Publicacións en colaboración con investigadores/as de University of Copenhagen (12)

2021

  1. Association of Rare CYP39A1 Variants with Exfoliation Syndrome Involving the Anterior Chamber of the Eye

    JAMA - Journal of the American Medical Association, Vol. 325, Núm. 8, pp. 753-764

2018

  1. Early human dispersals within the Americas

    Science (New York, N.Y.), Vol. 362, Núm. 6419

2017

  1. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

    Nature Genetics, Vol. 49, Núm. 7, pp. 993-1004

2015

  1. Genome-wide ancestry of 17th-century enslaved Africans from the Caribbean

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 112, Núm. 12, pp. 3669-3673

  2. Mosaic maternal ancestry in the Great Lakes region of East Africa

    Human Genetics, Vol. 134, Núm. 9, pp. 1013-1027

2014

  1. A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

    Forensic Science International: Genetics, Vol. 12, pp. 12-23

  2. DNA Commission of the International Society for Forensic Genetics: Revised and extended guidelines for mitochondrial DNA typing

    Forensic Science International: Genetics, Vol. 13, pp. 134-142

2008

  1. Identification of West Eurasian mitochondrial haplogroups by mtDNA SNP screening: Results of the 2006-2007 EDNAP collaborative exercise

    Forensic Science International: Genetics, Vol. 2, Núm. 1, pp. 61-68

2007

  1. Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs

    Forensic Science International: Genetics, Vol. 1, Núm. 3-4, pp. 273-280

2006

  1. A compact population analysis test using 32 SNPs with highly diverse allele frequency distributions

    International Congress Series, Vol. 1288, pp. 58-60

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

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

2001

  1. Fluorescent SSCP of overlapping fragments (FSSCP-OF): A highly sensitive method for the screening of mitochondrial DNA variation

    Forensic Science International, Vol. 124, Núm. 2-3, pp. 97-103