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OpenAlex Citation Counts

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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:

Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2
Merel Stemerdink, Belén García‐Bohórquez, Renske Schellens, et al.
Human Genetics (2021) Vol. 141, Iss. 3-4, pp. 737-758
Closed Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

Personalized genetic counseling for Stargardt disease: Offspring risk estimates based on variant severity
Stéphanie S. Cornelis, Esmee H. Runhart, Miriam Bauwens, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 3, pp. 498-507
Open Access | Times Cited: 42
A Knockin Model with the Mouse Equivalent to the c.2299delG Mutation in Usherin Exhibits Early-Onset Hearing Loss and Progressive Retinal Degeneration
Lars Tebbe, Muayyad R. Al-Ubaidi, Muna I. Naash
Advances in experimental medicine and biology (2025), pp. 253-257
Closed Access | Times Cited: 1
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants
Hedwig M. Velde, Janine Reurink, Sebastian Held, et al.
Human Genetics (2022) Vol. 141, Iss. 11, pp. 1723-1738
Open Access | Times Cited: 35
A systematic review of inherited retinal dystrophies in Pakistan: updates from 1999 to April 2023
Asad Munir, Salma Afsar, Atta Ur Rehman
BMC Ophthalmology (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 7
Retinal Phenotypes and Single-cell Sequencing Analysis of Ush2a Knockout Mice
Yifan Ning, Longhao Kuang, Tao Huang, et al.
Experimental Eye Research (2025), pp. 110247-110247
Closed Access
Vestibular Deficits in Deafness: Clinical Presentation, Animal Modeling, and Treatment Solutions
Audrey Maudoux, Sandrine Vitry, A. Amraoui
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 19
Phenotypic Distinctions Between EYS- and USH2A-Associated Retinitis Pigmentosa in an Asian Population
Erik Yeo, Taro Kominami, Tien‐En Tan, et al.
Translational Vision Science & Technology (2025) Vol. 14, Iss. 2, pp. 16-16
Open Access
Improving personalised genetic counselling for ABCA4 -associated retinopathy: Updated recurrence risk estimates
Stéphanie S. Cornelis, Frans P.M. Cremers
Medizinische Genetik (2025) Vol. 37, Iss. 1, pp. 19-25
Closed Access
Usher Syndrome: New Insights into Classification, Genotype–Phenotype Correlation, and Management
Fabiana D’Esposito, Giuseppe Gagliano, Caterina Gagliano, et al.
Genes (2025) Vol. 16, Iss. 3, pp. 332-332
Open Access
Affinity Proteomics Identifies Interaction Partners and Defines Novel Insights into the Function of the Adhesion GPCR VLGR1/ADGRV1
Barbara Knapp, Jens Roedig, Heiko Roedig, et al.
Molecules (2022) Vol. 27, Iss. 10, pp. 3108-3108
Open Access | Times Cited: 16
Retinal organoids and microfluidic chip-based approaches to explore the retinitis pigmentosa with USH2A mutations
Ting Su, Liying Liang, Lan Zhang, et al.
Frontiers in Bioengineering and Biotechnology (2022) Vol. 10
Open Access | Times Cited: 16
Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
Yuqin Liang, Xihao Sun, Chunwen Duan, et al.
Stem Cell Research & Therapy (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Pathogenesis and Treatment of Usher Syndrome Type IIA
Khine Zaw, Lívia S. Carvalho, May T. Aung-Htut, et al.
Asia-Pacific Journal of Ophthalmology (2022) Vol. 11, Iss. 4, pp. 369-379
Open Access | Times Cited: 12
The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1
Lars Tebbe, Maggie L. Mwoyosvi, Ryan Crane, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 6
Usher syndrome IIIA: a review of the disorder and preclinical research advances in therapeutic approaches
Azmi Marouf, Benjamin Johnson, Kumar N. Alagramam
Human Genetics (2022) Vol. 141, Iss. 3-4, pp. 759-783
Closed Access | Times Cited: 9
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher Syndrome
Malena Daich Varela, Shiao Wei Wong, Gülünay Kıray, et al.
American Journal of Ophthalmology (2023) Vol. 256, pp. 186-195
Open Access | Times Cited: 4
Usher syndrome: Genetic diagnosis and current therapeutic approaches
Beatriz Rocha Cuzzuol, Jonathan Santos Apolonio, Ronaldo Teixeira da Silva Júnior, et al.
World Journal of Otorhinolaryngology (2024) Vol. 11, Iss. 1, pp. 1-17
Open Access | Times Cited: 1
Syndromic Retinitis Pigmentosa
Jessica S. Karuntu, Hind Almushattat, Xuan‐Thanh‐An Nguyen, et al.
Progress in Retinal and Eye Research (2024), pp. 101324-101324
Open Access | Times Cited: 1
Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization
Ryan Crane, Lars Tebbe, Maggie L. Mwoyosvi, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 3
Allelic hierarchy for USH2A influences auditory and visual phenotypes in South Korean patients
Dong Woo Nam, Yong Keun Song, Jeong Hun Kim, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 3
Developing Non-Human Primate Models of Inherited Retinal Diseases
Ivan Seah, Debbie Goh, Hwei Wuen Chan, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 344-344
Open Access | Times Cited: 5
Induced Pluripotent Stem Cells, a Stepping Stone to In Vitro Human Models of Hearing Loss
María Beatriz Durán Alonso, Hrvoje Petković
Cells (2022) Vol. 11, Iss. 20, pp. 3331-3331
Open Access | Times Cited: 5
Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2a
Jessie M. Hendricks, Juriaan R. Metz, Hedwig M. Velde, et al.
Ophthalmology Science (2023) Vol. 3, Iss. 4, pp. 100323-100323
Open Access | Times Cited: 2
A systematic review of inherited retinal dystrophies in Pakistan: Updates from 1999 to April 2023
Asad Munir, Salma Afsar, Atta Ur Rehman
Research Square (Research Square) (2023)
Open Access | Times Cited: 2
Otolith function in Usher type II syndrome
Ana Margarida Amorim, Diliana Rebelo, Ana Beatriz Ramada, et al.
Acta Oto-Laryngologica (2024) Vol. 144, Iss. 9, pp. 485-490
Closed Access
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