Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Family studies to find rare high risk variants in migraine
Rikke Dyhr Hansen, Anne Francke Christensen, Jes Olesen
The Journal of Headache and Pain (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 23

Showing 23 citing articles:

Advances in genetics of migraine
Heidi G. Sutherland, Cassie L. Albury, Lyn R. Griffiths
The Journal of Headache and Pain (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 175
Migraine and neuroinflammation: the inflammasome perspective
Oğuzhan Kurşun, Müge Yemişçi, Arn M. J. M. van den Maagdenberg, et al.
The Journal of Headache and Pain (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 163
Migraine Burden of Disease: From the Patient's Experience to a Socio‐Economic View
R. Agosti
Headache The Journal of Head and Face Pain (2018) Vol. 58, Iss. S1, pp. 17-32
Open Access | Times Cited: 148
Clinical Features, Familial History, and Migraine Precursors in Patients With Definite Vestibular Migraine: The VM‐Phenotypes Projects
Roberto Teggi, Bruno Colombo, Roberto Albera, et al.
Headache The Journal of Head and Face Pain (2017) Vol. 58, Iss. 4, pp. 534-544
Open Access | Times Cited: 96
Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance
Aquillah M. Kanzi, James Emmanuel San, Benjamin Chimukangara, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 84
Exploring the Hereditary Nature of Migraine
Charlene Bron, Heidi G. Sutherland, Lyn R. Griffiths
Neuropsychiatric Disease and Treatment (2021) Vol. Volume 17, pp. 1183-1194
Open Access | Times Cited: 40
Functional gene networks reveal distinct mechanisms segregating in migraine families
Andreas Rasmussen, Lisette J. A. Kogelman, David M. Kristensen, et al.
Brain (2020) Vol. 143, Iss. 10, pp. 2945-2956
Open Access | Times Cited: 27
Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes
Phillip E. Melton, Matthew P. Johnson, Dnyanada Gokhale-Agashe, et al.
Journal of Hypertension (2019) Vol. 37, Iss. 5, pp. 997-1011
Closed Access | Times Cited: 23
Rare GPR37L1 Variants Reveal Potential Association between GPR37L1 and Disorders of Anxiety and Migraine
Gerda E. Breitwieser, Andrea Cippitelli, Yingcai Wang, et al.
Journal of Neuroscience (2024) Vol. 44, Iss. 19, pp. e1226232024-e1226232024
Closed Access | Times Cited: 2
Clinical Features of Headache in Patients With Diagnosis of Definite Vestibular Migraine: The VM-Phenotypes Projects
Roberto Teggi, Bruno Colombo, Roberto Albera, et al.
Frontiers in Neurology (2018) Vol. 9
Open Access | Times Cited: 20
Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine
Marta Kowalska, Michał Prendecki, Magdalena Kapelusiak-Pielok, et al.
Current Genomics (2020) Vol. 21, Iss. 3, pp. 224-236
Open Access | Times Cited: 16
Familial analysis reveals rare risk variants for migraine in regulatory regions
Tanya Ramdal Techlo, Andreas Rasmussen, Peter Möller, et al.
Neurogenetics (2020) Vol. 21, Iss. 3, pp. 149-157
Open Access | Times Cited: 14
Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease
Daniela Felício, Miguel Alves‐Ferreira, Mariana Santos, et al.
Briefings in Functional Genomics (2023) Vol. 23, Iss. 2, pp. 138-149
Closed Access | Times Cited: 4
Rare Mutations in CCDC7 Contribute to Early-Onset Preeclampsia by Inhibiting Trophoblast Migration and Invasion
Hu Tan, Yu Li, Jingsi Chen, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 3, pp. 253-253
Open Access | Times Cited: 1
Current Update on Categorization of Migraine Subtypes on the Basis of Genetic Variation: a Systematic Review
Kashish Goel, Aakash Chhetri, Abhilash Ludhiadch, et al.
Molecular Neurobiology (2023) Vol. 61, Iss. 7, pp. 4804-4833
Closed Access | Times Cited: 3
Genetic Epidemiology of Complex Phenotypes
Darren D. O’Rielly, Proton Rahman
Methods in molecular biology (2021), pp. 335-367
Closed Access | Times Cited: 4
Revisão Sistemática sobre Cefaleia em Salvas: Explorando as Correlações com Variáveis Ambientais e Genética
Maria Kéren Ribeiro Sousa, Luanna de Souza Côrtes Cremonez, Myllena Alves Rodrigues, et al.
Brazilian Journal of Implantology and Health Sciences (2024) Vol. 6, Iss. 1, pp. 02-16
Open Access
Genetic architecture of preeclampsia
Aarthi Manoharan, Vishnu Bhat Ballambattu, Ramya Palani
Clinica Chimica Acta (2024) Vol. 558, pp. 119656-119656
Closed Access
Investigate the causality and genetic association between migraine and Parkinson’s disease
Ming‐Gang Deng, Xiuxiu Zhou, Fang Liu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility
Daniela Felício, Andreia Dias, Sandra Martins, et al.
The Journal of Headache and Pain (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Rare GPR37L1 variants reveal potential roles in anxiety and migraine disorders
Gerda E. Breitwieser, Andrea Cippitelli, Yingcai Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Identification of Pre-eclampsia susceptibility genes
Dnyanada Gokhale-Agashe
(2018)
Closed Access
Rare risk variants associate with epigenetic dysregulation in migraine
Tanya Ramdal Techlo, Mona Ameri Chalmer, Peter Möller, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
Page 1

Scroll to top