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Author Details

Jacob L McCauley
2003
95
37
PMIDPaper TitleJournal TitlePublished Year
35253861Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans.Brain2023
36448302Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity.Brain2023
37255344Patients' views on HCC biospecimen research: Understanding the role of race and culture through interviews.2023
37162822Deep resequencing of the 1q22 locus in non-lobar intracerebral hemorrhage.medRxiv2023
35207439Plasma Protein Levels Analysis in Multiple Sclerosis Sardinian Families Identified C9 and CYP24A1 as Candidate Biomarkers.Life2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
35963264Genetics of multiple sclerosis: lessons from polygenicity.Lancet Neurology, The2022
35505219Revisiting the Latino Epidemiologic Paradox: an Analysis of Data from the All of Us Research Program.J Gen Intern Med2022
35443984Initial antihypertensive agent effects on acute blood pressure after intracerebral haemorrhage.Stroke Vasc Neurol2022
35888189Heritability Estimation of Multiple Sclerosis Related Plasma Protein Levels in Sardinian Families with Immunochip Genotyping Data.Life2022
36061955Lamina Propria Phagocyte Profiling Reveals Targetable Signaling Pathways in Refractory Inflammatory Bowel Disease.2022
36548255Ancestral risk modification for multiple sclerosis susceptibility detected across the Major Histocompatibility Complex in a multi-ethnic population.PLoS One2022
35289861Risk Factors Associated With Mortality and Neurologic Disability After Intracerebral Hemorrhage in a Racially and Ethnically Diverse Cohort.JAMA Netw Open2022
34424302Ethnic and Racial Variation in Intracerebral Hemorrhage Risk Factors and Risk Factor Burden.JAMA Netw Open2021
33717502Effectiveness of film as a health communication tool to improve perceptions and attitudes in multiple sclerosis.Multiple Sclerosis Journal - Experimental, Translational and Clinical2021
33600772Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.Am J Hum Genet2021
34889895Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families.Current Issues in Molecular Biology2021
31368393The genetic diversity of multiple sclerosis risk among Hispanic and African American populations living in the United States.Mult Scler2020
32432099Investigating the Causal Effect of Brain Expression of , , , , Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach.Frontiers in Bioengineering and Biotechnology2020
31857710Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.Nat Neurosci2020
31965878Race and ethnicity on MS presentation and disease course.Multiple Sclerosis Journal2020
32231680Understanding Participation in Genetic Research Among Patients With Multiple Sclerosis: The Influences of Ethnicity, Gender, Education, and Age.Frontiers in Genetics2020
32385188Validation of serum neurofilaments as prognostic and potential pharmacodynamic biomarkers for ALS.Neurology2020
33037294Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans.Sci Rep2020
33088910A How-to Guide to Building a Robust SARS-CoV-2 Testing Program at a University-Based Health System.Academic Pathology2020
32517581Combining Imaging and Genetics to Predict Recurrence of Anticoagulation-Associated Intracerebral Hemorrhage.Stroke2020
31275353The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach.Frontiers in Genetics2019
31768050Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein.Nat Neurosci2019
31703377Fine-Mapping Array Design for Multi-Ethnic Studies of Multiple Sclerosis.Genes2019
29558868Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case report.Amyotroph Lateral Scler Frontotemporal Degener2018
28933650Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.Multiple Sclerosis Journal2018
29982988Hispanics Coming to the US Adopt US Cultural Behaviors and Eat Less Healthy: Implications for Development of Inflammatory Bowel Disease.Digestive Diseases and Sciences2018
29888042Somatic T-cell Receptor Diversity in a Chronic Kidney Disease PatientPopulation Linked to Electronic Health Records.AMIA Jt Summits Transl Sci Proc2018
30480030Native ancestry is associated with optic neuritis and age of onset in hispanics with multiple sclerosis.Annals of Clinical and Translational Neurology2018
30517106Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations.PLoS Genet2018
28275670Data characterizing the ZMIZ1 molecular phenotype of multiple sclerosis.Data Brief2017
28979795MS in self-identified Hispanic/Latino individuals living in the US.Multiple Sclerosis Journal - Experimental, Translational and Clinical2017
28406493Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort.Clinical and Translational Gastroenterology2017
28524546Inflammatory bowel disease is presenting sooner after immigration in more recent US immigrants from Cuba.Alimentary Pharmacology and Therapeutics2017
28063629The autoimmune risk gene ZMIZ1 is a vitamin D responsive marker of a molecular phenotype of multiple sclerosis.J Autoimmun2017
27861356A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants.Medicine (United States)2016
25959749Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype.Clinical Genetics2016
26754803European multiple sclerosis risk variants in the south Asian population.Multiple Sclerosis Journal2016
27377463A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.Gastroenterology2016
27046481Colorectal Tumors From Different Racial and Ethnic Minorities Have Similar Rates of Mismatch Repair Deficiency.Clinical Gastroenterology and Hepatology2016
27278126GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis.Genes Immun2016
27039700Power estimation for non-standardized multisite studies.Neuroimage2016
26343388Class II HLA interactions modulate genetic risk for multiple sclerosis.Nat Genet2015
25921054Enrichment for Northern European-derived multiple sclerosis risk alleles in Sardinia.Multiple Sclerosis Journal2015
25818868An ImmunoChip study of multiple sclerosis risk in African Americans.Brain2015
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