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:
The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes
William Davies
European Journal of Medical Genetics (2021) Vol. 64, Iss. 4, pp. 104169-104169
Open Access | Times Cited: 8
William Davies
European Journal of Medical Genetics (2021) Vol. 64, Iss. 4, pp. 104169-104169
Open Access | Times Cited: 8
Showing 8 citing articles:
Organ Abnormalities Caused by Turner Syndrome
Sang Hoon Yoon, Ga Yeon Kim, Gyu Tae Choi, et al.
Cells (2023) Vol. 12, Iss. 10, pp. 1365-1365
Open Access | Times Cited: 16
Sang Hoon Yoon, Ga Yeon Kim, Gyu Tae Choi, et al.
Cells (2023) Vol. 12, Iss. 10, pp. 1365-1365
Open Access | Times Cited: 16
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report
Ingrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, et al.
The Italian Journal of Pediatrics/Italian journal of pediatrics (2022) Vol. 48, Iss. 1
Open Access | Times Cited: 15
Ingrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, et al.
The Italian Journal of Pediatrics/Italian journal of pediatrics (2022) Vol. 48, Iss. 1
Open Access | Times Cited: 15
Sex-linked genetic mechanisms and atrial fibrillation risk
Georgina H. Wren, William Davies
European Journal of Medical Genetics (2022) Vol. 65, Iss. 4, pp. 104459-104459
Open Access | Times Cited: 10
Georgina H. Wren, William Davies
European Journal of Medical Genetics (2022) Vol. 65, Iss. 4, pp. 104459-104459
Open Access | Times Cited: 10
The good, the bad, and the ugly: Evolutionary and pathological aspects of gene dosage alterations
M. Felicia Basilicata, Claudia Isabelle Keller Valsecchi
PLoS Genetics (2021) Vol. 17, Iss. 12, pp. e1009906-e1009906
Open Access | Times Cited: 13
M. Felicia Basilicata, Claudia Isabelle Keller Valsecchi
PLoS Genetics (2021) Vol. 17, Iss. 12, pp. e1009906-e1009906
Open Access | Times Cited: 13
Turner Syndrome: An Update Review
Jahangir Alam, Devarakonda Shalini
International Journal of Innovative Science and Research Technology (IJISRT) (2024), pp. 3640-3645
Open Access | Times Cited: 1
Jahangir Alam, Devarakonda Shalini
International Journal of Innovative Science and Research Technology (IJISRT) (2024), pp. 3640-3645
Open Access | Times Cited: 1
Xp22.31 copy number variations in 87 fetuses: refined genotype–phenotype correlations by prenatal and postnatal follow-up
Huamei Hu, Yulin Huang, Renke Hou, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Huamei Hu, Yulin Huang, Renke Hou, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Integrative epigenome profiling of 47XXY provides insights into whole genomic DNA hypermethylation and active chromatin accessibility
Nan Miao, Zhiwei Zeng, Trevor Lee, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 1
Nan Miao, Zhiwei Zeng, Trevor Lee, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 1
Prenatally detected six duplications at Xp22.33-p11.22: a case report
Xue Zhang, Jian Li, Lan Zhang, et al.
BMC Pregnancy and Childbirth (2023) Vol. 23, Iss. 1
Open Access
Xue Zhang, Jian Li, Lan Zhang, et al.
BMC Pregnancy and Childbirth (2023) Vol. 23, Iss. 1
Open Access
