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Marcio Augusto Afonso de Almeida
Marcio Augusto Afonso de Almeida
Verified email at txbiomedgenetics.org
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Cited by
Year
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552-561, 2012
7022012
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
5862020
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
AR Majithia, J Flannick, P Shahinian, M Guo, MA Bray, P Fontanillas, ...
Proceedings of the National Academy of Sciences 111 (36), 13127-13132, 2014
1762014
Genetic and molecular basis of drug resistance and species-specific drug action in schistosome parasites
CLL Valentim, D Cioli, FD Chevalier, X Cao, AB Taylor, SP Holloway, ...
Science 342 (6164), 1385-1389, 2013
1702013
Brazilian urban population genetic structure reveals a high degree of admixture
SR Giolo, JMP Soler, SC Greenway, MAA Almeida, M De Andrade, ...
European Journal of Human Genetics 20 (1), 111-116, 2012
1452012
Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility
RA Toledo, R Hatakana, DM Lourenço Jr, SC Lindsey, CP Camacho, ...
Endocrine-related cancer 22 (1), 65-76, 2015
1192015
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees
L Almasy, TD Dyer, JM Peralta, G Jun, AR Wood, C Fuchsberger, ...
BMC proceedings 8, 1-9, 2014
812014
A kernel of truth: statistical advances in polygenic variance component models for complex human pedigrees
J Blangero, VP Diego, TD Dyer, M Almeida, J Peralta, JW Kent Jr, ...
Advances in genetics 81, 1-31, 2013
812013
Prosaposin is a regulator of progranulin levels and oligomerization
AM Nicholson, NCA Finch, M Almeida, RB Perkerson, M Van Blitterswijk, ...
Nature communications 7 (1), 11992, 2016
792016
Human plasma lipidome is pleiotropically associated with cardiovascular risk factors and death
C Bellis, H Kulkarni, M Mamtani, JW Kent Jr, G Wong, JM Weir, CK Barlow, ...
Circulation: Cardiovascular Genetics 7 (6), 854-863, 2014
662014
Omics-squared: human genomic, transcriptomic and phenotypic data for Genetic Analysis Workshop 19
J Blangero, TM Teslovich, X Sim, MA Almeida, G Jun, TD Dyer, ...
BMC proceedings 10, 71-77, 2016
572016
Enhancing NeuroImaging genetics through metaanalysis consortium (ENIGMA)-genetics working group. The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
452020
Genome‐wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition
EEM Knowles, MA Carless, MAA de Almeida, JE Curran, DR McKay, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 …, 2014
432014
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees
G Jun, A Manning, M Almeida, M Zawistowski, AR Wood, TM Teslovich, ...
Proceedings of the National Academy of Sciences 115 (2), 379-384, 2018
402018
TRAK2, a novel regulator of ABCA1 expression, cholesterol efflux and HDL biogenesis
NJ Lake, RL Taylor, H Trahair, KN Harikrishnan, JE Curran, M Almeida, ...
European Heart Journal 38 (48), 3579-3587, 2017
302017
Insights into the organization of dorsal spinal cord pathways from an evolutionarily conserved raldh2 intronic enhancer
HA Castillo, RM Cravo, AP Azambuja, MS Simões-Costa, S Sura-Trueba, ...
Development 137 (3), 507-518, 2010
302010
Recurrent major depression and right hippocampal volume: a bivariate linkage and association study
SR Mathias, EEM Knowles, JW Kent Jr, DR Mckay, JE Curran, ...
Human brain mapping 37 (1), 191-202, 2016
282016
Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression
EEM Knowles, JW Kent Jr, DR McKay, E Sprooten, SR Mathias, ...
Journal of affective disorders 191, 123-131, 2016
272016
Exome sequence data from multigenerational families implicate AMPA receptor trafficking in neurocognitive impairment and schizophrenia risk
MZ Kos, MA Carless, J Peralta, A Blackburn, M Almeida, D Roalf, ...
Schizophrenia bulletin 42 (2), 288-300, 2016
252016
Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway [S]
NB Blackburn, LF Michael, PJ Meikle, JM Peralta, M Mosior, S McAhren, ...
Journal of lipid research 60 (9), 1630-1639, 2019
222019
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