A

Asadollahi, Reza ORCID: 0000-0002-1497-0564 , Delvendahl, Igor, Muff, Rebecca, Tan, Ge, Rodríguez, Daymé González, Turan, Soeren, Russo, Martina, Oneda, Beatrice, Joset, Pascal, Boonsawat, Paranchai, Masood, Rahim, Mocera, Martina, Ivanovski, Ivan, Baumer, Alessandra, Bachmann-Gagescu, Ruxandra, Schlapbach, Ralph, Rehrauer, Hubert, Steindl, Katharina, Begemann, Anaïs, Reis, André, Winkler, Jürgen, Winner, Beate, Müller, Martin and Rauch, Anita (2023) Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons. Human Molecular Genetics, 32 (13). pp. 2192-2204. ISSN 0964-6906 (Print), 1460-2083 (Online) (doi:https://doi.org/10.1093/hmg/ddad048)

H

Huang, Yuqing, Wang, Yiru A, Sluijs, Lisa van, Vogels, Demi H J, Chen, Yuzhi, Tegelbeckers, Vivian I P, Schoonderwoerd, Steven, Riksen, Joost A G, Kammenga, Jan E, Harvey, Simon C ORCID: 0000-0002-7504-2227 and Sterken, Mark G (2024) eQTL mapping in transgenic alpha-synuclein carrying caenorhabditis elegans recombinant inbred lines. Human Molecular Genetics. ISSN 0964-6906 (Print), 1460-2083 (Online) (doi:https://doi.org/10.1093/hmg/ddae148)