Cargando…

Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands

BACKGROUND: High blood pressure or hypertension is a major risk factor involved in the development of cardiovascular diseases. We conducted genome-wide variance component linkage analyses to search for loci influencing five blood pressure related traits including the quantitative traits systolic blo...

Descripción completa

Detalles Bibliográficos
Autores principales:	Åberg, Karolina, Dai, Feng, Viali, Satupaitea, Tuitele, John, Sun, Guangyun, Indugula, Subba R, Deka, Ranjan, Weeks, Daniel E, McGarvey, Stephen T
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2009
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770055/ https://www.ncbi.nlm.nih.gov/pubmed/19852796 http://dx.doi.org/10.1186/1471-2350-10-107

Ejemplares similares

Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population
por: Tsai, Hui-Ju, et al.
Publicado: (2004)

Stratified randomization controls better for batch effects in 450K methylation analysis: a cautionary tale
por: Buhule, Olive D., et al.
Publicado: (2014)

Evolutionary history of modern Samoans
por: Harris, Daniel N., et al.
Publicado: (2020)

A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans
por: Deka, Ranjan, et al.
Publicado: (2009)

CREBRF missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesian peoples living in Samoa and Aotearoa New Zealand
por: Russell, Emily M, et al.
Publicado: (2022)

The missense variant, rs373863828, in CREBRF plays a role in longitudinal changes in body mass index in Samoans
por: Fu, Haoyi, et al.
Publicado: (2022)

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Genome-Wide Linkage Scan of a Pedigree with Familial Hypercholesterolemia Suggests Susceptibility Loci on Chromosomes 3q25-26 and 21q22
por: Wang, Xu, et al.
Publicado: (2011)

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

ECHS1 disease in two unrelated families of Samoan descent: Common variant ‐ rare disorder
por: Simon, Mariella T., et al.
Publicado: (2020)

Gestational weight gain among American Samoan women and its impact on delivery and infant outcomes
por: Hawley, Nicola L, et al.
Publicado: (2015)

Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions
por: Casselbrant, Margaretha L, et al.
Publicado: (2009)

Exploring the Paradoxical Relationship of a Creb 3 Regulatory Factor Missense Variant With Body Mass Index and Diabetes Among Samoans: Protocol for the Soifua Manuia (Good Health) Observational Cohort Study
por: Hawley, Nicola L, et al.
Publicado: (2020)

The extensive networks of frequent population mobility in the Samoan Islands and their implications for infectious disease transmission
por: Xu, Zhijing, et al.
Publicado: (2018)

Finding Missing Heritability in Less Significant Loci and Allelic Heterogeneity: Genetic Variation in Human Height
por: Zhang, Ge, et al.
Publicado: (2012)

A stop-gain variant in BTNL9 is associated with atherogenic lipid profiles
por: Carlson, Jenna C., et al.
Publicado: (2022)

Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans
por: Yoon, Se Chang, et al.
Publicado: (2016)

Extent of Height Variability Explained by Known Height-Associated Genetic Variants in an Isolated Population of the Adriatic Coast of Croatia
por: Zhang, Ge, et al.
Publicado: (2011)

Diffuse panbronchiolitis in a Samoan man
por: Gibson, Justine, et al.
Publicado: (2017)

Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip
por: Woo, Jessica G, et al.
Publicado: (2007)

Analysis of 2 men with t(8;22)(q13;q13) and t(8;14)(q13;q22) chromosomal translocation karyotypes
por: Sun, Qijia, et al.
Publicado: (2022)

Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion
por: PANAGOPOULOS, IOANNIS, et al.
Publicado: (2013)

Deposits, flow characteristics, and landscape change resulting from the September 2009 South Pacific tsunami in the Samoan islands
por: Richmond, Bruce M., et al.
Publicado: (2011)

Systemic mastocytosis associated with t(8;21)(q22;q22) acute myeloid leukemia
por: Pullarkat, Sheeja T., et al.
Publicado: (2009)

Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia
por: Roberts, Aedan, et al.
Publicado: (2010)

A Polynesian-specific missense CETP variant alters the lipid profile
por: Moors, Jaye, et al.
Publicado: (2023)

伴继发性t（9;22）（q34;q11）的t（8;21）（q22;q22）急性髓系白血病一例报告及文献复习
Publicado: (2017)

Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis
por: Woo, Jessica G, et al.
Publicado: (2012)

The remittances of migrant Tongan and Samoan nurses from Australia
por: Connell, John, et al.
Publicado: (2004)

A subduction and mantle plume origin for Samoan volcanism
por: Strak, Vincent, et al.
Publicado: (2018)

The ‘Influenza’ Vaccine Used during the Samoan Pandemic of 1918
por: Shanks, G. Dennis
Publicado: (2018)

Exploring Food Literacy Domains in an Adult Samoan Population
por: Kammholz, Grace, et al.
Publicado: (2021)

Pure interstitial dup(6)(q22.31q22.31) – a case report
por: Sheth, Frenny, et al.
Publicado: (2015)

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease
por: Butcher, Nancy J., et al.
Publicado: (2017)

Significant Evidence of Linkage for a Gene Predisposing to Colorectal Cancer and Multiple Primary Cancers on 22q11
por: Teerlink, Craig, et al.
Publicado: (2014)

Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
por: Rasmussen-Torvik, Laura J, et al.
Publicado: (2009)

Cytogenetical and hematological analysis of chronic myelogenous leukemia patients with a novel case 52XX, t (1;9;22) (q23.3; q34; q11.2), +6, +8, i(9) (q10;q10), +18,+19,+21+der22 t(9;22)(q34;q11)
por: Asif, Muhammad, et al.
Publicado: (2022)

8q22.2q22.3 Microdeletion Syndrome Associated with Hearing Loss and Intractable Epilepsy
por: Rincon, Alejandra, et al.
Publicado: (2019)

A novel t (5; 17) (q35; q21) associated with t (8; 21) (q22; q22) in a patient with acute myeloid leukemia: case report and review of literature
por: Zahra, Kmira, et al.
Publicado: (2023)

The need for translation and cultural adaptation of audiology questionnaires to enable the development of hearing healthcare policies in the Pacific Islands: a Samoan perspective
por: Kaspar, Annette, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_dfn3k3kt4mpjcet4f3q5au5s41