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:
Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses
Ewelina Bukowska‐Olech, Anna Materna‐Kiryluk, Joanna Walczak‐Sztulpa, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 12
Ewelina Bukowska‐Olech, Anna Materna‐Kiryluk, Joanna Walczak‐Sztulpa, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 12
Showing 12 citing articles:
Genotype-phenotype associations in microtia: a systematic review
Siti Isya Wahdini, Fina Idamatussilmi, Rachmaniar Pramanasari, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 4
Siti Isya Wahdini, Fina Idamatussilmi, Rachmaniar Pramanasari, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 4
Unveiling the Phenotypic Spectrum of Miller Syndrome: A Systematic Review
V L van Roey, Saranda Ombashi, Idilay Kaymaz, et al.
Journal of Craniofacial Surgery (2025)
Closed Access
V L van Roey, Saranda Ombashi, Idilay Kaymaz, et al.
Journal of Craniofacial Surgery (2025)
Closed Access
Optimal Diagnostic and Treatment Practices for Facial Dysostosis Syndromes: A Clinical Consensus Statement Among European Experts
V L van Roey, Willemijn Irvine
Journal of Craniofacial Surgery (2024) Vol. 35, Iss. 5, pp. 1315-1324
Open Access | Times Cited: 3
V L van Roey, Willemijn Irvine
Journal of Craniofacial Surgery (2024) Vol. 35, Iss. 5, pp. 1315-1324
Open Access | Times Cited: 3
Further phenotypic delineation of the auriculocondylar syndrome type 2 with literature review
Ewelina Bukowska‐Olech, Anna Sowińska‐Seidler, Filip Łojek, et al.
Journal of Applied Genetics (2020) Vol. 62, Iss. 1, pp. 107-113
Open Access | Times Cited: 13
Ewelina Bukowska‐Olech, Anna Sowińska‐Seidler, Filip Łojek, et al.
Journal of Applied Genetics (2020) Vol. 62, Iss. 1, pp. 107-113
Open Access | Times Cited: 13
AI-based diagnosis in mandibulofacial dysostosis with microcephaly using external ear shapes
Quentin Hennocq, Thomas Bongibault, Sandrine Marlin, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 5
Quentin Hennocq, Thomas Bongibault, Sandrine Marlin, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 5
Molecular mechanisms of hearing loss in Nager syndrome
Santosh Kumar Maharana, Jean‐Pierre Saint‐Jeannet
Developmental Biology (2021) Vol. 476, pp. 200-208
Open Access | Times Cited: 10
Santosh Kumar Maharana, Jean‐Pierre Saint‐Jeannet
Developmental Biology (2021) Vol. 476, pp. 200-208
Open Access | Times Cited: 10
Treacher Collins Syndrome (mandibulofacial dysostosis) – A case report
Praveen Sharma, Ajina Sam, Iffath Misbah, et al.
Romanian Journal of Neurology (2024) Vol. 23, Iss. 2, pp. 197-203
Open Access | Times Cited: 1
Praveen Sharma, Ajina Sam, Iffath Misbah, et al.
Romanian Journal of Neurology (2024) Vol. 23, Iss. 2, pp. 197-203
Open Access | Times Cited: 1
Clinical and molecular delineation of mandibulofacial dysostosis with microcephaly in six Korean patients: When to consider EFTUD2 analysis?
Jae Hui Ryu, Hwa Young Kim, Jung Min Ko, et al.
European Journal of Medical Genetics (2022) Vol. 65, Iss. 5, pp. 104478-104478
Closed Access | Times Cited: 5
Jae Hui Ryu, Hwa Young Kim, Jung Min Ko, et al.
European Journal of Medical Genetics (2022) Vol. 65, Iss. 5, pp. 104478-104478
Closed Access | Times Cited: 5
Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population
Kai Yang, Li‐Man Fu, Xiaoyang Chu, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 7
Open Access | Times Cited: 2
Kai Yang, Li‐Man Fu, Xiaoyang Chu, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 7
Open Access | Times Cited: 2
Dual diagnosis of achondroplasia and mandibulofacial dysostosis with microcephaly
Ekaterina Lyulcheva, Christopher J. Kershaw, Eleanor Baker, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access
Ekaterina Lyulcheva, Christopher J. Kershaw, Eleanor Baker, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access
A mild skeletal phenotype with overlapping features of Miller syndrome and functional characterisation of two new variants of human dihydroorotate dehydrogenase
Inger‐Lise Mero, Juan Manuel Orozco Rodriguez, Kathrine Bjørgo, et al.
Heliyon (2024) Vol. 10, Iss. 19, pp. e38659-e38659
Open Access
Inger‐Lise Mero, Juan Manuel Orozco Rodriguez, Kathrine Bjørgo, et al.
Heliyon (2024) Vol. 10, Iss. 19, pp. e38659-e38659
Open Access
Clinical and molecular characterization of craniofrontonasal syndrome: new symptoms and novel pathogenic variants in the EFNB1 gene
Ewelina Bukowska‐Olech, Paweł Gawliński, Anna Jakubiuk‐Tomaszuk, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Ewelina Bukowska‐Olech, Paweł Gawliński, Anna Jakubiuk‐Tomaszuk, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 3
The First Description of Monozygotic Twin Females Discordant for the Craniofrontonasal Syndrome Phenotype and the Report of Four Novel Pathogenic Variants in the EFNB1 Gene
Ewelina Bukowska‐Olech, Paweł Gawliński, Anna Jakubiuk‐Tomaszuk, et al.
Research Square (Research Square) (2021)
Open Access
Ewelina Bukowska‐Olech, Paweł Gawliński, Anna Jakubiuk‐Tomaszuk, et al.
Research Square (Research Square) (2021)
Open Access
