Detalhe da pesquisa
1.
Copy number variation underlies complex phenotypes in domestic dog breeds and other canids.
Genome Res
; 31(5): 762-774, 2021 05.
Artigo
Inglês
| MEDLINE | ID: mdl-33863806
2.
Copy number variation analysis in the great apes reveals species-specific patterns of structural variation.
Genome Res
; 21(10): 1626-39, 2011 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-21824994
3.
The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild.
BMC Genomics
; 14: 363, 2013 May 31.
Artigo
Inglês
| MEDLINE | ID: mdl-23721540
4.
How to analyze many contingency tables simultaneously in genetic association studies.
Stat Appl Genet Mol Biol
; 11(4)2012 Jul 27.
Artigo
Inglês
| MEDLINE | ID: mdl-22850061
5.
Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management.
Bioinformatics
; 27(13): 1871-2, 2011 Jul 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21586520
6.
Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosis.
J Immunol
; 185(9): 5392-404, 2010 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-20921521
7.
Population dynamics and genetic connectivity in recent chimpanzee history.
Cell Genom
; 2(6): None, 2022 Jun 08.
Artigo
Inglês
| MEDLINE | ID: mdl-35711737
8.
Recent human evolution has shaped geographical differences in susceptibility to disease.
BMC Genomics
; 12: 55, 2011 Jan 24.
Artigo
Inglês
| MEDLINE | ID: mdl-21261943
9.
Mapping co-ancestry connections between the genome of a Medieval individual and modern Europeans.
Sci Rep
; 10(1): 6843, 2020 04 22.
Artigo
Inglês
| MEDLINE | ID: mdl-32321996
10.
Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD.
BMC Genomics
; 10: 338, 2009 Jul 28.
Artigo
Inglês
| MEDLINE | ID: mdl-19638193
11.
SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data.
Bioinformatics
; 24(14): 1643-4, 2008 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18515823
12.
Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies.
Sci Rep
; 6: 36671, 2016 11 28.
Artigo
Inglês
| MEDLINE | ID: mdl-27892471
13.
Pharmacogenomic study in patients with multiple sclerosis: Responders and nonresponders to IFN-ß.
Neurol Neuroimmunol Neuroinflamm
; 2(5): e154, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26445728
14.
New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.
JAMA Neurol
; 70(6): 764-71, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23700170
15.
Select your SNPs (SYSNPs): a web tool for automatic and massive selection of SNPs.
Int J Data Min Bioinform
; 6(3): 324-34, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23155765
16.
Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis.
Arch Neurol
; 66(8): 972-8, 2009 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-19667218
17.
The measurement of the lactonase activity of paraoxonase-1 in the clinical evaluation of patients with chronic liver impairment.
Clin Biochem
; 42(1-2): 91-8, 2009 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-18977341