Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Edmond Wonkam‐Tingang, et al.
Genes (2023) Vol. 14, Iss. 2, pp. 399-399
Open Access | Times Cited: 10

Showing 10 citing articles:

An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population
Alberto M. Parra‐Perez, Álvaro Gallego-Martinez, José A. López‐Escámez
Human Genetics (2024) Vol. 143, Iss. 3, pp. 423-435
Open Access | Times Cited: 3
Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA
Yan Yang, Haiyan Luo, Lijuan Pan, et al.
Human Molecular Genetics (2024)
Open Access | Times Cited: 2
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
В.Г. Пшенникова, Fedor M. Teryutin, Alexandra M. Cherdonova, et al.
Genes (2023) Vol. 14, Iss. 5, pp. 1001-1001
Open Access | Times Cited: 4
Novel, pathogenic insertion variant of GSDME associates with autosomal dominant hearing loss in a large Chinese pedigree
Jingliang Cheng, Ting Li, Qi Tan, et al.
Journal of Cellular and Molecular Medicine (2023) Vol. 28, Iss. 1
Open Access | Times Cited: 4
The historical demography of the Martha’s Vineyard signing community
Justin Power, Richard P. Meier
The Journal of Deaf Studies and Deaf Education (2024) Vol. 29, Iss. 3, pp. 295-321
Open Access | Times Cited: 1
Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis
Masoome Alerasool, Atieh Eslahi, Barbara Vona, et al.
Clinical Genetics (2024) Vol. 106, Iss. 6, pp. 693-701
Closed Access | Times Cited: 1
Comprehensive analysis, diagnosis, prognosis, and cordycepin (CD) regulations for GSDME expressions in pan-cancers
Jiewen Fu, Dabing Li, Lianmei Zhang, et al.
Cancer Cell International (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Pathogenic variant c.35delG of the GJB2 gene associated with nonsyndromic prelingual deafness
Estela Morales Peralta, Mercedes Arceo Alvarez, Yuledmi Perdomo Chacón, et al.
Salud Ciencia y Tecnología (2024) Vol. 4, pp. 766-766
Open Access
An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European descendant population
José A. López‐Escámez, Alberto M. Parra‐Perez, Álvaro Gallego-Martinez
Research Square (Research Square) (2023)
Open Access
Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA
Yan Yang, Haiyan Luo, Lijuan Pan, et al.
Research Square (Research Square) (2023)
Open Access
Page 1

Scroll to top