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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:

Diagnostic value of exome and whole genome sequencing in craniosynostosis
Kerry A. Miller, Stephen R.F. Twigg, Simon J. McGowan, et al.
Journal of Medical Genetics (2016) Vol. 54, Iss. 4, pp. 260-268
Open Access | Times Cited: 113

Showing 1-25 of 113 citing articles:

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Kandamurugu Manickam, Monica R. McClain, Laurie Demmer, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 11, pp. 2029-2037
Open Access | Times Cited: 396
A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis
Tobias Schwerd, Stephen R.F. Twigg, Dominik Aschenbrenner, et al.
The Journal of Experimental Medicine (2017) Vol. 214, Iss. 9, pp. 2547-2562
Open Access | Times Cited: 180
Clinical genetics of craniosynostosis
Andrew O.M. Wilkie, David Johnson, Steven A. Wall
Current Opinion in Pediatrics (2017) Vol. 29, Iss. 6, pp. 622-628
Open Access | Times Cited: 175
Hiding in Plain Sight: Interleukin-11 Emerges as a Master Regulator of Fibrosis, Tissue Integrity, and Stromal Inflammation
Stuart A. Cook, Sebastian Schäfer
Annual Review of Medicine (2020) Vol. 71, Iss. 1, pp. 263-276
Open Access | Times Cited: 139
Interleukin-11 signaling underlies fibrosis, parenchymal dysfunction, and chronic inflammation of the airway
Benjamin Ng, Stuart A. Cook, Sebastian Schäfer
Experimental & Molecular Medicine (2020) Vol. 52, Iss. 12, pp. 1871-1878
Open Access | Times Cited: 88
Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability
Jennifer Malinowski, David T. Miller, Laurie Demmer, et al.
Genetics in Medicine (2020) Vol. 22, Iss. 6, pp. 986-1004
Open Access | Times Cited: 73
IL‐11 in cardiac and renal fibrosis: Late to the party but a central player
Benjamin Corden, Eleonora Adami, Mark Sweeney, et al.
British Journal of Pharmacology (2020) Vol. 177, Iss. 8, pp. 1695-1708
Open Access | Times Cited: 72
Influences of the IL-6 cytokine family on bone structure and function
Natalie A. Sims
Cytokine (2021) Vol. 146, pp. 155655-155655
Closed Access | Times Cited: 62
Understanding interleukin 11 as a disease gene and therapeutic target
Stuart A. Cook
Biochemical Journal (2023) Vol. 480, Iss. 23, pp. 1987-2008
Open Access | Times Cited: 26
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome
Kerry A. Miller, David A. Cruz Walma, Daniel M. Pinkas, et al.
Journal of Medical Genetics (2024), pp. jmg-109531
Open Access | Times Cited: 8
HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients
Stéphanie Moortgat, Siren Berland, Ingvild Aukrust, et al.
European Journal of Human Genetics (2017) Vol. 26, Iss. 1, pp. 64-74
Open Access | Times Cited: 83
Genetic Causes of Craniosynostosis: An Update
Jacqueline A.C. Goos, Irene M. J. Mathijssen
Molecular Syndromology (2018) Vol. 10, Iss. 1-2, pp. 6-23
Open Access | Times Cited: 64
Human hyper-IgE syndrome: singular or plural?
Qian Zhang, Bertrand Boisson, Vivien Béziat, et al.
Mammalian Genome (2018) Vol. 29, Iss. 7-8, pp. 603-617
Open Access | Times Cited: 63
De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies
Konrad Platzer, Heinrich Sticht, Stacey L. Edwards, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 2, pp. 203-212
Open Access | Times Cited: 63
Skeletal stem and progenitor cells maintain cranial suture patency and prevent craniosynostosis
Siddharth Menon, Ankit Salhotra, Siny Shailendra, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 42
Appetite- and Weight-Regulating Neuroendocrine Circuitry in Hypothalamic Obesity
Hoong‐Wei Gan, Manuela Cerbone, Mehul Dattani
Endocrine Reviews (2023) Vol. 45, Iss. 3, pp. 309-342
Open Access | Times Cited: 20
Cranial Neural Crest Cells and Their Role in the Pathogenesis of Craniofacial Anomalies and Coronal Craniosynostosis
Erica Siismets, Nan Hatch
Journal of Developmental Biology (2020) Vol. 8, Iss. 3, pp. 18-18
Open Access | Times Cited: 46
Recent Advances in Craniosynostosis
Elanur Yılmaz, Ercan Mıhçı, Banu Nur, et al.
Pediatric Neurology (2019) Vol. 99, pp. 7-15
Closed Access | Times Cited: 43
Roles of the HUWE1 ubiquitin ligase in nervous system development, function and disease
Andrew C. Giles, Brock Grill
Neural Development (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 40
Similarities and differences between IL11 and IL11RA1 knockout mice for lung fibro-inflammation, fertility and craniosynostosis
Benjamin Ng, Anissa A. Widjaja, Sivakumar Viswanathan, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 39
The cytokine interleukin-11 crucially links bone formation, remodeling and resorption
Birte Kespohl, Tim Schumertl, Jessica Bertrand, et al.
Cytokine & Growth Factor Reviews (2021) Vol. 60, pp. 18-27
Closed Access | Times Cited: 33
The value of genome-wide analysis in craniosynostosis
Alexandra Topa, Anna Rohlin, André Fehr, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 5
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability
Mark Hamilton, Richard Caswell, Natalie Canham, et al.
Journal of Medical Genetics (2017) Vol. 55, Iss. 1, pp. 28-38
Open Access | Times Cited: 42
The phenotypic spectrum of Xia‐Gibbs syndrome
Yunyun Jiang, Michael F. Wangler, Amy L. McGuire, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 6, pp. 1315-1326
Open Access | Times Cited: 42
IL-11 Is Elevated and Drives the Profibrotic Phenotype Transition of Orbital Fibroblasts in Thyroid-Associated Ophthalmopathy
Pengsen Wu, Bingying Lin, Siyu Huang, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 21
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