Raza MH - Search Results

1

Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.

Raza MH, Riazuddin S, Drayna D. Raza MH, et al. Hum Genet. 2010 Oct;128(4):461-3. doi: 10.1007/s00439-010-0871-y. Epub 2010 Aug 13. Hum Genet. 2010. PMID: 20706738 Free PMC article.

2

Population studies for STR loci (D3S1358, D5S818, D7S820, D18S51 and FGA) in NWFP and Sindhi populations of Pakistan for forensic use.

Saqib Shahzad M, Abbas Bokhari SY, Rao AQ, Raza MH, Ullah O, Zia-Ur-rahman, Shahid AA, Ahmad Z, Riazuddin S. Saqib Shahzad M, et al. Among authors: raza mh. Arch Med Sadowej Kryminol. 2004 Oct-Dec;54(4):215-22. Arch Med Sadowej Kryminol. 2004. PMID: 15782779

3

Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q.

Raza MH, Amjad R, Riazuddin S, Drayna D. Raza MH, et al. Hum Genet. 2012 Feb;131(2):311-3. doi: 10.1007/s00439-011-1134-2. Epub 2011 Dec 29. Hum Genet. 2012. PMID: 22205390 Free PMC article.

4

Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance.

Raza MH, Gertz EM, Mundorff J, Lukong J, Kuster J, Schäffer AA, Drayna D. Raza MH, et al. Hum Genet. 2013 Apr;132(4):385-96. doi: 10.1007/s00439-012-1252-5. Epub 2012 Dec 13. Hum Genet. 2013. PMID: 23239121 Free PMC article. Clinical Trial.

5

Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes.

Raza MH, Domingues CE, Webster R, Sainz E, Paris E, Rahn R, Gutierrez J, Chow HM, Mundorff J, Kang CS, Riaz N, Basra MA, Khan S, Riazuddin S, Moretti-Ferreira D, Braun A, Drayna D. Raza MH, et al. Eur J Hum Genet. 2016 Apr;24(4):529-34. doi: 10.1038/ejhg.2015.154. Epub 2015 Jul 1. Eur J Hum Genet. 2016. PMID: 26130485 Free PMC article.

6

Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering.

Raza MH, Mattera R, Morell R, Sainz E, Rahn R, Gutierrez J, Paris E, Root J, Solomon B, Brewer C, Basra MA, Khan S, Riazuddin S, Braun A, Bonifacino JS, Drayna D. Raza MH, et al. Am J Hum Genet. 2015 Nov 5;97(5):715-25. doi: 10.1016/j.ajhg.2015.10.007. Am J Hum Genet. 2015. PMID: 26544806 Free PMC article.

7

A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).

Andres EM, Hafeez H, Yousaf A, Riazuddin S, Rice ML, Basra MAR, Raza MH. Andres EM, et al. Among authors: raza mh. Eur J Hum Genet. 2019 Aug;27(8):1274-1285. doi: 10.1038/s41431-019-0398-1. Epub 2019 Apr 11. Eur J Hum Genet. 2019. PMID: 30976110 Free PMC article.

8

Somatic embryogenesis in wild relatives of cotton (Gossypium Spp.).

Rao AQ, Hussain SS, Shahzad MS, Bokhari SY, Raza MH, Rakha A, Majeed A, Shahid AA, Saleem Z, Husnain T, Riazuddin S. Rao AQ, et al. Among authors: raza mh. J Zhejiang Univ Sci B. 2006 Apr;7(4):291-8. doi: 10.1631/jzus.2006.B0291. J Zhejiang Univ Sci B. 2006. PMID: 16532531 Free PMC article.

9

Whole Genome Analysis in Consanguineous Families Reveals New Loci for Speech Sound Disorder (SSD).

Yasmin T, Sadia A, Nadeem L, Basra MAR, Rice ML, Raza MH. Yasmin T, et al. Among authors: raza mh. Genes (Basel). 2024 Aug 13;15(8):1069. doi: 10.3390/genes15081069. Genes (Basel). 2024. PMID: 39202429 Free PMC article.

10

Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment.

Andres EM, Earnest KK, Smith SD, Rice ML, Raza MH. Andres EM, et al. Among authors: raza mh. J Speech Lang Hear Res. 2020 Dec 14;63(12):4046-4061. doi: 10.1044/2020_JSLHR-20-00102. Epub 2020 Nov 13. J Speech Lang Hear Res. 2020. PMID: 33186502 Free PMC article.

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