Special Issue “Genetics and Epigenetics in Endocrine Disorders”-Reference-Cited by-同舟云学术

Special Issue “Genetics and Epigenetics in Endocrine Disorders”

Published:2023-09-05 Issue:9 Volume:14 Page:1763
ISSN:2073-4425
Container-title:Genes
language:en
Short-container-title:Genes

Author:

Trebušak Podkrajšek Katarina¹²^ORCID,Kotnik Primož³⁴^ORCID

Affiliation:

1. Laboratory for Translational Medical Biochemistry, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia

2. Clinical Institute for Special Laboratory Diagnostics, University Children’s Hospital, University Medical Centre Ljubljana, Vrazov trg 1, 1000 Ljubljana, Slovenia

3. Department of Endocrinology, Diabetes, and Metabolic Diseases, University Children’s Hospital, University Medical Centre Ljubljana, Bohoriceva Ulica 20, 1000 Ljubljana, Slovenia

4. Chair of Pediatrics, Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia

Abstract

In the last decade, the development of high-throughput sequencing methodologies has significantly improved the gathering of genomic information and consequent under-standing of the genetic and epigenetic background of complex and monogenetic endocrine disorders [...]

Funder

Slovenian Research Agency

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Link

https://www.mdpi.com/2073-4425/14/9/1763/pdf

Reference10 articles.

1. Zajec, A., Trebušak Podkrajšek, K., Tesovnik, T., Šket, R., Čugalj Kern, B., Jenko Bizjan, B., Šmigoc Schweiger, D., Battelino, T., and Kovač, J. (2022). Pathogenesis of Type 1 Diabetes: Established Facts and New Insights. Genes, 13.

2. Lee, C.-M., Yang, Y.-S., Kornelius, E., Huang, C.-N., Hsu, M.-Y., Lee, C.-Y., Peng, S.-Y., and Yang, S.-F. (2022). Association of Long Non-Coding RNA Growth Arrest-Specific 5 Genetic Variants with Diabetic Retinopathy. Genes, 13.

3. Al-Adsani, A.M., Al-Otaibi, A.N., Barhoush, S.A., Al-Qattan, K.K., and Al-Bustan, S.A. (2022). Expression Profiling of Pdx1, Ngn3, and MafA in the Liver and Pancreas of Recovering Streptozotocin-Induced Diabetic Rats. Genes, 13.

4. Hassan, S.S., Abdullah, M., Podkrajsek, K.T., Musa, S., Ibrahim, A., Babiker, O., Kovac, J., Battelino, T., and Stefanija, M.A. (2022). A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees. Genes, 13.

5. Stritar, J., Stavber, L., Ficko, M., Kotnik, P., Battelino, T., Podkrajšek, K.T., and Hovnik, T. (2021). Detection of del/dup inside shox/par1 region in children and young adults with idiopathic short stature. Genes, 12.