| An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations U Dube, JL Del-Aguila, Z Li, JP Budde, S Jiang, S Hsu, L Ibanez, ... Nature neuroscience 22 (11), 1903-1912, 2019 | 264 | 2019 |
| Meningeal lymphatics affect microglia responses and anti-Aβ immunotherapy S Da Mesquita, Z Papadopoulos, T Dykstra, L Brase, FG Farias, M Wall, ... Nature 593 (7858), 255-260, 2021 | 211 | 2021 |
| The MS4A gene cluster is a key modulator of soluble TREM2 and Alzheimer’s disease risk Y Deming, F Filipello, F Cignarella, C Cantoni, S Hsu, R Mikesell, Z Li, ... Science translational medicine 11 (505), eaau2291, 2019 | 210 | 2019 |
| A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers FHG Farias, R Zeng, GS Johnson, FA Wininger, JF Taylor, RD Schnabel, ... Neurobiology of disease 42 (3), 468-474, 2011 | 144 | 2011 |
| Clonal polymorphism and high heterozygosity in the celibate genome of the Amazon molly WC Warren, R García-Pérez, S Xu, KP Lampert, D Chalopin, M Stöck, ... Nature ecology & evolution 2 (4), 669-679, 2018 | 130 | 2018 |
| Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders C Yang, FHG Farias, L Ibanez, A Suhy, B Sadler, MV Fernandez, F Wang, ... Nature neuroscience 24 (9), 1302-1312, 2021 | 124 | 2021 |
| Chi3l1/YKL-40 is controlled by the astrocyte circadian clock and regulates neuroinflammation and Alzheimer’s disease pathogenesis BV Lananna, CA McKee, MW King, JL Del-Aguila, JM Dimitry, FHG Farias, ... Science translational medicine 12 (574), eaax3519, 2020 | 114 | 2020 |
| A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism RM Buckley, BW Davis, WA Brashear, FHG Farias, K Kuroki, T Graves, ... PLoS Genetics 16 (10), e1008926, 2020 | 95 | 2020 |
| An ADAMTS17 splice donor site mutation in dogs with primary lens luxation FHG Farias, GS Johnson, JF Taylor, E Giuliano, ML Katz, DN Sanders, ... Investigative Ophthalmology & Visual Science 51 (9), 4716-4721, 2010 | 94 | 2010 |
| A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund DN Sanders, FH Farias, GS Johnson, V Chiang, JR Cook, DP O’Brien, ... Molecular genetics and metabolism 100 (4), 349-356, 2010 | 88 | 2010 |
| Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis K Tengvall, M Kierczak, K Bergvall, M Olsson, M Frankowiack, FHG Farias, ... PLoS genetics 9 (5), e1003475, 2013 | 82 | 2013 |
| A Missense Mutation in Canine CLN6 in an Australian Shepherd with Neuronal Ceroid Lipofuscinosis ML Katz, FH Farias, DN Sanders, R Zeng, S Khan, GS Johnson, ... BioMed Research International 2011, 2011 | 82 | 2011 |
| TREM2 brain transcript-specific studies in AD and TREM2 mutation carriers JL Del-Aguila, BA Benitez, Z Li, U Dube, KA Mihindukulasuriya, JP Budde, ... Molecular neurodegeneration 14, 1-13, 2019 | 68 | 2019 |
| The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion Z Li, FHG Farias, U Dube, JL Del-Aguila, KA Mihindukulasuriya, ... Acta neuropathologica 139 (1), 45-61, 2020 | 55 | 2020 |
| Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease D Eriksson, M Bianchi, N Landegren, J Nordin, F Dalin, A Mathioudaki, ... Journal of internal medicine 280 (6), 595-608, 2016 | 52 | 2016 |
| A Truncated Retrotransposon Disrupts the GRM1 Coding Sequence in Coton de Tulear Dogs with Bandera's Neonatal Ataxia R Zeng, FHG Farias, GS Johnson, SD McKay, RD Schnabel, JE Decker, ... Journal of veterinary internal medicine 25 (2), 267-272, 2011 | 48 | 2011 |
| Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing JK Sandling, P Pucholt, LH Rosenberg, FHG Farias, SV Kozyrev, ... Annals of the rheumatic diseases 80 (1), 109-117, 2021 | 47 | 2021 |
| The novel evolution of the sperm whale genome WC Warren, L Kuderna, A Alexander, J Catchen, JG Pérez-Silva, ... Genome Biology and Evolution 9 (12), 3260-3264, 2017 | 37 | 2017 |
| Genetic and clinical basis for two distinct subtypes of primary Sjögren’s syndrome GE Thorlacius, L Hultin-Rosenberg, JK Sandling, M Bianchi, ... Rheumatology 60 (2), 837-848, 2021 | 36 | 2021 |
| African Americans have differences in CSF soluble TREM2 and associated genetic variants SE Schindler, C Cruchaga, A Joseph, L McCue, FHG Farias, CH Wilkins, ... Neurology: Genetics 7 (2), e571, 2021 | 32 | 2021 |
