OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Sex chromosome aneuploidies give rise to changes in the circular RNA profile: A circular transcriptome-wide study of Turner and Klinefelter syndrome across different tissues
Emma B. Johannsen, Jesper Just, Mette Viuff, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 18
Emma B. Johannsen, Jesper Just, Mette Viuff, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 18
Showing 18 citing articles:
Clinical practice guidelines for the care of girls and women with Turner syndrome
Claus Højbjerg Gravholt, N.H. Andersen, Sophie Christin‐Maître, et al.
European Journal of Endocrinology (2024) Vol. 190, Iss. 6, pp. G53-G151
Open Access | Times Cited: 46
Claus Højbjerg Gravholt, N.H. Andersen, Sophie Christin‐Maître, et al.
European Journal of Endocrinology (2024) Vol. 190, Iss. 6, pp. G53-G151
Open Access | Times Cited: 46
Elevated levels of neutrophils with a pro-inflammatory profile in Turner syndrome across karyotypes
Jesper Just, Lukas Ochsner Ridder, Emma B. Johannsen, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 1
Jesper Just, Lukas Ochsner Ridder, Emma B. Johannsen, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 1
The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development
Jenifer P. Suntharalingham, Ignacio del Valle, Federica Buonocore, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access | Times Cited: 1
Jenifer P. Suntharalingham, Ignacio del Valle, Federica Buonocore, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access | Times Cited: 1
X chromosome dosage and the genetic impact across human tissues
Mette Viuff, Anne Skakkebæk, Emma B. Johannsen, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 22
Mette Viuff, Anne Skakkebæk, Emma B. Johannsen, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 22
Sex-Chromosome Abnormalities
Claus Højbjerg Gravholt
Elsevier eBooks (2024), pp. 139-178
Closed Access | Times Cited: 4
Claus Højbjerg Gravholt
Elsevier eBooks (2024), pp. 139-178
Closed Access | Times Cited: 4
Non‐Invasive Prenatal Testing by Cell‐Free DNA (cfNIPT ) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal Outcomes
Ivonne Bedei, Johanna Bruder, Ida Charlotte Bay Lund, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2025)
Open Access
Ivonne Bedei, Johanna Bruder, Ida Charlotte Bay Lund, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2025)
Open Access
More than the SRY: The Non-Coding Landscape of the Y Chromosome and Its Importance in Human Disease
Emily S Rice, Michael T. Winters, Travis W. Rawson, et al.
Non-Coding RNA (2024) Vol. 10, Iss. 2, pp. 21-21
Open Access | Times Cited: 2
Emily S Rice, Michael T. Winters, Travis W. Rawson, et al.
Non-Coding RNA (2024) Vol. 10, Iss. 2, pp. 21-21
Open Access | Times Cited: 2
Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome
Ivonne Bedei, Karl‐Philipp Gloning, Luc Joyeux, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 2, pp. 183-191
Open Access | Times Cited: 6
Ivonne Bedei, Karl‐Philipp Gloning, Luc Joyeux, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 2, pp. 183-191
Open Access | Times Cited: 6
New developments and future trajectories in supernumerary sex chromosome abnormalities: a summary of the 2022 3rd International Workshop on Klinefelter Syndrome, Trisomy X, and XYY
Claus Højbjerg Gravholt, Alberto Ferlin, Joerg Gromoll, et al.
Endocrine Connections (2023) Vol. 12, Iss. 3
Open Access | Times Cited: 5
Claus Højbjerg Gravholt, Alberto Ferlin, Joerg Gromoll, et al.
Endocrine Connections (2023) Vol. 12, Iss. 3
Open Access | Times Cited: 5
Individuals with numerical and structural variations of sex chromosomes: interdisciplinary management with focus on fertility potential
Anders Juul, Claus Højbjerg Gravholt, Michel De Vos, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 5
Anders Juul, Claus Højbjerg Gravholt, Michel De Vos, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 5
The multi-omic landscape of sex chromosome abnormalities: current status and future directions
Helene Bandsholm Leere Tallaksen, Emma B. Johannsen, Jesper Just, et al.
Endocrine Connections (2023) Vol. 12, Iss. 9
Open Access | Times Cited: 5
Helene Bandsholm Leere Tallaksen, Emma B. Johannsen, Jesper Just, et al.
Endocrine Connections (2023) Vol. 12, Iss. 9
Open Access | Times Cited: 5
Dosage of the pseudoautosomal gene SLC25A6 is implicated in QTc interval duration
Anne Skakkebæk, Kasper Kjær-Sørensen, Vladimir V. Matchkov, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 5
Anne Skakkebæk, Kasper Kjær-Sørensen, Vladimir V. Matchkov, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 5
Analysis of genetic variability in Turner syndrome linked to long-term clinical features
Jenifer P. Suntharalingham, Miho Ishida, Antoinette Cameron‐Pimblett, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 5
Jenifer P. Suntharalingham, Miho Ishida, Antoinette Cameron‐Pimblett, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 5
The testicular microvasculature in Klinefelter syndrome is immature with compromised integrity and characterized by excessive inflammatory cross-talk
Emma B. Johannsen, Anne Skakkebæk, Joanna Kalucka, et al.
Human Reproduction (2023) Vol. 38, Iss. 12, pp. 2339-2349
Open Access | Times Cited: 3
Emma B. Johannsen, Anne Skakkebæk, Joanna Kalucka, et al.
Human Reproduction (2023) Vol. 38, Iss. 12, pp. 2339-2349
Open Access | Times Cited: 3
Turner syndrome: fertility counselling in childhood and through the reproductive lifespan
Kassie Jean Bollig, Monica Mainigi, Suneeta Senapati, et al.
Current Opinion in Endocrinology Diabetes and Obesity (2022) Vol. 30, Iss. 1, pp. 16-26
Closed Access | Times Cited: 5
Kassie Jean Bollig, Monica Mainigi, Suneeta Senapati, et al.
Current Opinion in Endocrinology Diabetes and Obesity (2022) Vol. 30, Iss. 1, pp. 16-26
Closed Access | Times Cited: 5
The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development
Jenifer P. Suntharalingham, Ignacio del Valle, Federica Buonocore, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Jenifer P. Suntharalingham, Ignacio del Valle, Federica Buonocore, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
X chromosome rearrangement associated with premature ovarian insufficiency as diagnosed by molecular cytogenetic methods: a case report and review of the literature
Zhifang Peng, Renqi Yang, Qing Liu, et al.
Molecular Cytogenetics (2024) Vol. 17, Iss. 1
Open Access
Zhifang Peng, Renqi Yang, Qing Liu, et al.
Molecular Cytogenetics (2024) Vol. 17, Iss. 1
Open Access
Non-coding rnas in Turner syndrome: a systematic review
Júlio César Carvalho de Oliveira, Eldevan da Silva Barbosa, Nathaniel Batista Silva, et al.
Revista Paulista de Pediatria (2024) Vol. 43
Closed Access
Júlio César Carvalho de Oliveira, Eldevan da Silva Barbosa, Nathaniel Batista Silva, et al.
Revista Paulista de Pediatria (2024) Vol. 43
Closed Access
