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:

Exome sequencing in paediatric patients with movement disorders
Anna Ka‐Yee Kwong, Mandy Ho‐Yin Tsang, Jasmine Lee‐Fong Fung, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 22

Showing 22 citing articles:

Next-generation sequencing and bioinformatics in rare movement disorders
Michael Zech, J C Winkelmann
Nature Reviews Neurology (2024) Vol. 20, Iss. 2, pp. 114-126
Closed Access | Times Cited: 12
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder
Khemika K. Sudnawa, Alison Garber, Ryan Cohen, et al.
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 523-532
Closed Access | Times Cited: 9
Genetic Testing of Movements Disorders: A Review of Clinical Utility
Dennis Yeow, Laura Ivete Rudaks, Sue‐Faye Siow, et al.
Tremor and Other Hyperkinetic Movements (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 5
Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies
Jan M. Friedman, Peter van Essen, Clara van Karnebeek
Molecular Genetics and Metabolism (2021) Vol. 137, Iss. 4, pp. 399-419
Open Access | Times Cited: 29
PURA-related neurodevelopmental disorders: a systematic review on genotype-phenotype correlations
Naoyuki Taniguchi, Keisuke Watanuki, Daisuke Nakato, et al.
Journal of Medical Genetics (2025), pp. jmg-110379
Closed Access
A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan
Meng-Chen Wu, Yung‐Yee Chang, Min‐Yu Lan, et al.
Journal of Molecular Diagnostics (2022) Vol. 24, Iss. 3, pp. 262-273
Closed Access | Times Cited: 13
A 25 Mainland Chinese cohort of patients with PURA-related neurodevelopmental disorders: clinical delineation and genotype–phenotype correlations
Weiqian Dai, Yu Sun, Yanjie Fan, et al.
European Journal of Human Genetics (2022) Vol. 31, Iss. 1, pp. 112-121
Open Access | Times Cited: 13
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant
Jonna Komulainen‐Ebrahim, Salla M. Kangas, Estrella López‐Martín, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 6, pp. 708-715
Open Access | Times Cited: 2
Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies
Jana Domínguez Carral, Carola Reinhard, Darius Ebrahimi‐Fakhari, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 2
PSMF1variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways
Francesca Magrinelli, Christelle Tesson, Plamena R. Angelova, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
KMT2B-Related Dystonia in Indian Patients With Literature Review and Emphasis on Asian Cohort
Debjyoti Dhar, Vikram V. Holla, Riyanka Kumari, et al.
Journal of Movement Disorders (2023) Vol. 16, Iss. 3, pp. 285-294
Open Access | Times Cited: 4
Genetically altered animal models forATP1A3-related disorders
Hannah Wai Yiu Ng, Jennifer A. Ogbeta, Steven J. Clapcote
Disease Models & Mechanisms (2021) Vol. 14, Iss. 10
Open Access | Times Cited: 8
Dystonia‐Deafness Syndrome: ACTB Pathogenic Variant in an Argentinean Family
Lucía Zavala, Gabriela Ziegler, Dolores González Morón, et al.
Movement Disorders Clinical Practice (2021) Vol. 9, Iss. 1, pp. 122-124
Open Access | Times Cited: 7
RNA sequencing reveals a complete picture of a homozygous missense variant in a patient with VPS13D movement disorder: a case report and review of the literature
Elizabeth Baker, Jingfen Han, William A. Langley, et al.
Molecular Genetics and Genomics (2023) Vol. 298, Iss. 5, pp. 1185-1199
Closed Access | Times Cited: 2
Limitations of Multigene Next-Generation Sequencing Panel for “Cerebral Palsy” Phenotype and Other Complex Movement Disorders
Marina Eskandar, Laura Tochen, Mi Ran Shin, et al.
Pediatric Neurology (2023) Vol. 149, pp. 15-18
Closed Access | Times Cited: 1
A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients
Lidangzhi Mo, Xiaoling Tie, Fengyu Che, et al.
Pediatric Neurology (2024) Vol. 152, pp. 200-208
Closed Access
Clinical Response of Levodopa in CTNNB1-Related Dystonia
Anna Revert Barberà, Loreto Martorell, Cristina Martínez Boix, et al.
Journal of Pediatric Neurology (2024) Vol. 22, Iss. 06, pp. 466-469
Closed Access
Translating Genetic Discovery into a Mechanistic Understanding of Pediatric Movement Disorders: Lessons from Genetic Dystonias and Related Disorders
Wei‐Sheng Lin
Advanced Genetics (2022) Vol. 4, Iss. 2
Open Access | Times Cited: 2
Integrative Multi-Omics Research in Cerebral Palsy: Current Progress and Future Prospects
Chengqi Xin, Xin Guan, Liang Wang, et al.
Neurochemical Research (2022) Vol. 48, Iss. 5, pp. 1269-1279
Closed Access | Times Cited: 1
Dyskinetic Crisis in GNAO1-Related Disorder: A Comprehensive International Delphi Study
J. Domínguez-Carral, Carola Reinhard, Darius Ebrahimi‐Fakhari, et al.
(2023)
Closed Access
Dystonia
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, et al.
Elsevier eBooks (2022), pp. 229-262
Closed Access
Dystonia‐Deafness Syndrome Response to Subthalamic Nucleus Stimulation
Yi Zhang, Ying Huang, Lin Wang, et al.
Movement Disorders Clinical Practice (2022) Vol. 9, Iss. 8, pp. 1124-1127
Open Access
Page 1

Scroll to top