6.
  
    Tukel R, Polat A, Ozdemir O, Aksut D, Turksoy N
    
    . Comorbid conditions in obsessive-compulsive disorder. Compr Psychiatry. 2002; 43(3):204-9.
    
          DOI: 10.1053/comp.2002.32355.
    
    
View
   
 
                                          
  7.
  
    de Mathis M, Diniz J, Shavitt R, Torres A, Ferrao Y, Fossaluza V
    
    . Early onset obsessive-compulsive disorder with and without tics. CNS Spectr. 2009; 14(7):362-70.
    
          DOI: 10.1017/s1092852900023014.
    
    
View
   
 
                                          
  8.
  
    Alemany-Navarro M, Cruz R, Real E, Segalas C, Bertolin S, Rabionet R
    
    . Looking into the genetic bases of OCD dimensions: a pilot genome-wide association study. Transl Psychiatry. 2020; 10(1):151.
          PMC: 7235014.
    
          DOI: 10.1038/s41398-020-0804-z.
    
    
View
   
 
                                          
  9.
  
    Fu J, Satterstrom F, Peng M, Brand H, Collins R, Dong S
    
    . Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nat Genet. 2022; 54(9):1320-1331.
          PMC: 9653013.
    
          DOI: 10.1038/s41588-022-01104-0.
    
    
View
   
 
                                          
  10.
  
    Miguel E, Ferrao Y, do Rosario M, de Mathis M, Torres A, Fontenelle L
    
    . The Brazilian Research Consortium on Obsessive-Compulsive Spectrum Disorders: recruitment, assessment instruments, methods for the development of multicenter collaborative studies and preliminary results. Braz J Psychiatry. 2008; 30(3):185-96.
    
          DOI: 10.1590/s1516-44462008000300003.
    
    
View
   
 
                                          
  11.
  
    Mataix-Cols D, Boman M, Monzani B, Ruck C, Serlachius E, Langstrom N
    
    . Population-based, multigenerational family clustering study of obsessive-compulsive disorder. JAMA Psychiatry. 2013; 70(7):709-17.
    
          DOI: 10.1001/jamapsychiatry.2013.3.
    
    
View
   
 
                                          
  12.
  
    Slomp C, Morris E, Inglis A, Lehman A, Austin J
    
    . Patient outcomes of genetic counseling: Assessing the impact of different approaches to family history collection. Clin Genet. 2017; 93(4):830-836.
    
          DOI: 10.1111/cge.13176.
    
    
View
   
 
                                          
  13.
  
    Geller D, Biederman J, Jones J, Shapiro S, Schwartz S, Park K
    
    . Obsessive-compulsive disorder in children and adolescents: a review. Harv Rev Psychiatry. 1998; 5(5):260-73.
    
          DOI: 10.3109/10673229809000309.
    
    
View
   
 
                                          
  14.
  
    Berends D, Dissanayake C, Lawson L
    
    . Differences in Cognition and Behaviour in Multiplex and Simplex Autism: Does Prior Experience Raising a Child with Autism Matter?. J Autism Dev Disord. 2019; 49(8):3401-3411.
    
          DOI: 10.1007/s10803-019-04052-7.
    
    
View
   
 
                                          
  15.
  
    Grove J, Ripke S, Als T, Mattheisen M, Walters R, Won H
    
    . Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019; 51(3):431-444.
          PMC: 6454898.
    
          DOI: 10.1038/s41588-019-0344-8.
    
    
View
   
 
                                          
  16.
  
    Virkud Y, Todd R, Abbacchi A, Zhang Y, Constantino J
    
    . Familial aggregation of quantitative autistic traits in multiplex versus simplex autism. Am J Med Genet B Neuropsychiatr Genet. 2008; 150B(3):328-34.
          PMC: 2819431.
    
          DOI: 10.1002/ajmg.b.30810.
    
    
View
   
 
                                          
  17.
  
    de Mathis M, Diniz J, Hounie A, Shavitt R, Fossaluza V, Ferrao Y
    
    . Trajectory in obsessive-compulsive disorder comorbidities. Eur Neuropsychopharmacol. 2012; 23(7):594-601.
    
          DOI: 10.1016/j.euroneuro.2012.08.006.
    
    
View
   
 
                                          
  18.
  
    Wang S, Mandell J, Kumar Y, Sun N, Morris M, Arbelaez J
    
    . De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Rep. 2018; 24(13):3441-3454.e12.
          PMC: 6475626.
    
          DOI: 10.1016/j.celrep.2018.08.082.
    
    
View
   
 
                                          
  19.
  
    Mahjani B, Klei L, Hultman C, Larsson H, Devlin B, Buxbaum J
    
    . Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder. Biol Psychiatry. 2020; 87(12):1045-1051.
          PMC: 8023336.
    
          DOI: 10.1016/j.biopsych.2020.01.006.
    
    
View
   
 
                                          
  20.
  
    Riehm K, Keyes K, Susser E
    
    . Social determinants of health and selection bias in genome-wide association studies. World Psychiatry. 2023; 22(1):160-161.
          PMC: 9840488.
    
          DOI: 10.1002/wps.21047.
    
    
View