Chromosomal abnormalities and copy number variations in children with idiopathic mental illness by O. S. Kurinnaia, I. Y. Iourov, S. G. Vorsanova

Subjects: “…chromosomal abnormalities, copy number variations, mental illness, molecular karyotyping…”
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Insight into the Mechanisms and Clinical Relevance of Antifungal Heteroresistance by Yanyu Su, Yi Li, Qiaolian Yi, Yingchun Xu, Tianshu Sun, Yingxing Li

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Genome Architecture and Its Roles in Human Copy Number Variation by Lu Chen, Weichen Zhou, Ling Zhang, Feng Zhang

Subjects: “…DNA copy number variations…”
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Genome-Wide Scan for Copy Number Variations in Chinese Merino Sheep Based on Ovine High-Density 600K SNP Arrays by Yuezhen Tian, Jing An, Xinning Zhang, Jiang Di, Junmin He, Ayinuer Yasen, Yanpin Ma, Gaohaer Sailikehan, Xixia Huang, Kechuan Tian

Subjects: “…copy number variations…”
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Optical Genome Mapping ( OGM) : Looking beyond karyotyping by Ruby Dhar, Arun Kumar, Subhradip Karmakar

Subjects: “…structural variants; optical genome mapping; genomics; copy number variations; karyotyping…”
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Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients by Yilun Tao, Yilun Tao, Hongzhi Guo, Dong Han, Miao Yang, Ting Lun, Lihong Wang, Wenxia Song, Haiwei Wang, Xiaoze Li

Subjects: “…copy number variations…”
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A Systematic Review of the Advances and New Insights into Copy Number Variations in Plant Genomes by Saimire Silaiyiman, Jiaxuan Liu, Jiaxin Wu, Lejun Ouyang, Zheng Cao, Chao Shen

Subjects: “…copy number variations…”
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Population-level gene copy number variations reveal distinct genetic properties of different Malus species by Aafreen Sakina, Can Alkan, Awais Khan

Subjects: “…Copy number variations (CNVs)…”
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Outcomes associated with fetal nuchal translucency between 3.0 and 3.4 mm in the first trimester by Manon D. E. Vriendt, Caroline Rooryck, Hugo Madar, Frédéric Coatleven, Marie Vincienne, Perrine Prier, Sophie Naudion, Loïc Sentilhes, Hanane Bouchghoul

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Genome-wide copy number variation regions in indigenous (Bos indicus) cattle breeds of Tamil Nadu, India by S. Vani, D. Balasubramanyam, K. G. Tirumurugaan, A. Gopinathan, S. M. K. Karthickeyan

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Genome-wide search for copy number variations associated with blood parameters in Large White pigs by M. A. Kolosova, L. V. Getmantseva, S. Yu. Bakoev, A. Yu. Kolosov

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Novel Copy Number Deletion Involving NUS1 Associated With Epilepsy, Tremor, and Intellectual Disability by Jing Y. Hsu, Daniah H. Ibrahim, Riza Ali, Elaine Marchi, Maureen Gavin, Karen Amble, Gholson J. Lyon

Subjects: “…DNA copy number variations…”
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Genetic and neuro-epigenetic effects of divergent artificial selection for feather pecking behaviour in chickens by Elske N. de Haas, Fábio Pértille, Joergen B. Kjaer, Per Jensen, Carlos Guerrero-Bosagna

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Structural variations in oil crops: Types, and roles on domestication and breeding by Xiaobo Cui, Miao Yao, Meili Xie, Ming Hu, Shengyi Liu, Lijiang Liu, Chaobo Tong

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Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis by Qinxin Zhang, Yan Wang, Yiyun Xu, Ran Zhou, Mingtao Huang, Fengchang Qiao, Lulu Meng, An Liu, Jing Zhou, Li Li, Xiuqing Ji, Zhengfeng Xu, Ping Hu

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Long-Read Sequencing and Structural Variant Detection: Unlocking the Hidden Genome in Rare Genetic Disorders by Efthalia Moustakli, Panagiotis Christopoulos, Anastasios Potiris, Athanasios Zikopoulos, Despoina Mavrogianni, Grigorios Karampas, Nikolaos Kathopoulis, Ismini Anagnostaki, Ekaterini Domali, Alexandros T. Tzallas, Peter Drakakis, Sofoklis Stavros

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Genetic Evaluation of Early Pregnancy Loss by Chromosomal Microarray Analysis: A Retrospective Analysis by Hu Ding, Honglei Duan, Xiangyu Zhu, Wei Liu, Leilei Gu, Chunxiang Zhou, Jie Li

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Copy number variations within fibroblast growth factor 13 gene influence growth traits and alternative splicing in cattle by Hanfang Cai, Xin Li, Xinran Niu, Jing Li, Xianyong Lan, Chuzhao Lei, Yongzhen Huang, Huifen Xu, Ming Li, Hong Chen

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A retrospective study for the diagnostic value of chromosomal microarray analysis in fetuses with high-risk prenatal indications by Hui Xiao, Junfang Xiao, Huan Zhang, Shuhui Huang, Qing Lu, Huizhen Yuan, Yongyi Zou, Bicheng Yang, Yanqiu Liu

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Copy number variations in the Brazilian High-Risk Cohort for Mental Conditions by Júlia Arendt, Malú Zamariolli, Liriel Almodobar, Lucas Toshio Ito, Rafaella Ormond, Adrielle M. Oliveira, Vanessa Kiyomi Ota, Luis Augusto Rohde, Euripedes Constantino Miguel, Pedro Mario Pan, Rodrigo Affonseca Bressan, Giovanni Salum, Sintia Belangero, Marcos Leite Santoro

Subjects: “…Copy number variations (CNVs)…”
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