
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:
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
Susan M. Motch Perrine, Meng Wu, Greg Holmes, et al.
Journal of Developmental Biology (2020) Vol. 8, Iss. 4, pp. 30-30
Open Access | Times Cited: 19
Susan M. Motch Perrine, Meng Wu, Greg Holmes, et al.
Journal of Developmental Biology (2020) Vol. 8, Iss. 4, pp. 30-30
Open Access | Times Cited: 19
Showing 19 citing articles:
Precise modulation of transcription factor levels identifies features underlying dosage sensitivity
Sahin Naqvi, Seungsoo Kim, Hanne Hoskens, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 841-851
Open Access | Times Cited: 67
Sahin Naqvi, Seungsoo Kim, Hanne Hoskens, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 841-851
Open Access | Times Cited: 67
Characterization of upper airway airflow dynamics in young adults with isolated Robin sequence: An exploratory investigation
Maria Noel Marzano‐Rodrigues, Sérgio Henrique Kiemle Trindade, Ivy Kiemle Trindade‐Suedam
Journal of Oral Biology and Craniofacial Research (2025) Vol. 15, Iss. 2, pp. 234-239
Open Access
Maria Noel Marzano‐Rodrigues, Sérgio Henrique Kiemle Trindade, Ivy Kiemle Trindade‐Suedam
Journal of Oral Biology and Craniofacial Research (2025) Vol. 15, Iss. 2, pp. 234-239
Open Access
Epigenetic regulation of craniofacial development and disease
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 7
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 7
Cleft Palate in Apert Syndrome
Delayna Willie, Greg Holmes, Ethylin Wang Jabs, et al.
Journal of Developmental Biology (2022) Vol. 10, Iss. 3, pp. 33-33
Open Access | Times Cited: 8
Delayna Willie, Greg Holmes, Ethylin Wang Jabs, et al.
Journal of Developmental Biology (2022) Vol. 10, Iss. 3, pp. 33-33
Open Access | Times Cited: 8
Precise modulation of transcription factor levels reveals drivers of dosage sensitivity
Sahin Naqvi, Seungsoo Kim, Hanne Hoskens, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
Sahin Naqvi, Seungsoo Kim, Hanne Hoskens, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
Epidemiology of Robin sequence: geographical variation in the UK/Ireland
Giles Atton, Diana Baralle
Archives of Disease in Childhood (2024) Vol. 109, Iss. 3, pp. 177-178
Open Access
Giles Atton, Diana Baralle
Archives of Disease in Childhood (2024) Vol. 109, Iss. 3, pp. 177-178
Open Access
Mandibular Deformation
John M. Graham, Pedro A. Sanchez‐Lara
Elsevier eBooks (2024), pp. 182-190
Closed Access
John M. Graham, Pedro A. Sanchez‐Lara
Elsevier eBooks (2024), pp. 182-190
Closed Access
Orofacial clefts in Costa Rica, 1996–2021: Analysis of surveillance data
María de la Paz Barboza‐Argüello, Adriana Benavides‐Lara
Birth Defects Research (2024) Vol. 116, Iss. 8
Closed Access
María de la Paz Barboza‐Argüello, Adriana Benavides‐Lara
Birth Defects Research (2024) Vol. 116, Iss. 8
Closed Access
Regulatory mechanisms of palate and tongue development
Carolina Parada, Tingwei Guo, Jifan Feng, et al.
Elsevier eBooks (2024), pp. 347-360
Closed Access
Carolina Parada, Tingwei Guo, Jifan Feng, et al.
Elsevier eBooks (2024), pp. 347-360
Closed Access
Deficiency of Fam20b-Catalyzed Glycosaminoglycan Chain Synthesis in Neural Crest Leads to Cleft Palate
Xiaohong Chen, Nan Li, Ping Hu, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 11, pp. 9634-9634
Open Access | Times Cited: 1
Xiaohong Chen, Nan Li, Ping Hu, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 11, pp. 9634-9634
Open Access | Times Cited: 1
The Impact of Mandibular Distraction Osteogenesis on Cephalometric Measurements in Infants with Pierre Robin Sequence.
Dang Hoang Thom, Vũ Ngọc Lâm, Trần Thiết Sơn
PubMed (2023) Vol. 69, Iss. 3, pp. E106-E114
Closed Access | Times Cited: 1
Dang Hoang Thom, Vũ Ngọc Lâm, Trần Thiết Sơn
PubMed (2023) Vol. 69, Iss. 3, pp. E106-E114
Closed Access | Times Cited: 1
Advances in Understanding the Pathogenesis of Craniofacial Birth Defects
André L. P. Tavares, Sally A. Moody
Journal of Developmental Biology (2022) Vol. 10, Iss. 3, pp. 27-27
Open Access | Times Cited: 2
André L. P. Tavares, Sally A. Moody
Journal of Developmental Biology (2022) Vol. 10, Iss. 3, pp. 27-27
Open Access | Times Cited: 2
Augmented BMP4 signal impairs tongue myogenesis
Jian Zhang, Chensheng Lin, Yingnan Song, et al.
Journal of Molecular Histology (2021) Vol. 52, Iss. 4, pp. 651-659
Closed Access | Times Cited: 2
Jian Zhang, Chensheng Lin, Yingnan Song, et al.
Journal of Molecular Histology (2021) Vol. 52, Iss. 4, pp. 651-659
Closed Access | Times Cited: 2
Sedation, pediatric dentistry, propofol, nitrous oxide, midazolam, dexmedetomidine
a .
International Journal of Applied Dental Sciences (2022) Vol. 8, Iss. 2, pp. 182-185
Open Access | Times Cited: 1
a .
International Journal of Applied Dental Sciences (2022) Vol. 8, Iss. 2, pp. 182-185
Open Access | Times Cited: 1
Use of Mandibular Distraction Osteogenesis to Correct Micrognathia and Airway Obstruction in Newborn Female with Pierre Robin Sequence and Neonatal Abstinence Syndrome in Rural Appalachia
Seneca Williams, Adam Van Horn
Marshall Journal of Medicine (2022) Vol. 8, Iss. 2
Open Access | Times Cited: 1
Seneca Williams, Adam Van Horn
Marshall Journal of Medicine (2022) Vol. 8, Iss. 2
Open Access | Times Cited: 1
Pierre Robin Syndrome: A Literature Review
Maria Yolanda Yunga-Picón, Marilyn Dayana Argudo-Velastegui, Jeny Maricela Bermeo-Cabrera, et al.
World Journal of Advanced Research and Reviews (2023) Vol. 19, Iss. 1, pp. 110-116
Open Access
Maria Yolanda Yunga-Picón, Marilyn Dayana Argudo-Velastegui, Jeny Maricela Bermeo-Cabrera, et al.
World Journal of Advanced Research and Reviews (2023) Vol. 19, Iss. 1, pp. 110-116
Open Access
Genetics of Pierre Robin Syndrome/Sequence
Dominic Augustine, SV Sowmya, Vanishri C. Haragannavar, et al.
Encyclopedia of Life Sciences (2022), pp. 1-10
Closed Access
Dominic Augustine, SV Sowmya, Vanishri C. Haragannavar, et al.
Encyclopedia of Life Sciences (2022), pp. 1-10
Closed Access
Dysmorphology and Developmental Delay in a Dizygotic Twin With an Incidental Finding of Chimerism or Mosaicism: Case Report With Analysis of Molecular Diagnostics and Genetic Counseling Issues
Misha Bano Asif
(2021)
Closed Access
Misha Bano Asif
(2021)
Closed Access
Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a NovelLOXL3Mutation
Anubhuti Sood, Uzma Shamim, Om Prakash Kharbanda, et al.
The Cleft Palate-Craniofacial Journal (2021) Vol. 59, Iss. 11, pp. 1329-1339
Closed Access
Anubhuti Sood, Uzma Shamim, Om Prakash Kharbanda, et al.
The Cleft Palate-Craniofacial Journal (2021) Vol. 59, Iss. 11, pp. 1329-1339
Closed Access