BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Fox MD, Carson VJ, Feng HZ, Lawlor MW, Gray JT, Brigatti KW, Jin JP, Strauss KA. TNNT1 nemaline myopathy: natural history and therapeutic frontier. Hum Mol Genet 2018;27:3272-82. [PMID: 29931346 DOI: 10.1093/hmg/ddy233] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Streff H, Bi W, Colón AG, Adesina AM, Miyake CY, Lalani SR. Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child. Eur J Med Genet 2019;62:103567. [PMID: 30395933 DOI: 10.1016/j.ejmg.2018.11.001] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
2 Sewry CA, Laitila JM, Wallgren-Pettersson C. Nemaline myopathies: a current view. J Muscle Res Cell Motil. 2019;40:111-126. [PMID: 31228046 DOI: 10.1007/s10974-019-09519-9] [Cited by in Crossref: 47] [Cited by in F6Publishing: 38] [Article Influence: 15.7] [Reference Citation Analysis]
3 van de Locht M, Borsboom TC, Winter JM, Ottenheijm CAC. Troponin Variants in Congenital Myopathies: How They Affect Skeletal Muscle Mechanics. Int J Mol Sci 2021;22:9187. [PMID: 34502093 DOI: 10.3390/ijms22179187] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Wang S, Tian W, Pan D, Liu L, Xu C, Ma Y, Wang D, Jiang L. A Comprehensive Analysis of the Myocardial Transcriptome in ZBED6-Knockout Bama Xiang Pigs. Genes 2022;13:1382. [DOI: 10.3390/genes13081382] [Reference Citation Analysis]
5 Laitila J, Wallgren-Pettersson C. Recent advances in nemaline myopathy. Neuromuscul Disord 2021;31:955-67. [PMID: 34561123 DOI: 10.1016/j.nmd.2021.07.012] [Reference Citation Analysis]
6 Laflamme N, Lace B, Thonta Setty S, Rioux N, Labrie Y, Droit A, Chrestian N, Rivest S. A Homozygous Deep Intronic Mutation Alters the Splicing of Nebulin Gene in a Patient With Nemaline Myopathy. Front Neurol 2021;12:660113. [PMID: 34211429 DOI: 10.3389/fneur.2021.660113] [Reference Citation Analysis]
7 Lynch MT, Maloney KA, Pollin TI, Streeten EA, Xu H, Shuldiner AR, Van Hout CV, Gonzaga-Jauregui C, Mitchell BD; Regeneron Genetics Center. The burden of pathogenic variants in clinically actionable genes in a founder population. Am J Med Genet A 2021;185:3476-84. [PMID: 34467620 DOI: 10.1002/ajmg.a.62472] [Reference Citation Analysis]
8 Rasmussen M, Jin JP. Troponin Variants as Markers of Skeletal Muscle Health and Diseases. Front Physiol 2021;12:747214. [PMID: 34733179 DOI: 10.3389/fphys.2021.747214] [Reference Citation Analysis]
9 Miles AM, Posbergh CJ, Huson HJ. Direct Phenotyping and Principal Component Analysis of Type Traits Implicate Novel QTL in Bovine Mastitis through Genome-Wide Association. Animals (Basel) 2021;11:1147. [PMID: 33920522 DOI: 10.3390/ani11041147] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
10 Hoshino A, Kanegane H, Nishi M, Tsuge I, Tokuda K, Kobayashi I, Imai K, Morio T, Takagi M. Identification of autoantibodies using human proteome microarrays in patients with IPEX syndrome. Clinical Immunology 2019;203:9-13. [DOI: 10.1016/j.clim.2019.03.011] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
11 Calame DG, Fatih J, Herman I, Akdemir ZC, Du H, Jhangiani SN, Gibbs RA, Marafi D, Pehlivan D, Posey JE, Lotze T, Mancias P, Bhattacharjee MB, Lupski JR. Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. Neurol Genet 2021;7:e589. [PMID: 33977145 DOI: 10.1212/NXG.0000000000000589] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
12 Christophers B, Lopez MA, Gupta VA, Vogel H, Baylies M. Pediatric Nemaline Myopathy: A Systematic Review Using Individual Patient Data. J Child Neurol 2022;37:652-63. [DOI: 10.1177/08830738221096316] [Reference Citation Analysis]
13 Petrucci A, Primiano G, Savarese M, Sancricca C, Udd B, Servidei S. Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patient. Neuromuscul Disord 2021;31:532-8. [PMID: 33832840 DOI: 10.1016/j.nmd.2021.03.001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
14 Lu J, Li H, Zhang H, Lin Z, Xu C, Xu X, Hu L, Luan Z, Lou Y, Tang S. The distal arthrogryposis-linked p.R63C variant promotes the stability and nuclear accumulation of TNNT3. J Clin Lab Anal 2021;35:e24089. [PMID: 34766372 DOI: 10.1002/jcla.24089] [Reference Citation Analysis]
15 Pellerin D, Aykanat A, Ellezam B, Troiano EC, Karamchandani J, Dicaire MJ, Petitclerc M, Robertson R, Allard-Chamard X, Brunet D, Konersman CG, Mathieu J, Warman Chardon J, Gupta VA, Beggs AH, Brais B, Chrestian N. Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians. Ann Neurol 2020;87:568-83. [PMID: 31970803 DOI: 10.1002/ana.25685] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
16 Zhang Y, Yan H, Liu J, Yan H, Ma Y, Wei C, Wang Z, Xiong H, Chang X. Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre. BMC Pediatr 2022;22:65. [PMID: 35081925 DOI: 10.1186/s12887-021-03024-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Oki K, Wei B, Feng HZ, Jin JP. The loss of slow skeletal muscle isoform of troponin T in spindle intrafusal fibres explains the pathophysiology of Amish nemaline myopathy. J Physiol 2019;597:3999-4012. [PMID: 31148174 DOI: 10.1113/JP278119] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
18 Lee S, Eum J, Park S, Ki S, Hwang BJ, Kee Y, Chae JH. TNNT1 myopathy with novel compound heterozygous mutations. Neuromuscular Disorders 2021. [DOI: 10.1016/j.nmd.2021.12.003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Zambon AA, Abel F, Linnane B, O'rourke D, Phadke R, Sewry CA, Sarkozy A, Manzur A, Muntoni F. Troponin-T type 1 (TNNT1)-related nemaline myopathy: unique respiratory phenotype and muscle pathology findings. Neuromuscular Disorders 2022. [DOI: 10.1016/j.nmd.2022.01.014] [Reference Citation Analysis]
20 Géraud J, Dieterich K, Rendu J, Uro Coste E, Dobrzynski M, Marcorelle P, Ioos C, Romero NB, Baudou E, Brocard J, Coville AC, Fauré J, Koenig M, Juntas Morales R, Lacène E, Madelaine A, Marty I, Pegeot H, Theze C, Siegfried A, Cossee M, Cances C. Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy. J Med Genet 2021;58:602-8. [PMID: 32994279 DOI: 10.1136/jmedgenet-2019-106714] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]