Detalhe da pesquisa
1.
Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.
PLoS Genet
; 18(9): e1009923, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36112662
2.
Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes.
Genet Epidemiol
; 47(6): 450-460, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37158367
3.
Do children with mathematical learning disabilities use the inversion principle to solve three-term arithmetic problems?: The impact of presentation mode.
J Exp Child Psychol
; 216: 105343, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34968744
4.
Collection and storage of human white blood cells for analysis of DNA damage and repair activity using the comet assay in molecular epidemiology studies.
Mutagenesis
; 36(3): 193-212, 2021 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33755160
5.
Mixed logistic regression in genome-wide association studies.
BMC Bioinformatics
; 21(1): 536, 2020 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-33228527
6.
Rare variant association testing for multicategory phenotype.
Genet Epidemiol
; 43(6): 646-656, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31087445
7.
First genome-wide association study of non-severe malaria in two birth cohorts in Benin.
Hum Genet
; 138(11-12): 1341-1357, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31667592
8.
Time knowledge acquisition in children aged 6 to 11 years and its relationship with numerical skills.
J Exp Child Psychol
; 143: 1-13, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26590852
9.
The Use of the Linear Mixed Model in Human Genetics.
Hum Hered
; 80(4): 196-206, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27576760
10.
A Bagged, Partially Linear, Tree-Based Regression Procedure for Prediction and Variable Selection.
Hum Hered
; 79(3-4): 182-93, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26201703
11.
A new scoring system in cancer genetics: application to criteria for BRCA1 and BRCA2 mutation screening.
J Med Genet
; 51(2): 114-21, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24343917
12.
Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III.
Hum Hered
; 77(1-4): 49-62, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25060269
13.
Using affected sib-pairs to uncover rare disease variants.
Hum Hered
; 74(3-4): 129-41, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23594491
14.
Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?
Hum Hered
; 74(3-4): 142-52, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23594492
15.
Comorbidity and metabolic context are crucial factors determining neurological sequelae of hypoglycaemia.
Dev Med Child Neurol
; 54(11): 1012-7, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22924392
16.
Extension of SKAT to multi-category phenotypes through a geometrical interpretation.
Eur J Hum Genet
; 29(5): 736-744, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33446828
17.
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death.
Sci Rep
; 11(1): 16793, 2021 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34408182
18.
Adipose Tissue Properties in Tumor-Bearing Breasts.
Front Oncol
; 10: 1506, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32974182
19.
Detecting the dominance component of heritability in isolated and outbred human populations.
Sci Rep
; 8(1): 18048, 2018 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30575761
20.
Validation of Gelbond® high-throughput alkaline and Fpg-modified comet assay using a linear mixed model.
Environ Mol Mutagen
; 59(7): 595-602, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30091211