Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Clinical overview on RASopathies
Martin Zenker
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 414-424
Open Access | Times Cited: 49

Showing 26-50 of 49 citing articles:

Biomarker Landscape in RASopathies
Noemi Ferrito, Juan Báez-Flores, Mario Rodríguez-Martín, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8563-8563
Open Access
Plastic Bronchitis in Noonan Syndrome: Further Evidence Suggesting a Higher Risk of Lymphatic Abnormalities in Individuals Harboring Variants in PTPN11 Residue p.Phe285
Lucas Vieira Lacerda Pires, Eduardo Da Cás, Letícia Cole de Melo, et al.
Molecular Syndromology (2024), pp. 1-6
Closed Access
Variants of the PTPN11 Gene in Mexican Patients with Noonan Syndrome
Paola Montserrat Zepeda-Olmos, Eduardo Esparza-García, Kiabeth Robles-Espinoza, et al.
Genes (2024) Vol. 15, Iss. 11, pp. 1379-1379
Open Access
New Insights Into the Spectrum of RASopathies: Clinical and Genetic Data in a Cohort of 121 Spanish Patients
Ana Isabel Sánchez Barbero, Irene Valenzuela, Paula Fernández‐Álvarez, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
Autism and Social Behavior in RASopathies
Allison M. H. Foy, Rebekah L. Hudock, Elizabeth I. Pierpont
(2024), pp. 611-634
Closed Access
Irritability in Children with Rasopathies, Insights into Emotional Dysregulation and Social Skills Impairments
Yaffa Serur, Naomi Fuhrman, Odeya Russo, et al.
Research Square (Research Square) (2024)
Closed Access
Clinical features and molecular genetics of patients with RASopathies: expanding the phenotype with rare genes and novel variants
Ceren Yılmaz Uzman, Semra Gürsoy, Behzat Özkan, et al.
European Journal of Pediatrics (2024) Vol. 184, Iss. 1
Closed Access
The first case of a point pathogenic variant in the RREB1 gene in Noonan‐like Rasopathy
Olga Shatokhina, Fatima Bostanova, Maria Bulakh, et al.
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 573-580
Closed Access
Nerve enlargement in patients with Noonan syndrome: A retrospective cohort study
Fieke Draaisma, Erika Leenders, Corrie E. Erasmus, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 11
Open Access
Cardiac Phenotype and Gene Mutations in RASopathies
Maria Felicia Faienza, Giovanni Meliota, Donatella Mentino, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1015-1015
Open Access
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules
Gioia Mastromoro, Claudia Santoro, Marialetizia Motta, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 11, pp. 101241-101241
Closed Access
Germline Predisposition to MDS and AML
Majd Khiami, Marcin W. Włodarski
Pediatric oncology (2024), pp. 37-55
Closed Access
A Strong Candidate Gene for Nonsyndromic Intellectual Disability Phenotype: SGSM3
Ayberk Türkyılmaz, Kübra Adanur Sağlam, Mustafa Yılmaz, et al.
Clinical Genetics (2024)
Open Access
Genomic ascertainment to quantify prevalence and cancer risk in adults with pathogenic and likely pathogenic germline variants in RASopathy genes
Jung Kim, Gina M. Ney, Megan N. Frone, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Thyrotoxic Myopathy with Nonspecific Ophthalmopathy in a Two-Year-Old Child: Case Report and Literature Review
Katarzyna Smółka, Lidia Perenc, Joanna Pelc, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 20, pp. 6180-6180
Open Access
Speech-Language Pathology in the RASopathies
Heather L. Thompson
(2024), pp. 653-678
Closed Access
Drosophila Models of RASopathies
Robert A. Marmion, Alison G. Simpkins, Stanislav Y. Shvartsman
(2024), pp. 819-832
Closed Access
Cognitive Development and Learning in RASopathies
Alana M. McNeill, Dante J. Rogers, Elizabeth I. Pierpont
(2024), pp. 571-596
Closed Access
Epilepsy in the RASopathies
Danilo Bernardo
(2024), pp. 635-651
Closed Access
Precision Medicine in RASopathies: Tailored Disease Management Through Enhanced Approaches, Disease Delineation, and Pathway-Specific Therapies
Vanina Taliercio, David Viskochil
(2024), pp. 319-328
Closed Access
Behavioral Profile in RASopathies
Marni E. Axelrad, Jennifer M. Katzenstein, David D. Schwartz
(2024), pp. 597-609
Closed Access
Do children with a Noonan syndrome-like RASopathy and avoidant/restrictive food intake disorder benefit from behavioral therapy?
Éric Dumont, Dagmar K. Tiemens, Jos Draaisma, et al.
European Journal of Pediatrics (2024) Vol. 184, Iss. 1
Closed Access
Hsp70/Hsp90 organizing protein (HOP) maintains CRAF kinase activity and regulates MAPK signaling by enhancing Hsp90-CRAF association
Nilanjan Gayen, Sahana Mitra, S.C. Roy, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Editorial: Identifying the isoform-specific roles of RAS paralogs in health and disease
Saeideh Nakhaei‐Rad, Anna Fejtová
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access
An incomplete LEOPARD syndrome presented with generalized lentigines
Tianzi Wang, Yan Lin, Lele Sun, et al.
Journal of Cosmetic Dermatology (2023) Vol. 23, Iss. 2, pp. 711-713
Open Access
Previous Page - Page 2

Scroll to top