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Publications
The full list of publications can be viewed here
Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
Contrastive Learning Improves Critical Event Prediction in COVID-19 Patients
Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure
Using Deep-Learning Algorithms to Simultaneously Identify Right and Left Ventricular Dysfunction From the Electrocardiogram
Acute COVID-19 gene-expression profiles show multiple etiologies of long-term sequelae
Genetic discovery and risk characterization in type 2 diabetes across diverse populations
Phe2vec: Automated disease phenotyping based on unsupervised embeddings from electronic health records
Evaluation and management of COVID-19-related severity in people with type 2 diabetes
Prognostic value of polygenic risk scores for adults with psychosis
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Development and validation of techniques for phenotyping ST-elevation myocardial infarction encounters from electronic health records
Continuous Kidney Replacement Therapy of the Future: Innovations in Information Technology, Data Analytics, and Quality Assurance Systems
Downregulation of exhausted cytotoxic T cells in gene expression networks of multisystem inflammatory syndrome in children
Factors Associated With Longitudinal Psychological and Physiological Stress in Health Care Workers During the COVID-19 Pandemic: Observational Study Using Apple Watch Data
Acute Kidney Injury in Patients Hospitalized With COVID-19 in New York City: Temporal Trends From March 2020 to April 2021
Albuminuria Testing in Hypertension and Diabetes: An Individual-Participant Data Meta-Analysis in a Global Consortium
Metabolite Biomarkers of CKD Progression in Children
Development of a federated learning approach to predict acute kidney injury in adult hospitalized patients with COVID-19 in New York City
Performance of crisis standards of care guidelines in a cohort of critically ill COVID-19 patients in the United States
Rare Coding Variants Associated with Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-ancestry Analysis
Genome sequencing unveils a regulatory landscape of platelet reactivity
Variant-specific inflation factors for assessing population stratification at the phenotypic variance level
Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19
Multi-Institutional Implementation of Clinical Decision Support for APOL1, NAT2, and YEATS4 Genotyping in Antihypertensive Management
The trans-ancestral genomic architecture of glycemic traits
Predictive Approaches for Acute Dialysis Requirement and Death in COVID-19
Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries
Identification of Distinct Clinical Subphenotypes in Critically Ill Patients With COVID-19
Molecular Analysis of the Kidney From a Patient With COVID-19-Associated Collapsing Glomerulopathy
Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium
A Resilience-Building App to Support the Mental Health of Health Care Workers in the COVID-19 Era: Design Process, Distribution, and Evaluation
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
Neonatal outcomes during the COVID-19 pandemic in New York City
Derivation and validation of a machine learning risk score using biomarker and electronic patient data to predict progression of diabetic kidney disease
Relational Learning Improves Prediction of Mortality in COVID-19 in the Intensive Care Unit
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Genetically Downregulated Interleukin-6 Signaling Is Associated With a Favorable Cardiometabolic Profile: A Phenome-Wide Association Study
Gemcitabine plus nab-paclitaxel versus FOLFIRINOX for unresected pancreatic cancer: Comparative effectiveness and evaluation of tumor growth in veterans
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Genome-wide polygenic risk score for retinopathy of type 2 diabetes
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