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

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

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Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment von 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.

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Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network von Lewis, Anna C.F., Chisholm, Rex L., Connolly, John J., Esplin, Edward D., Glessner, Joe, Gordon, Adam, Green, Robert C., Hakonarson, Hakon, Harr, Margaret, Holm, Ingrid A., Jarvik, Gail P., Karlson, Elizabeth, Kenny, Eimear E., Kottyan, Leah, Lennon, Niall, Linder, Jodell E., Luo, Yuan, Martin, Lisa J., Perez, Emma, Puckelwartz, Megan J., Rasmussen-Torvik, Laura J., Sabatello, Maya, Sharp, Richard R., Smoller, Jordan W., Sterling, Rene, Terek, Shannon, Wei, Wei-Qi, Fullerton, Stephanie M.

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

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Lessons learned from the eMERGE Network: balancing genomics in discovery and practice

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