| An efficient CRISPR-based strategy to insert small and large fragments of DNA using short homology arms O Kanca, J Zirin, J Garcia-Marques, SM Knight, D Yang-Zhou, G Amador, ... Elife 8, e51539, 2019 | 131 | 2019 |
| IRF2BPL is associated with neurological phenotypes PC Marcogliese, V Shashi, RC Spillmann, N Stong, JA Rosenfeld, ... The American Journal of Human Genetics 103 (2), 245-260, 2018 | 101 | 2018 |
| Loss-or gain-of-function mutations in ACOX1 cause axonal loss via different mechanisms H Chung, MF Wangler, PC Marcogliese, J Jo, TA Ravenscroft, Z Zuo, ... Neuron 106 (4), 589-606. e6, 2020 | 96 | 2020 |
| Mutations in ANKLE2, a ZIKA virus target, disrupt an asymmetric cell division pathway in Drosophila neuroblasts to cause microcephaly N Link, H Chung, A Jolly, M Withers, B Tepe, BR Arenkiel, PS Shah, ... Developmental cell 51 (6), 713-729. e6, 2019 | 86 | 2019 |
| Drosophila Schip1 links expanded and Tao-1 to regulate hippo signaling HL Chung, GJ Augustine, KW Choi Developmental Cell 36 (5), 511-524, 2016 | 38 | 2016 |
| De novo variants in CDK19 are associated with a syndrome involving intellectual disability and epileptic encephalopathy H Chung, X Mao, H Wang, YJ Park, PC Marcogliese, JA Rosenfeld, ... The American Journal of Human Genetics 106 (5), 717-725, 2020 | 36 | 2020 |
| Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases PC Marcogliese, SL Deal, J Andrews, JM Harnish, VH Bhavana, ... Cell reports 38 (11), 2022 | 35* | 2022 |
| Bi-allelic loss-of-function variants in DNMBP cause infantile cataracts M Ansar, H Chung, RL Taylor, A Nazir, S Imtiaz, MT Sarwar, ... The American Journal of Human Genetics 103 (4), 568-578, 2018 | 35 | 2018 |
| Bi-allelic variants in IQSEC1 cause intellectual disability, developmental delay, and short stature M Ansar, H Chung, A Al-Otaibi, MN Elagabani, TA Ravenscroft, ... The American Journal of Human Genetics 105 (5), 907-920, 2019 | 31 | 2019 |
| Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3 M Ansar, H Chung, YM Waryah, P Makrythanasis, E Falconnet, AR Rao, ... Human molecular genetics 27 (15), 2703-2711, 2018 | 27 | 2018 |
| Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation H Chung, Q Ye, YJ Park, Z Zuo, JW Mok, O Kanca, SG Tattikota, S Lu, ... Cell metabolism 35 (5), 855-874. e5, 2023 | 26 | 2023 |
| Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures S Lu, R Hernan, PC Marcogliese, Y Huang, TS Gertler, M Akcaboy, S Liu, ... The American Journal of Human Genetics 109 (4), 571-586, 2022 | 25 | 2022 |
| Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling PC Marcogliese, D Dutta, SS Ray, NDP Dang, Z Zuo, Y Wang, D Lu, ... Science advances 8 (3), eabl5613, 2022 | 20 | 2022 |
| Phosphatidylserine synthase plays an essential role in glia and affects development, as well as the maintenance of neuronal function YJ Park, S Kim, HP Shim, JH Park, G Lee, TY Kim, MC Jo, AY Kwon, ... Iscience 24 (8), 2021 | 18 | 2021 |
| ABCD1 and Xlinked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models J Manor, H Chung, PK Bhagwat, MF Wangler Journal of neuroscience research 99 (12), 3170-3181, 2021 | 16 | 2021 |
| De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in Drosophila HL Chung, P Rump, D Lu, MR Glassford, JW Mok, J Fatih, A Basal, ... Human Molecular Genetics 31 (19), 3231-3244, 2022 | 14 | 2022 |
| De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies SN Manivannan, J Roovers, N Smal, CT Myers, D Turkdogan, F Roelens, ... Brain 145 (5), 1684-1697, 2022 | 10 | 2022 |
| The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival M Ma, X Zhang, Y Zheng, S Lu, X Pan, X Mao, H Pan, H Chung, H Wang, ... Human Molecular Genetics 32 (6), 984-997, 2023 | 6 | 2023 |
| Schip1, a new upstream regulator of Hippo signaling HL Chung, KW Choi Cell Cycle 15 (16), 2097-2098, 2016 | 5 | 2016 |
| Calx, a sodium/calcium exchanger, may affect lifespan in Drosophila melanogaster JW Mok, H Chung, KW Choi Micropublication Biology 2020, 2020 | 3* | 2020 |
