Literature DB >> 11262873

The origins, patterns and implications of human spontaneous mutation.

J F Crow1.   

Abstract

The germline mutation rate in human males, especially older males, is generally much higher than in females, mainly because in males there are many more germ-cell divisions. However, there are some exceptions and many variations. Base substitutions, insertion-deletions, repeat expansions and chromosomal changes each follow different rules. Evidence from evolutionary sequence data indicates that the overall rate of deleterious mutation may be high enough to have a large effect on human well-being. But there are ways in which the impact of deleterious mutations can be mitigated.

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Year:  2000        PMID: 11262873     DOI: 10.1038/35049558

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  288 in total

1.  One hundred years of mouse genetics: an intellectual history. II. The molecular revolution (1981-2002).

Authors:  Kenneth Paigen
Journal:  Genetics       Date:  2003-04       Impact factor: 4.562

Review 2.  Chromosomal translocations and palindromic AT-rich repeats.

Authors:  Takema Kato; Hiroki Kurahashi; Beverly S Emanuel
Journal:  Curr Opin Genet Dev       Date:  2012-03-06       Impact factor: 5.578

3.  Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening.

Authors:  Juanliang Cai; Barbara K Goodman; Ankita S Patel; John B Mulliken; Lionel Van Maldergem; George E Hoganson; William A Paznekas; Ziva Ben-Neriah; Ruth Sheffer; Michael L Cunningham; Donna L Daentl; Ethylin Wang Jabs
Journal:  Hum Genet       Date:  2003-09-25       Impact factor: 4.132

4.  Parental genotypes in the risk of a complex disease.

Authors:  Damian Labuda; Maja Krajinovic; Audrey Sabbagh; Claire Infante-Rivard; Daniel Sinnett
Journal:  Am J Hum Genet       Date:  2002-06-07       Impact factor: 11.025

5.  Is the rate of insertion and deletion mutation male biased?: Molecular evolutionary analysis of avian and primate sex chromosome sequences.

Authors:  Hannah Sundström; Matthew T Webster; Hans Ellegren
Journal:  Genetics       Date:  2003-05       Impact factor: 4.562

Review 6.  Rett syndrome and MeCP2: linking epigenetics and neuronal function.

Authors:  Mona D Shahbazian; Huda Y Zoghbi
Journal:  Am J Hum Genet       Date:  2002-11-19       Impact factor: 11.025

7.  Insertions and deletions are male biased too: a whole-genome analysis in rodents.

Authors:  Kateryna D Makova; Shan Yang; Francesca Chiaromonte
Journal:  Genome Res       Date:  2004-04       Impact factor: 9.043

Review 8.  Measuring genome instability in aging - a mini-review.

Authors:  Wenge Li; Jan Vijg
Journal:  Gerontology       Date:  2011-12-10       Impact factor: 5.140

9.  De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalance.

Authors:  Charlene Sibbons; Joan K Morris; John A Crolla; Patricia A Jacobs; N Simon Thomas
Journal:  Eur J Hum Genet       Date:  2011-09-28       Impact factor: 4.246

10.  Functional constraints and frequency of deleterious mutations in noncoding DNA of rodents.

Authors:  Peter D Keightley; Daniel J Gaffney
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-03       Impact factor: 11.205

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