Finding specific genes that cause autism: a combination of approaches will be needed to maximize power (Q50301508)

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scientific article published in October 1998

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Language	Label	Description	Also known as
English	Finding specific genes that cause autism: a combination of approaches will be needed to maximize power	scientific article published in October 1998

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

review article

1 reference

stated in

Europe PubMed Central

title

Finding specific genes that cause autism: a combination of approaches will be needed to maximize power (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

main subject

autism

0 references

author name string

S E Folstein

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

E Bisson

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

S L Santangelo

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

J Piven

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

language of work or name

English

0 references

publication date

1 October 1998

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

published in

Journal of Autism and Developmental Disorders

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

volume

28

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

page(s)

439-445

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

cites work

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Social language use in parents of autistic individuals

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Personality characteristics of the parents of autistic individuals

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage and mental disorders: an update on analytic methodologies.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translating the genetic library: the goals, methods, and applications of the Human Genome Project

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic variation of human serotonin transporter gene expression

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extreme discordant sib pairs for mapping quantitative trait loci in humans

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combining information within and between pedigrees for mapping complex traits.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polygenic disease: methods for mapping complex disease traits

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The affected-pedigree-member method of linkage analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catecholaminergic metabolism and autism.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of linkage between the serotonin transporter and autistic disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete multipoint sib-pair analysis of qualitative and quantitative traits

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and genetics: clinical approach and association study with two markers of HRAS gene

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequencing the human genome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9813779

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1026008606672

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

Dimensions Publication ID

1013233448

0 references

PubMed publication ID

9813779

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9813779

retrieved

2 March 2018

reference URL

http://europepmc.org/abstract/MED/9813779

 

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