Literature DB >> 20706738

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

Muhammad Hashim Raza1, Sheikh Riazuddin, Dennis Drayna.   

Abstract

Stuttering is a common speech disorder with substantial genetic contributions. To better understand the genetic factors involved in stuttering, we performed a genome-wide linkage study in a newly-ascertained consanguineous stuttering family from Pakistan. A linkage scan in this family using parametric linkage analysis revealed significant linkage only on chromosome 3q13.2-3q13.33, with a maximum two-point LOD score of 4.23 under an autosomal recessive model of inheritance.

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Year:  2010        PMID: 20706738      PMCID: PMC3030966          DOI: 10.1007/s00439-010-0871-y

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  Results of a genome-wide linkage scan for stuttering.

Authors:  Yin Yao Shugart; Jennifer Mundorff; James Kilshaw; Kimberly Doheny; Betty Doan; Jacqueline Wanyee; Eric D Green; Dennis Drayna
Journal:  Am J Med Genet A       Date:  2004-01-15       Impact factor: 2.802

2.  Genomewide significant linkage to stuttering on chromosome 12.

Authors:  Naveeda Riaz; Stacy Steinberg; Jamil Ahmad; Anna Pluzhnikov; Sheikh Riazuddin; Nancy J Cox; Dennis Drayna
Journal:  Am J Hum Genet       Date:  2005-02-15       Impact factor: 11.025

3.  easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data.

Authors:  K Hoffmann; T H Lindner
Journal:  Bioinformatics       Date:  2005-07-12       Impact factor: 6.937

4.  Genetic studies of stuttering in a founder population.

Authors:  Jacqueline K Wittke-Thompson; Nicoline Ambrose; Ehud Yairi; Cheryl Roe; Edwin H Cook; Carole Ober; Nancy J Cox
Journal:  J Fluency Disord       Date:  2006-12-30       Impact factor: 2.538

5.  New complexities in the genetics of stuttering: significant sex-specific linkage signals.

Authors:  Rathi Suresh; Nicoline Ambrose; Cheryl Roe; Anna Pluzhnikov; Jacqueline K Wittke-Thompson; Maggie C-Y Ng; Xiaolin Wu; Edwin H Cook; Cecilia Lundstrom; Marie Garsten; Ruth Ezrati; Ehud Yairi; Nancy J Cox
Journal:  Am J Hum Genet       Date:  2006-02-01       Impact factor: 11.025

6.  Mutations in the lysosomal enzyme-targeting pathway and persistent stuttering.

Authors:  Changsoo Kang; Sheikh Riazuddin; Jennifer Mundorff; Donna Krasnewich; Penelope Friedman; James C Mullikin; Dennis Drayna
Journal:  N Engl J Med       Date:  2010-02-10       Impact factor: 91.245

7.  Association between dopaminergic genes (SLC6A3 and DRD2) and stuttering among Han Chinese.

Authors:  Jie Lan; Manshu Song; Chunhui Pan; Guoqing Zhuang; Youxin Wang; Wenzhan Ma; Qiaoyun Chu; Qingxuan Lai; Feng Xu; Yanli Li; Lixin Liu; Wei Wang
Journal:  J Hum Genet       Date:  2009-07-10       Impact factor: 3.172

  7 in total
  16 in total

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

Authors:  M Hashim Raza; Rafael Mattera; Robert Morell; Eduardo Sainz; Rachel Rahn; Joanne Gutierrez; Emily Paris; Jessica Root; Beth Solomon; Carmen Brewer; M Asim Raza Basra; Shaheen Khan; Sheikh Riazuddin; Allen Braun; Juan S Bonifacino; Dennis Drayna
Journal:  Am J Hum Genet       Date:  2015-11-05       Impact factor: 11.025

2.  Characteristics of Fluency and Speech in Two Families With High Incidences of Stuttering.

Authors:  Sheila V Stager; Frances J Freeman; Allen Braun
Journal:  J Speech Lang Hear Res       Date:  2015-10       Impact factor: 2.297

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

Authors:  Erin M Andres; Huma Hafeez; Adnan Yousaf; Sheikh Riazuddin; Mabel L Rice; Muhammad Asim Raza Basra; Muhammad Hashim Raza
Journal:  Eur J Hum Genet       Date:  2019-04-11       Impact factor: 4.246

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

Authors:  Muhammad Hashim Raza; Rana Amjad; Sheikh Riazuddin; Dennis Drayna
Journal:  Hum Genet       Date:  2011-12-29       Impact factor: 4.132

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

Authors:  M Hashim Raza; E Michael Gertz; Jennifer Mundorff; Joseph Lukong; Judith Kuster; Alejandro A Schäffer; Dennis Drayna
Journal:  Hum Genet       Date:  2012-12-13       Impact factor: 4.132

6.  Are variants in sex hormone metabolizing genes associated with stuttering?

Authors:  Carlos E Frigerio Domingues; Katherine Grainger; Hui Cheng; Danilo Moretti-Ferreira; Sheikh Riazuddin; Dennis Drayna
Journal:  Brain Lang       Date:  2019-02-22       Impact factor: 2.381

7.  Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case.

Authors:  Aline L Petrin; Célia M Giacheti; Luciana P Maximino; Dagma V M Abramides; Sthella Zanchetta; Natalia F Rossi; Antônio Richieri-Costa; Jeffrey C Murray
Journal:  Am J Med Genet A       Date:  2010-12       Impact factor: 2.802

8.  A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.

Authors:  Tae-Un Han; John Park; Carlos F Domingues; Danilo Moretti-Ferreira; Emily Paris; Eduardo Sainz; Joanne Gutierrez; Dennis Drayna
Journal:  Neurobiol Dis       Date:  2014-05-05       Impact factor: 5.996

Review 9.  Genetic advances in the study of speech and language disorders.

Authors:  D F Newbury; A P Monaco
Journal:  Neuron       Date:  2010-10-21       Impact factor: 17.173

Review 10.  A role for inherited metabolic deficits in persistent developmental stuttering.

Authors:  Changsoo Kang; Dennis Drayna
Journal:  Mol Genet Metab       Date:  2012-07-28       Impact factor: 4.797

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