Mixed phenotype acute leukemia in a child associated with a NUP98‐NSD1 fusion and NRAS p.Gly61Arg mutation

by Shireen S. Ganapathi, Sunil S. Raikar, Svetlana A. Yatsenko, Miroslav Djokic, Andrew Bukowinski
Published 2021-08-01

High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions.

by Tianjiao Chu, Suveyda Yeniterzi, Svetlana A Yatsenko, Mary Dunkel, Patricia A Shaw, Kimberly D Bunce, David G Peters
Published 2016-01-01

Correction: High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions.

by Tianjiao Chu, Suveyda Yeniterzi, Svetlana A Yatsenko, Mary Dunkel, Patricia A Shaw, Kimberly D Bunce, David G Peters
Published 2016-01-01

Correction: Hormad1 Mutation Disrupts Synaptonemal Complex Formation, Recombination, and Chromosome Segregation in Mammalian Meiosis

by Yong-Hyun Shin, Youngsok Choi, Serpil Uckac Erdin, Svetlana A. Yatsenko, Malgorzata Kloc, Fang Yang, P. Jeremy Wang, Marvin L. Meistrich, Aleksandar Rajkovic
Published 2011-02-01

Correction: Mutation Disrupts Synaptonemal Complex Formation, Recombination, and Chromosome Segregation in Mammalian Meiosis.

by Yong-Hyun Shin, Youngsok Choi, Serpil Uckac Erdin, Svetlana A. Yatsenko, Malgorzata Kloc, Fang Yang, P. Jeremy Wang, Marvin L. Meistrich, Aleksandar Rajkovic
Published 2011-02-01

Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis.

by Yong-Hyun Shin, Youngsok Choi, Serpil Uckac Erdin, Svetlana A Yatsenko, Malgorzata Kloc, Fang Yang, P Jeremy Wang, Marvin L Meistrich, Aleksandar Rajkovic
Published 2010-11-01

Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials.

by Xunda Luo, Artur V Cideciyan, Alessandro Iannaccone, Alejandro J Roman, Lauren C Ditta, Barbara J Jennings, Svetlana A Yatsenko, Rebecca Sheplock, Alexander Sumaroka, Malgorzata Swider, Sharon B Schwartz, Bernd Wissinger, Susanne Kohl, Samuel G Jacobson
Published 2015-01-01

Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea

by Jun Liao, Keith A. Coffman, Joseph Locker, Quasar S. Padiath, Bruce Nmezi, Robyn A. Filipink, Jie Hu, Malini Sathanoori, Suneeta Madan‐Khetarpal, Marianne McGuire, Allison Schreiber, Rocio Moran, Neil Friedman, Lori Hoffner, Aleksandar Rajkovic, Svetlana A. Yatsenko, Urvashi Surti
Published 2021-04-01

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.

by Xinyan Lu, Chad A Shaw, Ankita Patel, Jiangzhen Li, M Lance Cooper, William R Wells, Cathy M Sullivan, Trilochan Sahoo, Svetlana A Yatsenko, Carlos A Bacino, Pawel Stankiewicz, Zhishu Ou, A Craig Chinault, Arthur L Beaudet, James R Lupski, Sau W Cheung, Patricia A Ward
Published 2007-01-01