Epigenetics and genomics in Turner syndrome-Reference-Cited by-同舟云学术

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Epigenetics and genomics in Turner syndrome

Published:2019-02-27 Issue:1 Volume:181 Page:125-132
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Viuff Mette¹²,Skakkebæk Anne¹³,Nielsen Morten M.²,Chang Simon¹⁴,Gravholt Claus H.¹²^ORCID

Affiliation:

1. Department of Endocrinology and Internal Medicine (MEA)Aarhus University Hospital Aarhus Denmark

2. Department of Molecular MedicineAarhus University Hospital Aarhus Denmark

3. Department of Clinical GeneticsAarhus University Hospital Aarhus Denmark

4. Department of Clinical BiochemistryEsbjerg Sygehus Denmark

Funder

Aarhus Universitet

Aase og Ejnar Danielsens Fond

Augustinus Fonden

Familien Hede Nielsens Fond

Fonden til Lægevidenskabens Fremme

Lundbeckfonden

Novo Nordisk Fonden

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31683

Reference82 articles.

1. Genomic imprinting: recognition and marking of imprinted loci

2. Chromosome Imbalance as a Driver of Sex Disparity in Disease

3. Epigenetics in Turner syndrome

4. The importance of having two X chromosomes

5. X-Chromosome Gene Dosage and the Risk of Diabetes in Turner Syndrome

Cited by 42 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. Visual Impairment in Women with Turner Syndrome—A 49-Year Literature Review;Journal of Clinical Medicine;2024-09-13

2. Clinical practice guidelines for the care of girls and women with Turner syndrome;European Journal of Endocrinology;2024-05-15

3. Heritable thoracic aortic disease: a literature review on genetic aortopathies and current surgical management;General Thoracic and Cardiovascular Surgery;2024-03-14

4. Methodological advances in patient-centered rare disease research: the UTHealth Houston Turner Syndrome Society of the United States research registry;Orphanet Journal of Rare Diseases;2024-03-11

5. The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development;2024-03-04

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