| 36436147 | Additive or Interactive Associations of Food Allergies with Glutathione S-Transferase Genes in Relation to ASD and ASD Severity in Jamaican Children. | J Autism Dev Disord | 2024 |
| 37170952 | Metabolomic Signatures of Sedentary Behavior and Cardiometabolic Traits in US Hispanics/Latinos: Results from HCHS/SOL. | Med Sci Sports Exerc | 2023 |
| 37804200 | Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. | J Am Heart Assoc | 2023 |
| 37777527 | Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality. | Nat Commun | 2023 |
| 37461703 | Polygenic Risk Score Associates with Atherosclerotic Plaque Characteristics at Autopsy. | bioRxiv | 2023 |
| 35010728 | Additive and Interactive Associations of Environmental and Sociodemographic Factors with the Genotypes of Three Glutathione S-Transferase Genes in Relation to the Blood Arsenic Concentrations of Children in Jamaica. | Int J Environ Res Public Health | 2022 |
| 35591888 | A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data. | NAR Genom Bioinform | 2022 |
| 36292793 | Interactions between Environmental Factors and Glutathione S-Transferase (GST) Genes with Respect to Detectable Blood Aluminum Concentrations in Jamaican Children. | Genes (Basel) | 2022 |
| 35741737 | Detoxification Role of Metabolic Glutathione S-Transferase (GST) Genes in Blood Lead Concentrations of Jamaican Children with and without Autism Spectrum Disorder. | Genes (Basel) | 2022 |
| 34127525 | Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies. | Gut | 2022 |
| 34570667 | Longitudinal change in blood DNA epigenetic signature after smoking cessation. | Epigenetics | 2022 |
| 35232957 | Correction: Association of low-frequency and rare coding variants with information processing speed. | Transl Psychiatry | 2022 |
| 34415308 | Epigenome-wide association study of mitochondrial genome copy number. | Hum Mol Genet | 2021 |
| 33546147 | Associations of Metabolic Genes (<i>GSTT1</i>, <i>GSTP1</i>, <i>GSTM1</i>) and Blood Mercury Concentrations Differ in Jamaican Children with and without Autism Spectrum Disorder. | Int J Environ Res Public Health | 2021 |
| 33909500 | A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease. | Am J Physiol Lung Cell Mol Physiol | 2021 |
| 33748830 | Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality. | Eur Heart J | 2021 |
| 34230475 | Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids. | Nat Commun | 2021 |
| 34002480 | Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants. | Alzheimers Dement | 2021 |
| 33727701 | Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2021 |
| 34183656 | A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids. | Nat Commun | 2021 |
| 32892263 | Interaction of Blood Manganese Concentrations with GSTT1 in Relation to Autism Spectrum Disorder in Jamaican Children. | J Autism Dev Disord | 2021 |
| 34864818 | Association of low-frequency and rare coding variants with information processing speed. | Transl Psychiatry | 2021 |
| 35036986 | Association of mitochondrial DNA copy number with cardiometabolic diseases. | Cell Genom | 2021 |
| 34887417 | Meta-analyses identify DNA methylation associated with kidney function and damage. | Nat Commun | 2021 |
| 34887389 | Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus. | Nat Commun | 2021 |
| 34542373 | Correlation between concentrations of four heavy metals in cord blood and childhood blood of Jamaican children. | J Environ Sci Health A Tox Hazard Subst Environ Eng | 2021 |
| 31538260 | Perinatal Factors Associated with Autism Spectrum Disorder in Jamaican Children. | J Autism Dev Disord | 2020 |
| 31630168 | Epigenetic Age Acceleration and Cognitive Function in African American Adults in Midlife: The Atherosclerosis Risk in Communities Study. | J Gerontol A Biol Sci Med Sci | 2020 |
| 32004343 | Evaluation of mitochondrial DNA copy number estimation techniques. | PLoS One | 2020 |
| 31727850 | GSTM1 Deletion Exaggerates Kidney Injury in Experimental Mouse Models and Confers the Protective Effect of Cruciferous Vegetables in Mice and Humans. | J Am Soc Nephrol | 2020 |
| 32479199 | Mitochondrial DNA Copy Number and Incident Heart Failure: The Atherosclerosis Risk in Communities (ARIC) Study. | Circulation | 2020 |
| 32469399 | Serum sphingolipids and incident diabetes in a US population with high diabetes burden: the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). | Am J Clin Nutr | 2020 |
| 32436959 | Analysis of putative cis-regulatory elements regulating blood pressure variation. | Hum Mol Genet | 2020 |
| 33313427 | Corrigendum to 'Association of sickle cell trait with measures of cognitive function and dementia in African Americans' <i>eNeurologicalSci,</i> Vol. 16 (2019), 100,201. | eNeurologicalSci | 2020 |
| 32988399 | Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs. | Genome Med | 2020 |
| 33193808 | Interaction between a Mixture of Heavy Metals (Lead, Mercury, Arsenic, Cadmium, Manganese, Aluminum) and <i>GSTP1, GSTT1,</i> and <i>GSTM1</i> in Relation to Autism Spectrum Disorder. | Res Autism Spectr Disord | 2020 |
| 33031748 | A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. | Am J Hum Genet | 2020 |
| 33186364 | Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. | PLoS One | 2020 |
| 33230300 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2020 |
| 32661462 | Association of Polychlorinated Biphenyls and Organochlorine Pesticides with Autism Spectrum Disorder in Jamaican Children. | Res Autism Spectr Disord | 2020 |
| 31532792 | Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers. | PLoS One | 2019 |
| 30571559 | HFE H63D Polymorphism and the Risk for Systemic Hypertension, Myocardial Remodeling, and Adverse Cardiovascular Events in the ARIC Study. | Hypertension | 2019 |
| 30624610 | Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample. | Hum Mol Genet | 2019 |
| 31068470 | Multiple <i>SCN5A</i> variant enhancers modulate its cardiac gene expression and the QT interval. | Proc Natl Acad Sci U S A | 2019 |
| 31261817 | Concentrations of Lead, Mercury, Arsenic, Cadmium, Manganese, and Aluminum in Blood of Romanian Children Suspected of Having Autism Spectrum Disorder. | Int J Environ Res Public Health | 2019 |
| 31384675 | Association of sickle cell trait with measures of cognitive function and dementia in African Americans. | eNeurologicalSci | 2019 |
| 31160809 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2019 |
| 31058353 | A generalized weighted quantile sum approach for analyzing correlated data in the presence of interactions. | Biom J | 2019 |
| 30930959 | Interaction between manganese and <i>GSTP1</i> in relation to autism spectrum disorder while controlling for exposure to mixture of lead, mercury, arsenic, and cadmium. | Res Autism Spectr Disord | 2018 |
| 30175238 | Meta-analysis of exome array data identifies six novel genetic loci for lung function. | Wellcome Open Res | 2018 |