Author details

Full Name

Ryan L Minster

Affiliation

ORCID

Career Start Year

2000

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36340932	A stop-gain variant in is associated with atherogenic lipid profiles.	Human Genetics and Genomics Advances	2023
37961708	Improving imputation quality in Samoans through the integration of population-specific sequences into existing reference panels.		2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
37250494	A Polynesian<i>-</i>specific missense CETP variant alters the lipid profile.	HGG Adv	2023
36864286	Association of rs9939609 in FTO with BMI among Polynesian peoples living in Aotearoa New Zealand and other Pacific nations.		2023
36799557	Compound heterozygous splicing variants expand the genotypic spectrum of EMC1-related disorders.		2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
36428275	Validity of anthropometric equation-based estimators of fat mass in Samoan adults.	American Journal of Human Biology	2023
36352773	Multivariate analysis of a missense variant in CREBRF reveals associations with measures of adiposity in people of Polynesian ancestries.	Genetic Epidemiology	2023
36193739	Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney Function.	Hypertension	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	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
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
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
36284436	The protective effect of rs373863828 on type 2 diabetes does not operate through a body composition pathway in adult Samoans.		2022
34504188	Pleiotropic effects between cardiovascular disease risk factors and measures of cognitive and physical function in long-lived adults.	Scientific Reports	2021
33571193	The impact of global and local Polynesian genetic ancestry on complex traits in Native Hawaiians.	PLoS Genet	2021
33180942	Relationship Between Serum IGF-1 and BMI Differs by Age.	J Gerontol A Biol Sci Med Sci	2021
33112498	ECHS1 disease in two unrelated families of Samoan descent: Common variant - rare disorder.	Am J Med Genet A	2021
32759990	Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.	Journal of Human Genetics	2021
35083470	Iron homeostasis pathway DNA methylation trajectories reveal a role for STEAP3 metalloreductase in patient outcomes after aneurysmal subarachnoid hemorrhage.	Epigenetics Commun	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
32190945	A missense variant in CREBRF is associated with taller stature in Samoans.	American Journal of Human Biology	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
32291332	Evolutionary history of modern Samoans.	Proceedings of the National Academy of Sciences of the United States of America	2020
32246437	Genetic Variability in the Iron Homeostasis Pathway and Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage.	Neurocrit Care	2020
31332674	Heterogeneity of healthy aging: comparing long-lived families across five healthy aging phenotypes of blood pressure, memory, pulmonary function, grip strength, and metabolism.	Geroscience	2019
31634740	Genome-wide linkage analysis of carotid artery traits in exceptionally long-lived families.	Atherosclerosis	2019
29511321	Re: "Widespread prevalence of a CREBRF variant among MÄori and Pacific children is associated with weight and height in early childhood".	Int J Obes (Lond)	2018
28837423	A novel healthy blood pressure phenotype in the Long Life Family Study.	J Hypertens	2018
29721634	Discordant association of the CREBRF rs373863828 A allele with increased BMI and protection from type 2 diabetes in MÄori and Pacific (Polynesian) people living in Aotearoa/New Zealand.	Diabetologia	2018
28329217	Genomewide Association Scan of a Mortality Associated Endophenotype for a Long and Healthy Life in the Long Life Family Study.		2017
28422589	Energy Expenditure in Vinyasa Yoga Versus Walking.	Journal of Physical Activity and Health	2017
27294813	Association Between Mortality and Heritability of the Scale of Aging Vigor in Epidemiology.		2016
27455349	A thrifty variant in CREBRF strongly influences body mass index in Samoans.	Nature Genetics	2016
25758594	Genome-Wide Association Study and Linkage Analysis of the Healthy Aging Index.	J Gerontol A Biol Sci Med Sci	2015
24430505	Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.	Hum Mol Genet	2014
23913930	Heritability of and mortality prediction with a longevity phenotype: the healthy aging index.	J Gerontol A Biol Sci Med Sci	2014
25409777	Genetic variants associated with lung function: the long life family study.	Respiratory Research	2014
25352862	Stratified randomization controls better for batch effects in 450K methylation analysis: a cautionary tale.	Frontiers in Genetics	2014
24929828	Genome-wide association analysis identifies six new loci associated with forced vital capacity.	Nat Genet	2014
24844858	Biomechanical properties of the skin in cutis laxa.		2014
24799123	Prevalence of adiposity and associated cardiometabolic risk factors in the Samoan genome-wide association study.	American Journal of Human Biology	2014
22005931	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Mol Psychiatry	2012
20570404	Association of CLU and PICALM variants with Alzheimer's disease.	Neurobiol Aging	2012
22832961	Genome-wide association study of Alzheimer's disease.	Transl Psychiatry	2012