Publicacións en colaboración con investigadores/as de Johannes Gutenberg University of Mainz (31)

2017

  1. ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development

    Scientific Reports, Vol. 7

2014

  1. Ancient human genomes suggest three ancestral populations for present-day Europeans

    Nature, Vol. 513, Núm. 7518, pp. 409-413

2011

  1. Immunogenicity of a combination vaccine containing diphtheria toxoid, tetanus toxoid, three-component acellular pertussis, hepatitis B, inactivated polio virus, and Haemophilus influenzae type b when given concomitantly with 13-valent pneumococcal conjugate vaccine

    Vaccine, Vol. 29, Núm. 35, pp. 6042-6048

2008

  1. Forensic typing of autosomal SNPs with a 29 SNP-multiplex-Results of a collaborative EDNAP exercise

    Forensic Science International: Genetics, Vol. 2, Núm. 3, pp. 176-183

2007

  1. Forensic validation of the SNPforID 52-plex assay

    Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 186-190

2006

  1. A multiplex assay with 52 single nucleotide polymorphisms for human identification

    Electrophoresis, Vol. 27, Núm. 9, pp. 1713-1724

  2. A sensitive issue: Pyrosequencing as a valuable forensic SNP typing platform

    International Congress Series, Vol. 1288, pp. 52-54

  3. Analysis of 29 Y-chromosome SNPs in a single multiplex useful to predict the geographic origin of male lineages

    International Congress Series, Vol. 1288, pp. 13-15

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

    Forensic Science International, Vol. 164, Núm. 1, pp. 33-44

  5. Application of whole genome amplification for forensic analysis

    International Congress Series, Vol. 1288, pp. 725-727

  6. Development of a multiplex PCR assay detecting 52 autosomal SNPs

    International Congress Series, Vol. 1288, pp. 67-69

  7. Mixture analysis using SWaP™ SNPs and non-biallelic SNPs

    International Congress Series, Vol. 1288, pp. 34-36

  8. Rapid microarray-based typing of forensic SNPs

    International Congress Series, Vol. 1288, pp. 37-39

  9. The effect of whole genome amplification on samples originating from more than one donor

    International Congress Series, Vol. 1288, pp. 722-724

2005

  1. Introduction of an single nucleotide polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

    Electrophoresis, Vol. 26, Núm. 23, pp. 4411-4420

2004

  1. Results of a collaborative study of the EDNAP group regarding mitochondrial DNA heteroplasmy and segregation in hair shafts

    Forensic Science International, Vol. 140, Núm. 1, pp. 1-11

  2. The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: Organisation, results and perspectives

    Forensic Science International, Vol. 139, Núm. 2-3, pp. 215-226

  3. Whole genome amplification—the solution for a common problem in forensic casework?

    International Congress Series, Vol. 1261, Núm. C, pp. 24-26

2003

  1. Paternity Testing Commission of the International Society of Forensic Genetics: Recommendations on genetic investigations in paternity cases

    International Journal of Legal Medicine, Vol. 117, Núm. 1, pp. 51-61

2002

  1. Paternity Testing Commission of the International Society of Forensic Genetics: Recommendations on genetic investigations in paternity cases

    Forensic Science International, Vol. 129, Núm. 3, pp. 148-157