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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:

A new case of Smith‐Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth
Diana Carli, Giovanni Battista Ferrero, Anna Fusillo, et al.
Clinical Genetics (2021) Vol. 99, Iss. 5, pp. 719-723
Closed Access | Times Cited: 12

Showing 12 citing articles:

Quantification of Lateralized Overgrowth and Genotype‐Driven Tissue Composition
Andrea Gazzin, G.J. Reynolds, Damiano Allegro, et al.
Clinical Genetics (2025)
Open Access
Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros)
G.J. Reynolds, Simona Cardaropoli, Diana Carli, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 11, pp. 1333-1336
Open Access | Times Cited: 9
The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowth
Maria Luca, Marilidia Piglionica, Rosanna Bagnulo, et al.
Genes Chromosomes and Cancer (2023) Vol. 62, Iss. 12, pp. 703-709
Open Access | Times Cited: 5
Molecular Basis and Diagnostic Approach to Isolated and Syndromic Lateralized Overgrowth in Childhood
Simone Bellucca, Diana Carli, Andrea Gazzin, et al.
The Journal of Pediatrics (2024) Vol. 274, pp. 114177-114177
Open Access | Times Cited: 1
Clinical and functional studies of MTOR variants in Smith-Kingsmore syndrome reveal deficits of circadian rhythm and sleep-wake behavior
Andrew C. Liu, Yang Shen, Carolyn R. Serbinski, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 4, pp. 100333-100333
Open Access | Times Cited: 1
Detailed Clinical and Functional Studies of New MTOR Variants in Smith-Kingsmore Syndrome Reveal Deficits of Circadian and Sleep Homeostasis
Andrew C. Liu, Yang Shen, Destino Roman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Midline non-ictal rhythmic waveforms as possible electroencephalographic biomarkers of Smith-Klingsmore syndrome in children
Valerio Simonelli, Anna Rita Ferrari, Roberta Battini, et al.
Clinical Neurophysiology Practice (2024) Vol. 9, pp. 102-105
Open Access
Smith-Kingsmore Syndrome (SKS)
Cena Aram
Springer eBooks (2024), pp. 1-6
Closed Access
Unique presentation of a novel gain-of-function mutation in MTOR
Samira Slimani, Alex G.I. Gagnon, Simon V. Schreiber, et al.
Genes & Diseases (2024) Vol. 12, Iss. 2, pp. 101405-101405
Open Access
Correspondence on “Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities,” by Carmignac et al.
Nicoletta Resta, Olga Calabrese, Valentina Grossi, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2223-2224
Open Access | Times Cited: 2
Smith-Kingsmore syndrome with nystagmus as the initial symptom
Meiling Cai, Yanfei Zhao, He Wang, et al.
Acta Epileptologica (2023) Vol. 5, Iss. 1
Open Access
Response to Resta et al.
Virginie Carmignac, P. Vabres
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2225-2225
Open Access
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