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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 Recurrent Mosaic Mutation in SMO , Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome
Stephen R.F. Twigg, Robert B. Hufnagel, Kerry A. Miller, et al.
The American Journal of Human Genetics (2016) Vol. 98, Iss. 6, pp. 1256-1265
Open Access | Times Cited: 82

Showing 1-25 of 82 citing articles:

Medulloblastoma
Paul A. Northcott, Giles Robinson, Christian P. Kratz, et al.
Nature Reviews Disease Primers (2019) Vol. 5, Iss. 1
Closed Access | Times Cited: 484
Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
Tim Ripperger, Stefan Bielack, Arndt Borkhardt, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 1017-1037
Closed Access | Times Cited: 244
Medulloblastoma in the age of molecular subgroups: a review
Kyle Juraschka, Michael D. Taylor
Journal of Neurosurgery Pediatrics (2019) Vol. 24, Iss. 4, pp. 353-363
Open Access | Times Cited: 209
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
Hedgehog Signaling and Truncated GLI1 in Cancer
Daniel Doheny, Sara G. Manore, Grace L. Wong, et al.
Cells (2020) Vol. 9, Iss. 9, pp. 2114-2114
Open Access | Times Cited: 149
Cell fate decisions, transcription factors and signaling during early retinal development
Raven Diacou, Prithviraj Nandigrami, András Fiser, et al.
Progress in Retinal and Eye Research (2022) Vol. 91, pp. 101093-101093
Open Access | Times Cited: 78
Relating enhancer genetic variation across mammals to complex phenotypes using machine learning
Irene M. Kaplow, Alyssa J. Lawler, Daniel E. Schäffer, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 43
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
Hedgehog Signal and Genetic Disorders
Noriaki Sasai, Michinori Toriyama, Tôru Kondo
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 105
Genomic testing, tumor microenvironment and targeted therapy of Hedgehog-related human cancers
Masaru Katoh
Clinical Science (2019) Vol. 133, Iss. 8, pp. 953-970
Closed Access | Times Cited: 90
The Molecular Basis of Human Anophthalmia and Microphthalmia
Philippa Harding, Mariya Moosajee
Journal of Developmental Biology (2019) Vol. 7, Iss. 3, pp. 16-16
Open Access | Times Cited: 71
Structural basis of sterol recognition by human hedgehog receptor PTCH1
Chao Qi, Giulio Di Minin, Irene Vercellino, et al.
Science Advances (2019) Vol. 5, Iss. 9
Open Access | Times Cited: 70
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
Genetics of anophthalmia and microphthalmia. Part 2: Syndromes associated with anophthalmia–microphthalmia
Anne Slavotinek
Human Genetics (2018) Vol. 138, Iss. 8-9, pp. 831-846
Closed Access | Times Cited: 61
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: 54
Genetic Predisposition to Solid Pediatric Cancers
Mario Capasso, Annalaura Montella, Matilde Tirelli, et al.
Frontiers in Oncology (2020) Vol. 10
Open Access | Times Cited: 51
Clinical and genetic heterogeneity of primary ciliopathies (Review)
Ina Ofelia Focșa, Magdalena Budișteanu, Mihaela Bălgrădean
International Journal of Molecular Medicine (2021) Vol. 48, Iss. 3
Open Access | Times Cited: 48
Lessons learnt from prenatal exome sequencing
Natalie Chandler, Elizabeth Scotchman, Rhiannon Mellis, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 7, pp. 831-844
Open Access | Times Cited: 33
The hedgehog pathway and ocular developmental anomalies
Florencia Cavodeassi, Sophie Creuzet, Heather Etchevers
Human Genetics (2018) Vol. 138, Iss. 8-9, pp. 917-936
Open Access | Times Cited: 57
Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling
Anna Kutkowska‐Kaźmierczak, Monika Goś, Ewa Obersztyn
Journal of Applied Genetics (2018) Vol. 59, Iss. 2, pp. 133-147
Closed Access | Times Cited: 56
Medulloblastoma genomics in the modern molecular era
Rahul Kumar, Anthony P. Y. Liu, Paul A. Northcott
Brain Pathology (2019) Vol. 30, Iss. 3, pp. 679-690
Open Access | Times Cited: 52
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects
Roberta De Mori, Marta Romani, Stefano D’Arrigo, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 4, pp. 552-563
Open Access | Times Cited: 51
Hypothalamic Hamartomas
Nathan T. Cohen, J. Helen Cross, Alexis Arzimanoglou, et al.
Neurology (2021) Vol. 97, Iss. 18, pp. 864-873
Open Access | Times Cited: 33
Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes
Aman George, Tiziana Cogliati, Brian P. Brooks
Experimental Eye Research (2020) Vol. 193, pp. 107940-107940
Open Access | Times Cited: 33
Optic cup morphogenesis across species and related inborn human eye defects
Marcos J. Cardozo, Elena Sánchez-Bustamante, Paola Bovolenta
Development (2023) Vol. 150, Iss. 2
Open Access | Times Cited: 12
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