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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 1-25 of 71 citing articles:

Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation
Scott R. Plotkin, Ludwine Messiaen, Eric Legius, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 9, pp. 1967-1977
Open Access | Times Cited: 141
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases
Taiki Abe, Ikumi Umeki, Shin‐ichiro Kanno, et al.
Cell Death and Differentiation (2019) Vol. 27, Iss. 3, pp. 1023-1035
Open Access | Times Cited: 101
RIT1 oncoproteins escape LZTR1-mediated proteolysis
Pau Castel, Alice Cheng, Antonio Cuevas-Navarro, et al.
Science (2019) Vol. 363, Iss. 6432, pp. 1226-1230
Open Access | Times Cited: 96
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
Integrative molecular and clinical profiling of acral melanoma links focal amplification of 22q11.21 to metastasis
Farshad Farshidfar, Kahn Rhrissorrakrai, Chaya Levovitz, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 41
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Ludovica Montanucci, David Lewis‐Smith, Ryan L. Collins, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 30
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
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
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
Clinical and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort
Hao Chen, Xin Li, Xiaoliang Liu, et al.
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 40
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 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
Nerve Enlargement in Patients with INF2 Variants Causing Peripheral Neuropathy and Focal Segmental Glomerulosclerosis
Tran Thuy Huong Quynh, Linh Tran, Hiroko Ueda, et al.
Biomedicines (2025) Vol. 13, Iss. 1, pp. 127-127
Open Access
Classification of schwannomas and the new naming convention for “neurofibromatosis-2”: Genetic updates and international consensus recommendation
Pranjal Rai, Girish Bathla, Neetu Soni, et al.
The Neuroradiology Journal (2025)
Open Access
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 tumor suppressor LZTR1: Its expression, purification and characterization
Yifang Sun, Yuxuan Jiang, Meng Zhang, et al.
Protein Expression and Purification (2025), pp. 106716-106716
Closed 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
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
Undiagnosed RASopathies in infertile men
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
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
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
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
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
Abnormalities of pubertal development and gonadal function in Noonan syndrome
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 7
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