(Q37167768)

18 August 2017

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title

Common and rare alleles as causes of complex phenotypes (English)

1 reference

18 August 2017

Constantin Polychronakos

object named as

Constantin Polychronakos

series ordinal

1

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publication date

1 June 2008

1 reference

Current Atherosclerosis Reports

18 August 2017

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18 August 2017

10

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18 August 2017

3

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18 August 2017

194-200

1 reference

https://scigraph.springernature.com/pub.10.1007/s11883-008-0031-1

18 August 2017

0 references

cites work

Lack of MEF2A mutations in coronary artery disease

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0031-1

The Body-Mass Index of Twins Who Have Been Reared Apart

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0031-1

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

21 January 2018

1 reference

12 December 2020

A frameshift mutation in human MC4R is associated with a dominant form of obesity

1 reference

12 December 2020

Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.

1 reference

12 December 2020

Monogenic and other unusual causes of diabetes mellitus

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12 December 2020

The diploid genome sequence of an individual human

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12 December 2020

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

1 reference

12 December 2020

A second generation human haplotype map of over 3.1 million SNPs

1 reference

12 December 2020

Twin study of genetic and environmental effects on lipid levels

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12 December 2020

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

1 reference

12 December 2020

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

1 reference

12 December 2020

Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650)

1 reference

12 December 2020

Highly parallel genomic assays

1 reference

12 December 2020

Genetics of susceptibility to human infectious disease

1 reference

12 December 2020

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

1 reference

12 December 2020

Are rare variants responsible for susceptibility to complex diseases?

1 reference

12 December 2020

Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

1 reference

12 December 2020

Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.

1 reference

12 December 2020

Global variation in copy number in the human genome

1 reference

12 December 2020

Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods

1 reference

12 December 2020

A map of recent positive selection in the human genome

1 reference

12 December 2020

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

12 December 2020

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

12 December 2020

Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"?

1 reference

12 December 2020

Medical sequencing at the extremes of human body mass

1 reference

12 December 2020

HNF-1alpha G319S, a transactivation-deficient mutant, is associated with altered dynamics of diabetes onset in an Oji-Cree community

1 reference

12 December 2020

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

12 December 2020

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

1 reference

12 December 2020

Genetic epidemiology of diabetes

1 reference

12 December 2020

New perspectives for the elucidation of genetic disorders

1 reference

12 December 2020

Remapping the insulin gene/IDDM2 locus in type 1 diabetes.

1 reference

12 December 2020

10.1007/S11883-008-0031-1

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18489846