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)

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

Daniel Greene, Rodrigo Mendez, Jon Lees

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Frequent Collaborators

Kathleen Freson

Willem H Ouwehand

Kathy Stirrups

Hana Lango Allen

James E D Thaventhiran

3 joint publications

Christopher J Penkett

Andrew Mumford

Adrian J Thrasher

Salih Tuna

Wei Wei

Frequent Collaborators

Kathleen Freson

Willem H Ouwehand

Kathy Stirrups

Hana Lango Allen