| DJ-1 protects the nigrostriatal axis from the neurotoxin MPTP by modulation of the AKT pathway H Aleyasin, MWC Rousseaux, PC Marcogliese, SJ Hewitt, I Irrcher, ... Proceedings of the National Academy of Sciences 107 (7), 3186-3191, 2010 | 200 | 2010 |
| Regulation of myeloid cell phagocytosis by LRRK2 via WAVE2 complex stabilization is altered in Parkinson’s disease KS Kim, PC Marcogliese, J Yang, SM Callaghan, V Resende, ... Proceedings of the National Academy of Sciences 115 (22), E5164-E5173, 2018 | 114* | 2018 |
| Sphingolipids in the Pathogenesis of Parkinson’s Disease and Parkinsonism G Lin, L Wang, PC Marcogliese, HJ Bellen Trends in Endocrinology & Metabolism 30 (2), 106-117, 2019 | 104 | 2019 |
| Progressive dopaminergic cell loss with unilateral-to-bilateral progression in a genetic model of Parkinson disease MWC Rousseaux, PC Marcogliese, D Qu, SJ Hewitt, S Seang, RH Kim, ... Proceedings of the National Academy of Sciences 109 (39), 15918-15923, 2012 | 101 | 2012 |
| 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 | 98 | 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 | 92 | 2020 |
| Lrrk2 alleles modulate inflammation during microbial infection of mice in a sex-dependent manner B Shutinoski, M Hakimi, IE Harmsen, M Lunn, J Rocha, N Lengacher, ... Science translational medicine 11 (511), eaas9292, 2019 | 92 | 2019 |
| Neuronal ROS-induced glial lipid droplet formation is altered by loss of Alzheimer’s disease–associated genes MJ Moulton, S Barish, I Ralhan, J Chang, LD Goodman, JG Harland, ... Proceedings of the National Academy of Sciences 118 (52), e2112095118, 2021 | 86 | 2021 |
| BAG2 gene-mediated regulation of PINK1 protein is critical for mitochondrial translocation of PARKIN and neuronal survival D Qu, A Hage, K Don-Carolis, E Huang, A Joselin, F Safarpour, ... Journal of Biological Chemistry 290 (51), 30441-30452, 2015 | 60 | 2015 |
| Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders H Guo, E Bettella, PC Marcogliese, R Zhao, JC Andrews, TJ Nowakowski, ... Nature communications 10 (1), 4679, 2019 | 59 | 2019 |
| Drosophila voltage-gated sodium channels are only expressed in active neurons and are localized to distal axonal initial segment-like domains TA Ravenscroft, J Janssens, PT Lee, B Tepe, PC Marcogliese, ... Journal of Neuroscience 40 (42), 7999-8024, 2020 | 48 | 2020 |
| Unaltered Striatal Dopamine Release Levels in Young Parkin Knockout, Pink1 Knockout, DJ-1 Knockout and LRRK2 R1441G Transgenic Mice G Sanchez, RK Varaschin, H Büeler, PC Marcogliese, DS Park, ... PLoS One 9 (4), e94826, 2014 | 44 | 2014 |
| 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 | 35 | 2020 |
| DJ-1 modulates the unfolded protein response and cell death via upregulation of ATF4 following ER stress J Yang, KS Kim, GO Iyirhiaro, PC Marcogliese, SM Callaghan, D Qu, ... Cell Death & Disease 10 (2), 135, 2019 | 34 | 2019 |
| 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 | 32* | 2022 |
| De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment D Dutta, LC Briere, O Kanca, PC Marcogliese, MA Walker, FA High, ... Human Molecular Genetics 29 (9), 1568-1579, 2020 | 32 | 2020 |
| 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 | 30 | 2019 |
| Missense variants in CTNNB1 can be associated with vitreoretinopathy—Seven new cases of CTNNB1‐associated neurodevelopmental disorder including a … LZ Rossetti, MR Bekheirnia, AM Lewis, HC Mefford, K Golden‐Grant, ... Molecular Genetics & Genomic Medicine 9 (1), e1542, 2021 | 25 | 2021 |
| 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 | 24 | 2022 |
| LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in Drosophila PC Marcogliese, S Abuaish, G Kabbach, E Abdel-Messih, S Seang, G Li, ... Human molecular genetics 26 (7), 1247-1257, 2017 | 24 | 2017 |
Hugo BellenProfessor, Developmental biology, Genetics, and Neuroscience在 bcm.edu 的电子邮件经过验证
