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:

Improving clinical trial readiness to accelerate development of new therapeutics for Rett syndrome
Helen Leonard, Wendy Gold, Rodney C. Samaco, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 16

Showing 16 citing articles:

Psychometric Assessment of the Rett Syndrome Caregiver Assessment of Symptom Severity (RCASS)
Melissa Raspa, Angela Gwaltney, Carla Bann, et al.
Journal of Autism and Developmental Disorders (2024)
Closed Access | Times Cited: 7

Rett syndrome
Wendy Gold, Alan K. Percy, Jeffrey L. Neul, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 5

Patient-advocate-led global coalition adapting fit-for-purpose outcomes measures to assure meaningful inclusion of DEEs in clinical trials
JayEtta Hecker, Gabrielle Conecker, Chere A. T. Chapman, et al.
Therapeutic Advances in Rare Disease (2024) Vol. 5
Open Access | Times Cited: 4

What does better look like in individuals with severe neurodevelopmental impairments? A qualitative descriptive study on SCN2A-related developmental and epileptic encephalopathy
Jenny Downs, Natasha N. Ludwig, Mary Wojnaroski, et al.
Quality of Life Research (2023) Vol. 33, Iss. 2, pp. 519-528
Open Access | Times Cited: 8

Characterizing the autism spectrum phenotype in DYRK1A‐related syndrome
Evangeline C. Kurtz‐Nelson, Hannah M. Rea, Aiva C. Petriceks, et al.
Autism Research (2023) Vol. 16, Iss. 8, pp. 1488-1500
Closed Access | Times Cited: 7

Associations between genotype, phenotype and behaviours measured by the Rett syndrome behaviour questionnaire in Rett syndrome
Jenny Downs, Kingsley Wong, Helen Leonard
Journal of Neurodevelopmental Disorders (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 2

Validation of the Observer-Reported Communication Ability (ORCA) measure for individuals with Rett syndrome
Bryce B. Reeve, Nicole Lucas, Dandan Chen, et al.
European Journal of Paediatric Neurology (2023) Vol. 46, pp. 74-81
Closed Access | Times Cited: 6

Multidimensional analysis of a social behavior identifies regression and phenotypic heterogeneity in a female mouse model for Rett syndrome
Michael Mykins, Benjamin B. Bridges, Angela Jo, et al.
Journal of Neuroscience (2024), pp. e1078232023-e1078232023
Open Access | Times Cited: 2

Advances in iPSC Technology in Neural Disease Modeling, Drug Screening, and Therapy
Sihan Dai, Linhui Qiu, Vishnu Priya Veeraraghavan, et al.
Current Stem Cell Research & Therapy (2023) Vol. 19, Iss. 6, pp. 809-819
Closed Access | Times Cited: 4

Using Precision Medicine to Disentangle Genotype–Phenotype Relationships in Twins with Rett Syndrome: A Case Report
Jatinder Singh, Georgina Wilkins, Ella Goodman-Vincent, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 8, pp. 8424-8440
Open Access | Times Cited: 1

Development and Psychometric Properties of the Multi-System Profile of Symptoms Scale in Patients with Rett Syndrome
Jatinder Singh, Federico Fiori, Mei Lin Law, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 17, pp. 5094-5094
Open Access | Times Cited: 7

Auditory event-related potential differentiates girls with Rett syndrome from their typically-developing peers with high accuracy: Machine learning study
Maxim Sharaev, Maxim Nekrashevich, Daria Kostanian, et al.
Cognitive Systems Research (2024) Vol. 85, pp. 101214-101214
Closed Access

Psychometric Assessment of the Rett Syndrome Caregiver Assessment of Symptom Severity (RCASS)
Melissa Raspa, Angela Gqaltney, Carla Bann, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1

Development of an International Database for a Rare Genetic Disorder: The MECP2 Duplication Database (MDBase)
Daniel Ta, Jenny Downs, Gareth Baynam, et al.
Children (2022) Vol. 9, Iss. 8, pp. 1111-1111
Open Access | Times Cited: 1

Multidimensional analysis of a social behavior identifies regression and phenotypic heterogeneity in a female mouse model for Rett syndrome
Michael Mykins, Benjamin B. Bridges, Angela Jo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access

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