Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications-Reference-Cited by-同舟云学术

Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications

Published:2019-11-15 Issue:1 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Myers Lynnea¹,Blyth Moira²,Moradkhani Kamran³,Hranilović Dubravka⁴,Polesie Sam⁵⁶,Isaksson Johan¹⁷,Nordgren Ann⁸⁹,Bucan Maja¹⁰,Vincent Marie¹¹,Bölte Sven¹¹²,Anderlid Britt‐Marie⁸⁹,Tammimies Kristiina¹^ORCID

Affiliation:

1. Center of Neurodevelopmental Disorders (KIND) Centre for Psychiatry Research Department of Women’s and Children’s Health Karolinska Institutet & Child and Adolescent Psychiatry Stockholm Health Care Services Stockholm County Council Stockholm Sweden

2. Department of Clinical Genetics Chapel Allerton Hospital Leeds UK

3. CHU Nantes Service de Génétique Médicale Nantes France

4. Department of Biology Faculty of Science University of Zagreb Zagreb Croatia

5. Department of Dermatology and Venereology Institute of Clinical Sciences Sahlgrenska Academy University of Gothenburg Gothenburg Sweden

6. Department of Dermatology and Venereology Region Västra Götaland Sahlgrenska University Hospital Gothenburg Sweden

7. Department of Neuroscience, Child and Adolescent Psychiatry and Psychiatry Unit Uppsala University Uppsala Sweden

8. Department of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden

9. Department of Clinical Genetics Karolinska University Hospital Stockholm Sweden

10. Department of Genetics and Psychiatry Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

11. Centre Hospitalier University of Nantes Nantes France

12. Curtin Autism Research Group School of Occupational Therapy, Social Work and Speech Pathology Curtin University Perth Western Australia Australia

Funder

Hjärnfonden

Åke Wiberg Stiftelse

Vetenskapsrådet

Stiftelsen för Strategisk Forskning

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1013

Reference37 articles.

1. A family with a 1.17 Mb deletion of 12q12: Refining genotype-phenotype correlation

2. The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

3. Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype

4. Haploinsufficiency ofANO6, NELL2andDBX2in a boy with intellectual disability and growth delay

5. DNA deletion and duplication and the associated genetic disorders;Clancy S.;Nature Education,2008

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Guest editorial: Overview, implications, and directions of twin design research exploring neurodevelopmental conditions;JCPP Advances;2022-11-17

2. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System—A Close Look at Chromosome 15;International Journal of Molecular Sciences;2020-03-09