Ernest Turro

27PUBLICATIONS
210CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Aerodynamics (excl. hypersonic aerodynamics)
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Publications (27)

|May 29, 2026
Reduced platelet formation associated with serine metabolic dysregulation in integrin αIIbβ3-deficient megakaryocytes.

|Apr 23, 2026
Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

|Mar 30, 2026
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Daniel Greene, Rodrigo Mendez, Jon Lees

|Jan 20, 2026
Understanding how a highly prevalent GRK5 polymorphism affects platelets and enhances thrombotic risk.

Yanki Yarman, Xuefei Zhao, Hyunsook Ahn

|Oct 16, 2025
Human missense variants in F3 impair the initiation of blood coagulation.

Shabbir A Ansari, Marisa A Brake, Nishtha Pathak

|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

7 joint publications

Kathleen Freson

5 joint publications

Willem H Ouwehand

4 joint publications

Kathy Stirrups

3 joint publications

Hana Lango Allen