A unified genetic theory for sporadic and inherited autism (Q24684315)

5

0 references

Jonathan Sebat

object named as

Jonathan Sebat

10

0 references

Catherine Lord

9

object named as

Catherine Lord

0 references

author name string

Xiaoyue Zhao

1

0 references

Anthony Leotta

2

0 references

Vlad Kustanovich

3

0 references

Clara Lajonchere

4

0 references

Kiely Law

6

0 references

Paul Law

7

0 references

Shanping Qiu

8

0 references

Kenny Ye

Proceedings of the National Academy of Sciences of the United States of America

11

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language of work or name

English

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publication date

31 July 2007

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published in

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volume

104

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issue

31

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page(s)

12831-6

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cites work

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A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

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A genomic screen of autism: evidence for a multilocus etiology

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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Advancing paternal age and autism

7 April 2017

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Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

7 April 2017

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Identification and characterization of the tuberous sclerosis gene on chromosome 16

7 April 2017

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Autism as a strongly genetic disorder: evidence from a British twin study

7 April 2017

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Sex differences in the brain: implications for explaining autism

28 September 2017

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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

28 September 2017

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28 September 2017

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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28 November 2018

Identifiers

DOI

10.1073/PNAS.0705803104

1 reference

1041725

ADS bibcode

2007PNAS..10412831Z

0 references

1041725

1 reference

1 reference

1 reference