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María Brion
María Brion
Instituto de investigación Sanitaria de Santiago, Complejo Hospitalario Universitario de Santiago,
Verified email at usc.es
Title
Cited by
Cited by
Year
SNPs in forensic genetics: a review on SNP typing methodologies
B Sobrino, M Brión, A Carracedo
Forensic science international 154 (2-3), 181-194, 2005
6052005
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
W Chen, D Stambolian, AO Edwards, KE Branham, M Othman, ...
Proceedings of the National Academy of Sciences 107 (16), 7401-7406, 2010
5682010
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ...
Nature genetics 46 (8), 826-836, 2014
2802014
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula
SM Adams, E Bosch, PL Balaresque, SJ Ballereau, AC Lee, E Arroyo, ...
The American Journal of Human Genetics 83 (6), 725-736, 2008
2762008
Ancestry analysis in the 11-M Madrid bomb attack investigation
C Phillips, L Prieto, M Fondevila, A Salas, A Gómez-Tato, J Álvarez-Dios, ...
PloS one 4 (8), e6583, 2009
1402009
Hierarchical analysis of 30 Y-chromosome SNPs in European populations
M Brion, B Sobrino, A Blanco-Verea, MV Lareu, A Carracedo
International Journal of Legal Medicine 119, 10-15, 2005
1312005
Molecular genetics of sudden cardiac death
MS Rodríguez-Calvo, M Brion, C Allegue, L Concheiro, A Carracedo
Forensic science international 182 (1-3), 1-12, 2008
1062008
Robustness of the Y STRs DYS19, DYS389 I and II, DYS390 and DYS393: optimization of a PCR pentaplex
L Gusmao, A Gonzalez-Neira, C Pestoni, M Brion, MV Lareu, A Carracedo
Forensic science international 106 (3), 163-172, 1999
1021999
Forensic validation of the SNPforID 52-plex assay
E Musgrave-Brown, D Ballard, K Balogh, K Bender, B Berger, M Bogus, ...
Forensic Science International: Genetics 1 (2), 186-190, 2007
992007
Introduction of an single nucleodite polymorphism‐based “Major Y‐chromosome haplogroup typing kit” suitable for predicting the geographical origin of male lineages
M Brión, JJ Sanchez, K Balogh, C Thacker, A Blanco‐Verea, C Børsting, ...
Electrophoresis 26 (23), 4411-4420, 2005
882005
Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome
R Franken, G Teixido-Tura, M Brion, A Forteza, J Rodriguez-Palomares, ...
Heart 103 (22), 1795-1799, 2017
792017
RAS gene polymorphisms, classical risk factors and the advent of coronary artery disease in the Portuguese population
AI Freitas, I Mendonça, M Brión, MM Sequeira, RP Reis, A Carracedo, ...
BMC Cardiovascular Disorders 8 (1), 1-12, 2008
672008
D. Syndercombe-Court, H. Schmitter, B. Stradmann-Bellinghausen, K. Bender, P. Gill, Analysis of artificially degraded DNA using STRs and SNPs–results of a collaborative …
LA Dixon, AE Dobbins, HK Pulker, JM Butler, PM Vallone, MD Coble, ...
Forensic Sci. Int 164 (1), 33-44, 2006
592006
Sarcomeric gene mutations in sudden infant death syndrome (SIDS)
M Brion, C Allegue, M Santori, R Gil, A Blanco-Verea, C Haas, C Bartsch, ...
Forensic science international 219 (1-3), 278-281, 2012
582012
Genetic association study of age‐related macular degeneration in the Spanish population
M Brión, M Sanchez‐Salorio, M Cortón, M de la Fuente, B Pazos, ...
Acta ophthalmologica 89 (1), e12-e22, 2011
562011
A strong genetic association between the tumor necrosis factor locus and proliferative vitreoretinopathy: the retina 4 project
J Rojas, I Fernandez, JC Pastor, MT Garcia-Gutierrez, MR Sanabria, ...
Ophthalmology 117 (12), 2417-2423. e2, 2010
552010
Genetic analysis of arrhythmogenic diseases in the era of NGS: the complexity of clinical decision-making in Brugada syndrome
C Allegue, M Coll, J Mates, O Campuzano, A Iglesias, B Sobrino, M Brion, ...
PloS one 10 (7), e0133037, 2015
512015
Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe
C Capelli, V Onofri, F Brisighelli, I Boschi, F Scarnicci, M Masullo, G Ferri, ...
European journal of human genetics 17 (6), 848-852, 2009
492009
Insights into Iberian population origins through the construction of highly informative Y‐chromosome haplotypes using biallelic markers, STRs, and the MSY1 minisatellite
M Brion, A Salas, A González‐Neira, MV Lareu, A Carracedo
American Journal of Physical Anthropology: The Official Publication of the …, 2003
492003
A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy
J Rojas, I Fernandez, JC Pastor, RE MacLaren, Y Ramkissoon, S Harsum, ...
Investigative ophthalmology & visual science 54 (3), 1665-1678, 2013
482013
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