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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:

A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair
Karen W. Gripp, Kimberly A. Aldinger, James T. Bennett, et al.
American Journal of Medical Genetics Part A (2016) Vol. 170, Iss. 9, pp. 2237-2247
Open Access | Times Cited: 138

Showing 26-50 of 138 citing articles:

Genotype and phenotype spectrum of NRAS germline variants
Franziska Altmüller, Christina Lißewski, Débora Romeo Bertola, et al.
European Journal of Human Genetics (2017) Vol. 25, Iss. 7, pp. 823-831
Open Access | Times Cited: 47
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms
Giulio Calcagni, Marta Unolt, M. Cristina Digilio, et al.
Expert Review of Molecular Diagnostics (2017) Vol. 17, Iss. 9, pp. 861-870
Closed Access | Times Cited: 44
MRAS: A Close but Understudied Member of the RAS Family
Lucy C. Young, Pablo Rodriguez‐Viciana
Cold Spring Harbor Perspectives in Medicine (2018) Vol. 8, Iss. 12, pp. a033621-a033621
Open Access | Times Cited: 42
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
The sixth international RASopathies symposium: Precision medicine—From promise to practice
Karen W. Gripp, Lisa Schill, Lisa Schoyer, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 3, pp. 597-606
Open Access | Times Cited: 38
Protein phosphatase 1 in tumorigenesis: is it worth a closer look?
Juliana Felgueiras, Cármen Jerónimo, Margarida Fardilha
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (2020) Vol. 1874, Iss. 2, pp. 188433-188433
Closed Access | Times Cited: 33
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability
Chaofan Zhang, Angad Jolly, Brian J. Shayota, et al.
Human Genetics and Genomics Advances (2021) Vol. 3, Iss. 1, pp. 100074-100074
Open Access | Times Cited: 29
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
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 954-963
Closed Access | Times Cited: 4
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
Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature
Aurore Siegfried, Claude Cancès, Marie Denuelle, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 1061-1065
Closed Access | Times Cited: 35
A Leucine-Rich Repeat Protein Provides a SHOC2 the RAS Circuit: a Structure-Function Perspective
Jason J. Kwon, William C. Hahn
Molecular and Cellular Biology (2021) Vol. 41, Iss. 4
Open Access | Times Cited: 24
Cancer incidence and surveillance strategies in individuals withRASopathies
Gina M. Ney, Andrea M. Gross, Alicia A. Livinski, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 530-540
Open Access | Times Cited: 17
RASopathies – what they reveal about RAS/MAPK signaling in skeletal muscle development
Katherine A. Rauen, William E. Tidyman
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 3
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease
Lijiang Ma, Yavuz Bayram, Heather M. McLaughlin, et al.
Human Genetics (2016) Vol. 135, Iss. 12, pp. 1399-1409
Open Access | Times Cited: 31
The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan‐like syndrome individual: Broadening the clinical phenotype
Débora Romeo Bertola, Guilherme Lopes Yamamoto, Michelle Buscarilli, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 3, pp. 824-828
Closed Access | Times Cited: 30
New Noonan syndrome model mice with RIT1 mutation exhibit cardiac hypertrophy and susceptibility to β-adrenergic stimulation-induced cardiac fibrosis
Shingo Takahara, Shinichi Inoue, Sachiko Miyagawa‐Tomita, et al.
EBioMedicine (2019) Vol. 42, pp. 43-53
Open Access | Times Cited: 28
Expanding the molecular spectrum of pathogenicSHOC2variants underlying Mazzanti syndrome
Marialetizia Motta, Maja Šolman, Adeline Bonnard, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. 16, pp. 2766-2778
Open Access | Times Cited: 15
Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp
Débora Romeo Bertola, Michelle Buscarilli, Deborah L. Stabley, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 5, pp. 1309-1318
Open Access | Times Cited: 26
Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair
Regina M. Zambrano, Michael Marble, Stuart A. Chalew, et al.
American Journal of Medical Genetics Part A (2016) Vol. 173, Iss. 2, pp. 565-567
Closed Access | Times Cited: 24
RASopathies: The musculoskeletal consequences and their etiology and pathogenesis
John L. Fowlkes, Kathryn M. Thrailkill, R. Clay Bunn
Bone (2021) Vol. 152, pp. 116060-116060
Open Access | Times Cited: 18
Systemic lupus erythematosus in a patient with Noonan syndrome‐like disorder with loose anagen hair 1: More than a chance association
Tomoko Uehara, Naoki Hosogaya, Nobutake Matsuo, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 7, pp. 1662-1666
Closed Access | Times Cited: 22
Cellular interplay via cytokine hierarchy causes pathological cardiac hypertrophy in RAF1-mutant Noonan syndrome
Jiani C. Yin, Mathew J. Platt, Xixi Tian, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 22
Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencing
Elizabeth Bhoj, Zhenming Yu, Qiaoning Guan, et al.
Genetics in Medicine (2016) Vol. 19, Iss. 6, pp. 715-718
Open Access | Times Cited: 20
Clinical and functional characterization of a novel RASopathy‐causingSHOC2mutation associated with prenatal‐onset hypertrophic cardiomyopathy
Marialetizia Motta, Aldo Giancotti, Gioia Mastromoro, et al.
Human Mutation (2019)
Open Access | Times Cited: 20

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