Detalhe da pesquisa
1.
A multi-ancestry genome-wide association study in type 1 diabetes.
Hum Mol Genet
; 33(11): 958-968, 2024 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38453145
2.
PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity.
Mult Scler
; 27(9): 1332-1340, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33566725
3.
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
4.
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
5.
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
6.
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
7.
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
8.
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
9.
GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.
Bioinformatics
; 31(22): 3682-4, 2015 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26209433
10.
Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing.
CRISPR J
; 7(1): 53-67, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38353623
11.
Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 hours.
bioRxiv
; 2023 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333221
12.
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
Pediatr Nephrol
; 32(7): 1285, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28349212
13.
Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach.
Nat Commun
; 13(1): 2337, 2022 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35484151
14.
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes.
Nat Genet
; 53(7): 962-971, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34127860
15.
Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes.
J Endocr Soc
; 4(11): bvaa121, 2020 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33150273
16.
Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families.
Diabetes
; 68(4): 847-857, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30655385
17.
Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score.
Diabetes Care
; 42(3): 406-415, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30659077
18.
Genetics of type 1 diabetes.
Curr Opin Genet Dev
; 50: 7-16, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29453110