All Stories

  1. Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3′ splice acceptor site of intron 2

    Article • Congenital Anomalies, October 2018, Wiley

    Dr Haiba Kaul

  2. Fine mapping of chromosome 9 locus associated with congenital cataract

    Article • International Ophthalmology, June 2017, Springer Science + Business Media

    Dr Haiba Kaul

  3. In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma

    Article • International Ophthalmology, April 2017, Springer Science + Business Media

    Dr Haiba Kaul

  4. Interleukin 6 Receptor (IL6-R) Gene Polymorphisms Underlie Susceptibility to Rheumatoid Arthritis

    Article • Clinical Laboratory, January 2017, Clinical Laboratory Publications

    Dr Haiba Kaul

  5. Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

    Article • PLoS ONE, November 2016, PLOS

    Dr Haiba Kaul

  6. Determination of Serum Trace Elements (Zn, Cu, and Fe) in Pakistani Patients with Rheumatoid Arthritis

    Article • Biological Trace Element Research, May 2016, Springer Science + Business Media

    Dr Haiba Kaul

  7. Missense mutation inSLC4A11in two Pakistani families affected with congenital hereditary endothelial dystrophy (CHED2)

    Article • Clinical and Experimental Optometry, August 2015, Wiley

    Dr Haiba Kaul

  8. Ectopia Lentis in a Consanguineous Pakistani Family and a Novel Locus on Chromosome 8q

    Article • Archives of Ophthalmology, August 2010, American Medical Association (AMA)

    Dr Haiba Kaul