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:
Mutations in the Endothelin Receptor Type A Cause Mandibulofacial Dysostosis with Alopecia
Christopher T. Gordon, K. Nicole Weaver, Roseli Maria Zechi‐Ceide, et al.
The American Journal of Human Genetics (2015) Vol. 96, Iss. 4, pp. 519-531
Open Access | Times Cited: 44
Christopher T. Gordon, K. Nicole Weaver, Roseli Maria Zechi‐Ceide, et al.
The American Journal of Human Genetics (2015) Vol. 96, Iss. 4, pp. 519-531
Open Access | Times Cited: 44
Showing 26-50 of 44 citing articles:
A consensus single-cell transcriptomic atlas of dermal fibroblast heterogeneity
Alex M. Ascensión, Ander Izeta
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Alex M. Ascensión, Ander Izeta
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Nkx2.5 regulates endothelin converting enzyme‐1 during pharyngeal arch patterning
Jennifer M. Iklé, André L. P. Tavares, M S King, et al.
genesis (2017) Vol. 55, Iss. 3
Open Access | Times Cited: 9
Jennifer M. Iklé, André L. P. Tavares, M S King, et al.
genesis (2017) Vol. 55, Iss. 3
Open Access | Times Cited: 9
Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
Yukiko Kurihara, Toru Ekimoto, Christopher T. Gordon, et al.
Journal of Clinical Investigation (2023) Vol. 133, Iss. 4
Open Access | Times Cited: 3
Yukiko Kurihara, Toru Ekimoto, Christopher T. Gordon, et al.
Journal of Clinical Investigation (2023) Vol. 133, Iss. 4
Open Access | Times Cited: 3
Transcriptomic analysis reveals the role of SIX1 in mouse cranial neural crest patterning and bone development
Aparna B. Baxi, Karyn Jourdeuil, Timothy C. Cox, et al.
Developmental Dynamics (2023) Vol. 252, Iss. 10, pp. 1303-1315
Open Access | Times Cited: 3
Aparna B. Baxi, Karyn Jourdeuil, Timothy C. Cox, et al.
Developmental Dynamics (2023) Vol. 252, Iss. 10, pp. 1303-1315
Open Access | Times Cited: 3
Homology modeling, molecular dynamics and virtual screening of endothelin-A receptor for the treatment of pulmonary arterial hypertension
Xi Gu, Ying Wang, Hanxun Wang, et al.
Journal of Biomolecular Structure and Dynamics (2020) Vol. 39, Iss. 11, pp. 3912-3923
Open Access | Times Cited: 7
Xi Gu, Ying Wang, Hanxun Wang, et al.
Journal of Biomolecular Structure and Dynamics (2020) Vol. 39, Iss. 11, pp. 3912-3923
Open Access | Times Cited: 7
Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation
Sibylle Sabrautzki, Michael A. Sandholzer, Bettina Lorenz‐Depiereux, et al.
Mammalian Genome (2016) Vol. 27, Iss. 11-12, pp. 587-598
Open Access | Times Cited: 6
Sibylle Sabrautzki, Michael A. Sandholzer, Bettina Lorenz‐Depiereux, et al.
Mammalian Genome (2016) Vol. 27, Iss. 11-12, pp. 587-598
Open Access | Times Cited: 6
Interstitial 4q Deletion Syndrome Including <b><i>NR3C2</i></b> Causing Pseudohypoaldosteronism
Amanda Barone Pritchard, Alyssa Ritter, Hutton M. Kearney, et al.
Molecular Syndromology (2019) Vol. 10, Iss. 6, pp. 327-331
Open Access | Times Cited: 6
Amanda Barone Pritchard, Alyssa Ritter, Hutton M. Kearney, et al.
Molecular Syndromology (2019) Vol. 10, Iss. 6, pp. 327-331
Open Access | Times Cited: 6
Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review
Henrique Regonaschi Serigatto, Nancy Mizue Kokitsu‐Nakata, Siulan Vendramini‐Pittoli, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 10, pp. 2493-2507
Closed Access | Times Cited: 2
Henrique Regonaschi Serigatto, Nancy Mizue Kokitsu‐Nakata, Siulan Vendramini‐Pittoli, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 10, pp. 2493-2507
Closed Access | Times Cited: 2
A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
Khawla El Fizazi, Abdelhamid Bouramtane, Meriame Abbassi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 11, pp. 2673-2678
Open Access | Times Cited: 2
Khawla El Fizazi, Abdelhamid Bouramtane, Meriame Abbassi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 11, pp. 2673-2678
Open Access | Times Cited: 2
The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies
Santiago Cerrizuela, Guillermo A. Vega‐López, Karla Méndez‐Maldonado, et al.
WIREs Mechanisms of Disease (2021) Vol. 14, Iss. 1
Closed Access | Times Cited: 5
Santiago Cerrizuela, Guillermo A. Vega‐López, Karla Méndez‐Maldonado, et al.
WIREs Mechanisms of Disease (2021) Vol. 14, Iss. 1
Closed Access | Times Cited: 5
Welfare Assessment of Adult Laboratory Zebrafish: A Practical Guide
Sibylle Sabrautzki, Manuel Miller, Érika Kague, et al.
Zebrafish (2021) Vol. 18, Iss. 4, pp. 282-292
Closed Access | Times Cited: 4
Sibylle Sabrautzki, Manuel Miller, Érika Kague, et al.
Zebrafish (2021) Vol. 18, Iss. 4, pp. 282-292
Closed Access | Times Cited: 4
Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome via alteration of metabolic signaling
Kimberly A. Chapman, Farid Ullah, Zachary A Yahiku, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Kimberly A. Chapman, Farid Ullah, Zachary A Yahiku, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
The Gq/11 family of Gα subunits is necessary and sufficient for lower jaw development
Stanley M. Kanai, Chloe R. Garcia, MaCalia R. Augustus, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Stanley M. Kanai, Chloe R. Garcia, MaCalia R. Augustus, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
WITHDRAWN: Endothelin signaling in bone
Jasmin Kristianto, Michael G. Johnson, Rafia Afzal, et al.
Translational research (2016)
Closed Access
Jasmin Kristianto, Michael G. Johnson, Rafia Afzal, et al.
Translational research (2016)
Closed Access
Cleft 6
P. Pellerin, Nivaldo Alonso, Renato da Silva Freitas, et al.
Springer eBooks (2023), pp. 215-250
Closed Access
P. Pellerin, Nivaldo Alonso, Renato da Silva Freitas, et al.
Springer eBooks (2023), pp. 215-250
Closed Access
Mandibulofacial dysostosis Bauru type: Refining the phenotype
Priscila Padilha Moura, Nancy Mizue Kokitsu‐Nakata, Marília Yatabe, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 7, pp. 1747-1753
Closed Access
Priscila Padilha Moura, Nancy Mizue Kokitsu‐Nakata, Marília Yatabe, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 7, pp. 1747-1753
Closed Access
Caracterização morfológica de arco zigomático, maxila e mandíbula em indivíduos com disostose mandibulofacial
Priscila Padilha Moura
(2017)
Open Access
Priscila Padilha Moura
(2017)
Open Access
Faculty Opinions recommendation of Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β.
Michail S. Lionakis
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature (2020)
Open Access
Michail S. Lionakis
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature (2020)
Open Access
Genetics of craniofacial anomalies
Andrew O.M. Wilkie
Oxford University Press eBooks (2021), pp. 691-696
Closed Access
Andrew O.M. Wilkie
Oxford University Press eBooks (2021), pp. 691-696
Closed Access
