Dopamine receptor D4 (DRD) polymorphisms with reduced functional potency intensify atrophy in syndrome-specific sites of frontotemporal dementia von Butler, P.M., Chiong, W., Perry, D.C., Miller, Z.A., Gennatas, E.D., Brown, J.A., Pasquini, L., Karydas, A., Dokuru, D., Coppola, G., Sturm, V.E., Boxer, A.L., Gorno-Tempini, M.L., Rosen, H.J., Kramer, J.H., Miller, B.L., Seeley, W.W.

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Dopamine receptor D 4 (DRD 4 ) polymorphisms with reduced functional potency intensify atrophy in syndrome-specific sites of frontotemporal dementia von Butler, P M, Chiong, W, Perry, D C, Miller, Z A, Gennatas, E D, Brown, J A, Pasquini, L, Karydas, A, Dokuru, D, Coppola, G, Sturm, V E, Boxer, A L, Gorno-Tempini, M L, Rosen, H J, Kramer, J H, Miller, B L, Seeley, W W

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Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia von Geier, Ethan G., Bourdenx, Mathieu, Storm, Nadia J., Cochran, J. Nicholas, Sirkis, Daniel W., Hwang, Ji-Hye, Bonham, Luke W., Ramos, Eliana Marisa, Diaz, Antonio, Van Berlo, Victoria, Dokuru, Deepika, Nana, Alissa L., Karydas, Anna, Balestra, Maureen E., Huang, Yadong, Russo, Silvia P., Spina, Salvatore, Grinberg, Lea T., Seeley, William W., Myers, Richard M., Miller, Bruce L., Coppola, Giovanni, Lee, Suzee E., Cuervo, Ana Maria, Yokoyama, Jennifer S.

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Exploring Relationships Between Internalizing Problems and Risky Sexual Behavior: A Twin Study von Paulich, Katie N., Freis, Samantha M., Dokuru, Deepika R., Alexander, Jordan D., Vrieze, Scott I., Corley, Robin P., McGue, Matt, Hewitt, John K., Stallings, Michael C.

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Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers von Lee, Suzee E, Sias, Ana C, Mandelli, Maria Luisa, Brown, Jesse A, Brown, Alainna B, Khazenzon, Anna M, Vidovszky, Anna A, Zanto, Theodore P, Karydas, Anna M, Pribadi, Mochtar, Dokuru, Deepika, Coppola, Giovanni, Geschwind, Dan H, Rademakers, Rosa, Gorno-Tempini, Maria Luisa, Rosen, Howard J, Miller, Bruce L, Seeley, William W

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Neurodegenerative Disease Caregivers’ 5-HTTLPR Genotype Moderates the Effect of Patients’ Empathic Accuracy Deficits on Caregivers’ Well-Being von Wells, Jenna L., Brown, Casey L., Hua, Alice Y., Soyster, Peter D., Chen, Kuan-Hua, Dokuru, Deepika R., Coppola, Giovanni, Haase, Claudia M., Levenson, Robert W.

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South Asia: The Missing Diverse in Diversity von Dokuru, Deepika R., Horwitz, Tanya B., Freis, Samantha M., Stallings, Michael C., Ehringer, Marissa A.

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Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family von Ramos, Eliana Marisa, Roca, Alessandro, Chumchim, Noravit, Dokuru, Deepika Reddy, Van Berlo, Victoria, De Michele, Giovanna, Lieto, Maria, Tedeschi, Enrico, De Michele, Giuseppe, Coppola, Giovanni

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A Quantitative Kinetic Study of Polysorbate Autoxidation: The Role of Unsaturated Fatty Acid Ester Substituents von Yao, Jia, Dokuru, Dushyanth K., Noestheden, Matthew, Park, SungAe S., Kerwin, Bruce A., Jona, Janan, Ostovic, Drazen, Reid, Darren L.

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Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases von Ramos, Eliana Marisa, Dokuru, Deepika Reddy, Van Berlo, Victoria, Wojta, Kevin, Wang, Qing, Huang, Alden Y., Deverasetty, Sandeep, Qin, Yue, Blitterswijk, Marka, Jackson, Jazmyne, Appleby, Brian, Bordelon, Yvette, Brannelly, Patrick, Brushaber, Danielle E., Dickerson, Bradford, Dickinson, Susan, Domoto‐Reilly, Kimiko, Faber, Kelley, Fields, Julie, Fong, Jamie, Foroud, Tatiana, Forsberg, Leah K., Gavrilova, Ralitza, Ghoshal, Nupur, Goldman, Jill, Graff‐Radford, Jonathan, Graff‐Radford, Neill, Grant, Ian, Grossman, Murray, Heuer, Hilary W., Hsiung, Ging‐Yuek R., Huey, Edward, Irwin, David, Kantarci, Kejal, Karydas, Anna, Kaufer, Daniel, Kerwin, Diana, Knopman, David, Kornak, John, Kramer, Joel H., Kremers, Walter, Kukull, Walter, Litvan, Irene, Ljubenkov, Peter, Lungu, Codrin, Mackenzie, Ian, Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi, Pantelyat, Alexander, Pearlman, Rodney, Petrucelli, Len, Potter, Madeline, Rankin, Katherine P., Rascovsky, Katya, Roberson, Erik D., Rogalski, Emily, Shaw, Leslie, Syrjanen, Jeremy, Tartaglia, Maria Carmela, Tatton, Nadine, Taylor, Joanne, Toga, Arthur, Trojanowski, John Q., Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew, Rademakers, Rosa, Boeve, Brad F., Rosen, Howard J., Boxer, Adam L., Coppola, Giovanni

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Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich's ataxia patients von Nachun, Daniel, Gao, Fuying, Isaacs, Charles, Strawser, Cassandra, Yang, Zhongan, Dokuru, Deepika, Van Berlo, Victoria, Sears, Renee, Farmer, Jennifer, Perlman, Susan, Lynch, David R, Coppola, Giovanni

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Frontotemporal dementia spectrum: first genetic screen in a Greek cohort von Ramos, Eliana Marisa, Koros, Christos, Dokuru, Deepika Reddy, Van Berlo, Victoria, Kroupis, Christos, Wojta, Kevin, Wang, Qing, Andronas, Nikolaos, Matsi, Stavroula, Beratis, Ion N., Huang, Alden Y., Lee, Suzee E., Bonakis, Anastasios, Florou-Hatziyiannidou, Chryseis, Fragkiadaki, Stella, Kontaxopoulou, Dionysia, Agiomyrgiannakis, Dimitrios, Kamtsadeli, Vasiliki, Tsinia, Niki, Papastefanopoulou, Vasiliki, Stamelou, Maria, Miller, Bruce L., Stefanis, Leonidas, Papatriantafyllou, John D., Papageorgiou, Sokratis G., Coppola, Giovanni

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Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression von Lin, Amy, Forsyth, Jennifer K., Hoftman, Gil D., Kushan-Wells, Leila, Jalbrzikowski, Maria, Dokuru, Deepika, Coppola, Giovanni, Fiksinski, Ania, Zinkstok, Janneke, Vorstman, Jacob, Nachun, Daniel, Bearden, Carrie E.

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Genetic screen in a large series of patients with primary progressive aphasia von Ramos, Eliana Marisa, Dokuru, Deepika Reddy, Van Berlo, Victoria, Wojta, Kevin, Wang, Qing, Huang, Alden Y., Miller, Zachary A., Karydas, Anna M., Bigio, Eileen H., Rogalski, Emily, Weintraub, Sandra, Rader, Benjamin, Miller, Bruce L., Gorno-Tempini, Maria Luisa, Mesulam, Marek-Marsel, Coppola, Giovanni

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Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia von Olney, Nicholas T., Alquezar, Carolina, Ramos, Eliana Marisa, Nana, Alissa L., Fong, Jamie C., Karydas, Anna M., Taylor, Joanne B., Stephens, Melanie L., Argouarch, Andrea R., Van Berlo, Victoria A., Dokuru, Deepika R., Sherr, Elliott H., Jicha, Gregory A., Dillon, William P., Desikan, Rahul S., De May, Mary, Seeley, William W., Coppola, Giovanni, Miller, Bruce L., Kao, Aimee W.

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Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression von Lin, Amy, Forsyth, Jennifer K, Hoftman, Gil D, Kushan-Wells, Leila, Jalbrzikowski, Maria, Dokuru, Deepika, Coppola, Giovanni, Fiksinski, Ania, Zinkstok, Janneke, Vorstman, Jacob, Nachun, Daniel, Bearden, Carrie E

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Historical Migration revealed through a Case of Autosomal Dominant Alzheimer's Disease von Poblete, JoAnna, Dokuru, Deepika, Coppola, Giovanni, Ortiz, Freddy, Medina, Luis D, Vinters, Harry V, Ringman, John M

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Progranulin levels in blood in Alzheimer's disease and mild cognitive impairment von Cooper, Yonatan A., Nachun, Daniel, Dokuru, Deepika, Yang, Zhongan, Karydas, Anna M., Serrero, Ginette, Yue, Binbin, Boxer, Adam L., Miller, Bruce L., Coppola, Giovanni

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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects von Howe, Laurence J, Nivard, Michel G, Morris, Tim T, Hansen, Ailin F, Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A, van der Zee, Matthijs D, Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M, Bielak, Lawrence F, Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A, Reynolds, Chandra A, Balbona, Jared V, Andreassen, Ole A, Ask, Helga, Baras, Aris, Bauer, Christopher R, Boomsma, Dorret I, Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth, Dahm, Christina C, Dokuru, Deepika R, Evans, Luke M, de Geus, Eco JC, Giddaluru, Sudheer, Gordon, Scott D, Harden, K Paige, Hill, W David, Hughes, Amanda, Kerr, Shona M, Kim, Yongkang, Kweon, Hyeokmoon, Latvala, Antti, Lawlor, Deborah A, Li, Liming, Lin, Kuang, Magnus, Per, Magnusson, Patrik KE, Mallard, Travis T, Martikainen, Pekka, Mills, Melinda C, Njølstad, Pål Rasmus, Overton, John D, Pedersen, Nancy L, Porteous, David J, Reid, Jeffrey, Silventoinen, Karri, Southey, Melissa C, Stoltenberg, Camilla, Tucker-Drob, Elliot M, Social Science Genetic Association Consortium, Within Family Consortium, Hewitt, John K, Keller, Matthew C, Stallings, Michael C, Lee, James J, Christensen, Kaare, Kardia, Sharon LR, Peyser, Patricia A, Smith, Jennifer A, Wilson, James F, Hopper, John L, Hägg, Sara, Spector, Tim D, Pingault, Jean-Baptiste, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G, Oskarsson, Sven, Justice, Anne E, Millwood, Iona Y, Hveem, Kristian, Naess, Øyvind, Willer, Cristen J, Åsvold, Bjørn Olav, Koellinger, Philipp D, Kaprio, Jaakko, Medland, Sarah E, Walters, Robin G, Benjamin, Daniel J, Turley, Patrick, Evans, David M, Davey Smith, George, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil M

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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects von Howe, Laurence J, Nivard, Michel G, Morris, Tim T, Hansen, Ailin F, Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A, van der Zee, Matthijs D, Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M, Bielak, Lawrence F, Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A, Reynolds, Chandra A, Balbona, Jared V, Andreassen, Ole A, Ask, Helga, Baras, Aris, Bauer, Christopher R, Boomsma, Dorret I, Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth, Dahm, Christina C, Dokuru, Deepika R, Evans, Luke M, de Geus, Eco JC, Giddaluru, Sudheer, Gordon, Scott D, Harden, K Paige, Hill, W David, Hughes, Amanda, Kerr, Shona M, Kim, Yongkang, Kweon, Hyeokmoon, Latvala, Antti, Lawlor, Deborah A, Li, Liming, Lin, Kuang, Magnus, Per, Magnusson, Patrik KE, Mallard, Travis T, Martikainen, Pekka, Mills, Melinda C, Njølstad, Pål Rasmus, Overton, John D, Pedersen, Nancy L, Porteous, David J, Reid, Jeffrey, Silventoinen, Karri, Southey, Melissa C, Stoltenberg, Camilla, Tucker-Drob, Elliot M, Social Science Genetic Association Consortium, Within Family Consortium, Hewitt, John K, Keller, Matthew C, Stallings, Michael C, Lee, James J, Christensen, Kaare, Kardia, Sharon LR, Peyser, Patricia A, Smith, Jennifer A, Wilson, James F, Hopper, John L, Hägg, Sara, Spector, Tim D, Pingault, Jean-Baptiste, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G, Oskarsson, Sven, Justice, Anne E, Millwood, Iona Y, Hveem, Kristian, Naess, Øyvind, Willer, Cristen J, Åsvold, Bjørn Olav, Koellinger, Philipp D, Kaprio, Jaakko, Medland, Sarah E, Walters, Robin G, Benjamin, Daniel J, Turley, Patrick, Evans, David M, Davey Smith, George, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil M

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