(Q34136776)

31 July 2017

title

The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism (English)

1 reference

31 July 2017

The NADH‐ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism (English)

1 reference

https://api.crossref.org/works/10.1111/J.1600-0447.2010.01600.X

9 July 2024

0 references

10

K. Kasai

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

author name string

T. Marui

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

I. Funatogawa

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

S. Koishi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

K. Yamamoto

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

H. Matsumoto

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

O. Hashimoto

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

S. Jinde

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

H. Nishida

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

T. Sugiyama

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

K. Watanabe

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

Y. Kano

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

N. Kato

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20825370

9 July 2024

language of work or name

English

0 references

publication date

5 September 2010

1 reference

full work available at URL

31 July 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1600-0447.2010.01600.x

1 reference

https://api.crossref.org/works/10.1111/J.1600-0447.2010.01600.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1600-0447.2010.01600.x

9 July 2024

1 reference

https://api.crossref.org/works/10.1111/J.1600-0447.2010.01600.X

Acta Psychiatrica Scandinavica

9 July 2024

published in

1 reference

31 July 2017

volume

123

1 reference

31 July 2017

issue

2

1 reference

31 July 2017

page(s)

118-124

1 reference

Genetics of austim: complex aetiology for a heterogeneous disorder

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Autism: a mitochondrial disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

The biochemical basis of mitochondrial diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Autism and lactic acidosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Mitochondrial DNA abnormalities and autistic spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Mitochondrial dysfunction in autistic patients with 15q inverted duplication

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Transmission/disequilibrium tests for extended marker haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Candidate-gene approaches for studying complex genetic traits: practical considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

From age correction to genome-wide association

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Association study designs for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

A survey of haplotype variants at several disease candidate genes: the importance of rare variants for complex diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

No association between the neuronal pentraxin II gene polymorphism and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

Oxidative metabolism in Rett syndrome: 1. Clinical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0447.2010.01600.X

21 January 2018

Identifiers

1 reference

31 July 2017

1 reference