(Q57161547)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

review article

1 reference

title

Mendelian disorders and multifactorial traits: the big divide or one for all? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

author

Stilianos Antonarakis

1

1 reference

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31 January 2020

author name string

Aravinda Chakravarti

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

John Hardy

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Jonathan C Cohen

3

1 reference

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31 January 2020

publication date

1 May 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

published in

Nature Reviews Genetics

1 reference

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31 January 2020

volume

11

1 reference

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31 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

page(s)

380-384

1 reference

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https://scigraph.springernature.com/pub.10.1038/nrg2793

31 January 2020

exact match

0 references

cites work

Application of genome-wide single nucleotide polymorphism typing: simple association and beyond

1 reference

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans

31 March 2020

1 reference

Targeted capture and massively parallel sequencing of 12 human exomes

31 March 2020

1 reference

The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases

31 March 2020

1 reference

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

31 March 2020

1 reference

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

31 March 2020

1 reference

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

31 March 2020

1 reference

Inflammation, the complement system and the diseases of aging

31 March 2020

1 reference

The complement cascade: Yin-Yang in neuroinflammation--neuro-protection and -degeneration

31 March 2020

1 reference

Finding the missing heritability of complex diseases

31 March 2020

1 reference

Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias.

31 March 2020

1 reference

A polymorphic DNA marker genetically linked to Huntington's disease

31 March 2020

1 reference

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

31 March 2020

1 reference

Initial sequencing and analysis of the human genome

31 March 2020

1 reference

The Sequence of the Human Genome

31 March 2020

1 reference

Initial sequencing and comparative analysis of the mouse genome

31 March 2020

1 reference

A haplotype map of the human genome

31 March 2020

1 reference

Exome sequencing identifies the cause of a mendelian disorder

31 March 2020

1 reference

Genetic mapping in human disease

31 March 2020

1 reference

Conserved non-genic sequences - an unexpected feature of mammalian genomes

31 March 2020

1 reference

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20395971

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRG2793

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20395971%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference