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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:

Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome
Alistair T. Pagnamenta, Pamela J. Kaisaki, Fenella Bennett, et al.
Clinical Genetics (2019) Vol. 95, Iss. 6, pp. 693-703
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype
Marialetizia Motta, Giulia Fasano, Sina Gredy, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 11, pp. 2112-2129
Open Access | Times Cited: 57
The molecular genetics of RASopathies: An update on novel disease genes and new disorders
Marco Tartaglia, Yoko Aoki, Bruce D. Gelb
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 425-439
Open Access | Times Cited: 43
Preclinical evaluation of CRISPR-based therapies for Noonan syndrome caused by deep-intronic LZTR1 variants
Carolin Knauer, Henrike Haltern, Eric Schoger, et al.
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 1, pp. 102123-102123
Open Access | Times Cited: 5
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
Marialetizia Motta, Lena Sagi‐Dain, Oliver H.F. Krumbach, et al.
Human Molecular Genetics (2019) Vol. 29, Iss. 11, pp. 1772-1783
Closed Access | Times Cited: 42
Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene Variants
Ellen Wingbermühle, Renée L. Roelofs, Wouter Oomens, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 16, pp. 4735-4735
Open Access | Times Cited: 19
The pathogenesis of Noonan syndrome is modulated by NOC2L, a novel interactor of LZTR1 leading to impaired p53 signalling
Sumana Chatterjee, Miho Ishida, Débora Romeo Bertola, et al.
Research Square (Research Square) (2025)
Closed Access
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
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking
Raj Nayan Sewduth, Silvia Pandolfi, Mikhail Steklov, et al.
Circulation Research (2020) Vol. 126, Iss. 10, pp. 1379-1393
Open Access | Times Cited: 28
Venus: Elucidating the Impact of Amino Acid Variants on Protein Function Beyond Structure Destabilisation
Matteo P. Ferla, Alistair T. Pagnamenta, Leonidas Koukouflis, et al.
Journal of Molecular Biology (2022) Vol. 434, Iss. 11, pp. 167567-167567
Open Access | Times Cited: 16
Phenotypic Expansion of Autosomal Dominant LZTR1-Related Disorders with Special Emphasis on Adult-Onset Features
Vera Uliana, Enrico Ambrosini, Antonietta Taiani, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 916-916
Open Access | Times Cited: 3
MichelaNglo: sculpting protein views on web pages without coding
Matteo P. Ferla, Alistair T. Pagnamenta, David Damerell, et al.
Bioinformatics (2020) Vol. 36, Iss. 10, pp. 3268-3270
Open Access | Times Cited: 26
LZTR1: A promising adaptor of the CUL3 family (Review)
Hui Zhang, Xinyi Cao, Jian Wang, et al.
Oncology Letters (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 22
Inside the Noonan “universe”: Literature review on growth, GH/IGF axis and rhGH treatment: Facts and concerns
Stefano Stagi, Vittorio Ferrari, Marta Ferrari, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 15
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis
Kirsten M. Farncombe, Emily Thain, Carolina Barnett‐Tapia, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Gonadal dysfunction in a man with Noonan syndrome from the LZTR1 variant: case report and review of literature
Francesca Orsolini, Luisa Pignata, Fulvia Baldinotti, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 2
<b><i>LZTR1</i></b>: Genotype Expansion in Noonan Syndrome
María Güemes, Álvaro Martín‐Rivada, Nelmar Valentina Ortiz‐Cabrera, et al.
Hormone Research in Paediatrics (2019) Vol. 92, Iss. 4, pp. 269-275
Closed Access | Times Cited: 18
Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors
Heather B. Radtke, Amanda Bergner, Allison L. Goetsch, et al.
Journal of Genetic Counseling (2020) Vol. 29, Iss. 5, pp. 692-714
Open Access | Times Cited: 18
Phenotype–genotype analysis of 242 individuals with RASopathies: 18‐year experience of a tertiary center in Brazil
Débora Romeo Bertola, Matheus Augusto Araújo Castro, Guilherme Lopes Yamamoto, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2020) Vol. 184, Iss. 4, pp. 896-911
Closed Access | Times Cited: 18
Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study
Ahmed Alhendi, Derek Lim, Shane McKee, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 6, pp. 613-622
Open Access | Times Cited: 15
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
Noonan syndrome: rhGH treatment and PTPN11 mutation
Xian Wu, Jiali Wu, Yi Yuan, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 11
Open Access | Times Cited: 5
Neurological features of Noonan syndrome and related RASopathies: Pain and nerve enlargement characterized by nerve ultrasound
Willem De Ridder, Baziel G.M. van Engelen, Nens van Alfen
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 6, pp. 1801-1807
Closed Access | Times Cited: 8
Biventricular outflow tract obstruction due to hypertrophy related to compound heterozygous variants in LZTR1
Shuai Wang, Daoquan Peng
ESC Heart Failure (2024) Vol. 11, Iss. 6, pp. 4450-4455
Open Access | Times Cited: 1
A homozygous variant in growth and differentiation factor 2 (GDF2) may cause lymphatic dysplasia with hydrothorax and nonimmune hydrops fetalis
Sietse Aukema, Gerdien A. ten Brinke, Wim Timens, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 9, pp. 2152-2160
Open Access | Times Cited: 9
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