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:
Additional causal SNRPE mutations in hereditary hypotrichosis simplex
Pan Cheng, Aytaj Humbatova, Lan Zheng, et al.
British Journal of Dermatology (2021) Vol. 185, Iss. 2, pp. 439-441
Open Access | Times Cited: 4
Pan Cheng, Aytaj Humbatova, Lan Zheng, et al.
British Journal of Dermatology (2021) Vol. 185, Iss. 2, pp. 439-441
Open Access | Times Cited: 4
Showing 4 citing articles:
Update of recent findings in genetic hair disorders
Ryota Hayashi, Yutaka Shimomura
The Journal of Dermatology (2021) Vol. 49, Iss. 1, pp. 55-67
Closed Access | Times Cited: 17
Ryota Hayashi, Yutaka Shimomura
The Journal of Dermatology (2021) Vol. 49, Iss. 1, pp. 55-67
Closed Access | Times Cited: 17
Hereditary hypotrichosis simplex with SNRPE gene mutation
Yumi Won, Byung Soo Kim, Moon-Bum Kim, et al.
Indian Journal of Dermatology Venereology and Leprology (2024), pp. 1-3
Open Access
Yumi Won, Byung Soo Kim, Moon-Bum Kim, et al.
Indian Journal of Dermatology Venereology and Leprology (2024), pp. 1-3
Open Access
Novel blended SNRPE ‐related spliceosomopathy phenotype characterized by microcephaly and congenital atrichia
Shivarajan Amudhavalli, Victoria Paolillo, Caitlin E. Lawson, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 5, pp. 1425-1429
Closed Access | Times Cited: 1
Shivarajan Amudhavalli, Victoria Paolillo, Caitlin E. Lawson, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 5, pp. 1425-1429
Closed Access | Times Cited: 1
A novel pathogenic CDH3 variant underlying heredity hypotrichosis simplex detected by whole-exome sequencing (WES)—a case report
Ayat Kadhi, Lamiaa Hamie, Christel Tamer, et al.
Molecular Case Studies (2022) Vol. 8, Iss. 5, pp. a006225-a006225
Open Access | Times Cited: 2
Ayat Kadhi, Lamiaa Hamie, Christel Tamer, et al.
Molecular Case Studies (2022) Vol. 8, Iss. 5, pp. a006225-a006225
Open Access | Times Cited: 2
