(Q34043497)

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Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes

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1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

0 references

8

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

John A.L. Armour

9

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

author name string

Danielle Carpenter

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Sugandha Dhar

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Laura M Mitchell

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Beiyuan Fu

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Jess Tyson

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Nzar A A Shwan

6

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Fengtang Yang

7

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

publication date

18 March 2015

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

24

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

12

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

3472-3480

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Large multiallelic copy number variations in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Ancient human genomes suggest three ancestral populations for present-day Europeans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

The Role of Copy Number Variation in African Americans with Type 2 Diabetes-Associated End Stage Renal Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

The genomic signature of dog domestication reveals adaptation to a starch-rich diet

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

A mechanistic basis for amplification differences between samples and between genome regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Correlating multiallelic copy number polymorphisms with disease susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Accuracy and differential bias in copy number measurement of CCL3L1 in association studies with three auto-immune disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Diversity of human copy number variation and multicopy genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Experimental aspects of copy number variant assays at CCL3L1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Origins and functional impact of copy number variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Diet and the evolution of human amylase gene copy number variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Hotspots for copy number variation in chimpanzees and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Detection of large-scale variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Dynamic molecular combing: stretching the whole human genome for high-resolution studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Evidence of duplication of the human salivary amylase gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

The human alpha-amylase multigene family consists of haplotypes with variable numbers of genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Evolution of the human alpha-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossovers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Selective deficiency of pancreatic amylase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

New Genetic Variants of Parotid Salivary Amylase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498156

5 July 2018

Low copy number of the salivary amylase gene predisposes to obesity.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV098

21 January 2018

Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV098

21 January 2018

Amylase gene structures in primates: retroposon insertions and promoter evolution

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV098

21 January 2018

Association of higher DEFB4 genomic copy number with Crohn's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV098

21 January 2018

Familial occurrence of diminished pancreatic amylase in serum--a "silent" Amy-2 allelic variant?

1 reference

https://pubmed.ncbi.nlm.nih.gov/25788522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiplex Paralogue Ratio Tests for accurate measurement of multiallelic CNVs

1 reference

https://pubmed.ncbi.nlm.nih.gov/25788522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human amylase-encoding genes amy2 and amy3 are identical to AMY2A and AMY2B

1 reference

https://pubmed.ncbi.nlm.nih.gov/25788522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interpretation of polymorphic DNA patterns in the human alpha-amylase multigene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/25788522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in gene copy number and polymorphism of the human salivary amylase isoenzyme system in Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/25788522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDV098

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25788522%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

ResearchGate publication ID

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