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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:

Novel therapeutic approaches for the treatment of achondroplasia
Laurence Legeai‐Mallet, Ravi Savarirayan
Bone (2020) Vol. 141, pp. 115579-115579
Open Access | Times Cited: 49

Showing 1-25 of 49 citing articles:

International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia
Ravi Savarirayan, Penny Ireland, Melita Irving, et al.
Nature Reviews Endocrinology (2021) Vol. 18, Iss. 3, pp. 173-189
Open Access | Times Cited: 110
New developments in the biology of fibroblast growth factors
David M. Ornitz, Nobuyuki Itoh
WIREs Mechanisms of Disease (2022) Vol. 14, Iss. 4
Open Access | Times Cited: 96
New treatments for children with achondroplasia
Ravi Savarirayan, Julie Hoover‐Fong, Patrick Yap, et al.
The Lancet Child & Adolescent Health (2024) Vol. 8, Iss. 4, pp. 301-310
Closed Access | Times Cited: 9
Molecular and Genetic Mechanisms of Spinal Stenosis Formation: Systematic Review
Vadim A. Byvaltsev, А. А. Калинин, Phillip A. Hernandez, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13479-13479
Open Access | Times Cited: 28
Hypochondroplasia gain-of-function mutation in FGFR3 causes defective bone mineralization in mice
Léa Loisay, Davide Komla‐Ebri, Anne Morice, et al.
JCI Insight (2023) Vol. 8, Iss. 12
Open Access | Times Cited: 22
Advantages and Disadvantages of Different Treatment Methods in Achondroplasia: A Review
Wiktoria Wrobel, E Pach, Iwona Beń‐Skowronek
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 11, pp. 5573-5573
Open Access | Times Cited: 33
Experiences of children and adolescents living with achondroplasia and their caregivers
Renée Shediac, Olga Moshkovich, Heather Gerould, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 4
Open Access | Times Cited: 19
Fgfr3 enhancer deletion markedly improves all skeletal features in a mouse model of achondroplasia
Marco Angelozzi, Arnaud Molin, Anirudha Karvande, et al.
Journal of Clinical Investigation (2025) Vol. 135, Iss. 2
Closed Access
Clinical and economic burden of achondroplasia in the United States: results from a retrospective, observational study
Nadia Merchant, José Alvir, Paulette Negron Ericksen, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Rationale, design, and methods of a randomized, controlled, open-label clinical trial with open-label extension to investigate the safety of vosoritide in infants, and young children with achondroplasia at risk of requiring cervicomedullary decompression surgery
Ravi Savarirayan, Melita Irving, Wirginia Maixner, et al.
Science Progress (2021) Vol. 104, Iss. 1
Open Access | Times Cited: 24
Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhood
Hwa Young Kim, Jung Min Ko
Annals of Pediatric Endocrinology & Metabolism (2022) Vol. 27, Iss. 2, pp. 90-97
Open Access | Times Cited: 13
Cardiovascular risk factors and body composition in adults with achondroplasia
Svein O. Fredwall, Jennifer Linge, Olof Dahlqvist Leinhard, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 4, pp. 732-739
Open Access | Times Cited: 20
Natural disease course modeling of achondroplasia to evaluate the efficacy of recifercept in the absence of a placebo control arm in phase II study
Wenlian Qiao, Martin Boucher, Alison Slade, et al.
CPT Pharmacometrics & Systems Pharmacology (2024) Vol. 13, Iss. 7, pp. 1103-1116
Open Access | Times Cited: 2
Discovery of TYRA-300: First Oral Selective FGFR3 Inhibitor for the Treatment of Urothelial Cancers and Achondroplasia
Robert L. Hudkins, Eric Allen, Alexandra Balcer, et al.
Journal of Medicinal Chemistry (2024)
Closed Access | Times Cited: 2
Fat infiltration in the thigh muscles is associated with symptomatic spinal stenosis and reduced physical functioning in adults with achondroplasia
Svein O. Fredwall, Jennifer Linge, Olga de Vries, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Craniofacial growth and function in achondroplasia: a multimodal 3D study on 15 patients
Anne Morice, M.A.M. Taverne, Sophie Eché, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Quality of Life in Children With Achondroplasia Undergoing Paired Limb Lengthening With an External Fixator and Modified Distraction Control: Observational Nonrandomized Study
Vitaliy Trofimchuk, Bolatbek Dossanov, Vassiliy Lozovoy, et al.
JMIR Rehabilitation and Assistive Technologies (2024) Vol. 11, pp. e49261-e49261
Open Access | Times Cited: 1
Mutational analysis of consanguineous families and their targeted therapy against dwarfism
Feroz Khan, Sarmir Khan, Nehal Rana, et al.
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-18
Closed Access | Times Cited: 1
Promising horizons in achondroplasia along with the development of new drugs
Keiichi Ozono, Takuo Kubota, Toshimi Michigami
Endocrine Journal (2024) Vol. 71, Iss. 7, pp. 643-650
Open Access | Times Cited: 1
Natural history of spinal cord compression stage AFMS3 in infants with achondroplasia: retrospective cohort study
Moira Cheung, Alessandra Cocca, Charlotte Harvey, et al.
Archives of Disease in Childhood (2024) Vol. 109, Iss. 12, pp. 1025-1028
Closed Access | Times Cited: 1
Foetal Achondroplasia: Prenatal Diagnosis, Outcome and Perspectives
Alberto Vallin, D. Grévent, Bettina Bessières, et al.
Journal of Gynecology Obstetrics and Human Reproduction (2024) Vol. 54, Iss. 2, pp. 102891-102891
Closed Access | Times Cited: 1
Theobroma cacao improves bone growth by modulating defective ciliogenesis in a mouse model of achondroplasia
Ludovic Martin, Nabil Kaci, Catherine Benoist-Lasselin, et al.
Bone Research (2022) Vol. 10, Iss. 1
Open Access | Times Cited: 7
A long-acting C-natriuretic peptide for achondroplasia
Eric L. Schneider, Christopher W. Carreras, Ralph R. Reid, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 30
Open Access | Times Cited: 7
Higher rates of non-skeletal complications and greater healthcare needs in achondroplasia compared to the general UK population: a matched cohort study using the CPRD database
Jeanne M. Pimenta, Melita Irving, Moira Cheung, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 3
Hearing loss in Norwegian adults with achondroplasia
Svein O. Fredwall, Björn Åberg, Hanne Berdal, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 5
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