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:

Rubinstein–Taybi syndrome in diverse populations
Cedrik Tekendo‐Ngongang, Babajide Owosela, Nicole Fleischer, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 12, pp. 2939-2950
Closed Access | Times Cited: 25

Showing 25 citing articles:

Analysis of large-language model versus human performance for genetics questions
Dat Duong, Benjamin D. Solomon
European Journal of Human Genetics (2023) Vol. 32, Iss. 4, pp. 466-468
Open Access | Times Cited: 99

Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
Julien Van‐Gils, Frédérique Magdinier, Patricia Fergelot, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 968-968
Open Access | Times Cited: 66

Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement
Didier Lacombe, Agnès Bloch‐Zupan, Cecilie Bredrup, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 6, pp. 503-519
Open Access | Times Cited: 12

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16

Recognition of Genetic Conditions After Learning With Images Created Using Generative Artificial Intelligence
Rebekah L. Waikel, Amna A. Othman, Tanviben Patel, et al.
JAMA Network Open (2024) Vol. 7, Iss. 3, pp. e242609-e242609
Open Access | Times Cited: 4

Rubinstein-Taybi syndrome with ganglioneuroblastoma: a case report and literature review
Jiaji Zhou, Dan Tang, Lan Zeng, et al.
BMC Pediatrics (2025) Vol. 25, Iss. 1
Open Access

Approximating facial expression effects on diagnostic accuracy via generative AI in medical genetics
Tanviben Patel, Amna A. Othman, Ömer Sümer, et al.
Bioinformatics (2024) Vol. 40, Iss. Supplement_1, pp. i110-i118
Open Access | Times Cited: 3

Perspectives on the future of dysmorphology
Benjamin D. Solomon, Margaret P Adam, Chin‐To Fong, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 3, pp. 659-671
Closed Access | Times Cited: 15

Neurobiology of puberty and its disorders
Selma F. Witchel, Tony M. Plant
Handbook of clinical neurology (2021), pp. 463-496
Closed Access | Times Cited: 20

Generative Methods for Pediatric Genetics Education
Rebekah L. Waikel, Amna A. Othman, Tanviben Patel, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5

Can artificial intelligence save medical genetics?
Benjamin D. Solomon
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 397-399
Closed Access | Times Cited: 11

Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome
Naye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 10
Open Access | Times Cited: 10

Application of facial analysis Technology in Clinical Genetics: Considerations for diverse populations
Paul Kruszka, Cedrik Tekendo‐Ngongang
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Closed Access | Times Cited: 3

Artificial intelligence and the impact on medical genetics
Benjamin D. Solomon, Wendy K. Chung
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access | Times Cited: 3

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome
Qian Wang, Cong Wang, Wen Bin Wei, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 5

Facial clues to the photosensitive trichothiodystrophy phenotype in childhood
Giulia Pascolini, Federica Gaudioso, Marina Baldi, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 6, pp. 437-443
Closed Access | Times Cited: 2

The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know
Silvia Ciancia, Simona Filomena Madeo, Olga Calabrese, et al.
Children (2024) Vol. 11, Iss. 5, pp. 578-578
Open Access

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Research Square (Research Square) (2024)
Open Access

Evolving technologies in medical genetics and genomics
Benjamin D. Solomon
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2021) Vol. 187, Iss. 1, pp. 5-6
Closed Access | Times Cited: 2

Privacy, bias and the clinical use of facial recognition technology: A survey of genetics professionals
Elias Aboujaoude, Janice Light, Julia E. H. Brown, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access

Artificial intelligence in medical genetics
Rebekah L. Waikel, Dat Duong, Benjamin D. Solomon
Elsevier eBooks (2023), pp. 329-339
Closed Access

Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome
Yasuhito Nagai, M. Nishioka, Tatsuki Tanaka, et al.
Psychiatry and Clinical Neurosciences Reports (2022) Vol. 1, Iss. 3
Open Access

Síndrome de Rubinstein-Taybi, genética e clínica: uma revisão integrativa
Ana Flávia Wendpap Chueire, Marcelle Lupi Gasparini, Clarissa Torresan
Brazilian Journal of Health Review (2022) Vol. 5, Iss. 5, pp. 21727-21742
Open Access

Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update
Alejandro Carlos de la Parte Serna, Ricardo Ortega-Soria, Gonzalo Oliván-Gonzalvo
Iberoamerican Journal of Medicine (2021) Vol. 3, Iss. 2, pp. 169-172
Open Access

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