Alejandro Q. Nato, Jr.
Titel
Citeret af
Citeret af
År
Genetic studies of body mass index yield new insights for obesity biology [member of PAGE Consortium]
AE Locke, B Kahali, SI Berndt, ..., PAGEConsortium, et al.
Nature 518 (7538), 197-206, 2015
33192015
Defining the role of common variation in the genomic and biological architecture of adult human height [member of PAGE Consortium]
AR Wood, T Esko, J Yang, ..., PAGE Consortium, et al.
Nature genetics 46 (11), 1173-1186, 2014
17062014
New genetic loci link adipose and insulin biology to body fat distribution [member of PAGE Consortium]
D Shungin, TW Winkler, DC Croteau-Chonka, ..., PAGEConsortium, et al.
Nature 518 (7538), 187-196, 2015
11242015
Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study [member of PAGE Consortium]
CS Carlson, TC Matise, KE North, CA Haiman, MD Fesinmeyer, S Buyske, ...
PLoS Biol 11 (9), e1001661, 2013
1912013
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes
NH Chapman, AQ Nato, R Bernier, K Ankenman, H Sohi, J Munson, ...
Human genetics 134 (10), 1055-1068, 2015
502015
Genetic candidate variants in two multigenerational families with childhood apraxia of speech
B Peter, EM Wijsman, AQ Nato Jr, ...
PloS one 11 (4), e0153864, 2016
342016
Association of rare coding mutations with Alzheimer disease and other dementias among adults of European ancestry
D Patel, J Mez, BN Vardarajan, L Staley, J Chung, X Zhang, JJ Farrell, ...
JAMA network open 2 (3), e191350-e191350, 2019
282019
The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation
BI Li, PG Matteson, MF Ababon, AQ Nato Jr, Y Lin, V Nanda, TC Matise, ...
Developmental biology 402 (1), 17-31, 2015
272015
Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using …
L Zhang, P Buzkova, CL Wassel, MJ Roman, KE North, DC Crawford, ...
Atherosclerosis 228 (2), 390-399, 2013
272013
Divergent haplotypes and human history as revealed in a worldwide survey of X-linked DNA sequence variation
MK Shimada, K Panchapakesan, SA Tishkoff, AQ Nato Jr, J Hey
Molecular biology and evolution 24 (3), 687-698, 2007
272007
Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and …
MD Fesinmeyer, JB Meigs, KE North, FR Schumacher, P Bůžková, ...
BMC medical genetics 14 (1), 1-8, 2013
252013
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease
X Zhang, C Zhu, G Beecham, BN Vardarajan, Y Ma, D Lancour, JJ Farrell, ...
Alzheimer's & Dementia 15 (3), 441-452, 2019
232019
Analysis of whole-exome sequencing data for Alzheimer disease stratified by APOE genotype
Y Ma, GR Jun, X Zhang, J Chung, AC Naj, Y Chen, C Bellenguez, ...
JAMA neurology 76 (9), 1099-1108, 2019
182019
Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease [member of Alzheimer's Disease Sequencing Project]
BN Vardarajan, S Barral, J Jaworski, ..., ...
Annals of Clinical and Translational Neurology 5 (4), 406-417, 2018
182018
Genetic variation in genes underlying diverse dementias may explain a small proportion of cases in the Alzheimer’s Disease Sequencing Project
EE Blue, JC Bis, MO Dorschner, DW Tsuang, SM Barral, G Beecham, ...
Dementia and geriatric cognitive disorders 45 (1), 1-17, 2018
172018
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project
AC Naj, H Lin, BN Vardarajan, S White, D Lancour, Y Ma, M Schmidt, ...
Genomics 111 (4), 808-818, 2019
122019
Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error
W Kim, D Londono, L Zhou, J Xing, AQ Nato, A Musolf, TC Matise, ...
Human heredity 74 (3-4), 172-183, 2012
122012
Comparison and Assessment of Family-and Population-Based Genotype Imputation Methods in Large Pedigrees
E Ullah, R Mall, MM Abbas, K Kunji, AQ Nato Jr, H Bensmail, EM Wijsman, ...
Genome Research, 2018
112018
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease
GW Beecham, B Vardarajan, E Blue, W Bush, J Jaworski, S Barral, ...
Neurology Genetics 4 (6), 2018
102018
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders
DT Truong, LD Shriberg, SD Smith, KL Chapman, AR Scheer-Cohen, ...
Human genetics 135 (12), 1329-1341, 2016
92016
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Artikler 1–20