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Kristiina Rannikmäe

7PUBLICATIONS

63CO-AUTHORS

Behavioural neuroscienceHaematologyCardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)

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Publications (7)

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|Mar 06, 2026

Reply to Comment on "Delayed Disease Onset Report in UK Biobank: Implications for Prodromal Studies in Parkinson's Disease".

Trycia Kouchache, Sheida Zolfaghari, Sarah Bouhadoun

|Mar 14, 2025

Genetic Insights Into Hemorrhagic Stroke and Vascular Malformations: Pathogenesis and Emerging Therapeutic Strategies.

Pazhanichamy Kalailingam, Kristiina Rannikmae, Moran Hausman-Kedem

|May 15, 2023

Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes.

Ana Villaplana-Velasco, Marie Pigeyre, Justin Engelmann

|Jun 14, 2022

Systematic Review of Cerebral Phenotypes Associated With Monogenic Cerebral Small-Vessel Disease.

Ed Whittaker, Sophie Thrippleton, Liza Y W Chong

|Oct 09, 2021

Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities.

Rainer Malik, Nathalie Beaufort, Simon Frerich

|Dec 23, 2020

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.

Mark K Bakker, Rick A A van der Spek, Wouter van Rheenen

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Frequent Collaborators

3 joint publications

Ynte M Ruigrok

2 joint publications

Mark K Bakker

2 joint publications

Wouter van Rheenen

2 joint publications

Sandrine Morel

2 joint publications

Isabel C Hostettler

2 joint publications

Masaru Koido

2 joint publications

Chikashi Terao

2 joint publications

Koichi Matsuda

2 joint publications

Robin G Walters

2 joint publications

Zhengming Chen

Frequent Collaborators

3 joint publications

Ynte M Ruigrok

2 joint publications

Mark K Bakker

2 joint publications

Wouter van Rheenen

2 joint publications

Sandrine Morel

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