Detalhe da pesquisa
1.
Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program.
PLoS Genet
; 19(3): e1010623, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36940203
2.
Nontargeted Plasma Proteomic Analysis of Renal Disease and Pulmonary Hypertension in Patients with Sickle Cell Disease.
J Proteome Res
; 23(3): 1039-1048, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38353026
3.
Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Am J Hum Genet
; 108(1): 100-114, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33352116
4.
Variation and impact of polygenic hematologic traits in monogenic sickle cell disease.
Haematologica
; 108(3): 870-881, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36226494
5.
A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci.
Mol Psychiatry
; 27(4): 2264-2272, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35347246
6.
Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.
Blood Cells Mol Dis
; 86: 102504, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32949984
7.
Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis.
Haematologica
; 106(6): 1749-1753, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33179474
8.
Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Am J Hum Genet
; 108(3): 530-531, 2021 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667397
9.
Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Am J Hum Genet
; 108(2): 368, 2021 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33545031
10.
Sex differences in progression of kidney disease in sickle cell disease.
Haematologica
; 108(5): 1436-1441, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36546431
11.
Clinical and metabolomic risk factors associated with rapid renal function decline in sickle cell disease.
Am J Hematol
; 93(12): 1451-1460, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30144150
12.
In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress.
PLoS Genet
; 11(7): e1005349, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26147622
13.
The association of single-nucleotide polymorphisms in the oxytocin receptor and G protein-coupled receptor kinase 6 (GRK6) genes with oxytocin dosing requirements and labor outcomes.
Am J Obstet Gynecol
; 217(3): 367.e1-367.e9, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28526450
14.
Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma.
PLoS Genet
; 10(5): e1004372, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24875647
15.
Epigenome-wide association of PTSD from heterogeneous cohorts with a common multi-site analysis pipeline.
Am J Med Genet B Neuropsychiatr Genet
; 174(6): 619-630, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28691784
16.
Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.
BMC Genomics
; 16: 11, 2015 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-25609184
17.
Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease.
Hepatology
; 59(2): 471-82, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23913408
18.
Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.
Blood
; 122(3): 434-42, 2013 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-23719301
19.
Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival.
Transfusion
; 55(6 Pt 2): 1378-87, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25444611
20.
Pregnancy continuation and organizational religious activity following prenatal diagnosis of a lethal fetal defect are associated with improved psychological outcome.
Prenat Diagn
; 35(8): 761-768, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25872901