What makes you tic?: A new lead in Tourette syndrome genetics

gan Fernandez, Thomas V.
Cyhoeddwyd yn Biol Psychiatry (2016)

Tourette Syndrome: Bridging the Gap between Genetics and Biology

gan Richer, Petra, Fernandez, Thomas V.
Cyhoeddwyd yn Mol Neuropsychiatry (2015)

Genetic Insights Into ADHD Biology

gan Hayman, Victoria, Fernandez, Thomas V.
Cyhoeddwyd yn Front Psychiatry (2018)

The Origins of Obsessive-Compulsive Disorder: Prenatal and Perinatal Risk Factors and the Promise of Birth Cohort Studies

gan Fernandez, Thomas V., Leckman, James F.
Cyhoeddwyd yn JAMA Psychiatry (2016)

The Origins of Tourette Syndrome: Prenatal Risk Factors and the Promise of Birth Cohort Studies

gan Leckman, James F., Fernandez, Thomas V.
Cyhoeddwyd yn J Am Acad Child Adolesc Psychiatry (2016)

From Bedside to Bench and Back Again: Tourette Syndrome and Translational Clinical Science

gan Fernandez, Thomas V., King, Robert A., Pittenger, Christopher
Cyhoeddwyd yn J Am Acad Child Adolesc Psychiatry (2015)

Motor Stereotypies: A Pathophysiological Review

gan Péter, Zsanett, Oliphant, Melody E., Fernandez, Thomas V.
Cyhoeddwyd yn Front Neurosci (2017)

Genetic Susceptibility and Neurotransmitters in Tourette Syndrome

gan Paschou, Peristera, Fernandez, Thomas V., Sharp, Frank, Heiman, Gary A., Hoekstra, Pieter J.
Cyhoeddwyd yn Int Rev Neurobiol (2013)

Leveraging aggression risk gene expression in the developing and adult human brain to guide future precision interventions

gan Kim, Ahra, Rader, Sarah L., Fernandez, Thomas V., Vandekar, Simon N., Lewis, Alan S.
Cyhoeddwyd yn Mol Psychiatry (2020)

The Inheritance of Tourette Disorder: A review

gan Pauls, David L., Fernandez, Thomas V., Mathews, Carol A., State, Matthew W., Scharf, Jeremiah M.
Cyhoeddwyd yn J Obsessive Compuls Relat Disord (2014)

Empiric Recurrence Risk Estimates for Chronic Tic Disorders: Implications for Genetic Counseling

gan Heiman, Gary A., Rispoli, Jessica, Seymour, Christine, Leckman, James F., King, Robert A., Fernandez, Thomas V.
Cyhoeddwyd yn Front Neurol (2020)

The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods

gan Dietrich, Andrea, Fernandez, Thomas V., King, Robert A., State, Matthew W., Tischfield, Jay A., Hoekstra, Pieter J., Heiman, Gary A.
Cyhoeddwyd 2014

Gene variants associated with antisocial behaviour: A latent variable approach

gan Bentley, Mary Jane, Lin, Haiqun, Fernandez, Thomas V., Lee, Maria, Yrigollen, Carolyn M., Pakstis, Andrew J., Katsovich, Liliya, Olds, David L., Grigorenko, Elena L., Leckman, James F.
Cyhoeddwyd 2013

Transcriptome analysis of the human striatum in Tourette syndrome

gan Lennington, Jessica B., Coppola, Gianfilippo, Kataoka-Sasaki, Yuko, Fernandez, Thomas V., Palejev, Dean, Li, Yifan, Huttner, Anita, Pletikos, Mihovil, Ŝestan, Nenad, Leckman, James F., Vaccarino, Flora M.
Cyhoeddwyd yn Biol Psychiatry (2014)

Early developmental asymmetries in cell lineage trees in living individuals

gan Fasching, Liana, Jang, Yeongjun, Tomasi, Simone, Schreiner, Jeremy, Tomasini, Livia, Brady, Melanie, Bae, Taejeong, Sarangi, Vivekananda, Vasmatzis, Nikolaos, Wang, Yifan, Szekely, Anna, Fernandez, Thomas V., Leckman, James F., Abyzov, Alexej, Vaccarino, Flora M.
Cyhoeddwyd yn Science (2021)

De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism

gan Cappi, Carolina, Oliphant, Melody E., Péter, Zsanett, Zai, Gwyneth, do Rosário, Maria Conceição, Sullivan, Catherine A. W., Gupta, Abha R., Hoffman, Ellen J., Virdee, Manmeet, Olfson, Emily, Abdallah, Sarah B., Willsey, A. Jeremy, Shavitt, Roseli G., Miguel, Euripedes C., Kennedy, James L., Richter, Margaret A., Fernandez, Thomas V.
Cyhoeddwyd yn Biol Psychiatry (2019)

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders

gan Gupta, Abha R, Pirruccello, Michelle, Cheng, Feng, Kang, Hyo Jung, Fernandez, Thomas V, Baskin, Jeremy M, Choi, Murim, Liu, Li, Ercan-Sencicek, Adife Gulhan, Murdoch, John D, Klei, Lambertus, Neale, Benjamin M, Franjic, Daniel, Daly, Mark J, Lifton, Richard P, De Camilli, Pietro, Zhao, Hongyu, Šestan, Nenad, State, Matthew W
Cyhoeddwyd 2014

No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti...

gan Murdoch, John D., Gupta, Abha R., Sanders, Stephan J., Walker, Michael F., Keaney, John, Fernandez, Thomas V., Murtha, Michael T., Anyanwu, Samuel, Ober, Gordon T., Raubeson, Melanie J., DiLullo, Nicholas M., Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A. Jeremy, Choe, So-Yeon, Neale, Benjamin M., Daly, Mark J., State, Matthew W.
Cyhoeddwyd yn PLoS Genet (2015)

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

gan 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.
Cyhoeddwyd yn Neuron (2017)

Neurogenetic analysis of childhood disintegrative disorder

gan Gupta, Abha R., Westphal, Alexander, Yang, Daniel Y. J., Sullivan, Catherine A. W., Eilbott, Jeffrey, Zaidi, Samir, Voos, Avery, Vander Wyk, Brent C., Ventola, Pam, Waqar, Zainulabedin, Fernandez, Thomas V., Ercan-Sencicek, A. Gulhan, Walker, Michael F., Choi, Murim, Schneider, Allison, Hedderly, Tammy, Baird, Gillian, Friedman, Hannah, Cordeaux, Cara, Ristow, Alexandra, Shic, Frederick, Volkmar, Fred R., Pelphrey, Kevin A.
Cyhoeddwyd yn Mol Autism (2017)