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

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

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

http://www.wikidata.org/entity/Q35764851

about

Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism.The SLC6A14 gene shows evidence of association with obesity Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart Study Search for genetic factors predisposing to atherogenic dyslipidemia.Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses.An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study WWOX gene is associated with HDL cholesterol and triglyceride levels.Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q Effect of HDL composition and particle size on the resistance of HDL to the oxidation.Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease Association of a common LAMA5 variant with anthropometric and metabolic traits in an Italian cohort of healthy elderly subjects Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism.A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI.Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL.Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia.Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects The WWOX gene modulates high-density lipoprotein and lipid metabolism.Genetic evaluation for coronary artery disease.A male-specific quantitative trait locus on 1p21 controlling human stature.Compendium of genome-wide scans of lipid-related phenotypes: adding a new genome-wide search of apolipoprotein levels.Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population?Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family Unraveling the complex genetics of familial combined hyperlipidemia.WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension Genetic variation and atherosclerosis.Admixture mapping of quantitative trait loci for blood lipids in African-Americans.Genetic determinants of obesity-related lipid traits.Single nucleotide polymorphisms in protein tyrosine phosphatase 1beta (PTPN1) are associated with essential hypertension and obesity.A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia.The genetics of familial combined hyperlipidaemia.Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia.QTL mapping for genetic determinants of lipoprotein cholesterol levels in combined crosses of inbred mouse strains.Determinants of low HDL levels in familial combined hyperlipidemia.Low HDL cholesterol concentration is associated with increased intima-media thickness independent of arterial stiffness in healthy subjects from families with low HDL cholesterol.Genome-wide linkage scan reveals multiple susceptibility loci influencing lipid and lipoprotein levels in the Quebec Family Study.Multivariate linkage scan for metabolic syndrome traits in families with type 2 diabetes.

P2860

Q21144978-523F2686-482D-43EB-A295-9EAE66CAE275 Q24650988-B86BBE2C-1647-4BBD-8089-6958767167C5 Q24654114-CE19BBB7-202E-4CF8-BA55-FE216EF4EB49 Q31049201-159FCFED-D323-4F9B-B996-1E124E4B11D9 Q31049239-B3D4C9EB-7B10-4A02-9CA1-8730275FAB61 Q33198443-20693AF6-FC7C-413B-8ED9-1A2F117CE813 Q33298456-A6C92B09-BE35-4DB2-82DC-A04C66220E77 Q33717629-6AFF8000-F32A-4C84-A76A-DD4CF9DAAEB0 Q33905086-8AFF09A6-BA39-46A1-A18F-8158EC43F385 Q34198872-2B18EFC9-7F7A-4074-94AF-1CDE866002E7 Q34329091-35D587A9-F6C6-450B-8C7F-DD085F11E4A7 Q34388414-1F425F04-EB2A-4075-B9E1-C5A743CD16AA Q34390616-937B190C-0C28-40A4-A325-57DF69F5D597 Q34476897-3CD553FE-5468-4677-9792-747CBEFC556B Q34559909-6E45A782-BC3C-4C87-A5BC-A390A2AF07A8 Q34610302-CEB001A9-8500-4D83-8014-7817693FCE71 Q34761622-A6F2D37E-8D4E-4736-BD7E-A143557547D5 Q34943973-45688DC1-383B-4310-B0EA-651978AEA375 Q35008788-2C785964-4AAE-4BD6-AE9F-6DA69E458511 Q35042693-013B6B62-032B-43CB-9ACC-2FEC01DCA588 Q35179025-C08E8B60-6EFB-400A-A9B5-C6900F16339B Q35447506-06ACCFA2-4DFC-4034-A959-00866B4C6528 Q35890892-C2B6F541-AFFA-4572-92C5-DAFB789907C8 Q35936516-A72B3897-2BB7-4CD5-B398-E67AF570806D Q36448832-2BBE645F-9742-44A2-BDC9-A07967BF2978 Q36580345-D7C02B5D-056B-48AE-8C1C-6E32B7C5166D Q36808835-724E65F0-B78E-4EA6-AC24-6666E7907577 Q37144556-6B4C65E1-D784-4F34-8726-31B840179561 Q37172163-28383FE4-C38F-47F1-B50B-C5313984C483 Q37292958-648AE494-C030-4365-B455-4FE8C1C8566B Q37408308-0BFE40D6-2A4D-4E43-8EDC-222C7627EAD2 Q37412376-7637E18B-B1C9-4552-918E-04EB71D12F2A Q37475639-295C2C6B-4134-4FD9-A783-B14300901B02 Q37983699-8E0AFAA0-7CE5-4D6E-A9E3-43245A005CA9 Q42631637-09EDF446-B959-47FF-BC69-29A19EE4A45F Q42685371-8425FBE0-3F8D-4303-BBFF-D1F403928FE8 Q44460212-0ABE35E5-8FA0-4314-B210-66C93E84390D Q44471147-E50A7D22-2FF5-434E-BB6E-E0BD2CEE2F72 Q44695915-2240970F-E328-4C25-9AED-E1ED745A1AB5 Q44704567-B666A826-900D-4BD7-BC9D-224980B99F12

P2860

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

http://www.wikidata.org/entity/Q35764851

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu

2002年论文

@zh

2002年论文

@zh-cn

name

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@ast

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@en

type

label

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@ast

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@en

prefLabel

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@ast

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@en

P1433

Q35764851-D950FCBC-6DC8-4085-B00E-B1F4B08F4739

P1476

Q35764851-4703A00C-65EF-457E-9FAA-1ABF662807AE

P2093

Q35764851-0AC4ED0B-7BB4-4FFD-ABB8-94A3AC81CF3D

Q35764851-25ABE8D7-B3AB-4985-ACEB-136F82D49327

Q35764851-6205292B-4977-4778-964D-6791C3B63F64

Q35764851-95626516-3C05-4402-800F-6744EB0DF675

Q35764851-969FE61C-B6C3-429E-8C76-E1B65819CD24

Q35764851-BE854EAF-FBD1-4083-9F49-323A1B19033B

Q35764851-DD40BB29-B593-4CD1-8CEA-9CB74E474854

Q35764851-FEE2DE53-3418-4898-934E-D63109990A65

P2860

Q35764851-0919CCB3-2487-4A93-B962-0AA85AF3AC13

Q35764851-17214B91-705C-4ED0-B805-A463C25DE2D4

Q35764851-19912784-B4CC-43AF-9335-D2534B50EC6A

Q35764851-1B3855D8-7866-4D14-A17B-9E7A48A274D2

Q35764851-374C76D5-BF5A-4CBA-B491-FB43184B4867

Q35764851-3D1E7371-10E0-4E85-984C-23B4C8776DF8

Q35764851-4AC9CCCD-05F8-40D3-B329-20DD27EE8538

Q35764851-4DD428B7-945E-4383-B392-C3CFC8A69F2A

Q35764851-56769738-831D-477D-BFB8-0FA6F8B9C322

Q35764851-58994F05-7464-4E07-8376-9C7CF3BDC8C1

P304

Q35764851-1CDC75AB-6BE0-4CC6-8888-746F1CC75362

P31

Q35764851-51B9B333-D258-4EF7-BE48-D418DFA0D631

Q35764851-fe56d654-bf8f-431d-af22-c21e690ef7dc

P356

Q35764851-ED117F27-16D8-44A1-A288-6F98B606EA25

P407

Q35764851-09B8D670-DB63-4D06-91F4-F3CE291EADB7

P433

Q35764851-3F9A8E1E-AD49-4DFF-AE68-F56CB017D144

P478

Q35764851-51B902B5-A925-4F72-8564-5ADDADC57F58

P50

Q35764851-0AF20B82-FF18-4630-8058-32DCFD123271

Q35764851-2295E5E1-4885-4D6A-A3DB-84F98F3FA22B

Q35764851-6BAF7E4A-E156-46CE-901C-C42BFF8C1A78

P577

Q35764851-EA1BC7F5-FD2B-47D0-BA28-CC19A6D901D5

P5875

Q35764851-FF9FBFE7-8DC2-495C-B650-3B281183793D

P698

Q35764851-CA40470F-E3D5-403B-A88B-6891F09B6257

P921

Q35764851-0A4EC924-C498-4D2A-B2A4-090899A904C0

P932

Q35764851-BA2F4944-7DA3-44DD-87A5-562A196DCA07

P356

P1433

American Journal of Human Genetics

P1476

Genome scans provide evidence ...... 20q13.11 in Finnish families.

@en

P2093

Aino Soro

http://www.w3.org/2001/XMLSchema#string

Heidi E Lilja

http://www.w3.org/2001/XMLSchema#string

Jorma S A Viikari

http://www.w3.org/2001/XMLSchema#string

Kati Ylitalo

http://www.w3.org/2001/XMLSchema#string

Marja-Riitta Taskinen

http://www.w3.org/2001/XMLSchema#string

Päivi Pajukanta

http://www.w3.org/2001/XMLSchema#string

Rita M Cantor

http://www.w3.org/2001/XMLSchema#string

Tero Hiekkalinna

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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

Strategies for multilocus linkage analysis in humans

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

Multipoint quantitative-trait linkage analysis in general pedigrees

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

Faster sequential genetic linkage computations

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

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease.

P304

1333-1340

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1086/339988

http://www.w3.org/2001/XMLSchema#string

P407

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

70

http://www.w3.org/2001/XMLSchema#string

P50

Leena Peltonen-Palotie

Tero Hiekkalinna

P577

2002-03-12T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

11471010

http://www.w3.org/2001/XMLSchema#string

P698

11891617

http://www.w3.org/2001/XMLSchema#string

P921

P932

447608

http://www.w3.org/2001/XMLSchema#string