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

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

共 50 条

[11] Phenotypic spectrum associated with copy - number variation of chromosome 16p11.2 p12.2 locus [J].

Haltrich, Iren ;

Piko, Henriett ;

Tihanyi, Mariann ;

Toth, Zsuzsa ;

Beke, Artur ;

Karcagi, Veronika ;

Fekete, Gyorgy .

MOLECULAR CYTOGENETICS, 2017, 10

[12] Atypical neural variability in carriers of 16p11.2 copy number variants [J].

Al-Jawahiri, Reem ;

Jones, Myles ;

Milne, Elizabeth .

AUTISM RESEARCH, 2019, 12 (09) :1322-1333

[13] Psychotic symptoms in 16p11.2 copy-number variant carriers [J].

Jutla, Amandeep ;

Turner, J. Blake ;

Snyder, LeeAnne Green ;

Chung, Wendy K. ;

Veenstra-VanderWeele, Jeremy .

AUTISM RESEARCH, 2020, 13 (02) :187-198

[14] Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia [J].

Ida E. Sønderby ;

Ómar Gústafsson ;

Nhat Trung Doan ;

Derrek P. Hibar ;

Sandra Martin-Brevet ;

Abdel Abdellaoui ;

David Ames ;

Katrin Amunts ;

Michael Andersson ;

Nicola J. Armstrong ;

Manon Bernard ;

Nicholas Blackburn ;

John Blangero ;

Dorret I. Boomsma ;

Janita Bralten ;

Hans-Richard Brattbak ;

Henry Brodaty ;

Rachel M. Brouwer ;

Robin Bülow ;

Vince Calhoun ;

Svenja Caspers ;

Gianpiero Cavalleri ;

Chi-Hua Chen ;

Sven Cichon ;

Simone Ciufolini ;

Aiden Corvin ;

Benedicto Crespo-Facorro ;

Joanne E. Curran ;

Anders M. Dale ;

Shareefa Dalvie ;

Paola Dazzan ;

Eco J. C. de Geus ;

Greig I. de Zubicaray ;

Sonja M. C. de Zwarte ;

Norman Delanty ;

Anouk den Braber ;

Sylvane Desrivières ;

Gary Donohoe ;

Bogdan Draganski ;

Stefan Ehrlich ;

Thomas Espeseth ;

Simon E. Fisher ;

Barbara Franke ;

Vincent Frouin ;

Masaki Fukunaga ;

Thomas Gareau ;

David C. Glahn ;

Hans Grabe ;

Nynke A. Groenewold ;

Jan Haavik .

Molecular Psychiatry, 2020, 25 :692-695

[15] The use of pyrosequencing to identify copy number variation of 16p11.2 in euchromatic variant carriers and the normal population [J].

Hall, Victoria ;

Maloney, V. K. ;

White, H. ;

Liehr, T. ;

Volleth, M. ;

Barber, J. C. K. .

JOURNAL OF MEDICAL GENETICS, 2006, 43 :S98-S98

[16] Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2 [J].

Owen, Julia P. ;

Bukshpun, Polina ;

Pojman, Nicholas ;

Thieu, Tony ;

Chen, Qixuan ;

Lee, Jihui ;

D'Angelo, Debra ;

Glenn, Orit A. ;

Hunter, Jill V. ;

Berman, Jeffrey I. ;

Roberts, Timothy P. ;

Buckner, Randy ;

Nagarajan, Srikantan S. ;

Mukherjee, Pratik ;

Sherr, Elliott H. .

RADIOLOGY, 2018, 286 (01) :217-226

[17] Phenotypic differences in facial features of individuals with the 16p11.2 copy number variant [J].

Pang, Tim .

BEHAVIOR GENETICS, 2015, 45 (06) :678-678

[18] Phenotypes Associated with 16p11.2 Copy Number Gains and Losses at a Single Institution [J].

Chu, Caleb ;

Wu, Haotian ;

Xu, Fangling ;

Ray, Joseph W. ;

Britt, Allison ;

Robinson, Sally S. ;

Lupo, Pamela J. ;

Murphy, Christine R. C. ;

Dreyer, Charles F. ;

Lee, Phillip D. K. ;

Hu, Peter C. ;

Dong, Jianli .

LABORATORY MEDICINE, 2020, 51 (06) :642-648

[19] Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations [J].

Cardenas-de-la-Parra, Alonso ;

Martin-Brevet, Sandra ;

Moreau, Clara ;

Rodriguez-Herreros, Borja ;

Fonov, Vladimir S. ;

Maillard, Anne M. ;

Zurcher, Nicole R. ;

Hadjikhani, Nouchine ;

Beckmann, Jacques S. ;

Reymond, Alexandre ;

Draganski, Bogdan ;

Jacquemont, Sebastien ;

Collins, D. Louis .

NEUROIMAGE, 2019, 203

[20] Evaluation of the 16p11.2 proximal copy number variants in patients with neurodevelopmental disorders [J].

Pohovski, Leona Morozin ;

Measic, Ana-Maria ;

Bobinec, Adriana ;

Sansovic, Ivona ;

Vulin, Katarina ;

Odak, Ljubica ;

Kero, Mijana ;

Lozic, Bernarda ;

Puseljic, Silvija ;

Tomac, Visnja .

EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 :464-465

← 1 2 3 4 5 →