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Adolfo López de Munain

Researcher at University of the Basque Country

Publications -  219
Citations -  11470

Adolfo López de Munain is an academic researcher from University of the Basque Country. The author has contributed to research in topics: Medicine & Myotonic dystrophy. The author has an hindex of 42, co-authored 195 publications receiving 8963 citations. Previous affiliations of Adolfo López de Munain include Ministry of Science and Innovation & Autonomous University of Barcelona.

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Journal ArticleDOI

Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease

Coro Paisán-Ruiz, +20 more
- 18 Nov 2004 - 
TL;DR: The cloning of a novel gene that contains missense mutations segregating with PARK8-linked PD in five families from England and Spain is described and this protein is named dardarin, derived from the Basque word dardara, meaning tremor, because of the tremor observed in PD.
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

Vivianna M. Van Deerlin, +107 more
- 01 Mar 2010 - 
TL;DR: It is found that FTLD-TDP associates with multiple SNPs mapping to a single linkage disequilibrium block on 7p21 that contains TMEM 106B, which implicate variants in TMEM106B as a strong risk factor for FTLD, suggesting an underlying pathogenic mechanism.
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New insights into the genetic etiology of Alzheimer’s disease and related dementias

Céline Bellenguez, +401 more
- 01 Apr 2022 - 
TL;DR: This paper performed a two-stage genome-wide association study with 111,326 clinically diagnosed/proxy AD cases and 677,663 controls and found 75 risk loci, of which 42 were new at the time of analysis.
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Association between total, processed, red and white meat consumption and all-cause, CVD and IHD mortality: a meta-analysis of cohort studies.

Itziar Abete, +4 more
- 14 Sep 2014 - 
TL;DR: The results of the present meta-analysis indicate that processed meat consumption could increase the risk of mortality from any cause and CVD, while red meat consumption is positively but weakly associated with CVD mortality.
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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

José Manuel Morante-Redolat, +26 more
- 01 May 2002 - 
TL;DR: It is demonstrated that the LGI1 protein, which contains several leucine-rich repeats, is expressed ubiquitously in the neuronal cell compartment of the brain and provides evidence for genetic heterogeneity within this disorder.