Ryan Sun

发表

Methods for High-Dimensional Inference in Genetic Association Studies

Xihong Lin, Ryan Sun, 2019 .

Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic

Gary D Bader, Xihong Lin, P. Kraft, 2018, bioRxiv.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility

Xihong Lin, Hongbing Shen, H. Brenner, 2020, medRxiv.

Integration of multiomic annotation data to prioritize and characterize inflammation and immune‐related risk variants in squamous cell lung cancer

Y. Bossé, L. Kiemeney, Xihong Lin, 2020, Genetic epidemiology.

Set-Based Tests for Genetic Association Using the Generalized Berk-Jones Statistic

Xihong Lin, Ryan Sun, 2017, 1710.02469.

Identification of Novel Loci Associated with Infant Cognitive Ability

Xihong Lin, D. Christiani, L. Su, 2018, Molecular Psychiatry.

Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment

Xihong Lin, D. Christiani, Chaolong Wang, 2017, Environmental Health.

Differences in set-based tests for sparse alternatives when testing sets of outcomes compared to sets of explanatory factors in genetic association studies.

Xihong Lin, Ryan Sun, A. Shi, 2022, Biostatistics.

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

Marshall W. Anderson, J. Witte, Y. Bossé, 2022, Nature Genetics.

Title: Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility

Aldrich, Mattias, Walsh, 2020 .

Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk

Kristen S Purrington, Y. Bossé, Hongbing Shen, 2021, Human molecular genetics.

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2022, Nature Genetics.

Genetic Variant Set-Based Tests Using the Generalized Berk–Jones Statistic With Application to a Genome-Wide Association Study of Breast Cancer

Xihong Lin, Ryan Sun, 2019, Journal of the American Statistical Association.

Leveraging a surrogate outcome to improve inference on a partially missing target outcome

Xihong Lin, Ryan Sun, Z. McCaw, 2022, bioRxiv.

Cross-tissue eQTL mapping in the presence of missing data via surrogate outcome analysis

Xihong Lin, Zachary R. McCaw, Sheila M. Gaynor, 2020 .

Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis

Manal M. Hassan, K. Siminovitch, T. Karlsen, 2023, Nature Communications.

A multi-dimensional integrative scoring framework for predicting functional variants in the human genome.

Martin Jinye Zhang, Xihong Lin, I. Ionita-Laza, 2022, American Journal of Human Genetics.

A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

May E. Montasser, Nicholette D. Palmer, A. Reiner, 2021, bioRxiv.

Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic

Gary D. Bader, Gary D Bader, Ryan Sun, 2018, bioRxiv.

A Multi-dimensional Integrative Scoring Framework for Predicting Functional Regions in the Human Genome

Xihong Lin, I. Ionita-Laza, Zilin Li, 2021, bioRxiv.

Testing for gene–environment interaction under exposure misspecification

Ryan Sun, Raymond J Carroll, David C Christiani, 2018, Biometrics.

MicroRNA-124 Reduces Arsenic-induced Endoplasmic Reticulum Stress and Neurotoxicity and is Linked with Neurodevelopment in Children

D. Christiani, Q. Lu, Ryan Sun, 2020, Scientific Reports.

Identification of differentially expressed gene sets using the Generalized Berk-Jones statistic

Ryan Sun, Xihong Lin, John Quackenbush, 2019, Bioinform..

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2020, Nature Genetics.

Testing a Large Number of Composite Null Hypotheses Using Conditionally Symmetric Multidimensional Gaussian Mixtures in Genome-Wide Studies

Ryan Sun, Z. McCaw, Xihong Lin, 2023, 2309.12584.

A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

Benjamin D. Heavner, May E. Montasser, Nicholette D. Palmer, 2021, bioRxiv.

A Multi-dimensional Integrative Scoring Framework for Predicting Functional Regions in the Human Genome

Martin Jinye Zhang, Xihong Lin, I. Ionita-Laza, 2021, bioRxiv.

Inference for set‐based effects in genetic association studies with interval‐censored outcomes

L. Robison, Ryan Sun, Y. Yasui, 2022, Biometrics.

Identification of Novel Loci Associated with Infant Cognitive Ability

Xihong Lin, D. Christiani, Q. Lu, 2018, Molecular Psychiatry.