Rodrigo Mendez

10PUBLICATIONS
131CO-AUTHORS
Gene mappingCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (10)

|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 <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorder.

Daniel Greene, Rodrigo Mendez, Jon Lees

|Apr 29, 2025
Saturation genome editing of <i>RNU4-2</i> reveals distinct dominant and recessive neurodevelopmental disorders.

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji

|Jan 13, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies.

Maggie T Arriaga, Rodrigo Mendez, Rachel A Ungar

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Frequent Collaborators

6 joint publications

Matthew T Wheeler

6 joint publications

Jonathan A Bernstein

4 joint publications

Elsa Leitão

4 joint publications

Nicola Whiffin