants in Human Brain Development. Genes. 11. PMID 32403330 DOI: 10.3390/genes11050535 |
0.441 |
|
| 2020 |
Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G, Sousa AMM, Tebbenkamp ATN, Kaur N, Gulden FO, Breen MS, Liang L, et al. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Reports. 31: 107489. PMID 32268104 DOI: 10.1016/J.Celrep.2020.03.053 |
0.788 |
|
| 2020 |
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, Peng M, Collins R, Grove J, Klei L, Stevens C, Reichert J, Mulhern MS, Artomov M, Gerges S, et al. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell. PMID 31981491 DOI: 10.1016/J.Cell.2019.12.036 |
0.752 |
|
| 2018 |
An JY, Lin K, Zhu L, Werling DM, Dong S, Brand H, Wang HZ, Zhao X, Schwartz GB, Collins RL, Currall BB, Dastmalchi C, Dea J, Duhn C, Gilson MC, et al. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362. PMID 30545852 DOI: 10.1126/Science.Aat6576 |
0.796 |
|
| 2018 |
Williams SM, An JY, Edson J, Watts M, Murigneux V, Whitehouse AJO, Jackson CJ, Bellgrove MA, Cristino AS, Claudianos C. An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder. Molecular Psychiatry. PMID 29703944 DOI: 10.1038/S41380-018-0049-X |
0.821 |
|
| 2018 |
Werling DM, Brand H, An JY, Stone MR, Zhu L, Glessner JT, Collins RL, Dong S, Layer RM, Markenscoff-Papadimitriou E, Farrell A, Schwartz GB, Wang HZ, Currall BB, Zhao X, et al. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics. PMID 29700473 DOI: 10.1038/S41588-018-0107-Y |
0.806 |
|
| 2018 |
Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, et al. Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. PMID 29549319 DOI: 10.1038/S41593-018-0102-8 |
0.757 |
|
| 2017 |
Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, et al. Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. 20: 1661-1668. PMID 29184211 DOI: 10.1038/S41593-017-0017-9 |
0.798 |
|
| 2017 |
An JY, Sanders SJ. Appreciating the Population-wide Impact of Copy Number Variants on Cognition. Biological Psychiatry. 82: 78-80. PMID 28645357 DOI: 10.1016/J.Biopsych.2017.05.010 |
0.484 |
|
| 2017 |
Collins RL, Brand H, Redin CE, Hanscom C, Antolik C, Stone MR, Glessner JT, Mason T, Pregno G, Dorrani N, Mandrile G, Giachino D, Perrin D, Walsh C, Cipicchio M, ... ... An JY, et al. Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome. Genome Biology. 18: 36. PMID 28260531 DOI: 10.1186/S13059-017-1158-6 |
0.603 |
|
| 2016 |
An JY, Claudianos C. Genetic heterogeneity in autism: From single gene to a pathway perspective. Neuroscience and Biobehavioral Reviews. PMID 27317861 DOI: 10.1016/J.Neubiorev.2016.06.013 |
0.707 |
|
| 2014 |
An JY, Cristino AS, Zhao Q, Edson J, Williams SM, Ravine D, Wray J, Marshall VM, Hunt A, Whitehouse AJ, Claudianos C. Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach. Translational Psychiatry. 4: e394. PMID 24893065 DOI: 10.1038/Tp.2014.38 |
0.785 |
|
| 2014 |
Cristino AS, Williams SM, Hawi Z, An JY, Bellgrove MA, Schwartz CE, Costa Lda F, Claudianos C. Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system. Molecular Psychiatry. 19: 294-301. PMID 23439483 DOI: 10.1038/Mp.2013.16 |
0.805 |
|
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