Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts
NPJ Genom Med
.
2023 May 24;8(1):9.
doi: 10.1038/s41525-023-00354-z.
Authors
Giuliana Giannuzzi
1
2
,
Nicolas Chatron
3
4
5
,
Katrin Mannik
3
6
,
Chiara Auwerx
3
7
8
9
,
Sylvain Pradervand
3
,
Gilles Willemin
3
,
Kendra Hoekzema
10
,
Xander Nuttle
11
12
13
,
Jacqueline Chrast
3
,
Marie C Sadler
7
8
9
,
Eleonora Porcu
3
8
9
;
16p11.2 Consortium
;
Yann Herault
14
,
Bertrand Isidor
15
,
Brigitte Gilbert-Dussardier
16
,
Evan E Eichler
10
17
,
Zoltan Kutalik
7
8
9
,
Alexandre Reymond
3
Collaborators
16p11.2 Consortium
:
Katrin Männik
,
Damien Sanlaville
,
Caroline Schluth-Bolard
,
Cédric Le Caignec
,
Mathilde Nizon
,
Sandra Martin
,
Sébastien Jacquemont
,
Armand Bottani
,
Marion Gérard
,
Sacha Weber
,
Aurélia Jacquette
,
Catherine Vincent-Delorme
,
Aurora Currò
,
Francesca Mari
,
Alessandra Renieri
,
Alfredo Brusco
,
Giovanni Battista Ferrero
Affiliations
1
Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. giuliana.giannuzzi@unimi.it.
2
Department of Biosciences, University of Milan, Milan, Italy. giuliana.giannuzzi@unimi.it.
3
Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
4
Service de génétique, Hospices Civils de Lyon, Lyon, France.
5
University of Lyon, Université Claude Bernard Lyon 1, CNRS UMR-5310, INSERM U-1217, Institut NeuroMyoGène, F-69008, Lyon, France.
6
Health 2030 Genome Center, Foundation Campus Biotech, Geneva, Switzerland.
7
Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
8
Center for Primary Care and Public Health, University of Lausanne, Lausanne, Switzerland.
9
Swiss Institute of Bioinformatics, Lausanne, Switzerland.
10
Department of Genome Sciences, University of Washington, Seattle, WA, USA.
11
Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
12
Department of Neurology, Harvard Medical School, Boston, MA, USA.
13
Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA, USA.
14
University of Strasbourg, CNRS, INSERM, PHENOMIN-ICS, Institute of Genetics and Molecular and Cellular Biology, Illkirch, France.
15
Service de Génétique Médicale, CHU de Nantes, Nantes, France.
16
Service de Génétique, CHU de Poitiers, Poitiers, France.
17
Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.
PMID:
37225732
PMCID:
PMC10209113
DOI:
10.1038/s41525-023-00354-z
No abstract available
Publication types
Published Erratum