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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:

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population
Sirui Zhou, Amirthagowri Ambalavanan, Daniel Rochefort, et al.
The American Journal of Human Genetics (2016) Vol. 99, Iss. 5, pp. 1072-1085
Open Access | Times Cited: 60

Showing 1-25 of 60 citing articles:

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Mark K. Bakker, Rick A. A. van der Spek, Wouter van Rheenen, et al.
Nature Genetics (2020) Vol. 52, Iss. 12, pp. 1303-1313
Open Access | Times Cited: 257
Intracranial Aneurysms: Pathology, Genetics, and Molecular Mechanisms
Zhen Xu, Yan‐Ning Rui, John P. Hagan, et al.
NeuroMolecular Medicine (2019) Vol. 21, Iss. 4, pp. 325-343
Open Access | Times Cited: 102
The Genetic Basis of Moyamoya Disease
Robert Mertens, Mariona Graupera, Holger Gerhardt, et al.
Translational Stroke Research (2021) Vol. 13, Iss. 1, pp. 25-45
Open Access | Times Cited: 95
Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians
Stéphanie Guey, Markus Kraemer, Dominique Hervé, et al.
European Journal of Human Genetics (2017) Vol. 25, Iss. 8, pp. 995-1003
Open Access | Times Cited: 94
Genetics of Intracranial Aneurysms
Mark K. Bakker, Ynte M. Ruigrok
Stroke (2021) Vol. 52, Iss. 9, pp. 3004-3012
Open Access | Times Cited: 59
Moyamoya Disease Susceptibility Gene RNF213 Regulates Endothelial Barrier Function
Vincent Roy, Jay P. Ross, Rémy Pépin, et al.
Stroke (2022) Vol. 53, Iss. 4, pp. 1263-1275
Open Access | Times Cited: 43
Genetics of Intracranial Aneurysms
Sirui Zhou, Patrick A. Dion, Guy A. Rouleau
Stroke (2018) Vol. 49, Iss. 3, pp. 780-787
Open Access | Times Cited: 78
Novel Multifaceted Roles for RNF213 Protein
Giuliana Pollaci, Gemma Gorla, Antonella Potenza, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 9, pp. 4492-4492
Open Access | Times Cited: 33
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans
Tanyeri Barak, Emma Ristori, A. Gulhan Ercan‐Sencicek, et al.
Nature Medicine (2021) Vol. 27, Iss. 12, pp. 2165-2175
Open Access | Times Cited: 41
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm
Romain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud, et al.
The American Journal of Human Genetics (2018) Vol. 102, Iss. 1, pp. 133-141
Open Access | Times Cited: 43
RNF213-Associated Vascular Disease: A Concept Unifying Various Vasculopathies
Takahiro Hiraide, Hisato Suzuki, Mizuki Momoi, et al.
Life (2022) Vol. 12, Iss. 4, pp. 555-555
Open Access | Times Cited: 22
Genetic basis of intracranial aneurysm formation and rupture: clinical implications in the postgenomic era
Nardin Samuel, Ivan Radovanovic
Neurosurgical FOCUS (2019) Vol. 47, Iss. 1, pp. E10-E10
Open Access | Times Cited: 33
Hereditary Haemorrhagic Cerebrovascular Disease: Implications for Clinical Management
Wanting Hou, Y. Hou, Xiangshan Ren, et al.
Annals of Neurosciences (2025)
Open Access
Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage
Thomas Sauvigny, Malik Alawi, Linda Krause, et al.
Journal of Neurology (2020) Vol. 267, Iss. 9, pp. 2533-2545
Open Access | Times Cited: 22
The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea
Young Min Park, Hui Jeong An, Jung Oh Kim, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 11, pp. 2477-2477
Open Access | Times Cited: 22
Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressure
Shan Liu, Mengwei Liu, Qian Li, et al.
Bioscience Reports (2019) Vol. 39, Iss. 12
Open Access | Times Cited: 21
Mutations of RNF213 are responsible for sporadic cerebral cavernous malformation and lead to a mulberry-like cluster in zebrafish
Jing Lin, Jie Liang, Jun Wen, et al.
Journal of Cerebral Blood Flow & Metabolism (2020) Vol. 41, Iss. 6, pp. 1251-1263
Open Access | Times Cited: 19
Rho Guanine Nucleotide Exchange Factor ARHGEF17 Is a Risk Gene for Intracranial Aneurysms
Xinyu Yang, Jiani Li, Yabo Fang, et al.
Circulation Genomic and Precision Medicine (2018) Vol. 11, Iss. 7
Open Access | Times Cited: 20
RNF213 Variant Diversity Predisposes Distinct Populations to Dissimilar Cerebrovascular Diseases
Jing Lin, Wenli Sheng
BioMed Research International (2018) Vol. 2018, pp. 1-7
Open Access | Times Cited: 20
Genetic architecture and adaptations of Nunavik Inuit
Sirui Zhou, Pingxing Xie, Amélie Quoibion, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 32, pp. 16012-16017
Open Access | Times Cited: 18
Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis
Hiroki Hongo, Satoru Miyawaki, Hideaki Imai, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 13
Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm
Yunsun Song, Jong‐Keuk Lee, Jin‐Ok Lee, et al.
Korean Journal of Radiology (2021) Vol. 23, Iss. 1, pp. 101-101
Open Access | Times Cited: 12
Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease
Hiroyuki Akagawa, Maki Mukawa, Tadashi Nariai, et al.
Human Genome Variation (2018) Vol. 5, Iss. 1
Open Access | Times Cited: 13
Exome sequencing reveals a novel variant inNFX1causing intracranial aneurysm in a Chinese family
Xinghuan Ding, Sen Zhao, Qianqian Zhang, et al.
Journal of NeuroInterventional Surgery (2019) Vol. 12, Iss. 2, pp. 221-226
Open Access | Times Cited: 11
<i>RNF213</i>-Related Vasculopathy: Various Systemic Vascular Diseases Involving <i>RNF213</i> Gene Mutations: Review
Yasuo Murai, Fumihiro Matano, Asami Kubota, et al.
Journal of Nippon Medical School (2024) Vol. 91, Iss. 2, pp. 140-145
Open Access | Times Cited: 1
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