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| 36864286 | Association of rs9939609 in FTO with BMI among Polynesian peoples living in Aotearoa New Zealand and other Pacific nations. | | 2023 |
| 36352773 | Multivariate analysis of a missense variant in CREBRF reveals associations with measures of adiposity in people of Polynesian ancestries. | Genetic Epidemiology | 2023 |
| 36029021 | Advancing Nursing Research Through Interactive Data Visualization With R Shiny. | | 2023 |
| 36340932 | A stop-gain variant in is associated with atherogenic lipid profiles. | Human Genetics and Genomics Advances | 2023 |
| 36428275 | Validity of anthropometric equation-based estimators of fat mass in Samoan adults. | American Journal of Human Biology | 2023 |
| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 37986966 | Characterization of Per- and Polyfluoroalkyl Substance (PFAS) concentrations in a community-based sample of infants from Samoa. | | 2023 |
| 37961708 | Improving imputation quality in Samoans through the integration of population-specific sequences into existing reference panels. | | 2023 |
| 36764636 | Brain-derived neurotrophic factor (BDNF) epigenomic modifications and brain-related phenotypes in humans: A systematic review. | Neurosci Biobehav Rev | 2023 |
| 36702996 | Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing. | Nat Genet | 2023 |
| 37250494 | A Polynesian<i>-</i>specific missense CETP variant alters the lipid profile. | HGG Adv | 2023 |
| 37063698 | A longitudinal epigenome-wide association study of preeclamptic and normotensive pregnancy. | Epigenetics Commun | 2023 |
| 36869285 | dbGaPCheckup: pre-submission checks of dbGaP-formatted subject phenotype files. | | 2023 |
| 35144939 | missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesian peoples living in Samoa and Aotearoa New Zealand. | BMJ Open Diabetes Research and Care | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 35642557 | Post hoc power is not informative. | Genetic Epidemiology | 2022 |
| 35442418 | A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes. | J Exp Med | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36284436 | The protective effect of rs373863828 on type 2 diabetes does not operate through a body composition pathway in adult Samoans. | | 2022 |
| 36338277 | Correlates of daytime sleepiness and insomnia among adults in Samoa. | Sleep Epidemiol | 2022 |
| 36193739 | Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney Function. | Hypertension | 2022 |
| 35606300 | The missense variant, rs373863828, in CREBRF plays a role in longitudinal changes in body mass index in Samoans. | Obesity Research and Clinical Practice | 2022 |
| 35028889 | Decreased DNA Methylation of RGMA is Associated with Intracranial Hypertension After Severe Traumatic Brain Injury: An Exploratory Epigenome-Wide Association Study. | Neurocrit Care | 2022 |
| 35083469 | Characterization of cerebrospinal fluid DNA methylation age during the acute recovery period following aneurysmal subarachnoid hemorrhage. | | 2021 |
| 35359917 | <i>ANGPT1</i> methylation and delayed cerebral ischemia in aneurysmal subarachnoid hemorrhage patients. | Epigenetics Commun | 2021 |
| 34167372 | Acute <i>Brain-Derived</i> <i>Neurotrophic Factor</i> DNA Methylation Trajectories in Cerebrospinal Fluid and Associations With Outcomes Following Severe Traumatic Brain Injury in Adults. | Neurorehabil Neural Repair | 2021 |
| 33848002 | AMD Genetics: Methods and Analyses for Association, Progression, and Prediction. | Advances in Experimental Medicine and Biology | 2021 |
| 34003914 | Genome-Wide Association Studies-Based Machine Learning for Prediction of Age-Related Macular Degeneration Risk. | Transl Vis Sci Technol | 2021 |
| 33846329 | Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. | Nat Commun | 2021 |
| 33877642 | An Exploratory Study of Epigenetic Age in Preeclamptic and Normotensive Pregnancy Reveals Differences by Self-Reported Race but Not Pregnancy Outcome. | Reprod Sci | 2021 |
| 33720349 | Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. | Genetics | 2021 |
| 34323937 | CHIT: an allele-specific method for testing the association between molecular quantitative traits and phenotype-genotype interaction. | | 2021 |
| 34321704 | Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration. | J Am Stat Assoc | 2021 |
| 32884101 | A missense variant in CREBRF, rs373863828, is associated with fat-free mass, not fat mass in Samoan infants. | International Journal of Obesity | 2021 |
| 32759990 | Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels. | Journal of Human Genetics | 2021 |
| 33112498 | ECHS1 disease in two unrelated families of Samoan descent: Common variant - rare disorder. | Am J Med Genet A | 2021 |
| 34520472 | A murine model of the human CREBRFR457Q obesity-risk variant does not influence energy or glucose homeostasis in response to nutritional stress. | PLoS ONE | 2021 |
| 34697971 | An exploratory study of white blood cell proportions across preeclamptic and normotensive pregnancy by self-identified race in individuals with overweight or obesity. | Hypertens Pregnancy | 2021 |
| 35083470 | Iron homeostasis pathway DNA methylation trajectories reveal a role for STEAP3 metalloreductase in patient outcomes after aneurysmal subarachnoid hemorrhage. | Epigenetics Commun | 2021 |
| 31346934 | Genetic Variability and Trajectories of DNA Methylation May Support a Role for HAMP in Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage. | Neurocrit Care | 2020 |
| 32190945 | A missense variant in CREBRF is associated with taller stature in Samoans. | American Journal of Human Biology | 2020 |
| 32246437 | Genetic Variability in the Iron Homeostasis Pathway and Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage. | Neurocrit Care | 2020 |
| 32291332 | Evolutionary history of modern Samoans. | Proceedings of the National Academy of Sciences of the United States of America | 2020 |
| 32285025 | Deep-learning-based Prediction of Late Age-Related Macular Degeneration Progression. | Nat Mach Intell | 2020 |
| 32088307 | Transcriptome-wide and differential expression network analyses of childhood asthma in nasal epithelium. | Journal of Allergy and Clinical Immunology | 2020 |
| 32706746 | Exploring the Paradoxical Relationship of a Creb 3 Regulatory Factor Missense Variant With Body Mass Index and Diabetes Among Samoans: Protocol for the Soifua Manuia (Good Health) Observational Cohort Study. | JMIR Res Protoc | 2020 |
| 32670358 | Methylation Data Processing Protocol and Comparison of Blood and Cerebral Spinal Fluid Following Aneurysmal Subarachnoid Hemorrhage. | Frontiers in Genetics | 2020 |
| 30657194 | Spinning convincing stories for both true and false association signals. | Genetic Epidemiology | 2019 |
| 30158665 | Y chromosome mosaicism is associated with age-related macular degeneration. | Eur J Hum Genet | 2019 |
| 30584054 | DNA methylation in nasal epithelium, atopy, and atopic asthma in children: a genome-wide study. | Lancet Respiratory Medicine,The | 2019 |