Detalhe da pesquisa
1.
E-Pedigrees: a large-scale automatic family pedigree prediction application.
Bioinformatics
; 37(21): 3966-3968, 2021 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34086863
2.
Kidney failure in Bardet-Biedl syndrome.
Clin Genet
; 101(4): 429-441, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35112343
3.
Medical Records-Based Genetic Studies of the Complement System.
J Am Soc Nephrol
; 32(8): 2031-2047, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33941608
4.
Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.
Lupus
; 30(8): 1264-1272, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33977795
5.
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
World J Surg
; 44(1): 84-94, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31605180
6.
Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations.
Hum Genet
; 138(10): 1155-1169, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31342140
7.
Applying family analyses to electronic health records to facilitate genetic research.
Bioinformatics
; 34(4): 635-642, 2018 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28968884
8.
Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission.
J Med Virol
; 90(3): 436-446, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29053189
9.
Phenome-wide association study maps new diseases to the human major histocompatibility complex region.
J Med Genet
; 53(10): 681-9, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287392
10.
Application of clinical text data for phenome-wide association studies (PheWASs).
Bioinformatics
; 31(12): 1981-7, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25657332
11.
Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity.
Circ Res
; 115(12): 1017-25, 2014 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25326128
12.
SeqHBase: a big data toolset for family based sequencing data analysis.
J Med Genet
; 52(4): 282-8, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25587064
13.
Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort.
Genet Epidemiol
; 38(8): 692-8, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25250975
14.
The challenges, advantages and future of phenome-wide association studies.
Immunology
; 141(2): 157-65, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24147732
15.
Assessment of the current status of real-world pharmacogenomic testing: informed consent, patient education, and related practices.
Front Pharmacol
; 15: 1355412, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38410134
16.
The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease after antenatal betamethasone administration.
Am J Obstet Gynecol
; 208(3): 215.e1-6, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23295978
17.
Estimating the efficacy of pharmacogenomics over a lifetime.
Front Med (Lausanne)
; 10: 1006743, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38020121
18.
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.
Circ Genom Precis Med
; 16(2): e003816, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37071725
19.
Serine hydroxymethyltransferase 1 and 2: gene sequence variation and functional genomic characterization.
J Neurochem
; 120(6): 881-90, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22220685
20.
Human liver methionine cycle: MAT1A and GNMT gene resequencing, functional genomics, and hepatic genotype-phenotype correlation.
Drug Metab Dispos
; 40(10): 1984-92, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22807109