PAPA-1 Is a Nuclear Binding Partner of IGFBP-2 and Modulates Its Growth-Promoting Actions

Por Miyako, Kenichi, Cobb, Laura J., Francis, Malik, Huang, Alden, Peng, Bonnie, Pintar, John E., Ariga, Hiroyoshi, Cohen, Pinchas
Publicado em 2009

Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder

Por Jalbrzikowski, Maria, Lazaro, Maria T., Gao, Fuying, Huang, Alden, Chow, Carolyn, Geschwind, Daniel H., Coppola, Giovanni, Bearden, Carrie E.
Publicado no PLoS One (2015)

Mutations In Rare Ataxia Genes Are Uncommon Causes of Sporadic Cerebellar Ataxia

Por Fogel, Brent L., Lee, Ji Yong, Lane, Jessica, Wahnich, Amanda, Chan, Sandy, Huang, Alden, Osborn, Greg E., Klein, Eric, Mamah, Catherine, Perlman, Susan, Geschwind, Daniel H., Coppola, Giovanni
Publicado em 2012

Disseminated Coccidioidomycosis Treated with Interferon-γ and Dupilumab.

Por Tsai, Monica, Thauland, Timothy J., Huang, Alden Y., Bun, Chantana, Fitzwater, Sean, Krogstad, Paul, Douine, Emilie D., Nelson, Stanley F., Lee, Hane, Garcia-Lloret, Maria I., Butte, Manish J.
Publicado no N Engl J Med (2020)

Activity-Dependent Regulation of Alternative Cleavage and Polyadenylation During Hippocampal Long-Term Potentiation

Por Fontes, Mariana M., Guvenek, Aysegul, Kawaguchi, Riki, Zheng, Dinghai, Huang, Alden, Ho, Victoria M., Chen, Patrick B., Liu, Xiaochuan, O’Dell, Thomas J., Coppola, Giovanni, Tian, Bin, Martin, Kelsey C.
Publicado no Sci Rep (2017)

Neurodegenerative disease biomarkers Aβ(1–40), Aβ(1–42), tau, and p‐tau(181) in the vervet monkey cerebrospinal fluid: Relation to normal aging, genetic influences, and cerebral am...

Por Chen, Jason A., Fears, Scott C., Jasinska, Anna J., Huang, Alden, Al‐Sharif, Noor B., Scheibel, Kevin E., Dyer, Thomas D., Fagan, Anne M., Blangero, John, Woods, Roger, Jorgensen, Matthew J., Kaplan, Jay R., Freimer, Nelson B., Coppola, Giovanni
Publicado no Brain Behav (2018)

Genetic screen in a large series of patients with primary progressive aphasia

Por 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
Publicado no Alzheimers Dement (2019)

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

Por Willsey, A. Jeremy, Fernandez, Thomas V., Yu, Dongmei, King, Robert A., Dietrich, Andrea, Xing, Jinchuan, Sanders, Stephan J., Mandell, Jeffrey D., Huang, Alden Y., Richer, Petra, Smith, Louw, Dong, Shan, Samocha, Kaitlin E., Neale, Benjamin M., Coppola, Giovanni, Mathews, Carol A., Tischfield, Jay A., Scharf, Jeremiah M., State, Matthew W., Heiman, Gary A.
Publicado no Neuron (2017)

Familial Cortical Myoclonus with a Mutation in NOL3

Por Russell, Jonathan F., Steckley, Jamie L., Coppola, Giovanni, Hahn, Angelika F.G., Howard, MacKenzie A., Kornberg, Zachary, Huang, Alden, Mirsattari, Seyed M., Merriman, Barry, Klein, Eric, Choi, Murim, Lee, Hsien-Yang, Kirk, Andrew, Nelson-Williams, Carol, Gibson, Gillian, Baraban, Scott C., Lifton, Richard P., Geschwind, Daniel H., Fu, Ying-Hui, Ptáček, Louis J.
Publicado em 2012

Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

Por Chen, Jason A., Chen, Zhongbo, Won, Hyejung, Huang, Alden Y., Lowe, Jennifer K., Wojta, Kevin, Yokoyama, Jennifer S., Bensimon, Gilbert, Leigh, P. Nigel, Payan, Christine, Shatunov, Aleksey, Jones, Ashley R., Lewis, Cathryn M., Deloukas, Panagiotis, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-Francois, Ludolph, Albert, Boxer, Adam L., Bronstein, Jeff M., Al-Chalabi, Ammar, Geschwind, Daniel H., Coppola, Giovanni
Publicado no Mol Neurodegener (2018)

Frontotemporal dementia spectrum: first genetic screen in a Greek cohort

Por 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
Publicado no Neurobiol Aging (2018)

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Por Wang, Sheng, Mandell, Jeffrey D., Kumar, Yogesh, Sun, Nawei, Morris, Montana T., Arbelaez, Juan, Nasello, Cara, Dong, Shan, Duhn, Clif, Zhao, Xin, Yang, Zhiyu, Padmanabhuni, Shanmukha S., Yu, Dongmei, King, Robert A., Dietrich, Andrea, Khalifa, Najah, Dahl, Niklas, Huang, Alden Y., Neale, Benjamin M., Coppola, Giovanni, Mathews, Carol A., Fernandez, Thomas V., Buxbaum, Joseph D., De Rubeis, Silvia, Grice, Dorothy E., Xing, Jinchuan, Heiman, Gary A., Tischfield, Jay A., Paschou, Peristera, Willsey, A. Jeremy, State, Matthew W.
Publicado no Cell Rep (2018)

Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

Por Lee, Hane, Huang, Alden Y., Wang, Lee-kai, Yoon, Amanda J., Renteria, Genecee, Eskin, Ascia, Signer, Rebecca H., Dorrani, Naghmeh, Nieves-Rodriguez, Shirley, Wan, Jijun, Douine, Emilie D., Woods, Jeremy D., Dell’Angelica, Esteban C., Fogel, Brent L., Martin, Martin G., Butte, Manish J., Parker, Neil H., Wang, Richard T., Shieh, Perry B., Wong, Derek A., Gallant, Natalie, Singh, Kathryn E., Asher, Y. Jane Tavyev, Sinsheimer, Janet S., Krakow, Deborah, Loo, Sandra K., Allard, Patrick, Papp, Jeanette C., Palmer, Christina G. S., Martinez-Agosto, Julian A., Nelson, Stanley F.
Publicado no Genet Med (2019)

A Multiancestral Genome-Wide Exome Array Study of Alzheimer Disease, Frontotemporal Dementia, and Progressive Supranuclear Palsy

Por Chen, Jason A., Wang, Qing, Davis-Turak, Jeremy, Li, Yun, Karydas, Anna M., Hsu, Sandy C., Sears, Renee L., Chatzopoulou, Doxa, Huang, Alden Y., Wojta, Kevin J., Klein, Eric, Lee, Jason, Beekly, Duane L., Boxer, Adam, Faber, Kelley M., Haase, Claudia M., Miller, Josh, Poon, Wayne W., Rosen, Ami, Rosen, Howard, Sapozhnikova, Anna, Shapira, Jill, Varpetian, Arousiak, Foroud, Tatiana M., Levenson, Robert W., Levey, Allan I., Kukull, Walter A., Mendez, Mario F., Ringman, John, Chui, Helena, Cotman, Carl, DeCarli, Charles, Miller, Bruce L., Geschwind, Daniel H., Coppola, Giovanni
Publicado no JAMA Neurol (2015)

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

Por Sul, Jae Hoon, Service, Susan K., Huang, Alden Y., Ramensky, Vasily, Hwang, Sun-Goo, Teshiba, Terri M., Park, YoungJun, Ori, Anil P. S., Zhang, Zhongyang, Mullins, Niamh, Olde Loohuis, Loes M., Fears, Scott C., Araya, Carmen, Araya, Xinia, Spesny, Mitzi, Bejarano, Julio, Ramirez, Margarita, Castrillón, Gabriel, Gomez-Makhinson, Juliana, Lopez, Maria C., Montoya, Gabriel, Montoya, Claudia P., Aldana, Ileana, Escobar, Javier I., Ospina-Duque, Jorge, Kremeyer, Barbara, Bedoya, Gabriel, Ruiz-Linares, Andres, Cantor, Rita M., Molina, Julio, Coppola, Giovanni, Ophoff, Roel A., Macaya, Gabriel, Lopez-Jaramillo, Carlos, Reus, Victor, Bearden, Carrie E., Sabatti, Chiara, Freimer, Nelson B.
Publicado no Transl Psychiatry (2020)

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

Por Hsu, Sandy Chan, Sears, Renee L., Lemos, Roberta R., Quintáns, Beatriz, Huang, Alden, Spiteri, Elizabeth, Nevarez, Lisette, Mamah, Catherine, Zatz, Mayana, Pierce, Kerrie D., Fullerton, Janice M., Adair, John C., Berner, Jon E., Bower, Matthew, Brodaty, Henry, Carmona, Olga, Dobricić, Valerija, Fogel, Brent L., García-Estevez, Daniel, Goldman, Jill, Goudreau, John L., Hopfer, Suellen, Janković, Milena, Jaumà, Serge, Jen, Joanna C., Kirdlarp, Suppachok, Klepper, Joerg, Kostić, Vladimir, Lang, Anthony E., Linglart, Agnès, Maisenbacher, Melissa K., Manyam, Bala V., Mazzoni, Pietro, Miedzybrodzka, Zofia, Mitarnun, Witoon, Mitchell, Philip B., Mueller, Jennifer, Novaković, Ivana, Paucar, Martin, Paulson, Henry, Simpson, Sheila A., Svenningsson, Per, Tuite, Paul, Vitek, Jerrold, Wetchaphanphesat, Suppachok, Williams, Charles, Yang, Michele, Schofield, Peter R., de Oliveira, João R. M., Sobrido, María-Jesús, Geschwind, Daniel H., Coppola, Giovanni
Publicado em 2013

Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

Por Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Muller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott, Pato, Carlos N., Pato, Michele T., Knowles, James A, Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M., Coppola, Giovanni
Publicado no Neuron (2017)

GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder

Por Shieh, Christine, Jones, Natasha, Vanle, Brigitte, Au, Margaret, Huang, Alden Y., Silva, Ana P.G., Lee, Hane, Douine, Emilie D., Otero, Maria G., Choi, Andrew, Grand, Katheryn, Taff, Ingrid P., Delgado, Mauricio R., Hajianpour, MJ, Seeley, Andrea, Rohena, Luis, Vernon, Hilary, Gripp, Karen W., Vergano, Samantha A., Mahida, Sonal, Naidu, Sakkubai, Sousa, Ana Berta, Wain, Karen E., Challman, Thomas D., Beek, Geoffrey, Basel, Donald, Ranells, Judith, Smith, Rosemarie, Yusupov, Roman, Freckmann, Mary-Louise, Ohden, Lisa, Davis-Keppen, Laura, Chitayat, David, Dowling, James J., Finkel, Richard, Dauber, Andrew, Spillmann, Rebecca, Pena, Loren D.M., Metcalfe, Kay, Splitt, Miranda, Lachlan, Katherine, McKee, Shane A., Hurst, Jane, Fitzpatrick, David R., Morton, Jenny E.V., Cox, Helen, Venkateswaran, Sunita, Young, Juan I., Marsh, Eric D., Nelson, Stanley F., Martinez, Julian A., Graham, John M., Kini, Usha, Mackay, Joel P., Pierson, Tyler Mark
Publicado no Genet Med (2020)

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

Por Ramos, Eliana Marisa, Dokuru, Deepika Reddy, Van Berlo, Victoria, Wojta, Kevin, Wang, Qing, Huang, Alden Y., Deverasetty, Sandeep, Qin, Yue, van 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
Publicado no Alzheimers Dement (2020)

Synaptic processes and immune-related pathways implicated in Tourette syndrome

Por Tsetsos, Fotis, Yu, Dongmei, Sul, Jae Hoon, Huang, Alden Y., Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Muller-Vahl, Kirsten R., Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy A., Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L., Grados, Marco A., Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Rizzo, Renata, Lyon, Gholson J., McMahon, William M., Batterson, James R., Cath, Danielle C., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Dietrich, Andrea, Hoekstra, Pieter J., Kuperman, Samuel, Zinner, Samuel H., Wagner, Michael, Knowles, James A., Jeremy Willsey, A., Tischfield, Jay A., Heiman, Gary A., Cox, Nancy J., Freimer, Nelson B., Neale, Benjamin M., Davis, Lea K., Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Paschou, Peristera, Barr, Cathy L., Batterson, James R., Berlin, Cheston, Budman, Cathy L., Cath, Danielle C., Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Davis, Lea K., Dion, Yves, Freimer, Nelson B., Grados, Marco A., Greenberg, Erica, Hirschtritt, Matthew E., Huang, Alden Y., Illmann, Cornelia, King, Robert A., Kurlan, Roger, Leckman, James F., Lyon, Gholson J., Malaty, Irene A., Mathews, Carol A., McMahon, William M., Neale, Benjamin M., Okun, Michael S., Osiecki, Lisa, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Scharf, Jeremiah M., Singer, Harvey S., Smit, Jan H., Sul, Jae Hoon, Yu, Dongmei, Aschauer, Harald Aschauer Harald, Barta, Csaba, Budman, Cathy L., Cath, Danielle C., Depienne, Christel, Hartmann, Andreas, Hebebrand, Johannes, Konstantinidis, Anastasios, Mathews, Carol A., Müller-Vahl, Kirsten, Nagy, Peter, Nöthen, Markus M., Paschou, Peristera, Rizzo, Renata, Rouleau, Guy A., Sandor, Paul, Scharf, Jeremiah M., Schlögelhofer, Monika, Stamenkovic, Mara, Stuhrmann, Manfred, Tsetsos, Fotis, Tarnok, Zsanett, Wolanczyk, Tomasz, Worbe, Yulia, Brown, Lawrence, Cheon, Keun-Ah, Coffey, Barbara J., Dietrich, Andrea, Fernandez, Thomas V., Garcia-Delgar, Blanca, Gilbert, Donald, Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hoekstra, Pieter J., Huyser, Chaim, Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett L., Madruga-Garrido, Marcos, Mir, Pablo, Morer, Astrid, Münchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Tischfield, Jay A., Willsey, A. Jeremy, Zinner, Samuel, Aschauer, Harald, Barr, Cathy L., Barta, Csaba, Batterson, James R., Berlin, Cheston, Brown, Lawrence, Budman, Cathy L., Cath, Danielle C., Coffey, Barbara J., Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Davis, Lea K., Depienne, Christel, Dietrich, Andrea, Dion, Yves, Fernandez, Thomas, Freimer, Nelson B., Gilbert, Donald, Grados, Marco A., Greenberg, Erica, Hartmann, Andreas, Hebebrand, Johannes, Heiman, Gary, Hirschtritt, Matthew E., Hoekstra, Pieter, Huang, Alden Y., Illmann, Cornelia, Jankovic, Joseph, King, Robert A., Kuperman, Samuel, Lee, Paul C., Lyon, Gholson J., Malaty, Irene A., Mathews, Carol A., McMahon, William M., Müller-Vahl, Kirsten, Nagy, Peter, Neale, Benjamin M., Nöthen, Markus M., Okun, Michael S., Osiecki, Lisa, Paschou, Peristera, Rizzo, Renata, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Scharf, Jeremiah M., Schlögelhofer, Monika, Singer, Harvey S., Stamenkovic, Mara, Stuhrmann, Manfred, Sul, Jae Hoon, Tarnok, Zsanett, Tischfield, Jay, Tsetsos, Fotis, Willsey, A. Jeremy, Woods, Douglas, Worbe, Yulia, Yu, Dongmei, Zinner, Samuel
Publicado no Transl Psychiatry (2021)