Detalhe da pesquisa
1.
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations.
Hum Mol Genet
; 32(6): 907-916, 2023 03 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36168886
2.
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk.
Proc Natl Acad Sci U S A
; 118(51)2021 12 21.
Artigo
Inglês
| MEDLINE | ID: mdl-34916285
3.
Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases.
Clin Proteomics
; 20(1): 31, 2023 Aug 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37550624
4.
Development and characterization of microsatellite primers for Triops granarius (Branchiopoda: Notostraca) using MiSeq technology.
Mol Biol Rep
; 49(10): 10121-10125, 2022 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-36057875
5.
Defining the genetic control of human blood plasma N-glycome using genome-wide association study.
Hum Mol Genet
; 28(12): 2062-2077, 2019 06 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31163085
6.
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida.
Genet Med
; 23(7): 1211-1218, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33686259
7.
Single nucleotide variant counts computed from RNA sequencing and cellular traffic into human kidney allografts.
Am J Transplant
; 18(10): 2429-2442, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-29659169
8.
Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry.
BMC Genomics
; 16: 92, 2015 Feb 18.
Artigo
Inglês
| MEDLINE | ID: mdl-25765185
9.
Nanoparticle enrichment mass-spectrometry proteomics identifies protein-altering variants for precise pQTL mapping.
Nat Commun
; 15(1): 989, 2024 Feb 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38307861
10.
Standardization and Interpretation of RNA-sequencing for Transplantation.
Transplantation
; 107(10): 2155-2167, 2023 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37026702
11.
Identification of PCSK9-like human gene knockouts using metabolomics, proteomics, and whole-genome sequencing in a consanguineous population.
Cell Genom
; 3(1): 100218, 2023 Jan 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36777185
12.
Retinal nerve fibre layer thinning and corneal nerve loss in patients with Bardet-Biedl syndrome.
BMC Med Genomics
; 16(1): 301, 2023 11 23.
Artigo
Inglês
| MEDLINE | ID: mdl-37996899
13.
Defining the landscape of metabolic dysregulations in cancer metastasis.
Clin Exp Metastasis
; 39(2): 345-362, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34921655
14.
Ratios of Acetaminophen Metabolites Identify New Loci of Pharmacogenetic Relevance in a Genome-Wide Association Study.
Metabolites
; 12(6)2022 May 30.
Artigo
Inglês
| MEDLINE | ID: mdl-35736429
15.
Detection of infiltrating fibroblasts by single-cell transcriptomics in human kidney allografts.
PLoS One
; 17(6): e0267704, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35657798
16.
Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits.
Nat Commun
; 12(1): 1250, 2021 02 23.
Artigo
Inglês
| MEDLINE | ID: mdl-33623009
17.
Deep sequencing of DNA from urine of kidney allograft recipients to estimate donor/recipient-specific DNA fractions.
PLoS One
; 16(4): e0249930, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33857204
18.
Identification of genetic variants controlling RNA editing and their effect on RNA structure stabilization.
Eur J Hum Genet
; 28(12): 1753-1762, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32651550
19.
Epigenetics meets proteomics in an epigenome-wide association study with circulating blood plasma protein traits.
Nat Commun
; 11(1): 15, 2020 01 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31900413
20.
Partners in Crime: Inferring Cell-to-cell Interactions in Kidney Allograft Rejection From Single-cell RNA Sequencing.
Transplantation
; 108(2): 325-326, 2024 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37638872