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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:

Providing more evidence on LZTR1 variants in Noonan syndrome patients
Josefina Chinton, Victoria Huckstadt, Mafalda Mucciolo, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 2, pp. 409-414
Closed Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Genotype‐cardiac phenotype correlations in a large single‐center cohort of patients affected by RASopathies: Clinical implications and literature review
Chiara Leoni, Rita Blandino, Angelica Bibiana Delogu, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 431-445
Closed Access | Times Cited: 43
The heart in RASopathies
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 440-451
Closed 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
Molecular genetics of congenital heart disease
Xiaoqing Zhang, Ming Qi, Qihua Fu
Science China Life Sciences (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
Protein-losing enteropathy and multiple vasculature dysplasia in LZTR1-related Noonan syndrome: A case report and review of literature
Qiuju Tian, Lujia Zhang, Qun Zhang, et al.
World Journal of Gastroenterology (2025) Vol. 31, Iss. 17
Closed Access
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot
Miriam S. Reuter, Rajiv Chaturvedi, Rebekah Jobling, et al.
Circulation Genomic and Precision Medicine (2021) Vol. 14, Iss. 4
Open Access | Times Cited: 24
The Genetics of Neurodevelopment in Congenital Heart Disease
Eli Patt, Asmita Singhania, Amy E. Roberts, et al.
Canadian Journal of Cardiology (2022) Vol. 39, Iss. 2, pp. 97-114
Open Access | Times Cited: 17
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
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
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
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?
Luca Ferrari, Eleonora Mangano, Maria Teresa Bonati, et al.
European Journal of Human Genetics (2020) Vol. 28, Iss. 10, pp. 1432-1445
Open Access | Times Cited: 13
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
Transient Myeloproliferative Disorder (TMD), Acute Lymphoblastic Leukemia (ALL), and Juvenile Myelomonocytic Leukemia (JMML) in a Child with Noonan Syndrome: Sequential Occurrence, Single Center Experience, and Review of the Literature
Marta Arrabito, Nicolò Li Volsi, Manuela La Rosa, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1191-1191
Open Access | Times Cited: 1
Enrichment of cancer-predisposing germline variants in adult and pediatric patients with acute lymphoblastic leukemia
Suvi P. M. Douglas, Atte Lahtinen, Jessica R. Koski, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 7
Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1
Dilek Uludağ Alkaya, Christina Lißewski, Gözde Yeşil, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 12, pp. 3623-3633
Closed Access | Times Cited: 8
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review
Xiu Zhao, Zhuoguang Li, Li Wang, et al.
BMC Endocrine Disorders (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 7
Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone
Dongye He, Yanying Li, Wanling Yang, et al.
Clinica Chimica Acta (2021) Vol. 524, pp. 1-10
Closed Access | Times Cited: 6
Case Report: Molecular autopsy underlie COVID-19-associated sudden, unexplained child mortality
Kana Unuma, Dan Tomomasa, Kosuke Noma, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 2
RASopathy Cohort of Patients Enrolled in a Brazilian Reference Center for Rare Diseases: A Novel Familial LZTR1 Variant and Recurrent Mutations
Natana Chaves Rabelo, Maria E.S. Gomes, Isabelle de Oliveira Moraes, et al.
The Application of Clinical Genetics (2022) Vol. Volume 15, pp. 153-170
Open Access | Times Cited: 4
Ventricular arrhythmia and Noonan Syndrome with LZTR1 Mutations: Expanding the Phenotype with a Case Report and Review of the Literature
Zhuyuan Liu, Yan Huang, Jinxi Wang, et al.
Research Square (Research Square) (2024)
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
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
Cardiovascular Disease in the RASopathies
Kathryn C. Chatfield
(2024), pp. 551-569
Closed Access
Integrated in silico MS-based phosphoproteomics and network enrichment analysis of RASopathy proteins
Javier‐Fernando Montero‐Bullón, Óscar González-Velasco, María Isidoro‐García, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 3
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