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 Mouse Splice-Site Mutant and Individuals with Atypical Chromosome 22q11.2 Deletions Demonstrate the Crucial Role for Crkl in Craniofacial and Pharyngeal Development
Kerry A. Miller, Tiong Yang Tan, Megan F. Welfare, et al.
Molecular Syndromology (2014) Vol. 5, Iss. 6, pp. 276-286
Open Access | Times Cited: 11
Kerry A. Miller, Tiong Yang Tan, Megan F. Welfare, et al.
Molecular Syndromology (2014) Vol. 5, Iss. 6, pp. 276-286
Open Access | Times Cited: 11
Showing 11 citing articles:
Oculo-auriculo-vertebral spectrum: Clinical and molecular analysis of 51 patients
Ana Beleza‐Meireles, Rachel Hart, Jill Clayton‐Smith, et al.
European Journal of Medical Genetics (2015) Vol. 58, Iss. 9, pp. 455-465
Closed Access | Times Cited: 104
Ana Beleza‐Meireles, Rachel Hart, Jill Clayton‐Smith, et al.
European Journal of Medical Genetics (2015) Vol. 58, Iss. 9, pp. 455-465
Closed Access | Times Cited: 104
In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
Zahra Motahari, Sally A. Moody, Thomas M. Maynard, et al.
Journal of Neurodevelopmental Disorders (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 70
Zahra Motahari, Sally A. Moody, Thomas M. Maynard, et al.
Journal of Neurodevelopmental Disorders (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 70
Craniofacial Microsomia
K. Brandstetter, Krishna G. Patel
Facial Plastic Surgery Clinics of North America (2016) Vol. 24, Iss. 4, pp. 495-515
Closed Access | Times Cited: 59
K. Brandstetter, Krishna G. Patel
Facial Plastic Surgery Clinics of North America (2016) Vol. 24, Iss. 4, pp. 495-515
Closed Access | Times Cited: 59
Exploring the Underlying Genetics of Craniofacial Morphology through Various Sources of Knowledge
Jasmien Roosenboom, Greet Hens, Brooke C. Mattern, et al.
BioMed Research International (2016) Vol. 2016, pp. 1-9
Open Access | Times Cited: 56
Jasmien Roosenboom, Greet Hens, Brooke C. Mattern, et al.
BioMed Research International (2016) Vol. 2016, pp. 1-9
Open Access | Times Cited: 56
SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia
Zornitza Stark, Joanna Behrsin, Trent Burgess, et al.
American Journal of Medical Genetics Part A (2015) Vol. 167, Iss. 10, pp. 2319-2326
Closed Access | Times Cited: 20
Zornitza Stark, Joanna Behrsin, Trent Burgess, et al.
American Journal of Medical Genetics Part A (2015) Vol. 167, Iss. 10, pp. 2319-2326
Closed Access | Times Cited: 20
Rare single‐nucleotide variants in oculo‐auriculo‐vertebral spectrum (OAVS)
Malú Zamariolli, Mileny Esbravatti Stephano Colovati, Mariana Moysés‐Oliveira, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 10
Open Access | Times Cited: 11
Malú Zamariolli, Mileny Esbravatti Stephano Colovati, Mariana Moysés‐Oliveira, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 10
Open Access | Times Cited: 11
Identification of a novel CYP26A1 mutation in a Chinese family with congenital microtia
Peipei Guo, Zhonglei Ji, Haiyue Jiang, et al.
International Journal of Pediatric Otorhinolaryngology (2020) Vol. 139, pp. 110488-110488
Closed Access | Times Cited: 8
Peipei Guo, Zhonglei Ji, Haiyue Jiang, et al.
International Journal of Pediatric Otorhinolaryngology (2020) Vol. 139, pp. 110488-110488
Closed Access | Times Cited: 8
Heterozygosity of murine Crkl does not recapitulate behavioral dimensions of human 22q11.2 hemizygosity
Takahira Yamauchi, Gina Kang, Noboru Hiroi
Genes Brain & Behavior (2020) Vol. 20, Iss. 5
Open Access | Times Cited: 8
Takahira Yamauchi, Gina Kang, Noboru Hiroi
Genes Brain & Behavior (2020) Vol. 20, Iss. 5
Open Access | Times Cited: 8
Determination of Extra Craniofacial Abnormalities in Patients With Craniofacial Microsomia
Barbara Kawano Raposo, Guilherme Bail Ferreira, Alfredo Benjamin Duarte e Silva, et al.
Journal of Craniofacial Surgery (2021) Vol. 33, Iss. 1, pp. 230-232
Closed Access | Times Cited: 3
Barbara Kawano Raposo, Guilherme Bail Ferreira, Alfredo Benjamin Duarte e Silva, et al.
Journal of Craniofacial Surgery (2021) Vol. 33, Iss. 1, pp. 230-232
Closed Access | Times Cited: 3
Crk adaptor proteins are necessary for the development of the zebrafish retina
Helaina R. Stergas, Zoë Kalbag, Riley M. St. Clair, et al.
Developmental Dynamics (2021) Vol. 251, Iss. 2, pp. 362-376
Open Access | Times Cited: 1
Helaina R. Stergas, Zoë Kalbag, Riley M. St. Clair, et al.
Developmental Dynamics (2021) Vol. 251, Iss. 2, pp. 362-376
Open Access | Times Cited: 1
22q11.2 Deletion Syndrome
Brianne Barnett Roby, Michael Broderick, Lauren A. Bohm
Elsevier eBooks (2021), pp. 154-163
Closed Access | Times Cited: 1
Brianne Barnett Roby, Michael Broderick, Lauren A. Bohm
Elsevier eBooks (2021), pp. 154-163
Closed Access | Times Cited: 1
