Cover, Volume 41, Issue 10,Human Mutation

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Cover, Volume 41, Issue 10
Human Mutation ( IF 3.3 ) Pub Date : 2020-09-28 , DOI: 10.1002/humu.24115
Simranpreet Kaur _{1,

2} , Nicole J. Van Bergen _{1,

2} , Kristen J. Verhey ₃ , Cameron J. Nowell ₄ , Breane Budaitis ₅ , Yang Yue ₃ , Carolyn Ellaway _{6,

7} , Nicola Brunetti‐Pierri _{8,

9} , Gerarda Cappuccio _{8,

9} , Irene Bruno ₁₀ , Lia Boyle ₁₁ , Vincenzo Nigro ₁₀ , Annalaura Torella ₁₀ , Tony Roscioli _{12,

13} , Mark J. Cowley _{14,

15,

16} , Sean Massey ₁ , Rhea Sonawane ₁₇ , Matthew D. Burton ₁₈ , Bitten Schonewolf‐Greulich ₁₉ , Zeynep Tümer ₁₉ , Wendy K. Chung ₂₀ , Wendy A. Gold _{21,

22,

23} , John Christodoulou _{1,

2,

6,

24}

Affiliation

Brain and Mitochondrial Research Group, Murdoch Children's Research Institute Royal Children's Hospital Melbourne Victoria Australia
Department of Paediatrics University of Melbourne Melbourne Victoria Australia
Department of Cell and Developmental Biology University of Michigan Medical School Ann Arbor Michigan
Drug Discover Biology, Monash Institute of Pharmaceutical Sciences Monash University Melbourne Victoria Australia
Cellular and Molecular Biology Program University of Michigan Medical School Ann Arbor Michigan
Discipline of Genomic Medicine, School of Medical Sciences, Faculty of Medicine and Health University of Sydney Sydney New South Wales Australia
Western Sydney Genetics Program Children's Hospital at Westmead Westmead New South Wales Australia
Department of Translational Medicine University of Naples “Federico II” Naples Italy
Telethon Institute of Genetics and Medicine Pozzuoli Italy
Department of Precision Medicine University of Campania “Luigi Vanvitelli” Naples Italy
Division of Molecular Genetics Columbia University Irving Medical Center New York New York
New South Wales Health Pathology Randwick New South Wales Australia
Neuroscience Research Australia University of New South Wales Sydney New South Wales Australia
Kinghorn Centre for Clinical Genomics Garvan Institute of Medical Research Sydney New South Wales Australia
St Vincent's Clinical School UNSW Sydney Sydney New South Wales Australia
Children's Cancer Institute, Lowy Cancer Research Centre UNSW Sydney New South Wales Australia
Faculty of Science, Engineering and Built Environment Deakin University Melbourne Australia
Flow Cytometry and Imaging Facility, Murdoch Children's Research Institute Royal Children's Hospital Melbourne Victoria Australia
Department of Clinical Genetics, Kennedy Center Copenhagen University Hospital, Rigshospitalet Glostrup Denmark
Departments of Paediatrics and Medicine Columbia University Medical Center New York New York
Molecular Neurobiology Research Laboratory, Kids Research Children's Hospital at Westmead, and The Children's Medical Research Institute Westmead New South Wales Australia
Kids Neuroscience Centre, Kids Research Children's Hospital at Westmead Westmead New South Wales Australia
School of Medical Sciences and Discipline of Child and Adolescent Health, Faculty of Medicine and Health The University of Sydney Sydney New South Wales Australia
Victorian Clinical Genetics Services Royal Children's Hospital Melbourne Victoria Australia

The cover image is based on the Research Article Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A) by Simranpreet Kaur et al., https://doi.org/10.1002/humu.24079.