Prevalence of autism spectrum disorders in China

por Cubells, Joseph F.
Publicado 2013

Substance Use Disorders Assessed Using the Kreek–McHugh–Schluger–Kellogg (KMSK) Scale in an Urban Low-Income and Predominantly African American Sample of Primary Care Patients...

por Tang, Yi-lang, Khoury, Lamya, Bradley, Bekh, Gillespie, Charles F, Ressler, Kerry J, Cubells, Joseph F
Publicado 2011

Adaptive behavior deficits in individuals with 3q29 deletion syndrome

por Pollak, Rebecca M, Burrell, T Lindsey, Cubells, Joseph F, Klaiman, Cheryl, Murphy, Melissa M, Saulnier, Celine A, Walker, Elaine F, White, Stormi Pulver, Mulle, Jennifer G
Publicado 2023

Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a multilevel approach to defining core disease processes

por Parker, David A., Cubells, Joseph F., Imes, Sid L., Ruban, Gabrielle A., Henshey, Brett T., Massa, Nicholas M., Walker, Elaine F., Duncan, Erica J., Ousley, Opal Y.
Publicado 2023

Polymorphisms in CRHR1 and the Serotonin Transporter Loci: Gene × Gene × Environment Interactions on Depressive Symptoms

por Ressler, Kerry J, Bradley, Bekh, Mercer, Kristina B, Deveau, Todd C, Smith, Alicia K, Gillespie, Charles F, Nemeroff, Charles B, Cubells, Joseph F, Binder, Elisabeth B
Publicado 2010

Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome

por Pollak, Rebecca M., Pincus, Jordan E., Burrell, T. Lindsey, Cubells, Joseph F., Klaiman, Cheryl, Murphy, Melissa M., Saulnier, Celine A., Walker, Elaine F., White, Stormi Pulver, Mulle, Jennifer G.
Publicado 2022

Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report

por Murphy, Melissa M., Burrell, T. Lindsey, Cubells, Joseph F., Epstein, Michael T., Espana, Roberto, Gambello, Michael J., Goines, Katrina, Klaiman, Cheryl, Koh, Sookyong, Russo, Rossana Sanchez, Saulnier, Celine A., Walker, Elaine, Mulle, Jennifer Gladys
Publicado 2020

Association of a Polymorphism in the Indoleamine-2,3-Dioxygenase Gene and Interferon-α-Induced Depression in Patients with Chronic Hepatitis C

por Smith, Alicia K., Simon, Jason S., Gustafson, Eric L., Noviello, Stephanie, Cubells, Joseph F., Epstein, Michael P., Devlin, David J., Qiu, Ping, Albrecht, Janice K., Brass, Clifford A., Sulkowski, Mark S., McHutchinson, John G., Miller, Andrew H.
Publicado 2011

Human Bacterial Artificial Chromosome (BAC) Transgenesis Fully Rescues Noradrenergic Function in Dopamine β-Hydroxylase Knockout Mice

por Cubells, Joseph F., Schroeder, Jason P., Barrie, Elizabeth S., Manvich, Daniel F., Sadee, Wolfgang, Berg, Tiina, Mercer, Kristina, Stowe, Taylor A., Liles, L. Cameron, Squires, Katherine E., Mezher, Andrew, Curtin, Patrick, Perdomo, Dannie L., Szot, Patricia, Weinshenker, David
Publicado 2016

Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome

por Murphy, Melissa M., Lindsey Burrell, T., Cubells, Joseph F., España, Roberto Antonio, Gambello, Michael J., Goines, Katrina C. B., Klaiman, Cheryl, Li, Longchuan, Novacek, Derek M., Papetti, Ava, Sanchez Russo, Rossana Lucia, Saulnier, Celine A., Shultz, Sarah, Walker, Elaine, Mulle, Jennifer Gladys
Publicado 2018

Predictors of remission in depression to individual and combined treatments (PReDICT): study protocol for a randomized controlled trial

por Dunlop, Boadie W, Binder, Elisabeth B, Cubells, Joseph F, Goodman, Mark M, Kelley, Mary E, Kinkead, Becky, Kutner, Michael, Nemeroff, Charles B, Newport, D Jeffrey, Owens, Michael J, Pace, Thaddeus W W, Ritchie, James C, Rivera, Vivianne Aponte, Westen, Drew, Craighead, W Edward, Mayberg, Helen S
Publicado 2012

Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care

por Sanchez Russo, Rossana, Gambello, Michael J., Murphy, Melissa M., Aberizk, Katrina, Black, Emily, Burrell, T. Lindsey, Carlock, Grace, Cubells, Joseph F., Epstein, Michael T., Espana, Roberto, Goines, Katrina, Guest, Ryan M., Klaiman, Cheryl, Koh, Sookyong, Leslie, Elizabeth J., Li, Longchuan, Novacek, Derek M., Saulnier, Celine A., Sefik, Esra, Shultz, Sarah, Walker, Elaine, White, Stormi Pulver, Mulle, Jennifer Gladys
Publicado 2021

An epigenetic clock for gestational age at birth based on blood methylation data

por Knight, Anna K., Craig, Jeffrey M., Theda, Christiane, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Hansen, Christine S., Hollegaard, Mads V., Hougaard, David M., Mortensen, Preben B., Weinsheimer, Shantel M., Werge, Thomas M., Brennan, Patricia A., Cubells, Joseph F., Newport, D. Jeffrey, Stowe, Zachary N., Cheong, Jeanie L. Y., Dalach, Philippa, Doyle, Lex W., Loke, Yuk J., Baccarelli, Andrea A., Just, Allan C., Wright, Robert O., Téllez-Rojo, Mara M., Svensson, Katherine, Trevisi, Letizia, Kennedy, Elizabeth M., Binder, Elisabeth B., Iurato, Stella, Czamara, Darina, Räikkönen, Katri, Lahti, Jari M. T., Pesonen, Anu-Katriina, Kajantie, Eero, Villa, Pia M., Laivuori, Hannele, Hämäläinen, Esa, Park, Hea Jin, Bailey, Lynn B., Parets, Sasha E., Kilaru, Varun, Menon, Ramkumar, Horvath, Steve, Bush, Nicole R., LeWinn, Kaja Z., Tylavsky, Frances A., Conneely, Karen N., Smith, Alicia K.
Publicado 2016

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

por Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A.S., Bearden, Carrie E., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J., Chopra, Pankaj, Cutler, David J., Duncan, Richard, Kotlar, Alex V., Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Holmans, Peter, Pardinas, Antonio, Walters, James T.R., Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J., Costain, Gregory A., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A.M.J, van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vergaelen, Elfi, Vogels, Annick, Crowley, T. Blaine, McGinn, Daniel E., Moss, Edward M., Sharkus, Robert J., Unolt, Marta, Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Moss, Hayley, Niarchou, Maria, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan G., Buzzanca, Antonio, Di Fabio, Fabio, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Schneider, Maude, Béna, Frédérique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, García-Miñaúr, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suñer, Damià H., Raventos-Simic, Jasna, Epstein, Michael P., Williams, Nigel M., Bassett, Anne S.
Publicado 2020