Admin – Page 6 – Raheel Qamar

Patients HLA DRB1* and DQB1* allele and haplotype association with Hepatitis C virus persistence and clearance.

Ali, L., Mansoor, A., Ahmad, N., Siddiqi, S., Mazhar, K., Muazzam, A.G., Qamar, R. and Khan K.M. Journal of General Virology 91:1931-1938 (2010).

Further considerations in investigating the association of ABO and Rh (D) blood groups with glaucoma—Author reply.

Qamar, R. Canadian Journal of Ophthalmology, 45:178 (2010).

Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia.

Ajmal M., Ahmed W., Sadeque A., Ali SHB., Bukhari SH., Ahmed N., Qamar R. Molecular Biology Reports, 37:3869-75 (2010).

May 18, 2021

A novel familial BBS12 mutation associated with a mild phenotype: implications for clinical and molecular diagnostic strategies.

Pawlik B., Mir A., Iqbal H., Li Y., Nürnberg G., Becker C., Qamar R., Nürnberg, P., Wollnik B. Molecular Syndromology, 1:27-34 (2010).

May 18, 2021

Association of eNOS and HSP70 gene polymorphism with Glaucoma.

Ayub, H., Imran, M., Michael, S., Akhter, F., Ajmal, M., Shafique, S., den Hollander, A.I., Ahmed, A., Qamar, R. Molecular Vision, 16:18-25 (2010).

May 18, 2021

Association of Tumor Necrosis Factor Alpha gene polymorphism G-308A with Pseudoexfoliative Glaucoma in Pakistani population.

Khan, M.I., Micheal, S., Rana, N., Akhtar, F., den Hollander, A.I., Ahmed, A., Qamar, R. Molecular Vision, 15:2861-2867 (2009).

May 18, 2021

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

Azam, M., Khan, M.I., Gal, A., Hussain, A., Shah, S.T.A., Khan, M.S., Sadeque, A., Bokhari, H., Collin, R.W.J., Orth, U., van Genderen,M.M., den Hollander, A.I., Cremers, F.P.M. and Qamar, R. Molecular Vision, 15:2526-2534 (2009).

May 18, 2021

MTHFR Gene C677T and A1298C Polymorphisms and Homocysteine Levels in Primary Open Angle and Primary Closed Angle Glaucoma.

Micheal, S., Qamar, R., Akhtar, F., Khan, M.I., Khan, W.A. and Ahmed, A. Molecular Vision, 15:2268-2278 (2009).

Association of ABO Blood Groups with Glaucoma in the Pakistani Population.

Khan, M.I., Micheal, S., Akhtar, F., Naveed, A., Ahmed, A., Qamar, R. Canadian Journal of Ophthalmology, 44:582-586 (2009).

May 18, 2021

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.

Azam, M., Collin, R.W.J., Khan, M.I., Shah, S.T.A., Qureshi, N., Ajmal, M., den Hollander, A.I., Qamar, R. and Cremers, F.P.M. Molecular Vision, 15:1788-1793 (2009).

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