(Q36605965)

15 August 2017

1 reference

title

The genetics of health (English)

1 reference

15 August 2017

2

1 reference

15 August 2017

Joseph H Nadeau

1

1 reference

PubMed ID

17006459

15 August 2017

language of work or name

English

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publication date

1 October 2006

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15 August 2017

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15 August 2017

38

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15 August 2017

10

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15 August 2017

1095-1098

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https://scigraph.springernature.com/pub.10.1038/ng1006-1095

15 August 2017

0 references

cites work

Modifier genes in mice and humans

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

The genetics of exceptional human longevity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Inheritance and drug response

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

The genetics of human obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Appetite-suppressant drugs and the risk of primary pulmonary hypertension. International Primary Pulmonary Hypertension Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Arthritis medicines and cardiovascular events--"house of coxibs".

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Cardiotoxicity of the cancer therapeutic agent imatinib mesylate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Complement factor H polymorphism and age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Complement factor H variant increases the risk of age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

The Ter mutation in the dead end gene causes germ cell loss and testicular germ cell tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Sensitized polygenic trait analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

SCNM1, a putative RNA splicing factor that modifies disease severity in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

A natural allele of Nxf1 suppresses retrovirus insertional mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Modification of human hearing loss by plasma-membrane calcium pump PMCA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

PTEN: one gene, many syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

A male germ cell tumor-susceptibility-determining locus, pgct1, identified on murine chromosome 13

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Genetic modifiers interact with Cpe(fat) to affect body weight, adiposity, and hyperglycemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Identification of major quantitative trait loci controlling body weight variation in ob/ob mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

The origins, patterns and implications of human spontaneous mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Genetics of recurrent pregnancy loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

From genotype to phenotype: buffering mechanisms and the storage of genetic information

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Hsp90 as a capacitor of phenotypic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

A vision for the future of genomics research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

Statistical false positive or true disease pathway?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

DNA pooling as a quick method for finding candidate linkages in multigenic trait analysis: an example involving susceptibility to germ cell tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

7 January 2021

Genetic modifiers of atherosclerosis in mice

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

7 January 2021

In silico quantitative trait locus map for atherosclerosis susceptibility in apolipoprotein E-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

7 January 2021

Quantitative trait locus mapping of genetic modifiers of metabolic syndrome and atherosclerosis in low-density lipoprotein receptor-deficient mice: identification of a locus for metabolic syndrome and increased atherosclerosis on chromosome 4.

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

7 January 2021

Genetic background alters the spectrum of tumors that develop in p53-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FNG1006-1095

7 January 2021

Identifiers

DOI

10.1038/NG1006-1095

1 reference

PubMed ID

17006459

Dimensions Publication ID

15 August 2017

0 references

1 reference

PubMed ID

17006459