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Page 1
Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes.
Ann Hum Biol. 2023 Feb;50(1):100-107. doi: 10.1080/03014460.2023.2180087.
Ann Hum Biol. 2023.
PMID: 36786444
Free PMC article.
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.
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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Innovative Family-Based Genetically Informed Series of Analyses of Whole-Exome Data Supports Likely Inheritance for Grammar in Children with Specific Language Impairment.
Andres EM, Earnest KK, Xuan H, Zhong C, Rice ML, Raza MH.
Andres EM, et al.
Children (Basel). 2023 Jun 28;10(7):1119. doi: 10.3390/children10071119.
Children (Basel). 2023.
PMID: 37508616
Free PMC article.
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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.
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.
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Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in BUD13, a Component of the Retention and Splicing (RES) Complex.
Andres EM, Earnest KK, Zhong C, Rice ML, Raza MH.
Andres EM, et al.
Brain Sci. 2021 Dec 30;12(1):47. doi: 10.3390/brainsci12010047.
Brain Sci. 2021.
PMID: 35053791
Free PMC article.
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Study of rare genetic variants in TM4SF20, NFXL1, CNTNAP2, and ATP2C2 in Pakistani probands and families with language impairment.
Andres EM, Neely HL, Hafeez H, Yasmin T, Kausar F, Basra MAR, Raza MH.
Andres EM, et al.
Meta Gene. 2021 Dec;30:100966. doi: 10.1016/j.mgene.2021.100966. Epub 2021 Aug 27.
Meta Gene. 2021.
PMID: 34540591
Free PMC article.
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