A polymorphism in the thyroid hormone receptor gene is associated with bronchodilator response in asthmatics von Duan, Q L, Du, R, Lasky-Su, J, Klanderman, B J, Partch, A B, Peters, S P, Irvin, C G, Hanrahan, J P, Lima, J J, Blake, K V, Liggett, S B, Litonjua, A A, Tantisira, K G

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CK1δ/ε protein kinase primes the PER2 circadian phosphoswitch von Narasimamurthy, Rajesh, Hunt, Sabrina R., Lu, Yining, Fustin, Jean-Michel, Okamura, Hitoshi, Partch, Carrie L., Forger, Daniel B., Kim, Jae Kyoung, Virshup, David M.

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Ketogenesis impact on liver metabolism revealed by proteomics of lysine β-hydroxybutyrylation von Koronowski, Kevin B., Greco, Carolina M., Huang, He, Kim, Jin-Kwang, Fribourgh, Jennifer L., Crosby, Priya, Mathur, Lavina, Ren, Xuelian, Partch, Carrie L., Jang, Cholsoon, Qiao, Feng, Zhao, Yingming, Sassone-Corsi, Paolo

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CRY2 missense mutations suppress P53 and enhance cell growth von Chan, Alanna B., Parico, Gian Carlo G., Fribourgh, Jennifer L., Ibrahim, Lara H., Bollong, Michael J., Partch, Carrie L., Lamia, Katja A.

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Reassessment of Risk Genotypes (GRN, TMEM106B, and ABCC9 Variants) Associated With Hippocampal Sclerosis of Aging Pathology von Nelson, Peter T, Wang, Wang-Xia, Partch, Amanda B, Monsell, Sarah E, Valladares, Otto, Ellingson, Sally R, Wilfred, Bernard R, Naj, Adam C, Wang, Li-San, Kukull, Walter A, Fardo, David W

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Analysis of concordance in blastulation between partners of same-sex male couples using sibling oocytes from a sigle ovum donor von Moskovtsev, S., Partch, T., Hemalal, S., Chamas, B., Millman, N., Balakier, H., Librach, C.L.

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Regulating the ARNT/TACC3 Axis: Multiple Approaches to Manipulating Protein/Protein Interactions with Small Molecules von Guo, Yirui, Partch, Carrie L, Key, Jason, Card, Paul B, Pashkov, Victor, Patel, Anjana, Bruick, Richard K, Wurdak, Heiko, Gardner, Kevin H

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CK1d/e protein kinase primes the PER2 circadian phosphoswitch von Narasimamurthy, Rajesh, Hunt, Sabrina R, Lu, Yining, Fustin, Jean-Michel, Okamura, Hitoshi, Partch, Carrie L, ger, Daniel B, Kim, Jae Kyoung, Virshup, David M

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ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology von Nelson, Peter T., Estus, Steven, Abner, Erin L., Parikh, Ishita, Malik, Manasi, Neltner, Janna H., Ighodaro, Eseosa, Wang, Wang-Xia, Wilfred, Bernard R., Wang, Li-San, Kukull, Walter A., Nandakumar, Kannabiran, Farman, Mark L., Poon, Wayne W., Corrada, Maria M., Kawas, Claudia H., Cribbs, David H., Bennett, David A., Schneider, Julie A., Larson, Eric B., Crane, Paul K., Valladares, Otto, Schmitt, Frederick A., Kryscio, Richard J., Jicha, Gregory A., Smith, Charles D., Scheff, Stephen W., Sonnen, Joshua A., Haines, Jonathan L., Pericak-Vance, Margaret A., Mayeux, Richard, Farrer, Lindsay A., Van Eldik, Linda J., Horbinski, Craig, Green, Robert C., Gearing, Marla, Poon, Leonard W., Kramer, Patricia L., Woltjer, Randall L., Montine, Thomas J., Partch, Amanda B., Rajic, Alexander J., Richmire, KatieRose, Monsell, Sarah E., Schellenberg, Gerard D., Fardo, David W.

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The Three Rs of Transcription: Recruit, Retain, and Recycle von Motta-Mena, Laura B., Partch, Carrie L., Gardner, Kevin H.

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Multiple deletion copy number variants (CNVs) are associated with late-onset Alzheimer's disease: The Alzheimer’s disease genetics consortium von Wang, Weixin, Lin, Chiao-Feng, Partch, Amanda B, Valladares, Otto, Cantwell, Laura, Naj, Adam C, Wang, Li-San, Schellenberg, Gerard D

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HIGH-RESOLUTION IMPUTATION IN GENOME-WIDE ASSOCIATION STUDIES OF LATE-ONSET ALZHEIMER'S DISEASE IDENTIFIES NOVEL RARE VARIANT ASSOCIATIONS von Naj, Adam C, Zhao, Yi, van der Lee, Sven J, Hamilton, Kara L, Kunkle, Brian W, Partch, Amanda B, Valladares, Otto, Beecham, Gary W, Martin, Eden R, Wang, Li-San, Haines, Jonathan L, Mayeux, Richard, Farrer, Lindsay A, Pericak-Vance, Margaret A, Schellenberg, Gerard D

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Nia genetics of Alzheimer’s disease data storage site (NIAGADS): 2015 update von Partch, Amanda B, Laufer, Daniel, Valladares, Otto, Iodice, John, Greenfest-Allen, Emily, Childress, Daniel Micah, Malamon, John, Gangadharan, Prabhakaran, Arnold, Steven E, Stoeckert, Christian J, Schellenberg, Gerard D, Wang, Li-San

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Analysis of the need for facilities to provide adequate highter educational opportunities for veterans and for graduates of secondary schools von Partch, Clarence E. b. 1884

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O3‐05‐03: Multiple deletion copy number variants (CNVs) are associated with late‐onset Alzheimer's disease: The Alzheimer's disease genetics consortium von Wang, Weixin, Lin, Chiao-Feng, Partch, Amanda B., Valladares, Otto, Cantwell, Laura, Naj, Adam C., Wang, Li-San, Schellenberg, Gerard D.

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NIA GENETICS OF ALZHEIMER’S DISEASE DATA STORAGE SITE (NIAGADS): 2016 UPDATE von Gangadharan, Prabhakaran, Partch, Amanda B., Valladares, Otto, Greenfest-Allen, Emily, Childress, Daniel Micah, Cweibel, Rebecca, Malamon, John, Lin, Han-Jen, Zhao, Yi, Khaladkar, Mugdha, Naj, Adam C., Stoeckert, Christian J., Schellenberg, Gerard D., Wang, Li-San

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P1‐061: Nia genetics of Alzheimer's disease data storage site (NIAGADS): 2015 update von Partch, Amanda B., Laufer, Daniel, Valladares, Otto, Iodice, John, Greenfest-Allen, Emily, Childress, Daniel Micah, Malamon, John, Gangadharan, Prabhakaran, Arnold, Steven E., Stoeckert, Christian J., Schellenberg, Gerard D., Wang, Li-San

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O1‐03‐05: High‐Resolution Imputation in Genome‐Wide Association Studies of Late‐Onset Alzheimer's Disease Identifies Novel Rare Variant Associations von Naj, Adam C., Zhao, Yi, van der Lee, Sven J., Hamilton, Kara L., Kunkle, Brian W., Partch, Amanda B., Valladares, Otto, Beecham, Gary W., Martin, Eden R., Wang, Li-San, Haines, Jonathan L., Mayeux, Richard, Farrer, Lindsay A., Pericak-Vance, Margaret A., Schellenberg, Gerard D.

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P2‐097: The Alzheimer’s Disease Sequencing Project (ADSP): Data Production, Management, and Availability von Partch, Amanda B., DeStefano, Anita L., Cantwell, Laura, Faber, Kelley, Feolo, Mike, Stine, Adam, Gupta, Namrata, Salerno, William, Kobolt, Dan, Valladares, Otto, Bis, Joshua C., Childress, Daniel Micah, Cweibel, Rebecca, Dugan-Rocha, Shannon, Gangadharan, Prabhakaran, Choi, Seung Hoan, Stiening, Shannon, Reyes-Dumeyer, Dolly, Boerwinkle, Eric, Schellenberg, Gerard D., Seshadri, Sudha, Foroud, Tatiana M., Wang, Li-San

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F1‐01‐02: Alzheimer's Disease Sequencing Project: Search for Alzheimer's Disease Resilience Genes That May Modify Disease Susceptibility in Specific Apoe Genotype Backgrounds von Marcora, Eduardo, Renton, Alan E., Beecham, Gary W., Boerwinkle, Eric, Cantwell, Laura, Cruchaga, Carlos, Cweibel, Rebecca, Felsenfeld, Adam, Fornage, Myriam, Kapoor, Manav, Kauwe, Keoni, Khaladkar, Mugdha, Kobolt, Dan, Ma, Yiyi, Mayeux, Richard, Miller, Marilyn, Naj, Adam C., Partch, Amanda B., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Seshadri, Sudha, Vardarajan, Badri N., Wang, Li-San, Bis, Joshua C., Farrer, Lindsay A., Goate, Alison M.

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