(Q33905086)

English

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

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scholarly article

1 reference

Europe PubMed Central

29 July 2017

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q (English)

1 reference

Europe PubMed Central

29 July 2017

0 references

HDL cholesterol

0 references

susceptibility locus

1 reference

based on heuristic

inferred from title

Jerome I Rotter

11

object named as

Jerome I Rotter

1 reference

Europe PubMed Central

29 July 2017

Aldons Jake Lusis

14

object named as

Aldons J Lusis

1 reference

Europe PubMed Central

29 July 2017

10

object named as

Markku Laakso

1 reference

Europe PubMed Central

29 July 2017

Leena Peltonen-Palotie

15

object named as

Leena Peltonen

1 reference

Europe PubMed Central

29 July 2017

Marja-Riitta Taskinen

8

object named as

Marja-Riitta Taskinen

1 reference

Europe PubMed Central

29 July 2017

Päivi Pajukanta

1

object named as

Päivi Pajukanta

1 reference

Europe PubMed Central

29 July 2017

9

object named as

Ilpo Nuotio

1 reference

Europe PubMed Central

29 July 2017

13

object named as

Rita M Cantor

1 reference

Europe PubMed Central

29 July 2017

author name string

Hooman Allayee

2

1 reference

Europe PubMed Central

29 July 2017

Kelly L Krass

3

1 reference

Europe PubMed Central

29 July 2017

Ali Kuraishy

4

1 reference

Europe PubMed Central

29 July 2017

Aino Soro

5

1 reference

Europe PubMed Central

29 July 2017

Heidi E Lilja

6

1 reference

Europe PubMed Central

29 July 2017

Rebecca Mar

7

1 reference

Europe PubMed Central

29 July 2017

Tjerk W A de Bruin

12

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29 July 2017

language of work or name

0 references

publication date

12 March 2003

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Europe PubMed Central

29 July 2017

number of pages

15

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American Journal of Human Genetics

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Europe PubMed Central

29 July 2017

72

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Europe PubMed Central

29 July 2017

903-917

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Europe PubMed Central

29 July 2017

4

1 reference

Europe PubMed Central

29 July 2017

Evaluating the results of genomewide linkage scans of complex traits by locus counting

1 reference

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Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

1 reference

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5 July 2018

The structure of haplotype blocks in the human genome

1 reference

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Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia

1 reference

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5 July 2018

A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program

1 reference

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5 July 2018

Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families

1 reference

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Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig

1 reference

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5 July 2018

Genetic dissection of familial combined hyperlipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance

1 reference

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5 July 2018

Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

1 reference

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5 July 2018

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups

1 reference

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5 July 2018

Linkage disequilibrium in humans: models and data

1 reference

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5 July 2018

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

1 reference

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5 July 2018

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Linkage disequilibrium 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=1180353

5 July 2018

International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Use of population isolates for mapping complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Initial sequencing and analysis of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

The Sequence of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

How many diseases does it take to map a gene with SNPs?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

All LODs are not created equal

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Gamete-competition models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Replication of linkage studies of complex traits: an examination of variation in location estimates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes

1 reference

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Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Faster sequential genetic linkage computations

1 reference

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5 July 2018

Disease gene mapping in isolated human populations: the example of Finland

1 reference

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5 July 2018

Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

5 July 2018

Genetic dissection of complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

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Linkage detection under heterogeneity and the mixture problem.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180353

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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

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Strategies for multilocus linkage analysis in humans

1 reference

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Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

1 reference

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1 reference

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A comprehensive linkage analysis for myocardial infarction and its related risk factors

1 reference

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1 reference

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High-resolution haplotype structure in the human genome

1 reference

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29 October 2018

Significance levels in complex inheritance

1 reference

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29 October 2018

Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III.

1 reference

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29 October 2018

A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method.

1 reference

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Avoiding recomputation in linkage analysis.

1 reference

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29 October 2018

Age and gender specific serum lipid and apolipoprotein fractiles of Finnish children and young adults. The Cardiovascular Risk in Young Finns Study.

1 reference

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

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29 October 2018

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family study of serum lipids and lipoproteins in coronary heart-disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of familial hypercholesterolemia by assaying functional low-density-lipoprotein receptors on lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Model misspecification and multipoint linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Twenty-year trends in coronary risk factors in north Karelia and in other areas of Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

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based on heuristic

inferred from PubMed ID database lookup

Haplotype tagging for the identification of common disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12638083

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

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