Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts

被引：0

作者：

Giuliana Giannuzzi

Nicolas Chatron

Katrin Mannik

Chiara Auwerx

Sylvain Pradervand

Gilles Willemin

Kendra Hoekzema

Xander Nuttle

Jacqueline Chrast

Marie C. Sadler

Eleonora Porcu

Yann Herault

Bertrand Isidor

Brigitte Gilbert-Dussardier

Evan E. Eichler

Zoltan Kutalik

Alexandre Reymond

机构：

[1] University of Lausanne,Center for Integrative Genomics

[2] University of Milan,Department of Biosciences

[3] Hospices Civils de Lyon,Service de génétique

[4] University of Lyon,Department of Computational Biology

[5] Université Claude Bernard Lyon 1,Center for Primary Care and Public Health

[6] CNRS UMR-5310,Department of Genome Sciences

[7] INSERM U-1217,Center for Genomic Medicine

[8] Institut NeuroMyoGène,Department of Neurology

[9] University of Lausanne,Howard Hughes Medical Institute

[10] University of Lausanne,Department of Genetic Medicine and Development

[11] Swiss Institute of Bioinformatics,Medical Genetics

[12] University of Washington,Department of Medical Sciences

[13] Massachusetts General Hospital,Department of Clinical and Biological Sciences

[14] Harvard Medical School,undefined

[15] Program in Medical and Population Genetics and Stanley Center for Psychiatric Research,undefined

[16] Broad Institute,undefined

[17] University of Strasbourg,undefined

[18] CNRS,undefined

[19] INSERM,undefined

[20] PHENOMIN-ICS,undefined

[21] Institute of Genetics and Molecular and Cellular Biology,undefined

[22] Service de Génétique Médicale,undefined

[23] CHU de Nantes,undefined

[24] Service de Génétique,undefined

[25] CHU de Poitiers,undefined

[26] University of Washington,undefined

[27] Centre Hospitalier Universitaire Vaudois,undefined

[28] University of Lausanne,undefined

[29] University of Montreal,undefined

[30] University of Geneva Medical School,undefined

[31] Service de Génétique Medicale,undefined

[32] CHU de Caen,undefined

[33] Service de Génétique Clinique,undefined

[34] CHU Paris-GH La Pitié Salpêtrière,undefined

[35] Service de Génétique Clinique,undefined

[36] CHU de Lille,undefined

[37] University of Siena,undefined

[38] University of Turin,undefined

[39] University of Turin,undefined

[40] Health 2030 Genome Center,undefined

[41] Foundation Campus Biotech,undefined

来源：

npj Genomic Medicine | / 8卷

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[1] Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts
Giuliana Giannuzzi
Nicolas Chatron
Katrin Mannik
Chiara Auwerx
Sylvain Pradervand
Gilles Willemin
Kendra Hoekzema
Xander Nuttle
Jacqueline Chrast
Marie C. Sadler
Eleonora Porcu
Yann Herault
Bertrand Isidor
Brigitte Gilbert-Dussardier
Evan E. Eichler
Zoltan Kutalik
Alexandre Reymond
npj Genomic Medicine, 7
[2] 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
NPJ GENOMIC MEDICINE, 2022, 7 (01)
[3] Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts (vol 7, 38, 2022)
Giannuzzi, Giuliana
Chatron, Nicolas
Mannik, Katrin
Auwerx, Chiara
Pradervand, Sylvain
Willemin, Gilles
Hoekzema, Kendra
Nuttle, Xander
Chrast, Jacqueline
Sadler, Marie C.
Porcu, Eleonora
Maennik, Katrin
Herault, Yann
Isidor, Bertrand
Gilbert-Dussardier, Brigitte E.
Eichler, Evan E.
Kutalik, Zoltan
Reymond, Alexandre
NPJ GENOMIC MEDICINE, 2023, 8 (01)
[4] Motor difficulties in 16p11.2 copy number variation
Jutla, Amandeep
Harvey, Loraine
Veenstra-VanderWeele, Jeremy
Chung, Wendy K.
AUTISM RESEARCH, 2024, 17 (05) : 906 - 916
[5] Developmental Trajectories for Young Children With 16p11.2 Copy Number Variation
Bernier, Raphael
Hudac, Caitlin M.
Chen, Qixuan
Zeng, Chubing
Wallace, Arianne Stevens
Gerdts, Jennifer
Earl, Rachel
Peterson, Jessica
Wolken, Anne
Peters, Alana
Hanson, Ellen
Goin-Kochel, Robin P.
Kanne, Stephen
Snyder, LeeAnne Green
Chung, Wendy K.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2017, 174 (04) : 367 - 380
[6] 16P11.2 Copy Number Variations and Neurodevelopmental Disorders
Rein, Benjamin
Yan, Zhen
TRENDS IN NEUROSCIENCES, 2020, 43 (11) : 886 - 901
[7] Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development
Qiu, Yuqi
Arbogast, Thomas
Lorenzo, Sandra Martin
Li, Hongying
Tang, Shih C.
Richardson, Ellen
Hong, Oanh
Cho, Shawn
Shanta, Omar
Pang, Timothy
Corsello, Christina
Deutsch, Curtis K.
Chevalier, Claire
Davis, Erica E.
Iakoucheva, Lilia M.
Herault, Yann
Katsanis, Nicholas
Messer, Karen
Sebat, Jonathan
CELL REPORTS, 2019, 28 (13): : 3320 - +
[8] Copy number variation and brain structure: lessons learned from chromosome 16p11.2
Stein, Jason L.
GENOME MEDICINE, 2015, 7
[9] Copy number variation and brain structure: lessons learned from chromosome 16p11.2
Jason L Stein
Genome Medicine, 7
[10] Altered neurite density and dispersion in the white matter of carriers of 16p11.2 copy number variants
Villalon-Reina, J.
Moreau, C.
Nir, T. M.
Jahanshad, N.
Lippe, S.
Maillard, A.
Romascano, D.
Bodgan, D.
Bearden, C. E.
Thompson, P. M.
Jacquemont, S.
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2020, 40 : S284 - S285

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