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Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.
Giannuzzi, Giuliana; Chatron, Nicolas; Mannik, Katrin; Auwerx, Chiara; Pradervand, Sylvain; Willemin, Gilles; Hoekzema, Kendra; Nuttle, Xander; Chrast, Jacqueline; Sadler, Marie C; Porcu, Eleonora; Herault, Yann; Isidor, Bertrand; Gilbert-Dussardier, Brigitte; Eichler, Evan E; Kutalik, Zoltan; Reymond, Alexandre.
Afiliação
  • Giannuzzi G; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. giuliana.giannuzzi@unimi.it.
  • Chatron N; Department of Biosciences, University of Milan, Milan, Italy. giuliana.giannuzzi@unimi.it.
  • Mannik K; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Auwerx C; Service de génétique, Hospices Civils de Lyon, Lyon, France.
  • Pradervand S; University of Lyon, Université Claude Bernard Lyon 1, CNRS UMR-5310, INSERM U-1217, Institut NeuroMyoGène, F-69008, Lyon, France.
  • Willemin G; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Hoekzema K; Health 2030 Genome Center, Foundation Campus Biotech, Geneva, Switzerland.
  • Nuttle X; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Chrast J; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
  • Sadler MC; Center for Primary Care and Public Health, University of Lausanne, Lausanne, Switzerland.
  • Porcu E; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  • Herault Y; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Isidor B; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Gilbert-Dussardier B; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Eichler EE; Department of Neurology, Harvard Medical School, Boston, MA, USA.
  • Kutalik Z; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA, USA.
  • Reymond A; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
NPJ Genom Med ; 8(1): 9, 2023 May 24.
Article em En | MEDLINE | ID: mdl-37225732
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: NPJ Genom Med Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: NPJ Genom Med Ano de publicação: 2023 Tipo de documento: Article