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Items: 11

1.

A Novel Calsequestrin 2 Deletion Causing Catecholaminergic Polymorphic Ventricular Tachycardia and Sudden Cardiac Death.

Blanco-Verea A, Ramos-Luis E, García-Seara J, Carracedo Á, González-Juanatey JR, Brion M.

Rev Esp Cardiol (Engl Ed). 2018 Aug 20. pii: S1885-5857(18)30313-X. doi: 10.1016/j.rec.2018.07.005. [Epub ahead of print] English, Spanish. No abstract available.

PMID:
30139651
2.

CD19+ B-Cells, a New Biomarker of Mortality in Hemodialysis Patients.

Molina M, Allende LM, Ramos LE, Gutiérrez E, Pleguezuelo DE, Hernández ER, Ríos F, Fernández C, Praga M, Morales E.

Front Immunol. 2018 Jun 15;9:1221. doi: 10.3389/fimmu.2018.01221. eCollection 2018.

3.

Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.

Gago-Díaz M, Ramos-Luis E, Zoppis S, Zorio E, Molina P, Braza-Boïls A, Giner J, Sobrino B, Amigo J, Blanco-Verea A, Carracedo Á, Brion M.

Int J Legal Med. 2017 Sep;131(5):1211-1219. doi: 10.1007/s00414-017-1583-9. Epub 2017 Apr 8.

PMID:
28391405
4.

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders.

Brion M, Blanco-Verea A, Sobrino B, Santori M, Gil R, Ramos-Luis E, Martinez M, Amigo J, Carracedo A.

Electrophoresis. 2014 Nov;35(21-22):3111-6. doi: 10.1002/elps.201400148. Epub 2014 Aug 6.

PMID:
24981977
5.

Y-chromosomal DNA analysis in French male lineages.

Ramos-Luis E, Blanco-Verea A, Brión M, Van Huffel V, Sánchez-Diz P, Carracedo A.

Forensic Sci Int Genet. 2014 Mar;9:162-8. doi: 10.1016/j.fsigen.2013.12.008. Epub 2013 Dec 29.

PMID:
24528594
6.

Evidence of pre-Roman tribal genetic structure in Basques from uniparentally inherited markers.

Martínez-Cruz B, Harmant C, Platt DE, Haak W, Manry J, Ramos-Luis E, Soria-Hernanz DF, Bauduer F, Salaberria J, Oyharçabal B, Quintana-Murci L, Comas D; Genographic Consortium.

Mol Biol Evol. 2012 Sep;29(9):2211-22. Epub 2012 Mar 12.

PMID:
22411853
7.

The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269.

Busby GB, Brisighelli F, Sánchez-Diz P, Ramos-Luis E, Martinez-Cadenas C, Thomas MG, Bradley DG, Gusmão L, Winney B, Bodmer W, Vennemann M, Coia V, Scarnicci F, Tofanelli S, Vona G, Ploski R, Vecchiotti C, Zemunik T, Rudan I, Karachanak S, Toncheva D, Anagnostou P, Ferri G, Rapone C, Hervig T, Moen T, Wilson JF, Capelli C.

Proc Biol Sci. 2012 Mar 7;279(1730):884-92. doi: 10.1098/rspb.2011.1044. Epub 2011 Aug 24.

8.

Forensic validation of the SNPforID 52-plex assay.

Musgrave-Brown E, Ballard D, Balogh K, Bender K, Berger B, Bogus M, Børsting C, Brion M, Fondevila M, Harrison C, Oguzturun C, Parson W, Phillips C, Proff C, Ramos-Luis E, Sanchez JJ, Sánchez Diz P, Sobrino Rey B, Stradmann-Bellinghausen B, Thacker C, Carracedo A, Morling N, Scheithauer R, Schneider PM, Syndercombe Court D.

Forensic Sci Int Genet. 2007 Jun;1(2):186-90. doi: 10.1016/j.fsigen.2007.01.004. Epub 2007 Mar 6.

PMID:
19083753
9.

Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel.

Phillips C, Fang R, Ballard D, Fondevila M, Harrison C, Hyland F, Musgrave-Brown E, Proff C, Ramos-Luis E, Sobrino B, Carracedo A, Furtado MR, Syndercombe Court D, Schneider PM; SNPforID Consortium.

Forensic Sci Int Genet. 2007 Jun;1(2):180-5. doi: 10.1016/j.fsigen.2007.02.007. Epub 2007 Mar 23.

PMID:
19083752
10.

Analysis of artificially degraded DNA using STRs and SNPs--results of a collaborative European (EDNAP) exercise.

Dixon LA, Dobbins AE, Pulker HK, Butler JM, Vallone PM, Coble MD, Parson W, Berger B, Grubwieser P, Mogensen HS, Morling N, Nielsen K, Sanchez JJ, Petkovski E, Carracedo A, Sanchez-Diz P, Ramos-Luis E, Briōn M, Irwin JA, Just RS, Loreille O, Parsons TJ, Syndercombe-Court D, Schmitter H, Stradmann-Bellinghausen B, Bender K, Gill P.

Forensic Sci Int. 2006 Dec 1;164(1):33-44. Epub 2005 Dec 15.

PMID:
16343834
11.

Mutation rates at Y chromosome specific microsatellites.

Gusmão L, Sánchez-Diz P, Calafell F, Martín P, Alonso CA, Alvarez-Fernández F, Alves C, Borjas-Fajardo L, Bozzo WR, Bravo ML, Builes JJ, Capilla J, Carvalho M, Castillo C, Catanesi CI, Corach D, Di Lonardo AM, Espinheira R, Fagundes de Carvalho E, Farfán MJ, Figueiredo HP, Gomes I, Lojo MM, Marino M, Pinheiro MF, Pontes ML, Prieto V, Ramos-Luis E, Riancho JA, Souza Góes AC, Santapa OA, Sumita DR, Vallejo G, Vidal Rioja L, Vide MC, Vieira da Silva CI, Whittle MR, Zabala W, Zarrabeitia MT, Alonso A, Carracedo A, Amorim A.

Hum Mutat. 2005 Dec;26(6):520-8.

PMID:
16220553

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