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For: Maclachlan A, Watson SP, Morgan NV. Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing. Platelets 2017;28:14-9. [PMID: 27348543 DOI: 10.1080/09537104.2016.1195492] [Cited by in Crossref: 24] [Cited by in F6Publishing: 19] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
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5 Hou Y, Shao L, Zhou H, Liu Y, Fisk DG, Spiteri E, Zehnder JL, Peng J, Zhang BM, Hou M. Identification of a pathogenic TUBB1 variant in a Chinese family with congenital macrothrombocytopenia through whole genome sequencing. Platelets 2021;:1-5. [PMID: 33400601 DOI: 10.1080/09537104.2020.1869714] [Reference Citation Analysis]
6 Alharby E, Bakhsh MA, Albalawi AM, Almutairi SO, Hashmi JA, Basit S. A novel missense variant in the RASGRP2 gene in patients with moderate to severe bleeding disorder. Platelets 2020;31:646-51. [PMID: 32609603 DOI: 10.1080/09537104.2019.1663803] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Mundell SJ, Mumford A. TBXA2R gene variants associated with bleeding. Platelets 2018;29:739-42. [PMID: 30089223 DOI: 10.1080/09537104.2018.1499888] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
8 Rao AK. Editorial: Platelet Genomics and Disorders of Platelet Number and Function. Platelets 2017;28:2. [PMID: 28095213 DOI: 10.1080/09537104.2016.1262013] [Reference Citation Analysis]
9 Romasko EJ, Devkota B, Biswas S, Jayaraman V, Rajagopalan R, Dulik MC, Thom CS, Choi J, Jairam S, Scarano MI, Krantz ID, Spinner NB, Conlin LK, Lambert MP. Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders. Am J Hematol 2018;93:8-16. [PMID: 28960434 DOI: 10.1002/ajh.24917] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 3.0] [Reference Citation Analysis]
10 Greinacher A, Eekels JJM. Simplifying the diagnosis of inherited platelet disorders? The new tools do not make it any easier. Blood 2019;133:2478-83. [PMID: 30858232 DOI: 10.1182/blood-2019-01-852350] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 5.3] [Reference Citation Analysis]
11 Eicher JD, Chen MH, Pitsillides AN, Lin H, Veeraraghavan N, Brody JA, Metcalf GA, Muzny DM, Gibbs RA, Becker DM, Becker LC, Faraday N, Mathias RA, Yanek LR, Boerwinkle E, Cupples LA, Johnson AD. Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation. Thromb Haemost 2017;117:1083-92. [PMID: 28300864 DOI: 10.1160/TH16-09-0677] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
12 Körholz J, Lucas N, Boiti F, Althaus K, Tiebel O, Fang M, Berner R, Lee-Kirsch MA, Knöfler R. Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation. TH Open 2020;4:e413-6. [PMID: 33376940 DOI: 10.1055/s-0040-1718910] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
13 Ghosh K, Patel P, Mishra K, Ghosh K. Inherited Thrombocytopenias: Combining High-Throughput Sequencing With Other Relevant Data. Clin Appl Thromb Hemost 2019;25:1076029618820164. [PMID: 30808217 DOI: 10.1177/1076029618820164] [Reference Citation Analysis]
14 Mohan G, Malayala SV, Mehta P, Balla M. A Comprehensive Review of Congenital Platelet Disorders, Thrombocytopenias and Thrombocytopathies. Cureus 2020;12:e11275. [PMID: 33274150 DOI: 10.7759/cureus.11275] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Kim B. Diagnostic workup of inherited platelet disorders. Blood Res 2022;57:11-9. [PMID: 35483920 DOI: 10.5045/br.2022.2021223] [Reference Citation Analysis]
16 Eicher JD, Lettre G, Johnson AD. The genetics of platelet count and volume in humans. Platelets. 2018;29:125-130. [PMID: 28649937 DOI: 10.1080/09537104.2017.1317732] [Cited by in Crossref: 22] [Cited by in F6Publishing: 20] [Article Influence: 4.4] [Reference Citation Analysis]
17 Zaninetti C, Wolff M, Greinacher A. Diagnosing Inherited Platelet Disorders: Modalities and Consequences. Hamostaseologie 2021. [PMID: 34391210 DOI: 10.1055/a-1515-0813] [Reference Citation Analysis]
18 Nessle CN, Ghosal S, Mathews C, Taylor D, Myers J, Raj A, Panigrahi A. Weak correlation of bleeding scores to platelet electron microscopy: A retrospective chart review of pediatric patients with delta-storage pool disorder. Pediatr Blood Cancer 2019;66:e27505. [PMID: 30345617 DOI: 10.1002/pbc.27505] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
19 Fager Ferrari M, Zetterberg E, Rossing M, Manon-Jensen T, Pehrsson M, Karsdal MA, Lykkesfeldt J, Leinoe E. Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen-related genes. Haemophilia 2021;27:e69-77. [PMID: 33161638 DOI: 10.1111/hae.14195] [Reference Citation Analysis]
20 Kumm EJ, Pagel O, Gambaryan S, Walter U, Zahedi RP, Smolenski A, Jurk K. The Cell Cycle Checkpoint System MAST(L)-ENSA/ARPP19-PP2A is Targeted by cAMP/PKA and cGMP/PKG in Anucleate Human Platelets. Cells 2020;9:E472. [PMID: 32085646 DOI: 10.3390/cells9020472] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
21 Negahdari S, Zamani M, Seifi T, Sedighzadeh S, Mazaheri N, Zeighami J, Sedaghat A, Saberi A, Hamid M, Keikhaei B, Radpour R, Shariati G, Galehdari H. Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing. Int J Prev Med 2020;11:117. [PMID: 33088445 DOI: 10.4103/ijpvm.IJPVM_462_19] [Reference Citation Analysis]
22 Ross JE, Zhang BM, Lee K, Mohan S, Branchford BR, Bray P, Dugan SN, Freson K, Heller PG, Kahr WHA, Lambert MP, Luchtman-Jones L, Luo M, Perez Botero J, Rondina MT, Ryan G, Westbury S, Bergmeier W, Di Paola J. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel. Blood Adv 2021;5:414-31. [PMID: 33496739 DOI: 10.1182/bloodadvances.2020003712] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]