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.
Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma.
Blood
; 141(11): 1293-1307, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35977101
3.
Soluble urokinase plasminogen activator receptor is associated with kidney disease and its progression in sickle cell anemia.
Haematologica
; 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38695132
4.
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
Am J Med Genet A
; 188(8): 2303-2314, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35451555
5.
Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anaemia: SCCRIP cohort study results.
Br J Haematol
; 194(2): 469-473, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34137022
6.
Optimal sequencing strategies for identifying disease-associated singletons.
PLoS Genet
; 13(6): e1006811, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28640830
7.
Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease.
Curr Res Transl Med
; 72(2): 103433, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38244277
8.
Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis.
JAMA Netw Open
; 6(10): e2337484, 2023 10 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37851445
9.
Fetal hemoglobin modulates neurocognitive performance in sickle cell anemiaâ°,â°â°.
Curr Res Transl Med
; 70(3): 103335, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35303690
10.
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden.
J Natl Cancer Inst
; 114(8): 1159-1166, 2022 08 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35511172
11.
Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts.
Nat Commun
; 12(1): 970, 2021 02 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33579919
12.
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility.
Cancer Res
; 81(7): 1695-1703, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33293427
13.
A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease.
Blood Adv
; 5(14): 2839-2851, 2021 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34283174
14.
Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction.
Nat Commun
; 11(1): 6084, 2020 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33247094
15.
The landscape of host genetic factors involved in immune response to common viral infections.
Genome Med
; 12(1): 93, 2020 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33109261
16.
The landscape of host genetic factors involved in immune response to common viral infections.
medRxiv
; 2020 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32511533
17.
Genomewide Meta-Analysis Validates a Role for S1PR1 in Microtubule Targeting Agent-Induced Sensory Peripheral Neuropathy.
Clin Pharmacol Ther
; 108(3): 625-634, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32562552
18.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Nat Commun
; 11(1): 4423, 2020 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32887889
19.
Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility.
Nat Commun
; 11(1): 27, 2020 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31911640
20.
A Pharmacogenetic Prediction Model of Progression-Free Survival in Breast Cancer using Genome-Wide Genotyping Data from CALGB 40502 (Alliance).
Clin Pharmacol Ther
; 105(3): 738-745, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30260474