BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Marchini A, Ogata T, Rappold GA. A Track Record on SHOX: From Basic Research to Complex Models and Therapy. Endocr Rev 2016;37:417-48. [PMID: 27355317 DOI: 10.1210/er.2016-1036] [Cited by in Crossref: 46] [Cited by in F6Publishing: 46] [Article Influence: 7.7] [Reference Citation Analysis]
Number Citing Articles
1 Tian Y, Wang W, Lautrup S, Zhao H, Li X, Law PWN, Dinh N, Fang EF, Cheung HH, Chan W. WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome. Nat Commun 2022;13. [DOI: 10.1038/s41467-022-33012-6] [Reference Citation Analysis]
2 Satoh M, Hasegawa Y. Factors affecting prepubertal and pubertal bone age progression. Front Endocrinol 2022;13:967711. [DOI: 10.3389/fendo.2022.967711] [Reference Citation Analysis]
3 Fukami M, Shindo J, Ogata T, Kageyama I, Kamimaki T. SHOX far-downstream deletion in a patient with nonsyndromic short stature. Am J Med Genet A 2022. [PMID: 35319168 DOI: 10.1002/ajmg.a.62734] [Reference Citation Analysis]
4 Willems M, Amouroux C, Barat-houari M, Salles J, Edouard T. Exploring the genetic causes of isolated short stature. What has happened to idiopathic short stature? Archives de Pédiatrie 2022;28:28/8S27-32. [DOI: 10.1016/s0929-693x(22)00040-9] [Reference Citation Analysis]
5 Mastromauro C, Chiarelli F; Department of Paediatrics, University of Chieti, Chieti, Italy, Department of Paediatrics, University of Chieti, Chieti, Italy. Novel Insights Into the Genetic Causes of Short Stature in Children. Endocrinology 2022;18:49. [DOI: 10.17925/ee.2022.18.1.49] [Reference Citation Analysis]
6 Stritar J, Stavber L, Ficko M, Kotnik P, Battelino T, Trebušak Podkrajšek K, Hovnik T. Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature. Genes (Basel) 2021;12:1546. [PMID: 34680940 DOI: 10.3390/genes12101546] [Reference Citation Analysis]
7 Marí-Beffa M, Mesa-Román AB, Duran I. Zebrafish Models for Human Skeletal Disorders. Front Genet 2021;12:675331. [PMID: 34490030 DOI: 10.3389/fgene.2021.675331] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
8 Li N, Zeng Y, Tai M, Lin B, Zhu D, Luo Y, Ren X, Zhu X, Li L, Wu H, Huang J. Analysis of the Prognostic Value and Gene Expression Mechanism of SHOX2 in Lung Adenocarcinoma. Front Mol Biosci 2021;8:688274. [PMID: 34262939 DOI: 10.3389/fmolb.2021.688274] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
9 Santana González L, Artibani M, Ahmed AA. Studying Müllerian duct anomalies - from cataloguing phenotypes to discovering causation. Dis Model Mech 2021;14:dmm047977. [PMID: 34160006 DOI: 10.1242/dmm.047977] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
10 Weiss B, Eberle B, Roeth R, de Bruin C, Lui JC, Paramasivam N, Hinderhofer K, van Duyvenvoorde HA, Baron J, Wit JM, Rappold GA. Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes. Front Endocrinol (Lausanne) 2021;12:660731. [PMID: 34194391 DOI: 10.3389/fendo.2021.660731] [Reference Citation Analysis]
11 Hoffmann S, Roeth R, Diebold S, Gogel J, Hassel D, Just S, Rappold GA. Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes. Front Genet 2021;12:688808. [PMID: 34122528 DOI: 10.3389/fgene.2021.688808] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Maxeiner S, Gebhardt S, Schweizer F, Venghaus AE, Krasteva-Christ G. Of mice and men - and guinea pigs? Ann Anat 2021;238:151765. [PMID: 34000371 DOI: 10.1016/j.aanat.2021.151765] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Marin F, Jodar E, Sánchez Del Pozo J. Coexistence of dyschondrosteosis associated to SHOX deficiency, pseudohypoparathyroidism 1B, and chronic autoimmune thyroiditis: a case report. J Pediatr Endocrinol Metab 2021;34:531-4. [PMID: 33818044 DOI: 10.1515/jpem-2020-0419] [Reference Citation Analysis]
14 Mintz CS, Seaver LH, Irons M, Grimberg A, Lozano R; ACMG Professional Practice and Guidelines Committee. Focused Revision: ACMG practice resource: Genetic evaluation of short stature. Genet Med 2021;23:813-5. [PMID: 33514815 DOI: 10.1038/s41436-020-01046-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
15 Bieg M, Moskalev EA, Will R, Hebele S, Schwarzbach M, Schmeck S, Hohenberger P, Jakob J, Kasper B, Gaiser T, Ströbel P, Wardelmann E, Kontny U, Braunschweig T, Sirbu H, Grützmann R, Meidenbauer N, Ishaque N, Eils R, Wiemann S, Hartmann A, Agaimy A, Fritchie K, Giannini C, Haller F. Gene Expression in Solitary Fibrous Tumors (SFTs) Correlates with Anatomic Localization and NAB2-STAT6 Gene Fusion Variants. Am J Pathol 2021;191:602-17. [PMID: 33497701 DOI: 10.1016/j.ajpath.2020.12.015] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 6.0] [Reference Citation Analysis]
16 Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M, Santana L, Honjo RS, Kim CA, de Zegher F, Idkowiak J, Gilligan LC, Arlt W, Funari MFDA, Jorge AADL, Mendonca BB, Netchine I, Brito VN, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction 2021;36:506-18. [DOI: 10.1093/humrep/deaa306] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
17 Vannelli S, Baffico M, Buganza R, Verna F, Vinci G, Tessaris D, Di Rosa G, Borraccino A, de Sanctis L. SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators. Ital J Pediatr 2020;46:163. [PMID: 33143726 DOI: 10.1186/s13052-020-00927-z] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
18 Wang D, Pan X, Wang X. Metabolic syndrome coexists with adult Léri-Weill dyschondrosteosis: A case report. J Diabetes Investig 2021;12:446-9. [PMID: 32633455 DOI: 10.1111/jdi.13350] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Babu D, Vannelli S, Fanelli A, Mellone S, Baffico AM, Corrado L, Essa WA, Grandone A, Bellone S, Monzani A, Vinci G, De Sanctis L, Stuppia L, Prodam F, Giordano M. Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency. Eur J Hum Genet 2021;29:110-21. [PMID: 32647378 DOI: 10.1038/s41431-020-0676-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 7] [Article Influence: 0.5] [Reference Citation Analysis]
20 Faienza MF, Chiarito M, Brunetti G, D'Amato G. Growth plate gene involment and isolated short stature. Endocrine 2021;71:28-34. [PMID: 32504378 DOI: 10.1007/s12020-020-02362-w] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
21 Li N, Zeng Y, Huang J. Signaling pathways and clinical application of RASSF1A and SHOX2 in lung cancer. J Cancer Res Clin Oncol. 2020;146:1379-1393. [PMID: 32266538 DOI: 10.1007/s00432-020-03188-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
22 Sun Y, Luo Y, Qian Y, Chen M, Wang L, Li H, Zou Y, Dong M. Heterozygous Deletion of the SHOX Gene Enhancer in two Females With Clinical Heterogeneity Associating With Skewed XCI and Escaping XCI. Front Genet 2019;10:1086. [PMID: 31781162 DOI: 10.3389/fgene.2019.01086] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 Argente J, Tatton-Brown K, Lehwalder D, Pfäffle R. Genetics of Growth Disorders-Which Patients Require Genetic Testing? Front Endocrinol (Lausanne) 2019;10:602. [PMID: 31555216 DOI: 10.3389/fendo.2019.00602] [Cited by in Crossref: 10] [Cited by in F6Publishing: 20] [Article Influence: 3.3] [Reference Citation Analysis]
24 Pellegrin MC, Tornese G, Barbi E. Pubertal boy presenting with mild disproportionate short stature. Arch Dis Child Educ Pract Ed 2021;106:149-51. [PMID: 31467065 DOI: 10.1136/archdischild-2019-317564] [Reference Citation Analysis]
25 Del Pino M, Aza-Carmona M, Medino-Martín D, Gomez A, Heath KE, Fano V, Obregon MG. SHOX Deficiency in Argentinean Cohort: Long-Term Auxological Follow-Up and a Family's New Mutation. J Pediatr Genet 2019;8:123-32. [PMID: 31406617 DOI: 10.1055/s-0039-1691788] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
26 Farahmand SK, Emadzadeh M, Hassankhani GG, Mirbirjandian M, Rafiezadeh T, Abasalti Z, Khayyatzadeh SS, Bahrami A, Tabatabaeizadeh SA, Tayefi M, Ferns GA, Gonoodi K, Moslem A, Ghayour-Mobarhan M. The relationship between short stature and menstrual pattern in a large cohort of Iranian girls. J Obstet Gynaecol 2020;40:228-32. [PMID: 31339388 DOI: 10.1080/01443615.2019.1621806] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
27 Funari MFA, de Barros JS, Santana LS, Lerario AM, Freire BL, Homma TK, Vasques GA, Mendonca BB, Nishi MY, Jorge AAL. Evaluation of SHOX defects in the era of next-generation sequencing. Clin Genet 2019;96:261-5. [PMID: 31219618 DOI: 10.1111/cge.13587] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
28 Caputo M, Mele C, Zavattaro M, Samà MT, Giordano M, Umari P, Volpe A, Aimaretti G, Prodam F. Ovotesticular Disorder of Sex Development: A Rare Case of Lateral Subtype 45X/46XY kariotype Diagnosed in Adulthood. Urology 2019;129:68-70. [DOI: 10.1016/j.urology.2019.04.008] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
29 Gravholt CH, Viuff MH, Brun S, Stochholm K, Andersen NH. Turner syndrome: mechanisms and management. Nat Rev Endocrinol 2019;15:601-14. [PMID: 31213699 DOI: 10.1038/s41574-019-0224-4] [Cited by in Crossref: 78] [Cited by in F6Publishing: 60] [Article Influence: 26.0] [Reference Citation Analysis]
30 Finken MJJ, van der Steen M, Smeets CCJ, Walenkamp MJE, de Bruin C, Hokken-Koelega ACS, Wit JM. Children Born Small for Gestational Age: Differential Diagnosis, Molecular Genetic Evaluation, and Implications. Endocr Rev 2018;39:851-94. [PMID: 29982551 DOI: 10.1210/er.2018-00083] [Cited by in Crossref: 35] [Cited by in F6Publishing: 56] [Article Influence: 11.7] [Reference Citation Analysis]
31 San Roman AK, Page DC. A strategic research alliance: Turner syndrome and sex differences. Am J Med Genet C Semin Med Genet 2019;181:59-67. [PMID: 30790449 DOI: 10.1002/ajmg.c.31677] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
32 Arnold AP. The mouse as a model of fundamental concepts related to Turner syndrome. Am J Med Genet C Semin Med Genet 2019;181:76-85. [PMID: 30779420 DOI: 10.1002/ajmg.c.31681] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
33 Collett-solberg PF, Jorge AA, Boguszewski MC, Miller BS, Choong CSY, Cohen P, Hoffman AR, Luo X, Radovick S, Saenger P. Growth hormone therapy in children; research and practice – A review. Growth Hormone & IGF Research 2019;44:20-32. [DOI: 10.1016/j.ghir.2018.12.004] [Cited by in Crossref: 16] [Cited by in F6Publishing: 25] [Article Influence: 5.3] [Reference Citation Analysis]
34 Monzani A, Babu D, Mellone S, Genoni G, Fanelli A, Prodam F, Bellone S, Giordano M. Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies. BMC Med Genomics 2019;12:5. [PMID: 30626445 DOI: 10.1186/s12920-018-0445-8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
35 Freire BL, Homma TK, Funari MFA, Lerario AM, Vasques GA, Malaquias AC, Arnhold IJP, Jorge AAL. Multigene Sequencing Analysis of Children Born Small for Gestational Age With Isolated Short Stature. The Journal of Clinical Endocrinology & Metabolism 2019;104:2023-30. [DOI: 10.1210/jc.2018-01971] [Cited by in Crossref: 21] [Cited by in F6Publishing: 29] [Article Influence: 7.0] [Reference Citation Analysis]
36 Oberg KC. Classification of congenital upper limb anomalies: towards improved communication, diagnosis, and discovery. J Hand Surg Eur Vol 2019;44:4-14. [PMID: 30269619 DOI: 10.1177/1753193418801280] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
37 Skuplik I, Benito-Sanz S, Rosin JM, Bobick BE, Heath KE, Cobb J. Identification of a limb enhancer that is removed by pathogenic deletions downstream of the SHOX gene. Sci Rep 2018;8:14292. [PMID: 30250174 DOI: 10.1038/s41598-018-32565-1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
38 Vasques GA, Funari MFA, Ferreira FM, Aza-Carmona M, Sentchordi-Montané L, Barraza-García J, Lerario AM, Yamamoto GL, Naslavsky MS, Duarte YAO, Bertola DR, Heath KE, Jorge AAL. IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy. J Clin Endocrinol Metab 2018;103:604-14. [PMID: 29155992 DOI: 10.1210/jc.2017-02026] [Cited by in Crossref: 26] [Cited by in F6Publishing: 30] [Article Influence: 6.5] [Reference Citation Analysis]
39 Blum WF, Alherbish A, Alsagheir A, El Awwa A, Kaplan W, Koledova E, Savage MO. The growth hormone-insulin-like growth factor-I axis in the diagnosis and treatment of growth disorders. Endocr Connect 2018;7:R212-22. [PMID: 29724795 DOI: 10.1530/EC-18-0099] [Cited by in Crossref: 27] [Cited by in F6Publishing: 43] [Article Influence: 6.8] [Reference Citation Analysis]
40 Montalbano A, Juergensen L, Fukami M, Thiel CT, Hauer NH, Roeth R, Weiss B, Naiki Y, Ogata T, Hassel D, Rappold GA. Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature. Eur J Hum Genet 2018;26:1113-20. [PMID: 29706635 DOI: 10.1038/s41431-018-0148-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
41 Hori YS, Ohkura T, Ebisudani Y, Umakoshi M, Ishi M, Oda K, Aoi M, Inoue T, Furujo M, Tanaka H, Fukuhara T. Hypertensive Cerebral Hemorrhage in a Patient with Turner Syndrome Caused by Deletion in the Short Arm of the X Chromosome. Pediatr Neurosurg 2018;53:167-70. [DOI: 10.1159/000485252] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
42 Tung YC, Lee NC, Hwu WL, Liu SY, Lee CT, Chien YH, Tsai WY. SHOX deficiency in short Taiwanese children: A single-center experience. J Formos Med Assoc 2018;117:909-14. [PMID: 29254682 DOI: 10.1016/j.jfma.2017.11.014] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
43 Yokokura T, Kamei H, Shibano T, Yamanaka D, Sawada-Yamaguchi R, Hakuno F, Takahashi SI, Shimizu T. The Short-Stature Homeobox-Containing Gene (shox/SHOX) Is Required for the Regulation of Cell Proliferation and Bone Differentiation in Zebrafish Embryo and Human Mesenchymal Stem Cells. Front Endocrinol (Lausanne) 2017;8:125. [PMID: 28642734 DOI: 10.3389/fendo.2017.00125] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
44 Albuquerque EVA, Scalco RC, Jorge AAL. MANAGEMENT OF ENDOCRINE DISEASE: Diagnostic and therapeutic approach of tall stature. Eur J Endocrinol 2017;176:R339-53. [PMID: 28274950 DOI: 10.1530/EJE-16-1054] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 3.0] [Reference Citation Analysis]
45 Montalbano A, Juergensen L, Roeth R, Weiss B, Fukami M, Fricke-Otto S, Binder G, Ogata T, Decker E, Nuernberg G, Hassel D, Rappold GA. Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. EMBO Mol Med 2016;8:1455-69. [PMID: 27861128 DOI: 10.15252/emmm.201606623] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
46 Sharma D, Sharma P, Shastri S. Genetic, metabolic and endocrine aspect of intrauterine growth restriction: an update. The Journal of Maternal-Fetal & Neonatal Medicine 2017;30:2263-75. [DOI: 10.1080/14767058.2016.1245285] [Cited by in Crossref: 20] [Cited by in F6Publishing: 27] [Article Influence: 3.3] [Reference Citation Analysis]