Setmelanotide Administration Improves Cardiac Systolic Function in Sirtuin-3 Deficient Mice by Nelson, Benjamin, Omoto, Ana C. M, Espinoza, Micaela, Nall, John, Chen, Jian-Xiong, Zeng, Heng, do Carmo, Jussara

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Young-Nall House, County Highway 40 at Lake Berry Road, Burkville, Lowndes County, AL by Historic American Buildings Survey

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Eight-Second Delay Fin Release Mechanism for Use with MAU-91B/B Bomb Fin by Lesikar, John Nall

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GREAT YARMOUTH AND LOWESTOFT; A HANDBOOK FOR VISITORS AND RESIDENTS by NALL, JOHN GREAVES

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Spondylitis in Diana Guenon Monkey by Nall, John D., Bartels, J. E.

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Short Research Article: Do demographic, socioeconomic and clinical characteristics influence the number of psychological intervention sessions attended by young people in need of m... by Meddings, John, Harries, Anthony D., Michelet, Felix, Nall‐Evans, Sharleen, Pender, Fiona, Jaydeokar, Sujeet

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Hepatitis in a Gorilla by Nall, John D., Lindsey, J. Russell, Baker, Henry J., Truett, F. Robert

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Community Engaged Cumulative Risk Assessment of Exposure to Inorganic Well Water Contaminants, Crow Reservation, Montana by Eggers, Margaret J, Doyle, John T, Lefthand, Myra J, Young, Sara L, Moore-Nall, Anita L, Kindness, Larry, Medicine, Roberta Other, Ford, Timothy E, Dietrich, Eric, Parker, Albert E, Hoover, Joseph H, Camper, Anne K

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The transcriptional landscape of age in human peripheral blood by Peters, Marjolein J., Joehanes, Roby, Pilling, Luke C., Schurmann, Claudia, Conneely, Karen N., Powell, Joseph, Reinmaa, Eva, Sutphin, George L., Zhernakova, Alexandra, Schramm, Katharina, Wilson, Yana A., Kobes, Sayuko, Ramos, Yolande F., Göring, Harald H. H., Fornage, Myriam, Liu, Yongmei, Gharib, Sina A., Stranger, Barbara E., Aviv, Abraham, Levy, Daniel, Murabito, Joanne M., Munson, Peter J., Huan, Tianxiao, Hofman, Albert, Uitterlinden, André G., Rivadeneira, Fernando, van Rooij, Jeroen, Stolk, Lisette, Broer, Linda, Verbiest, Michael M. P. J., Jhamai, Mila, Arp, Pascal, Metspalu, Andres, Milani, Lili, Kasela, Silva, Codd, Veryan, Peters, Annette, Herder, Christian, Waldenberger, Melanie, Roden, Michael, Zeilinger, Sonja, Illig, Thomas, Homuth, Georg, Grabe, Hans-Jörgen, Völzke, Henry, Steil, Leif, Kocher, Thomas, Murray, Anna, Melzer, David, Yaghootkar, Hanieh, Bandinelli, Stefania, Moses, Eric K., Kent, Jack W., Williams-Blangero, Sarah, Westra, Harm-Jan, McRae, Allan F., Smith, Jennifer A., Kardia, Sharon L. R., Hovatta, Iiris, Perola, Markus, Salomaa, Veikko, Henders, Anjali K., Martin, Nicholas G., Smith, Alicia K., Mehta, Divya, Binder, Elisabeth B., Nylocks, K Maria, Kennedy, Elizabeth M., Ding, Jingzhong, Suchy-Dicey, Astrid M., Enquobahrie, Daniel A., Brody, Jennifer, Rotter, Jerome I., Chen, Yii-Der I., Houwing-Duistermaat, Jeanine, Kloppenburg, Margreet, Slagboom, P. Eline, Helmer, Quinta, den Hollander, Wouter, Bean, Shannon, Raj, Towfique, Wang, Qiao Ping, Oyston, Lisa J., Tracy, Russell P., Montgomery, Grant W., Turner, Stephen T., Blangero, John, Meulenbelt, Ingrid, Ressler, Kerry J., Franke, Lude, Kettunen, Johannes, Visscher, Peter M., Neely, G. Gregory, Korstanje, Ron, Hanson, Robert L., Prokisch, Holger, Esko, Tonu, Teumer, Alexander, van Meurs, Joyce B. J., Johnson, Andrew D.

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Widespread sex differences in gene expression and splicing in the adult human brain by Trabzuni, Daniah, Ramasamy, Adaikalavan, Imran, Sabaena, Walker, Robert, Smith, Colin, Weale, Michael E., Hardy, John, Ryten, Mina

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Potential Health Risks from Uranium in Home Well Water: An Investigation by the Apsaalooke (Crow) Tribal Research Group by Eggers, Margaret, Moore-Nall, Anita, Doyle, John, Lefthand, Myra, Young, Sara, Bends, Ada, Committee, Crow, Camper, Anne

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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome by Storm, Catherine S., Kia, Demis A., Almramhi, Mona M., Bandres-Ciga, Sara, Finan, Chris, Hingorani, Aroon D., Wood, Nicholas W.

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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies by Broce, Iris, Karch, Celeste M, Wen, Natalie, Fan, Chun C, Wang, Yunpeng, Tan, Chin Hong, Kouri, Naomi, Ross, Owen A, Höglinger, Günter U, Muller, Ulrich, Hardy, John, Momeni, Parastoo, Hess, Christopher P, Dillon, William P, Miller, Zachary A, Bonham, Luke W, Rabinovici, Gil D, Rosen, Howard J, Schellenberg, Gerard D, Franke, Andre, Karlsen, Tom H, Veldink, Jan H, Ferrari, Raffaele, Yokoyama, Jennifer S, Miller, Bruce L, Andreassen, Ole A, Dale, Anders M, Desikan, Rahul S, Sugrue, Leo P

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The Impact of Internal Medicine Clerkship Characteristics and NBME Subject Exams on USMLE Step 2 Clinical Knowledge Exam Performance by Fitz, Matthew, Adams, William, Heincelman, Marc, Haist, Steve, Whelan, Karina, Cox, LeeAnn, Cao, Uyen-Thi, Hingle, Susan, Raff, Amanda, Houghton, Bruce, Fitzpatrick, Janet, Nall, Ryan, Foster, Jennifer, Appelbaum, Jonathan, Grum, Cyril, Donovan, Anna, Kiken, Stuart, Abraham, Reeni, Hlafka, Marti, Miller, Chad, Bansal, Saurabh, Paauw, Douglas, Lai, Cindy J, Pincavage, Amber, Agarwal, Gauri, Burns, Cynthia, Holzer, Horatio, Lappé, Katie, John, Viju, Barker, Blake, Mingioni, Nina, Rao, Deepti, Zakowski, Laura, Chakraborti, Chayan, Williams, Winter, Kelly, William

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MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study by Valentino, Rebecca R, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Real, Raquel, Mok, Kin, Christopher, Elizabeth A, Lee, Edward B, Frosch, Matthew P, Molina-Porcel, Laura, Gefen, Tamar, Robinson, Andrew C, Kobylecki, Christopher, Rowe, James B, Beach, Thomas G, Teich, Andrew F, Keith, Julia L, Bodi, Istvan, Gearing, Marla, Arzberger, Thomas, Morris, Christopher M, White, Charles L, Mechawar, Naguib, MacKenzie, Ian R, McLean, Catriona, Wang, Shih-Hsiu J, Nagra, Rashed M, Kovacs, Gabor G, Giaccone, Giorgio, Ang, Lee-Cyn, Morris, Huw R, Hardy, John A, Dickson, Dennis W, Ross, Owen A, Warner, Thomas T, Boeve, Bradley F, Duara, Ranjan, Josephs, Keith A, Murray, Melissa E, Lyons, Kelly E, Whitwell, Jennifer L, Miller, Bruce, Schlereth, Athena, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Aldecoa, Iban, Gelpi, Ellen, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Bigio, Eileen H, Weintraub, Sandra, Schneider, Julie A, Chang, Koping, Troncoso, Juan C, Jones, Matthew, Richardson, Anna, Roncaroli, Federico, Snowden, Julie, Serrano, Geidy E, Goldman, James E, Leskinen, Sandra P, Masellis, Mario, King, Andrew, Al-Sarraj, Safa, Troakes, Claire, Hodges, John R, Kril, Jillian J, Kwok, John B, Roeber, Sigrun, Attems, Johannes, Thomas, Alan J, Evers, Bret M., Bieniek, Kevin F, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, Castellani, Rudolph J, Chaffee, Ann, Franklin, Erin, Jacobsen, Max, Keene, Dirk, Latimer, Caitlin S, Purohit, Dushyant P, Schantz, Aimee, Walker, Jamie, De Deyn, Peter P, Duyckaerts, Charles, Seilhean, Danielle, Turbant-Leclere, Sabrina, Nennesmo, Inger, Riehl, James, Nacmias, Benedetta, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

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Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score by Iwaki, Hirotaka, Makarious, Mary B., Bandrés‐Ciga, Sara, Leonard, Hampton L., Gibbs, J. Raphael, Singleton, Andrew B., Middlehurst, Ben, Kia, Demis A, Houlden, Henry, Morris, Huw R, Plun‐Favreau, Helene, Quinn, John, Mok, Kin Y, Kinghorn, Kerri J., Wood, Nicholas W, Lewis, Patrick, Lovering, Ruth, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott‐Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Morrison, Karen E., Clarke, Carl, Brice, Alexis, Danjou, Fabrice, Lesage, Suzanne, Martinez, Maria, Simón‐Sánchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Gasser, Thomas, Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Craig, David W., Billingsley, Kimberley, Narendra, Derek, Raphael Gibbs, J, Shulman, Joshua M., Iwaki, Hirotaka, Leonard, Hampton L., Nalls, Mike A., Finkbeiner, Steven, Lungu, Codrin, Singleton, Andrew B, Gan‐Or, Ziv, Rouleau, Guy A., Krohn, Lynne, Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Barrero, Francisco Javier, Yarza, Jesús Alberto Bergareche, Bonilla‐Toribio, Marta, Boungiorno, María Teresa, Buiza‐Rueda, Dolores, Cámara, Ana, Carrillo, Fátima, Carrión‐Claro, Mario, Cerdan, Debora, Diez‐Fairen, Monica, Dols‐Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla‐Sevilla, Francisco, Feliz, Cici, Fernández, Manel, Gonzalez‐Aramburu, Isabel, Pagola, Ana Gorostidi, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Jimenez‐Escrig, Adriano, Kulisevsky, Jaime, Labrador‐Espinosa, Miguel A., Lopez‐Sendon, Jose Luis, Torres, Irene Martínez, Mir, Pablo, Rezola, Elisabet Mondragon, Periñán‐Tocino, Teresa, Ruiz‐Martínez, Javier, Ruz, Clara, Rodriguez, Antonio Sanchez, Tabernero, Cesar, Tartari, Juan Pablo, Tolosa, Eduard, Valldeoriola, Francesc, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Koks, Sulev, Siitonen, Ari, Kaiyrzhanov, Coordinator ‐ Rauan, Zharkinbekova, Nazira, Aitkulova, Akbota, Kaishybayeva, Gulnaz, Karimova, Altynay

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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight by Ahmed, Sarah, Jesús, Silvia, Méndez‐del‐Barrio, Carlota, Vargas‐González, Laura, Tartari, Juan Pablo, Mondragon, Elisabet, Vinagre‐Aragon, Ana, Dols‐Icardo, Oriol, Pascual‐Sedano, Berta, Ezquerra, Mario, Cámara, Ana, Compta, Yaroslau, Fernández, Manel, Sierra, María, Menéndez‐González, Manuel, García‐Ruiz, Pedro, Vela‐Desojo, Lydia, Barrero, Francisco Javier, Mínguez‐Castellanos, Adolfo, Cerdan, Debora, Gomez Heredia, Maria Jose, Feliz, Cici, Lopez‐Sendon, Jose Luis, Martínez Torres, Irene, Kim, Jonggeol Jeffrey, Botia, Juan A., Morrison, Karen E., Morris, Huw, Edsall, Connor, Vives, Francisco, Duran, Raquel, Hoenicka, Janet, Alvarez, Victoria, Marti, Maria José, Singleton, Andrew, Noyce, Alastair J, Holmans, Peter, Trabzuni, Daniah, Bras, Jose, Wood, Nicholas W, Guerreiro, Rita, Guelfi, Sebastian, Chelban, Viorica, Foltynie, Thomas, Morrison, Karen E., Brockmann, Kathrin, Gasser, Thomas, Cookson, Mark R, Blauwendraat, Cornelis, Craig, David W., Faghri, Faraz, Gibbs, J Raphael, Shulman, Joshua M., Leonard, Hampton L., Nalls, Mike A., Robak, Laurie, Lubbe, Steven, Mencacci, Niccolo E., Alcalay, Roy N., Krohn, Lynne, Aguilar, Miquel, Alvarez, Ignacio, Yarza, Jesús Alberto Bergareche, Blazquez, Marta, Botía, Juan A., Boungiorno, María Teresa, Buiza-Rueda, Dolores, Clarimón, Jordi, Casa, Beatríz, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Fernández, Manel, Heredia, Maria Jose Gomez, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Jimenez-Escrig, Adriano, Arregui, Adolfo López de Munain, Marín, Juan, Mata, Marina, Mínguez, Adolfo, Mir, Pablo, Pascual-Sedano, Berta, Pastor, Pau, Errazquin, Francisco Perez, Ruiz-Martínez, Javier, Rodriguez, Antonio Sanchez, Sierra, María, Suarez-Sanmartin, Esther, Tolosa, Eduard, Valldeoriola, Francesc, Vargas-González, Laura, Zimprich, Alexander, Taba, Pille, Dalgard, Clifton L., Adeleye, Adelani, Soltis, Anthony R., Bacikova, Dagmar, Wilkerson, Matthew D.

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Identification of sixteen novel candidate genes for late onset Parkinson's disease by Gialluisi, Alessandro, Reccia, Mafalda Giovanna, Modugno, Nicola, Nutile, Teresa, Lombardi, Alessia, Di Giovannantonio, Luca Giovanni, Pietracupa, Sara, Ruggiero, Daniela, Scala, Simona, Gambardella, Stefano, Iacoviello, Licia, Gianfrancesco, Fernando, Acampora, Dario, D'Esposito, Maurizio, Simeone, Antonio, Ciullo, Marina, Esposito, Teresa

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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases by Nalls, Mike A, Bras, Jose, Hernandez, Dena G, Keller, Margaux F, Majounie, Elisa, Renton, Alan E, Saad, Mohamad, Jansen, Iris, Guerreiro, Rita, Lubbe, Steven, Plagnol, Vincent, Gibbs, J. Raphael, Schulte, Claudia, Pankratz, Nathan, Sutherland, Margaret, Bertram, Lars, Lill, Christina M, DeStefano, Anita L, Faroud, Tatiana, Eriksson, Nicholas, Tung, Joyce Y, Edsall, Connor, Nichols, Noah, Brooks, Janet, Arepalli, Sampath, Pliner, Hannah, Letson, Chris, Heutink, Peter, Martinez, Maria, Gasser, Thomas, Traynor, Bryan J, Wood, Nick, Hardy, John, Singleton, Andrew B

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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia by Mishra, Aniket, Ferrari, Raffaele, Heutink, Peter, Hardy, John, Pijnenburg, Yolande, Posthuma, Danielle

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