| For: | Kaufman CS, Butler MG. Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome. World J Med Genet 2016; 6(2): 17-21 [PMID: 28344932 DOI: 10.5496/wjmg.v6.i2.17] |
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| URL: | https://www.wjgnet.com/2220-3184/full/v6/i2/17.htm |
| Number | Citing Articles |
| 1 |
Ian M. Clapp, Katlynn M. Paul, Edward C. Beck, Shane J. Nho. Hypermobile Disorders and Their Effects on the Hip Joint. Frontiers in Surgery 2021; 8 doi: 10.3389/fsurg.2021.596971
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| 2 |
Tatsiana Sergeevna Pratasevich, Valentina Alexandrovna Zhemoytiak, Natalya Ivanovna Denisik, Hashini Promodhya Thenabadu, Ayesh Riqaq Mohamed Hajzab, Ranasingha Arachchige Shanika Lakmini, Muthuthanthrige Supuni Sanjana Perera, Iryna Nikolaevna Matsiuk, Santhiyapu Hewa Chamodya Hemali Thathsarani. Some Neonates with Congenital Adrenal Hyperplasia may Need Disproportionately High Doses of Mineralocorticoids. Newborn 2025; 4(2) doi: 10.5005/jp-journals-11002-0128
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| 3 |
Krystal VanderJagt, Merlin G. Butler. Ehlers–Danlos syndrome and other heritable connective tissue disorders that impact pregnancies can be detected using next-generation DNA sequencing. Archives of Gynecology and Obstetrics 2019; 300(3) doi: 10.1007/s00404-019-05226-5
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| 4 |
Kathryne Holmes, Pearl Shah, Melanie Jones, Ryan Langston, Faizal Asumda, Jack Yu. Delayed Wound Healing in a Young Patient with TNXB Variants and the Role of WES. FACE 2024; 5(4) doi: 10.1177/27325016241274964
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| 5 |
Yinjie Gao, Lin Lu, Bingqing Yu, Jiangfeng Mao, Xi Wang, Min Nie, Xueyan Wu. The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers–Danlos Syndrome with 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism 2020; 105(7) doi: 10.1210/clinem/dgaa199
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| 6 |
Vidyanand Anaparti, Prasoon Agarwal, Irene Smolik, Neeloffer Mookherjee, Hani El-Gabalawy. Whole Blood Targeted Bisulfite Sequencing and Differential Methylation in the C6ORF10 Gene of Patients with Rheumatoid Arthritis. The Journal of Rheumatology 2020; 47(11) doi: 10.3899/jrheum.190376
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| 7 |
Samantha Beckley, Roopam Dey, Shaun Stinton, Willem van der Merwe, Thomas Branch, Alison V. September, Michael Posthumus, Malcolm Collins. The Association of Genetic Variants Within the Type XII Collagen and Tenascin C Genes with Knee Joint Laxity Measurements. Genes 2025; 16(2) doi: 10.3390/genes16020164
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| 8 |
Lucia Micale, Vito Guarnieri, Bartolomeo Augello, Orazio Palumbo, Emanuele Agolini, Valentina Maria Sofia, Tommaso Mazza, Antonio Novelli, Massimo Carella, Marco Castori. Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome. Genes 2019; 10(12) doi: 10.3390/genes10120967
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| 9 |
Negin Yekkalam, Mehmed Novo, Anders Wänman. Treatments related to temporomandibular disorders among patients with prevalent types of Ehlers-Danlos syndrome in Sweden. CRANIO® 2025; 43(4) doi: 10.1080/08869634.2024.2319565
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| 10 |
Cortney Gensemer, Randall Burks, Steven Kautz, Daniel P. Judge, Mark Lavallee, Russell A. Norris. Hypermobile Ehlers‐Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes. Developmental Dynamics 2021; 250(3) doi: 10.1002/dvdy.220
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| 11 |
Haohuan Li, Hailong Xie, Jiaman Zhang, Chuang Tang, Shibo Tian, Peng Yuan, Chenglu Sun, Chao Cui, Qin Zhong, Funeng Xu, Xiao-xia Liang, Hualin Fu, Long Jin, Keren Long, Lu Lu, Xun Zhou, Jiaxue Cao, Jianlin Yuan, Juan Deng, Dengfeng Gao, Bo Huang, Mingzhou Li. Hydrogel-Based Sequential Photodynamic Therapy Promotes Wound Healing by Targeting Wound Infection and Inflammation. Nano Letters 2025; 25(32) doi: 10.1021/acs.nanolett.5c00014
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| 12 |
Anna Junkiert-Czarnecka, Maria Pilarska-Deltow, Magdalena Kacprzak, Agnieszka Łobodzińska, Agnieszka Sobczyńska-Tomaszewska, Katarzyna Linkowska, Tomasz Grzybowski, Olga Haus. Insights into TNXB-Related Classical-Like Ehlers–Danlos Syndrome: A Study of Polish Patients. Open Access Rheumatology: Research and Reviews 2026; doi: 10.2147/OARRR.S574513
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| 13 |
Shota Tomida, Hironori Okuhata, Tamaki Ishima, Ryozo Nagai, Kenichi Aizawa. Loss of Myh11 K1256 Dysregulates the Extracellular Matrix and Focal Adhesion by Inhibiting Zyxin-Activated Transcription. International Journal of Molecular Sciences 2025; 26(16) doi: 10.3390/ijms26167853
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| 14 |
A. Bauer, M. de Lucia, F. Leuthard, V. Jagannathan, T. Leeb. Compound heterozygosity for TNXB genetic variants in a mixed‐breed dog with Ehlers‐Danlos syndrome. Animal Genetics 2019; 50(5) doi: 10.1111/age.12830
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| 15 |
Victoria Sergeevna Shchekina, Nikita Aleksandrovich Batashkov, Anna Arkadievna Maznina, Julia Aleksandrovna Krupinova, Viktor Pavlovich Bogdanov, Anna Vasilievna Korobeinikova, Dmitry Igorevich Tychinin, Olga Valentinovna Glushkova, Ekaterina Sergeevna Petriaikina, Dmitry Vladimirovich Svetlichnyy, Mary Woroncow, Vladimir Sergeevich Yudin, Anton Arturovich Keskinov, Sergey Mikhailovich Yudin, Veronika Igorevna Skvortsova, Dmitry Vyacheslavovich Tabakov, Andrei Andreevich Deviatkin, Pavel Yu. Volchkov. Identifying a Common Autoimmune Gene Core as a Tool for Verifying Biological Significance and Applicability of Polygenic Risk Scores. International Journal of Molecular Sciences 2026; 27(1) doi: 10.3390/ijms27010543
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| 16 |
Paola Concolino, Alessandra Costella. Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene. Molecular Diagnosis & Therapy 2018; 22(3) doi: 10.1007/s40291-018-0319-y
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| 17 |
Komal Preet, Methma Udawatta, Courtney Duong, Quinton Gopen, Isaac Yang. Bilateral Superior Semicircular Canal Dehiscence Associated with Ehlers-Danlos Syndrome: A Report of 2 Cases. World Neurosurgery 2019; 122 doi: 10.1016/j.wneu.2018.10.126
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| 18 |
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| 19 |
. 2021; doi: 10.70675/b46879dez8548z48b4z8ea5z01fc12172485
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| 20 |
Olivia J. Veatch, Jacob Steinle, Waheeda A. Hossain, Merlin G. Butler. Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study. BMC Medical Genomics 2022; 15(1) doi: 10.1186/s12920-022-01321-w
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| 21 |
Anne Martin. An acquired or heritable connective tissue disorder? A review of hypermobile Ehlers Danlos Syndrome. European Journal of Medical Genetics 2019; 62(7) doi: 10.1016/j.ejmg.2019.103672
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| 22 |
Talal M. Al‐Harbi, Haya Al‐Rammah, Naif Al‐Zahrani, Yichuan Liu, Patrick M. A. Sleiman, Walid Dridi, Hakon Hakonarson. Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene. American Journal of Medical Genetics Part A 2022; 188(2) doi: 10.1002/ajmg.a.62539
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| 23 |
Yajing Shuai, Jieyu Xing, Xiaoxian Liu, Zijing Song, Siqi Lin, Chengyu Lu, Weiwei Zeng, Guixiang Wang. Atractylodes macrocephala polysaccharide orchestrates anti-tumor immunity via a dual-network mechanism targeting the gut microbiota and spleen. npj Biofilms and Microbiomes 2026; 12(1) doi: 10.1038/s41522-026-01013-8
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| 24 |
Luke Dreher, Hussein Abdul Nabi, Ramzi Ibrahim, Mahmoud Abdelnabi, Omar Baqal, Christopher N. Kanaan, Min Choon Tan, Linnea M. Baudhuin, Fadi E. Shamoun, Hicham Z. El Masry. Connective tissue disorders and cardiac arrhythmias: genetic pathways, mechanistic bridges, and clinical implications. Frontiers in Cardiovascular Medicine 2026; 13 doi: 10.3389/fcvm.2026.1860012
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| 25 |
Merlin G Butler. Classic Ehlers-Danlos syndrome and cardiac transplantation - Is there a connection?. World Journal of Cardiology 2020; 12(8): 368-372 doi: 10.4330/wjc.v12.i8.368
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| 26 |
Samla M.F. Cunha, Flavio S. Schenkel, Ricardo V. Ventura, Gordon Vander Voort, Ángela Cánovas. Genome-wide association study identifies major histocompatibility complex genes linked to resistance to gastrointestinal nematodes in grazing Rideau Arcott sheep. Canadian Journal of Animal Science 2026; 106 doi: 10.1139/cjas-2025-0083
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