Publikationen in Zusammenarbeit mit Forschern von University of Copenhagen (23)

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

2019

  1. Development and validation of the EUROFORGEN NAME (North African and Middle Eastern) ancestry panel

    Forensic Science International: Genetics, Vol. 42, pp. 260-267

2018

  1. Early human dispersals within the Americas

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

  2. Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

    Forensic Science International: Genetics, Vol. 37, pp. 241-251

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

2016

  1. Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™

    Forensic Science International: Genetics, Vol. 23, pp. 178-189

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. Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set

    Forensic Science International: Genetics, Vol. 11, Núm. 1, pp. 13-25

  3. 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

  4. Euroforgen-NoE collaborative exercise on LRmix to demonstrate standardization of the interpretation of complex DNA profiles

    Forensic Science International: Genetics, Vol. 9, Núm. 1, pp. 47-54

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

2004

  1. Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications

    Forensic Science International, Vol. 140, Núm. 2-3, pp. 241-250

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

1999

  1. Results of a collaborative study regarding the standardization of the Y-linked STR system DYS385 by the European DNA Profiling (EDNAP) group

    Forensic Science International, Vol. 102, Núm. 2-3, pp. 159-165

1998

  1. Report of the European DNA profiling group (EDNAP)-an investigation of the hypervariable STR loci ACTBP2, APOAI1 and D11S554 and the compound loci D12S391 and D1S1656

    Forensic Science International, Vol. 98, Núm. 3, pp. 193-200