Rezultaty - Rabinowitz, Matthew
- Rezultaty 1 - 20 Rezultaty od 24
- Idź do następnej strony
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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 od Rabinowitz, Matthew, Banjevic, Milena, Chan, A.S., Myers, Lance, Wolkowicz, Roland, Haberer, Jessica, Singer, Joshua
Wydane 2005Text -
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An Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population od Benn, Peter, Curnow, Kirsten J., Chapman, Steven, Michalopoulos, Steven N., Hornberger, John, Rabinowitz, Matthew
Wydane 2015Text -
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Onset of azoospermia in man treated with ipilimumab/nivolumab for BRAF negative metastatic melanoma od Rabinowitz, Matthew J., Kohn, Taylor P., Peña, Vanessa N., Samarska, Iryna V., Matoso, Andres, Herati, Amin S.
Wydane 2020Text -
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Non-Invasive Prenatal Detection of Trisomy 13 Using a Single Nucleotide Polymorphism- and Informatics-Based Approach od Hall, Megan P., Hill, Matthew, Zimmermann, Bernhard, Sigurjonsson, Styrmir, Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Wydane 2014Text -
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Resident involvement in the prostatic urethral lift: implementing innovative technology in an academic setting od Alam, Ridwan, Rabinowitz, Matthew J, Kohn, Taylor P, Peña, Vanessa N, Liu, James L, Bhanji, Yasin, Herati, Amin S
Wydane 2021Text -
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Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics od Lathi, Ruth B., Loring, Megan, Massie, Jamie A. M., Demko, Zachary P., Johnson, David, Sigurjonsson, Styrmir, Gemelos, George, Rabinowitz, Matthew
Wydane 2012Text -
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Correction: Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics od Lathi, Ruth B., Massie, Jamie A. M., Loring, Megan, Demko, Zachary P., Johnson, David, Sigurjonsson, Styrmir, Gemelos, George, Rabinowitz, Matthew
Wydane 2012Text -
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Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryos od McCoy, Rajiv C., Demko, Zachary, Ryan, Allison, Banjevic, Milena, Hill, Matthew, Sigurjonsson, Styrmir, Rabinowitz, Matthew, Fraser, Hunter B., Petrov, Dmitri A.
Wydane 2015Text -
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Non-invasive prenatal aneuploidy testing at chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci od Zimmermann, Bernhard, Hill, Matthew, Gemelos, George, Demko, Zachary, Banjevic, Milena, Baner, Johan, Ryan, Allison, Sigurjonsson, Styrmir, Chopra, Nikhil, Dodd, Michael, Levy, Brynn, Rabinowitz, Matthew
Wydane 2012Text -
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SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy od Samango-Sprouse, Carole, Banjevic, Milena, Ryan, Allison, Sigurjonsson, Styrmir, Zimmermann, Bernhard, Hill, Matthew, Hall, Megan P., Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Wydane 2013Text -
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Whole genome prediction for preimplantation genetic diagnosis od 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
Wydane 2015Text -
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Correction: Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach od 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
Wydane 2020Text -
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Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach od 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
Wydane 2020Text -
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CIRCULATE‐Japan: Circulating tumor DNA–guided adaptive platform trials to refine adjuvant therapy for colorectal cancer od 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
Wydane 2021Text -
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Whole-genome risk prediction of common diseases in human preimplantation embryos od 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
Wydane 2022Text -
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Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort od 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
Wydane 2014Text