Genetics of Obsessive-Compulsive Disorder and Related Disorders

Por Browne, Heidi A., Gair, Shannon L., Scharf, Jeremiah M., Grice, Dorothy E.
Publicado em 2014

Diagnostic validity of early-onset obsessive-compulsive disorder in the Danish Psychiatric Central Register: findings from a cohort sample

Por Nissen, Judith, Powell, Shelagh, Koch, Susanne V, Crowley, James J, Matthiesen, Manuel, Grice, Dorothy E, Thomsen, Per H, Parner, E
Publicado no BMJ Open (2017)

Transcriptional profiling of C57 and DBA strains of mice in the absence and presence of morphine

Por Grice, Dorothy E, Reenilä, Ilkka, Männistö, Pekka T, Brooks, Andrew I, Smith, George G, Golden, Greg T, Buxbaum, Joseph D, Berrettini, Wade H
Publicado em 2007

Identification of five mouse μ-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon

Por Doyle, Glenn A., Sheng, X. Rebecca, Lin, Sharon S.J., Press, Danielle M., Grice, Dorothy E., Buono, Russell J., Ferraro, Thomas N., Berrettini, Wade H.
Publicado em 2007

Characterization of SLITRK1 Variation in Obsessive-Compulsive Disorder

Por Ozomaro, Uzoezi, Cai, Guiqing, Kajiwara, Yuji, Yoon, Seungtai, Makarov, Vladimir, Delorme, Richard, Betancur, Catalina, Ruhrmann, Stephan, Falkai, Peter, Grabe, Hans Jörgen, Maier, Wolfgang, Wagner, Michael, Lennertz, Leonhard, Moessner, Rainald, Murphy, Dennis L., Buxbaum, Joseph D., Züchner, Stephan, Grice, Dorothy E.
Publicado em 2013

Common genetic variants, acting additively, are a major source of risk for autism

Por Klei Lambertus, Sanders Stephan J, Murtha Michael T, Hus Vanessa, Lowe Jennifer K, Willsey A, Moreno-De-Luca Daniel, Yu Timothy W, Fombonne Eric, Geschwind Daniel, Grice Dorothy E, Ledbetter David H, Lord Catherine, Mane Shrikant M, Martin Christa, Martin Donna M, Morrow Eric M, Walsh Christopher A, Melhem Nadine M, Chaste Pauline, Sutcliffe James S, State Matthew W, Cook Edwin H, Roeder Kathryn, Devlin Bernie
Publicado em 2012-10-01

Common genetic variants, acting additively, are a major source of risk for autism

Por Klei, Lambertus, Sanders, Stephan J, Murtha, Michael T, Hus, Vanessa, Lowe, Jennifer K, Willsey, A Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E, Ledbetter, David H, Lord, Catherine, Mane, Shrikant M, Martin, Christa Lese, Martin, Donna M, Morrow, Eric M, Walsh, Christopher A, Melhem, Nadine M, Chaste, Pauline, Sutcliffe, James S, State, Matthew W, Cook, Edwin H, Roeder, Kathryn, Devlin, Bernie
Publicado em 2012

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

Por Chaste, Pauline, Klei, Lambertus, Sanders, Stephan J., Murtha, Michael T., Hus, Vanessa, Lowe, Jennifer K., Willsey, A. Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W., Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E., Ledbetter, David H., Lord, Catherine, Mane, Shrikant M., Martin, Christa Lese, Martin, Donna M., Morrow, Eric M., Walsh, Christopher A., Sutcliffe, James S., State, Matthew W., Devlin, Bernie, Cook, Edwin H., Kim, Soo-Jeong
Publicado em 2013

A genomewide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

Por Chaste, Pauline, Klei, Lambertus, Sanders, Stephan J., Hus, Vanessa, Murtha, Michael T., Lowe, Jennifer K., Willsey, A. Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W., Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E., Ledbetter, David H., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Walsh, Christopher A., Sutcliffe, James S., Martin, Christa Lese, Beaudet, Arthur L., Lord, Catherine, State, Matthew W., Cook, Edwin H., Devlin, Bernie
Publicado no Biol Psychiatry (2014)

Genomewide Linkage Analyses of Bipolar Disorder: A New Sample of 250 Pedigrees from the National Institute of Mental Health Genetics Initiative

Por Dick, Danielle M., Foroud, Tatiana, Flury, Leah, Bowman, Elizabeth S., Miller, Marvin J., Rau, N. Leela, Moe, P. Ryan, Samavedy, Nalini, El-Mallakh, Rif, Manji, Husseini, Glitz, Debra A., Meyer, Eric T., Smiley, Carrie, Hahn, Rhoda, Widmark, Clifford, McKinney, Rebecca, Sutton, Laura, Ballas, Christos, Grice, Dorothy, Berrettini, Wade, Byerley, William, Coryell, William, DePaulo, Raymond, MacKinnon, Dean F., Gershon, Elliot S., Kelsoe, John R., McMahon, Francis J., McInnis, Melvin, Murphy, Dennis L., Reich, Theodore, Scheftner, William, Nurnberger Jr., John I.
Publicado em 2003

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

Por Abdulkadir, Mohamed, Londono, Douglas, Gordon, Derek, Fernandez, Thomas V., Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Elzerman, Lonneke, Fremer, Carolin, Fründt, Odette, Garcia-Delgar, Blanca, Gilbert, Donald L., Grice, Dorothy E., Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Ibanez-Gomez, Laura, Jakubovski, Ewgeni, Kim, Young Key, Kim, Young Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett, Ludolph, Andrea G., Madruga-Garrido, Marcos, Maras, Athanasios, Mir, Pablo, Morer, Astrid, Müller-Vahl, Kirsten, Münchau, Alexander, Murphy, Tara L., Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Tübing, Jennifer, van den Ban, Els, Visscher, Frank, Wanderer, Sina, Woods, Martin, Zinner, Samuel H., King, Robert A., Tischfield, Jay A., Heiman, Gary A., Hoekstra, Pieter J., Dietrich, Andrea
Publicado no Eur Arch Psychiatry Clin Neurosci (2017)

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Por Sanders, Stephan J., He, Xin, Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, Samocha, Kaitlin E., Cicek, A. Ercument, Murtha, Michael T., Bal, Vanessa H., Bishop, Somer L., Dong, Shan, Goldberg, Arthur P., Jinlu, Cai, Keaney, John F., Klei, Lambertus, Mandell, Jeffrey D., Moreno-De-Luca, Daniel, Poultney, Christopher S., Robinson, Elise B., Smith, Louw, Solli-Nowlan, Tor, Su, Mack Y., Teran, Nicole A., Walker, Michael F., Werling, Donna M., Beaudet, Arthur L., Cantor, Rita M., Fombonne, Eric, Geschwind, Daniel H., Grice, Dorothy E., Lord, Catherine, Lowe, Jennifer K., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Talkowski, Michael E., Sutcliffe, James S., Walsh, Christopher A., Yu, Timothy W., Ledbetter, David H., Martin, Christa Lese, Cook, Edwin H., Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, State, Matthew W.
Publicado no Neuron (2015)

Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder

Por Abdulkadir, Mohamed, Tischfield, Jay A., King, Robert A., Fernandez, Thomas V., Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., de Bruijn, Sebastian F. T. M., Elzerman, Lonneke, Garcia-Delgar, Blanca, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Lamerz, Andreas, Leventhal, Bennett, Ludolph, Andrea G., Madruga-Garrido, Marcos, Maras, Athanasios, Messchendorp, Marieke D., Mir, Pablo, Morer, Astrid, Münchau, Alexander, Murphy, Tara L., Openneer, Thaïra J. C., Plessen, Kerstin J., Rath, Judith J. G., Roessner, Veit, Fründt, Odette, Shin, Eun-Young, Sival, Deborah A., Song, Dong-Ho, Song, Jungeun, Stolte, Anne-Marie, Tübing, Jennifer, van den Ban, Els, Visscher, Frank, Wanderer, Sina, Woods, Martin, Zinner, Samuel H., State, Matthew W., Heiman, Gary A., Hoekstra, Pieter J., Dietrich, Andrea
Publicado no J Psychiatr Res (2016)

Multiple recurrent de novo copy number variations (CNVs), including duplications of the 7q11.23 Williams-Beuren syndrome region, are strongly associated with autism

Por Sanders, Stephan J., Ercan-Sencicek, A. Gulhan, Hus, Vanessa, Luo, Rui, Murtha, Michael T., Moreno-De-Luca, Daniel, Chu, Su H., Moreau, Michael P., Gupta, Abha R., Thomson, Susanne A., Mason, Christopher E., Bilguvar, Kaya, Celestino-Soper, Patricia B. S., Choi, Murim, Crawford, Emily L., Davis, Lea, Wright, Nicole R. Davis, Dhodapkar, Rahul M., DiCola, Michael, DiLullo, Nicholas M., Fernandez, Thomas V., Fielding-Singh, Vikram, Fishman, Daniel O., Frahm, Stephanie, Garagaloyan, Rouben, Goh, Gerald S., Kammela, Sindhuja, Klei, Lambertus, Lowe, Jennifer K., Lund, Sabata C., McGrew, Anna D., Meyer, Kyle A., Moffat, William J., Murdoch, John D., O'Roak, Brian J., Ober, Gordon T., Pottenger, Rebecca S., Raubeson, Melanie J., Song, Youeun, Wang, Qi, Yaspan, Brian L., Yu, Timothy W., Yurkiewicz, Ilana R., Beaudet, Arthur L., Cantor, Rita M., Curland, Martin, Grice, Dorothy E., Günel, Murat, Lifton, Richard P., Mane, Shrikant M., Martin, Donna M., Shaw, Chad A., Sheldon, Michael, Tischfield, Jay A., Walsh, Christopher A., Morrow, Eric M., Ledbetter, David H., Fombonne, Eric, Lord, Catherine, Martin, Christa Lese, Brooks, Andrew I., Sutcliffe, James S., Cook, Edwin H., Geschwind, Daniel, Roeder, Kathryn, Devlin, Bernie, State, Matthew W.
Publicado em 2011