Skip to main content
Advertisement
  • Neurology.org
  • Journals
    • Neurology
    • Clinical Practice
    • Education
    • Genetics
    • Neuroimmunology & Neuroinflammation
  • Online Sections
    • Neurology Video Journal Club
    • Inclusion, Diversity, Equity, Anti-racism, & Social Justice (IDEAS)
    • Innovations in Care Delivery
    • Practice Buzz
    • Practice Current
    • Residents & Fellows
    • Without Borders
  • Collections
    • COVID-19
    • Disputes & Debates
    • Health Disparities
    • Infographics
    • Null Hypothesis
    • Patient Pages
    • Translations
    • Topics A-Z
  • Podcast
  • CME
  • About
    • About the Journals
    • Contact Us
    • Editorial Board
  • Authors
    • Submit a Manuscript
    • Author Center

Advanced Search

Main menu

  • Neurology.org
  • Journals
    • Neurology
    • Clinical Practice
    • Education
    • Genetics
    • Neuroimmunology & Neuroinflammation
  • Online Sections
    • Neurology Video Journal Club
    • Inclusion, Diversity, Equity, Anti-racism, & Social Justice (IDEAS)
    • Innovations in Care Delivery
    • Practice Buzz
    • Practice Current
    • Residents & Fellows
    • Without Borders
  • Collections
    • COVID-19
    • Disputes & Debates
    • Health Disparities
    • Infographics
    • Null Hypothesis
    • Patient Pages
    • Translations
    • Topics A-Z
  • Podcast
  • CME
  • About
    • About the Journals
    • Contact Us
    • Editorial Board
  • Authors
    • Submit a Manuscript
    • Author Center
  • Home
  • Articles
  • Issues

User menu

  • My Alerts
  • Log in

Search

  • Advanced search
Neurology Genetics
Home
A peer-reviewed clinical and translational neurology open access journal
  • My Alerts
  • Log in
Site Logo
  • Home
  • Articles
  • Issues

Share

June 2015; 1 (1)

Share

The Helix

  • Open Access
    Welcome to Neurology: Genetics
    Stefan M. Pulst
    • Full Text
    • Full Text (PDF)

Editor's Note

  • Open Access
    Spotlight on the June 2015 issue
    Stefan M. Pulst
    • Full Text
    • Full Text (PDF)

Editorial

  • Open Access
    Are migraineurs naturally born “well-hearted”?
    Anne Ducros
    • Full Text
    • Full Text (PDF)

Articles

  • Open Access
    Genetic analysis for a shared biological basis between migraine and coronary artery disease
    Bendik 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
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Open Access
    CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease
    Mari Auranen, Emil Ylikallio, Maria Shcherbii, Anders Paetau, Sari Kiuru-Enari, Jussi P. Toppila, Henna Tyynismaa
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Open Access
    Phenotypic and molecular analyses of primary lateral sclerosis
    Hiroshi 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
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Open Access
    Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis
    Ryan 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
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Open Access
    Epilepsy with auditory featuresA heterogeneous clinico-molecular disease
    Tommaso 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
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Open Access
    Respiratory chain deficiency in nonmitochondrial disease
    Angela 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
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Open Access
    PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistry
    Mari Auranen, Johanna Palmio, Emil Ylikallio, Sanna Huovinen, Anders Paetau, Satu Sandell, Hannu Haapasalo, Kati Viitaniemi, Päivi Piirilä, Henna Tyynismaa, Bjarne Udd
    • Abstract
    • Full Text
    • Full Text (PDF)

Clinical/Scientific Notes

  • Open Access
    Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
    Suzanne 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)
    • Full Text
    • Full Text (PDF)
Back to top
Next
Next Issue
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
Subscribe to e-Alerts
RSS
Advertisement
Popular on
Neurology: Genetics
  • Most Read
  • Most Cited
Loading
  • Neurodevelopmental Disorder, Obesity, Pancytopenia, Diabetes Mellitus, Cirrhosis, and Renal Failure in ACBD6-Associated SyndromeA Case Report
  • Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation
  • Severe Cerebral Small Vessel Disease Caused by the Uniallelic p.A252T Variant of HTRA1
  • Identification of Sex-Specific Genetic Variants Associated With Tau PET
  • RFC1-Related DiseaseMolecular and Clinical Insights
More...

Preferences and User Experiences of Wearable Devices in Epilepsy A Systematic Review and Mixed-Methods Synthesis

Dr. Daniel Friedman and Dr. Sharon Chiang

► Watch

Advertisement
Neurology Genetics: 9 (2)

Articles

  • Articles
  • Issues
  • Popular Articles

About

  • About the Journals
  • Ethics Policies
  • Editors & Editorial Board
  • Contact Us
  • Advertise

Submit

  • Author Center
  • Submit a Manuscript
  • Information for Reviewers
  • AAN Guidelines
  • Permissions

Subscribers

  • Subscribe
  • Sign up for eAlerts
  • RSS Feed
Site Logo
  • Visit neurology Template on Facebook
  • Follow neurology Template on Twitter
  • Visit Neurology on YouTube
  • Neurology
  • Neurology: Clinical Practice
  • Neurology: Education
  • Neurology: Genetics
  • Neurology: Neuroimmunology & Neuroinflammation
  • AAN.com
  • AANnews
  • Continuum
  • Brain & Life
  • Neurology Today

Wolters Kluwer Logo

Neurology: Genetics | Online ISSN: 2376-7839

© 2023 American Academy of Neurology

  • Privacy Policy
  • Feedback
  • Advertise