(Q56262863)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Missing heritability: paternal age effect mutations and selfish spermatogonia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

Andrew Oliver Mungo Wilkie

7 February 2020

series ordinal

2

object named as

Andrew O. M. Wilkie

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

publication date

1 August 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

published in

Nature Reviews Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

589

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634812%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nrg2809-c1

7 February 2020

exact match

0 references

cites work

Paternal factors and schizophrenia risk: de novo mutations and imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Missing heritability and strategies for finding the underlying causes of complex disease

21 January 2018

1 reference

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Common and rare variants in multifactorial susceptibility to common diseases

31 March 2020

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Uncovering the roles of rare variants in common disease through whole-genome sequencing

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Evidence for selective advantage of pathogenic FGFR2 mutations in the male germ line

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

The molecular anatomy of spontaneous germline mutations in human testes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Hyperactive Ras in developmental disorders and cancer

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

MAP'ing CNS development and cognition: an ERKsome process

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Risk of autism and increasing maternal and paternal age in a large north American population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Ethnic ancestry and increased paternal age are risk factors for breast cancer before the age of 40 years.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Exclusive paternal origin of new mutations in Apert syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Age and sex effects on human mutation rates: an old problem with new complexities

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRG2809-C1

Functional impact of global rare copy number variation in autism spectrum disorders

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20634812