(Q47677207)

4 February 2018

title

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes (English)

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4 February 2018

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5

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Johanne Marie Justesen

11

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Henrik Vestergaard

18

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Allan Linneberg

19

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Daníel F. Guðbjartsson

31

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Hafdis Helgadottir

Hafdis T Helgadottir

7

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Rafn Benediktsson

Rafn Benediktsson

27

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Marit E. Jørgensen

Marit E Jørgensen

13

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Torben Hansen

Torben Hansen

21

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Oluf Borbye Pedersen

Oluf Pedersen

32

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Torben Jørgensen

Torben Jørgensen

Valgerdur Steinthorsdottir

20

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Valgerdur Steinthorsdottir

1

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Unnur Þorsteinsdóttir

33

Unnur Thorsteinsdottir

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4 February 2018

Augustine Kong

30

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Gudmar Thorleifsson

2

Gudmar Thorleifsson

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4 February 2018

26

Fereidoun Azizi

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4 February 2018

Patrick Sulem

3

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34

Kari Stefansson

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4 February 2018

Ivan Brandslund

15

Ivan Brandslund

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4 February 2018

Annelli Sandbaek

16

Annelli Sandbæk

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4 February 2018

Gísli Másson

28

Gisli Masson

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4 February 2018

Cramer Christensen

14

Cramer Christensen

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4 February 2018

Astradur B Hreidarsson

24

Astradur B Hreidarsson

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4 February 2018

Asgeir Sigurdsson

6

Asgeir Sigurdsson

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4 February 2018

Torsten Lauritzen

17

Torsten Lauritzen

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4 February 2018

author name string

Hannes Helgason

4

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4 February 2018

Hrefna Johannsdottir

8

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4 February 2018

Olafur T Magnusson

9

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4 February 2018

Sigurjon A Gudjonsson

10

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4 February 2018

Marie N Harder

12

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4 February 2018

Maryam S Daneshpour

22

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Mohammad-Sadegh Fallah

23

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4 February 2018

Gunnar Sigurdsson

25

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4 February 2018

Agnar Helgason

29

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4 February 2018

language of work or name

English

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publication date

26 January 2014

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4 February 2018

published in

Nature Genetics

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4 February 2018

volume

46

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4 February 2018

issue

3

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4 February 2018

page(s)

294-298

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4 February 2018

https://scigraph.springernature.com/pub.10.1038/ng.2882

exact match

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cites work

Detection of sharing by descent, long-range phasing and haplotype imputation

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Parental origin of sequence variants associated with complex diseases

21 January 2018

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Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

21 January 2018

1 reference

MODY in Iceland is associated with mutations in HNF-1alpha and a novel mutation in NeuroD1.

21 January 2018

1 reference

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

21 January 2018

1 reference

Common variants in WFS1 confer risk of type 2 diabetes

21 January 2018

1 reference

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

21 January 2018

1 reference

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

21 January 2018

1 reference

Cyclins D2 and D1 are essential for postnatal pancreatic beta-cell growth

21 January 2018

1 reference

Genetics of gene expression and its effect on disease

21 January 2018

1 reference

Deletion of peptide amidation enzymatic activity leads to edema and embryonic lethality in the mouse

21 January 2018

1 reference

Probing the production of amidated peptides following genetic and dietary copper manipulations

21 January 2018

1 reference

Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes

21 January 2018

1 reference

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

21 January 2018

1 reference

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

21 January 2018

1 reference

A randomized non-pharmacological intervention study for prevention of ischaemic heart disease: baseline results Inter99.

21 January 2018

1 reference

The prevalence and morbidity of sensitization to fragrance mix I in the general population.

21 January 2018

1 reference

Prevention of non-communicable disease in a population in nutrition transition: Tehran Lipid and Glucose Study phase II.

21 January 2018

1 reference

A novel endonuclease IV post-PCR genotyping system

21 January 2018

1 reference

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.

21 January 2018

1 reference

NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

21 January 2018

1 reference

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

21 January 2018

1 reference

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke

21 January 2018

1 reference

The human genome browser at UCSC

21 January 2018

1 reference

12 December 2020

Beta cell replication is the primary mechanism for maintaining postnatal beta cell mass.

1 reference

12 December 2020

Early-onset type-II diabetes mellitus (MODY4) linked to IPF1

1 reference

12 December 2020

The biosynthesis of neuropeptides: peptide alpha-amidation

1 reference

12 December 2020

Statistical aspects of the analysis of data from retrospective studies of disease

1 reference

12 December 2020

The ADDITION study: proposed trial of the cost-effectiveness of an intensive multifactorial intervention on morbidity and mortality among people with Type 2 diabetes detected by screening

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.2882

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4 February 2018

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4 February 2018