Search Results - Hakker, Inessa
- Showing 1 - 11 results of 11
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Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies by Jobanputra, Vaidehi, Andrews, Peter, Felice, Vanessa, Abhyankar, Avinash, Kozon, Lukasz, Robinson, Dino, London, Ferrah, Hakker, Inessa, Wrzeszczynski, Kazimierz, Ronemus, Michael
Published 2020Text -
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Overexpression of Neprilysin Reduces Alzheimer Amyloid-β42 (Aβ42)-induced Neuron Loss and Intraneuronal Aβ42 Deposits but Causes a Reduction in cAMP-responsive Element-binding Pr... by Iijima-Ando, Kanae, Hearn, Stephen A., Granger, Linda, Shenton, Christopher, Gatt, Anthony, Chiang, Hsueh-Cheng, Hakker, Inessa, Zhong, Yi, Iijima, Koichi
Published 2008Text -
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Aβ42 Mutants with Different Aggregation Profiles Induce Distinct Pathologies in Drosophila by Iijima, Koichi, Chiang, Hsueh-Cheng, Hearn, Stephen A., Hakker, Inessa, Gatt, Anthony, Shenton, Christopher, Granger, Linda, Leung, Amy, Iijima-Ando, Kanae, Zhong, Yi
Published 2008Text -
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DNA copy number variations in children with vesicoureteral reflux and urinary tract infections by Liang, Dong, McHugh, Kirk M., Brophy, Pat D., Shaikh, Nader, Manak, J. Robert, Andrews, Peter, Hakker, Inessa, Wang, Zihua, Schwaderer, Andrew L., Hains, David S.
Published 2019Text -
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Utility of single cell genomics in diagnostic evaluation of prostate cancer by Alexander, Joan, Kendall, Jude, McIndoo, Jean, Rodgers, Linda, Aboukhalil, Robert, Levy, Dan, Stepansky, Asya, Sun, Guoli, Chobardjiev, Lubomir, Riggs, Michael, Cox, Hilary, Hakker, Inessa, Nowak, Dawid G., Laze, Juliana, Llukani, Elton, Srivastava, Abhishek, Gruschow, Siobhan, Yadav, Shalini S., Robinson, Brian, Atwal, Gurinder, Trotman, Lloyd, Lepor, Herbert, Hicks, James, Wigler, Michael, Krasnitz, Alexander
Published 2017Text -
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De Novo Gene Disruptions in Children on the Autistic Spectrum by Iossifov, Ivan, Ronemus, Michael, Levy, Dan, Wang, Zihua, Hakker, Inessa, Rosenbaum, Julie, Yamrom, Boris, Lee, Yoon-ha, Narzisi, Giuseppe, Leotta, Anthony, Kendall, Jude, Grabowska, Ewa, Ma, Beicong, Marks, Steven, Rodgers, Linda, Stepansky, Asya, Troge, Jennifer, Andrews, Peter, Bekritsky, Mitchell, Pradhan, Kith, Ghiban, Elena, Kramer, Melissa, Parla, Jennifer, Demeter, Ryan, Fulton, Lucinda L., Fulton, Robert S., Magrini, Vincent J., Ye, Kenny, Darnell, Jennifer C., Darnell, Robert B., Mardis, Elaine R., Wilson, Richard K., Schatz, Michael C., McCombie, W. Richard, Wigler, Michael
Published 2012Text -
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The contribution of de novo coding mutations to autism spectrum disorder by Iossifov, Ivan, O’Roak, Brian J., Sanders, Stephan J., Ronemus, Michael, Krumm, Niklas, Levy, Dan, Stessman, Holly A., Witherspoon, Kali, Vives, Laura, Patterson, Karynne E., Smith, Joshua D., Paeper, Bryan, Nickerson, Deborah A., Dea, Jeanselle, Dong, Shan, Gonzalez, Luis E., Mandell, Jefferey D., Mane, Shrikant M., Murtha, Michael T., Sullivan, Catherine A., Walker, Michael F., Waqar, Zainulabedin, Wei, Liping, Willsey, A. Jeremy, Yamrom, Boris, Lee, Yoon-ha, Grabowska, Ewa, Dalkic, Ertugrul, Wang, Zihua, Marks, Steven, Andrews, Peter, Leotta, Anthony, Kendall, Jude, Hakker, Inessa, Rosenbaum, Julie, Ma, Beicong, Rodgers, Linda, Troge, Jennifer, Narzisi, Giuseppe, Yoon, Seungtai, Schatz, Michael C., Ye, Kenny, McCombie, W. Richard, Shendure, Jay, Eichler, Evan E., State, Matthew W., Wigler, Michael
Published 2014Text