Detalhe da pesquisa
1.
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.
Hum Mol Genet;
33(10): 919-929, 2024 May 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38339995
2.
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.
Genet Epidemiol;
46(1): 51-62, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34672391
3.
Medical Advice for Commercial Air Travel.
Am Fam Physician;
104(4): 403-410, 2021 10 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34652099
4.
Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers.
BMC Bioinformatics;
20(1): 610, 2019 Nov 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31775616
5.
Molecular phylogeny and patterns of diversification in syngnathid fishes.
Mol Phylogenet Evol;
107: 388-403, 2017 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27989632
6.
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy.
Circ Genom Precis Med;
16(1): e003716, 2023 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36598836
7.
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.
Circ Genom Precis Med;
16(3): 207-215, 2023 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37017090
8.
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.
medRxiv;
2023 Feb 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36778260
9.
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.
Nat Commun;
14(1): 1411, 2023 03 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36918541
10.
Clinical pharmacokinetic assessment of an anti-MAdCAM monoclonal antibody therapeutic by LC-MS/MS.
Anal Chem;
84(14): 5959-67, 2012 Jul 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22816779
11.
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
Nat Genet;
54(12): 1803-1815, 2022 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36474045
12.
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Nat Genet;
53(2): 135-142, 2021 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33495597
13.
The complexity, relative value, and financial worth of curbside consultations in an academic infectious diseases unit.
Clin Infect Dis;
51(6): 651-5, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20687842
14.
Assessing immunogenicity in the presence of excess protein therapeutic using immunoprecipitation and quantitative mass spectrometry.
Anal Chem;
80(18): 6907-14, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18702532
15.
Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease.
Sci Rep;
8(1): 7102, 2018 05 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29740026
16.
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
Nat Genet;
49(9): 1385-1391, 2017 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28714975
17.
Elevated Biomarkers of Inflammation and Coagulation in Patients with HIV Are Associated with Higher Framingham and VACS Risk Index Scores.
PLoS One;
10(12): e0144312, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26641655
18.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
Nat Genet;
47(10): 1121-1130, 2015 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26343387
19.
CDR-restricted engineering of native human scFvs creates highly stable and soluble bifunctional antibodies for subcutaneous delivery.
MAbs;
5(6): 882-95, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23995618
20.
Improving the pharmacokinetic properties of biologics by fusion to an anti-HSA shark VNAR domain.
MAbs;
4(6): 673-85, 2012.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23676205