Canlyniadau Chwilio - S A Yatsenko

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  1. 1
    Genetics of human female infertility†

    Genetics of human female infertility† gan Svetlana A. Yatsenko, Aleksandar Rajkovic

    Cyhoeddwyd 2019
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    Revisão
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  2. 2
    Discrepancies between sex prediction and fetal sex after prenatal non-invasive cell-free DNA screening

    Discrepancies between sex prediction and fetal sex after prenatal non-invasive cell-free DNA screening gan Selma F. Witchel, Aleksandar Rajkovic, Svetlana A. Yatsenko

    Cyhoeddwyd 2025
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    Revisão
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  3. 3
    Med12 gain-of-function mutation causes leiomyomas and genomic instability

    Med12 gain-of-function mutation causes leiomyomas and genomic instability gan Priya Mittal, Yong‐Hyun Shin, Svetlana A. Yatsenko, Carlos Iregui, Urvashi Surti, Aleksandar Rajkovic

    Cyhoeddwyd 2015
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    Artigo
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  4. 4
    CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

    CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders gan Jie Hu, Jun Liao, Malini Sathanoori, Sally J. Kochmar, Jessica Sebastian, Svetlana A. Yatsenko, Urvashi Surti

    Cyhoeddwyd 2015
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  5. 5
    Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure

    Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure gan Sunita Katari, Michelle A. Wood, Huaiyang Jiang, Eve Justine Kalynchuk, Radhika Muzumdar, Svetlana A. Yatsenko, A Rajkovic

    Cyhoeddwyd 2015
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    Artigo
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  6. 6
    Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome

    Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome gan Svetlana A. Yatsenko, Ellen K. Brundage, Erin K. Roney, Sau Wai Cheung, A. Craig Chinault, James R. Lupski

    Cyhoeddwyd 2009
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    Artigo
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  7. 7
    Highly heterogeneous genomic landscape of uterine leiomyomas by whole exome sequencing and genome-wide arrays

    Highly heterogeneous genomic landscape of uterine leiomyomas by whole exome sequencing and genome-wide arrays gan Svetlana A. Yatsenko, Priya Mittal, Michelle A. Wood, Mirka W. Jones, Urvashi Surti, Robert P. Edwards, Anil K. Sood, Aleksandar Rajkovic

    Cyhoeddwyd 2016
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  8. 8
    Hormad1 Mutation Disrupts Synaptonemal Complex Formation, Recombination, and Chromosome Segregation in Mammalian Meiosis

    Hormad1 Mutation Disrupts Synaptonemal Complex Formation, Recombination, and Chromosome Segregation in Mammalian Meiosis gan Yong-Hyun Shin, Youngsok Choi, Serpil Uckac Erdin, Svetlana A. Yatsenko, Małgorzata Kloc, Yang Fang, P. Jeremy Wang, Marvin L. Meistrich, Aleksandar Rajkovic

    Cyhoeddwyd 2010
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  9. 9
    Single-cell morphological and transcriptome analysis unveil inhibitors of polyploid giant breast cancer cells in vitro

    Single-cell morphological and transcriptome analysis unveil inhibitors of polyploid giant breast cancer cells in vitro gan Mengli Zhou, Yushu Ma, Chun‐Cheng Chiang, Edwin C. Rock, Samuel Charles Butler, Rajiv Anne, Svetlana A. Yatsenko, Yi‐Nan Gong, Yu‐Chih Chen

    Cyhoeddwyd 2023
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    Artigo
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  10. 10
    Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome

    Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome gan David G. Peters, Tianjiao Chu, Svetlana A. Yatsenko, Nancy W. Hendrix, W. Allen Hogge, Urvashi Surti, Kimberly Bunce, Mary K. Dunkel, Patricia Shaw, Aleksandar Rajkovic

    Cyhoeddwyd 2011
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    Carta
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  11. 11
    Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants

    Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants gan Mona Amin‐Beidokhti, Jia-Hua Qu, Shweta Belur, Hakan Çakmak, Eleni A. Greenwood, Ruth B. Lathi, Marina Sirota, M Snyder, Svetlana A. Yatsenko, Aleksandar Rajkovic

    Cyhoeddwyd 2024
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    Artigo
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  12. 12
    Identification of De Novo Copy Number Variants Associated with Human Disorders of Sexual Development

    Identification of De Novo Copy Number Variants Associated with Human Disorders of Sexual Development gan Mounia Tannour‐Louet, Shuo Han, Sean T. Corbett, Jean‐François Louet, Svetlana A. Yatsenko, Lindsay Meyers, Chad A. Shaw, Sung‐Hae Kang, Sau Wai Cheung, Dolores J. Lamb

    Cyhoeddwyd 2010
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  13. 13
    Comprehensive 5-Year Study of Cytogenetic Aberrations in 668 Infertile Men

    Comprehensive 5-Year Study of Cytogenetic Aberrations in 668 Infertile Men gan Alexander N. Yatsenko, Svetlana A. Yatsenko, John Weedin, Amy E. Lawrence, Ankita Patel, Sandra Peacock, Martin M. Matzuk, Dolores J. Lamb, Sau Wai Cheung, Larry I. Lipshultz

    Cyhoeddwyd 2010
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    Artigo
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  14. 14
    X-Linked <i>TEX11</i> Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

    X-Linked <i>TEX11</i> Mutations, Meiotic Arrest, and Azoospermia in Infertile Men gan Alexander N. Yatsenko, Andrew Georgiadis, Albrecht Röpke, Andrea J. Berman, Thomas Jaffe, Marta Olszewska, Birgit Westernströer, Joseph S. Sanfilippo, Maciej Kurpisz, Aleksandar Rajkovic, Svetlana A. Yatsenko, Sabine Kliesch, Stefan Schlatt, Frank Tüttelmann

    Cyhoeddwyd 2015
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    Artigo
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  15. 15
    Reproductive outcomes in individuals with chromosomal reciprocal translocations

    Reproductive outcomes in individuals with chromosomal reciprocal translocations gan Angela M. Verdoni, Jie Hu, Urvashi Surti, Melanie Babcock, Elizabeth Sheehan, Michele Clemens, Sarah Drewes, Leslie Walsh, Rebecca I. Clark, Sunita Katari, Joe Sanfilippo, Devereux N. Saller, Aleksandar Rajkovic, Svetlana A. Yatsenko

    Cyhoeddwyd 2021
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  16. 16
    Development and validation of a CGH microarray for clinical cytogenetic diagnosis

    Development and validation of a CGH microarray for clinical cytogenetic diagnosis gan Sau Wai Cheung, Chad A. Shaw, Wei Yu, Jiangzham Li, Zhishuo Ou, Ankita Patel, Svetlana A. Yatsenko, M. Lance Cooper, Patti Furman, P Stankiewicz, James R. Lupski, A. Craig Chinault, Arthur L. Beaudet

    Cyhoeddwyd 2005
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  17. 17
    MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability

    MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability gan Michelle A. Wood, Fatih Gürbüz, Svetlana A. Yatsenko, Elizabeth P. Jeffries, Leman Damla Kotan, Urvashi Surti, Deborah M. Ketterer, Jelena Matic, Jacqueline Chipkin, Huaiyang Jiang, Michael A. Trakselis, A. Kemal Topaloğlu, Aleksandar Rajkovic

    Cyhoeddwyd 2014
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    Artigo
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  18. 18
    Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability

    Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability gan Saleh AlAsiri, Sulman Basit, Michelle A. Wood, Svetlana A. Yatsenko, Elizabeth P. Jeffries, Urvashi Surti, Deborah M. Ketterer, Sibtain Afzal, Khushnooda Ramzan, Muhammad Faiyaz-Ul Haque, Huaiyang Jiang, Michael A. Trakselis, Aleksandar Rajkovic

    Cyhoeddwyd 2014
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    Artigo
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  19. 19
    Identification of critical regions for clinical features of distal 10q deletion syndrome

    Identification of critical regions for clinical features of distal 10q deletion syndrome gan S A Yatsenko, M.D. and Colin M. Roberts Michael C. Kruer, PI Bader, D Corzo, Jane L. Schuette, CE Keegan, Beata Nowakowska, Sandra Peacock, WW Cai, DA Peiffer, KL Gunderson, Zhishuo Ou, AC Chinault, SW Cheung

    Cyhoeddwyd 2009
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    Artigo
    Ychwanegu at ffefrynnau
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  20. 20
    Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

    Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases gan Lina Shao, Chad A. Shaw, Xinyan Lu, Trilochan Sahoo, Carlos A. Bacino, Seema R. Lalani, Paweł Stankiewicz, Svetlana A. Yatsenko, Yinfeng Li, Sarah E. Neill, Amber N. Pursley, A. Craig Chinault, Ankita Patel, Arthur L. Beaudet, James R. Lupski, Sau Wai Cheung

    Cyhoeddwyd 2008
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    Artigo
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