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B J Traynor

Explore the profile of B J Traynor including associated specialties, affiliations and a list of published articles. Areas
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Articles 20
Citations 1315
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Recent Articles
1.
Bandres-Ciga S, Saez-Atienzar S, Kim J, Makarious M, Faghri F, Diez-Fairen M, et al.
Acta Neuropathol . 2021 May; 142(1):223-224. PMID: 33944973
No abstract available.
2.
Bandres-Ciga S, Saez-Atienzar S, Kim J, Makarious M, Faghri F, Diez-Fairen M, et al.
Acta Neuropathol . 2020 Jul; 140(3):341-358. PMID: 32601912
Polygenic inheritance plays a central role in Parkinson disease (PD). A priority in elucidating PD etiology lies in defining the biological basis of genetic risk. Unraveling how risk leads to...
3.
Chio A, Logroscino G, Traynor B, Collins J, Simeone J, Goldstein L, et al.
Neuroepidemiology . 2013 Jul; 41(2):118-30. PMID: 23860588
Background: Amyotrophic lateral sclerosis (ALS) is relatively rare, yet the economic and social burden is substantial. Having accurate incidence and prevalence estimates would facilitate efficient allocation of healthcare resources. Objective:...
4.
Taes I, Goris A, Lemmens R, van Es M, van den Berg L, Chio A, et al.
Neurology . 2010 May; 74(21):1687-93. PMID: 20498436
Background: The microtubule-associated protein tau is thought to play a pivotal role in neurodegeneration. Mutations in the tau coding gene MAPT are a cause of frontotemporal dementia, and the H1/H1...
5.
Nalls M, Guerreiro R, Simon-Sanchez J, Bras J, Traynor B, Gibbs J, et al.
Neurogenetics . 2009 Mar; 10(3):183-90. PMID: 19271249
Large tracts of extended homozygosity are more prevalent in outbred populations than previously thought. With the advent of high-density genotyping platforms, regions of extended homozygosity can be accurately located allowing...
6.
Chio A, Traynor B, Lombardo F, Fimognari M, Calvo A, Ghiglione P, et al.
Neurology . 2008 Feb; 70(7):533-7. PMID: 18268245
Background: Five to 10% of amyotrophic lateral sclerosis (ALS) cases are reported to be familial (FALS), and mutations of SOD1 account for 20% of these cases. However, estimates of SOD1...
7.
Logroscino G, Traynor B, Hardiman O, Chio A, Couratier P, Mitchell J, et al.
J Neurol Neurosurg Psychiatry . 2007 Dec; 79(1):6-11. PMID: 18079297
Amyotrophic lateral sclerosis (ALS) is a relatively rare disease with a reported population incidence of between 1.5 and 2.5 per 100,000 per year. Over the past 10 years, the design...
8.
Schymick J, Talbot K, Traynor B
Hum Mol Genet . 2007 Oct; 16 Spec No. 2:R233-42. PMID: 17911166
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized clinically by rapidly progressive paralysis leading ultimately to death from respiratory failure. There is substantial evidence suggesting that ALS is...
9.
OToole O, Traynor B, Brennan P, Sheehan C, Frost E, Corr B, et al.
J Neurol Neurosurg Psychiatry . 2007 Jul; 79(1):30-2. PMID: 17634215
Background: We conducted a prospective, population based study to examine trends in incidence and prevalence of amyotrophic lateral sclerosis (ALS) in Ireland from 1995 to 2004. Methods: The Irish ALS...
10.
Schymick J, Yang Y, Andersen P, Vonsattel J, Greenway M, Momeni P, et al.
J Neurol Neurosurg Psychiatry . 2007 Mar; 78(7):754-6. PMID: 17371905
Objective: Mutations in the progranulin (PGRN) gene were recently described as the cause of ubiquitin positive frontotemporal dementia (FTD). Clinical and pathological overlap between amyotrophic lateral sclerosis (ALS) and FTD...