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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:

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

Showing 1-25 of 44 citing articles:

Neurocristopathies: New insights 150 years after the neural crest discovery
Guillermo A. Vega‐López, Santiago Cerrizuela, Celeste Tríbulo, et al.
Developmental Biology (2018) Vol. 444, pp. S110-S143
Open Access | Times Cited: 180
New insights into craniofacial malformations
Stephen R.F. Twigg, Andrew O.M. Wilkie
Human Molecular Genetics (2015) Vol. 24, Iss. R1, pp. R50-R59
Open Access | Times Cited: 144
Mutations in G Protein–Coupled Receptors: Mechanisms, Pathophysiology and Potential Therapeutic Approaches
Torsten Schöneberg, Ines Liebscher
Pharmacological Reviews (2020) Vol. 73, Iss. 1, pp. 89-119
Open Access | Times Cited: 100
De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder
Sébastien Küry, Thomas Besnard, Frédéric Ebstein, et al.
The American Journal of Human Genetics (2017) Vol. 100, Iss. 2, pp. 352-363
Open Access | Times Cited: 97
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features
Paweł Stankiewicz, Tahir Naeem Khan, Przemysław Szafrański, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 4, pp. 503-515
Open Access | Times Cited: 82
News from the endothelin-3/EDNRB signaling pathway: Role during enteric nervous system development and involvement in neural crest-associated disorders
Nadège Bondurand, Sylvie Dufour, Véronique Pingault
Developmental Biology (2018) Vol. 444, pp. S156-S169
Open Access | Times Cited: 71
The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data
Eric Van Otterloo, Trevor Williams, Kristin Artinger
Developmental Biology (2016) Vol. 415, Iss. 2, pp. 171-187
Open Access | Times Cited: 67
Endothelin and the Cardiovascular System: The Long Journey and Where We Are Going
Andreas Haryono, Risa Ramadhiani, Gusty Rizky Teguh Ryanto, et al.
Biology (2022) Vol. 11, Iss. 5, pp. 759-759
Open Access | Times Cited: 30
Neural crest contributions to the ear: Implications for congenital hearing disorders
Kristina Ritter, Donna M. Martin
Hearing Research (2018) Vol. 376, pp. 22-32
Open Access | Times Cited: 51
The ontogeny of Robin sequence
Robrecht J. H. Logjes, Corstiaan C. Breugem, Gijs van Haaften, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 6, pp. 1349-1368
Open Access | Times Cited: 49
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β
Juan Li, Marco Ritelli, S. Cindy, et al.
Science Immunology (2019) Vol. 4, Iss. 41
Open Access | Times Cited: 46
Genomic amplification of the caprine EDNRA locus might lead to a dose dependent loss of pigmentation
Fiona Menzi, Irene Keller, Irene Reber, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 40
The role of teratogens in neural crest development
Santiago Cerrizuela, Guillermo A. Vega‐López, Manuel J. Aybar
Birth Defects Research (2020) Vol. 112, Iss. 8, pp. 584-632
Closed Access | Times Cited: 28
Specification of jaw identity by the Hand2 transcription factor
Noriko Funato, Hiroki Kokubo, Masataka Nakamura, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 29
Angiotensin and Endothelin Receptor Structures With Implications for Signaling Regulation and Pharmacological Targeting
David Speck, Gunnar Kleinau, Michal Szczepek, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 16
Review of the Genetic Basis of Jaw Malformations
Mairaj K. Ahmed, Xiaoqian Ye, Peter J. Taub
Journal of Pediatric Genetics (2016) Vol. 05, Iss. 04, pp. 209-219
Open Access | Times Cited: 18
Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants
Stanley M. Kanai, Caleb Heffner, Timothy C. Cox, et al.
Disease Models & Mechanisms (2022) Vol. 15, Iss. 4
Open Access | Times Cited: 11
Modulating Vertebrate Physiology by Genomic Fine-Tuning of GPCR Functions
Torsten Schöneberg
Physiological Reviews (2024) Vol. 105, Iss. 1, pp. 383-439
Closed Access | Times Cited: 2
Endothelin signaling in development
Stanley M. Kanai, David E. Clouthier
Development (2023) Vol. 150, Iss. 24
Open Access | Times Cited: 5
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
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
ITPR1 Mutation Contributes to Hemifacial Microsomia Spectrum
Zhixu Liu, Hao Sun, Jiewen Dai, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 11
High Endothelin Receptor Type A Expression as an Independent Prognostic Biomarker and Correlated with Immune Infiltrates in Stomach Adenocarcinoma
Yanhua Yan, Kechao Nie, Junhui Zheng, et al.
Cancer Management and Research (2021) Vol. Volume 13, pp. 5013-5026
Open Access | Times Cited: 11
Endothelin 2: a key player in ovulation and fertility
CheMyong Ko, Yoon Min Cho, Eugene Ham, et al.
Reproduction (2022) Vol. 163, Iss. 4, pp. R71-R80
Open Access | Times Cited: 8
Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
Amanda Barone Pritchard, Stanley M. Kanai, Bryan L. Krock, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 5, pp. 1104-1116
Open Access | Times Cited: 11
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