| Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer’s disease EF Fang, Y Hou, K Palikaras, BA Adriaanse, JS Kerr, B Yang, S Lautrup, ... Nature neuroscience 22 (3), 401-412, 2019 | 1149 | 2019 |
| Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ... Nature genetics 48 (8), 856-866, 2016 | 730 | 2016 |
| Mitophagy and Alzheimer’s disease: cellular and molecular mechanisms JS Kerr, BA Adriaanse, NH Greig, MP Mattson, MZ Cader, VA Bohr, ... Trends in neurosciences 40 (3), 151-166, 2017 | 666 | 2017 |
| A highly efficient human pluripotent stem cell microglia model displays a neuronal-co-culture-specific expression profile and inflammatory response W Haenseler, SN Sansom, J Buchrieser, SE Newey, CS Moore, ... Stem cell reports 8 (6), 1727-1742, 2017 | 457 | 2017 |
| A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis MR Lincoln, A Montpetit, MZ Cader, J Saarela, DA Dyment, M Tiislar, ... Nature genetics 37 (10), 1108-1112, 2005 | 423 | 2005 |
| A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura RG Lafrenière, MZ Cader, JF Poulin, I Andres-Enguix, M Simoneau, ... Nature medicine 16 (10), 1157-1160, 2010 | 417 | 2010 |
| Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance DA Dyment, BM Herrera, MZ Cader, CJ Willer, MR Lincoln, AD Sadovnick, ... Human molecular genetics 14 (14), 2019-2026, 2005 | 296 | 2005 |
| Rare variants in the CYP27B1 gene are associated with multiple sclerosis SV Ramagopalan, DA Dyment, MZ Cader, KM Morrison, G Disanto, ... Annals of neurology 70 (6), 881-886, 2011 | 288 | 2011 |
| Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model AH Németh, AC Kwasniewska, S Lise, R Parolin Schnekenberg, ... Brain 136 (10), 3106-3118, 2013 | 201 | 2013 |
| Neuropilins lock secreted semaphorins onto plexins in a ternary signaling complex BJC Janssen, T Malinauskas, GA Weir, MZ Cader, C Siebold, EY Jones Nature structural & molecular biology 19 (12), 1293-1299, 2012 | 200 | 2012 |
| Reproducibility of molecular phenotypes after long-term differentiation to human iPSC-derived neurons: a multi-site omics study V Volpato, J Smith, C Sandor, JS Ried, A Baud, A Handel, SE Newey, ... Stem cell reports 11 (4), 897-911, 2018 | 151 | 2018 |
| Significant linkage to migraine with aura on chromosome 11q24 ZM Cader, S Noble-Topham, DA Dyment, SS Cherny, JD Brown, ... Human molecular genetics 12 (19), 2511-2517, 2003 | 128 | 2003 |
| Functional analysis of missense variants in the TRESK (KCNK18) K+ channel I Andres-Enguix, L Shang, PJ Stansfeld, JM Morahan, MSP Sansom, ... Scientific reports 2 (1), 237, 2012 | 114 | 2012 |
| Assessing similarity to primary tissue and cortical layer identity in induced pluripotent stem cell-derived cortical neurons through single-cell transcriptomics AE Handel, S Chintawar, T Lalic, E Whiteley, J Vowles, A Giustacchini, ... Human molecular genetics 25 (5), 989-1000, 2016 | 111 | 2016 |
| Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development S Lise, Y Clarkson, E Perkins, A Kwasniewska, E Sadighi Akha, ... PLoS genetics 8 (12), e1003074, 2012 | 110 | 2012 |
| An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus JL Steckley, GC Ebers, MZ Cader, RS McLachlan Neurology 57 (8), 1499-1502, 2001 | 110 | 2001 |
| HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth disease V Benoy, L Van Helleputte, R Prior, C d’Ydewalle, W Haeck, N Geens, ... Brain 141 (3), 673-687, 2018 | 106 | 2018 |
| An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy F Achilli, V Bros-Facer, HP Williams, GT Banks, M AlQatari, R Chia, ... Disease models & mechanisms 2 (7-8), 359-373, 2009 | 101 | 2009 |
| Cellular uptake and gene delivery using layered double hydroxide nanoparticles S Li, J Li, CJ Wang, Q Wang, MZ Cader, J Lu, DG Evans, X Duan, ... Journal of Materials Chemistry B 1 (1), 61-68, 2013 | 95 | 2013 |
| Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene PA James, MZ Cader, F Muntoni, AM Childs, YJ Crow, K Talbot Neurology 67 (9), 1710-1712, 2006 | 88 | 2006 |
