| Epigenomic signatures of neuronal diversity in the mammalian brain A Mo, EA Mukamel, FP Davis, C Luo, GL Henry, S Picard, MA Urich, ... Neuron 86 (6), 1369-1384, 2015 | 656 | 2015 |
| Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease H Wu, J Luo, H Yu, A Rattner, A Mo, Y Wang, PM Smallwood, B Erlanger, ... Neuron 81 (1), 103-119, 2014 | 213 | 2014 |
| Age, CAG repeat length, and clinical progression in Huntington's disease A Rosenblatt, BV Kumar, A Mo, CS Welsh, RL Margolis, CA Ross Movement disorders 27 (2), 272-276, 2012 | 142 | 2012 |
| Epigenomic landscapes of retinal rods and cones A Mo, C Luo, FP Davis, EA Mukamel, GL Henry, JR Nery, MA Urich, ... Elife 5, e11613, 2016 | 116 | 2016 |
| Characterization of multiple spiral wave dynamics as a stochastic predator-prey system NF Otani, A Mo, S Mannava, FH Fenton, EM Cherry, S Luther, ... Physical Review E 78 (2), 021913, 2008 | 19 | 2008 |
| 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 | 8 | 2023 |
| Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST A Mo, A Saffari, M Kellner, M Döbler‐Neumann, C Jordan, S Srivastava, ... Movement Disorders 37 (12), 2440-2446, 2022 | 8 | 2022 |
| The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15 A Saffari, M Kellner, C Jordan, H Rosengarten, A Mo, B Zhang, O Strelko, ... Brain 146 (5), 2003-2015, 2023 | 7 | 2023 |
| Exome sequencing and the identification of new genes and shared mechanisms in polymicrogyria SK Akula, AY Chen, JE Neil, DD Shao, A Mo, NK Hylton, S DiTroia, ... JAMA neurology 80 (9), 980-988, 2023 | 4 | 2023 |
| Neurodevelopmental profile of HIVEP2‐related disorder A Mo, LG Snyder, O Babington, WK Chung, M Sahin, S Srivastava Developmental Medicine & Child Neurology 64 (5), 654-661, 2022 | 4 | 2022 |
| A recurrent de novo variant in NUSAP1 escapes nonsense‐mediated decay and leads to microcephaly, epilepsy, and developmental delay A Mo, E Paz‐Ebstein, S Yanovsky‐Dagan, A Lai, H Mor‐Shaked, T Gilboa, ... Clinical Genetics 104 (1), 73-80, 2023 | 3 | 2023 |
| The Clinical And Molecular Spectrum Of ZFYVE26-Associated Hereditary Spastic Paraplegia (SPG15)(P13-11.005) A Saffari, C Jordan, A Mo, B Zhang, M Sahin, C Blackstone, E Yang, ... Neurology 100 (17 Supplement 2), 2023 | | 2023 |
| Chapter 12: Movement Disorders A Mo, D Ebrahimi-Fakhari Neurology 100 (16_Supplement_1), S158-S159, 2023 | | 2023 |
| Blended Phenotype of Prader-Willi Syndrome and HSP-SPG11 Caused by Maternal Uniparental Isodisomy AR Kunta, J Jueng, C Jordan, J Kojic, A Mo, D Ebrahimi-Fakhari Neurology: Genetics 8 (6), e200041, 2022 | | 2022 |
| Further Evidence for Early-Onset, Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST A Mo, A Saffari, A Soldatos, K Alter, O Strelko, C Jordan, S Srivastava, ... ANNALS OF NEUROLOGY 92, S127-S127, 2022 | | 2022 |
| Upper motor neuron signs and early onset gait abnormalities in young children with bi‐allelic VWA1 variants DL Gable, A Mo, E Estrella, A Saffari, PS Ghosh, D Ebrahimi‐Fakhari American Journal of Medical Genetics Part A, 2022 | | 2022 |
| Child Neurology: Recurrent Brainstem Strokes and Aphthous Ulcers in a Child With Mutations in the ADA2 Gene A Mo, S Donatelli, LA Benson, PY Lee, MJ Rivkin Neurology 97 (14), 696-699, 2021 | | 2021 |
