Mahmood Baig S - Search Results

1

Compound heterozygous ASPM mutations in Pakistani MCPH families.

Muhammad F, Mahmood Baig S, Hansen L, Sajid Hussain M, Anjum Inayat I, Aslam M, Anver Qureshi J, Toilat M, Kirst E, Wajid M, Nürnberg P, Eiberg H, Tommerup N, Kjaer KW. Muhammad F, et al. Among authors: mahmood baig s. Am J Med Genet A. 2009 May;149A(5):926-30. doi: 10.1002/ajmg.a.32749. Am J Med Genet A. 2009. PMID: 19353628

2

β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan.

Mahmood Baig S, Sabih D, Rahim MK, Azhar A, Tariq M, Sajid Hussain M, Saqlan Naqvi SM, Raja GK, Khan TN, Jameel M, Iram Z, Noor S, Baig UR, Qureshi JA, Baig SA, Bakhtiar SM. Mahmood Baig S, et al. J Pediatr Hematol Oncol. 2012 Mar;34(2):90-2. doi: 10.1097/MPH.0b013e31823752f3. J Pediatr Hematol Oncol. 2012. PMID: 22258353

3

A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family.

Abdullah U, Farooq M, Mang Y, Marriam Bakhtiar S, Fatima A, Hansen L, Kjaer KW, Larsen LA, Faryal S, Tommerup N, Mahmood Baig S. Abdullah U, et al. Among authors: mahmood baig s. Eur J Med Genet. 2017 Dec;60(12):627-630. doi: 10.1016/j.ejmg.2017.07.017. Epub 2017 Aug 2. Eur J Med Genet. 2017. PMID: 28778786

4

Genome-Wide Supported Risk Variants in MIR137, CACNA1C, CSMD1, DRD2, and GRM3 Contribute to Schizophrenia Susceptibility in Pakistani Population.

Fatima A, Farooq M, Abdullah U, Tariq M, Mustafa T, Iqbal M, Tommerup N, Mahmood Baig S. Fatima A, et al. Among authors: mahmood baig s. Psychiatry Investig. 2017 Sep;14(5):687-692. doi: 10.4306/pi.2017.14.5.687. Epub 2017 Sep 11. Psychiatry Investig. 2017. PMID: 29042896 Free PMC article.

5

Identification of a novel variant in GPR56/ADGRG1 gene through whole exome sequencing in a consanguineous Pakistani family.

Zulfiqar S, Tariq M, Ramzan S, Khan A, Sher M, Ali Z, Dahl N, Abdullah U, Mahmood Baig S. Zulfiqar S, et al. Among authors: mahmood baig s. J Clin Neurosci. 2021 Dec;94:8-12. doi: 10.1016/j.jocn.2021.09.027. Epub 2021 Sep 30. J Clin Neurosci. 2021. PMID: 34863467

6

Recurrence mutation in RBBP8 gene causing non-syndromic autosomal recessive primary microcephaly; geometric simulation approach for insight into predicted computational models.

Batool T, Irshad S, Riaz M, Mahmood Baig S, Nuernberg P, Hussain MS. Batool T, et al. Among authors: mahmood baig s. J Hum Genet. 2023 Jul;68(7):469-475. doi: 10.1038/s10038-023-01132-6. Epub 2023 Mar 3. J Hum Genet. 2023. PMID: 36864288

7

A Novel MAG Variant Causes Hereditary Spastic Paraplegia in a Consanguineous Pakistani Family.

Akram R, Anwar H, Muzaffar H, Turchetti V, Lau T, Vona B, Makhdoom EUH, Iqbal J, Mahmood Baig S, Hussain G, Efthymiou S, Houlden H. Akram R, et al. Among authors: mahmood baig s. Genes (Basel). 2024 Sep 13;15(9):1203. doi: 10.3390/genes15091203. Genes (Basel). 2024. PMID: 39336794 Free PMC article.

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