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What will diabetes genomes tell us?
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Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
title
What will diabetes genomes tell us?
(English)
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Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
author
Karen L Mohlke
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1
object named as
Karen L Mohlke
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Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
author name string
Laura J Scott
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2
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Europe PubMed Central
PMCID
3489976
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13 August 2017
publication date
1 December 2012
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Europe PubMed Central
PMCID
3489976
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13 August 2017
published in
Current diabetes report
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stated in
Europe PubMed Central
PMCID
3489976
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13 August 2017
volume
12
1 reference
stated in
Europe PubMed Central
PMCID
3489976
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13 August 2017
issue
6
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Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
page(s)
643-650
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Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
exact match
https://scigraph.springernature.com/pub.10.1007/s11892-012-0321-4
0 references
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1 reference
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1 reference
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1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3489976
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1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3489976
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3489976
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PubMed Central
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30 September 2017
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
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30 September 2017
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PubMed Central
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30 September 2017
A new multipoint method for genome-wide association studies by imputation of genotypes
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30 September 2017
Medical sequencing at the extremes of human body mass
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30 September 2017
Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment
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30 September 2017
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
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30 September 2017
Genetic cause of hyperglycaemia and response to treatment in diabetes
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30 September 2017
Low-coverage sequencing: implications for design of complex trait association studies
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28 June 2018
The functional Thr130Ile and Val255Met polymorphisms of the hepatocyte nuclear factor-4alpha (HNF4A): gene associations with type 2 diabetes or altered beta-cell function among Danes.
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Computational neuroanatomy of speech production.
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T130I mutation in HNF-4alpha gene is a loss-of-function mutation in hepatocytes and is associated with late-onset Type 2 diabetes mellitus in Japanese subjects
1 reference
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PubMed
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retrieved
12 December 2020
based on heuristic
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Identifiers
DOI
10.1007/S11892-012-0321-4
1 reference
stated in
Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
PMCID
3489976
1 reference
stated in
Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
PubMed ID
22983892
1 reference
stated in
Europe PubMed Central
PMCID
3489976
retrieved
13 August 2017
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