Detalhe da pesquisa
1.
LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants.
BMC Genomics
; 25(1): 115, 2024 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38279154
2.
Scalable approaches for functional analyses of whole-genome sequencing non-coding variants.
Hum Mol Genet
; 31(R1): R62-R72, 2022 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35943817
3.
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies.
Am J Hum Genet
; 108(5): 919-928, 2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33789087
4.
NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge.
Alzheimers Dement
; 20(2): 1123-1136, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37881831
5.
Asian Cohort for Alzheimer's Disease (ACAD) pilot study on genetic and non-genetic risk factors for Alzheimer's disease among Asian Americans and Canadians.
Alzheimers Dement
; 20(3): 2058-2071, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38215053
6.
Perspectives toward biosimilars among oncologists: A Malaysian survey.
J Oncol Pharm Pract
; : 10781552221104773, 2022 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35698761
7.
Tangram: a comprehensive toolbox for mobile element insertion detection.
BMC Genomics
; 15: 795, 2014 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-25228379
8.
A comprehensive map of mobile element insertion polymorphisms in humans.
PLoS Genet
; 7(8): e1002236, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21876680
9.
Human whole-exome genotype data for Alzheimer's disease.
Nat Commun
; 15(1): 684, 2024 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38263370
10.
A comparative study of structural variant calling in WGS from Alzheimer's disease families.
Life Sci Alliance
; 7(5)2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38418088
11.
Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease.
medRxiv
; 2023 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38014121
12.
The prediction of Alzheimer's disease through multi-trait genetic modeling.
Front Aging Neurosci
; 15: 1168638, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37577355
13.
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects.
Res Sq
; 2023 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37886469
14.
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects.
medRxiv
; 2023 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37745545
15.
Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.
medRxiv
; 2023 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37693521
16.
Extended genome-wide association study employing the African Genome Resources Panel identifies novel susceptibility loci for Alzheimer's Disease in individuals of African ancestry.
medRxiv
; 2023 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37693582
17.
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies LRRC4C, LHX5-AS1 and nominates ancestry-specific loci PTPRK , GRB14 , and KIAA0825 as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium.
medRxiv
; 2023 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37461624
18.
The role of structural variations in Alzheimer's disease and other neurodegenerative diseases.
Front Aging Neurosci
; 14: 1073905, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36846102
19.
Polygenic Risk Scores in Alzheimer's Disease Genetics: Methodology, Applications, Inclusion, and Diversity.
J Alzheimers Dis
; 89(1): 1-12, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35848019
20.
Comprehensive Analysis of Alternative Splicing in Gastric Cancer Identifies Epithelial-Mesenchymal Transition Subtypes Associated with Survival.
Cancer Res
; 82(4): 543-555, 2022 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34903603