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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 26-50 of 71 citing articles:

LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretion
Taiki Abe, Shin-ichiro Kanno, Tetsuya Niihori, et al.
Cell Death and Disease (2023) Vol. 14, Iss. 8
Open Access | Times Cited: 7
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis
Kirsten M. Farncombe, Emily Thain, Carolina Barnett‐Tapia, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome
Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 7
Open Access | Times Cited: 11
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
Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome
Yasuko Shoji, Shinobu Ida, Tetsuya Niihori, et al.
Endocrine Journal (2019) Vol. 66, Iss. 11, pp. 983-994
Open Access | Times Cited: 19
<b><i>LZTR1</i></b>: Genotype Expansion in Noonan Syndrome
María Güemes, Álvaro Martín‐Rivada, Nelmar Valentina Ortiz‐Cabrera, et al.
Hormone Research in Paediatrics (2019) Vol. 92, Iss. 4, pp. 269-275
Closed Access | Times Cited: 18
Serine/threonine phosphatases in osteoclastogenesis and bone resorption
Ismael Y. Karkache, Jeyaram R. Damodaran, David H. H. Molstad, et al.
Gene (2020) Vol. 771, pp. 145362-145362
Open Access | Times Cited: 15
miRNA Genetic Variants Alter Their Secondary Structure and Expression in Patients With RASopathies Syndromes
Joseane Biso de Carvalho, Guilherme Loss de Morais, Thays Cristine dos Santos Vieira, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 14
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
Noonan syndrome‐associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafish
Yu Nakagama, Norihiko Takeda, Seishi Ogawa, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 8, Iss. 3
Open Access | Times Cited: 13
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome
Yasuko Shoji, Ayaha Hata, Takatoshi Maeyama, et al.
Clinical Pediatric Endocrinology (2024) Vol. 33, Iss. 2, pp. 50-58
Open Access | Times Cited: 1
Macrocephaly and Finger Changes: A Narrative Review
Cecilia Lazea, Romana Vulturar, Adina Chiş, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5567-5567
Open Access | Times Cited: 1
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
The RASopathies: Biology, genetics and therapeutic options
Jody Fromm Longo, Steven L. Carroll
Advances in cancer research (2022), pp. 305-341
Closed Access | Times Cited: 7
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1
Yuqi Wang, Jianong Zhang, Pingzhao Zhang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 9
Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center
Tuğba Saraç Sivrikoz, Seher Başaran, Recep Has, et al.
Archives of Gynecology and Obstetrics (2021) Vol. 305, Iss. 2, pp. 323-342
Closed Access | Times Cited: 9
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
PP1β opposes classic PP1 function, inhibiting spine maturation and promoting LTP
Karl Foley, Cody McKee, Abigail Mayer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
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
Cardiac features of Noonan syndrome in Japanese patients
Yasuhiro Ichikawa, Hiroyuki Kuroda, Takeshi Ikegawa, et al.
Cardiology in the Young (2022) Vol. 33, Iss. 4, pp. 564-569
Closed Access | Times Cited: 4
Case report: Identification and clinical phenotypic analysis of novel mutation of the PPP1CB gene in NSLH2 syndrome
Xuemei He, Xiuli Ma, Jing Wang, et al.
Frontiers in Behavioral Neuroscience (2022) Vol. 16
Open Access | Times Cited: 4
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
A case report of Noonan syndrome‐like disorder with loose anagen hair 2 treated with recombinant human growth hormone
Ping Zhou, Lin Zhu, Qiongli Fan, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 8, pp. 1967-1971
Closed Access | Times Cited: 4
Genetics of FASD: Confounding Rare Craniofacial and Neurodevelopmental Disorders May Identify Ethanol-Sensitizing Genetic Variants of FASD
Leo McKay, Berardino Petrelli, Albert E. Chudley, et al.
Neuromethods (2022), pp. 77-117
Closed Access | Times Cited: 3
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

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