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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:

Genotype–phenotype correlation in Phelan‐McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes
Arianna Ricciardello, Pasquale Tomaiuolo, Antonio M. Persico
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 7, pp. 2211-2233
Open Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H. Foss‐Feig, Catalina Betancur, et al.
Human Molecular Genetics (2021) Vol. 31, Iss. 4, pp. 625-637
Open Access | Times Cited: 47
Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals
Julián Nevado, Sixto García‐Miñaúr, María Palomares‐Bralo, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 36
Simultaneous CRISPR screening and spatial transcriptomics reveals intracellular, intercellular, and functional transcriptional circuits
Loïc Binan, Serwah Danquah, Vera Valakh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18
PharmVar Tutorial on CYP2D6 Structural Variation Testing and Recommendations on Reporting
Amy Turner, Charity Nofziger, Bronwyn Ramey-Hartung, et al.
Clinical Pharmacology & Therapeutics (2023) Vol. 114, Iss. 6, pp. 1220-1237
Open Access | Times Cited: 16
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome
Aline Vitrac, Claire S. Leblond, Thomas Rolland, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 5, pp. 104732-104732
Open Access | Times Cited: 15
Postsynaptic autism spectrum disorder genes and synaptic dysfunction
Paola Bonsi, Antonella De Jaco, Laurent Fasano, et al.
Neurobiology of Disease (2021) Vol. 162, pp. 105564-105564
Open Access | Times Cited: 32
Lactobacillus plantarum PS128 and Other Probiotics in Children and Adolescents with Autism Spectrum Disorder: A Real-World Experience
Martina Maria Mensi, Chiara Rogantini, Michele Marchesi, et al.
Nutrients (2021) Vol. 13, Iss. 6, pp. 2036-2036
Open Access | Times Cited: 31
Evidence for common mechanisms of pathology between SHANK3 and other genes of Phelan‐McDermid syndrome
Andrew R. Mitz, Luigi Boccuto, Audrey Thurm
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 459-469
Open Access | Times Cited: 4
Identification of a cryptic unbalanced translocation Der(22)t(12;22)(q24.33;q13.33) in a large Chinese family with Phelan-McDermid syndrome by nanopore sequencing
Xingwu Wu, Qiang Xu, Chen Ge, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Orofacial Lymphedema in Phelan–McDermid Syndrome: A Case of Hemifacial Involvement and a Scoping Review
Domenico De Falco, Dario Di Stasio, D Lauritano, et al.
Applied Sciences (2025) Vol. 15, Iss. 4, pp. 2195-2195
Open Access
Aberrant Notch Signaling Pathway as a Potential Mechanism of Central Precocious Puberty
Young Suk Shim, Hae Sang Lee, Jin Soon Hwang
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 6, pp. 3332-3332
Open Access | Times Cited: 17
Co-occurrence of Phelan-McDermid syndrome and metachromatic leukodystrophy
Snehal Mallakmir, Ambalam M. Chandrasekaran, Katy Phelan, et al.
International Journal of Scientific Reports (2025) Vol. 11, Iss. 2, pp. 80-84
Open Access
Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome
Odelia Chorin, Lior Greenbaum, Shelly Lev-Hochberg, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Lymphedema is associated with CELSR1 in Phelan–McDermid syndrome
Marie S. Smith, Sara M. Sarasua, Curtis Rogers, et al.
Clinical Genetics (2023) Vol. 104, Iss. 4, pp. 472-478
Open Access | Times Cited: 7
Loss of ctnnd2b affects neuronal differentiation and behavior in zebrafish
Raquel Vaz, Steven Edwards, Alfredo Dueñas-Rey, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 7
Yield of array‐CGH analysis in Tunisian children with autism spectrum disorder
Fethia Chehbani, Pasquale Tomaiuolo, Chiara Picinelli, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 8
Open Access | Times Cited: 12
The emerging roles of Shank3 in cardiac function and dysfunction
Yoonhee Kim, Tae Hee Ko, Chunmei Jin, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 7
Two Genetic Mechanisms in Two Siblings with Intellectual Disability, Autism Spectrum Disorder, and Psychosis
Yu‐Shu Huang, Ting-Hsuan Fang, Belle Kung, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 6, pp. 1013-1013
Open Access | Times Cited: 10
Genetic and metabolic profiling of individuals with Phelan‐McDermid syndrome presenting with seizures
Lavanya Jain, Lindsay M. Oberman, Laura Curr Beamer, et al.
Clinical Genetics (2021) Vol. 101, Iss. 1, pp. 87-100
Closed Access | Times Cited: 14
State of the Science for Kidney Disorders in Phelan-McDermid Syndrome: UPK3A, FBLN1, WNT7B, and CELSR1 as Candidate Genes
Megan D. McCoy, Sara M. Sarasua, Jane M. DeLuca, et al.
Genes (2022) Vol. 13, Iss. 6, pp. 1042-1042
Open Access | Times Cited: 9
Prenatal and postnatal diagnosis of Phelan–McDermid syndrome: A report of 21 cases from a medical center and review of the literature
Ying Hao, Yang Liu, Yang Jingxin, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 7
Clinical, developmental and serotonemia phenotyping of a sample of 70 Italian patients with Phelan-McDermid Syndrome
Lisa Asta, Arianna Ricciardello, Francesca Cucinotta, et al.
Journal of Neurodevelopmental Disorders (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Phenotypic Variability in Phelan–McDermid Syndrome and Its Putative Link to Environmental Factors
Luigi Boccuto, Andrew R. Mitz, Ludovico Abenavoli, et al.
Genes (2022) Vol. 13, Iss. 3, pp. 528-528
Open Access | Times Cited: 6
Living with and managing seizures among parents of children diagnosed with Phelan-McDermid syndrome: a qualitative study using in-depth interviews
Cristina García‐Bravo, Rosa M. Martínez-Piédrola, Sara García‐Bravo, et al.
European Journal of Pediatrics (2023) Vol. 183, Iss. 1, pp. 253-262
Closed Access | Times Cited: 3
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