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Thomas Fernandez - Publications

Affiliations: 
Yale Med Sch, New Haven, CT, United States 
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51 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Lima MO, Saraiva LC, Ramos VR, Oliveira MC, Costa DLC, Fernandez TV, Crowley JJ, Storch EA, Shavitt RG, Miguel EC, Cappi C. Clinical characteristics of probands with obsessive-compulsive disorder from simplex and multiplex families. Psychiatry Research. 331: 115627. PMID 38113811 DOI: 10.1016/j.psychres.2023.115627  0.305
2023 Wang S, Wang B, Drury V, Drake S, Sun N, Alkhairo H, Arbelaez J, Duhn C, Bal VH, Langley K, Martin J, Hoekstra PJ, Dietrich A, Xing J, Heiman GA, ... ... Fernandez TV, et al. Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD. Nature Communications. 14: 8077. PMID 38057346 DOI: 10.1038/s41467-023-43776-0  0.65
2023 Fernandez TV, Williams ZP, Kline T, Rajendran S, Augustine F, Wright N, Sullivan CAW, Olfson E, Abdallah SB, Liu W, Hoffman EJ, Gupta AR, Singer HS. Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. Plos One. 18: e0291978. PMID 37788244 DOI: 10.1371/journal.pone.0291978  0.738
2022 Olfson E, Lebowitz ER, Hommel G, Pashankar N, Silverman WK, Fernandez TV. Whole-exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants. Depression and Anxiety. PMID 35312124 DOI: 10.1002/da.23251  0.415
2021 Abdulkadir M, Yu D, Osiecki L, King RA, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, Garcia-Delgar B, Gilbert DL, Grice DE, Hagstrøm J, Hedderly T, Heyman I, Hong HJ, et al. Investigation of gene-environment interactions in relation to tic severity. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 34389898 DOI: 10.1007/s00702-021-02396-y  0.344
2021 Cao X, Zhang Y, Abdulkadir M, Deng L, Fernandez TV, Garcia-Delgar B, Hagstrøm J, Hoekstra PJ, King RA, Koesterich J, Kuperman S, Morer A, Nasello C, Plessen KJ, Thackray JK, et al. Whole-exome sequencing identifies genes associated with Tourette's disorder in multiplex families. Molecular Psychiatry. PMID 33837273 DOI: 10.1038/s41380-021-01094-1  0.407
2021 Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA, Aschauer H, Stamenkovic M, ... ... Fernandez TV, ... ... Fernandez TV, ... ... Fernandez T, et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational Psychiatry. 11: 56. PMID 33462189 DOI: 10.1038/s41398-020-01082-z  0.354
2020 Heiman GA, Rispoli J, Seymour C, Leckman JF, King RA, Fernandez TV. Empiric Recurrence Risk Estimates for Chronic Tic Disorders: Implications for Genetic Counseling. Frontiers in Neurology. 11: 770. PMID 32849224 DOI: 10.3389/fneur.2020.00770  0.339
2019 Cappi C, Oliphant ME, Péter Z, Zai G, Conceição do Rosário M, Sullivan CAW, Gupta AR, Hoffman EJ, Virdee M, Olfson E, Abdallah SB, Willsey AJ, Shavitt RG, Miguel EC, Kennedy JL, ... ... Fernandez TV, et al. De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. Biological Psychiatry. PMID 31771860 DOI: 10.1016/J.Biopsych.2019.09.029  0.754
2019 Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, ... ... Fernandez TV, et al. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227. PMID 30818990 DOI: 10.1176/Appi.Ajp.2018.18070857  0.762
2019 Abdallah S, Olfson E, Fernandez T. 42 EXPLORING POST-ZYGOTIC GENETIC VARIATION IN TOURETTE SYNDROME European Neuropsychopharmacology. 29: S82-S83. DOI: 10.1016/J.Euroneuro.2019.07.183  0.388
2019 Cappi C, Miguel EC, Pinto D, Fernandez T. SU78PROTEIN-PROTEIN INTERACTION (PPI) NETWORK ANALYSES OF DE NOVO VARIATION IN OBSESSIVE-COMPULSIVE DISORDER REVEAL OVERLAP WITH AUTISM RISK GENES European Neuropsychopharmacology. 29: S1308. DOI: 10.1016/J.Euroneuro.2018.08.442  0.452
2019 Willsey J, Fernandez T, Yu D, King R, Dietrich A, Xing J, Sanders S, Mandell J, Neale B, Coppola G, Mathews C, Tischfield J, Scharf J, State M, Heiman G. De Novo Coding Variants Are Strongly Associated with Tourette Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.065  0.774
2019 Abdallah S, Cappi C, Olfson E, Fernandez T. Exploring Post-Zygotic Variants in Obsessive-Compulsive Disorder Biological Psychiatry. 85. DOI: 10.1016/J.Biopsych.2019.03.563  0.451
2018 Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... Fernandez TV, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544. PMID 30566877 DOI: 10.1016/j.celrep.2018.12.024  0.772
2018 Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... Fernandez TV, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12. PMID 30257206 DOI: 10.1016/J.Celrep.2018.08.082  0.81
2018 Hayman V, Fernandez TV. Genetic Insights Into ADHD Biology. Frontiers in Psychiatry. 9: 251. PMID 29930523 DOI: 10.3389/fpsyt.2018.00251  0.326
2018 Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Fernandez T, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757  0.482
2018 Fernandez TV, Leckman JF, Pittenger C. Genetic susceptibility in obsessive-compulsive disorder. Handbook of Clinical Neurology. 148: 767-781. PMID 29478613 DOI: 10.1016/B978-0-444-64076-5.00049-1  0.435
2018 Fernandez TV, State MW, Pittenger C. Tourette disorder and other tic disorders. Handbook of Clinical Neurology. 147: 343-354. PMID 29325623 DOI: 10.1016/B978-0-444-63233-3.00023-3  0.702
2018 Fernandez TV. 5.1 Gene Discovery in Neuropsychiatric Disorders Journal of the American Academy of Child & Adolescent Psychiatry. 57: S276. DOI: 10.1016/j.jaac.2018.07.641  0.365
2018 Fernandez TV. 4.1 New Genetic Findings in Tourette’s and Tic Disorders Journal of the American Academy of Child & Adolescent Psychiatry. 57: S274. DOI: 10.1016/j.jaac.2018.07.635  0.328
2017 Willsey AJ, Fernandez TV, Yu D, King RA, Dietrich A, Xing J, Sanders SJ, Mandell JD, Huang AY, Richer P, Smith L, Dong S, Samocha KE, et al. De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron. 94: 486-499.e9. PMID 28472652 DOI: 10.1016/J.Neuron.2017.04.024  0.821
2017 Gupta AR, Westphal A, Yang DY, Sullivan CA, Eilbott J, Zaidi S, Voos A, Vander Wyk BC, Ventola P, Waqar Z, Fernandez TV, Ercan-Sencicek AG, Walker MF, Choi M, Schneider A, et al. Neurogenetic analysis of childhood disintegrative disorder. Molecular Autism. 8: 19. PMID 28392909 DOI: 10.1186/S13229-017-0133-0  0.637
2016 Abdulkadir M, Tischfield JA, King RA, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, de Bruijn SF, Elzerman L, Garcia-Delgar B, Gilbert DL, Grice DE, Hagstrøm J, Hedderly T, Heyman I, et al. Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder. Journal of Psychiatric Research. 82: 126-135. PMID 27494079 DOI: 10.1016/J.Jpsychires.2016.07.017  0.607
2016 Fernandez TV. 20.1 GENETIC INVESTIGATIONS OF A CORE PHENOTYPE FOR AUTISM SPECTRUM DISORDER Journal of the American Academy of Child & Adolescent Psychiatry. 55: S288. DOI: 10.1016/j.jaac.2016.07.232  0.379
2015 Castro-Chavira SA, Fernandez T, Nicolini H, Diaz-Cintra S, Prado-Alcala RA. Genetic markers in biological fluids for aging-related major neurocognitive disorder. Current Alzheimer Research. 12: 200-9. PMID 25731625 DOI: 10.2174/1567205012666150302155138  0.347
2015 Murdoch JD, Gupta AR, Sanders SJ, Walker MF, Keaney J, Fernandez TV, Murtha MT, Anyanwu S, Ober GT, Raubeson MJ, DiLullo NM, Villa N, Waqar Z, Sullivan C, Gonzalez L, et al. 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 Contactins. Plos Genetics. 11: e1004852. PMID 25621974 DOI: 10.1371/Journal.Pgen.1004852  0.758
2015 Fernandez TV, King RA, Pittenger C. Tourette's syndrome and translational clinical science. Journal of the American Academy of Child and Adolescent Psychiatry. 54: 6-8. PMID 25524784 DOI: 10.1016/j.jaac.2014.11.004  0.317
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Fernandez T, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306  0.555
2015 Dietrich A, Fernandez TV, King RA, State MW, Tischfield JA, Hoekstra PJ, Heiman GA. The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods. European Child & Adolescent Psychiatry. 24: 141-51. PMID 24771252 DOI: 10.1007/S00787-014-0543-X  0.668
2014 Pauls DL, Fernandez TV, Mathews CA, State MW, Scharf JM. The Inheritance of Tourette Disorder: A review. Journal of Obsessive-Compulsive and Related Disorders. 3: 380-385. PMID 25506544 DOI: 10.1016/J.Jocrd.2014.06.003  0.662
2014 Griesi-Oliveira K, Acab A, Gupta AR, Sunaga DY, Chailangkarn T, Nicol X, Nunez Y, Walker MF, Murdoch JD, Sanders SJ, Fernandez TV, Ji W, Lifton RP, Vadasz E, Dietrich A, et al. Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. Molecular Psychiatry. PMID 25385366 DOI: 10.1038/Mp.2014.141  0.776
2014 Lennington JB, Coppola G, Kataoka-Sasaki Y, Fernandez TV, Palejev D, Li Y, Huttner A, Pletikos M, Sestan N, Leckman JF, Vaccarino FM. Transcriptome Analysis of the Human Striatum in Tourette Syndrome. Biological Psychiatry. PMID 25199956 DOI: 10.1016/J.Biopsych.2014.07.018  0.455
2014 McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Fernandez TV, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/J.Jaac.2014.04.022  0.435
2014 Gupta AR, Pirruccello M, Cheng F, Kang HJ, Fernandez TV, Baskin JM, Choi M, Liu L, Ercan-Sencicek AG, Murdoch JD, Klei L, Neale BM, Franjic D, Daly MJ, Lifton RP, et al. Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. Molecular Autism. 5: 31. PMID 24860643 DOI: 10.1186/2040-2392-5-31  0.795
2013 Paschou P, Fernandez TV, Sharp F, Heiman GA, Hoekstra PJ. Genetic susceptibility and neurotransmitters in tourette syndrome International Review of Neurobiology. 112: 155-177. PMID 24295621 DOI: 10.1016/B978-0-12-411546-0.00006-8  0.336
2013 Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... Fernandez TV, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864  0.443
2013 Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Fernandez TV, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69  0.649
2012 Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, et al. Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biological Psychiatry. 71: 392-402. PMID 22169095 DOI: 10.1016/J.Biopsych.2011.09.034  0.757
2011 Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, ... ... Fernandez TV, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85. PMID 21658581 DOI: 10.1016/J.Neuron.2011.05.002  0.756
2010 Ercan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, ... ... Fernandez T, et al. L-histidine decarboxylase and Tourette's syndrome. The New England Journal of Medicine. 362: 1901-8. PMID 20445167 DOI: 10.1056/Nejmoa0907006  0.752
2010 Fernandez TV, State MW, Davalos-Rodriguez NO. Reply to 3p deletion and (skewed) literature review American Journal of Medical Genetics, Part A. 152: 1060. DOI: 10.1002/Ajmg.A.33150  0.48
2008 Fernandez TV, García-González IJ, Mason CE, Hernández-Zaragoza G, Ledezma-Rodríguez VC, Anguiano-Alvarez VM, E'Vega R, Gutiérrez-Angulo M, Maya ML, García-Bejarano HE, González-Cruz M, Barrios S, Atorga R, López-Cardona MG, Armendariz-Borunda J, et al. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature. American Journal of Medical Genetics. Part A. 146: 2746-52. PMID 18837054 DOI: 10.1002/Ajmg.A.32533  0.671
2008 Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. American Journal of Human Genetics. 82: 1385. PMID 18551756 DOI: 10.1016/j.ajhg.2008.04.021  0.638
2004 Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. American Journal of Human Genetics. 74: 1286-93. PMID 15106122 DOI: 10.1086/421474  0.704
2004 Fernandez T, State M. Genetics and Genomics of Neurobehavioral Disorders Journal of the American Academy of Child & Adolescent Psychiatry. 43: 370-371. DOI: 10.1097/00004583-200403000-00021  0.649
2000 Nicolson R, Lenane M, Singaracharlu S, Malaspina D, Giedd JN, Hamburger SD, Gochman P, Bedwell J, Thaker GK, Fernandez T, Wudarsky M, Hommer DW, Rapoport JL. Premorbid speech and language impairments in childhood-onset schizophrenia: association with risk factors. The American Journal of Psychiatry. 157: 794-800. PMID 10784474 DOI: 10.1176/Appi.Ajp.157.5.794  0.323
2000 Nicolson R, Lenane M, Hamburger SD, Fernandez T, Bedwell J, Rapoport JL. Lessons from childhood-onset schizophrenia. Brain Research Reviews. 31: 147-156. PMID 10719143 DOI: 10.1016/S0165-0173(99)00032-6  0.367
1999 Nicolson R, Giedd JN, Lenane M, Hamburger S, Singaracharlu S, Bedwell J, Fernandez T, Thaker GK, Malaspina D, Rapoport JL. Clinical and neurobiological correlates of cytogenetic abnormalities in childhood-onset schizophrenia American Journal of Psychiatry. 156: 1575-1579. PMID 10518169 DOI: 10.1176/Ajp.156.10.1575  0.302
1998 Kumra S, Wiggs E, Krasnewich D, Meck J, Smith AC, Bedwell J, Fernandez T, Jacobsen LK, Lenane M, Rapoport JL. Brief report: association of sex chromosome anomalies with childhood-onset psychotic disorders. Journal of the American Academy of Child and Adolescent Psychiatry. 37: 292-6. PMID 9519634 DOI: 10.1097/00004583-199803000-00014  0.352
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