Jacob McCauley

Professor

University of Miami Miller School of Medicine

United States

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Jacob McCauley is a Professor at the University of Miami Miller School of Medicine in the United States. His research focuses on social determinants of health, particularly in relation to multiple sclerosis and diverse populations. Recent publications include studies on disability in Hispanic individuals with multiple sclerosis, digital health research for diverse cohorts, and the heritability of plasma protein levels associated with the disease.

Articles (15)

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2025

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2025

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2024

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2022

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2022

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2022

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2022

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2021

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2021

Collaborators (8)

Sergio E Baranzini

University of California

UNITED STATES

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Carlo Berzuini

The University of Manchester

UNITED KINGDOM

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Mario Saporta

ASSOCIATE PROFESSOR

University of Miami School of Medicine

UNITED STATES

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Mary Fasano

Clinical Professor Medicine & Pediatrics

The University of Iowa Roy J and Lucille A Carver College of Medicine

UNITED STATES

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Nicholas Borja

Assistant Professor of Clinical Genetics

University of Miami Miller School of Medicine

UNITED STATES

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Paul Marcogliese

Assistant Professor

University of Manitoba

CANADA

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Mustafa Tekin

University of Miami

UNITED STATES

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LUISA BERNARDINELLI

Full Professor

University of Pavia

ITALY

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Jacob McCauley

Research Interests

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About

Articles (15)

Person-Centered Social Determinants and Neighborhood-Level Deprivation Associated With Disability in Hispanic People With Multiple Sclerosis

Building a Digital Health Research Platform to Enable Recruitment, Enrollment, Data Collection, and Follow-Up for a Highly Diverse Longitudinal US Cohort of 1 Million People in the All of Us Research Program: Design and Implementation Study

Multiple sclerosis in Colombia: A review of the literature

Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans

Patients’ views on HCC biospecimen research: Understanding the role of race and culture through interviews

Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling

Plasma Protein Levels Analysis in Multiple Sclerosis Sardinian Families Identified C9 and CYP24A1 as Candidate Biomarkers

Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant

Genome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic disease

Risk Factors Associated with Mortality and Neurologic Disability after Intracerebral Hemorrhage in a Racially and Ethnically Diverse Cohort

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder

Variable clinical severity in TANGO2 deficiency: Case series and literature review

Heritability Estimation of Multiple Sclerosis Related Plasma Protein Levels in Sardinian Families with Immunochip Genotyping Data.

Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families

A novel de novo intronic variant in ITPR1 causes Gillespie syndrome

Collaborators (8)

Sergio E Baranzini

Carlo Berzuini

Mario Saporta

Mary Fasano

Nicholas Borja

Paul Marcogliese

Mustafa Tekin

LUISA BERNARDINELLI

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