Anna-Elina Lehesjoki

7PUBLICATIONS
42CO-AUTHORS
Aboriginal and Torres Strait Islander artefactsMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)Microfluidics and nanofluidicsCell physiology
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Publications (7)

|Sep 18, 2026
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago.

|Nov 21, 2025
Novel, complex configurations of the MARCHF6 repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsy.

Mark F Bennett, Mark A Corbett, Thessa Kroes

|Dec 23, 2024
A conserved role for ALG10/ALG10B and the N -glycosylation pathway in the sleep-epilepsy axis.

Shubhroz Gill, Torrey R Mandigo, Ayse Deniz Elmali

|May 07, 2024
Heterogeneous genetic patterns in bilateral perisylvian polymicrogyria: insights from a Finnish family cohort.

Irma Järvelä, Ritva Paetau, Yasmin Rajendran

|Apr 04, 2022
Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy.

Marieke M van der Knoop, Reza Maroofian, Yuko Fukata

|Dec 15, 2021
Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.

Laura C Bott, Mitra Forouhan, Maria Lieto

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Frequent Collaborators

4 joint publications

Samuel F Berkovic

3 joint publications

Melanie Bahlo

2 joint publications

Nerses Bebek

2 joint publications

Karen L Oliver