(Q36761965)

English

A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height

scientific article published on February 2016

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

0 references

alpha-1-antitrypsin deficiency

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

6

object named as

Mika Kivimaki

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object named as

Andrew Wong

12

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object named as

Meena Kumari

7

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object named as

Ian J Deary

4

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Richard M Martin

object named as

Richard M Martin

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13

object named as

Diana Kuh

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Avan Aihie Sayer

object named as

Avan Aihie Sayer

10

0 references

Yoav Ben-Shlomo

object named as

Yoav Ben-Shlomo

2

0 references

3

object named as

Cyrus Cooper

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

author name string

Teri-Louise North

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

John Gallacher

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Alison Pattie

9

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

John M Starr

11

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Santiago Rodriguez

14

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Ian N M Day

15

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

language of work or name

0 references

publication date

1 February 2016

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

53

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Europe PubMed Central

PMC publication ID

16 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

280-288

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

SPARTA clinical trial design: exploring the efficacy and safety of two dose regimens of alpha1-proteinase inhibitor augmentation therapy in alpha1-antitrypsin deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Defining the role of common variation in the genomic and biological architecture of adult human height

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Role of alpha-1 antitrypsin in human health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Evidence of widespread selection on standing variation in Europe at height-associated SNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Molecular and population analysis of natural selection on the human haptoglobin duplication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Cohort profile: the 'children of the 90s'—the index offspring of the Avon Longitudinal Study of Parents and Children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Absence of association of a single-nucleotide polymorphism in the TERT-CLPTM1L locus with age-related phenotypes in a large multicohort study: the HALCyon programme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Objectively measured physical capability levels and mortality: systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Common SNPs explain a large proportion of the heritability for human height

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Development of predictive models for airflow obstruction in alpha-1-antitrypsin deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Does cognition predict mortality in midlife? Results from the Whitehall II cohort study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

A map of recent positive selection 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=4819619

29 September 2017

The selective advantage of alpha1-antitrypsin deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Chronic obstructive pulmonary disease in alpha1-antitrypsin PI MZ heterozygotes: a meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Phenylketonuria mutations in Europe

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

PAHdb 2003: what a locus-specific knowledgebase can do.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Detecting recent positive selection in the human genome from haplotype structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

The structure of haplotype blocks 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=4819619

29 September 2017

Estimating allele age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

Meta-analysis of continuous outcome data from individual patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

29 September 2017

PiSZ alpha-1 antitrypsin deficiency (AATD): pulmonary phenotype and prognosis relative to PiZZ AATD and PiMM COPD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

28 June 2018

Plasma phenylalanine levels in phenylketonuric heterozygous and normal adults administered aspartame at 34 mg/kg body weight

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

28 June 2018

alpha 1-antitrypsin phenotypes in rheumatoid arthritis and ankylosing spondylitis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

28 June 2018

A general framework for the use of logistic regression models in meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

5 September 2018

Clarification of the risk of chronic obstructive pulmonary disease in α1-antitrypsin deficiency PiMZ heterozygotes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

5 September 2018

A life course approach to healthy ageing: the HALCyon programme.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

5 September 2018

Ethnicity of children with homozygous c.985A>G medium-chain acyl-CoA dehydrogenase deficiency: findings from screening approximately 1.1 million newborn infants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

5 September 2018

Alpha1-antitrypsin as a risk for infant and adult respiratory outcomes in a national birth cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

5 September 2018

Patterns of haplotype diversity within the serpin gene cluster at 14q32.1: insights into the natural history of the alpha1-antitrypsin polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4819619

5 September 2018

Early influences on adult lung function in two national British cohorts

1 reference

https://pubmed.ncbi.nlm.nih.gov/26831755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lung function and respiratory symptoms in association with mortality: The HUNT Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/26831755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diagnosis of intermediate and severe alpha(1)-antitrypsin deficiency: MZ individuals with chronic obstructive pulmonary disease may have lower lung function than MM individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/26831755

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMEDGENET-2015-103342

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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