I. Ahmed

发表

TLR4 polymorphisms and disease susceptibility

Mamoona Noreen, M. Shah, Sheeba Murad Mall, 2012, Inflammation Research.

Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features.

J. Vincent, A. Caglayan, R. Abou Jamra, 2016, American journal of human genetics.

Association of Pro12Ala (rs1801282) variant of PPAR gamma with Rheumatoid Arthritis in a Pakistani population

A. Bhatti, P. John, I. Ahmed, 2014, Rheumatology International.

MAPPING OF GENES INVOLVED IN NEUROLOGICAL DISORDERS IN PAKISTANI FAMILIES

I. Ahmed, Iltaf Ahmed, 2015 .

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

J. Vincent, M. Rafiq, G. Rouleau, 2014, Human Genetics.

Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability

J. Vincent, M. Rafiq, A. Bhatti, 2016, Psychiatric genetics.

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

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

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

A. Noor, J. Vincent, M. Rafiq, 2017, Molecular Psychiatry.

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.

TLR4 polymorphisms and disease susceptibility

Mamoona Noreen, Sheeba Murad Mall, Shazia Choudhary, 2012, Inflammation Research.

Replication of European Rheumatoid Arthritis Loci in a Pakistani Population

Xingbin Wang, F. Demirci, M. Kamboh, 2013, The Journal of Rheumatology.

Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.

J. Vincent, H. Stehr, H. Ropers, 2015, Human molecular genetics.

Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families

J. Vincent, M. Rafiq, A. Bhatti, 2014, Acta Neuropsychiatrica.

Effects of gasoline engine emissions on health status of auto rickshaw drivers at DIR (L) Khyber Pukhtunkhwa

S. Ullah, A. Khan, I. Ahmed, 2012 .