(Q35784042)

10 August 2017

title

Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia (English)

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genome-wide association study

10 August 2017

main subject

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17

Robert A Hegele

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Aldons Jake Lusis

10

object named as

Aldons J Lusis

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10 August 2017

9

Margarete Mehrabian

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11

Sekar Kathiresan

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13

Salim Yusuf

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3

Adam D McIntyre

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14

Ann-Hwee Lee

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15

Laurie H Glimcher

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10 August 2017

author name string

Christopher T Johansen

1

1 reference

10 August 2017

Jian Wang

2

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10 August 2017

Rebecca A Martins

4

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Matthew R Ban

5

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Matthew B Lanktree

6

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Murray W Huff

7

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10 August 2017

Miklós Péterfy

8

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10 August 2017

Sonia S Anand

12

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10 August 2017

Henian Cao

16

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10 August 2017

publication date

1 December 2011

1 reference

Circulation: Cardiovascular Genetics

10 August 2017

published in

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10 August 2017

volume

5

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10 August 2017

issue

1

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10 August 2017

page(s)

66-72

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describes a project that uses

10 August 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

The transcription factor cyclic AMP-responsive element-binding protein H regulates triglyceride metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Testing for an unusual distribution of rare variants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Genetic determinants of plasma triglycerides

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Statistical analysis strategies for association studies involving rare variants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Biological, clinical and population relevance of 95 loci for blood lipids

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Pooled association tests for rare variants in exon-resequencing studies

27 July 2018

1 reference

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A method and server for predicting damaging missense mutations

27 July 2018

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Quantitative trait locus mapping and identification of Zhx2 as a novel regulator of plasma lipid metabolism.

27 July 2018

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Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defects

27 July 2018

1 reference

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Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia

27 July 2018

1 reference

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Finding the missing heritability of complex diseases

27 July 2018

1 reference

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A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia

27 July 2018

1 reference

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

27 July 2018

1 reference

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Plasma lipoproteins: genetic influences and clinical implications

27 July 2018

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Normal binding of lipoprotein lipase, chylomicrons, and apo-AV to GPIHBP1 containing a G56R amino acid substitution

27 July 2018

1 reference

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Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

27 July 2018

1 reference

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Apolipoprotein CIISt. Michael. Familial apolipoprotein CII deficiency associated with premature vascular disease

27 July 2018

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An apolipoprotein CII mutation, CIILys19----Thr' identified in patients with hyperlipidemia

27 July 2018

1 reference

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Bias due to selection of rare variants using frequency in controls.

27 July 2018

1 reference

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Regulation of hepatic gluconeogenesis by an ER-bound transcription factor, CREBH.

25 September 2018

1 reference

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Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Homozygous missense mutation (G56R) in glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPI-HBP1) in two siblings with fasting chylomicronemia (MIM 144650).

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 plays a critical role in the lipolytic processing of chylomicrons

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3288444

Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE)

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22135386

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Defining rare variants by their frequencies in controls may increase type I error

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22135386

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCGENETICS.111.960864

1 reference

10 August 2017

1 reference

10 August 2017

1 reference