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A genome-wide scan statistic framework for whole-genome sequence data analysis

Nature communications, 2019-07, Vol.10 (1), p.3018-11, Article 3018

2019

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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

Nature communications, 2021-05, Vol.12 (1), p.3152-3152, Article 3152

2021

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A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs

Nature communications, 2018-12, Vol.9 (1), p.5199-12, Article 5199

2018

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Molecular signatures underlying neurofibrillary tangle susceptibility in Alzheimer’s disease

Neuron (Cambridge, Mass.), 2022-09, Vol.110 (18), p.2929-2948.e8

2022

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FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications

American journal of human genetics, 2018-05, Vol.102 (5), p.920-942

2018

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BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data

Genome Biology, 2023-02, Vol.24 (1), p.24-24, Article 24

2023

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Spinal cord injury: a study protocol for a systematic review and meta-analysis of microRNA alterations

Systematic reviews, 2022-04, Vol.11 (1), p.61-61, Article 61

2022

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GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Nature communications, 2022-11, Vol.13 (1), p.7209-16, Article 7209

2022

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Stability of transcranial magnetic stimulation electroencephalogram evoked potentials in pediatric epilepsy

Scientific reports, 2024-04, Vol.14 (1), p.9045-9045, Article 9045

2024

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Multitrait GWAS to connect disease variants and biological mechanisms

PLoS genetics, 2021-08, Vol.17 (8), p.e1009713

2021

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Impaired 24-h activity patterns are associated with an increased risk of Alzheimer's disease, Parkinson's disease, and cognitive decline

Alzheimer's research & therapy, 2024-02, Vol.16 (1), p.35-11, Article 35

2024

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Peripheral T-Cells, B-Cells, and Monocytes from Multiple Sclerosis Patients Supplemented with High-Dose Vitamin D Show Distinct Changes in Gene Expression Profiles

Nutrients, 2022-11, Vol.14 (22), p.4737

2022

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A novel age-informed approach for genetic association analysis in Alzheimer's disease

Alzheimer's research & therapy, 2021-04, Vol.13 (1), p.72-72, Article 72

2021

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Loop diuretics association with Alzheimer's disease risk

Frontiers in aging, 2023-09, Vol.4, p.1211571

2023

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Improving genetic risk prediction across diverse population by disentangling ancestry representations

Communications biology, 2023-09, Vol.6 (1), p.964-9, Article 964

2023

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Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies

NPJ digital medicine, 2021-07, Vol.4 (1), p.116-116, Article 116

2021

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Association between Stress Response Genes and Features of Diurnal Cortisol Curves in the Multi-Ethnic Study of Atherosclerosis: A New Multi-Phenotype Approach for Gene-Based Association Tests

PloS one, 2015-05, Vol.10 (5), p.e0126637-e0126637

2015

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Summary statistics knockoffs inference with family-wise error rate control

Biometrics, 2024-07, Vol.80 (3)

2024

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Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data

American journal of human genetics, 2017-09, Vol.101 (3), p.340-352

2017

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Advances and challenges in quantitative delineation of the genetic architecture of complex traits

Quantitative biology, 2021-06, Vol.9 (2), p.168-184

2021

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Pediatric Functional Neurological Disorder: Investigating Demographic & Clinical Factors and Impacts on Management (P3-5.004)

Neurology, 2022-05, Vol.98 (18_supplement)

2022

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Do Steroids Matter? A Retrospective Review of Premedication for Taxane Chemotherapy and Hypersensitivity Reactions

Journal of clinical oncology, 2021-11, Vol.39 (32), p.3583-3590

2021

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Deep Learning for EEG‐Based Alzheimer’s Disease Diagnosis

Alzheimer's & dementia, 2023-12, Vol.19 (S15), p.n/a

2023

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Second-order group knockoffs with applications to genome-wide association studies

Bioinformatics (Oxford, England), 2024-10, Vol.40 (10)

2024

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Integration of expression QTLs with fine mapping via SuSiE

PLoS genetics, 2024-01, Vol.20 (1), p.e1010929-e1010929

2024

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A genome-wide scan statistic framework for whole-genome sequence data analysis

Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs

Molecular signatures underlying neurofibrillary tangle susceptibility in Alzheimer’s disease

FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications

BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data

Spinal cord injury: a study protocol for a systematic review and meta-analysis of microRNA alterations

GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Stability of transcranial magnetic stimulation electroencephalogram evoked potentials in pediatric epilepsy

Multitrait GWAS to connect disease variants and biological mechanisms

Impaired 24-h activity patterns are associated with an increased risk of Alzheimer's disease, Parkinson's disease, and cognitive decline

Peripheral T-Cells, B-Cells, and Monocytes from Multiple Sclerosis Patients Supplemented with High-Dose Vitamin D Show Distinct Changes in Gene Expression Profiles

A novel age-informed approach for genetic association analysis in Alzheimer's disease

Loop diuretics association with Alzheimer's disease risk

Improving genetic risk prediction across diverse population by disentangling ancestry representations

Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies

Association between Stress Response Genes and Features of Diurnal Cortisol Curves in the Multi-Ethnic Study of Atherosclerosis: A New Multi-Phenotype Approach for Gene-Based Association Tests

Summary statistics knockoffs inference with family-wise error rate control

Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data

Advances and challenges in quantitative delineation of the genetic architecture of complex traits

Pediatric Functional Neurological Disorder: Investigating Demographic & Clinical Factors and Impacts on Management (P3-5.004)

Do Steroids Matter? A Retrospective Review of Premedication for Taxane Chemotherapy and Hypersensitivity Reactions

Deep Learning for EEG‐Based Alzheimer’s Disease Diagnosis

Second-order group knockoffs with applications to genome-wide association studies

Integration of expression QTLs with fine mapping via SuSiE

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