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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 LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes
Ikumi Umeki, Tetsuya Niihori, Taiki Abe, et al.
Human Genetics (2018) Vol. 138, Iss. 1, pp. 21-35
Closed Access | Times Cited: 71

Showing 51-75 of 71 citing articles:

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
Functional CRISPR repair of induced pluripotent stem cells from patients with Noonan syndrome-associated cardiac hypertrophy
Lennart Roos
(2024)
Open Access
The Role of Genetics in Cardiomyopathy
Kazuki Kodo, Hiroyuki Yamagishi
Pediatric Cardiology (2024), pp. 2473-2502
Closed 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
LZTR1 loss-of-function variants associated with café au lait macules with or without freckling
Svea Horn, Teresa Neuhann, Corina Hennig, et al.
Frontiers in Neurology (2024) Vol. 15
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
Defining Pathogenic Variants in RASopathies
Trevor G. Smart, Hamsa D. Tadepally, Ryan Webb, et al.
(2024), pp. 241-262
Closed Access
The Noncanonical RAS/MAPK Pathway and the RASopathies
Stephanie Mo, Pau Castel
(2024), pp. 427-456
Closed Access
Cardiovascular Disease in the RASopathies
Kathryn C. Chatfield
(2024), pp. 551-569
Closed Access
Molecular Genetics of Noonan Syndrome and Other RASopathies
Marialetizia Motta, Elisabetta Flex, Simone Martinelli, et al.
(2024), pp. 263-305
Closed Access
Prenatal diagnosis of Noonan syndrome in a set of monozygotic twins- a case report
Wei Jian, Huizhen Yuan, Yu Liu, et al.
BMC Pregnancy and Childbirth (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 1
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes
Viviana Tritto, Daniele Capitanio, Cecilia Gelfi, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4035-4035
Open Access | Times Cited: 1
The Role of Genetics in Cardiomyopathy
Kazuki Kodo, Hiroyuki Yamagishi
Pediatric Cardiology (2023), pp. 1-31
Closed Access | Times Cited: 1
Structural Model for Recruitment of RIT1 to the LZTR1 E3 Ligase: Evidences from an Integrated Computational Approach
Antonella Paladino, Fulvio D’Angelo, Teresa Noviello, et al.
Journal of Chemical Information and Modeling (2021) Vol. 61, Iss. 4, pp. 1875-1888
Open Access | Times Cited: 3
Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
Mary Jo Talley, Diana Nardini, Nisha Shabbir, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 2
Integrative Molecular and Clinical Profiling of Acral Melanoma Identifies LZTR1 as a Key Tumor Promoter and Therapeutic Target
Ruth Halaban, Aaron M. Newman, Farshad Farshidfar, et al.
Research Square (Research Square) (2021)
Open Access | Times Cited: 1
Integrative molecular and clinical profiling of acral melanoma identifies LZTR1 as a key tumor promoter and therapeutic target
Farshad Farshidfar, Cong Peng, Chaya Levovitz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Genotype-Phenotype Correlation in Noonan Syndrome – Focus on LZTR1 and its Substrates
Alexandra Viktoria Busley
(2023)
Open Access
A rare case of Noonan syndrome associated with biallelic variants in the LZTR1
Л. А. Гандаева, В. Г. Каверина, Е. Н. Басаргина, et al.
L O Badalyan Neurological Journal (2023) Vol. 4, Iss. 3, pp. 120-129
Open Access
Electrocardiographic Changes with Age in Japanese Patients with Noonan Syndrome
Yasuhiro Ichikawa, Hiroyuki Kuroda, Takeshi Ikegawa, et al.
Journal of Cardiovascular Development and Disease (2023) Vol. 11, Iss. 1, pp. 10-10
Open Access
A Rare Heterozygous LZTR1 Mutation in an Infant with Noonan Syndrome Running Title: LZTR1 Variant in Noonan Syndrome
Dimitrios Rallis, Maria Baltogianni
Journal of Case Reports (2022), pp. 73-77
Open Access
Induced pluripotent stem cells for modeling Noonan, Noonan Syndrome with Multiple Lentigines, and Costello Syndromes
A. Gulhan Ercan‐Sencicek, Saravanakkumar Chennappan, Kelly Aromalaran, et al.
Elsevier eBooks (2021), pp. 65-110
Closed Access
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