381 related articles for article (PubMed ID: 31771860)
1. De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
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; Richter MA; Fernandez TV
Biol Psychiatry; 2020 Jun; 87(12):1035-1044. PubMed ID: 31771860
[TBL] [Abstract][Full Text] [Related]
2. Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways.
Cappi C; Brentani H; Lima L; Sanders SJ; Zai G; Diniz BJ; Reis VN; Hounie AG; Conceição do Rosário M; Mariani D; Requena GL; Puga R; Souza-Duran FL; Shavitt RG; Pauls DL; Miguel EC; Fernandez TV
Transl Psychiatry; 2016 Mar; 6(3):e764. PubMed ID: 27023170
[TBL] [Abstract][Full Text] [Related]
3. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
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; Illmann C; McGrath LM; Mayerfeld C; Arepalli S; Barlassina C; Barr CL; Bellodi L; Benarroch F; Berrió GB; Bienvenu OJ; Black DW; Bloch MH; Brentani H; Bruun RD; Budman CL; Camarena B; Campbell DD; Cappi C; Silgado JC; Cavallini MC; Chavira DA; Chouinard S; Cook EH; Cookson MR; Coric V; Cullen B; Cusi D; Delorme R; Denys D; Dion Y; Eapen V; Egberts K; Falkai P; Fernandez T; Fournier E; Garrido H; Geller D; Gilbert DL; Girard SL; Grabe HJ; Grados MA; Greenberg BD; Gross-Tsur V; Grünblatt E; Hardy J; Heiman GA; Hemmings SM; Herrera LD; Hezel DM; Hoekstra PJ; Jankovic J; Kennedy JL; King RA; Konkashbaev AI; Kremeyer B; Kurlan R; Lanzagorta N; Leboyer M; Leckman JF; Lennertz L; Liu C; Lochner C; Lowe TL; Lupoli S; Macciardi F; Maier W; Manunta P; Marconi M; McCracken JT; Mesa Restrepo SC; Moessner R; Moorjani P; Morgan J; Muller H; Murphy DL; Naarden AL; Nurmi E; Ochoa WC; Ophoff RA; Pakstis AJ; Pato MT; Pato CN; Piacentini J; Pittenger C; Pollak Y; Rauch SL; Renner T; Reus VI; Richter MA; Riddle MA; Robertson MM; Romero R; Rosário MC; Rosenberg D; Ruhrmann S; Sabatti C; Salvi E; Sampaio AS; Samuels J; Sandor P; Service SK; Sheppard B; Singer HS; Smit JH; Stein DJ; Strengman E; Tischfield JA; Turiel M; Valencia Duarte AV; Vallada H; Veenstra-VanderWeele J; Walitza S; Wang Y; Weale M; Weiss R; Wendland JR; Westenberg HG; Shugart YY; Hounie AG; Miguel EC; Nicolini H; Wagner M; Ruiz-Linares A; Cath DC; McMahon W; Posthuma D; Oostra BA; Nestadt G; Rouleau GA; Purcell S; Jenike MA; Heutink P; Hanna GL; Conti DV; Arnold PD; Freimer NB; Stewart SE; Knowles JA; Cox NJ; Pauls DL
Am J Psychiatry; 2015 Jan; 172(1):82-93. PubMed ID: 25158072
[TBL] [Abstract][Full Text] [Related]
4. Whole-exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants.
Olfson E; Lebowitz ER; Hommel G; Pashankar N; Silverman WK; Fernandez TV
Depress Anxiety; 2022 Jun; 39(6):474-484. PubMed ID: 35312124
[TBL] [Abstract][Full Text] [Related]
5. Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants.
Halvorsen M; Samuels J; Wang Y; Greenberg BD; Fyer AJ; McCracken JT; Geller DA; Knowles JA; Zoghbi AW; Pottinger TD; Grados MA; Riddle MA; Bienvenu OJ; Nestadt PS; Krasnow J; Goes FS; Maher B; Nestadt G; Goldstein DB
Nat Neurosci; 2021 Aug; 24(8):1071-1076. PubMed ID: 34183866
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.
Mahjani B; Birnbaum R; Buxbaum Grice A; Cappi C; Jung S; Avila MN; Reichenberg A; Sandin S; Hultman CM; Buxbaum JD; Grice DE
Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292681
[TBL] [Abstract][Full Text] [Related]
7. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
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; Gallagher P; Fagerness JA; Barr CL; Bellodi L; Benarroch F; Bienvenu OJ; Black DW; Bloch MH; Bruun RD; Budman CL; Camarena B; Cath DC; Cavallini MC; Chouinard S; Coric V; Cullen B; Delorme R; Denys D; Derks EM; Dion Y; Rosário MC; Eapen V; Evans P; Falkai P; Fernandez TV; Garrido H; Geller D; Grabe HJ; Grados MA; Greenberg BD; Gross-Tsur V; Grünblatt E; Heiman GA; Hemmings SM; Herrera LD; Hounie AG; Jankovic J; Kennedy JL; King RA; Kurlan R; Lanzagorta N; Leboyer M; Leckman JF; Lennertz L; Lochner C; Lowe TL; Lyon GJ; Macciardi F; Maier W; McCracken JT; McMahon W; Murphy DL; Naarden AL; Neale BM; Nurmi E; Pakstis AJ; Pato MT; Pato CN; Piacentini J; Pittenger C; Pollak Y; Reus VI; Richter MA; Riddle M; Robertson MM; Rosenberg D; Rouleau GA; Ruhrmann S; Sampaio AS; Samuels J; Sandor P; Sheppard B; Singer HS; Smit JH; Stein DJ; Tischfield JA; Vallada H; Veenstra-VanderWeele J; Walitza S; Wang Y; Wendland JR; Shugart YY; Miguel EC; Nicolini H; Oostra BA; Moessner R; Wagner M; Ruiz-Linares A; Heutink P; Nestadt G; Freimer N; Petryshen T; Posthuma D; Jenike MA; Cox NJ; Hanna GL; Brentani H; Scherer SW; Arnold PD; Stewart SE; Mathews CA; Knowles JA; Cook EH; Pauls DL; Wang K; Scharf JM
J Am Acad Child Adolesc Psychiatry; 2014 Aug; 53(8):910-9. PubMed ID: 25062598
[TBL] [Abstract][Full Text] [Related]
8. De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
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; ; ; Neale BM; Coppola G; Mathews CA; Tischfield JA; Scharf JM; State MW; Heiman GA
Neuron; 2017 May; 94(3):486-499.e9. PubMed ID: 28472652
[TBL] [Abstract][Full Text] [Related]
9. Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes.
Moya PR; Dodman NH; Timpano KR; Rubenstein LM; Rana Z; Fried RL; Reichardt LF; Heiman GA; Tischfield JA; King RA; Galdzicka M; Ginns EI; Wendland JR
Eur J Hum Genet; 2013 Aug; 21(8):850-4. PubMed ID: 23321619
[TBL] [Abstract][Full Text] [Related]
10. Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlates.
Lochner C; Hemmings SM; Kinnear CJ; Niehaus DJ; Nel DG; Corfield VA; Moolman-Smook JC; Seedat S; Stein DJ
Compr Psychiatry; 2005; 46(1):14-9. PubMed ID: 15714189
[TBL] [Abstract][Full Text] [Related]
11. Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
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
PLoS One; 2023; 18(10):e0291978. PubMed ID: 37788244
[TBL] [Abstract][Full Text] [Related]
12. Gilles de la Tourette's syndrome and obsessive-compulsive disorder. Evidence supporting a genetic relationship.
Pauls DL; Towbin KE; Leckman JF; Zahner GE; Cohen DJ
Arch Gen Psychiatry; 1986 Dec; 43(12):1180-2. PubMed ID: 3465280
[TBL] [Abstract][Full Text] [Related]
13. Conceptual and methodological issues in studies of obsessive-compulsive and Tourette's disorders.
Hollander E; Liebowitz MR; DeCaria CM
Psychiatr Dev; 1989; 7(4):267-96. PubMed ID: 2577300
[TBL] [Abstract][Full Text] [Related]
14. The relationship between types and severity of repetitive behaviors in Gilles de la Tourette's disorder and obsessive-compulsive disorder.
Cath DC; Spinhoven P; van de Wetering BJ; Hoogduin CA; Landman AD; van Woerkom TC; Roos RA; Rooijmans HG
J Clin Psychiatry; 2000 Jul; 61(7):505-13. PubMed ID: 10937609
[TBL] [Abstract][Full Text] [Related]
15. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
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; Khalifa N; Dahl N; Huang AY; Neale BM; Coppola G; Mathews CA; Scharf JM; ; ; ; Fernandez TV; Buxbaum JD; De Rubeis S; Grice DE; Xing J; Heiman GA; Tischfield JA; Paschou P; Willsey AJ; State MW
Cell Rep; 2018 Sep; 24(13):3441-3454.e12. PubMed ID: 30257206
[TBL] [Abstract][Full Text] [Related]
16. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
17. Tourette's syndrome, trichotillomania, and obsessive-compulsive disorder: how closely are they related?
Ferrão YA; Miguel E; Stein DJ
Psychiatry Res; 2009 Nov; 170(1):32-42. PubMed ID: 19801170
[TBL] [Abstract][Full Text] [Related]
18. Characterization of SLITRK1 variation in obsessive-compulsive disorder.
Ozomaro U; Cai G; Kajiwara Y; Yoon S; Makarov V; Delorme R; Betancur C; Ruhrmann S; Falkai P; Grabe HJ; Maier W; Wagner M; Lennertz L; Moessner R; Murphy DL; Buxbaum JD; Züchner S; Grice DE
PLoS One; 2013; 8(8):e70376. PubMed ID: 23990902
[TBL] [Abstract][Full Text] [Related]
19. Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome.
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; McGrath LM; McMahon WM; Lee PC; Delucchi KL; Scharf JM; Mathews CA;
Am J Psychiatry; 2017 Apr; 174(4):387-396. PubMed ID: 27809572
[TBL] [Abstract][Full Text] [Related]
20. Brain-derived neurotrophic factor: a genetic risk factor for obsessive-compulsive disorder and Tourette syndrome?
Klaffke S; König IR; Poustka F; Ziegler A; Hebebrand J; Bandmann O
Mov Disord; 2006 Jun; 21(6):881-3. PubMed ID: 16541456
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
