Literature DB >> 1346390

Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity.

O Steinlein1, A Anokhin, M Yping, E Schalt, F Vogel.   

Abstract

The localization of a gene responsible for a normal variant of the human electroencephalogram to the distal part of chromosome 20q is reported. A linkage analysis, including 17 families with 191 individuals, tested with 73 RFLPs and 22 blood and serological markers, was performed for the low-voltage electroencephalogram. This is a normal variant of the human electroencephalogram with an autosomal dominant mode of inheritance. The results present strong evidence for close linkage with the highly polymorphic marker CMM6 (D20S19) and for genetic heterogeneity.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1346390     DOI: 10.1016/0888-7543(92)90408-k

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  20 in total

1.  A genetic study of the human low-voltage electroencephalogram.

Authors:  A Anokhin; O Steinlein; C Fischer; Y Mao; P Vogt; E Schalt; F Vogel
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

Review 2.  Genetic analysis of sleep.

Authors:  Amanda Crocker; Amita Sehgal
Journal:  Genes Dev       Date:  2010-06-15       Impact factor: 11.361

Review 3.  Genetics of narcolepsy and other sleep disorders.

Authors:  E Mignot
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

Review 4.  Control of sleep and wakefulness.

Authors:  Ritchie E Brown; Radhika Basheer; James T McKenna; Robert E Strecker; Robert W McCarley
Journal:  Physiol Rev       Date:  2012-07       Impact factor: 37.312

Review 5.  Genetic psychophysiology: advances, problems, and future directions.

Authors:  Andrey P Anokhin
Journal:  Int J Psychophysiol       Date:  2014-04-13       Impact factor: 2.997

6.  Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population.

Authors:  Qian Peng; Nicholas J Schork; Kirk C Wilhelmsen; Cindy L Ehlers
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-04-24       Impact factor: 3.568

7.  Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q.

Authors:  O Steinlein; V Schuster; C Fischer; M Häussler
Journal:  Hum Genet       Date:  1995-04       Impact factor: 4.132

8.  Heritability of human brain functioning as assessed by electroencephalography.

Authors:  C E van Beijsterveldt; P C Molenaar; E J de Geus; D I Boomsma
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

9.  Low voltage alpha EEG phenotype is associated with reduced amplitudes of alpha event-related oscillations, increased cortical phase synchrony, and a low level of response to alcohol.

Authors:  Cindy L Ehlers; Derek N Wills; Evelyn Phillips; James Havstad
Journal:  Int J Psychophysiol       Date:  2015-07-04       Impact factor: 2.997

10.  EEG alpha phenotypes: linkage analyses and relation to alcohol dependence in an American Indian community study.

Authors:  Cindy L Ehlers; Ian R Gizer; Evelyn Phillips; Kirk C Wilhelmsen
Journal:  BMC Med Genet       Date:  2010-03-18       Impact factor: 2.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.