Alexandre Bolze

University of Nevada, Reno — United States

Medicine · Health Sciences

42h-index18.8kcitations127works3.62yr avg
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Research Topics

SARS-CoV-2 and COVID-19 Research(41), COVID-19 Clinical Research Studies(16), Genomics and Rare Diseases(16), Immunodeficiency and Autoimmune Disorders(16), interferon and immune responses(11)

Publications117 total

Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2
Nature Communications·2025· 1 citedOpen Access
Population Genomic Screening and Improved Lipid Management in Patients With Familial Hypercholesterolemia
Circulation Genomic and Precision Medicine·2025Open Access
Abstract 4370493: Hypercholesterolemia polygenic score modulates response to statin therapy
Circulation·2025
Abstract 4360588: Population Genomic Screening for Familial Hypercholesterolemia is Associated with Improved Lipid Management and Control
Circulation·2025
The seven enigmas of SARS-CoV-2: From the past to the future
Journal of Human Immunity·2025· 1 citedOpen Access
From Uncertain to Actionable: Significant Reduction in Variants of Uncertain Significance in Hereditary Germline Testing via Multi-Institutional Real-World Evidence
2025Open Access
Dominant negative <i>ADA2</i> mutations cause ADA2 deficiency in heterozygous carriers
The Journal of Experimental Medicine·2025· 2 citedOpen Access
Novel Method for Predicting Lp(a) From Genomic Testing Identifies ASCVD Risk Across a Diverse Cohort
JACC Basic to Translational Science·2025· 2 citedOpen Access
Tu1160: MINORITY POPULATIONS EXHIBIT DISTINCT CLINICAL AND GENETIC FEATURES OF CELIAC DISEASE IN THE UNITED STATES
Gastroenterology·2025
Hypertension increases PPV for polycystic kidney disease in PKD1 and PKD2 variant carriers
Human Genetics and Genomics Advances·2025Open Access
Population genomic screening leads to improved lipid management in patients with familial hypercholesterolemia
2025Open Access
Lynch syndrome in the general population: low clinical utility of genomic screening for <i>PMS2</i> pathogenic variants
2025Open Access
Response to Karp-Tatham et al.
Human Genetics and Genomics Advances·2025Open Access
P172: A framework to identify individuals at low risk of disease in the population*
Genetics in Medicine Open·2025Open Access
Human genetics of responses to vaccines
Clinical & Experimental Immunology·2025· 3 cited
P217: Solving for PS4
Genetics in Medicine Open·2025Open Access
P580: Comparing automated vs ACMG/AMP-based variant interpretation for the CDC Tier 1 conditions in a clinicogenomic cohort from US-based health systems
Genetics in Medicine Open·2025Open Access
P293: A novel method for predicting Lp(a) levels from routine outpatient genomic testing identifies those at risk of cardiovascular disease
Genetics in Medicine Open·2025Open Access
O20: Improved clinical management following diagnosis with familial hypercholesterolemia in the Helix Research Network Population Genomics Screening Program
Genetics in Medicine Open·2025Open Access
Integrative Modeling of Genetic and Clinical Risks to Improve Celiac Disease Prediction Across Diverse Populations
SSRN Electronic Journal·2025Open Access
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Frequent Co-authors

Laurent Abel(25), Jean‐Laurent Casanova(24), Elizabeth T. Cirulli(18), Nicole Washington(17), Kelly M. Schiabor Barrett(15), Anne Puel(13), Jacques Fellay(13), James T. Lu(13), Paul Bastard(12), Alessandro Aiuti(12), Filomeen Haerynck(12), Andrés A. Arias(12), Bertrand Boisson(12), Giorgio Casari(11), Petter Brodin(11), Carlos Rodríguez‐Gallego(11), Davood Mansouri(11), Giuseppe Novelli(11), Isabelle Meyts(11), Simon White(11)