Search details
1.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Cell
; 182(5): 1198-1213.e14, 2020 09 03.
Article
in English
| MEDLINE | ID: mdl-32888493
2.
Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 622(7984): 784-793, 2023 Oct.
Article
in English
| MEDLINE | ID: mdl-37821707
3.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36450978
4.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34662886
5.
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 626(8001): E18, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38332034
6.
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
Hum Mol Genet
; 31(13): 2279-2293, 2022 07 07.
Article
in English
| MEDLINE | ID: mdl-35022708
7.
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
; 31(3): 347-361, 2022 02 03.
Article
in English
| MEDLINE | ID: mdl-34553764
8.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-36807635
9.
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
; 17(10): e1009858, 2021 Oct.
Article
in English
| MEDLINE | ID: mdl-34662343
10.
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
; 17(5): e1009497, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33979322
11.
A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.
Genet Epidemiol
; 46(1): 3-16, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34779012
12.
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
PLoS Genet
; 16(6): e1008725, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32603359
13.
Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies.
BMC Med
; 20(1): 332, 2022 10 06.
Article
in English
| MEDLINE | ID: mdl-36199081
14.
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Ophthalmology
; 129(6): 626-636, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35031440
15.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
PLoS Genet
; 15(12): e1008500, 2019 12.
Article
in English
| MEDLINE | ID: mdl-31869403
16.
Extension of Mendelian Randomization to Identify Earliest Manifestations of Alzheimer Disease: Association of Genetic Risk Score for Alzheimer Disease With Lower Body Mass Index by Age 50 Years.
Am J Epidemiol
; 190(10): 2163-2171, 2021 10 01.
Article
in English
| MEDLINE | ID: mdl-33843952
17.
A polygenic risk score for asthma in a large racially diverse population.
Clin Exp Allergy
; 51(11): 1410-1420, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34459047
18.
Genetic variation in the SIM1 locus is associated with erectile dysfunction.
Proc Natl Acad Sci U S A
; 115(43): 11018-11023, 2018 10 23.
Article
in English
| MEDLINE | ID: mdl-30297428
19.
Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African American subjects in 2 large US cohorts.
J Allergy Clin Immunol
; 145(1): 192-198.e11, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31369801
20.
Eleven loci with new reproducible genetic associations with allergic disease risk.
J Allergy Clin Immunol
; 143(2): 691-699, 2019 02.
Article
in English
| MEDLINE | ID: mdl-29679657