Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans (Q40617961)

22 September 2017

Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans (English)

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genome-wide association study

22 September 2017

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Jerome I Rotter

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22 September 2017

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Lynne E Wagenknecht

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22 September 2017

7

Kent D Taylor

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22 September 2017

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Jill M Norris

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Carl D Langefeld

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Donald W Bowden

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Nicholette D Palmer

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Yii-Der Ida Chen

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Jacob M Keaton

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22 September 2017

Elizabeth K Speliotes

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object named as

Elizabeth K Speliotes

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Satria Sajuthi

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Jirong Long

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22 September 2017

Jacklyn Nikole Hellwege

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object named as

Jacklyn N Hellwege

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Gregory A Hawkins

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Latchezar Dimitrov

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Keri L Tabb

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22 September 2017

Maggie C Y Ng

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Carlos Lorenzo

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18 August 2016

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Journal of Human Genetics

22 September 2017

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22 September 2017

62

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22 September 2017

175-184

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2

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https://scigraph.springernature.com/pub.10.1038/jhg.2016.103

22 September 2017

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22 September 2017

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Genetic linkage analysis in the age of whole-genome sequencing

22 September 2017

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Structural basis of latrophilin-FLRT interaction

22 September 2017

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22 September 2017

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Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

22 September 2017

1 reference

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Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels

22 September 2017

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Cation-coupled bicarbonate transporters

22 September 2017

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22 September 2017

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RASAL2 activates RAC1 to promote triple-negative breast cancer progression

22 September 2017

1 reference

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RASAL2 down-regulation in ovarian cancer promotes epithelial-mesenchymal transition and metastasis

22 September 2017

1 reference

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Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing

22 September 2017

1 reference

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Chemokine-like receptor 1 deficiency does not affect the development of insulin resistance and nonalcoholic fatty liver disease in mice

22 September 2017

1 reference

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Identification of candidate susceptibility genes for colorectal cancer through eQTL analysis.

22 September 2017

1 reference

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Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk

22 September 2017

1 reference

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Identification of thyroid carcinoma related genes with mRMR and shortest path approaches

22 September 2017

1 reference

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Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans

22 September 2017

1 reference

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Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.

22 September 2017

1 reference

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Contribution of common genetic variants to obesity and obesity-related traits in mexican children and adults.

22 September 2017

1 reference

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Influence of a latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD).

22 September 2017

1 reference

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Chemerin: a potential endocrine link between obesity and type 2 diabetes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

FLRT proteins are endogenous latrophilin ligands and regulate excitatory synapse development

22 September 2017

1 reference

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Disruption of the chemokine-like receptor-1 (CMKLR1) gene is associated with reduced adiposity and glucose intolerance

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

A linear complexity phasing method for thousands of genomes

22 September 2017

1 reference

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Family-based designs for genome-wide association studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Chemerin is a novel adipocyte-derived factor inducing insulin resistance in primary human skeletal muscle cells.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Neuroblastoma-derived secretory protein is a novel secreted factor overexpressed in neuroblastoma

22 September 2017

1 reference

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Fast model-based estimation of ancestry in unrelated individuals

22 September 2017

1 reference

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

22 September 2017

1 reference

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LULL1 retargets TorsinA to the nuclear envelope revealing an activity that is impaired by the DYT1 dystonia mutation

22 September 2017

1 reference

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Neuroblastoma-derived secretory protein messenger RNA levels correlate with high-risk neuroblastoma

22 September 2017

1 reference

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Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelope

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

A chemotactic peptide from laminin alpha 5 functions as a regulator of inflammatory immune responses via TNF alpha-mediated signaling.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

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.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Multipoint quantitative-trait linkage analysis in general pedigrees

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

LPHN3 and attention-deficit/hyperactivity disorder: a susceptibility and pharmacogenetic study.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Borderline personality disorder and childhood maltreatment: a genome-wide methylation analysis.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

RASAL2 promotes lung cancer metastasis through epithelial-mesenchymal transition.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Effect of lifestyle modification on serum chemerin concentration and its association with insulin sensitivity in overweight and obese adults with type 2 diabetes.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Obesity susceptibility genetic variants identified from recent genome-wide association studies: implications in a chinese population

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference

20 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FJHG.2016.103

Genome-wide study of hypomethylated and induced genes in patients with liver cancer unravels novel anticancer targets

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5266668

Linkage and association mapping of a chromosome 1q21-q24 type 2 diabetes susceptibility locus in northern European Caucasians

2 December 2018

1 reference

12 December 2020

Keratins 8 and 18 are type II acute-phase responsive genes overexpressed in human liver disease

1 reference

12 December 2020

Gpr1 is an active chemerin receptor influencing glucose homeostasis in obese mice

1 reference

12 December 2020

Integration of linkage analyses and disease association studies

1 reference

12 December 2020

Identifiers

DOI

10.1038/JHG.2016.103

1 reference

22 September 2017

1 reference

22 September 2017

1 reference