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Copy number variation

The copy number variation and stroke (CaNVAS) risk and outcome study

John W. Cole, Taiwo Adigun, Rufus Akinyemi, Onoja Matthew Akpa, Steven Bell, Bowang Chen, Jordi Jimenez Conde, Uxue Lazcano Dobao, Israel Fernandez, Myriam Fornage, Cristina Gallego-Fabrega, Christina Jern, Michael Krawczak, Arne Lindgren, Hugh S. Markus, Olle Melander, Mayowa Owolabi, Kristina Schlicht, Martin Söderholm, Vinodh Srinivasasainagendra, Carolina Soriano Tárraga, Martin Stenman, Hemant Tiwari, Margaret Corasaniti, Natalie Fecteau, Beth Guizzardi, Haley Lopez, Kevin Nguyen, Brady Gaynor, Timothy O’Connor, O. Colin Stine, Steven J. Kittner, Patrick McArdle, Braxton D. Mitchell, Huichun Xu, Caspar Grond-Ginsbach

published 19 Apr 2021

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Prognostic value of integrated cytogenetic, somatic variation, and copy number variation analyses in Korean patients with newly diagnosed multiple myeloma

Nuri Lee, Sung-Min Kim, Youngeun Lee, Dajeong Jeong, Jiwon Yun, Sohee Ryu, Sung-Soo Yoon, Yong-Oon Ahn, Sang Mee Hwang, Dong Soon Lee

published 05 Feb 2021

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Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia

Maroua Boujemaa, Yosr Hamdi, Nesrine Mejri, Lilia Romdhane, Kais Ghedira, Hanen Bouaziz, Houda El Benna, Soumaya Labidi, Hamza Dallali, Olfa Jaidane, Sonia Ben Nasr, Abderrazek Haddaoui, Khaled Rahal, Sonia Abdelhak, Hamouda Boussen, Mohamed Samir Boubaker

published 27 Jan 2021

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Identification of a 6-gene signature for the survival prediction of breast cancer patients based on integrated multi-omics data analysis

Wenju Mo, Yuqin Ding, Shuai Zhao, Dehong Zou, Xiaowen Ding

published 10 Nov 2020

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Homogeneity among glyphosate-resistant Amaranthus palmeri in geographically distant locations

William T. Molin, Eric L. Patterson, Christopher A. Saski

published 09 Sep 2020

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Whole genome detection of sequence and structural polymorphism in six diverse horses

Mohammed Ali Al Abri, Heather Marie Holl, Sara E. Kalla, Nathan B. Sutter, Samantha A. Brooks

published 09 Apr 2020

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Comparing genome-scale DNA methylation and CNV marks between adult human cultured ITGA6+ testicular cells and seminomas to assess in vitro genomic stability

Robert B. Struijk, Lambert C. J. Dorssers, Peter Henneman, Martin A. Rijlaarsdam, Andrea Venema, Aldo Jongejan, Marcel M. A. M. Mannens, Leendert H. J. Looijenga, Sjoerd Repping, Ans M. M. van Pelt

published 16 Mar 2020

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CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders

Aditya Addepalli, Sakhare Kalyani, Minali Singh, Debashree Bandyopadhyay, K. Naga Mohan

published 29 Jan 2020

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HeLa-CCL2 cell heterogeneity studied by single-cell DNA and RNA sequencing

Wan-er Hu, Xin Zhang, Qiu-fang Guo, Jing-wei Yang, Yuan Yang, Shi-cheng Wei, Xiao-dong Su

published 02 Dec 2019

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Clade II Candida auris possess genomic structural variations related to an ancestral strain

Tsuyoshi Sekizuka, Shigekazu Iguchi, Takashi Umeyama, Yuba Inamine, Koichi Makimura, Makoto Kuroda, Yoshitsugu Miyazaki, Ken Kikuchi

published 09 Oct 2019

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DNA copy number variations in children with vesicoureteral reflux and urinary tract infections

Dong Liang, Kirk M. McHugh, Pat D. Brophy, Nader Shaikh, J. Robert Manak, Peter Andrews, Inessa Hakker, Zihua Wang, Andrew L. Schwaderer, David S. Hains

published 12 Aug 2019

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Association between polymorphisms in the SOX9 region and canine disorder of sex development (78,XX; SRY-negative) revisited in a multibreed case-control study

Joanna Nowacka-Woszuk, Izabela Szczerbal, Monika Stachowiak, Maciej Szydlowski, Wojciech Nizanski, Stanislaw Dzimira, Artur Maslak, Rita Payan-Carreira, Eline Wydooghe, Tomasz Nowak, Marek Switonski

published 20 Jun 2019

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Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease

Svetlana Frenkel, Charles N. Bernstein, Michael Sargent, Qin Kuang, Wenxin Jiang, John Wei, Bhooma Thiruvahindrapuram, Elizabeth Spriggs, Stephen W. Scherer, Pingzhao Hu

published 11 Jun 2019

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