BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Yu B, Long W, Yang Y, Wang Y, Jiang L, Cai Z, Wang H. Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population. Front Genet. 2018;9:509. [PMID: 30420871 DOI: 10.3389/fgene.2018.00509] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Citterio CE, Rivolta CM, Targovnik HM. Structure and genetic variants of thyroglobulin: Pathophysiological implications. Mol Cell Endocrinol 2021;528:111227. [PMID: 33689781 DOI: 10.1016/j.mce.2021.111227] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Albader N, Zou M, BinEssa HA, Abdi S, Al-Enezi AF, Meyer BF, Alzahrani AS, Shi Y. Insights of Non-canonical Splice-site Variants on RNA Splicing in Patients with Congenital Hypothyroidism. J Clin Endocrinol Metab 2021:dgab737. [PMID: 34632506 DOI: 10.1210/clinem/dgab737] [Reference Citation Analysis]
3 Zhang RJ, Sun F, Chen F, Fang Y, Yan CY, Zhang CR, Ying YX, Wang Z, Zhang CX, Wu FY, Han B, Liang J, Zhao SX, Song HD. The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism. Mol Cell Endocrinol 2020;506:110761. [PMID: 32088313 DOI: 10.1016/j.mce.2020.110761] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
4 Wang J, Zhang B, Zhou L, Zhou Q, Chen Y, Yu B. Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations. Front Genet 2021;12:665589. [PMID: 34335682 DOI: 10.3389/fgene.2021.665589] [Reference Citation Analysis]
5 Wang H, Liu S, Wang B, Yang Y, Yu B, Wang L, Wang T. 3-Methylcrotonyl-CoA carboxylase deficiency newborn screening in a population of 536,008: is routine screening necessary? J Pediatr Endocrinol Metab 2019;32:1321-6. [PMID: 31730530 DOI: 10.1515/jpem-2018-0536] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
6 Pio MG, Siffo S, Scheps KG, Molina MF, Adrover E, Abelleyro MM, Rivolta CM, Targovnik HM. Curating the gnomAD database: Report of novel variants in the thyrogobulin gene using in silico bioinformatics algorithms. Mol Cell Endocrinol 2021;534:111359. [PMID: 34119605 DOI: 10.1016/j.mce.2021.111359] [Reference Citation Analysis]
7 Acar S, Gürsoy S, Arslan G, Nalbantoğlu Ö, Hazan F, Köprülü Ö, Özkaya B, Özkan B. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7. J Endocrinol Invest 2021. [PMID: 34780050 DOI: 10.1007/s40618-021-01706-1] [Reference Citation Analysis]
8 Alfadhel M, Umair M, Almuzzaini B, Alsaif S, AlMohaimeed SA, Almashary MA, Alharbi W, Alayyar L, Alasiri A, Ballow M, AlAbdulrahman A, Alaujan M, Nashabat M, Al-Odaib A, Altwaijri W, Al-Rumayyan A, Alrifai MT, Alfares A, AlBalwi M, Tabarki B. Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening. Ann Clin Transl Neurol 2019;6:2097-103. [PMID: 31557427 DOI: 10.1002/acn3.50898] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 1.3] [Reference Citation Analysis]
9 Alcántara-Ortigoza MA, Sánchez-Verdiguel I, Fernández-Hernández L, Enríquez-Flores S, González-Núñez A, Hernández-Martínez NL, Sánchez C, González-Del Angel A. Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children (Basel) 2021;8:457. [PMID: 34070861 DOI: 10.3390/children8060457] [Reference Citation Analysis]
10 Targovnik HM, Scheps KG, Rivolta CM. Defects in protein folding in congenital hypothyroidism. Mol Cell Endocrinol 2020;501:110638. [PMID: 31751626 DOI: 10.1016/j.mce.2019.110638] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 4.3] [Reference Citation Analysis]
11 Yang Y, Wang Y, Zhou L, Long W, Yu B, Wang H. Molecular Genetic Screening of Neonatal Intensive Care Units: Hyperbilirubinemia as an Example. TACG 2022;Volume 15:39-48. [DOI: 10.2147/tacg.s362148] [Reference Citation Analysis]
12 Shi Y, Ma J, Xue Y, Wang J, Yu B, Wang T. The assessment of combined karyotype analysis and chromosomal microarray in pregnant women of advanced maternal age: a multicenter study. Ann Transl Med 2019;7:318. [PMID: 31475188 DOI: 10.21037/atm.2019.06.63] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
13 Anton-Paduraru DT, Bilha S, Miftode EG, Iliescu ML, Leustean L, Ungureanu MC. Screening of Congenital Hypothyroidism in North-East Romania. Benefits and Messages for Further Improvement. Acta Endocrinol (Buchar) 2020;16:437-42. [PMID: 34084234 DOI: 10.4183/aeb.2020.437] [Reference Citation Analysis]
14 Wang J, Tang XX, Zhou Q, Yang S, Shi Y, Yu B, Zhang B, Wang LL. Prenatal Diagnostic Testing Following High-Risk Result from Serological Screening: Which Shall We Select? Int J Womens Health 2021;13:879-88. [PMID: 34588820 DOI: 10.2147/IJWH.S324529] [Reference Citation Analysis]
15 Wang H, Wang W, Chen X, Shi H, Shi Y, Ding G. Screening and Functional Analysis of TPO Gene Mutations in a Cohort of Chinese Patients With Congenital Hypothyroidism. Front Endocrinol (Lausanne) 2021;12:774941. [PMID: 35002963 DOI: 10.3389/fendo.2021.774941] [Reference Citation Analysis]
16 Citterio CE, Siffo S, Moya CM, Pio MG, Molina MF, Scheps KG, Rey OA, Arvan P, Rivolta CM, Targovnik HM. p.L571P in the linker domain of rat thyroglobulin causes intracellular retention. Molecular and Cellular Endocrinology 2020;505:110719. [DOI: 10.1016/j.mce.2020.110719] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Huang M, Lu X, Dong G, Li J, Chen C, Yu Q, Li M, Su Y. Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population. Front Endocrinol (Lausanne) 2021;12:695426. [PMID: 34276565 DOI: 10.3389/fendo.2021.695426] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
18 Kopel J. A global perspective on newborn congenital hypothyroidism screening. Proc (Bayl Univ Med Cent) 2020;33:137-9. [PMID: 32063801 DOI: 10.1080/08998280.2019.1668715] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Xiao FF, Wang YZ, Dong F, Li XL, Zhang T. Congenital hepatic fibrosis in a young boy with congenital hypothyroidism: A case report. World J Clin Cases 2021; 9(6): 1475-1482 [PMID: 33644218 DOI: 10.12998/wjcc.v9.i6.1475] [Reference Citation Analysis]
20 Bruellman RJ, Watanabe Y, Ebrhim RS, Creech MK, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE. Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism. J Clin Endocrinol Metab 2020;105:dgz297. [PMID: 31867598 DOI: 10.1210/clinem/dgz297] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
21 Kollati Y, Akella RRD, Naushad SM, Thalla M, Reddy GB, Dirisala VR. The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism. 3 Biotech 2020;10:285. [PMID: 32550104 DOI: 10.1007/s13205-020-02273-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
22 Sorapipatcharoen K, Tim-Aroon T, Mahachoklertwattana P, Chantratita W, Iemwimangsa N, Sensorn I, Panthan B, Jiaranai P, Noojarern S, Khlairit P, Pongratanakul S, Suprasongsin C, Korwutthikulrangsri M, Sriphrapradang C, Poomthavorn P. DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients. Endocr Connect 2020;9:1121-34. [PMID: 33310921 DOI: 10.1530/EC-20-0411] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
23 Weichenberger CX, Rivera MT, Vanderpas J. Familial Aggregation of Endemic Congenital Hypothyroidism Syndrome in Congo (DR): Historical Data. Nutrients 2020;12:E3021. [PMID: 33023116 DOI: 10.3390/nu12103021] [Reference Citation Analysis]
24 Fang Y, Wan J, Zhang R, Sun F, Yang L, Zhao S, Dong M, Song H. Tpo knockout in zebrafish partially recapitulates clinical manifestations of congenital hypothyroidism and reveals the involvement of TH in proper development of glucose homeostasis. General and Comparative Endocrinology 2022;323-324:114033. [DOI: 10.1016/j.ygcen.2022.114033] [Reference Citation Analysis]
25 Li M, Li X, Wang F, Ren Y, Zhang X, Wang J, Shen L, Zhao D, ShiguoLiu. Genetic analysis of iodide transporter and recycling (NIS, PDS, SLC26A7, IYD) in patients with congenital hypothyroidism. Gene 2022;824:146402. [PMID: 35276235 DOI: 10.1016/j.gene.2022.146402] [Reference Citation Analysis]
26 Pio MG, Molina MF, Siffo S, Chiesa A, Rivolta CM, Targovnik HM. A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis. Mol Cell Endocrinol 2021;522:111124. [PMID: 33321114 DOI: 10.1016/j.mce.2020.111124] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
27 Asena M, Demiral M, Unal E, Öcal M, Demirbilek H, Özbek MN. Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism. J Clin Res Pediatr Endocrinol 2020;12:275-80. [PMID: 31990163 DOI: 10.4274/jcrpe.galenos.2020.2019.0170] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
28 Xu J, Xue Y, Wang J, Zhou Q, Zhang B, Yu B, Wang T. The Necessity of Prenatal Diagnosis by CMA for the Women with NIPS-Positive Results. Int J Genomics 2020;2020:2145701. [PMID: 32953872 DOI: 10.1155/2020/2145701] [Reference Citation Analysis]
29 Szczepanek-Parulska E, Budny B, Borowczyk M, Zhukov I, Szutkowski K, Zawadzka K, Tahir R, Minczykowski A, Niedziela M, Ruchała M. NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis. Int J Mol Sci 2022;23:3414. [PMID: 35328834 DOI: 10.3390/ijms23063414] [Reference Citation Analysis]
30 Tzifi F, Iliadi A, Voutetakis A, Platis D, Girginoudis P, Kanaka-Gantenbein C. Non-inferiority of liquid thyroxine in comparison to tablets formulation in the treatment of children with congenital hypothyroidism. J Pediatr Endocrinol Metab 2021. [PMID: 34653328 DOI: 10.1515/jpem-2021-0458] [Reference Citation Analysis]
31 Wu X, Yang Y, Zhou L, Long W, Yu B. Are We Ready for Newborn Genetic Screening? A Cross-Sectional Survey of Healthcare Professionals in Southeast China. Front Pediatr 2022;10:875229. [DOI: 10.3389/fped.2022.875229] [Reference Citation Analysis]
32 Park KS. Analysis of Worldwide Carrier Frequency and Predicted Genetic Prevalence of Autosomal Recessive Congenital Hypothyroidism Based on a General Population Database. Genes (Basel) 2021;12:863. [PMID: 34200080 DOI: 10.3390/genes12060863] [Reference Citation Analysis]