T. Nasr

发表

Self-reported health and smoking status, and body mass index: a case-control comparison based on GEN SCRIP (GENetics of SChizophRenia In Pakistan) data

Muntazir Mehdi, C. Pato, M. Pato, 2021, BMJ Open.

Study protocol of DIVERGE, the first genetic epidemiological study of major depressive disorder in Pakistan

J. Knowles, Farooq Naeem, M. Ayub, 2022, Psychiatric genetics.

Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan

J. Vincent, M. Rafiq, E. Schaftingen, 2015, Clinical genetics.

Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment.

J. Vincent, M. Rafiq, H. Sticht, 2015, Human molecular genetics.

Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation.

A. Noor, J. Vincent, R. Weksberg, 2009, American journal of human genetics.

Psychoeducation and the family burden in schizophrenia: a randomized controlled trial.

R. Kausar, T. Nasr, 2009, Annals of general psychiatry.

Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene GPR56 in Pakistani Intellectual Disability Families

J. Vincent, M. Rafiq, Farooq Naeem, 2017, Journal of Pediatric Genetics.

Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment.

M. Rafiq, H. Sticht, A. Reis, 2015, Human Molecular Genetics.