检索结果 - Glessner, Joe

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  1. 1
    CANOES: detecting rare copy number variants from whole exome sequencing data

    CANOES: detecting rare copy number variants from whole exome sequencing data 由 Backenroth, Daniel, Homsy, Jason, Murillo, Laura R., Glessner, Joe, Lin, Edwin, Brueckner, Martina, Lifton, Richard, Goldmuntz, Elizabeth, Chung, Wendy K., Shen, Yufeng

    出版 2014
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    Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities

    Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities 由 Shadrina, Alexandra S., Elgaeva, Elizaveta E., Stanaway, Ian B., Jarvik, Gail P., Namjou, Bahram, Wei, Wei-Qi, Glessner, Joe, Hakonarson, Hakon, Suri, Pradeep, Tsepilov, Yakov A.

    出版 2022
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    Genome-wide SNP Genotyping Identifies the Stereocilin (STRC) Gene as a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment

    Genome-wide SNP Genotyping Identifies the Stereocilin (STRC) Gene as a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment 由 Francey, Lauren J, Conlin, Laura K, Kadesch, Hanna E, Clark, Dinah, Berrodin, Donna, Sun, Yi, Glessner, Joe, Hakonarson, Hakon, Jalas, Chaim, Landau, Chaim, Spinner, Nancy B, Kenna, Margaret, Sagi, Michal, Rehm, Heidi L, Krantz, Ian D

    出版 2011
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