Number of items: 19.
Article
Targeted genetic Screen in amyotrophic lateral sclerosis reveals novel genetic variants with synergistic effect on clinical phenotype -
Johnathan Cooper-Knock,
Henry Robins,
Isabell Niedermoser,
Matthew Wyles,
Paul R. Heath,
Adrian Higginbottom,
Theresa Walsh,
Mbombe Kazoka,
Paul G. Ince,
Guillaume M. Hautbergue,
Christopher J. McDermott,
Janine Kirby and
Pamela J. Shaw
Type: Article
| 2017
Detection of long repeat expansions from PCR-free whole-genome sequence data -
Egor Dolzhenko,
Joke J.F.A. van Vugt,
Richard J Shaw,
Mitchell A Bekritsky,
Marka van Blitterswijk,
Giuseppe Narzisi,
Subramanian S. Ajay,
Vani Rajan,
Bryan R. Lajoie,
Nathan H. Johnson,
Zoya Kingsbury,
Sean J. Humphray,
Raymond D Schellevis,
William J. Brands,
Matt Baker,
Rosa Rademakers,
Maarten Kooyman,
Gijs H.P. Tazelaar,
Michael A. van Es,
Russell McLaughlin,
William Sproviero,
Aleksey Shatunov,
Ashley Jones,
Ahmad Al Khleifat,
Alan Pittman,
Sarah Morgan,
Orla Hardiman,
Ammar Al-Chalabi,
Chris Shaw,
Bradley Smith,
Edmund J. Neo,
Karen Morrison,
Pamela J. Shaw,
Catherine Reeves,
Lara Winterkorn,
Nancy S. Wexler,
David E. Housman,
Christopher W. Ng,
Alina L. Li,
Ryan J. Taft,
Leonard H. van den Berg,
David R. Bentley,
Jan H. Veldink and
Michael A. Eberle
Type: Article
| 2017
Type: Article
| 2017
| Item not available on this server.
Type: Article
| 2017
| Item not available on this server.
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing -
Iris E. Jansen,
Hui Ye,
Sasja Heetveld,
Marie C. Lechler,
Helen Michels,
Renée I. Seinstra,
Steven J. Lubbe,
Valérie Drouet,
Suzanne Lesage,
Elisa Majounie,
J. Raphael Gibbs,
Mike A. Nalls,
Mina Ryten,
Juan A. Botia,
Jana Vandrovcova,
Javier Simon-Sanchez,
Melissa Castillo-Lizardo,
Patrizia Rizzu,
Cornelis Blauwendraat,
Amit K. Chouhan,
Yarong Li,
Puja Yogi,
Najaf Amin,
Cornelia M. van Duijn,
Huw R. Morris,
Alexis Brice,
Della C. David,
Andrew B. Singleton,
Ellen A. Nollen,
Shushant Jain,
Joshua M. Shulman and
Peter Heutink
Type: Article
| 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK -
Sarah Morgan,
Aleksey Shatunov,
William Sproviero,
Ashley R. Jones,
Maryam Shoai,
Deborah Hughes,
Ahmad Al Khleifat,
Andrea Malaspina,
Karen E. Morrison,
Pamela J. Shaw,
Christopher E. Shaw,
Katie Sidle,
Richard W. Orrell,
Pietro Fratta,
John Hardy,
Alan Pittman and
Ammar Al-Chalabi
Type: Article
| 2017
Type: Article
| 2017
| Item not available on this server.
C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis -
James Rooney,
Isabella Fogh,
Henk-Jan Westeneng,
Alice Vajda,
Russell McLaughlin,
Mark Heverin,
Ashley Jones,
Ruben van Eijk,
Andrea Calvo,
Letizia Mazzini,
Christopher Shaw,
Karen Morrison,
Pamela J. Shaw,
Wim Robberecht,
Phillip Van Damme,
Ammar Al-Chalabi,
Leonard van den Berg,
Adriano Chio,
Jan Veldink and
Orla Hardiman
Type: Article
| 2017
| Item not available on this server.
Conference or Workshop Item
Type: Conference or Workshop Item
| 2017
| Item availability restricted.
Type: Conference or Workshop Item
| 2017
Review
Type: Review
| 2017
| Item not available on this server.
This list was generated on Tue Oct 15 02:25:47 2024 BST.