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 molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
Vanessa Luiza Romanelli Tavares, Roseli Maria Zechi‐Ceide, Débora Romeo Bertola, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 938-945
Closed Access | Times Cited: 14
Vanessa Luiza Romanelli Tavares, Roseli Maria Zechi‐Ceide, Débora Romeo Bertola, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 938-945
Closed Access | Times Cited: 14
Showing 14 citing articles:
Clinical Profiles and Genetic Spectra of 814 Chinese Children With Short Stature
Xin Li, Ruen Yao, Guoying Chang, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 107, Iss. 4, pp. 972-985
Open Access | Times Cited: 28
Xin Li, Ruen Yao, Guoying Chang, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 107, Iss. 4, pp. 972-985
Open Access | Times Cited: 28
Auriculocondylar syndrome 2 caused by a novel PLCB4 variant in a male Chinese neonate: A case report and review of the literature
Y L Zhang, Yuwei Zhao, Liying Dai, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 4
Open Access | Times Cited: 3
Y L Zhang, Yuwei Zhao, Liying Dai, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 4
Open Access | Times Cited: 3
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
Amira Nabil, Sahar El Shafei, Nihal M. El Shakankiri, et al.
European Journal of Medical Genetics (2020) Vol. 63, Iss. 6, pp. 103917-103917
Closed Access | Times Cited: 22
Amira Nabil, Sahar El Shafei, Nihal M. El Shakankiri, et al.
European Journal of Medical Genetics (2020) Vol. 63, Iss. 6, pp. 103917-103917
Closed Access | Times Cited: 22
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases
Nancy Végas, Zeynep Demir, Christopher T. Gordon, et al.
Human Mutation (2022) Vol. 43, Iss. 5, pp. 582-594
Open Access | Times Cited: 13
Nancy Végas, Zeynep Demir, Christopher T. Gordon, et al.
Human Mutation (2022) Vol. 43, Iss. 5, pp. 582-594
Open Access | Times Cited: 13
Auriculocondylar syndrome: Pathogenesis, clinical manifestations and surgical therapies
Qingqing Li, Zhiyuan Jiang, Liyuan Zhang, et al.
Journal of the Formosan Medical Association (2023) Vol. 122, Iss. 9, pp. 822-842
Open Access | Times Cited: 7
Qingqing Li, Zhiyuan Jiang, Liyuan Zhang, et al.
Journal of the Formosan Medical Association (2023) Vol. 122, Iss. 9, pp. 822-842
Open Access | Times Cited: 7
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
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
Zhixu Liu, Hao Sun, Jiewen Dai, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 11
Novel Anticoagulants for Stroke Prevention in Atrial Fibrillation: A Comprehensive Review
Prinka Perswani, Ritesh Croos Yogarajah, Mohammed Saifuddin, et al.
Cureus (2024)
Open Access | Times Cited: 1
Prinka Perswani, Ritesh Croos Yogarajah, Mohammed Saifuddin, et al.
Cureus (2024)
Open Access | Times Cited: 1
Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant
Lé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 4, pp. 1307-1310
Closed Access | Times Cited: 6
Lé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 4, pp. 1307-1310
Closed Access | Times Cited: 6
A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1
Kumiko Yanagi, Noriko Morimoto, Manami Iso, et al.
Journal of Human Genetics (2021) Vol. 66, Iss. 10, pp. 1029-1034
Open Access | Times Cited: 7
Kumiko Yanagi, Noriko Morimoto, Manami Iso, et al.
Journal of Human Genetics (2021) Vol. 66, Iss. 10, pp. 1029-1034
Open Access | Times Cited: 7
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
New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involvingTWIST1regulatory elements
Vanessa Luiza Romanelli Tavares, Sofia Ligia Guimarães-Ramos, Yan Zhou, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 9, pp. 895-905
Open Access | Times Cited: 5
Vanessa Luiza Romanelli Tavares, Sofia Ligia Guimarães-Ramos, Yan Zhou, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 9, pp. 895-905
Open Access | Times Cited: 5
Two Chinese Patients of Auriculocondylar Syndrome 2: A Novel PLCB4 Splicing Variant and 5-Year Follow-up
Yunting Lin, Ye Zhang, Jian Ma, et al.
The Cleft Palate-Craniofacial Journal (2024)
Closed Access
Yunting Lin, Ye Zhang, Jian Ma, et al.
The Cleft Palate-Craniofacial Journal (2024)
Closed Access
Investigação funcional do novo locus candidato, HDAC9, causativo da síndrome aurículo-condilar
Sofia Lígia Guimarães Ramos
(2021)
Open Access
Sofia Lígia Guimarães Ramos
(2021)
Open Access
