Roope Mannikko (Roope Männikkö)

ResearcherID Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 6

Top Venues

Scientific reports

Journal of neurology, neurosurgery, and psychiatry

Epilepsia

JCSM rapid communications

This page only lists publications with an associated author ORCID identifier.

Publications

Vincenzo Salpietro, Valentina Galassi Deforie, Stephanie Efthymiou, Emer O'Connor, Anna Marcé-Grau, Reza Maroofian, Pasquale Striano, Federico Zara, Michelle M Morrow, null null, Adi Reich, Amy Blevins, Júlia Sala-Coromina, Andrea Accogli, Sara Fortuna, Marie Alesandrini, Ping Yee Billie Au, Nilika Shah Singhal, Benjamin Cogne, Bertrand Isidor, Michael G Hanna, Alfons Macaya, Dimitri Michael Kullmann, Henry Houlden, Roope Mannikko
De novo KCNA6 variants with attenuated K V 1.6 channel deactivation in patients with epilepsy. Epilepsia (2022)
Karen J Suetterlin, S Veronica Tan, Roope Mannikko, Rahul Phadke, Michael Orford, Simon Eaton, Avan A Sayer, Miranda D Grounds, Emma Matthews, Linda Greensmith, Michael G Hanna
Ageing contributes to phenotype transition in a mouse model of periodic paralysis. JCSM rapid communications 4 (2) (2021)
Andoni Echaniz-Laguna, Valérie Biancalana, Aleksandra Nadaj-Pakleza, Emmanuel Fournier, Emma Matthews, Michael G Hanna, Roope Mannikko
Homozygous C-terminal loss-of-function NaV1.4 variant in a patient with congenital myasthenic syndrome. Journal of neurology, neurosurgery, and psychiatry 91 (8) (2020)
Vincenzo Salpietro, Christine L Dixon, Hui Guo, Oscar D Bello, Jana Vandrovcova, Stephanie Efthymiou, Reza Maroofian, Gali Heimer, Lydie Burglen, Stéphanie Valence, Erin Torti, Moritz Hacke, Julia Rankin, Huma Tariq, Estelle Colin, Vincent Procaccio, Pasquale Striano, Kshitij Mankad, Andreas Lieb, Sharon Chen, Laura Pisani, Conceicao Bettencourt, Roope Mannikko, Andreea Manole, Alfredo Brusco, Enrico Grosso, Giovanni Battista Ferrero, Judith Armstrong-Moron, Sophie Gueden, Omer Bar-Yosef, Michal Tzadok, Kristin G Monaghan, Teresa Santiago-Sim, Richard E Person, Megan T Cho, Rebecca Willaert, Yongjin Yoo, Jong-Hee Chae, Yingting Quan, Huidan Wu, Tianyun Wang, Raphael A Bernier, Kun Xia, Alyssa Blesson, Mahim Jain, Mohammad M Motazacker, Bregje Jaeger, Amy L Schneider, Katja Boysen, Alison M Muir, Candace T Myers, Ralitza H Gavrilova, Lauren Gunderson, Laura E Schultz-Rogers, Eric W Klee, David Dyment, Matthew Osmond, Mara Parellada, Cloe Llorente, Javier Gonzalez-Peñas, Angel Carracedo, Arie Van Haeringen, Claudia Ruivenkamp, Caroline Nava, Delphine Heron, Rosaria Nardello, Michele Iacomino, Carlo Minetti, Aldo Skabar, Antonella Fabretto, null null, Miquel Raspall-Chaure, Michael Chez, Anne Tsai, Emily Fassi, Marwan Shinawi, John N Constantino, Rita De Zorzi, Sara Fortuna, Fernando Kok, Boris Keren, Dominique Bonneau, Murim Choi, Bruria Benzeev, Federico Zara, Heather C Mefford, Ingrid E Scheffer, Jill Clayton-Smith, Alfons Macaya, James E Rothman, Evan E Eichler, Dimitri Michael Kullmann, Henry Houlden
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature communications 10 (1) (2019)
Michael G Thor, Vinojini Vivekanandam, Marisol Sampedro Castaneda, S Veronica Tan, Karen Suetterlin, Richa Sud, Siobhan Durran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna, Emma Matthews, Roope Mannikko
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation. Scientific reports 9 (1) (2019)
Sushan Luo, Marisol Sampedro Castañeda, Emma Matthews, Richa Sud, Michael G Hanna, Jian Sun, Jie Song, Jiahong Lu, Kai Qiao, Chongbo Zhao, Roope Mannikko
Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in NaV1.4. Scientific reports 8 (1) (2018)

Roope Mannikko.css-eqlu8i{font-size:small;padding-left:4px;} (Roope Männikkö)

Publication Activity (10 Years)

Top Topics

Top Venues

Roope Mannikko (Roope Männikkö)