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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.

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Showing 14 citing articles:

A novel davunetide (NAPVSIPQQ to NAPVSIPQE) point mutation in activity‐dependent neuroprotective protein (ADNP) causes a mild developmental syndrome
Illana Gozes, Shula Shazman
European Journal of Neuroscience (2023) Vol. 58, Iss. 2, pp. 2641-2652
Open Access | Times Cited: 14
NAP (Davunetide): The Neuroprotective ADNP Drug Candidate Penetrates Cell Nuclei Explaining Pleiotropic Mechanisms
Maram Ganaiem, Nina D. Gildor, Shula Shazman, et al.
Cells (2023) Vol. 12, Iss. 18, pp. 2251-2251
Open Access | Times Cited: 11
A convergent mechanism of high risk factors ADNP and POGZ in neurodevelopmental disorders
Megan Conrow-Graham, Jamal B. Williams, Jennifer A. Martin, et al.
Brain (2022) Vol. 145, Iss. 9, pp. 3250-3263
Open Access | Times Cited: 17
Distinct Impairments Characterizing Different ADNP Mutants Reveal Aberrant Cytoplasmic-Nuclear Crosstalk
Maram Ganaiem, Gidon Karmon, Yanina Ivashko‐Pachima, et al.
Cells (2022) Vol. 11, Iss. 19, pp. 2994-2994
Open Access | Times Cited: 17
Longitudinal Genotype-Phenotype (Vineland Questionnaire) Characterization of 15 ADNP Syndrome Cases Highlights Mutated Protein Length and Structural Characteristics Correlation with Communicative Abilities Accentuated in Males
Jospeh Levine, Alexandra Lobyntseva, Shula Shazman, et al.
Journal of Molecular Neuroscience (2024) Vol. 74, Iss. 1
Closed Access | Times Cited: 3
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van der Aa syndrome autopsy case
Claudio Peter D’Incal, Anke Van Dijck, Joe Ibrahim, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 3
Somatic Mutations and Alzheimer’s Disease
Jocelyn Downey, Jacqueline C. K. Lam, Victor O. K. Li, et al.
Journal of Alzheimer s Disease (2022) Vol. 90, Iss. 2, pp. 475-493
Closed Access | Times Cited: 13
Vineland Adaptive Behavior Scale in a Cohort of Four ADNP Syndrome Patients Implicates Age-Dependent Developmental Delays with Increased Impact of Activities of Daily Living
Joseph Levine, Fahed Hakim, R. Frank Kooy, et al.
Journal of Molecular Neuroscience (2022) Vol. 72, Iss. 8, pp. 1531-1546
Closed Access | Times Cited: 12
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
Claudio Peter D’Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Protective inherited mutations in activity-dependent neuroprotective protein (ADNP): the good, the bad, and the ugly
Illana Gozes, Shula Shazman, Eliezer Giladi, et al.
Genomic psychiatry : (2024), pp. 1-7
Closed Access | Times Cited: 1
Neuroprotective effect of the PACAP-ADNP axis on SOD1G93A mutant motor neuron death induced by trophic factors deprivation
Benedetta Magrì, Agata Grazia D’Amico, Grazia Maugeri, et al.
Neuropeptides (2023) Vol. 102, pp. 102386-102386
Closed Access | Times Cited: 2
In Search of the Hidden Protein: Optimization of Detection Strategies for autism-associated Activity-Dependent Neuroprotective Protein (ADNP) mutants.
Claudio Peter D’Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 3
An experimental framework for conjoint measures of olfaction, navigation, and motion as pre-clinical biomarkers of Alzheimer's disease
Katarina Biljman, Illana Gozes, Jacqueline C. K. Lam, et al.
Journal of Alzheimer s Disease Reports (2024) Vol. 8, Iss. 1, pp. 1722-1744
Open Access
Tracing the Invisible Mutant ADNP protein in Helsmoortel- Van der Aa Syndrome patients
Claudio Peter D’Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
Research Square (Research Square) (2023)
Open Access
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