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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:

Consensus recommendations on mental health issues in Phelan-McDermid syndrome
Ingrid D. C. van Balkom, Mónica Burdeus, Jennifer Cooke, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 6, pp. 104770-104770
Open Access | Times Cited: 12

Showing 12 citing articles:

Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome
Michael Schön, Pablo Lapunzina, Julián Nevado, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 7, pp. 104754-104754
Open Access | Times Cited: 27
Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey
Annemiek Landlust, Sylvia A. Koza, Maya J. Carbin, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 7, pp. 104771-104771
Open Access | Times Cited: 16
Behavioral and Psychiatric Disorders in Syndromic Autism
Ann Genovese, Merlin G. Butler
Brain Sciences (2024) Vol. 14, Iss. 4, pp. 343-343
Open Access | Times Cited: 4
Diagnosis and treatment of bipolar disorder in Phelan-McDermid syndrome: A case report and review of literature
Yongxue Sun, Yong Xia, Qianna Zhi, et al.
World Journal of Psychiatry (2025) Vol. 15, Iss. 2
Closed Access
Phenotype and psychometric characterization of Phelan-McDermid syndrome patients: pioneering towards personalized medicine
Julián Nevado, Filippo Ciceri, Cristina Bel‐Fenellós, et al.
Frontiers in Psychiatry (2025) Vol. 16
Open Access
Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome
Agnies M. van Eeghen, D. Stemkens, José Ramón Fernández‐Fructuoso, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 7, pp. 104747-104747
Open Access | Times Cited: 9
Consensus recommendations on communication, language and speech in Phelan-McDermid syndrome
Mónica Burdeus, Julián Nevado, Sabrina van Weering-Scholten, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 5, pp. 104745-104745
Open Access | Times Cited: 8
Editorial: Towards a European consensus guideline for Phelan-McDermid syndrome
Conny M.A. van Ravenswaaij‐Arts, Ingrid D. C. van Balkom, Sarah Jesse, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 5, pp. 104736-104736
Open Access | Times Cited: 8
Consensus recommendations on sleeping problems in Phelan-McDermid syndrome
Antonia San José Cáceres, Annemiek Landlust, J.M. Carbin, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 6, pp. 104750-104750
Open Access | Times Cited: 7
Phelan–McDermid Syndrome
Paige Hickey, Heli Patel, Ann M. Neumeyer
(2024), pp. 203-228
Closed Access | Times Cited: 1
Case study: bipolar disorder and catatonia in an adult autistic male with intellectual disability and Phelan-McDermid syndrome (22q13.33 deletion syndrome): psychopharmacological treatment and symptom trajectories
Maria Rognlid Skavås, Malin Rognlid, Arvid Nikolai Kildahl
International Journal of Developmental Disabilities (2024), pp. 1-12
Open Access
Spotted around the web: WNT pathway; Phelan-McDermid syndrome; haploinsufficiencies
Jill Adams
The Transmitter (2023)
Open Access
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