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For: Jäger AC, Alvarez ML, Davis CP, Guzmán E, Han Y, Way L, Walichiewicz P, Silva D, Pham N, Caves G, Bruand J, Schlesinger F, Pond SJK, Varlaro J, Stephens KM, Holt CL. Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories. Forensic Sci Int Genet 2017;28:52-70. [PMID: 28171784 DOI: 10.1016/j.fsigen.2017.01.011] [Cited by in Crossref: 131] [Cited by in F6Publishing: 110] [Article Influence: 26.2] [Reference Citation Analysis]
Number Citing Articles
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2 Vasiljevic N, Lim M, Humble E, Seah A, Kratzer A, Morf NV, Prost S, Ogden R. Developmental validation of Oxford Nanopore Technology MinION sequence data and the NGSpeciesID bioinformatic pipeline for forensic genetic species identification. Forensic Sci Int Genet 2021;53:102493. [PMID: 33770699 DOI: 10.1016/j.fsigen.2021.102493] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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5 Zhang Q, Zhou Z, Liu Q, Liu L, Shao L, Zhang M, Ding X, Gao Y, Wang S. Evaluation of the performance of Illumina's ForenSeq™ system on serially degraded samples. ELECTROPHORESIS 2018;39:2674-84. [DOI: 10.1002/elps.201800101] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
6 Lynch C, Fleming R. A review of direct polymerase chain reaction of DNA and RNA for forensic purposes. WIREs Forensic Sci 2019;1. [DOI: 10.1002/wfs2.1335] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 1.7] [Reference Citation Analysis]
7 Giampaoli S, De Vittori E, Frajese G, Paytuví A, Sanseverino W, Anselmo A, Barni F, Berti A. A semi-automated protocol for NGS metabarcoding and fungal analysis in forensic. Forensic Science International 2020;306:110052. [DOI: 10.1016/j.forsciint.2019.110052] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
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9 Arenas M, Pereira F, Oliveira M, Pinto N, Lopes AM, Gomes V, Carracedo A, Amorim A. Forensic genetics and genomics: Much more than just a human affair. PLoS Genet 2017;13:e1006960. [PMID: 28934201 DOI: 10.1371/journal.pgen.1006960] [Cited by in Crossref: 37] [Cited by in F6Publishing: 23] [Article Influence: 7.4] [Reference Citation Analysis]
10 Saedon NA, Saiman MZ, Ahmad N, Hashim R, Syed A.rahman SNH, Zainudin N, Azah MS, Che Amran MF, Husni Z, Khairi Othman H. DNA analysis on mass grave bone samples: Ops Wawasan Khas. Forensic Science International: Genetics Supplement Series 2017;6:e395-6. [DOI: 10.1016/j.fsigss.2017.09.164] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
11 Reid KM, Heathfield LJ. Evaluation of direct PCR for routine DNA profiling of non-decomposed deceased individuals. Sci Justice 2020;60:567-72. [PMID: 33077040 DOI: 10.1016/j.scijus.2020.08.004] [Reference Citation Analysis]
12 Pilli E, Tarallo R, Riccia P, Berti A, Novelletto A. Kinship assignment with the ForenSeq™ DNA Signature Prep Kit: Sources of error in simulated and real cases. Sci Justice 2022;62:1-9. [PMID: 35033321 DOI: 10.1016/j.scijus.2021.10.007] [Reference Citation Analysis]
13 Miao X, Li B, Shen Y, Yu H, Zhu G, Liang C, Fu X, Wang C, Li S, Zhang B. Development and Verification of an Economical Method of Custom Target Library Construction. ACS Omega 2020;5:13087-95. [PMID: 32548494 DOI: 10.1021/acsomega.0c01014] [Reference Citation Analysis]
14 Phillips C, Devesse L, Ballard D, van Weert L, de la Puente M, Melis S, Álvarez Iglesias V, Freire-aradas A, Oldroyd N, Holt C, Syndercombe Court D, Carracedo Á, Lareu MV. Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit. ELECTROPHORESIS 2018;39:2708-24. [DOI: 10.1002/elps.201800117] [Cited by in Crossref: 28] [Cited by in F6Publishing: 20] [Article Influence: 7.0] [Reference Citation Analysis]
15 McCord BR, Gauthier Q, Cho S, Roig MN, Gibson-Daw GC, Young B, Taglia F, Zapico SC, Mariot RF, Lee SB, Duncan G. Forensic DNA Analysis. Anal Chem 2019;91:673-88. [PMID: 30485738 DOI: 10.1021/acs.analchem.8b05318] [Cited by in Crossref: 17] [Cited by in F6Publishing: 11] [Article Influence: 4.3] [Reference Citation Analysis]
16 Senst A, Caliebe A, Scheurer E, Schulz I. Validation and beyond: Next generation sequencing of forensic casework samples including challenging tissue samples from altered human corpses using the MiSeq FGx system. J Forensic Sci 2022. [PMID: 35318655 DOI: 10.1111/1556-4029.15028] [Reference Citation Analysis]
17 Wu H, Ji AC, Liu YC, Kang KL, Zhang C, Li ZW, Ji AQ, Ye J, Nie SJ, Wang L. Massively parallel sequencing of STRs using a 29-plex panel reveals stutter sequence characteristics. Electrophoresis 2020;41:2029-35. [PMID: 32770833 DOI: 10.1002/elps.202000093] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
18 Xavier C, de la Puente M, Mosquera-miguel A, Freire-aradas A, Kalamara V, Vidaki A, E. Gross T, Revoir A, Pośpiech E, Kartasińska E, Spólnicka M, Branicki W, E. Ames C, M. Schneider P, Hohoff C, Kayser M, Phillips C, Parson W. Development and validation of the VISAGE AmpliSeq basic tool to predict appearance and ancestry from DNA. Forensic Science International: Genetics 2020;48:102336. [DOI: 10.1016/j.fsigen.2020.102336] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]
19 Truelsen D, Tvedebrink T, Mogensen HS, Farzad MS, Shan MA, Morling N, Pereira V, Børsting C. Assessment of the effectiveness of the EUROFORGEN NAME and Precision ID Ancestry panel markers for ancestry investigations. Sci Rep 2021;11:18595. [PMID: 34545122 DOI: 10.1038/s41598-021-97654-0] [Reference Citation Analysis]
20 Peng D, Zhang Y, Ren H, Li H, Li R, Shen X, Wang N, Huang E, Wu R, Sun H. Identification of sequence polymorphisms at 58 STRs and 94 iiSNPs in a Tibetan population using massively parallel sequencing. Sci Rep 2020;10:12225. [PMID: 32699278 DOI: 10.1038/s41598-020-69137-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
21 Oldoni F, Podini D. Forensic molecular biomarkers for mixture analysis. Forensic Science International: Genetics 2019;41:107-19. [DOI: 10.1016/j.fsigen.2019.04.003] [Cited by in Crossref: 20] [Cited by in F6Publishing: 15] [Article Influence: 6.7] [Reference Citation Analysis]
22 Ballard D, Winkler-Galicki J, Wesoły J. Massive parallel sequencing in forensics: advantages, issues, technicalities, and prospects. Int J Legal Med 2020;134:1291-303. [PMID: 32451905 DOI: 10.1007/s00414-020-02294-0] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 5.5] [Reference Citation Analysis]
23 Sharma V, Young B, Armogida L, Khan A, Wurmbach E. Evaluation of ArmedXpert software tools, MixtureAce and Mixture Interpretation, to analyze MPS-STR data. Forensic Sci Int Genet 2021;56:102603. [PMID: 34673336 DOI: 10.1016/j.fsigen.2021.102603] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Wu L, Chu X, Zheng J, Xiao C, Zhang Z, Huang G, Li D, Zhan J, Huang D, Hu P, Xiong B. Targeted capture and sequencing of 1245 SNPs for forensic applications. Forensic Science International: Genetics 2019;42:227-34. [DOI: 10.1016/j.fsigen.2019.07.006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
25 Li R, Budowle B, Sun H, Ge J. Linkage and linkage disequilibrium among the markers in the forensic MPS panels. J Forensic Sci 2021;66:1637-46. [PMID: 33885147 DOI: 10.1111/1556-4029.14724] [Reference Citation Analysis]
26 Li R, Li H, Peng D, Hao B, Wang Z, Huang E, Wu R, Sun H. Improved pairwise kinship analysis using massively parallel sequencing. Forensic Science International: Genetics 2019;38:77-85. [DOI: 10.1016/j.fsigen.2018.10.006] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 7.0] [Reference Citation Analysis]
27 Tyazhelova TV, Kuznetsova IL, Andreeva TV, Kunizheva SS, Rogaev EI. Application of Massive Parallel Sequencing Technology in Forensics: Comparative Analysis of Sequencing Platforms. Russ J Genet 2021;57:1430-42. [DOI: 10.1134/s1022795421120127] [Reference Citation Analysis]
28 Barbarić L, Horjan-Zanki I. Challenges in the recovery of the genetic data from human remains found on the Western Balkan migration route. Int J Legal Med 2022. [PMID: 35449468 DOI: 10.1007/s00414-022-02829-7] [Reference Citation Analysis]
29 Wu J, Li JL, Wang ML, Li JP, Zhao ZC, Wang Q, Yang SD, Xiong X, Yang JL, Deng YJ. Evaluation of the MiSeq FGx system for use in forensic casework. Int J Legal Med 2019;133:689-97. [PMID: 30604102 DOI: 10.1007/s00414-018-01987-x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
30 Köcher S, Müller P, Berger B, Bodner M, Parson W, Roewer L, Willuweit S. Inter-laboratory validation study of the ForenSeq™ DNA Signature Prep Kit. Forensic Science International: Genetics 2018;36:77-85. [DOI: 10.1016/j.fsigen.2018.05.007] [Cited by in Crossref: 26] [Cited by in F6Publishing: 22] [Article Influence: 6.5] [Reference Citation Analysis]
31 Hall CL, Kesharwani RK, Phillips NR, Planz JV, Sedlazeck FJ, Zascavage RR. Accurate profiling of forensic autosomal STRs using the Oxford Nanopore Technologies MinION device. Forensic Sci Int Genet 2022;56:102629. [PMID: 34837788 DOI: 10.1016/j.fsigen.2021.102629] [Reference Citation Analysis]
32 Just RS, Le J, Irwin JA. LUS+: Extension of the LUS designator concept to differentiate most sequence alleles for 27 STR loci. Forensic Science International: Reports 2020;2:100059. [DOI: 10.1016/j.fsir.2020.100059] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
33 Devesse L, Ballard D, Davenport L, Riethorst I, Mason-buck G, Syndercombe Court D. Concordance of the ForenSeq™ system and characterisation of sequence-specific autosomal STR alleles across two major population groups. Forensic Science International: Genetics 2018;34:57-61. [DOI: 10.1016/j.fsigen.2017.10.012] [Cited by in Crossref: 41] [Cited by in F6Publishing: 35] [Article Influence: 10.3] [Reference Citation Analysis]
34 Sharma V, Chow HY, Siegel D, Wurmbach E. Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™. PLoS One 2017;12:e0187932. [PMID: 29121662 DOI: 10.1371/journal.pone.0187932] [Cited by in Crossref: 22] [Cited by in F6Publishing: 17] [Article Influence: 4.4] [Reference Citation Analysis]
35 Butler JM, Willis S. Interpol review of forensic biology and forensic DNA typing 2016-2019. Forensic Sci Int Synerg 2020;2:352-67. [PMID: 33385135 DOI: 10.1016/j.fsisyn.2019.12.002] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 4.5] [Reference Citation Analysis]
36 Sharma V, Jani K, Khosla P, Butler E, Siegel D, Wurmbach E. Evaluation of ForenSeq™ Signature Prep Kit B on predicting eye and hair coloration as well as biogeographical ancestry by using Universal Analysis Software (UAS) and available web‐tools. ELECTROPHORESIS 2019;40:1353-64. [DOI: 10.1002/elps.201800344] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
37 Sidstedt M, Steffen CR, Kiesler KM, Vallone PM, Rådström P, Hedman J. The impact of common PCR inhibitors on forensic MPS analysis. Forensic Sci Int Genet 2019;40:182-91. [PMID: 30878722 DOI: 10.1016/j.fsigen.2019.03.001] [Cited by in Crossref: 19] [Cited by in F6Publishing: 11] [Article Influence: 6.3] [Reference Citation Analysis]
38 Bennett L, Oldoni F, Long K, Cisana S, Madella K, Wootton S, Chang J, Hasegawa R, Lagacé R, Kidd KK, Podini D. Mixture deconvolution by massively parallel sequencing of microhaplotypes. Int J Legal Med 2019;133:719-29. [PMID: 30758713 DOI: 10.1007/s00414-019-02010-7] [Cited by in Crossref: 20] [Cited by in F6Publishing: 15] [Article Influence: 6.7] [Reference Citation Analysis]
39 Truelsen D, Freire-Aradas A, Nazari M, Aliferi A, Ballard D, Phillips C, Morling N, Pereira V, Børsting C. Evaluation of a custom QIAseq targeted DNA panel with 164 ancestry informative markers sequenced with the Illumina MiSeq. Sci Rep 2021;11:21040. [PMID: 34702940 DOI: 10.1038/s41598-021-99933-2] [Reference Citation Analysis]
40 Müller P, Alonso A, Barrio PA, Berger B, Bodner M, Martin P, Parson W. Systematic evaluation of the early access applied biosystems precision ID Globalfiler mixture ID and Globalfiler NGS STR panels for the ion S5 system. Forensic Science International: Genetics 2018;36:95-103. [DOI: 10.1016/j.fsigen.2018.06.016] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [Reference Citation Analysis]
41 Gorden EM, Sturk-Andreaggi K, Marshall C. Capture enrichment and massively parallel sequencing for human identification. Forensic Sci Int Genet 2021;53:102496. [PMID: 33770700 DOI: 10.1016/j.fsigen.2021.102496] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Carrasco P, Inostroza C, Didier M, Godoy M, Holt CL, Tabak J, Loftus A. Optimizing DNA recovery and forensic typing of degraded blood and dental remains using a specialized extraction method, comprehensive qPCR sample characterization, and massively parallel sequencing. Int J Legal Med 2020;134:79-91. [PMID: 31414202 DOI: 10.1007/s00414-019-02124-y] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
43 Moura-Neto R, King JL, Mello I, Dias V, Crysup B, Woerner AE, Budowle B, Silva R. Evaluation of Promega PowerSeq™ Auto/Y systems prototype on an admixed sample of Rio de Janeiro, Brazil: Population data, sensitivity, stutter and mixture studies. Forensic Sci Int Genet 2021;53:102516. [PMID: 33878618 DOI: 10.1016/j.fsigen.2021.102516] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
44 Zajac BK, Zehner R, Scheiper S, Weissenberger M. Kit-dependent discrepancy in D16S539 and general considerations for database matches. Forensic Sci Int Genet 2018;34:148-51. [PMID: 29482104 DOI: 10.1016/j.fsigen.2018.02.012] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
45 Miao X, Shen Y, Gong X, Yu H, Li B, Chang L, Wang Y, Fan J, Liang Z, Tan B, Li S, Zhang B. A novel forensic panel of 186-plex SNPs and 123-plex STR loci based on massively parallel sequencing. Int J Legal Med 2021;135:709-18. [PMID: 32851473 DOI: 10.1007/s00414-020-02403-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
46 Ogden R, Vasiljevic N, Prost S. Nanopore sequencing in non-human forensic genetics. Emerg Top Life Sci 2021:ETLS20200287. [PMID: 34002773 DOI: 10.1042/ETLS20200287] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
47 Salvo NM, Janssen K, Kirsebom MK, Meyer OS, Berg T, Olsen GH. Predicting eye and hair colour in a Norwegian population using Verogen's ForenSeq™ DNA signature prep kit. Forensic Sci Int Genet 2022;56:102620. [PMID: 34735941 DOI: 10.1016/j.fsigen.2021.102620] [Reference Citation Analysis]
48 Beasley J, Shorrock G, Neumann R, May CA, Wetton JH. Massively parallel sequencing and capillary electrophoresis of a novel panel of falcon STRs: Concordance with minisatellite DNA profiles from historical wildlife crime. Forensic Sci Int Genet 2021;54:102550. [PMID: 34174583 DOI: 10.1016/j.fsigen.2021.102550] [Reference Citation Analysis]
49 Ge J, Budowle B. Forensic investigation approaches of searching relatives in DNA databases. J Forensic Sci 2021;66:430-43. [PMID: 33136341 DOI: 10.1111/1556-4029.14615] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
50 Huang E, Liu C, Zheng J, Han X, Du W, Huang Y, Li C, Wang X, Tong D, Ou X, Sun H, Zeng Z, Liu C. Genome-wide screen for universal individual identification SNPs based on the HapMap and 1000 Genomes databases. Sci Rep 2018;8:5553. [PMID: 29615764 DOI: 10.1038/s41598-018-23888-0] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
51 Staadig A, Tillmar A. An overall limited effect on the weight-of-evidence when taking STR DNA sequence polymorphism into account in kinship analysis. Forensic Science International: Genetics 2019;39:44-9. [DOI: 10.1016/j.fsigen.2018.11.020] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
52 Ragazzo M, Carboni S, Caputo V, Buttini C, Manzo L, Errichiello V, Puleri G, Giardina E. Interpreting Mixture Profiles: Comparison between Precision ID GlobalFiler™ NGS STR Panel v2 and Traditional Methods. Genes (Basel) 2020;11:E591. [PMID: 32466613 DOI: 10.3390/genes11060591] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
53 Kumar H, Haddish K, Lacerenza D, Aneli S, Di Gaetano C, Tewelemedhin G, Manukonda R, Futwi N, Alvarez-iglesias V, de la Puente M, Fondevila M, Lareu M, Phillips C, Robino C. Characterization of ancestry informative markers in the Tigray population of Ethiopia: A contribution to the identification process of dead migrants in the Mediterranean Sea. Forensic Science International: Genetics 2020;45:102207. [DOI: 10.1016/j.fsigen.2019.102207] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
54 Bulbul O, Filoglu G. Development of a SNP panel for predicting biogeographical ancestry and phenotype using massively parallel sequencing. ELECTROPHORESIS 2018;39:2743-51. [DOI: 10.1002/elps.201800243] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
55 Tao R, Qi W, Chen C, Zhang J, Yang Z, Song W, Zhang S, Li C. Pilot study for forensic evaluations of the Precision ID GlobalFiler™ NGS STR Panel v2 with the Ion S5™ system. Forensic Science International: Genetics 2019;43:102147. [DOI: 10.1016/j.fsigen.2019.102147] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 4.3] [Reference Citation Analysis]
56 Hölzl-Müller P, Bodner M, Berger B, Parson W. Exploring STR sequencing for forensic DNA intelligence databasing using the Austrian National DNA Database as an example. Int J Legal Med 2021;135:2235-46. [PMID: 34436655 DOI: 10.1007/s00414-021-02685-x] [Reference Citation Analysis]
57 Gomes I, Pinto N, Antão-Sousa S, Gomes V, Gusmão L, Amorim A. Twenty Years Later: A Comprehensive Review of the X Chromosome Use in Forensic Genetics. Front Genet 2020;11:926. [PMID: 33093840 DOI: 10.3389/fgene.2020.00926] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
58 Chen C, Jin X, Zhang X, Zhang W, Guo Y, Tao R, Chen A, Xu Q, Li M, Yang Y, Zhu B. Comprehensive Insights Into Forensic Features and Genetic Background of Chinese Northwest Hui Group Using Six Distinct Categories of 231 Molecular Markers. Front Genet 2021;12:705753. [PMID: 34721519 DOI: 10.3389/fgene.2021.705753] [Reference Citation Analysis]
59 Guo F, Yu J, Zhang L, Li J. Massively parallel sequencing of forensic STRs and SNPs using the Illumina ® ForenSeq™ DNA Signature Prep Kit on the MiSeq FGx™ Forensic Genomics System. Forensic Science International: Genetics 2017;31:135-48. [DOI: 10.1016/j.fsigen.2017.09.003] [Cited by in Crossref: 64] [Cited by in F6Publishing: 55] [Article Influence: 12.8] [Reference Citation Analysis]
60 Zeng X, King JL, Budowle B. Investigation of the STR loci noise distributions of PowerSeq™ Auto System. Croat Med J 2017;58:214-21. [PMID: 28613038 DOI: 10.3325/cmj.2017.58.214] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
61 Khubrani YM, Hallast P, Jobling MA, Wetton JH. Massively parallel sequencing of autosomal STRs and identity-informative SNPs highlights consanguinity in Saudi Arabia. Forensic Sci Int Genet 2019;43:102164. [PMID: 31585345 DOI: 10.1016/j.fsigen.2019.102164] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 4.3] [Reference Citation Analysis]
62 Zhang Q, Zhou Z, Wang L, Quan C, Liu Q, Tang Z, Liu L, Liu Y, Wang S. Pairwise kinship testing with a combination of STR and SNP loci. Forensic Science International: Genetics 2020;46:102265. [DOI: 10.1016/j.fsigen.2020.102265] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
63 Cho WK, Shin HR, Lee NY, Kim SK, Ahn MB, Baek IC, Kim TG, Suh BK. GPR174 and ITM2A Gene Polymorphisms rs3827440 and rs5912838 on the X chromosome in Korean Children with Autoimmune Thyroid Disease. Genes (Basel) 2020;11:E858. [PMID: 32727090 DOI: 10.3390/genes11080858] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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