Detalhe da pesquisa
1.
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease.
Cell
; 184(10): 2633-2648.e19, 2021 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33864768
2.
RNA Sequencing in Disease Diagnosis.
Annu Rev Genomics Hum Genet
; 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38360541
3.
Integration of rare expression outlier-associated variants improves polygenic risk prediction.
Am J Hum Genet
; 109(6): 1055-1064, 2022 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35588732
4.
Nonsense-mediated decay is highly stable across individuals and tissues.
Am J Hum Genet
; 108(8): 1401-1408, 2021 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34216550
5.
Effects of multicomponent primary care-based intervention on immunization rates and missed opportunities to vaccinate adults.
BMC Fam Pract
; 21(1): 46, 2020 02 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32113475
6.
Recruiting primary care practices for practice-based research: a case study of a group-randomized study (TRANSLATE CKD) recruitment process.
Fam Pract
; 35(1): 111-116, 2018 01 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28985294
7.
Missed opportunities for improving practice performance in adult immunizations: a meta-narrative review of the literature.
BMC Fam Pract
; 18(1): 108, 2017 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29272999
8.
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation.
medRxiv
; 2024 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38260377
9.
Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape.
Nat Commun
; 14(1): 4826, 2023 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37563143
10.
Stimulant Prescribing Error Assessment Rubric Development.
J Patient Saf
; 18(1): e282-e289, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32925567
11.
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics.
Nat Genet
; 53(3): 313-321, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33664507
12.
Properties of structural variants and short tandem repeats associated with gene expression and complex traits.
Nat Commun
; 11(1): 2927, 2020 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32522982
13.
Transcriptomic signatures across human tissues identify functional rare genetic variation.
Science
; 369(6509)2020 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32913073
14.
SNPs2ChIP: Latent Factors of ChIP-seq to infer functions of non-coding SNPs.
Pac Symp Biocomput
; 24: 184-195, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30864321
15.
Proficiency Testing of Standardized Samples Shows Very High Interlaboratory Agreement for Clinical Next-Generation Sequencing-Based Oncology Assays.
Arch Pathol Lab Med
; 143(4): 463-471, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30376374
16.
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.
Nat Med
; 25(6): 911-919, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31160820
17.
Preventing the voltage drop: keeping practice-based research network (PBRN) practices engaged in studies.
J Am Board Fam Med
; 27(1): 123-35, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24390894
18.
Protocol for the asthma tools study: a pragmatic practice-based research network trial.
Pragmat Obs Res
; 4: 7-18, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-27774020
19.
Preparing for and recovering from a natural disaster.
Fam Pract Manag
; 19(3): 15-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22612211