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Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

Author

Listed:
  • Xander Nuttle

    (University of Washington School of Medicine)

  • Giuliana Giannuzzi

    (Center for Integrative Genomics, University of Lausanne)

  • Michael H. Duyzend

    (University of Washington School of Medicine)

  • Joshua G. Schraiber

    (University of Washington School of Medicine)

  • Iñigo Narvaiza

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Peter H. Sudmant

    (University of Washington School of Medicine
    †Present address: Program in Computational and Systems Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.)

  • Osnat Penn

    (University of Washington School of Medicine)

  • Giorgia Chiatante

    (Università degli Studi di Bari ‘Aldo Moro’)

  • Maika Malig

    (University of Washington School of Medicine)

  • John Huddleston

    (University of Washington School of Medicine
    Howard Hughes Medical Institute)

  • Chris Benner

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Francesca Camponeschi

    (University of Florence)

  • Simone Ciofi-Baffoni

    (University of Florence
    Magnetic Resonance Center CERM, University of Florence)

  • Holly A. F. Stessman

    (University of Washington School of Medicine)

  • Maria C. N. Marchetto

    (Laboratory of Genetics, The Salk Institute for Biological Studies)

  • Laura Denman

    (University of Washington School of Medicine)

  • Lana Harshman

    (University of Washington School of Medicine)

  • Carl Baker

    (University of Washington School of Medicine)

  • Archana Raja

    (University of Washington School of Medicine
    Howard Hughes Medical Institute)

  • Kelsi Penewit

    (University of Washington School of Medicine)

  • Nicolette Janke

    (University of Washington School of Medicine)

  • W. Joyce Tang

    (Benaroya Research Institute at Virginia Mason)

  • Mario Ventura

    (Università degli Studi di Bari ‘Aldo Moro’)

  • Lucia Banci

    (University of Florence
    Magnetic Resonance Center CERM, University of Florence)

  • Francesca Antonacci

    (Università degli Studi di Bari ‘Aldo Moro’)

  • Joshua M. Akey

    (University of Washington School of Medicine)

  • Chris T. Amemiya

    (Benaroya Research Institute at Virginia Mason)

  • Fred H. Gage

    (Laboratory of Genetics, The Salk Institute for Biological Studies
    Center for Academic Research and Training in Anthropogeny (CARTA), 9500 Gilman Drive)

  • Alexandre Reymond

    (Center for Integrative Genomics, University of Lausanne)

  • Evan E. Eichler

    (University of Washington School of Medicine
    Howard Hughes Medical Institute)

Abstract

Reconstruction of the evolutionary history of the chromosome 16p11.2 locus and identification of bolA family member 2 (BOLA2) as a gene duplicated exclusively in Homo sapiens.

Suggested Citation

  • Xander Nuttle & Giuliana Giannuzzi & Michael H. Duyzend & Joshua G. Schraiber & Iñigo Narvaiza & Peter H. Sudmant & Osnat Penn & Giorgia Chiatante & Maika Malig & John Huddleston & Chris Benner & Fran, 2016. "Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility," Nature, Nature, vol. 536(7615), pages 205-209, August.
    • Handle: RePEc:nat:nature:v:536:y:2016:i:7615:d:10.1038_nature19075
    DOI: 10.1038/nature19075
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