Resultados da busca - Rabinowitz, Matthew
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Use of the l(1) Norm for Selection of Sparse Parameter Sets that Accurately Predict Drug Response Phenotype from Viral Genetic Sequences por Rabinowitz, Matthew, Banjevic, Milena, Chan, A.S., Myers, Lance, Wolkowicz, Roland, Haberer, Jessica, Singer, Joshua
Publicado em 2005Texto -
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An Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population por Benn, Peter, Curnow, Kirsten J., Chapman, Steven, Michalopoulos, Steven N., Hornberger, John, Rabinowitz, Matthew
Publicado em 2015Texto -
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The Impact of Telemedicine on Sexual Medicine at a Major Academic Center During the COVID-19 Pandemic por Rabinowitz, Matthew J., Kohn, Taylor P., Ellimoottil, Chad, Alam, Ridwan, Liu, James L., Herati, Amin S.
Publicado em 2021Texto -
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Onset of azoospermia in man treated with ipilimumab/nivolumab for BRAF negative metastatic melanoma por Rabinowitz, Matthew J., Kohn, Taylor P., Peña, Vanessa N., Samarska, Iryna V., Matoso, Andres, Herati, Amin S.
Publicado em 2020Texto -
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Non-Invasive Prenatal Detection of Trisomy 13 Using a Single Nucleotide Polymorphism- and Informatics-Based Approach por Hall, Megan P., Hill, Matthew, Zimmermann, Bernhard, Sigurjonsson, Styrmir, Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Publicado em 2014Texto -
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Resident involvement in the prostatic urethral lift: implementing innovative technology in an academic setting por Alam, Ridwan, Rabinowitz, Matthew J, Kohn, Taylor P, Peña, Vanessa N, Liu, James L, Bhanji, Yasin, Herati, Amin S
Publicado em 2021Texto -
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Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics por Lathi, Ruth B., Loring, Megan, Massie, Jamie A. M., Demko, Zachary P., Johnson, David, Sigurjonsson, Styrmir, Gemelos, George, Rabinowitz, Matthew
Publicado em 2012Texto -
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Correction: Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics por Lathi, Ruth B., Massie, Jamie A. M., Loring, Megan, Demko, Zachary P., Johnson, David, Sigurjonsson, Styrmir, Gemelos, George, Rabinowitz, Matthew
Publicado em 2012Texto -
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Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryos por McCoy, Rajiv C., Demko, Zachary, Ryan, Allison, Banjevic, Milena, Hill, Matthew, Sigurjonsson, Styrmir, Rabinowitz, Matthew, Fraser, Hunter B., Petrov, Dmitri A.
Publicado em 2015Texto -
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Non-invasive prenatal aneuploidy testing at chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci por Zimmermann, Bernhard, Hill, Matthew, Gemelos, George, Demko, Zachary, Banjevic, Milena, Baner, Johan, Ryan, Allison, Sigurjonsson, Styrmir, Chopra, Nikhil, Dodd, Michael, Levy, Brynn, Rabinowitz, Matthew
Publicado em 2012Texto -
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SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy por Samango-Sprouse, Carole, Banjevic, Milena, Ryan, Allison, Sigurjonsson, Styrmir, Zimmermann, Bernhard, Hill, Matthew, Hall, Megan P., Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Publicado em 2013Texto -
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Whole genome prediction for preimplantation genetic diagnosis por Kumar, Akash, Ryan, Allison, Kitzman, Jacob O, Wemmer, Nina, Snyder, Matthew W, Sigurjonsson, Styrmir, Lee, Choli, Banjevic, Milena, Zarutskie, Paul W, Lewis, Alexandra P, Shendure, Jay, Rabinowitz, Matthew
Publicado em 2015Texto -
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Correction: Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach por Westemeyer, Maggie, Saucier, Jennifer, Wallace, Jody, Prins, Sarah A., Shetty, Aparna, Malhotra, Meenakshi, Demko, Zachary P., Eng, Christine M., Weckstein, Louis, Boostanfar, Robert, Rabinowitz, Matthew, Benn, Peter, Keen-Kim, Dianne, Billings, Paul
Publicado em 2020Texto -
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Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach por Westemeyer, Maggie, Saucier, Jennifer, Wallace, Jody, Prins, Sarah A., Shetty, Aparna, Malhotra, Meenakshi, Demko, Zachary P., Eng, Christine M., Weckstein, Louis, Boostanfar, Robert, Rabinowitz, Matthew, Benn, Peter, Keen-Kim, Dianne, Billings, Paul
Publicado em 2020Texto -
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CIRCULATE‐Japan: Circulating tumor DNA–guided adaptive platform trials to refine adjuvant therapy for colorectal cancer por Taniguchi, Hiroya, Nakamura, Yoshiaki, Kotani, Daisuke, Yukami, Hiroki, Mishima, Saori, Sawada, Kentaro, Shirasu, Hiromichi, Ebi, Hiromichi, Yamanaka, Takeharu, Aleshin, Alexey, Billings, Paul R., Rabinowitz, Matthew, Oki, Eiji, Takemasa, Ichiro, Kato, Takeshi, Mori, Masaki, Yoshino, Takayuki
Publicado em 2021Texto -
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Whole-genome risk prediction of common diseases in human preimplantation embryos por Kumar, Akash, Im, Kate, Banjevic, Milena, Ng, Pauline C., Tunstall, Tate, Garcia, Geronimo, Galhardo, Luisa, Sun, Jiayi, Schaedel, Oren N., Levy, Brynn, Hongo, Donna, Kijacic, Dusan, Kiehl, Michelle, Tran, Nam D., Klatsky, Peter C., Rabinowitz, Matthew
Publicado em 2022Texto -
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Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort por Pergament, Eugene, Cuckle, Howard, Zimmermann, Bernhard, Banjevic, Milena, Sigurjonsson, Styrmir, Ryan, Allison, Hall, Megan P., Dodd, Michael, Lacroute, Phil, Stosic, Melissa, Chopra, Nikhil, Hunkapiller, Nathan, Prosen, Dennis E., McAdoo, Sallie, Demko, Zachary, Siddiqui, Asim, Hill, Matthew, Rabinowitz, Matthew
Publicado em 2014Texto