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Fabiana H G Farias
Fabiana H G Farias
Washington University
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Year
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
2632019
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
2082021
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
2082019
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
1442011
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
1292018
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
1222021
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
1122020
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
942010
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
922020
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
882010
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
822011
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
812013
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
682019
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
552020
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
522016
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
482011
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
472021
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
372017
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
362021
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
322021
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