The Helix
Editor's Note
Editorial
Articles
- Open AccessGenetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S. Winsvold, Christopher P. Nelson, Rainer Malik, Padhraig Gormley, Verneri Anttila, Jason Vander Heiden, Katherine S. Elliott, Line M. Jacobsen, Priit Palta, Najaf Amin, Boukje de Vries, Eija Hämäläinen, Tobias Freilinger, M. Arfan Ikram, Thorsten Kessler, Markku Koiranen, Lannie Ligthart, George McMahon, Linda M. Pedersen, Christina Willenborg, Hong-Hee Won, Jes Olesen, Ville Artto, Themistocles L. Assimes, Stefan Blankenberg, Dorret I. Boomsma, Lynn Cherkas, George Davey Smith, Stephen E. Epstein, Jeanette Erdmann, Michel D. Ferrari, Hartmut Göbel, Alistair S. Hall, Marjo-Riitta Jarvelin, Mikko Kallela, Jaakko Kaprio, Sekar Kathiresan, Terho Lehtimäki, Ruth McPherson, Winfried März, Dale R. Nyholt, Christopher J. O'Donnell, Lydia Quaye, Daniel J. Rader, Olli Raitakari, Robert Roberts, Heribert Schunkert, Markus Schürks, Alexandre F.R. Stewart, Gisela M. Terwindt, Unnur Thorsteinsdottir, Arn M.J.M. van den Maagdenberg, Cornelia van Duijn, Maija Wessman, Tobias Kurth, Christian Kubisch, Martin Dichgans, Daniel I. Chasman, Chris Cotsapas, John-Anker Zwart, Nilesh J. Samani, Aarno Palotie, For the CARDIoGRAM Consortium and the International Headache Genetics Consortium
- Open AccessCHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth diseaseMari Auranen, Emil Ylikallio, Maria Shcherbii, Anders Paetau, Sari Kiuru-Enari, Jussi P. Toppila, Henna Tyynismaa
- Open AccessPhenotypic and molecular analyses of primary lateral sclerosisHiroshi Mitsumoto, Peter L. Nagy, Chris Gennings, Jennifer Murphy, Howard Andrews, Raymond Goetz, Mary Kay Floeter, Jonathan Hupf, Jessica Singleton, Richard J. Barohn, Sharon Nations, Christen Shoesmith, Edward Kasarskis, Pam Factor-Litvak
- Open AccessEpileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosisRyan S. Dhindsa, Shelton S. Bradrick, Xiaodi Yao, Erin L. Heinzen, Slave Petrovski, Brian J. Krueger, Michael R. Johnson, Wayne N. Frankel, Steven Petrou, Rebecca M. Boumil, David B. Goldstein
- Open AccessEpilepsy with auditory featuresA heterogeneous clinico-molecular diseaseTommaso Pippucci, Laura Licchetta, Sara Baldassari, Flavia Palombo, Veronica Menghi, Romina D'Aurizio, Chiara Leta, Carlotta Stipa, Giovanni Boero, Giuseppe d'Orsi, Alberto Magi, Ingrid Scheffer, Marco Seri, Paolo Tinuper, Francesca Bisulli
- Open AccessRespiratory chain deficiency in nonmitochondrial diseaseAngela Pyle, Helen J. Nightingale, Helen Griffin, Angela Abicht, Janbernd Kirschner, Ivo Baric, Mario Cuk, Konstantinos Douroudis, Lea Feder, Markus Kratz, Birgit Czermin, Stephanie Kleinle, Mauro Santibanez-Koref, Veronika Karcagi, Elke Holinski-Feder, Patrick F. Chinnery, Rita Horvath
- Open AccessPFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, Sanna Huovinen, Anders Paetau, Satu Sandell, Hannu Haapasalo, Kati Viitaniemi, Päivi Piirilä, Henna Tyynismaa, Bjarne Udd
Clinical/Scientific Notes
- Open AccessLoss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, Christel Condroyer, Aude Nicolas, Lee Darwent, Rita Guerreiro, Elisa Majounie, Monica Federoff, Peter Heutink, Nicholas W. Wood, Thomas Gasser, John Hardy, François Tison, Andrew Singleton, Alexis Brice, For the French Parkinson's Disease Genetics Study Group (PDG) and the International Parkinson's Disease Genomics Consortium (IPDGC)
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