A. Pitsillides

发表

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Brian E. Cade, Zachary A. Szpiech, Shannon Kelly, 2019, Nature.

Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

Andrew Carroll, Eric Boerwinkle, Andrew D. Johnson, 2017, Nature Genetics.

Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases

R. Vasan, M. Feolo, P. Munson, 2022, Research square.

An evaluation of approaches for rare variant association analyses of binary traits in related samples

Qiong Yang, Ming-Huei Chen, A. Pitsillides, 2021, Scientific Reports.

The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk

M. Fornage, A. Reiner, Y. Zhang, 2022, medRxiv.

The power of genetic diversity in genome-wide association studies of lipids

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2021, Nature.

Association of mitochondrial DNA copy number with cardiometabolic diseases

M. Fornage, G. Abecasis, E. Boerwinkle, 2021, Cell genomics.

Association of mitochondrial DNA copy number with cardiometabolic diseases in a large cross-sectional study of multiple ancestries

M. Fornage, G. Abecasis, E. Boerwinkle, 2020, medRxiv.

Genome sequencing unveils a regulatory landscape of platelet reactivity

Benjamin D. Heavner, May E. Montasser, Nicholette D. Palmer, 2019, Nature Communications.

Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases

R. Vasan, M. Feolo, P. Munson, 2022, Scientific Reports.

Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation

Andrew D. Johnson, John D. Eicher, R. Gibbs, 2017, Thrombosis and Haemostasis.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

Christopher D. Brown, Aaron F. McDaid, Yan V. Sun, 2021, bioRxiv.

Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations

A. Uitterlinden, J. Manson, D. Mozaffarian, 2021, Circulation. Genomic and Precision Medicine.

Fine Mapping and Functional Studies of Risk Variants for Type 1 Diabetes at Chromosome 16p13.13

Wei-Min Chen, P. Concannon, S. Onengut-Gumuscu, 2014, Diabetes.

Whole genome sequence analyses of brain imaging measures in the Framingham Study

M. Fornage, C. DeCarli, R. Vasan, 2018, Neurology.

Association of genetic variations and gene expression in a family-based study

S. Choi, Honghuang Lin, Jaeyoung Hong, 2016, BMC Proceedings.

Elucidating the genetic architecture of DNA methylation to identify promising molecular mechanisms of disease

R. Vasan, M. Feolo, P. Munson, 2022, Scientific Reports.

Genome-Wide Meta-Analysis of Late-Onset Alzheimer's Disease Using Rare Variant Imputation in 324,809 Subjects Identifies Novel Rare Variant Locus NCK2: The International Genomics of Alzheimer's Project (IGAP)

Jennifer E. Phillips-Cremins, Pavel P. Kuksa, J. Haines, 2021, medRxiv.

Genome-wide gene–environment interactions on quantitative traits using family data

Josée Dupuis, Bruce M Psaty, Kenneth M Rice, 2015, European Journal of Human Genetics.

Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study

A. Reiner, M. Feolo, N. Sharopova, 2022, medRxiv.

Sugar-sweetened Beverage Consumption May Modify Associations between Genetic Variants in the CHREBP Locus and HDL-C and TG Concentrations.

A. Uitterlinden, J. Manson, D. Mozaffarian, 2021, Circulation. Genomic and precision medicine.

Network analysis of drug effect on triglyceride-associated DNA methylation

G. Peloso, A. DeStefano, Ching‐Ti Liu, 2018, BMC Proceedings.

Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function

J. Bressler, M. Fornage, L. Hou, 2023, Neurology.

Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus

Lynn K. Carmichael, Philip H. Schroeder, David E. Condon, 2023, medRxiv.

Association of Common and Rare Variants with Alzheimer’s Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer’s Disease Sequencing Project

Xiaoling, M. Fornage, J. Haines, 2023, medRxiv.

An efficient analytic approach in genome-wide identification of methylation quantitative trait loci response to fenofibrate treatment

L. Farrer, Virginia Fisher, Xiaoling Zhang, 2018, BMC Proceedings.

Key variants via Alzheimer’s Disease Sequencing Project whole genome sequence data

M. Fornage, E. Boerwinkle, J. Dupuis, 2023, medRxiv.

Null controllability and stabilization of linear systems subject to asymmetric actuator saturation

Tingshu Hu, Zongli Lin, Zongli Lin, 2000, Proceedings of the 39th IEEE Conference on Decision and Control (Cat. No.00CH37187).

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2022, American journal of human genetics.

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

M. Fornage, G. Abecasis, E. Boerwinkle, 2023, Journal of the American Heart Association.

Presence and Transmission of Mitochondrial Heteroplasmic Mutations in Human Populations of European and African Ancestry

G. Abecasis, R. Vasan, B. Cade, 2020, bioRxiv.

Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application.

G. Abecasis, D. Arking, Xiuqing Guo, 2024, Mitochondrion.