Author

Juan L. Rodríguez-Flores

Weill Cornell MedicineORCID 0000-0002-0394-8062Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3 Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 5 Assay:whole-genome sequencing· 4 Research Focus:variant calling· 3 Research Focus:GWAS / association mapping· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Ali Ait HssainiD· 2 shared Amal RobayiD· 2 shared Jason G. MezeyiD· 2 shared Mahboubeh R. RostamiiD· 2 shared Ronald G. CrystaliD· 2 shared Adam AutoniD· 1 shared Alan R. ShuldineriD· 1 shared Alexandra M. WeberiD· 1 shared

Activity by Year

2016-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Ali Ait HssainORCID

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 28, 2026

Genome-Wide Association Study of Sepsis Susceptibility in ICU Patients Identifies Arab Founder Loss-of-Function Variant in UBE2L3

Mahboubeh R. Rostami, Ali Ait Hssain, Amal Robay…·Juan L. Rodríguez-Flores

DOI 10.64898/2026.09.25.26363954

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintFeb 11, 2025

Population-specific Risk of Pharmacogenomics-related Inaccurate Drug Dosing of ICU Patients

Mahboubeh R. Rostami, Juan L. Rodríguez-Flores, Ali Ait Hssain…·Ronald G. Crystal

The paper assesses genetic risks of inaccurate ICU drug dosing in Qataris by analyzing whole genome sequencing data and identifies population-specific pharmacogenomics variants.

DOI 10.1101/2025.02.11.25321889

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintOct 5, 2023

NOTCH3 p.Arg1231Cys is Markedly Enriched in South Asians and Associated with Stroke

Juan L. Rodríguez-Flores, Shareef Khalid, Neelroop Parikshak…·Danish Saleheen

The paper identifies a NOTCH3 variant, p.Arg1231Cys, enriched in South Asians and strongly associated with stroke risk, highlighting the importance of genetic diversity in stroke research.

2 citations

humanwhole-exome sequencing

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GenomicsGigaSciencePeer-reviewedJan 1, 2021

Genome Diversity in Ukraine

Tarás K. Oleksyk, Walter Wolfsberger, Alexandra M. Weber…·Volodymyr Smolanka

This study provides genome-wide data for the Ukrainian population, identifying novel genetic variants and highlighting its unique genetic diversity.

27 citations

humanwhole-genome sequencing

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BioinformaticsbioRxivPreprintOct 18, 2016

False Negatives Are a Significant Feature of Next Generation Sequencing Callsets

Dean Bobo, Mikhail Lipatov, Juan L. Rodríguez-Flores…·Brenna M. Henn

The paper quantifies false negative rates in NGS data and introduces a tool to assess them, showing significant FN rates even in high-coverage datasets.

14 citations

humanwhole-genome sequencing

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