All Stories

  1. Parental Consanguineous Marriages are Associated with Early Age of Onset of Schizophrenia in a Pakistani Cohort
  2. Preliminary evaluation of a “formulation-driven cognitive behavioral guided self-help (fCBT-GSH)” for crisis and transitional case management clients
  3. A survey of eMedia-delivered interventions for schizophrenia used in randomized controlled trials
  4. Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability
  5. Clozapine for psychotic disorders in adults with intellectual disabilities
  6. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
  7. The UK10K project identifies rare variants in health and disease
  8. Mutations in the histamine N -methyltransferase gene, HNMT , are associated with nonsyndromic autosomal recessive intellectual disability
  9. Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features
  10. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
  11. Brief Culturally adapted CBT (CaCBT) for depression: A randomized controlled trial from Pakistan
  12. Brief culturally adapted CBT for psychosis (CaCBTp): A randomized controlled trial from a low income country
  13. Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment
  14. Interventions Following Traumatic Event in Children and Adolescents: An Evidence-Based Response
  15. Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families
  16. Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
  17. Rate and predictors of psychotic symptoms after Kashmir earthquake
  18. A Qualitative Study to Explore Patients’, Carers’ and Health Professionals’ Views to Culturally Adapt CBT for Psychosis (CBTp) in Pakistan
  19. Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder
  20. Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan
  21. Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability
  22. Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
  23. A multicentre randomised controlled trial of a carer supervised Culturally adapted CBT (CaCBT) based self-help for depression in Pakistan
  24. Domestic violence, mental illness and suicidal ideation – A study from Lahore, Pakistan
  25. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability
  26. Clozapine for psychotic disorders in adults with intellectual disabilities
  27. Homozygosity mapping of depressive disorder in a large family from Pakistan: Significant linkage on chromosome 6 and 9
  28. Views of Depressed Patients in Pakistan Concerning Their Illness, Its Causes, and Treatments
  29. Can watching traumatic events on TV cause PTSD symptoms? Evidence from Pakistan
  30. Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
  31. Identification of genomic deletions spanning thePCDH19gene in two unrelated girls with intellectual disability and seizures
  32. Psychological Morbidity in Children 18 months after Kashmir Earthquake of 2005
  33. Urdu translation of the ICD-10 chapter V (F), Research Diagnostic Criteria (RDC): Process and principles of translation
  34. Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability
  35. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms
  36. Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability
  37. Prevalence and psychosocial risk factors of PTSD: 18months after Kashmir earthquake in Pakistan
  38. Preliminary Evaluation of Culturally Sensitive CBT for Depression in Pakistan: Findings from Developing Culturally-Sensitive CBT Project (DCCP)
  39. The genetic basis of non-syndromic intellectual disability: a review
  40. Cognitive Behavior Therapy in Pakistan Interview Guide
  41. Psychologists experience of cognitive behaviour therapy in a developing country: a qualitative study from Pakistan
  42. Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation
  43. University students’ views about compatibility of cognitive behaviour therapy (CBT) with their personal, social and religious values (a study from Pakistan)
  44. Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3
  45. Psychiatric morbidity and domestic violence: a survey of married women in Lahore
  46. CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa
  47. Angry Wives, Abusive Husbands: Relationship Between Domestic Violence and Psychosocial Variables
  48. CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa
  49. Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment
  50. Linkage Analysis in a Large Family from Pakistan with Depression and a High Incidence of Consanguineous Marriages
  51. APPNA SEHAT: A description of the development of a health education programme in rural Pakistan
  52. Psychiatric Training in Pakistan