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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 26-50 of 60 citing articles:

Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms
Jinkwon Kim, Young Seok Park, Min-Hee Woo, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 6, pp. 1956-1956
Open Access | Times Cited: 9
A Rare Variant of ANK3 Is Associated With Intracranial Aneurysm
Junyu Liu, Xin Liao, Jilin Zhou, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 8
Dietary patterns among French-speaking men residing in Montreal, Canada
Karine Trudeau, Marie-Claude Rousseau, Ilona Csizmadi, et al.
Preventive Medicine Reports (2018) Vol. 13, pp. 205-213
Open Access | Times Cited: 8
Rare Neurovascular Diseases in Korea: Classification and Related Genetic Variants
Yunsun Song, Boseong Kwon, Abdulrahman Hamad Al-Abdulwahhab, et al.
Korean Journal of Radiology (2021) Vol. 22, Iss. 8, pp. 1379-1379
Open Access | Times Cited: 7
Association of Ring Finger Protein 213 Gene P.R4810k Polymorphism with Intracranial Major Artery Stenosis/Occlusion
Qian Zhang, Le‐Bao Yu, Peicong Ge, et al.
Journal of Stroke and Cerebrovascular Diseases (2018) Vol. 27, Iss. 6, pp. 1556-1564
Closed Access | Times Cited: 6
Rare and Low-Frequency Variants in RNF213 Confer Susceptibility to Moyamoya Syndrome Associated with Hyperthyroidism
Shunsuke Nomura, Hiroyuki Akagawa, Koji Yamaguchi, et al.
World Neurosurgery (2019) Vol. 127, pp. e460-e466
Closed Access | Times Cited: 6
Peptidomic profiling of cerebrospinal fluid from patients with intracranial saccular aneurysms
Gabriel Reis Sakaya, Carolina A. Parada, Rosangela A. S. Eichler, et al.
Journal of Proteomics (2021) Vol. 240, pp. 104188-104188
Closed Access | Times Cited: 6
Mystery(n) Phenotypic Presentation in Europeans: Report of Three Further Novel Missense RNF213 Variants Leading to Severe Syndromic Forms of Moyamoya Angiopathy and Literature Review
Claudia Santoro, Giuseppe Mirone, Mariateresa Zanobio, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 16, pp. 8952-8952
Open Access | Times Cited: 4
Biology, Physics and Genetics of Intracranial Aneurysm Formation: A Review
K. Ćmiel-Smorzyk, Piotr Ładziński, Wojciech Kaspera
Journal of Neurological Surgery Part A Central European Neurosurgery (2022)
Open Access | Times Cited: 4
The Genetic Landscape of Cerebral Steno-Occlusive Arteriopathy and Stroke in Sickle Cell Anemia
Catherine Amlie‐Lefond, Jonathan M. Flanagan, Julie Kanter, et al.
Journal of Stroke and Cerebrovascular Diseases (2018) Vol. 27, Iss. 11, pp. 2897-2904
Closed Access | Times Cited: 5
DNA Methylation Analysis Identifies Differentially Methylated Sites Associated with Early-Onset Intracranial Atherosclerotic Stenosis
Xinwei He, Ying Zhao, Yan-Hui Shi, et al.
Journal of Atherosclerosis and Thrombosis (2019) Vol. 27, Iss. 1, pp. 71-99
Open Access | Times Cited: 4
Familial Intracranial Aneurysm in Newfoundland: Clinical and Genetic Analysis
Amy E. Powell, Bridget A. Fernandez, Falah Maroun, et al.
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (2019) Vol. 46, Iss. 5, pp. 518-526
Open Access | Times Cited: 4
RNF213 rare variants and cerebral arteriovenous malformation in a Chinese population
Junyu Liu, Chongyu Hu, Jilin Zhou, et al.
Clinical Neurology and Neurosurgery (2021) Vol. 203, pp. 106582-106582
Closed Access | Times Cited: 4
Genetic Disorders of the Vasculature
Adam J. Brownstein, Bulat A. Ziganshin, John A. Elefteriades
Elsevier eBooks (2017), pp. 327-367
Closed Access | Times Cited: 3
Fatal brainstem injury following proton radiation in a patient with medulloblastoma and a germline variant in RNF213
Darren Klawinski, Catherine E. Cottrell, Kathleen M. Schieffer, et al.
Pediatric Blood & Cancer (2023) Vol. 71, Iss. 1
Closed Access | Times Cited: 1
RNF213 Polymorphisms in Intracranial Artery Dissection
Marialuisa Zedde, Ilaria Grisendi, Federica Assenza, et al.
Genes (2024) Vol. 15, Iss. 6, pp. 725-725
Open Access
Genetic Insights into the Enigma of Family Intracranial Aneurysms
Alimasi Abulizi, Riqing Su, Pengfei Wu, et al.
World Neurosurgery (2024) Vol. 193, pp. 135-140
Open Access
Gene Commonality in Arterial Circuits Throughout the Body
Lisa C. Harling, Mohammad A. Zafar, Bulat A. Ziganshin, et al.
Aorta (2024) Vol. 12, Iss. 01, pp. 008-012
Open Access
Exploring RNF213 in Ischemic Stroke and Moyamoya Disease: From Cellular Models to Clinical Insights
Benjamin Yong‐Qiang Tan, Charlene Kok, M. Ng, et al.
Biomedicines (2024) Vol. 13, Iss. 1, pp. 17-17
Open Access
Pericyte Ontogeny: The Use of Chimeras to Track a Cell Lineage of Diverse Germ Line Origins
Heather Etchevers
Methods in molecular biology (2021), pp. 61-87
Closed Access | Times Cited: 3
Association of rare RNF213 variants and intracranial aneurysm risk in a Chinese population
Yaqi Li, Junyu Liu, Chongyu Hu, et al.
Annals of Translational Medicine (2022) Vol. 10, Iss. 24, pp. 1336-1336
Open Access | Times Cited: 2
RNF213 c.14576G>A Is Associated with Intracranial Internal Carotid Artery Saccular Aneurysms
Yasuo Murai, Eitaro Ishisaka, Atsushi Watanabe, et al.
Genes (2021) Vol. 12, Iss. 10, pp. 1468-1468
Open Access | Times Cited: 2
Pericyte ontogeny: the use of chimeras to track a cell lineage of diverse germ line origins
Heather Etchevers
bioRxiv (Cold Spring Harbor Laboratory) (2017)
Open Access | Times Cited: 1
OBSOLETE: Genetic Disorders of the Vasculature
John A. Elefteriades
Elsevier eBooks (2017)
Closed Access | Times Cited: 1
RNF213 variation, a broader role in neurovascular disease in Caucasian and Japanese populations
Oswaldo Lorenzo‐Betancor, Patrick R. Blackburn, Luca Farrugia, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 1

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