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For: Ceulemans S, van der Ven K, Del-Favero J. Targeted screening and validation of copy number variations. Methods Mol Biol. 2012;838:311-328. [PMID: 22228019 DOI: 10.1007/978-1-61779-507-7_15] [Cited by in Crossref: 26] [Cited by in F6Publishing: 22] [Article Influence: 2.6] [Reference Citation Analysis]
Number Citing Articles
1 Rodriguez S, Al-Ghamdi OA, Guthrie PA, Shihab HA, McArdle W, Gaunt T, Alharbi KK, Day IN. Frequency of KLK3 gene deletions in the general population. Ann Clin Biochem 2017;54:472-80. [PMID: 27555663 DOI: 10.1177/0004563216666999] [Reference Citation Analysis]
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5 Di Filippo M, Collardeau Frachon S, Janin A, Rajan S, Marmontel O, Decourt C, Rubio A, Nony S, Dumont S, Cuerq C, Charrière S, Moulin P, Lachaux A, Hussain MM, Bozon D, Peretti N. Normal serum ApoB48 and red cells vitamin E concentrations after supplementation in a novel compound heterozygous case of abetalipoproteinemia. Atherosclerosis 2019;284:75-82. [PMID: 30875496 DOI: 10.1016/j.atherosclerosis.2019.02.016] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.7] [Reference Citation Analysis]
6 Li Z, Ding Y, Zhu Y, Yin M, Le X, Wang L, Yang Y, Zhang Q. Both gene deletion and promoter hyper-methylation contribute to the down-regulation of ZAC/PLAGL1 gene in gastric adenocarcinomas: a case control study. Clin Res Hepatol Gastroenterol 2014;38:744-50. [PMID: 25091631 DOI: 10.1016/j.clinre.2013.06.007] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
7 Wang J, Xiang J, Chen L, Luo H, Xu X, Li N, Cui C, Xu J, Song N, Peng J, Peng Z. Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach. Sci Rep 2021;11:4036. [PMID: 33597575 DOI: 10.1038/s41598-021-83493-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Whale AS, Cowen S, Foy CA, Huggett JF. Methods for applying accurate digital PCR analysis on low copy DNA samples. PLoS One 2013;8:e58177. [PMID: 23472156 DOI: 10.1371/journal.pone.0058177] [Cited by in Crossref: 96] [Cited by in F6Publishing: 86] [Article Influence: 10.7] [Reference Citation Analysis]
9 Landowski M, O'Donohue MF, Buros C, Ghazvinian R, Montel-Lehry N, Vlachos A, Sieff CA, Newburger PE, Niewiadomska E, Matysiak M, Glader B, Atsidaftos E, Lipton JM, Beggs AH, Gleizes PE, Gazda HT. Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia. Hum Genet 2013;132:1265-74. [PMID: 23812780 DOI: 10.1007/s00439-013-1326-z] [Cited by in Crossref: 74] [Cited by in F6Publishing: 74] [Article Influence: 8.2] [Reference Citation Analysis]
10 Yamamoto T, Shimada S, Shimojima K. Fiber-fluorescence in situ hybridization analyses as a diagnostic application for orientation of microduplications. World J Med Genet 2013; 3(2): 5-8 [DOI: 10.5496/wjmg.v3.i2.5] [Reference Citation Analysis]
11 Mei D, Parrini E, Marini C, Guerrini R. The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients. Mol Diagn Ther 2017;21:357-73. [DOI: 10.1007/s40291-017-0257-0] [Cited by in Crossref: 31] [Cited by in F6Publishing: 30] [Article Influence: 6.2] [Reference Citation Analysis]
12 Pócza T, Grolmusz VK, Papp J, Butz H, Patócs A, Bozsik A. Germline Structural Variations in Cancer Predisposition Genes. Front Genet 2021;12:634217. [PMID: 33936164 DOI: 10.3389/fgene.2021.634217] [Reference Citation Analysis]
13 Blesa S, Olivares MD, Alic AS, Serrano A, Lendinez V, González-Albert V, Olivares L, Martínez-Hervás S, Juanes JM, Marín P, Real JT, Navarro B, García-García AB, Chaves FJ, Ivorra C. Easy One-Step Amplification and Labeling Procedure for Copy Number Variation Detection. Clin Chem 2020;66:463-73. [PMID: 32068788 DOI: 10.1093/clinchem/hvaa002] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
14 Chillón MC, Jiménez C, García-Sanz R, Alcoceba M, Prieto I, García-Alvarez M, Antón A, Maldonado R, Hernández-Ruano M, González M, Gutiérrez NC, Sarasquete ME. Quantitative PCR: an alternative approach to detect common copy number alterations in multiple myeloma. Ann Hematol 2017;96:1699-705. [PMID: 28770277 DOI: 10.1007/s00277-017-3083-x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
15 Aydin AM, Chahoud J, Adashek JJ, Azizi M, Magliocco A, Ross JS, Necchi A, Spiess PE. Understanding genomics and the immune environment of penile cancer to improve therapy. Nat Rev Urol 2020;17:555-70. [DOI: 10.1038/s41585-020-0359-z] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
16 Pang JM, Gorringe KL, Wong SQ, Dobrovic A, Campbell IG, Fox SB. Appraisal of the technologies and review of the genomic landscape of ductal carcinoma in situ of the breast. Breast Cancer Res 2015;17:80. [PMID: 26078038 DOI: 10.1186/s13058-015-0586-z] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
17 Marcinkowska-swojak M, Uszczynska B, Figlerowicz M, Kozlowski P. An MLPA-Based Strategy for Discrete CNV Genotyping: CNV-miRNAs as an Example. Human Mutation 2013;34:763-73. [DOI: 10.1002/humu.22288] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 1.6] [Reference Citation Analysis]
18 Binversie EE, Baker LA, Engelman CD, Hao Z, Moran JJ, Piazza AM, Sample SJ, Muir P. Analysis of copy number variation in dogs implicates genomic structural variation in the development of anterior cruciate ligament rupture. PLoS One 2020;15:e0244075. [PMID: 33382735 DOI: 10.1371/journal.pone.0244075] [Reference Citation Analysis]
19 Rubio-piña J, Quiroz-moreno A, Sánchez-teyer LF. A quantitative PCR approach for determining the ribosomal DNA copy number in the genome of Agave tequila Weber. Electronic Journal of Biotechnology 2016;22:9-15. [DOI: 10.1016/j.ejbt.2016.05.002] [Cited by in Crossref: 4] [Article Influence: 0.7] [Reference Citation Analysis]
20 Bozsik A, Pócza T, Papp J, Vaszkó T, Butz H, Patócs A, Oláh E. Complex Characterization of Germline Large Genomic Rearrangements of the BRCA1 and BRCA2 Genes in High-Risk Breast Cancer Patients-Novel Variants from a Large National Center. Int J Mol Sci 2020;21:E4650. [PMID: 32629901 DOI: 10.3390/ijms21134650] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
21 Li W, Olivier M. Current analysis platforms and methods for detecting copy number variation. Physiol Genomics 2013;45:1-16. [PMID: 23132758 DOI: 10.1152/physiolgenomics.00082.2012] [Cited by in Crossref: 49] [Cited by in F6Publishing: 39] [Article Influence: 4.9] [Reference Citation Analysis]
22 Ebrahimizadeh W, Guérard KP, Rouzbeh S, Bramhecha YM, Scarlata E, Brimo F, Patel PG, Jamaspishvili T, Aprikian AG, Berman D, Bartlett JMS, Chevalier S, Lapointe J. Design and Development of a Fully Synthetic Multiplex Ligation-Dependent Probe Amplification-Based Probe Mix for Detection of Copy Number Alterations in Prostate Cancer Formalin-Fixed, Paraffin-Embedded Tissue Samples. J Mol Diagn 2020;22:1246-63. [PMID: 32763409 DOI: 10.1016/j.jmoldx.2020.07.003] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
23 Fowler A, Mahamdallie S, Ruark E, Seal S, Ramsay E, Clarke M, Uddin I, Wylie H, Strydom A, Lunter G, Rahman N. Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN. Wellcome Open Res 2016;1:20. [PMID: 28459104 DOI: 10.12688/wellcomeopenres.10069.1] [Cited by in Crossref: 41] [Cited by in F6Publishing: 32] [Article Influence: 6.8] [Reference Citation Analysis]
24 Fernández Asensio A, Iglesias T, Cotarelo A, Espina M, Blanco-gonzález E, Sierra L, Montes-bayón M. Multiplex polymerase chain reaction in combination with gel electrophoresis-inductively coupled plasma mass spectrometry: A powerful tool for the determination of gene copy number variations and gene expression changes. Analytica Chimica Acta 2018;1023:64-73. [DOI: 10.1016/j.aca.2018.03.047] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]