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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:

Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome
Yasuko Shoji, Shinobu Ida, Tetsuya Niihori, et al.
Endocrine Journal (2019) Vol. 66, Iss. 11, pp. 983-994
Open Access | Times Cited: 19

Showing 19 citing articles:

Update on the Clinical and Molecular Characterization of Noonan Syndrome and Other RASopathies: A Retrospective Study and Systematic Review
G.J. Reynolds, Andrea Gazzin, Diana Carli, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3515-3515
Open Access
Gene signatures and genotype-phenotype correlations of sensorineural hearing loss in Noonan syndrome and related RASopathies
Seung Jae Lee, Sun Young Jeong, Somin Lee, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Etiology and Treatment of Growth Delay in Noonan Syndrome
Fernándo Rodríguez, Ximena Gaete, Fernando Cassorla
Frontiers in Endocrinology (2021) Vol. 12
Open Access | Times Cited: 23
Lymphatic anomalies during lifetime in patients with Noonan syndrome: Retrospective cohort study
Jessie W. Swarts, Lotte E. R. Kleimeier, Erika Leenders, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 11, pp. 3242-3261
Open Access | Times Cited: 11
The Prevalence of Noonan Spectrum Disorders in Pediatric Patients with Pulmonary Valve Stenosis
Janet M. Bell, Ellen M. Considine, Leslie M. McCallen, et al.
The Journal of Pediatrics (2021) Vol. 234, pp. 134-141.e5
Closed Access | Times Cited: 14
Congenital sensorineural hearing loss as the initial presentation ofPTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms
Xue Gao, Shasha Huang, Shiwei Qiu, et al.
Journal of Medical Genetics (2020) Vol. 58, Iss. 7, pp. 465-474
Closed Access | Times Cited: 12
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome
Yasuko Shoji, Ayaha Hata, Takatoshi Maeyama, et al.
Clinical Pediatric Endocrinology (2024) Vol. 33, Iss. 2, pp. 50-58
Open Access | Times Cited: 1
Refractory Chylothorax and Ventricular Hypertrophy Treated with Trametinib in a Patient with Noonan Syndrome: 18-Month Follow-Up
Antonia Pascarella, Giuseppe Limongelli, Alessandro De Falco, et al.
Children (2024) Vol. 11, Iss. 11, pp. 1342-1342
Open Access | Times Cited: 1
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
Maja Šolman, Daniëlle T.J. Woutersen, Jeroen den Hertog
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
A PTPN11 mutation in a woman with Noonan syndrome and protein-losing enteropathy
Na Wang, Wen Shi, Yang Jiao
BMC Gastroenterology (2020) Vol. 20, Iss. 1
Open Access | Times Cited: 8
Cardiac features of Noonan syndrome in Japanese patients
Yasuhiro Ichikawa, Hiroyuki Kuroda, Takeshi Ikegawa, et al.
Cardiology in the Young (2022) Vol. 33, Iss. 4, pp. 564-569
Closed Access | Times Cited: 4
PTPN11 mutations in adult acute myeloid leukaemia: Prevalence and clinical implications in the context of NPM1 mutation
Jie Liu, Wei Qin, Biao Wang, et al.
Leukemia Research (2022) Vol. 118, pp. 106859-106859
Closed Access | Times Cited: 4
PTPN11 c.853T>C (p.Phe285Leu) mutation in Noonan syndrome with chylothorax.
Daisuke Watanabe, Yohei Hasebe, Shin Kasai, et al.
PubMed (2022) Vol. 84, Iss. 4, pp. 871-876
Closed Access | Times Cited: 3
Identification of genetic variants in two Vietnamese patients with hypertrophic cardiomyopathy by Whole exome sequencing
Nguyen Thi Kim Lien, Nguyen Van Tung, Le Thi Phuong Tu, et al.
Vietnam Journal of Biotechnology (2024) Vol. 22, Iss. 2, pp. 212-226
Closed Access
Case report: Distinctive cardiac features and phenotypic characteristics of Noonan syndrome with multiple lentigines among three generations in one family
Chon-Hou Chan, Man-Fong Chu, U Po Lam, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 1
Disruption of the glomerular basement membrane associated with nutcracker syndrome and double inferior vena cava in Noonan syndrome: a case report
Ayumi Omori, Kan Katayama, Ryosuke Saiki, et al.
BMC Nephrology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 2
A Chinese Family with Noonan Syndrome Associated with a Heterozygous LZTR1 Mutation
Xiu Hong Zhao, Li Wang, Zhangzhang Lan, et al.
Research Square (Research Square) (2020)
Open Access
New insights on Noonan syndrome’s clinical phenotype: a single center retrospective study
Francesco Baldo, Alice Fachin, Beatrice Da Re, et al.
Research Square (Research Square) (2022)
Open Access
Molecular characterization using exome sequencing of two probands with the undiagnosed developmental delay from Central Brazil
Irene Plaza Pinto, Ana Julia da Cunha Leite, Cristine Nascimento dos Santos, et al.
Conjecturas (2022) Vol. 22, Iss. 6, pp. 531-542
Open Access
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