Literature DB >> 22399792

Road to the chromosome 9p-linked ALS/FTD locus.

Bryan J Traynor1.   

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Year:  2012        PMID: 22399792      PMCID: PMC3513280          DOI: 10.1136/jnnp-2012-302429

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


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  8 in total

1.  Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.

Authors:  Mariely DeJesus-Hernandez; Ian R Mackenzie; Bradley F Boeve; Adam L Boxer; Matt Baker; Nicola J Rutherford; Alexandra M Nicholson; NiCole A Finch; Heather Flynn; Jennifer Adamson; Naomi Kouri; Aleksandra Wojtas; Pheth Sengdy; Ging-Yuek R Hsiung; Anna Karydas; William W Seeley; Keith A Josephs; Giovanni Coppola; Daniel H Geschwind; Zbigniew K Wszolek; Howard Feldman; David S Knopman; Ronald C Petersen; Bruce L Miller; Dennis W Dickson; Kevin B Boylan; Neill R Graff-Radford; Rosa Rademakers
Journal:  Neuron       Date:  2011-09-21       Impact factor: 17.173

2.  A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia.

Authors:  M Morita; A Al-Chalabi; P M Andersen; B Hosler; P Sapp; E Englund; J E Mitchell; J J Habgood; J de Belleroche; J Xi; W Jongjaroenprasert; H R Horvitz; L-G Gunnarsson; R H Brown
Journal:  Neurology       Date:  2006-01-18       Impact factor: 9.910

3.  Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.

Authors:  Hannu Laaksovirta; Terhi Peuralinna; Jennifer C Schymick; Sonja W Scholz; Shaoi-Lin Lai; Liisa Myllykangas; Raimo Sulkava; Lilja Jansson; Dena G Hernandez; J Raphael Gibbs; Michael A Nalls; David Heckerman; Pentti J Tienari; Bryan J Traynor
Journal:  Lancet Neurol       Date:  2010-10       Impact factor: 44.182

4.  Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

Authors:  Vivianna M Van Deerlin; Patrick M A Sleiman; Maria Martinez-Lage; Alice Chen-Plotkin; Li-San Wang; Neill R Graff-Radford; Dennis W Dickson; Rosa Rademakers; Bradley F Boeve; Murray Grossman; Steven E Arnold; David M A Mann; Stuart M Pickering-Brown; Harro Seelaar; Peter Heutink; John C van Swieten; Jill R Murrell; Bernardino Ghetti; Salvatore Spina; Jordan Grafman; John Hodges; Maria Grazia Spillantini; Sid Gilman; Andrew P Lieberman; Jeffrey A Kaye; Randall L Woltjer; Eileen H Bigio; Marsel Mesulam; Safa Al-Sarraj; Claire Troakes; Roger N Rosenberg; Charles L White; Isidro Ferrer; Albert Lladó; Manuela Neumann; Hans A Kretzschmar; Christine Marie Hulette; Kathleen A Welsh-Bohmer; Bruce L Miller; Ainhoa Alzualde; Adolfo Lopez de Munain; Ann C McKee; Marla Gearing; Allan I Levey; James J Lah; John Hardy; Jonathan D Rohrer; Tammaryn Lashley; Ian R A Mackenzie; Howard H Feldman; Ronald L Hamilton; Steven T Dekosky; Julie van der Zee; Samir Kumar-Singh; Christine Van Broeckhoven; Richard Mayeux; Jean Paul G Vonsattel; Juan C Troncoso; Jillian J Kril; John B J Kwok; Glenda M Halliday; Thomas D Bird; Paul G Ince; Pamela J Shaw; Nigel J Cairns; John C Morris; Catriona Ann McLean; Charles DeCarli; William G Ellis; Stefanie H Freeman; Matthew P Frosch; John H Growdon; Daniel P Perl; Mary Sano; David A Bennett; Julie A Schneider; Thomas G Beach; Eric M Reiman; Bryan K Woodruff; Jeffrey Cummings; Harry V Vinters; Carol A Miller; Helena C Chui; Irina Alafuzoff; Päivi Hartikainen; Danielle Seilhean; Douglas Galasko; Eliezer Masliah; Carl W Cotman; M Teresa Tuñón; M Cristina Caballero Martínez; David G Munoz; Steven L Carroll; Daniel Marson; Peter F Riederer; Nenad Bogdanovic; Gerard D Schellenberg; Hakon Hakonarson; John Q Trojanowski; Virginia M-Y Lee
Journal:  Nat Genet       Date:  2010-02-14       Impact factor: 38.330

5.  A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.

Authors:  Alan E Renton; Elisa Majounie; Adrian Waite; Javier Simón-Sánchez; Sara Rollinson; J Raphael Gibbs; Jennifer C Schymick; Hannu Laaksovirta; John C van Swieten; Liisa Myllykangas; Hannu Kalimo; Anders Paetau; Yevgeniya Abramzon; Anne M Remes; Alice Kaganovich; Sonja W Scholz; Jamie Duckworth; Jinhui Ding; Daniel W Harmer; Dena G Hernandez; Janel O Johnson; Kin Mok; Mina Ryten; Danyah Trabzuni; Rita J Guerreiro; Richard W Orrell; James Neal; Alex Murray; Justin Pearson; Iris E Jansen; David Sondervan; Harro Seelaar; Derek Blake; Kate Young; Nicola Halliwell; Janis Bennion Callister; Greg Toulson; Anna Richardson; Alex Gerhard; Julie Snowden; David Mann; David Neary; Michael A Nalls; Terhi Peuralinna; Lilja Jansson; Veli-Matti Isoviita; Anna-Lotta Kaivorinne; Maarit Hölttä-Vuori; Elina Ikonen; Raimo Sulkava; Michael Benatar; Joanne Wuu; Adriano Chiò; Gabriella Restagno; Giuseppe Borghero; Mario Sabatelli; David Heckerman; Ekaterina Rogaeva; Lorne Zinman; Jeffrey D Rothstein; Michael Sendtner; Carsten Drepper; Evan E Eichler; Can Alkan; Ziedulla Abdullaev; Svetlana D Pack; Amalia Dutra; Evgenia Pak; John Hardy; Andrew Singleton; Nigel M Williams; Peter Heutink; Stuart Pickering-Brown; Huw R Morris; Pentti J Tienari; Bryan J Traynor
Journal:  Neuron       Date:  2011-09-21       Impact factor: 17.173

6.  Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.

Authors:  Michael A van Es; Jan H Veldink; Christiaan G J Saris; Hylke M Blauw; Paul W J van Vught; Anna Birve; Robin Lemmens; Helenius J Schelhaas; Ewout J N Groen; Mark H B Huisman; Anneke J van der Kooi; Marianne de Visser; Caroline Dahlberg; Karol Estrada; Fernando Rivadeneira; Albert Hofman; Machiel J Zwarts; Perry T C van Doormaal; Dan Rujescu; Eric Strengman; Ina Giegling; Pierandrea Muglia; Barbara Tomik; Agnieszka Slowik; Andre G Uitterlinden; Corinna Hendrich; Stefan Waibel; Thomas Meyer; Albert C Ludolph; Jonathan D Glass; Shaun Purcell; Sven Cichon; Markus M Nöthen; H-Erich Wichmann; Stefan Schreiber; Sita H H M Vermeulen; Lambertus A Kiemeney; John H J Wokke; Simon Cronin; Russell L McLaughlin; Orla Hardiman; Katsumi Fumoto; R Jeroen Pasterkamp; Vincent Meininger; Judith Melki; P Nigel Leigh; Christopher E Shaw; John E Landers; Ammar Al-Chalabi; Robert H Brown; Wim Robberecht; Peter M Andersen; Roel A Ophoff; Leonard H van den Berg
Journal:  Nat Genet       Date:  2009-09-06       Impact factor: 38.330

7.  Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Authors:  Aleksey Shatunov; Kin Mok; Stephen Newhouse; Michael E Weale; Bradley Smith; Caroline Vance; Lauren Johnson; Jan H Veldink; Michael A van Es; Leonard H van den Berg; Wim Robberecht; Philip Van Damme; Orla Hardiman; Anne E Farmer; Cathryn M Lewis; Amy W Butler; Olubunmi Abel; Peter M Andersen; Isabella Fogh; Vincenzo Silani; Adriano Chiò; Bryan J Traynor; Judith Melki; Vincent Meininger; John E Landers; Peter McGuffin; Jonathan D Glass; Hardev Pall; P Nigel Leigh; John Hardy; Robert H Brown; John F Powell; Richard W Orrell; Karen E Morrison; Pamela J Shaw; Christopher E Shaw; Ammar Al-Chalabi
Journal:  Lancet Neurol       Date:  2010-10       Impact factor: 44.182

8.  Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

Authors:  Caroline Vance; Ammar Al-Chalabi; Deborah Ruddy; Bradley N Smith; Xun Hu; Jemeen Sreedharan; Teepu Siddique; H Jurgen Schelhaas; Benno Kusters; Dirk Troost; Frank Baas; Vianney de Jong; Christopher E Shaw
Journal:  Brain       Date:  2006-02-22       Impact factor: 13.501

  8 in total
  3 in total

1.  Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion.

Authors:  Hannah A Pliner; David M Mann; Bryan J Traynor
Journal:  Acta Neuropathol       Date:  2014-02-05       Impact factor: 17.088

2.  Assessment of Parkinson's disease risk loci in Greece.

Authors:  Eleanna Kara; Georgia Xiromerisiou; Cleanthe Spanaki; Maria Bozi; Georgios Koutsis; Marios Panas; Efthimios Dardiotis; Styliani Ralli; Jose Bras; Christopher Letson; Connor Edsall; Hannah Pliner; Sampath Arepalli; Kallirhoe Kalinderi; Liana Fidani; Sevasti Bostantjopoulou; Margaux F Keller; Nicholas W Wood; John Hardy; Henry Houlden; Leonidas Stefanis; Andreas Plaitakis; Dena Hernandez; Georgios M Hadjigeorgiou; Mike A Nalls; Andrew B Singleton
Journal:  Neurobiol Aging       Date:  2013-09-27       Impact factor: 4.673

Review 3.  Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia.

Authors:  Jennifer C Schymick; Bryan J Traynor
Journal:  Alzheimers Res Ther       Date:  2012-07-26       Impact factor: 6.982

  3 in total

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