Detalhe da pesquisa
1.
Plasma proteomic associations with genetics and health in the UK Biobank.
Nature
; 622(7982): 329-338, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794186
2.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450978
3.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662886
4.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
5.
External Validation and Comparison of a General Ward Deterioration Index Between Diversely Different Health Systems.
Crit Care Med
; 51(6): 775-786, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36927631
6.
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection.
N Engl J Med
; 380(20): 1918-1928, 2019 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31091373
7.
An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome.
Am J Hum Genet
; 103(2): 232-244, 2018 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30057032
8.
Disruption of the exocyst induces podocyte loss and dysfunction.
J Biol Chem
; 294(26): 10104-10119, 2019 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31073028
9.
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
; 101(5): 789-802, 2017 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29100090
10.
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
N Engl J Med
; 376(8): 742-754, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28121514
11.
Demonstrating the consequences of learning missingness patterns in early warning systems for preventative health care: A novel simulation and solution.
J Biomed Inform
; 110: 103528, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32795506
12.
Physician incivility in the health care workplace.
CMAJ
; 196(9): E295, 2024 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38467413
13.
Rapid breath analysis for acute respiratory distress syndrome diagnostics using a portable two-dimensional gas chromatography device.
Anal Bioanal Chem
; 411(24): 6435-6447, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31367803
14.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
J Am Soc Nephrol
; 29(7): 2000-2013, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29903748
15.
An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts.
Nephrol Dial Transplant
; 32(12): 2051-2058, 2017 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27638911
16.
APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts.
Nephrol Dial Transplant
; 32(6): 983-990, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27190333
17.
Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
Pediatr Nephrol
; 32(3): 467-476, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27766458
18.
Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.
J Am Soc Nephrol
; 27(7): 1970-83, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26534921
19.
Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.
J Am Soc Nephrol
; 27(3): 814-23, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26150607
20.
tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine.
BMC Bioinformatics
; 17(1): 233, 2016 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287006