| Year |
Citation |
Score |
| 2023 |
Miller-Fleming TW, Allos A, Gantz E, Yu D, Isaacs DA, Mathews CA, Scharf JM, Davis LK. Developing a Phenotype Risk Score for Tic Disorders in a Large, Clinical Biobank. Medrxiv : the Preprint Server For Health Sciences. PMID 36865201 DOI: 10.1101/2023.02.21.23286253 |
0.334 |
|
| 2023 |
Jain P, Miller-Fleming T, Topaloudi A, Yu D, Drineas P, Georgitsi M, Yang Z, Rizzo R, Müller-Vahl KR, Tumer Z, Mol Debes N, Hartmann A, Depienne C, Worbe Y, Mir P, ... ... Scharf JM, et al. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome. Translational Psychiatry. 13: 69. PMID 36823209 DOI: 10.1038/s41398-023-02341-5 |
0.376 |
|
| 2023 |
Tsetsos F, Topaloudi A, Jain P, Yang Z, Yu D, Kolovos P, Tumer Z, Rizzo R, Hartmann A, Depienne C, Worbe Y, Müller-Vahl KR, Cath DC, Boomsma DI, Wolanczyk T, ... ... Scharf JM, et al. Genome-wide Association Study points to novel locus for Gilles de la Tourette Syndrome. Biological Psychiatry. PMID 36738982 DOI: 10.1016/j.biopsych.2023.01.023 |
0.342 |
|
| 2022 |
Yang K, Essa A, Noriega D, Yu D, Osiecki L, Gauvin CA, Illmann C, Bortolato M, Dunn EC, Mathews CA, Scharf JM. Relationship between adverse childhood experiences and symptom severity in adult men with Tourette Syndrome. Journal of Psychiatric Research. 155: 252-259. PMID 36113395 DOI: 10.1016/j.jpsychires.2022.08.024 |
0.316 |
|
| 2021 |
Halvorsen M, Szatkiewicz J, Mudgal P, Yu D, Nordsletten AE, Mataix-Cols D, Mathews CA, Scharf JM, Mattheisen M, Robertson MM, McQuillin A, Crowley JJ. Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree. Molecular Psychiatry. PMID 34526668 DOI: 10.1038/s41380-021-01277-w |
0.326 |
|
| 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, ... ... Scharf JM, 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 |
0.31 |
|
| 2021 |
Yang Z, Wu H, Lee PH, Tsetsos F, Davis LK, Yu D, Lee SH, Dalsgaard S, Haavik J, Barta C, Zayats T, Eapen V, Wray NR, Devlin B, Daly M, ... ... Scharf J, et al. Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum. Biological Psychiatry. PMID 33714545 DOI: 10.1016/j.biopsych.2020.12.028 |
0.336 |
|
| 2020 |
Bralten J, Widomska J, Witte W, Yu D, Mathews CA, Scharf JM, Buitelaar J, Crosbie J, Schachar R, Arnold P, Lemire M, Burton CL, Franke B, Poelmans G. Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling. Translational Psychiatry. 10: 121. PMID 32341337 DOI: 10.1038/S41398-020-0793-Y |
0.386 |
|
| 2019 |
Rose O, Hartmann A, Worbe Y, Scharf JM, Black KJ. Tourette syndrome research highlights from 2018. F1000research. 8: 988. PMID 31508215 DOI: 10.12688/F1000Research.19542.1 |
0.326 |
|
| 2019 |
Mufford M, Cheung J, Jahanshad N, van der Merwe C, Ding L, Groenewold N, Koen N, Chimusa ER, Dalvie S, Ramesar R, Knowles JA, Lochner C, Hibar DP, Paschou P, ... ... Scharf JM, et al. Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational Psychiatry. 9: 120. PMID 30902966 DOI: 10.1038/S41398-019-0452-3 |
0.426 |
|
| 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, ... ... Scharf JM, 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 |
0.464 |
|
| 2019 |
Abdulkadir M, Mathews C, Scharf J, Yu D, Tischfield J, Heiman G, Hoekstra P, Dietrich A. Su67Polygenic Risk Scores Derived From A Tourette Syndrome Gwas Predict Presence Of Tics In The Avon Longitudinal Study Of Parents And Children (Alspac) Cohort European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.431 |
0.308 |
|
| 2019 |
Widomska J, Bralten J, Martens M, Witte WD, Vondervoort Ivd, Yu D, Mathews C, Scharf J, Buitelaar J, Glennon J, Franke B, Poelmans G. Determining The Genetic Overlap Between Tourette Syndrome (Ts), Obsessive Compulsive Disorder (Ocd) And Ocd/Tic-Related Traits European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.377 |
0.461 |
|
| 2019 |
Soda T, Crowley J, Bruer E, Bershader R, Collier S, Gantz E, Hucks D, Johnston R, Maxwell-Horn A, Soto-Freita A, Sutcliffe J, Mathews C, Scharf J, Cox N, Davis L. Validation Of Electronic Health Record-Based Ascertainment Of Obsessive Compulsive Disorder Cases And Controls European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.376 |
0.356 |
|
| 2019 |
Mathews C, Darrow S, Hirschtritt M, Yu D, Davis L, Scharf J. Symmetry and Disinhibition are Heritable Endophenotypes For Tourette Syndrome European Neuropsychopharmacology. 29: S738. DOI: 10.1016/J.Euroneuro.2017.06.067 |
0.405 |
|
| 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 |
0.408 |
|
| 2019 |
Scharf J, Yu D, Huang A, Tsetsos F, Paschou P, Coppola G, Mathews C. Collaborative Genome-Wide Association and Copy Number Variation Analysis of Tourette Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.064 |
0.428 |
|
| 2018 |
Abdulkadir M, Mathews CA, Scharf JM, Yu D, Tischfield JA, Heiman GA, Hoekstra PJ, Dietrich A. Polygenic Risk Scores Derived From a Tourette Syndrome Genome-wide Association Study Predict Presence of Tics in the Avon Longitudinal Study of Parents and Children Cohort. Biological Psychiatry. PMID 30424865 DOI: 10.1016/J.Biopsych.2018.09.011 |
0.414 |
|
| 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, ... ... Scharf JM, 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 |
0.431 |
|
| 2018 |
Yilmaz Z, Halvorsen M, Bryois J, Yu D, Thornton LM, Zerwas S, Micali N, Moessner R, Burton CL, Zai G, Erdman L, Kas MJ, Arnold PD, Davis LK, Knowles JA, ... ... Scharf JM, et al. Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. Molecular Psychiatry. PMID 30087453 DOI: 10.1038/S41380-018-0115-4 |
0.463 |
|
| 2018 |
Perez DL, Keshavan MS, Scharf JM, Boes AD, Price BH. Bridging the Great Divide: What Can Neurology Learn From Psychiatry? The Journal of Neuropsychiatry and Clinical Neurosciences. appineuropsych171002. PMID 29939105 DOI: 10.1176/Appi.Neuropsych.17100200 |
0.355 |
|
| 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, ... ... Scharf J, 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 |
0.455 |
|
| 2017 |
Greenberg E, Tung ES, Gauvin C, Osiecki L, Yang KG, Curley E, Essa A, Illmann C, Sandor P, Dion Y, Lyon GJ, King RA, Darrow S, Hirschtritt ME, Budman CL, ... ... Scharf JM, et al. Prevalence and predictors of hair pulling disorder and excoriation disorder in Tourette syndrome. European Child & Adolescent Psychiatry. PMID 29098466 DOI: 10.1007/S00787-017-1074-Z |
0.457 |
|
| 2017 |
Greenberg E, Grant JE, Curley EE, Lochner C, Woods DW, Tung ES, Stein DJ, Redden SA, Scharf JM, Keuthen NJ. Predictors of comorbid eating disorders and association with other obsessive-compulsive spectrum disorders in trichotillomania. Comprehensive Psychiatry. 78: 1-8. PMID 28667830 DOI: 10.1016/J.Comppsych.2017.06.008 |
0.423 |
|
| 2017 |
Hirschtritt ME, Darrow SM, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King RA, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, McGrath LM, ... ... Scharf JM, et al. Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome. Psychological Medicine. 1-15. PMID 28651666 DOI: 10.1017/S0033291717001672 |
0.407 |
|
| 2017 |
Darrow SM, Grados M, Sandor P, Hirschtritt ME, Illmann C, Osiecki L, Dion Y, King R, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, McMahon WM, Lee PC, ... ... Scharf JM, et al. Autism Spectrum Symptoms in a Tourette's Disorder Sample. Journal of the American Academy of Child and Adolescent Psychiatry. 56: 610-617.e1. PMID 28647013 DOI: 10.1016/J.Jaac.2017.05.002 |
0.403 |
|
| 2017 |
Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, ... ... Scharf JM, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010 |
0.434 |
|
| 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, ... ... Scharf JM, 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 |
0.457 |
|
| 2017 |
Leivonen S, Scharf JM, Mathews CA, Chudal R, Gyllenberg D, Sucksdorff D, Suominen A, Voutilainen A, Brown AS, Sourander A. Parental Psychopathology and Tourette Syndrome/Chronic Tic Disorder in Offspring: A Nationwide Case-Control Study. Journal of the American Academy of Child and Adolescent Psychiatry. 56: 297-303.e4. PMID 28335873 DOI: 10.1016/J.Jaac.2017.01.009 |
0.414 |
|
| 2017 |
Robertson MM, Eapen V, Singer HS, Martino D, Scharf JM, Paschou P, Roessner V, Woods DW, Hariz M, Mathews CA, Črnčec R, Leckman JF. Gilles de la Tourette syndrome. Nature Reviews. Disease Primers. 3: 16097. PMID 28150698 DOI: 10.1038/nrdp.2016.97 |
0.355 |
|
| 2017 |
Hirschtritt M, Darrow SM, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King RA, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, McGrath LM, ... ... Scharf JM, et al. 896. Genetic and Phenotypic Overlap of Specific Obsessive-Compulsive Subtypes with Tourette Syndrome Biological Psychiatry. 81: S361-S362. DOI: 10.1016/J.Biopsych.2017.02.621 |
0.386 |
|
| 2016 |
Keuthen NJ, Curley EE, Scharf JM, Woods DW, Lochner C, Stein DJ, Tung ES, Greenberg E, Stewart SE, Redden SA, Grant JE. Predictors of comorbid obsessive-compulsive disorder and skin-picking disorder in trichotillomania. Annals of Clinical Psychiatry : Official Journal of the American Academy of Clinical Psychiatrists. 28: 280-288. PMID 27901519 |
0.305 |
|
| 2016 |
Darrow SM, Hirschtritt ME, Davis LK, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King R, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, ... ... Scharf JM, et al. Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome. The American Journal of Psychiatry. appiajp201616020240. PMID 27809572 DOI: 10.1176/Appi.Ajp.2016.16020240 |
0.466 |
|
| 2016 |
Forde NJ, Kanaan AS, Widomska J, Padmanabhuni SS, Nespoli E, Alexander J, Rodriguez Arranz JI, Fan S, Houssari R, Nawaz MS, Rizzo F, Pagliaroli L, Zilhäo NR, Aranyi T, Barta C, ... ... Scharf JM, et al. TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome. Frontiers in Neuroscience. 10: 384. PMID 27601976 DOI: 10.3389/Fnins.2016.00384 |
0.44 |
|
| 2016 |
Georgitsi M, Willsey AJ, Mathews CA, State M, Scharf JM, Paschou P. The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery. Frontiers in Neuroscience. 10: 351. PMID 27536211 DOI: 10.3389/Fnins.2016.00351 |
0.452 |
|
| 2016 |
Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O'Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, Duncan LE, Estrada K, ... ... Scharf JM, et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 536: 285-291. PMID 27535533 DOI: 10.1038/Nature19057 |
0.325 |
|
| 2016 |
Hirschtritt ME, Dy ME, Yang KG, Scharf JM. Child Neurology: Diagnosis and treatment of Tourette syndrome. Neurology. 87: e65-7. PMID 27527544 DOI: 10.1212/Wnl.0000000000002977 |
0.348 |
|
| 2016 |
Lizano P, Popat-Jain A, Scharf JM, Berman NC, Widge A, Dougherty DD, Eskandar E. Challenges in Managing Treatment-Refractory Obsessive-Compulsive Disorder and Tourette's Syndrome. Harvard Review of Psychiatry. 24: 294-301. PMID 27384398 DOI: 10.1097/Hrp.0000000000000121 |
0.372 |
|
| 2016 |
Hirschtritt ME, Darrow SM, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King RA, Pauls DL, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, McGrath LM, ... ... Scharf JM, et al. Social disinhibition is a heritable subphenotype of tics in Tourette syndrome. Neurology. PMID 27371487 DOI: 10.1212/Wnl.0000000000002910 |
0.328 |
|
| 2016 |
Scharf JM. Parity in Tourette Syndrome: Reproducible Risk Factors for an Underrecognized Neurodevelopmental Disorder. The Journal of Pediatrics. PMID 26778098 DOI: 10.1016/J.Jpeds.2015.12.048 |
0.412 |
|
| 2015 |
Ben-Shlomo Y, Scharf JM, Miller LL, Mathews CA. Parental mood during pregnancy and post-natally is associated with offspring risk of Tourette syndrome or chronic tics: prospective data from the Avon Longitudinal Study of Parents and Children (ALSPAC). European Child & Adolescent Psychiatry. PMID 26174227 DOI: 10.1007/S00787-015-0742-0 |
0.303 |
|
| 2015 |
Darrow SM, Illmann C, Gauvin C, Osiecki L, Egan CA, Greenberg E, Eckfield M, Hirschtritt ME, Pauls DL, Batterson JR, Berlin CM, Malaty IA, Woods DW, Scharf JM, Mathews CA. Web-based phenotyping for Tourette Syndrome: Reliability of common co-morbid diagnoses. Psychiatry Research. PMID 26054936 DOI: 10.1016/J.Psychres.2015.05.017 |
0.43 |
|
| 2015 |
de Leeuw C, Goudriaan A, Smit AB, Yu D, Mathews CA, Scharf JM, Verheijen MH, Posthuma D. Involvement of astrocyte metabolic coupling in Tourette syndrome pathogenesis. European Journal of Human Genetics : Ejhg. PMID 25735483 DOI: 10.1038/Ejhg.2015.22 |
0.366 |
|
| 2015 |
Hirschtritt ME, Lee PC, Pauls DL, Dion Y, Grados MA, Illmann C, King RA, Sandor P, McMahon WM, Lyon GJ, Cath DC, Kurlan R, Robertson MM, Osiecki L, Scharf JM, et al. Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome. Jama Psychiatry. 72: 325-33. PMID 25671412 DOI: 10.1001/Jamapsychiatry.2014.2650 |
0.435 |
|
| 2015 |
Scharf JM, Miller LL, Gauvin CA, Alabiso J, Mathews CA, Ben-Shlomo Y. Population prevalence of Tourette syndrome: a systematic review and meta-analysis. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 221-8. PMID 25487709 DOI: 10.1002/Mds.26089 |
0.33 |
|
| 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, 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 |
0.495 |
|
| 2015 |
Davis LK, Lee SH, Gamazon ER, Im H, Yu D, Williams S, Sullivan PF, Mathews C, Knowles J, Scharf J, Wray N, Cox NJ. Characterizing an inverse axis between orthogonal sources of genetic risk Genetic Epidemiology. 39: 542-543. DOI: 10.1002/Gepi.21916 |
0.302 |
|
| 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 |
0.449 |
|
| 2014 |
Browne HA, Gair SL, Scharf JM, Grice DE. Genetics of obsessive-compulsive disorder and related disorders. The Psychiatric Clinics of North America. 37: 319-35. PMID 25150565 DOI: 10.1016/J.Psc.2014.06.002 |
0.471 |
|
| 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, ... ... Scharf JM, 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 |
0.48 |
|
| 2014 |
Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, ... ... Scharf JM, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of Neurology. 76: 310-5. PMID 25042818 DOI: 10.1002/Ana.24215 |
0.408 |
|
| 2014 |
Mathews CA, Scharf JM, Miller LL, Macdonald-Wallis C, Lawlor DA, Ben-Shlomo Y. Association between pre- and perinatal exposures and Tourette syndrome or chronic tic disorder in the ALSPAC cohort. The British Journal of Psychiatry : the Journal of Mental Science. 204: 40-5. PMID 24262815 DOI: 10.1192/Bjp.Bp.112.125468 |
0.415 |
|
| 2014 |
Miller LL, Scharf JM, Mathews CA, Ben-Shlomo Y. Tourette syndrome and chronic tic disorder are associated with lower socio-economic status: findings from the Avon Longitudinal Study of Parents and Children cohort. Developmental Medicine and Child Neurology. 56: 157-63. PMID 24138188 DOI: 10.1111/Dmcn.12318 |
0.381 |
|
| 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, ... ... Scharf JM, 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 |
0.487 |
|
| 2013 |
Stewart SE, Mayerfeld C, Arnold PD, Crane JR, O'Dushlaine C, Fagerness JA, Yu D, Scharf JM, Chan E, Kassam F, Moya PR, Wendland JR, Delorme R, Richter MA, Kennedy JL, et al. Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 367-79. PMID 23606572 DOI: 10.1002/Ajmg.B.32137 |
0.404 |
|
| 2013 |
Nag A, Bochukova EG, Kremeyer B, Campbell DD, Muller H, Valencia-Duarte AV, Cardona J, Rivas IC, Mesa SC, Cuartas M, Garcia J, Bedoya G, Cornejo W, Herrera LD, Romero R, ... ... Scharf JM, et al. CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. Plos One. 8: e59061. PMID 23533600 DOI: 10.1371/Journal.Pone.0059061 |
0.442 |
|
| 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, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69 |
0.438 |
|
| 2013 |
Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Davis LK, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, et al. Genome-wide association study of obsessive-compulsive disorder. Molecular Psychiatry. 18: 788-98. PMID 22889921 DOI: 10.1038/Mp.2012.85 |
0.409 |
|
| 2013 |
Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, Illman C, et al. Erratum: Genome-wide association study of obsessive-compulsive disorder Molecular Psychiatry. 18: 843-843. DOI: 10.1038/Mp.2013.15 |
0.321 |
|
| 2012 |
Egan CA, Marakovitz SE, O'Rourke JA, Osiecki L, Illmann C, Barton L, McLaughlin E, Proujansky R, Royal J, Cowley H, Rangel-Lugo M, Pauls DL, Scharf JM, Mathews CA. Effectiveness of a web-based protocol for the screening and phenotyping of individuals with Tourette syndrome for genetic studies. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 987-96. PMID 23090870 DOI: 10.1002/Ajmg.B.32107 |
0.414 |
|
| 2012 |
Scharf JM, Miller LL, Mathews CA, Ben-Shlomo Y. Prevalence of Tourette syndrome and chronic tics in the population-based Avon longitudinal study of parents and children cohort. Journal of the American Academy of Child and Adolescent Psychiatry. 51: 192-201.e5. PMID 22265365 DOI: 10.1016/J.Jaac.2011.11.004 |
0.396 |
|
| 2012 |
Scharf J, Yu D, Mathews C, Neale B, Stewart E, Fagerness J, Evans P, Gamazon E, Service S, Osiecki L, Illmann C, Cath D, King R, Dion Y, Sandor P, et al. Genome-Wide Association Study of Gilles de la Tourette Syndrome (IN10-1.002) Neurology. 78: IN10-1.002-IN10-1.00. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In10-1.002 |
0.386 |
|
| 2011 |
O'Rourke JA, Scharf JM, Platko J, Stewart SE, Illmann C, Geller DA, King RA, Leckman JF, Pauls DL. The familial association of tourette's disorder and ADHD: the impact of OCD symptoms. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 553-60. PMID 21557467 DOI: 10.1002/Ajmg.B.31195 |
0.351 |
|
| 2011 |
Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM. Family-based genetic association study of DLGAP3 in Tourette Syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 108-14. PMID 21184590 DOI: 10.1002/Ajmg.B.31134 |
0.443 |
|
| 2010 |
Scharf JM, Mathews CA. Copy number variation in Tourette syndrome: another case of neurodevelopmental generalist genes? Neurology. 74: 1564-5. PMID 20427746 DOI: 10.1212/Wnl.0B013E3181E24161 |
0.48 |
|
| 2009 |
O'Rourke JA, Scharf JM, Yu D, Pauls DL. The genetics of Tourette syndrome: a review. Journal of Psychosomatic Research. 67: 533-45. PMID 19913658 DOI: 10.1016/J.Jpsychores.2009.06.006 |
0.341 |
|
| 2008 |
Stewart SE, Rosario MC, Baer L, Carter AS, Brown TA, Scharf JM, Illmann C, Leckman JF, Sukhodolsky D, Katsovich L, Rasmussen S, Goodman W, Delorme R, Leboyer M, Chabane N, et al. Four-factor structure of obsessive-compulsive disorder symptoms in children, adolescents, and adults. Journal of the American Academy of Child and Adolescent Psychiatry. 47: 763-72. PMID 18520961 DOI: 10.1097/Chi.0B013E318172Ef1E |
0.337 |
|
| 2008 |
Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. Neurology. 70: 1495-6. PMID 18413575 DOI: 10.1212/01.Wnl.0000296833.25484.Bb |
0.44 |
|
| 2007 |
Stewart SE, Fagerness JA, Platko J, Smoller JW, Scharf JM, Illmann C, Jenike E, Chabane N, Leboyer M, Delorme R, Jenike MA, Pauls DL. Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 1027-33. PMID 17894418 DOI: 10.1002/Ajmg.B.30533 |
0.366 |
|
| 2007 |
Pauls D, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Scharf JM, Santangelo S, Stewart SE, Platko J, Pauls DL, Cox NJ, Robertson MM, Service S, et al. Genome scan for tourette disorder in affected-sibling-pair and multigenerational families American Journal of Human Genetics. 80: 265-272. PMID 17304708 DOI: 10.1086/511052 |
0.436 |
|
| 2000 |
Growney JD, Scharf JM, Kunkel LM, Dietrich WF. Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures. Genomics. 64: 62-81. PMID 10708519 DOI: 10.1006/Geno.1999.6111 |
0.302 |
|
| 1999 |
Endrizzi M, Huang S, Scharf JM, Kelter AR, Wirth B, Kunkel LM, Miller W, Dietrich WF. Comparative sequence analysis of the mouse and human Lgn1/SMA interval. Genomics. 60: 137-51. PMID 10486205 DOI: 10.1006/Geno.1999.5910 |
0.329 |
|
| 1998 |
Scharf JM, Endrizzi MG, Wetter A, Huang S, Thompson TG, Zerres K, Dietrich WF, Wirth B, Kunkel LM. Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics. Nature Genetics. 20: 83-6. PMID 9731538 DOI: 10.1038/1753 |
0.348 |
|
| 1996 |
Scharf JM, Damron D, Frisella A, Bruno S, Beggs AH, Kunkel LM, Dietrich WF. The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5. Genomics. 38: 405-17. PMID 8975718 DOI: 10.1006/Geno.1996.0644 |
0.332 |
|
| 1994 |
Boviatsis EJ, Scharf JM, Chase M, Harrington K, Kowall NW, Breakefield XO, Chiocca EA. Antitumor activity and reporter gene transfer into rat brain neoplasms inoculated with herpes simplex virus vectors defective in thymidine kinase or ribonucleotide reductase. Gene Therapy. 1: 323-31. PMID 7584098 |
0.338 |
|
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