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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 six-attribute classification of geneticmosaicism
Victor Martínez‐Glez, Jair Tenorio, Julián Nevado, et al.
Genetics in Medicine (2020) Vol. 22, Iss. 11, pp. 1743-1757
Open Access | Times Cited: 53

Showing 1-25 of 53 citing articles:

IVF outcomes of embryos with abnormal PGT-A biopsy previously refused transfer: a prospective cohort study
David H. Barad, David F. Albertini, Emanuela Molinari, et al.
Human Reproduction (2022) Vol. 37, Iss. 6, pp. 1194-1206
Open Access | Times Cited: 47
Genotoxicity assessment: opportunities, challenges and perspectives for quantitative evaluations of dose–response data
Jakob Menz, Mario E. Götz, Ulrike Gündel, et al.
Archives of Toxicology (2023) Vol. 97, Iss. 9, pp. 2303-2328
Open Access | Times Cited: 36
Human embryonic genetic mosaicism and its effects on development and disease
Sarah M. Waldvogel, Jennifer E. Posey, Margaret A. Goodell
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 12
Capillary malformations
Adrienne M. Hammill, Elisa Boscolo
Journal of Clinical Investigation (2024) Vol. 134, Iss. 8
Open Access | Times Cited: 9
A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease
Emma Ehn, Jesper Eisfeldt, José Miguel Laffita‐Mesa, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 1
De novo mutations, genetic mosaicism and human disease
Mohiuddin Mohiuddin, R. Frank Kooy, Christopher E. Pearson
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 37
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants
Alessandro Mussa, Chiara Leoni, Matteo Iacoviello, et al.
Journal of Medical Genetics (2022) Vol. 60, Iss. 2, pp. 163-173
Closed Access | Times Cited: 27
A Novel Deep Intronic Variant in NSD1 Causing Sotos Syndrome
Alejandro Parra, Mario Cazalla, Juan Andrés Jiménez-Estrada, et al.
American Journal of Medical Genetics Part A (2025)
Closed Access
Multifocal PIK3CA Related Congenital Hemangioma
Patricia Andres‐Ibarrola, Irune Méndez Maestro, Aitor Fernández Larrinoa Santamaria, et al.
Pediatric Dermatology (2025)
Closed Access
Cytogenomic characterization of mosaic X-ring chromosomes in seventeen patients with Turner syndrome (TS)-42 years of experience at a single-site institution
Anita Madison, Carolyn Applegate, Victoria Stinnett, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
The contribution of mosaicism to genetic diseases and de novo pathogenic variants
Rory J. Tinker, Lisa Bastarache, Kimberly Ezell, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 10, pp. 2482-2492
Open Access | Times Cited: 8
Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature
Valentina Trevisan, Anna Meroni, Chiara Leoni, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 346-346
Open Access | Times Cited: 2
Occurrence of mosaic Down syndrome and prevalence of co‐occurring conditions in Medicaid enrolled adults, 2016–2019
Eric Rubenstein, Salina Tewolde, Brian G. Skotko, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2024)
Closed Access | Times Cited: 2
Somatic mutations in autoinflammatory and autoimmune disease
Sofia Torreggiani, Flore S. Castellan, Ivona Aksentijevich, et al.
Nature Reviews Rheumatology (2024) Vol. 20, Iss. 11, pp. 683-698
Closed Access | Times Cited: 2
Mosaicism in Tumor Suppressor Gene Syndromes: Prevalence, Diagnostic Strategies, and Transmission Risk
Jillian L. Chen, David T. Miller, Laura S. Schmidt, et al.
Annual Review of Genomics and Human Genetics (2022) Vol. 23, Iss. 1, pp. 331-361
Open Access | Times Cited: 11
Delineation of the phenotypes and genotypes of facial infiltrating lipomatosis associated with PIK3CA mutations
Hongrui Chen, Bin Sun, Wei Gao, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Functional and structural analyses of novel Smith-Kingsmore Syndrome-Associated MTOR variants reveal potential new mechanisms and predictors of pathogenicity
Aaron D. Besterman, Thorsten Althoff, Peter Elfferich, et al.
PLoS Genetics (2021) Vol. 17, Iss. 7, pp. e1009651-e1009651
Open Access | Times Cited: 14
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
Revertant Mosaicism in Genodermatoses: Natural Gene Therapy Right before Your Eyes
Peter C. van den Akker, Maria C. Bolling, Anna M.G. Pasmooij
Biomedicines (2022) Vol. 10, Iss. 9, pp. 2118-2118
Open Access | Times Cited: 8
Segmental undergrowth is associated with pathogenic variants in vascular malformation genes: A retrospective case‐series study
Victor Martínez‐Glez, Lara Rodríguez‐Laguna, Vanesa Viana‐Huete, et al.
Clinical Genetics (2021) Vol. 101, Iss. 3, pp. 296-306
Closed Access | Times Cited: 11
Distal arthrogryposis in a girl arising from a novel TNNI2 variant inherited from paternal somatic mosaicism
Rie Seyama, Yuri Uchiyama, Yosuke Kaneshi, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 5, pp. 363-367
Closed Access | Times Cited: 4
Unexpected Findings in Hereditary Breast and Ovarian Cancer Syndrome: Low-Level Constitutional Mosaicism in BRCA2
Irene Hidalgo Mayoral, Ainhoa Almeida Santiago, Jose Manuel Sánchez-Zapardiel, et al.
Genes (2023) Vol. 14, Iss. 2, pp. 502-502
Open Access | Times Cited: 4
Mosaic trisomy 12 diagnosed in a female patient: clinical features, genetic analysis, and review of the literature
Daniela Hainz, Marcus Krüger, Daniela Reber, et al.
World Journal of Pediatrics (2021) Vol. 17, Iss. 4, pp. 438-448
Open Access | Times Cited: 6
Genomic Mosaicism of the Brain: Origin, Impact, and Utility
Jared H. Graham, Johannes C. M. Schlachetzki, Xiaoxu Yang, et al.
Neuroscience Bulletin (2023) Vol. 40, Iss. 6, pp. 759-776
Open Access | Times Cited: 2
Accuracy and depth evaluation of clinical low pass genome sequencing in the detection of mosaic aneuploidies and CNVs
Yanqiu Liu, Shengju Hao, Xueqin Guo, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 2
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