1. Angiosperm phylogeny website, Stevens, P., ver. 14,and more or less continuously updated since, , 2020
2. Genome evolution in polyploids, Wendel, J. F., 42, 225–249. https://doi. org/10.1023/A:1006392424384, , 2000
3. An update on chloroplast genomes, Khurana, P., Ravi, V., Khurana, J. P., Tyagi, A. K., 271, 101–122. https://doi. org/10.1007/s00606-007-0608-0, , 2008
4. Eukaryotic genome size databases, Gregory, T. R., Murray, B. G., Kullman, B., Nicol, J. A., Leitch, I. J., Kullman, K., Tamm, H., 35, D332–D338. https://doi. org/10.1093/nar/gkl828, , 2007
5. Satellite DNA: an evolving topic, Garrido-Ramos, M. A., Genes, 8, 230. https://doi. org/10.3390/genes8090230, , 2017
6. The chloroplast genome: a review, Dobrogojski, J., Luciński, R., Adamiec, M., Acta Physiol Plant, 42, 98. https://doi. org/10.1007/s11738-020-03089-x, , 2020
7. Dynamic evolution of Panax species, Waminal, N. E., Shim, H., Kim, H. H., Yang, T. J., 43(3), 209–215. https://doi. org/10.1007/s13258-021-01047-6, , 2021
8. Brief introduction of Panax ginseng, Yun T. K., 16, S3–S5. https://doi. org/10.3346/jkms.2001.16. S. S3, , 2001
9. Repetitive DNA in eukaryotic genomes, Biscotti, M. A., Heslop-Harrison, J. S., Olmo, E., 23, 415–420. https://doi. org/10.1007/s10577-015-9499-z, , 2015
10. Genome (in)stability at tandem repeats, Pelliccia, F., Balzano, E., Giunta, S., 113, 97-112. https://doi. org/10.1016/j. semcdb.2020.10.003, , 2021
11. The plastid genomes of flowering plants, Ruhlman, T. A., Jansen, R. K., 1132, 3– 38. https://doi. org/10.1007/978-1-62703-995-6_1, , 2014
12. Haploid induction and genome instability, Tan, E. H., Comai, L., Trends Genet TIG., 35(11), 791– 803. https://doi. org/10.1016/j. tig.2019.07.005, , 2019
13. Repetitive DNA sequences in plant genomes, Shcherban, A. B., 5, 159–167. https://doi. org/10.1134/S2079059715030168, , 2015
14. Centromere repeats: hidden gems of the genome, Hartley, G., O’neill, R. J., 10, 223. https://doi. org/10.3390/genes10030223, , 2019
15. Centromere identity from the DNA point of view, Plohl, M., Meštrović, N., Mravinac, B., Chromosoma, 123, 313–325. https://doi. org/10.1007/s00412-014-0462-0, , 2014
16. Ebb and flow of the chloroplast inverted repeat, Goulding, S. E., Morden, C. W., Wolfe, K. H., Olmstead, R. G., 252(1-2), 195–206. https://doi. org/10.1007/BF02173220, , 1996
17. Ginsenosides: a potential neuroprotective agent, Li, Y., Xu, F., Zheng, M., Guo, H., Xin, Y., Xi, X., 20, 8174345. https://doi. org/10.1155/2018/8174345, , 2018
18. Chloroplast genomes of photosynthetic eukaryotes, Green, B. R., 66(1), 34–44. https://doi. org/10.1111/j.1365-313X.2011.04541. x, , 2011
19. Competition of parental genomes in plant hybrids, Glombik, M., Bačovský, V., Hobza, R., Kopecký, D., 11, 200. https://doi. org/10.3389/fpls.2020.00200, , 2020
20. Flow cytometry: basic principles and applications, Adan, A., Alizada, G., Nalbant, A., Kiraz, Y., Baran, Y., 37(2), 163–176. https://doi. org/10.3109/07388551.2015.1128876, , 2016
21. Physical mapping of rDNA loci in Brassica species, Maluszynska, J., Heslop-Harrison, J., Genome, 36, 774–781. https://doi. org/10.1139/g93-102, , 1993
22. Ribosomal DNA instability and genome adaptability, Gerton, J. L., Salim, D., Chromosome Research, 27, 73–87. https://doi. org/10.1007/s10577-018-9599-7, , 2019
23. The advantages and disadvantages of being polyploid, Comai, L., 6, 836–846. https://doi. org/10.1038/nrg1711, , 2005
24. Chloroplast genome structure in Ilex (Aquifoliaceae), Yao, X., Jin, B, 6, 28559. https://doi. org/10.1038/srep28559, , 2016
25. Nomenclature for centromeric position on chromosomes, Fredga, K., Sandberg, A. A., Levan, A., Hereditas, 52, 201–220. https://doi. org/10.1111/j.1601-5223.1964. tb01953. x, , 1964
26. The use of ribosomal DNA for comparative cytogenetics, Yücel, G., Kolano, B., Senderowicz, M., 2672, 265–284. https://doi. org/10.1007/978-1-0716-3226-0_17, , 2023
27. Nuclear DNA content and genome size of trout and human, Dolezel, J., Voglmayr, H., Greilhuber, J., Bartos, J., 51(2), 127–129. https://doi. org/10.1002/cyto. a.10013, , 2003
28. Beyond genome: advanced omics progress of Panax ginseng, Yu, W., Hu, S., Cai, S., Xu, J., Zhao, J., Zang, C., Hu, L., 341, 112022. https://doi. org/10.1016/j. plantsci.2024.112022, , 2024
29. Chromatin dynamics during the cell cycle at centromeres, Almouzni, G., Müller, S., 18, 192–208. https://doi. org/10.1038/nrg.2016.157, , 2017
30. Chromoanagenesis: a piece of the macroevolution scenario, Gatinois, V., Pellestor, F., Mol Cytogenet., 13, 3. https://doi. org/10.1186/s13039-020-0470-0, , 2020
31. The molecular basis for centromere identity and function, McKinley, K., Cheeseman, I., 17, 16–29. https://doi. org/10.1038/nrm.2015.5, , 2016
32. Evolution of DNA amounts across land plants (embryophyta), Bennett, M. D., Soltis, D. E., Leitch, I. J.,, Soltis, P. S.,, 95(1), 207–217. https://doi. org/10.1093/aob/mci014, , 2005
33. Evolution of the angiosperms: calibrating the family tree, Chase, M. W., Savolainen, V., Wikström, N., 268(1482), 2211–2220. https://doi. org/10.1098/rspb.2001.1782, , 2001
34. The evolutionary dynamics of repetitive DNA in eukaryotes, Charlesworth, B., Stephan, W., Sniegowski, P., Nature, 371, 215–220. https://doi. org/10.1038/371215a0, , 1994
35. DNA replication stress restricts ribosomal DNA copy number, Wang, J., Gerton, J. L., Salim, D., Bradford, W. D., Pruitt, S. C., Cady, G., Freeland, A., 13(9), 1–20. https://doi. org/10.1371/journal. pgen.1007006, , 2017
36. Rapid and efficient FISH using pre-labeled oligomer probes, Waminal, N. E., Pellerin, R. J., Park, J. Y., Kim, N. S., Jayakodi, M., Yang, T. J., 8, 8224. https://doi. org/10.1038/s41598-018- 26667-z, , 2018
37. Rapid and efficient FISH using pre-labeled oligomer probes, Kim, N., Pellerin, R. J., Park, J. Y., Jayakodi, M., Waminal, N. E., Kim, H. H., Yang, T., 8(1), 1-10. https://doi. org/10.1038/s41598- 018-26667-z, , 2018
38. Numerical taxonomy of the genus Senna Mill. from Bangladesh, Begum, A., Rahman, Z., Oliur Rahman, M., 20(1), 77–83. https://doi. org/10.3329/bjpt. v20i1.15467, , 2013
39. Regulation of ribosomal DNA amplification by the TOR pathway, Ralser, M., Keller, M. A., Cruz, C., Houseley, J., Jack, C. V., Hull, R. M., 112(31), 9674–9679. https://doi. org/10.1073/pnas.1505015112, , 2015
40. Repetitive DNA elements as a major component of plant genomes, Schmidt, T., Kubis, S., Heslop-Harrison, J. S., 82, 45–55. https://doi. org/10.1006/anbo.1998.0779, , 1998
41. Chromosomal cytology and evolution in Eupatorieae (Asteraceae), Yahara, T., King, R. M., Ito, M., Yokoyama, J., Suzuki, T., Watanabe, K., 82, 581–592. https://doi. org/10.2307/2399838, , 1995
42. Plant DNA flow cytometry and estimation of nuclear genome size, Bartos, J., Dolezel, J., 95(1), 99–110. https://doi. org/10.1093/aob/mci005, , 2005
43. Ancient WGD events as drivers of key innovations in angiosperms, Soltis, D. E., Soltis, P. S., 30, 159-165. https://doi. org/10.1016/j. pbi.2016.03.015, , 2016
44. Estimation of nuclear DNA content in plants using flow cytometry, Dolezel, J., Suda, J., Greilhuber, J., 2(9), 2233–2244. https://doi. org/10.1038/nprot.2007.310, , 2007
45. Interstitial telomere-like repeats in the monocot family Araceae, Sousa, A., Renner, S. S., 177(1), 15–26. https://doi. org/10.1111/boj.12231, , 2015
46. Variation of 45S rDNA intergenic spacers in Arabidopsis thaliana, Havlová, K., Dvořáčková, M., Vansáčová, L., Abia, D., Peiro, R., Mozgová, I., 92, 457–471. https://doi. org/10.1007/S11103-016-0524-1, , 2016
47. Flow cytometric chromosome sorting in plants: the next generation, Kubaláková, M., Cíhalíková, J., Simková, H., Doležel, J., Vrána, J., Methods 57(3), 331–337. https://doi. org/10.1016/j. ymeth.2012.03.006, , 2012
48. Bulked oligo-FISH for chromosome painting and chromosome barcoding, Beránková D., Hřibová E., 2672, 445-463. https://doi. org/10.1007/978-1-0716-3226-0_27, , 2023
49. RbcL and matK earn two thumbs up as the core DNA barcode for Ferns, Li, W., Windham, M. D., Rothfels, C. J., Kuo, Y., Ebihara, A., Chiou, L., 6(10), e26597. https://doi. org/10.1371/journal. pone.0026597, , 2011
50. Chromosome numbers in plant cytotaxonomy: concepts and implications, Guerra, M., 120(3-4), 339–350. https://doi. org/10.1159/000121083, , 2008
51. Ethnobotanical description and biological activities of Senna alata, Adelowo, F. E., Oluyori, A. P., Oladeji, O. S., Evid-Based Complement. Alternat. Med., 2020, 2580259. https://doi. org/10.1155/2020/2580259, , 2020
52. Fast diploidization in close mesopolyploid relatives of Arabidopsis, Krzywinski, M., Mandáková, T., Lysaka, M. A., Mummenhoff, K., Joly, S., 22, 2277–2290. https://doi. org/10.1105/tpc.110.074526, , 2010
53. Genome size diversity and its impact on the evolution of land plants, Dodsworth, S., Pellicer, J., Hidalgo, O., Leitch, I. J., Genes, 9(2), 88. https://doi. org/10.3390/genes9020088, , 2018
54. Genome-enabled discovery of anthraquinone biosynthesis in Senna tora, Pandey, R. P., Sim, J. S., Lee, C. M., Jeong, J. T., Choi, B. S., Kang, S. H., al 11, 1–11. https://doi. org/10.1038/S41467-020-19681-1, , 2020
55. Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences, Doyle, J. J, Soltis, P. S., Soltis, D. E., 133(4), 381–461. https://doi. org/10.1006/bojl.2000.0380, , 2000
56. Structures of telomerase at several steps of telomere repeat synthesis, Sušac, L., Helmling, C., He, Y., Cheng, R., Liu, B., Wang, Y., Nature, 593(7859), 454-459. https://doi. org/10.1038/s41586-021-03529-9, , 2021
57. Cycles of satellite and transposon evolution in Arabidopsis centromeres, Naish, M., Burns, R., Scott, A., Rabanal, F. A., Primetis, E., Wlodzimierz, P., Nature, 618(7965), 557-565. https://doi. org/10.1038/s41586-023-06062-z, , 2023
58. Telomere sequence localization and karyotype evolution in higher plants, Fuchs, J., Schubert, I., Brandes, A., 196, 227–241. https://doi. org/10.1007/BF00982962, , 1995
59. Variability for sennoside A and B concentrations in eight Senna species, Bradley Morris, J., Wang, M. L., Tonnis, B. D., 139, 111489. https://doi. org/10.1016/j. indcrop.2019.111489, , 2019
60. Evolution and taxonomic split of the model grass Brachypodium distachyon, Mur, L. A., Müller, J., Langdon, T., Jenkins, G., Hasterok, R., Catalán, P., 109(2), 385–405. https://doi. org/10.1093/aob/mcr294, , 2012
61. Genome and evolution of the shade-requiring medicinal herb Panax ginseng, Jayakodi, M., Lee, J., Jang, W., Lee, S. C., Choi, B. S., Kim, N. H., 16(11), 1904–1917. https://doi. org/10.1111/pbi.12926, , 2018
62. Comparison of four nuclear isolation buffers for plant DNA flow cytometry, Rodriguez, E., Santos, C., Loureiro, J., Dolezel, J., 98(3), 679–689. https://doi. org/10.1093/aob/mcl141, , 2006
63. Centromeres: unique chromatin structures that drive chromosome segregation, Verdaasdonk, J., Bloom, K., 12, 320–332. https://doi. org/10.1038/nrm3107, , 2011
64. Post-polyploid diploidization and diversification through dysploid changes, Mandáková, T., Lysak, M. A., 42, 55–65. doi: 10.1016/j. pbi.2018.03.001, , 2018
65. Advances in plastid genome research: structure, evolution, and applications, Wu, S., Hu, H., Zhang, Y., 75, 189–210. https://doi. org/10.1146/annurev-arplant-080123-012456, , 2024
66. Plant genome size estimation by flow cytometry: inter-laboratory comparison, Lucretti, S., Obermayer, R., Nardi, L., Greilhuber, J., Meister, A., Doležel, J., Lysák, M. A., 82, 17-26. https://doi. org/10.1093/oxfordjournals. aob. a010312, , 1998
67. Endings in the middle: current knowledge of interstitial telomeric sequences, Yan, J., Lin, K. W., 658, 95–110. https://doi. org/10.1016/j. mrrev.2007.08.006, , 2008
68. Endings in the middle: current knowledge of interstitial telomeric sequences, Lin, K. W., Yan, J, 658(1-2), 95-110. https://doi. org/10.1016/j. mrrev.2007.08.006, , 2007
69. Plant polyploidy: origin, evolution, and its influence on crop domestication, Zhang, K., Cheng, F., Wang, X., 5(6), 231-239. https://doi. org/10.1016/j. hpj.2019.11.003, , 2019
70. Chromosome-specific painting in Cucumis species using bulked oligonucleotides, Thammapichai, P., Weng, Y., Zhang, T., Han, Y., Jiang, J., 200, 771–779. https://doi. org/10.1534/genetics.115.177642, , 2015
71. Comparative analysis of complete chloroplast genomes of 14 Asteraceae species, Wang, X., Sheng, S., Mahai, R., Cao, W., 51, 1094. https://doi. org/10.1007/s11033-024-10030-9, , 2024
72. Development of chloroplast genomic resources for Oryza species discrimination, Zhu, S., Chen, Y. Lv, J. Xu, J., Chen, N., Song, Y., Li, M., 8, 1854. https://doi. org/10.3389/fpls.2017.01854, , 2017
73. Phylogenetic implications of nuclear rRNA IGS variation in Stipa L. (Poaceae), Nowak, A., Sawicki, J., Szczecińska, M., Nobis, M., Krawczyk, K., 7, 11506. https://doi. org/10.1038/S41598- 017-11804-x, , 2017
74. Population genetic structures of Puccinia triticina in five provinces of China, Ma, Y., Liu, B., Gao, L., Liu, T., Chen, W., 156, 1135–1145. https://doi. org/10.1007/S10658-020- 01956-4, , 2020
75. Structure of centromere chromatin: from nucleosome to chromosomal architecture, Schalch, T., Steiner, F. A., Chromosoma, 126(4), 443–455. https://doi. org/10.1007/s00412-016-0620-7, , 2017
76. Telomeres, interstitial telomeric repeat sequences, and chromosomal aberrations, Bianchi, M. S., Bolzán, A. D., 612(3), 189–214. https://doi. org/10.1016/j. mrrev.2005.12.003, , 2006
77. Advances in chromatin and chromosome research: perspectives from multiple fields, Amitai, A., Agbleke, A. A., Chu, L., Hansen, A. S., Chakrabarti, A., Buenrostro, J. D., 79(6), 881-901. https://doi. org/10.1016/j. molcel.2020.07.003, , 2020
78. Engineering homoeologs provide a fine scale for quantitative traits in polyploid, Heo, J., Chougule, K. M., Bang, W. Y., Lee, E. S., Waminal, N. E., Hong, N. T., 21(12), 2458- 2472. https://doi. org/10.1111/pbi.14141, , 2023
79. Reconstructing the genome of the most recent common ancestor of flowering plants, Murat, F., Salse, J., Pont, C., Klopp, C., Armero, A., 49(4), 490–496. https://doi. org/10.1038/ng.3813, , 2017
80. The rDNA loci—intersections of replication, transcription, and repair pathways, Fajkus, J., Goffová, I., 22(3), 1302. https://doi. org/10.3390/ijms22031302, , 2021
81. Chloroplast microsatellites: new tools for studies in plant ecology and evolution, Hollingsworth, P. M., Powell, W., Provan, J., Trends Ecol. Evol., 16(3), 142–147. https://doi. org/10.1016/S0169- 5347(00)02097-8, , 2001
82. Polyspermy in angiosperms: its contribution to polyploid formation and speciation, Okamoto, T., Toda, E., Molecular reproduction and development, 87(3), 374–379. https://doi. org/10.1002/mrd.23295, , 2020
83. Tracing the evolution of the angiosperm genome from the cytogenetic point of view, Kolano, B., Trunova, D., Senderowicz, M., Plants, 11(6), 784. https://doi. org/10.3390/plants11060784, , 2021
84. Transgenerational inheritance of diet-induced genome rearrangements in Drosophila, Aldrich, J. C., Maggert, K. A., 11(4), 1–21. https://doi. org/10.1371/journal. pgen.1005148, , 2015
85. Chloroplast genomes: diversity, evolution, and applications in genetic engineering, Lin, C. S., Yu, M., Daniell, H., Chang, W. J., 17, 134. https://doi. org/10.1186/s13059-016-1004-2, , 2016
86. Editorial: the potential medicinal uses of Cassia tora Linn leaf and seed extracts, Puri, B. K., Rev. Recent. Clin. Trials., 13(1), 3–4 https://doi. org/10.2174/157488711301180131145359, , 2018
87. Whole-genome sequencing and analysis of the chinese herbal plant Panax notoginseng, Zhang, J., Zhu, S., Zhang, G., Kui, L., Wang, X., Chen, W., 10(6), 899–902. https://doi. org/10.1016/j. molp.2017.02.010, , 2017
88. Active components of Solanum nigrum and their antitumor effects: a literature review, Zheng, Q. S., Zhang, H., Lv, J. L., Li, J., 13:1329957. https://doi. org/10.3389/fonc.2023.1329957, , 2023
89. Active components of Solanum nigrum and their antitumor effects: a literature review, Li, J., Zhang, H., 13, 1329957. https://doi. org/10.3389/fonc.2023.1329957, , 2023
90. Diversification of Rosaceae since the late cretaceous based on plastid phylogenomics, Li, R., Zhang, S. D., Yang, Y., 214(3), 1355–1367. https://doi. org/10.1111/nph.14461, , 2017
91. Mechanisms of genomic rearrangements and gene expression changes in plant polyploids, Chen, Z. J., Ni, Z, 28(3), 240–252. https://doi. org/10.1002/bies.20374, , 2006
92. Dual-color FISH karyotype and rDNA distribution analyses on four Cucurbitaceae species, Kim, H. H., Waminal, N. E., 53, 49–56. https://doi. org/10.1007/s13580-012- 0105-4, , 2012
93. Dual-color oligo-FISH can reveal chromosomal variations and evolution in Oryza species, Yu, H., Sun, S., Liu, X., Wu, Y., Gu, S., Zhou, Y., 101(1), 112-121. https://doi. org/10.1111/tpj.14522, , 2019
94. Repetitive sequences in plant nuclear DNA: types, distribution, evolution and function, Mehrotra, S., Goyal, V., 12(4), 164-171. https://doi. org/10.1016/j. gpb.2014.07.003, , 2014
95. Comparison of the complete plastomes and the phylogenetic analysis of Paulownia species, Zhang, B., Lou, G., Cheng, Y., Cai, X., Li, P., Wang, H., 10(1), 1-9. https://doi. org/10.1038/s41598- 020-59204-y, , 2020
96. Interpretation of karyotype evolution should consider chromosome structural constraints, Schubert, I., Lysak, M. A., Trends. Genet, 27, 207–216. https://doi. org/10.1016/j. tig.2011.03.004, , 2011
97. Morpho-cytological studies and DNA barcoding in genus Senna (Fabaceae, Caesalpinoideae), Matthew, J. O., Abraham, O. G., Azeez, S. O., Ikhinmwin, I. V., Babayemi, O. S., 637(2), 165-176. https://doi. org/10.11646/phytotaxa.637.2.4, , 2024
98. Predicted roles of long non-coding RNAs in abiotic stress tolerance responses of plants, Hewadikaram, M., Imaduwage, I., 4, 20. https://doi. org/10.1186/s43897-024-00094-3, , 2024
99. Extrachromosomal circular DNA derived from tandemly repeated genomic sequences in plants, Houben, A., Segal, D., Cohen, S., 53, 1027–1034. https://doi. org/10.1111/j.1365- 313X.2007.03394. x, , 2008
100. Genome-wide characterization and analysis of WRKY transcription factors in Panax ginseng, Han, P., Yin, L., Di, P., Wang, P., Huang, X., Yan, M., 22(1), 834. https://doi. org/10.1186/s12864-021-08145-5, , 2021
101. Holocentric chromosomes: convergent evolution, meiotic adaptations, and genomic analysis, Korf, I. F., Melters, D. P., Chan, S. W., Paliulis, L. V., 20(5), 579–593. https://doi. org/10.1007/s10577-012-9292-1, , 2012
102. Repeatless and repeat-based centromeres in potato: implications for centromere evolution, Gong, Z., Torres, G. A., Wang, K., Wu, Y., Iovene, M., Koblížková, A., Neumann, P., 24(9), 3559-3574. https://doi. org/10.1105/tpc.112.100511, , 2012
103. Comparative and phylogenetic analyses of nine complete chloroplast genomes of Orchidaceae, Liu, L., Xu, J., Zhang, Q., 13(1), 1–16. https://doi. org/10.1038/s41598-023-48043-2, , 2023
104. Construction of a BAC library of Korean ginseng and initial analysis of BAC-end sequences, Park, Y. S., Lee, S. J., Hong, C. P., Park, J. Y., Lee, Y. K., Plaha, P., 271(6), 709–716. https://doi. org/10.1007/s00438-004-1021-9, , 2004
105. Fluorescence in situ hybridization in plants: recent developments and future applications, Jiang, J., 27(3), 153-165. https://doi. org/10.1007/s10577-019-09607-z, , 2019
106. The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation, Maffre, C., Robert, T., Brun, C., Guichard, V., Crimi, B., Bourbon, M., Nore, A., Science 351, 943-949. https://doi. org/aad5309, , 2016
107. The ups and downs of genome size evolution in polyploid species of Nicotiana (Solanaceae), Leitch, I. J., Kovarik, A., Leitch, A. R., Hanson, L., Chase, M. W., Clarkson, J. J., Lim, K. Y., 101(6), 805. https://doi. org/10.1093/aob/mcm326, , 2008
108. The comparison of RFLP, RAPD, AFLP and SSR (microsatellite) markers for germplasm analysis, Powell, W., Morgante, M., Vogel, J., Tingey, S. V., Rafalski, A. J., Andre, C., Hanafey, M. K., 2, 225–238. https://doi. org/10.1007/BF00564200, , 1996
109. Fluorescence in situ hybridization: cell-based genetic diagnostic and research applications, Shu, W., Cui, C., Li, P., 4, 89. https://doi. org/10.3389/fcell.2016.00089, , 2016
110. Saponins in the genus Panax L. (Araliaceae): a systematic review of their chemical diversity, Guo, D. A., Wu, W. Y., Ye, M., Yang, W. Z., Hu, Y., 106, 7–24. https://doi. org/10.1016/j. phytochem.2014.07.012, , 2014
111. A complex resistance locus in Solanum americanum recognizes a conserved Phytophthora effector, Steuernagel, B., Lin, X., Karki, H. S., Witek, A. I., Jupe, F., Witek, K., 7(2), 198-208. https://doi. org/10.1038/s41477-021-00854-9, , 2021
112. A cost-effective oligo-based barcode system for chromosome identification in longan and lychee, Wei, Y., Wang, B., Li, Y., Akbar, S., Zhuang, G., Yu, Z., Qi, Y., https://doi. org/10.1093/hr/uhae278, , 2024
113. De novo transcriptome sequence of Senna tora provides insights into anthraquinone biosynthesis, Han, S. R., Lee, C. M., Won, S. Y., Kang, S. H., Sim, J. S., Lee, W. H., al 15, e0225564. https://doi. org/10.1371/journal. pone.0225564, , 2020
114. Solanum nigrum Linn.: advances in anticancer activity and mechanism in digestive system tumors, Li, W., Sun, X., Pei, H., Yang, J., Xu, Y., Luo, X., 40(11), 311. https://doi. org/10.1007/s12032-023-02167-7, , 2023
115. MAFFT multiple sequence alignment software version 7: improvements in performance and usability, Katoh, K., Standley, D. M., 30(4), 772–780. https://doi. org/10.1093/molbev/mst010, , 2013
116. Silent sites in Drosophila genes are not neutral: evidence of selection among synonymous codons, Higgins, D. G., Wright, F., Shields, D. C., Sharp, P. M., 5(6), 704–716. https://doi. org/10.1093/oxfordjournals. molbev. a040525, , 1988
117. The evolution of the plastid chromosome in land plants: gene content, gene order, gene function, Müller, K. F., Schneeweiss, G. M., Wicke, S., dePamphilis, C. W., Quandt, D., 76(3-5), 273–297. https://doi. org/10.1007/s11103-011-9762-4, , 2011
118. An extraordinarily stable karyotype of the woody Populus species revealed by chromosome painting, Xi, M., Wu Y, Zhang, T., Xin, H., Zhang, W., Zhang, P., 101(2), 253–64, , 2020
119. Antioxidant activities of Solanum nigrum L. leaf extracts determined in in vitro cellular models, Santagati, N. A., Raciti, G., Rizzo, M., Campisi, A., Duro, A., Acquaviva, R., Foods, 8(2), 63. https://doi. org/10.3390/foods8020063, , 2019
120. Interstitial telomeric repeats are enriched in the centromeres of chromosomes in Solanum species, He, L., Torres, G. A., Liu, J., Xie, C., Jiang, J., Zhang, H., 21, 5–13. https://doi. org/10.1007/s10577-012-9332-x, , 2013
121. Sequence organization of the repeating units in the nucleus of wheat which contain 5S rRNA genes, Gerlach, W. L., Dyer, T. A., 8(21), 4851-4865. https://doi. org/10.1093/nar/8.21.4851, , 1980
122. Comparative and phylogenetic analysis of complete chloroplast genomes from five Artemisia species, Ren, Y., Zhao, M., Lan, T., 13, 1049209. https://doi. org/10.3389/fpls.2022.1049209, , 2022
123. Distribution of 45S rDNA sites in chromosomes of plants: structural and evolutionary implications, Roa, F., Guerra, M., 12, 225. https://doi. org/10.1186/1471-2148-12-225, , 2012
124. Senna (Cassia Angustifolia Vahl.): a comprehensive review of ethnopharmacology and phytochemistry, Rabadiya, K., Reddy, N. R. R., Thaker, K., Patoliya, J., Joshi, R., 1, 100003. https://doi. org/10.1016/j. prenap, , 2023
125. Molecular cytogenetic mapping of Cucumis sativus and C. melo using highly repetitive DNA sequences, Choi, D., Bang, J.-W., Nam, Y.-W., Koo, D.-H., De Jong, H., Hur, Y., 18, 325– 336. https://doi. org/10.1007/s10577-010-9116-0, , 2010
126. An assessment of karyotype restructuring in the neoallotetraploid Tragopogon miscellus (Asteraceae), Soltis, P. S., Gallagher, J. P., Chester, M., Soltis, D. E., Lipman, M. J., 21, 75– 852013 https://doi. org/10.1007/s10577-013-9339-y, , 2013
127. Current status and the future of fluorescence in situ hybridization (FISH) in plant genome research, Gill, B. S., Jiang, J., 49(9), 1057–1068. https://doi. org/10.1139/g06-076, , 2006
128. Combining FISH and model-based predictions to understand chromosome evolution in Typhonium (Araceae), Cusimano, N., Sousa, A., Renner, S. S., 113(4), 669–680. https://doi. org/10.1093/aob/mct302, , 2014
129. Comparative triple-color FISH mapping in eleven Senna species using rDNA and telomeric repeat probes, Campomayor, N. B., Ta, T. D., Pellerin, R. J., Waminal, N. E., Lee, D. S., Nguyen, T. H., Hortic. Environ. Biotechnol., 62, 927–935. https://doi. org/10.1007/S13580-021-00364-9, , 2021
130. Intra- and interspecific karyotypic variations of the genus Senna Mill. (Fabaceae, Caesalpinioideae), Felix, L. P., Cordeiro, J. M. P., 32(1), 128–134. https://doi. org/10.1590/0102- 33062017abb0274, , 2017
131. Widespread paleopolyploidy in model plant species inferred from age distributions of duplicate genes, Blanc, G., Wolfe, K. H., 16(7), 1667–1678. https://doi. org/10.1105/tpc.021345, , 2004
132. A refined Panax ginseng karyotype based on an ultra-high copy 167-bp tandem repeat and ribosomal DNAs, Jang, W., Park, J. Y., Waminal, N. E., Lee, J., Choi, H. I., Kim, N. H., 41(4), 469-476. https://doi. org/10.1016/j. jgr.2016.08.002, , 2017
133. Comparative chloroplast genomes of Argentina species: genome evolution and phylogenomic implications., Zhang, Z., Wen, J., Li, Q., 15, 1349358. https://doi. org/10.3389/fpls.2024.1349358, , 2024
134. Oligonucleotide fluorescence in situ hybridization: an efficient chromosome painting method in plants, Liu, H., Fang, Z., Song, S., Chen, C., Wen, X., Asghar, S., Harun, A., Plants 12(15), 2816. https://doi. org/10.3390/plants12152816, , 2022
135. Cladogenetic and anagenetic models of chromosome number evolution: a Bayesian model averaging approach, Freyman, W. A., Höhna, S., 67(2), 195-215. https://doi. org/10.1093/sysbio/syx065, , 2018
136. Complete chloroplast genomes provide insights into evolution and phylogeny of Zingiber (Zingiberaceae), Dong, S., Li, J., Cai, X., Liu, Y., Li, H. L., Xing, H., Xia, M., Jiang, D., Gong, M., Tian, S., Lin, J., 24(1), 30. doi:10.1186/s12864-023-09115-9, , 2023
137. FISH mapping for physical map improvement in the large genome of barley: a case study on chromosome 2H, Schmutzer, T., Ma, L., Poursarebani, N., Houben, A., Stein, N., Cytogenet Genome Res., 143(4), 275–279. https://doi. org/10.1159/000366028, , 2014
138. Plastid phylogenomics uncovers multiple species in Medicago truncatula (Fabaceae) germplasm accessions, Ruhlman, T. A., Wojciechowski, M. F., Jansen, R. K., Hopkins, A., Choi, I. S., Steele, K. P., 12(1), 1–10. https://doi. org/10.1038/s41598-022-25381-1, , 2022
139. Whole-chromosome paints in maize reveal rearrangements, nuclear domains, and chromosomal relationships, Rouillard, J. M., Kao, Y. H., Wang, C. R., Semrau, K., Zhang, T., Albert, P. S., 116, 1679–1685. https://doi. org/10.1073/pnas.1813957116, , 2019
140. Allopolyploid origin of Chenopodium album s. str. (Chenopodiaceae): a molecular and cytogenetic insight, Richter, S., Krak, K., Vasut, R. J., 11(8), e0161063. https://doi. org/10.1371/journal. pone.0161063, , 2016
141. Chromosomal evolution and evolutionary relationships of Lebiasina species (Characiformes, Lebiasinidae), Bertollo, L. A. C., Oliveira, E. A., Hatanaka, T., Nirchio, M., Marinho, M. M. F., Sassi, F. M. C., 20(12), 2944. https://doi. org/10.3390/ijms20122944, , 2019
142. Personal perspectives on plant ribosomal RNA genes research: from precursor-rRNA to molecular evolution, Kovarik, A., Volkov, R. A., Grierson, D., Borisjuk, N., Hemleben, V., 12, 797348. https://doi. org/10.3389/fpls.2021.797348, , 2021
143. Extraction of high-quality genomic DNA from different plant orders applying a modified CTAB-based method, Oraby, H. AS., Aboul-Maaty, N. AF., 43, 25. https://doi. org/10.1186/s42269-019-0066-1, , 2019
144. Extraordinarily conserved chromosomal synteny of Citrus species revealed by chromosome-specific painting, He, L., Yang, Z., Zhao, H., He, J., Chen, K., Guan, B., 103(6):2225–35. https://doi. org/10.1111/tpj.14894, , 2020
145. Reconstruction of karyotypic evolution in Saccharum spontaneum species by comparative oligo-FISH mapping, Li, H., Shen, H., Li, R., Xie, Q., Wang, F., Meng, Z., 22, 599. https://doi. org/10.1186/s12870-022-04008-7, , 2022
146. Ribosomal DNA deletions modulate genome-wide gene expression: rDNA-sensitive genes and natural variation, Paredes, S., Branco, A. T., Lemos, B., Maggert, K. A., Hartl, D. L., 7(4), 1– 10. https://doi. org/10.1371/journal. pgen.1001376, , 2011
147. Comparative chromosomal localization of 45S and 5S rDNA sites in 76 purple-fleshed sweet potato cultivars, Zhang, L., Gao, R., Sun, J., Chen, L., Han, Y., Su, D., Li, Z., Li, Q., Plants 9(7), 865. https://doi. org/10.3390/plants9070865, , 2020
148. Comparative chromosomal localization of 45S and 5S rDNAs and implications for genome evolution in Cucumis, Wang, Y. Z., Zhang, Z. T., Zhang, Y. X., Li, Z. A., Yang, S. Q., Cheng, C. Y., Genome, 59(7), 449–457. https://doi. org/10.1139/gen-2015-0207, , 2016
149. Taxonomic importance of the palynological features of some members of family Leguminosae-Caesalpinioideae, Bernard, T. T., Arogundade, O. O., Fatunmise, A. J., 21(3), 27–36. https://doi. org/10.4314/ijs. v21i3.3, , 2019
150. Chromosome fission associated with growth of ribosomal DNA in Neodiprion abietis (Hymenoptera: Diprionidae), Auger-Rozenberg, M. A., Lemeunier, F., Parker, J. S., Monti, L., Rousselet, J., 267(1455), 1819–1823. https://doi. org/10.1098/rspb.2000.1216, , 2000
151. Pre-labelled oligo probe-FISH karyotype analyses of four Araliaceae species using rDNA and telomeric repeat, Pellerin, R. J., Kim, H. H., Zhou, H. C., Yang, T. J., Waminal, N. E., 41(7), 839–847. https://doi. org/10.1007/s13258-019-00786-x, , 2019
152. Unraveling the sequence dynamics of the formation of genus-specific satellite DNAs in the family Solanaceae, Choi, D., Jo, S. H., Hur, C. G., Park, H. M., Kim, S. M., Kim, H. H., 106, 876–885. https://doi. org/10.1038/hdy.2010.131, , 2011
153. Chromoanasynthesis: another way for the formation of complex chromosomal abnormalities in human reproduction, Pellestor, F., Gatinois, V., 33, 1381–1387. https://doi. org/10.1093/humrep/dey231, , 2018
154. Complete chloroplast genomes of 14 subspecies of D. glomerata: Phylogenetic and comparative genomic analyses, Feng, G., Nie, G., Huang, L., Peng, Y., Li, Z., Jiao, Y., 13(9), 1621. https://doi. org/10.3390/genes13091621, , 2022
155. Origin and evolution of diploid and allopolyploid Camelina genomes were accompanied by chromosome shattering, Pouch, M., Mandáková, T., Lysak, M. A., Al-Shehbaz, I. A., Brock, J. R., 31(11), 2596–2612. https://doi. org/10.1105/tpc.19.00366, , 2019
156. Cytogenetics and cytotaxonomy of Brazilian species of Senna Mill. (Cassieae–Caesalpinioideae–Leguminosae), Elaine, B., De Castro, B, Miotto, S. T., Schifino-Wittmann, M. T., 58(2), 152– 163. https://doi. org/10.1080/00087114.2005.10589445, , 2005
157. Characterization of the chloroplast genome sequence of Acer miaotaiense: comparative and phylogenetic analyses, Chen, H., Xu, Y., Xi, L., Yang, J., Zhao, J., Zhang, J., Molecules 23(7), 1740. https://doi. org/10.3390/molecules23071740, , 2018
158. Chromosomal locations of 5S and 45S rDNA in Gossypium genus and its phylogenetic implications revealed by FISH, Wang, C., Gan, Y., Liu, F., Qin, Q., Chen, D., Wu, Q., 8(6), e68207. https://doi. org/10.1371/journal. pone.0068207, , 2013
159. Comparative FISH analysis of Senna tora tandem repeats revealed insights into the chromosome dynamics in Senna, Nguyen, T. H., Kim, H. H., Ta, T. D., Waminal, N. E., Pellerin, R. J., 43, 237–249. https://doi. org/10.1007/s13258-021-01051-w, , 2021
160. Decoding the role of satellite DNA in genome architecture and plasticity - an evolutionary and clinical affair, Lopes, M., Ferreira, D., Escudeiro, A., Louzada, S., Gama-Carvalho, M., Adega, F., Genes, 11, 72. https://doi. org/10.3390/genes11010072, , 2020
161. Fluorescent in situ hybridization using oligonucleotide-based probes Nielseneds In Situ Hybridization Protocols, In B. S., Braz, G. T., do Vale Martins, L., Yu, F., Jones J., Jiang, J., Methods in Molecular Biology, vol 2148. Humana, New York, NY. https://doi. org/10.1007/978-1- 0716-0623-0_4, , 2020
162. Chloroplast phylogenomic data support Eocene amphi-Pacific early radiation for the Asian Palmate core Araliaceae, Valcárcel, V., Wen, J., 57(6), 547-560. https://doi. org/10.1111/jse.12522, , 2019
163. Karyotype analysis of Panax ginseng C. A. Meyer, 1843 (Araliaceae) based on rDNA loci and DAPI band distribution, Park, H. M., Kim, H. H., Waminal, N. E.,, Ryu, K. B.,, Kim, J. H.,, Yang, T. J.,, 6(4), 425–441. https://doi. org/10.3897/CompCytogen. v6i4.3740, , 2012
164. Relative rates of synonymous substitutions in the mitochondrial, chloroplast, and nuclear genomes of seed plants, Daoud, H., Drouin, G., Xia, J., 49(3), 827–831. https://doi. org/10.1016/j. ympev.2008.09.009, , 2008
165. An efficient oligo-FISH painting system for revealing chromosome rearrangements and polyploidization in Triticeae, Wang, H., Zhang, T., Yang, Z., Li, G., Yu, Z., Yang, E., 105(4), 978-993. https://doi. org/10.1111/tpj.15081, , 2021
166. Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution, Melters, D. P., Bradnam, K. R., May, M. R., Young, H. A., Telis, N., Ruby, J. G., 14, R10. https://doi. org/10.1186/gb-2013-14-1-r10, , 2013
167. Comparative insights into the antimicrobial, antioxidant, and nutritional potential of the Solanum nigrum complex, Dera, A. A., Mohyuddin, A., Khan, Z., Javed, M., Kurniawan, T. A., Nadeem, S., Processes, 10(8):1455. https://doi. org/10.3390/PR10081455, , 2022
168. The genus Senna (Fabaceae): a review on its traditional uses, botany, phytochemistry, pharmacology and toxicology, Adelowo, F. E., Oladeji, O. S., Oluyori, A. P., 138, 1–32. https://doi. org/10.1016/j. sajb.2020.11.017, , 2021
169. An update of the angiosperm phylogeny group classification for the orders and families of flowering plants: APG IV, Byng, J. W., Soltis, D. E., Judd, W. S., Fay, M. F., Christenhusz, M. J. M., Chase, M. W., 181, 1-20. https://doi. org/10.1046/j.1095-8339.2003. t01-1-00158. x, , 2016
170. Interstitial telomeric-like repeats (ITR) in seed plants as assessed by molecular cytogenetic techniques: a review, Rosselló, J. A., Maravilla, A. J., Rosato, M., Plants, 10(11), 2541. https://doi. org/10.3390/plants10112541, , 2021
171. Solanum americanum genome-assisted discovery of immune receptors that detect potato late blight pathogen effectors, Olave-Achury, A., Sindalovskaya, M., Jia, Y., Lin, X., Heal, R., Prokchorchik, M., et al 55, 1579–1588. https://doi. org/10.1038/s41588-023-01486-9, , 2023
172. TAREAN: a computational tool for identification and characterization of satellite DNA from unassembled short reads, Neumann, P., Macas, J., Koblizková, A., Vrbová, I., Robledillo, L. A., Novák, P., 45, e111. https://doi. org/10.1093/nar/gkx257, , 2017
173. TAREAN: a computational tool for identification and characterization of satellite DNA from unassembled short reads, Robledillo, L.Á., Vrbová, I., Neumann, P., Koblížková, A., Novák, P., Macas, J., 45(12), e111. https://doi. org/10.1093/nar/gkx257, , 2017
174. The genus Senna (Fabaceae): a review on its traditional uses, botany, phytochemistry, pharmacology, and toxicology, Bankole, D. T., Sanni, D. M., Oladeji, O. S., 138, 1–32. https://doi. org/10.1016/j. sajb.2020.11.017, , 2021
175. Ancestral grass karyotype reconstruction unravels new mechanisms of genome shuffling as a source of plant evolution, Abrouk, M., Tannier, E., Guilhot, N., Murat, F., Xu, J. H., 20, 1545–1557. https://doi. org/10.1101/gr.109744.110, , 2010
176. Quantum speciation in Aegilops: molecular cytogenetic evidence from rDNA cluster variability in natural populations, Belyayev A., Nevo E., Raskina O., 101(41), 14818-23. doi: 10.1073/pnas.0405817101, , 2004
177. The dynamic interplay between ribosomal DNA and transposable elements: a perspective from genomics and cytogenetics, Mann, L., Schmidt, N., Pascual-Díaz, J. P., Garcia, S., Maiwald, S., Kovarik, A., 41(3), msae025. https://doi. org/10.1093/molbev/msae025, , 2024
178. Comparative oligo-FISH mapping: an efficient and powerful methodology to reveal karyotypic and chromosomal evolution, Braz, G. T., Zhang, T., Rouillard, J. M., He, L., Zhao, H., Semrau, K., 208(2), 513–523. https://doi. org/10.1534/genetics.117.300344, , 2018
179. Comparative oligo-FISH mapping: an efficient and powerful methodology to reveal karyotypic and chromosomal evolution, Semrau, K., Rouillard, J. M., Braz, G. T., He, L., Zhao, H. N., Zhang, T., Genetics, 208, 513–523. https://doi. org/10.1534/genetics.117.300344, , 2018
180. Interstitial telomeric sites and Robertsonian translocations in species of Ipheion and Nothoscordum (Amaryllidaceae), Guerra, M., Souza, G., Crosa, O., Vanzela, A. L. L., 144, 157–166. https://doi. org/10.1007/s10709-016-9886-1, , 2016
181. Ribosomal DNA stability is supported by many ‘buffer genes’— introduction to the yeast rDNA stability database, Sasaki, M., Kobayashi, T., 17, 1–8. https://doi. org/10.1093/femsyr/fox001, , 2017
182. Increasing phylogenetic resolution at low taxonomic levels using massively parallel sequencing of chloroplast genomes, Cronn, R., Parks, M., Liston, A., 7, 84. https://doi. org/10.1186/1741- 7007-7-84, , 2009
183. Inter- and intraspecific hypervariability in interstitial telomeric-like repeats (TTTAGGG)n in Anacyclus (Asteraceae), Feliner, G. N., Álvarez, I., Rosato, M., Rosselló, J. A., 122, 387–395. https://doi. org/10.1093/aob/mcy079, , 2018
184. Rapid amplification of four retrotransposon families promoted speciation and genome size expansion in the genus Panax, Perumal, S., Waminal, N. E., Lee, S. C., Choi, H. I., Nguyen, V. B., Lee, J., 7(1), 9045. https://doi. org/10.1038/s41598-017-08194-5, , 2017
185. Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau, Chen, S., Zhang, F., Chi, X., Cao, Q., Ma, X., Xing, R., Gao, Q., 22(1), 195. https://doi. org/10.1186/s12870-022-03577-x, , 2022
186. Robust, versatile DNA FISH probes for chromosome-specific repeats in Caenorhabditis elegans and Pristionchus pacificus, Adilardi, R. S., Dernburg, A. F., G3: Genes Genomes Genet. 12(7). https://doi. org/10.1093/g3journal/jkac121, , 2022
187. The comparisons of expression pattern reveal molecular regulation of fruit metabolites in S. nigrum and S. lycopersicum, Heo, J., Park, S., Jeong, J. C., Choi, S., Bang, W. Y., Lee, J. M., 12(1), 1-15. https://doi. org/10.1038/s41598-022-09032-z, , 2022
188. Thirteen Camellia chloroplast genome sequences determined by high-throughput sequencing: genome structure and phylogeny, Huang, H., Mao, S. Y., Gao, L. Z., Liu, Y., Shi, C., 10(6), 1347–1362. https://doi. org/10.1007/s11295-014-0778-6, , 2014
189. Chromosomal mapping of tandem repeats revealed massive chromosomal rearrangements and insights into Senna tora dysploidy, Kim, H. H., Waminal, N. E., Kang, S. H., Pellerin, R. J., 12, 629898. https://doi. org/10.3389/fpls.2021.629898, , 2021
190. Chromosomal mapping of tandem repeats revealed massive chromosomal rearrangements and insights into Senna tora dysploidy, Pellerin, R. J., Waminal, N. E., Kim, H. H., Kang, S., 12, 629898. https://doi. org/10.3389/fpls.2021.629898, , 2021
191. Telomere-centric genome repatterning determines recurring chromosome number reductions during the evolution of eukaryotes, Wang, X., Wang, Z., Wang, L., Jin, D., Guo, H., Zhang, L., New Phytol., 205, 378–389. https://doi. org/10.1111/nph.12985, , 2015
192. Agro-morphological, microanatomical and molecular cytogenetic characterization of the medicinal plant Chelidonium majus L., Konyaeva, E. A., Zoshchuk, S. A., Morozov, A. I., Hazieva, F. M., Yurkevich, O. Y., Samatadze, T. E., 9(10), 1396. https://doi. org/10.3390/plants9101396, , 2020
193. Insights into chloroplast genome structure and phylogenetic relationships within the Sesamum species complex (Pedaliaceae), Ahanhanzo, C., Azokpota, P., Zoclanclounon, Y. A., 14, 1207306. https://doi. org/10.3389/fgene.2023.1207306, , 2023
194. The origin, evolution and proposed stabilization of the terms 'genome size' and 'C-value' to describe nuclear DNA contents, Dolezel, J., Greilhuber, J., Lysák, M. A., Bennett, M. D., 95(1), 255–260. https://doi. org/10.1093/aob/mci019, , 2005
195. Major repeat components covering one-third of the ginseng (Panax ginseng C. A. Meyer) genome and evidence for allotetraploidy, Kim, N. H., Park, M., Park, H. M., Choi, B. S., Choi, H. I., Waminal, N. E., 77(6), 906–916. https://doi. org/10.1111/tpj.12441, , 2014
196. Revisiting the ethnomedicinal, ethnopharmacological, phytoconstituents and phytoremediation of the plant Solanum viarum Dunal, Das, P. P., Kumar, A, Thakur, M., Kumar, D., Verma, R., Dhalaria, R., 397 5513–5531. https://doi. org/10.1007/s00210-024- 03034-6, , 2024
197. The plant DNA C-values database (release 7.1): an updated online repository of plant genome size data for comparative studies, Pellicer, J., Leitch, I. J., 226(2), 301-305. https://doi. org/10.1111/nph.16261, , 2020
198. Panax ginseng and its ginsenosides: Potential candidates for the prevention and treatment of chemotherapy-induced side effects, Chen, L., Wang, J., Wan, Y., Tan, Y., Tang, F., Xu, J., 45(6), 617-630. https://doi. org/10.1016/j. jgr.2021.03.001, , 2021
199. Large-scale patterns of diversification in the widespread legume genus Senna and the evolutionary role of extrafloral nectaries, Michael, T., Marazzi, S., 64(12), 3570–3592. https://doi. org/10.1111/j.1558-5646.2010.01086. x, , 2010
200. Regulation of ribosomal RNA gene copy number and its role in modulating genome integrity and evolutionary adaptability in yeast, Kobayashi, T., 68, 1395–1403. https://doi. org/10.1007/s00018-010-0613-2, , 2011
201. Solanum fruits: phytochemicals, bioaccessibility and bioavailability, and their relationship with their health-promoting effects, Contreras-Angulo, L. A., Montoya-Inzunza, L. A., Elizalde-Romero, C. A., Heredia, J. B., Gutiérrez-Grijalva, E. P., 8, 790582. https://doi. org/10.3389/fnut.2021.790582, , 2021
202. Comparative triple-color FISH mapping and genome size advances understanding of the cytogenetic diversity in wild Solanum species, Nguyen, T. H., Kang, B. Y., Park, S. J., 64, 811–817. https://doi. org/10.1007/s13580-023-00522-1, , 2023
203. Comparative triple-color FISH mapping and genome size advances understanding of the cytogenetic diversity in wild Solanum species, Kang, B. Y., Nguyen, H. T., Kim H. H., Park, S. J., 64, 811–817. https://doi. org/10.1007/s13580-023-00522-1, , 2023
204. Ginsenoside Rg1 reduces cardiac inflammation against myocardial ischemia/reperfusion injury by inhibiting macrophage polarization, Zhang, M., Mao, C., Pei, K., Zhong, X., Wu, Q., Xu, X., 48(6), 570-580. https://doi. org/10.1016/j. jgr.2024.07.003, , 2024
205. Inferring the evolutionary mechanism of the chloroplast genome size by comparing whole-chloroplast genome sequences in seed plants, Ge, S., Zheng, X. M., 7(1), 1–10. https://doi. org/10.1038/s41598-017-01518-5, , 2017
206. Thousands of high-quality sequencing samples fail to show meaningful correlation between 5S and 45S ribosomal DNA arrays in humans, Hall, A. N., Turner, T. N., Queitsch, C., 11, 449. https://doi. org/10.1038/s41598-020-80049-y, , 2021
207. The complete chloroplast genome sequencing analysis revealed an unusual IRs reduction in three species of subfamily Zygophylloideae, Zhang, L., Li, R., Wang, X., 17(2), e0263253. https://doi. org/10.1371/journal. pone.0263253, , 2022
208. Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns, Cai, Z., Raubeson, L. A., Daniell, H., Leebens-Mack, J., Jansen, R. K., Depamphilis, C. W., 104(49), 19369–19374. https://doi. org/10.1073/pnas.0709121104, , 2007
209. Niche conservatism, divergence and polyploidy in Senna series Aphyllae (Fabaceae: Caesalpinioideae) from arid zones of South America, Fortunato, R. H., Moro Cordobés, F., Anton, A. M., Urdampilleta, J. D., Robbiati, F. O., 199(4), 773-789. https://doi. org/10.1093/botlinnean/boab105, , 2022
210. Chromosomal dynamics in Senna: comparative PLOP–FISH analysis of tandem repeats and flow cytometric nuclear genome size estimations, Kang, B. Y., Nguyen, T. H., Kim, H. H., 14, 1288220. https://doi. org/10.3389/fpls.2023.1288220, , 2023
211. The first complete chloroplast genome sequences of Ulmus species by de novo sequencing: Genome comparative and taxonomic position analysis, Zuo, H., Yang, Y., Dong, C., 12(2), e0171264. https://doi. org/10.1371/journal. pone.0171264, , 2017
212. Chloroplast genome analysis of resurrection tertiary relict Haberlea rhodopensis highlights genes important for desiccation stress response, Apostolova, E., Daskalova, E., Ivanova, Z., Sablok, G., Zahmanova, G., Yahubyan, G., 8, 204. https://doi. org/10.3389/fpls.2017.00204, , 2017
213. Chromosome painting facilitates anchoring reference genome sequence to chromosomes in situ and integrated karyotyping in Banana (Musa Spp.), Němečková, A., Swennen, R., Doležel, J., Uwimana, B., Hřibová, E., Karafiátová, M., Šimoníková, D., 10, 1503. https://doi. org/10.3389/fpls.2019.01503, , 2019
214. Chromosome-level genome assemblies of four wild peach species provide insights into genome evolution and genetic basis of stress resistance, Peng, Z., Li, Y., Cao, K., Zhao, X., Liu, K., Arus, P., 20, 139. https://doi. org/10.1186/s12915-022-01342-y, , 2022
215. Evolutionary relationship of Panax ginseng and P. quinquefolius inferred from sequencing and comparative analysis of expressed sequence tags, Choi, H. I., Kim, K. D., Choi, B. S., Lee, J., Park, J. Y., Kim, N. H., 60, 1377–1387. https://doi. org/10.1007/s10722-012-9926-3, , 2013
216. A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny: the Legume phylogeny working group (LPWG), Azani, N., Babineau, M., Pinto, R. B., Barbosa, A. R., Bailey, C. D., Banks, H., 66, 44–77. https://doi. org/10.12705/661.3, , 2017
217. Analysis of the giant genomes of Fritillaria (Liliaceae) indicates that a lack of DNA removal characterizes extreme expansions in genome size, Kelly, L. J., Renny-Byfield, S., Novák, P., Pellicer, J., Neumann, P., Macas, J., 208(2), 596-607. https://doi. org/10.1111/nph.13471, , 2015
218. Haplotype-resolved genome assembly and resequencing analysis provide insights into genome evolution and allelic imbalance in Pinus densiflora, Cho, H. J., Bae, E., Jung, S., Jang, M., Park, Y., Lee, H., 56(11), 2551-2561. https://doi. org/10.1038/s41588-024-01944-y, , 2024
219. Quantitative karyotyping of three diploid Brassica species by imaging methods and localization of 45S rDNA loci on the identified chromosomes, Fukui, K., Nakayama, S., Yoshiaki, H., Ohmido, N., Yamabe, M., 96, 325-30. https://doi. org/10.1007/s001220050744, , 1998
220. Structural variation and dynamics of the nuclear ribosomal intergenic spacer region in key members of the Gibberella fujikuroi species complex, González-Jaén, M. T., Jurado, M., Vázquez, C., Patiño, B., Mirete, S., Genome, 56(4), 205–213. https://doi. org/10.1139/gen-2013-0008, , 2013
221. Nuclear and chloroplast DNA variation provides insights into population structure and multiple origin of native aromatic rices of Odisha, India, Jena, S., Samal, R., Patnaik, S. S. C., Patnaik, A., Roy, P. S., Rao, G. J., 11(9), e0162268. https://doi. org/10.1371/journal. pone.0162268, , 2016
222. Satellite DNA in Vicia faba is characterized by remarkable diversity in its sequence composition, association with centromeres, and replication timing, Koblížková, A., Macas, J., Schubert, I., Böttinger, K., Vrbová, I., Neumann, P., Ávila Robledillo, L., Novák, P., 8(1), 1-11. https://doi. org/10.1038/s41598-018-24196-3, , 2018
223. At the beginning of the end and in the middle of the beginning: structure and maintenance of telomeric DNA repeats and interstitial telomeric sequences, Mirkin, S. M., Aksenova, A. Y., 10(2), 118. https://doi. org/10.3390/genes10020118, , 2019
224. Ethnopharmacological, phytochemical, pharmacological, and toxicological review on Senna auriculata (L.) Roxb.: A special insight to antidiabetic property, Nille, G. C., Mishra, S. K., Chaudhary, A. K., 12, 647887. https://doi. org/10.3389/fphar.2021.647887, , 2021
225. Repetitive DNA restructuring across multiple Nicotiana allopolyploidisation events shows a lack of strong cytoplasmic bias in influencing repeat turnover, Guignard, M. S., Dodsworth, S., Leitch, A. R., Struebig, M., Chase, M. W., Pérez-Escobar, O. A., Genes, 11(2), 216. https://doi. org/10.3390/genes11020216, , 2020
226. Insight into the chromosome structure of the cultivated tetraploid alfalfa (Medicago sativa subsp. sativa L.) by a combined use of GISH and FISH techniques, Falistocco, E., Plants, 9(4), 542. https://doi. org/10.3390/plants9040542, , 2020
227. Genome-wide association analysis and pathway enrichment provide insights into the genetic basis of photosynthetic responses to drought stress in Persian walnut, Sohrabi, S. S., Brown, P. J., Aliniaeifard, S., Abdollahi-Arpanahi, R., Askari, H., Arab, M. M., 9, 124. https://doi. org/10.1093/hr/uhac124, , 2022
228. Tracking the evolutionary trends among small-size fishes of the genus Pyrrhulina (Characiforme, Lebiasinidae): new insights from a molecular cytogenetic perspective, Bertollo, L. A., Viana, P. F., Marinho, M. M., Feldberg, E., de Moraes, R. L., Sassi, F. D., Front. Genet., 12, 769984. https://doi. org/10.3389/fgene.2021.769984, , 2021
229. The complete chloroplast genome of 17 individuals of pest species Jacobaea vulgaris: SNPs, microsatellites and barcoding markers for population and phylogenetic studies, Doorduin, L., Ariyurek, Y., Lammers, Y., Gravendeel, B., Vrieling, K., Chin-A-Woeng, T., 18(2), 93–105. https://doi. org/10.1093/dnares/dsr002, , 2011
230. Comparative analyses of chloroplast genomes from 13 Lagerstroemia (Lythraceae) species: identification of highly divergent regions and inference of phylogenetic relationships, Wu, Z., Chen, K., Gu, C., Ma, L., Wei, L., Zheng, G., 102, 659–676. https://doi. org/10.1007/s11103-020- 00972-6, , 2020
231. Comprehensive comparative analysis of chloroplast genomes from seven Panax species and development of an authentication system based on species-unique single nucleotide polymorphism markers, Park, H. S., Linh Giang, V. N., Jang, W., Nguyen, V. B., Kim, N. H., Waminal, N. E., , 2020
232. Exploring the medicinal potential of Senna siamea roots: an integrated study of antibacterial and antioxidant activities, phytochemical analysis, ADMET profiling, and molecular docking insights, Endale, M., Hunsen, M., Gebrehiwot, H., Ensermu, U., Dekebo, A., 67(1), 1–22. https://doi. org/10.1186/s13765-024-00899-2, , 2024