Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes-Reference-Cited by-同舟云学术

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Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes

Published:2023-01-02 Issue:1 Volume:50 Page:101-108
ISSN:0301-4460
Container-title:Annals of Human Biology
language:en
Short-container-title:Annals of Human Biology

Author:

Yasmin Tahira¹,Andres Erin M.²³,Ashraf Komal¹,Basra Muhammad Asim Raza¹,Raza Muhammad Hashim³

Affiliation:

1. Centre for Clinical and Nutritional Chemistry, School of Chemistry, University of The Punjab, Lahore, Pakistan

2. Thompson Center for Autism & Neurodevelopment, University of Missouri, Columbia, MO, USA

3. Child Language Doctoral Program (CLDP), University of Kansas, Lawrence, KS, USA

Funder

the National Institute on Deafness and Other Communication Disorders

Publisher

Informa UK Limited

Subject

Public Health, Environmental and Occupational Health,Genetics,Aging,Physiology,Epidemiology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03014460.2023.2180087

Reference58 articles.

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

2. Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in BUD13, a Component of the Retention and Splicing (RES) Complex

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

4. Study of rare genetic variants in TM4SF20, NFXL1, CNTNAP2, and ATP2C2 in Pakistani probands and families with language impairment

5. Association between genes regulating neural pathways for quantitative traits of speech and language disorders

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genome-Wide Mapping of Consanguineous Families Confirms Previously Implicated Gene Loci and Suggests New Loci in Specific Language Impairment (SLI);Children;2024-08-30

2. Insights from homozygous signatures of cervus nippon revealed genetic architecture for components of fitness;Mammalian Genome;2024-08-27

3. Whole Genome Analysis in Consanguineous Families Reveals New Loci for Speech Sound Disorder (SSD);Genes;2024-08-13

4. Assessment of inbreeding depression on morphometric traits among North Indian population cohorts;Discover Public Health;2024-06-24

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