Detalhe da pesquisa
1.
Epigenetic associations in HPA axis genes related to bronchopulmonary dysplasia and antenatal steroids.
Pediatr Res
; 2024 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38480856
2.
Childhood adversity, accelerated GrimAge, and associated health consequences.
J Behav Med
; 2024 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38762606
3.
Placental microRNAs relate to early childhood growth trajectories.
Pediatr Res
; 94(1): 341-348, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36380070
4.
Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth.
Pediatr Res
; 93(5): 1410-1418, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35906307
5.
Association between placental toxic metal exposure and NICU Network Neurobehavioral Scales (NNNS) profiles in the Rhode Island Child Health Study (RICHS).
Environ Res
; 204(Pt A): 111939, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34461121
6.
Seasonally variant gene expression in full-term human placenta.
FASEB J
; 34(8): 10431-10442, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32574425
7.
Epigenome-wide analysis identifies genes and pathways linked to acoustic cry variation in preterm infants.
Pediatr Res
; 89(7): 1848-1854, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32967004
8.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
Am J Hum Genet
; 99(1): 40-55, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346686
9.
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Am J Hum Genet
; 99(1): 8-21, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346685
10.
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.
Am J Hum Genet
; 99(1): 22-39, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346689
11.
Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.
Am J Hum Genet
; 97(4): 512-20, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26365338
12.
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Genome Res
; 25(3): 305-15, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25637381
13.
A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD.
Cardiol Young
; 28(1): 39-45, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28927471
14.
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
Genet Epidemiol
; 40(6): 470-4, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27229898
15.
Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.
Hum Genet
; 136(2): 165-178, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27848076
16.
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.
Am J Hum Genet
; 94(3): 349-60, 2014 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24560520
17.
Is "incidental finding" the best term?: a study of patients' preferences.
Genet Med
; 19(2): 176-181, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27490114
18.
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
; 174(4): 381-389, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28332277
19.
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.
Am J Hum Genet
; 93(6): 1035-45, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24268658
20.
Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome.
J Genet Couns
; 25(3): 515-9, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26637299