Membrane Mimetic Chemistry in Artificial Cells von Vance, Jacob A, Devaraj, Neal K

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Zeptomole Detection of C-Reactive Protein in Serum by a Nanoparticle Amplified Surface Plasmon Resonance Imaging Aptasensor von Vance, Stephen A., Sandros, Marinella G.

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Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Dise... von Vance, Jeffery M, Farrer, Lindsay A, Huang, Yadong, Cruchaga, Carlos, Hyman, Bradley T, Pericak-Vance, Margaret A, Goate, Alison M, Greicius, Michael D, Griswold, Anthony J, Haines, Jonathan L, Tcw, Julia, Schellenberg, Gerard D, Tsai, Li-Huei, Herz, Joachim, Holtzman, David M

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis von Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr

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Using Team-Based Learning to Teach Data Science von Vance, Eric A.

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Identification of TMEM230 mutations in familial Parkinson's disease von Deng, Han-Xiang, Shi, Yong, Yang, Yi, Ahmeti, Kreshnik B, Miller, Nimrod, Huang, Cao, Cheng, Lijun, Zhai, Hong, Deng, Sheng, Nuytemans, Karen, Corbett, Nicola J, Kim, Myung Jong, Deng, Hao, Tang, Beisha, Yang, Ziquang, Xu, Yanming, Chan, Piu, Huang, Bo, Gao, Xiao-Ping, Song, Zhi, Liu, Zhenhua, Fecto, Faisal, Siddique, Nailah, Foroud, Tatiana, Jankovic, Joseph, Ghetti, Bernardino, Nicholson, Daniel A, Krainc, Dimitri, Melen, Onur, Vance, Jeffery M, Pericak-Vance, Margaret A, Ma, Yong-Chao, Rajput, Ali H, Siddique, Teepu

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia von Deng, Han-Xiang, Chen, Wenjie, Hong, Seong-Tshool, Boycott, Kym M., Gorrie, George H., Siddique, Nailah, Yang, Yi, Fecto, Faisal, Shi, Yong, Zhai, Hong, Jiang, Hujun, Hirano, Makito, Rampersaud, Evadnie, Jansen, Gerard H., Donkervoort, Sandra, Bigio, Eileen H., Brooks, Benjamin R., Ajroud, Kaouther, Sufit, Robert L., Haines, Jonathan L., Mugnaini, Enrico, Pericak-Vance, Margaret A., Siddique, Teepu

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A von Vance, Jeffery M, Züchner, Stephan, Mersiyanova, Irina V, Muglia, Maria, Bissar-Tadmouri, Nisrine, Rochelle, Julie, Dadali, Elena L, Zappia, Mario, Nelis, Eva, Patitucci, Alessandra, Senderek, Jan, Parman, Yesim, Evgrafov, Oleg, Jonghe, Peter De, Takahashi, Yuji, Tsuji, Shoij, Pericak-Vance, Margaret A, Quattrone, Aldo, Battologlu, Esra, Polyakov, Alexander V, Timmerman, Vincent, Schröder, J Michael

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Relationship of cardiovascular disease risk and hearing loss in a clinical population von Baiduc, Rachael R., Sun, Joshua W., Berry, Caitlin M., Anderson, Melinda, Vance, Eric A.

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The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis von Chen, Han-Jou, Mitchell, Jacqueline C, Novoselov, Sergey, Miller, Jack, Nishimura, Agnes L, Scotter, Emma L, Vance, Caroline A, Cheetham, Michael E, Shaw, Christopher E

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Psychometric approaches to defining cognitive phenotypes in the Old Order Amish von Zaman, Andrew, Caywood, Laura, Prough, Michael, Clouse, Jason, Harrington, Sharlene, Adams, Larry, Fuzzell, Denise, Fuzzell, Sarada, Laux, Renee, Hochstetler, Sherri D., Ogrocki, Paula, Lerner, Alan, Vance, Jeffery M., Haines, Jonathan L., Scott, William K., Pericak‐Vance, Margaret A., Cuccaro, Michael L.

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Neuropsychiatric features in a multi‐ethnic population with Alzheimer disease and mild cognitive impairment von Celis, Katrina, Zaman, Andrew, Adams, Larry Deon, Gardner, Olivia, Farid, Rajabli, Starks, Takiyah D., Lacroix, Faina C., Hamilton‐Nelson, Kara, Mena, Pedro, Tejada, Sergio, Laux, Renee, Song, Yeunjoo E., Caban‐Holt, Allison, Feliciano‐Astacio, Briseida, Vance, Jeffery M., Haines, Jonathan L., Byrd, Goldie S., Beecham, Gary W., Pericak‐Vance, Margaret A., Cuccaro, Michael L.

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Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa von Züchner, Stephan, Dallman, Julia, Wen, Rong, Beecham, Gary, Naj, Adam, Farooq, Amjad, Kohli, Martin A., Whitehead, Patrice L., Hulme, William, Konidari, Ioanna, Edwards, Yvonne J.K., Cai, Guiqing, Peter, Inga, Seo, David, Buxbaum, Joseph D., Haines, Jonathan L., Blanton, Susan, Young, Juan, Alfonso, Eduardo, Vance, Jeffery M., Lam, Byron L., Peričak-Vance, Margaret A.

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Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics von Sariya, Sanjeev, Felsky, Daniel, Reyes‐Dumeyer, Dolly, Lali, Ricky, Lantigua, Rafael A., Vardarajan, Badri, Jiménez‐Velázquez, Ivonne Z., Haines, Jonathan L., Shellenberg, Gerard D., Pericak‐Vance, Margaret A, Paré, Guillaume, Mayeux, Richard, Tosto, Giuseppe

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Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons von DeRosa, Brooke A., El Hokayem, Jimmy, Artimovich, Elena, Garcia-Serje, Catherine, Phillips, Andre W., Van Booven, Derek, Nestor, Jonathan E., Wang, Lily, Cuccaro, Michael L., Vance, Jeffery M., Pericak-Vance, Margaret A., Cukier, Holly N., Nestor, Michael W., Dykxhoorn, Derek M.

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A neuronal signature for monogamous reunion von Scribner, Jennifer L., Vance, Eric A., Protter, David S. W., Sheeran, William M., Saslow, Elliott, Cameron, Ryan T., Klein, Eric M., Jimenez, Jessica C., Kheirbek, Mazen A., Donaldson, Zoe R.

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Assessment of intraretinal hyperreflective foci using multimodal imaging in eyes with age‐related macular degeneration von Oncel, Deniz, Corradetti, Giulia, He, Ye, Ashrafkhorasani, Maryam, Nittala, Muneeswar Gupta, Stambolian, Dwight, Pericak‐Vance, Margaret A., Haines, Jonathan L., Sadda, Srinivas R.

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Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 von Montenegro, Gladys, Rebelo, Adriana P, Connell, James, Allison, Rachel, Babalini, Carla, D'Aloia, Michela, Montieri, Pasqua, Schüle, Rebecca, Ishiura, Hiroyuki, Price, Justin, Strickland, Alleene, Gonzalez, Michael A, Baumbach-Reardon, Lisa, Deconinck, Tine, Huang, Jia, Bernardi, Giorgio, Vance, Jeffery M, Rogers, Mark T, Tsuji, Shoji, De Jonghe, Peter, Pericak-Vance, Margaret A, Schöls, Ludger, Orlacchio, Antonio, Reid, Evan, Züchner, Stephan

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DNA from multiple viral species is associated with Alzheimer's disease risk von Tejeda, Marlene, Farrell, John, Zhu, Congcong, Wetzler, Lee, Lunetta, Kathryn L., Bush, William S., Martin, Eden R., Wang, Li‐San, Schellenberg, Gerard D., Pericak‐Vance, Margaret A., Haines, Jonathan L., Farrer, Lindsay A., Sherva, Richard

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Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets von Nuytemans, Karen, Lipkin Vasquez, Marina, Wang, Liyong, Van Booven, Derek, Griswold, Antony J., Rajabli, Farid, Celis, Katrina, Oron, Oded, Hofmann, Natalia, Rolati, Sophie, Garcia‐Serje, Catherine, Zhang, Shanshan, Jin, Fulai, Argenziano, Mariana, Grant, Struan F.A., Chesi, Alessandra, Brown, Christopher D., Young, Juan I., Dykxhoorn, Derek M., Pericak‐Vance, Margaret A., Vance, Jeffery M.

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