Trisomy 13 and the risk of gestational hypertensive disorders: a population-based study by Dotters-Katz, Sarah K, Humphrey, Whitney M, Senz, Kayli L, Lee, Vanessa R, Shaffer, Brian L, Kuller, Jeffrey A, Caughey, Aaron B

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126: Trisomy 18 pregnancies: is there an increased maternal risk? by Dotters-Katz, Sarah K, Senz, Kayli, Humphrey, Whitney M, Lee, Vanessa R, Caughey, Aaron B

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765: The impact of trisomy 13 on perinatal outcomes by Senz, Kayli, Humphrey, Whitney M, Lee, Vanessa R, Shaffer, Brian L, Caughey, Aaron B

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460: The impact of 47,XXY on perinatal outcomes by Humphrey, Whitney M, Senz, Kayli, Lee, Vanessa R, Shaffer, Brian L, Caughey, Aaron B

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322: Microarray versus karyotype for pregnant women with anomalies found on ultrasonography by Humphrey, Whitney M, Griffin, Emily E, Shaffer, Brian L, Caughey, Aaron B

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118: The impact of 45,X on perinatal outcomes by Humphrey, Whitney M, Senz, Kayli, Lee, Vanessa R, Shaffer, Brian L, Caughey, Aaron B

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459: What is the best clinical approach after a non-invasive prenatal testing test failure in women at high risk for aneuploidy? by Humphrey, Whitney M, Griffin, Emily, Lee, Vanessa R, Aviram, Amir, Shaffer, Brian L, Caughey, Aaron B

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The impact of prenatally diagnosed Klinefelter Syndrome on obstetric and neonatal outcomes by Dotters-katz, Sarah K, Humphrey, Whitney M, Senz, Kayli L, Lee, Vanessa R, Shaffer, Brian L, Caughey, Aaron B

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119: What is the best clinical approach after a non-invasive prenatal testing test failure in women with low risk for aneuploidy? by Humphrey, Whitney M, Griffin, Emily, Lee, Vanessa R, Ameel, Britta M, Shaffer, Brian L, Caughey, Aaron B

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458: Routine amniocentesis vs standard serum screening for detection of aneuploidy in women in a low-risk population by Humphrey, Whitney M, Griffin, Emily E, Lee, Vanessa R, Aviram, Amir, Shaffer, Brian L, Caughey, Aaron B

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117: Routine amniocentesis versus serum screening for detection of aneuploidy in women of advanced maternal age by Humphrey, Whitney M, Griffin, Emily E, Senz, Kayli L, Shaffer, Brian L, Caughey, Aaron B

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Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes by Farrell, Kurt, Humphrey, Jack, Chang, Timothy, Zhao, Yi, Leung, Yuk Yee, Kuksa, Pavel P., Patil, Vishakha, Lee, Wan-Ping, Kuzma, Amanda B., Valladares, Otto, Cantwell, Laura B., Wang, Hui, Ravi, Ashvin, De Sanctis, Claudia, Han, Natalia, Christie, Thomas D., Afzal, Robina, Kandoi, Shrishtee, Whitney, Kristen, Krassner, Margaret M., Ressler, Hadley, Kim, SoongHo, Dangoor, Diana, Iida, Megan A., Casella, Alicia, Walker, Ruth H., Nirenberg, Melissa J., Renton, Alan E., Babrowicz, Bergan, Coppola, Giovanni, Raj, Towfique, Höglinger, Günter U., Müller, Ulrich, Golbe, Lawrence I., Morris, Huw R., Hardy, John, Revesz, Tamas, Warner, Tom T., Jaunmuktane, Zane, Mok, Kin Y., Rademakers, Rosa, Dickson, Dennis W., Ross, Owen A., Wang, Li-San, Goate, Alison, Schellenberg, Gerard, Geschwind, Daniel H., Crary, John F., Naj, Adam

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Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes by Farrell, Kurt, Humphrey, Jack, Chang, Timothy, Zhao, Yi, Leung, Yuk Yee, Kuksa, Pavel P., Patil, Vishakha, Lee, Wan-Ping, Kuzma, Amanda B., Valladares, Otto, Cantwell, Laura B., Wang, Hui, Ravi, Ashvin, De Sanctis, Claudia, Han, Natalia, Christie, Thomas D., Afzal, Robina, Kandoi, Shrishtee, Whitney, Kristen, Krassner, Margaret M., Ressler, Hadley, Kim, SoongHo, Dangoor, Diana, Iida, Megan A., Casella, Alicia, Walker, Ruth H., Nirenberg, Melissa J., Renton, Alan E., Babrowicz, Bergan, Coppola, Giovanni, Raj, Towfique, Höglinger, Günter U., Müller, Ulrich, Golbe, Lawrence I., Morris, Huw R., Hardy, John, Revesz, Tamas, Warner, Tom T., Jaunmuktane, Zane, Mok, Kin Y., Rademakers, Rosa, Dickson, Dennis W., Ross, Owen A., Wang, Li-San, Goate, Alison, Schellenberg, Gerard, Geschwind, Daniel H., Crary, John F., Naj, Adam

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Genome-wide association study and functional validation implicates JADE1 in tauopathy by Farrell, Kurt, Kim, SoongHo, Han, Natalia, Iida, Megan A., Gonzalez, Elias M., Otero-Garcia, Marcos, Walker, Jamie M., Richardson, Timothy E., Renton, Alan E., Andrews, Shea J., Fulton-Howard, Brian, Humphrey, Jack, Vialle, Ricardo A., Bowles, Kathryn R., de Paiva Lopes, Katia, Whitney, Kristen, Dangoor, Diana K., Walsh, Hadley, Marcora, Edoardo, Hefti, Marco M., Casella, Alicia, Sissoko, Cheick T., Kapoor, Manav, Novikova, Gloriia, Udine, Evan, Wong, Garrett, Tang, Weijing, Bhangale, Tushar, Hunkapiller, Julie, Ayalon, Gai, Graham, Robert R., Cherry, Jonathan D., Cortes, Etty P., Borukov, Valeriy Y., McKee, Ann C., Stein, Thor D., Vonsattel, Jean-Paul, Teich, Andy F., Gearing, Marla, Glass, Jonathan, Troncoso, Juan C., Frosch, Matthew P., Hyman, Bradley T., Dickson, Dennis W., Murray, Melissa E., Attems, Johannes, Flanagan, Margaret E., Mao, Qinwen, Mesulam, M.-Marsel, Weintraub, Sandra, Woltjer, Randy L., Pham, Thao, Kofler, Julia, Schneider, Julie A., Yu, Lei, Purohit, Dushyant P., Haroutunian, Vahram, Hof, Patrick R., Gandy, Sam, Sano, Mary, Beach, Thomas G., Poon, Wayne, Kawas, Claudia H., Corrada, María M., Rissman, Robert A., Metcalf, Jeff, Shuldberg, Sara, Salehi, Bahar, Nelson, Peter T., Trojanowski, John Q., Lee, Edward B., Wolk, David A., McMillan, Corey T., Keene, C. Dirk, Latimer, Caitlin S., Montine, Thomas J., Kovacs, Gabor G., Lutz, Mirjam I., Fischer, Peter, Perrin, Richard J., Cairns, Nigel J., Franklin, Erin E., Cohen, Herbert T., Raj, Towfique, Cobos, Inma, Frost, Bess, Goate, Alison, White III, Charles L., Crary, John F.

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