The Genetics of Tourette Syndrome: A review

Por O’Rourke, Julia A., Scharf, Jeremiah M., Yu, Dongmei, Pauls, David L.
Publicado em 2009

Prevalence of Tourette Syndrome and Chronic Tics in the Population-Based Avon Longitudinal Study of Parents and Children Cohort

Por Scharf, Jeremiah M., Miller, Laura L., Mathews, Carol A., Ben-Shlomo, Yoav
Publicado em 2012

Found in Feces: Differential Diagnosis, Workup, and Treatment

Por Stern, Theodore A., Pallais, J. Carl, Scharf, Jeremiah M., Schlozman, Steven C.
Publicado em 2012

Tourette syndrome and chronic tic disorder are associated with lower socio-economic status: findings from the Avon Longitudinal Study of Parents and Children cohort

Por Miller, Laura L, Scharf, Jeremiah M, Mathews, Carol A, Ben-Shlomo, Yoav
Publicado em 2014

Genetics of Obsessive-Compulsive Disorder and Related Disorders

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

Child Neurology: Diagnosis and treatment of Tourette syndrome

Por Hirschtritt, Matthew E., Dy, Marisela E., Yang, Kelly G., Scharf, Jeremiah M.
Publicado no Neurology (2016)

The Inheritance of Tourette Disorder: A review

Por Pauls, David L., Fernandez, Thomas V., Mathews, Carol A., State, Matthew W., Scharf, Jeremiah M.
Publicado no J Obsessive Compuls Relat Disord (2014)

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

Por Georgitsi, Marianthi, Willsey, A. Jeremy, Mathews, Carol A., State, Matthew, Scharf, Jeremiah M., Paschou, Peristera
Publicado no Front Neurosci (2016)

Family-based Genetic Association Study of DLGAP3 in Tourette Syndrome

Por Crane, Jacquelyn, Fagerness, Jesen, Osiecki, Lisa, Gunnell, Boyd, Stewart, S. Evelyn, Pauls, David L., Scharf, Jeremiah M.
Publicado em 2010

Association between pre- and perinatal exposures and Tourette syndrome or chronic tic disorder in the ALSPAC cohort†

Por Mathews, Carol A., Scharf, Jeremiah M., Miller, Laura L., Macdonald-Wallis, Corrie, Lawlor, Debbie A., Ben-Shlomo, Yoav
Publicado em 2014

Involvement of astrocyte metabolic coupling in Tourette syndrome pathogenesis

Por de Leeuw, Christiaan, Goudriaan, Andrea, Smit, August B, Yu, Dongmei, Mathews, Carol A, Scharf, Jeremiah M, Verheijen, Mark H G, Posthuma, Danielle
Publicado no Eur J Hum Genet (2015)

Effectiveness of a Web-Based Protocol for the Screening and Phenotyping of Individuals with Tourette Syndrome for Genetic Studies

Por Egan, Crystelle, Marakovitz, Susan, O’Rourke, Julia, Osiecki, Lisa, Illmann, Cornelia, Barton, Lauren, McLaughlin, Elizabeth, Proujansky, Rachel, Royal, Justin, Cowley, Heather, Rangel-Lugo, Martha, Pauls, David, Scharf, Jeremiah M., Mathews, Carol A.
Publicado em 2012

Lifetime Prevalence, Age of Risk, and Etiology of Comorbid Psychiatric Disorders in Tourette Syndrome

Por Hirschtritt, Matthew E., Lee, Paul C., Pauls, David L., Dion, Yves, Grados, Marco A., Illmann, Cornelia, King, Robert A., Sandor, Paul, McMahon, William M., Lyon, Gholson J., Cath, Danielle C., Kurlan, Roger, Robertson, Mary M., Osiecki, Lisa, Scharf, Jeremiah M., Mathews, Carol A.
Publicado no JAMA Psychiatry (2015)

Social disinhibition is a heritable subphenotype of tics in Tourette syndrome

Por Hirschtritt, Matthew E., Darrow, Sabrina M., Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert A., Pauls, David L., Budman, Cathy L., Cath, Danielle C., Greenberg, Erica, Lyon, Gholson J., Yu, Dongmei, McGrath, Lauren M., McMahon, William M., Lee, Paul C., Delucchi, Kevin L., Scharf, Jeremiah M., Mathews, Carol A.
Publicado no Neurology (2016)

Identification of two heritable cross-disorder endophenotypes for Tourette Syndrome

Por Darrow, Sabrina M., Hirschtritt, Matthew E., Davis, Lea K., Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert, Pauls, David, Budman, Cathy L., Cath, Danielle C., Greenberg, Erica, Lyon, Gholson J., Yu, Dongmei, McGrath, Lauren M., McMahon, William M., Lee, Paul C., Delucchi, Kevin L., Scharf, Jeremiah M., Mathews, Carol A.
Publicado no Am J Psychiatry (2016)

CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1

Por Nag, Abhishek, Bochukova, Elena G., Kremeyer, Barbara, Campbell, Desmond D., Muller, Heike, Valencia-Duarte, Ana V., Cardona, Julio, Rivas, Isabel C., Mesa, Sandra C., Cuartas, Mauricio, Garcia, Jharley, Bedoya, Gabriel, Cornejo, William, Herrera, Luis D., Romero, Roxana, Fournier, Eduardo, Reus, Victor I., Lowe, Thomas L., Farooqi, I. Sadaf, Mathews, Carol A., McGrath, Lauren M., Yu, Dongmei, Cook, Ed, Wang, Kai, Scharf, Jeremiah M., Pauls, David L., Freimer, Nelson B., Plagnol, Vincent, Ruiz-Linares, Andrés
Publicado em 2013

Genetic association signal near NTN4 in Tourette Syndrome

Por Paschou, Peristera, Yu, Dongmei, Gerber, Gloria, Evans, Patrick, Tsetsos, Fotis, Davis, Lea K., Karagiannidis, Iordanis, Chaponis, Jonathan, Gamazon, Eric, Mueller-Vahl, Kirsten, Stuhrmann, Manfred, Schloegelhofer, Monika, Stamenkovic, Mara, Hebebrand, Johannes, Noethen, Markus, Nagy, Peter, Barta, Csaba, Tarnok, Zsanett, Rizzo, Renata, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Cath, Danielle C., Budman, Cathy L., Sandor, Paul, Barr, Cathy, Wolanczyk, Thomas, Singer, Harvey, Chou, I-Ching, Grados, Marco, Posthuma, Danielle, Rouleau, Guy A., Aschauer, Harald, Freimer, Nelson B., Pauls, David L., Cox, Nancy J., Mathews, Carol A., Scharf, Jeremiah M.
Publicado em 2014

TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome

Por Forde, Natalie J., Kanaan, Ahmad S., Widomska, Joanna, Padmanabhuni, Shanmukha S., Nespoli, Ester, Alexander, John, Rodriguez Arranz, Juan I., Fan, Siyan, Houssari, Rayan, Nawaz, Muhammad S., Rizzo, Francesca, Pagliaroli, Luca, Zilhäo, Nuno R., Aranyi, Tamas, Barta, Csaba, Boeckers, Tobias M., Boomsma, Dorret I., Buisman, Wim R., Buitelaar, Jan K., Cath, Danielle, Dietrich, Andrea, Driessen, Nicole, Drineas, Petros, Dunlap, Michelle, Gerasch, Sarah, Glennon, Jeffrey, Hengerer, Bastian, van den Heuvel, Odile A., Jespersgaard, Cathrine, Möller, Harald E., Müller-Vahl, Kirsten R., Openneer, Thaïra J. C., Poelmans, Geert, Pouwels, Petra J. W., Scharf, Jeremiah M., Stefansson, Hreinn, Tümer, Zeynep, Veltman, Dick J., van der Werf, Ysbrand D., Hoekstra, Pieter J., Ludolph, Andrea, Paschou, Peristera
Publicado no Front Neurosci (2016)

Analysis of protein-coding genetic variation in 60,706 humans

Por Lek, Monkol, Karczewski, Konrad J, Minikel, Eric V, Samocha, Kaitlin E, Banks, Eric, Fennell, Timothy, O'Donnell-Luria, Anne H, Ware, James S, Hill, Andrew J, Cummings, Beryl B, Tukiainen, Taru, Birnbaum, Daniel P, Kosmicki, Jack A, Duncan, Laramie E, Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N, Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I, Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M, Poplin, Ryan, Rivas, Manuel A, Ruano-Rubio, Valentin, Rose, Samuel A, Ruderfer, Douglas M, Shakir, Khalid, Stenson, Peter D, Stevens, Christine, Thomas, Brett P, Tiao, Grace, Tusie-Luna, Maria T, Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M, Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C, Gabriel, Stacey B, Getz, Gad, Glatt, Stephen J, Hultman, Christina M, Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I, McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M, Palotie, Aarno, Purcell, Shaun M, Saleheen, Danish, Scharf, Jeremiah M, Sklar, Pamela, Sullivan, Patrick F, Tuomilehto, Jaakko, Tsuang, Ming T, Watkins, Hugh C, Wilson, James G, Daly, Mark J, MacArthur, Daniel G
Publicado no Nature (2016)

Genome-wide association study of Tourette Syndrome

Por Scharf, Jeremiah M., Yu, Dongmei, Mathews, Carol A., Neale, Benjamin M., Stewart, S. Evelyn, Fagerness, Jesen A, Evans, Patrick, Gamazon, Eric, Edlund, Christopher K., Service, Susan, Tikhomirov, Anna, Osiecki, Lisa, Illmann, Cornelia, Pluzhnikov, Anna, Konkashbaev, Anuar, Davis, Lea K, Han, Buhm, Crane, Jacquelyn, Moorjani, Priya, Crenshaw, Andrew T., Parkin, Melissa A., Reus, Victor I., Lowe, Thomas L., Rangel-Lugo, Martha, Chouinard, Sylvain, Dion, Yves, Girard, Simon, Cath, Danielle C, Smit, Jan H, King, Robert A., Fernandez, Thomas, Leckman, James F., Kidd, Kenneth K., Kidd, Judith R., Pakstis, Andrew J., State, Matthew, Herrera, Luis Diego, Romero, Roxana, Fournier, Eduardo, Sandor, Paul, Barr, Cathy L, Phan, Nam, Gross-Tsur, Varda, Benarroch, Fortu, Pollak, Yehuda, Budman, Cathy L., Bruun, Ruth D., Erenberg, Gerald, Naarden, Allan L, Lee, Paul C, Weiss, Nicholas, Kremeyer, Barbara, Berrío, Gabriel Bedoya, Campbell, Desmond, Silgado, Julio C. Cardona, Ochoa, William Cornejo, Restrepo, Sandra C. Mesa, Muller, Heike, Duarte, Ana V. Valencia, Lyon, Gholson J, Leppert, Mark, Morgan, Jubel, Weiss, Robert, Grados, Marco A., Anderson, Kelley, Davarya, Sarah, Singer, Harvey, Walkup, John, Jankovic, Joseph, Tischfield, Jay A., Heiman, Gary A., Gilbert, Donald L., Hoekstra, Pieter J., Robertson, Mary M., Kurlan, Roger, Liu, Chunyu, Gibbs, J. Raphael, Singleton, Andrew, Hardy, John, Strengman, Eric, Ophoff, Roel, Wagner, Michael, Moessner, Rainald, Mirel, Daniel B., Posthuma, Danielle, Sabatti, Chiara, Eskin, Eleazar, Conti, David V., Knowles, James A., Ruiz-Linares, Andres, Rouleau, Guy A., Purcell, Shaun, Heutink, Peter, Oostra, Ben A., McMahon, William, Freimer, Nelson, Cox, Nancy J., Pauls, David L.
Publicado em 2012