Rodrigo Mendez

12PUBLICATIONS
143CO-AUTHORS
Data models, storage and indexingGene mappingCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Publications (12)

|Oct 31, 2026
MetaDome 2027: a comprehensively updated resource for aggregating missense variant evidence across homologous human protein domains.

|Oct 24, 2026
MetaDome 2027: a comprehensively updated resource for aggregating missense variant evidence across homologous human protein domains.

|Apr 20, 2026
De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling.

|Apr 08, 2026
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders.

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji

|Nov 24, 2025
Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing.

Alexis Ferrasse, Rodrigo Mendez, John E Gorzynski

|Sep 05, 2025
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Daniel Greene, Rodrigo Mendez, Jon Lees

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Frequent Collaborators

8 joint publications

Jonathan A Bernstein

8 joint publications

Matthew T Wheeler

6 joint publications

Stephen B Montgomery

5 joint publications

Devon E Bonner