메뉴 건너뛰기




Volumn 516, Issue 2, 2013, Pages 198-203

Copy number variations of obesity relevant loci associated with body mass index in young Chinese

Author keywords

Body mass index; Case control study; Chinese young adult; Copy number variations; Obesity; Polymerase chain reaction

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; GAMMA GLUTAMYLTRANSFERASE; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN CHOLESTEROL; TRIACYLGLYCEROL;

EID: 84873277370     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2012.12.081     Document Type: Article
Times cited : (9)

References (36)
  • 1
    • 79954672317 scopus 로고    scopus 로고
    • Genome structural variation discovery and genotyping
    • Alkan C., Coe B.P., Eichler E.E. Genome structural variation discovery and genotyping. Nat. Rev. Genet. 2011, 12:363-376.
    • (2011) Nat. Rev. Genet. , vol.12 , pp. 363-376
    • Alkan, C.1    Coe, B.P.2    Eichler, E.E.3
  • 2
    • 0034611681 scopus 로고    scopus 로고
    • Genetics of body-weight regulation
    • Barsh G.S., Farooqi I.S., O'Rahilly S. Genetics of body-weight regulation. Nature 2000, 404:644-651.
    • (2000) Nature , vol.404 , pp. 644-651
    • Barsh, G.S.1    Farooqi, I.S.2    O'Rahilly, S.3
  • 3
    • 76349083132 scopus 로고    scopus 로고
    • Large, rare chromosomal deletions associated with severe early-onset obesity
    • Bochukova E.G., et al. Large, rare chromosomal deletions associated with severe early-onset obesity. Nature 2010, 463:666-670.
    • (2010) Nature , vol.463 , pp. 666-670
    • Bochukova, E.G.1
  • 4
    • 4544333509 scopus 로고    scopus 로고
    • Effect of liver fatty acid binding protein (FABP) T94A missense mutation on plasma lipoprotein responsiveness to treatment with fenofibrate
    • Brouillette C., Bosse Y., Perusse L., Gaudet D., Vohl M.C. Effect of liver fatty acid binding protein (FABP) T94A missense mutation on plasma lipoprotein responsiveness to treatment with fenofibrate. J. Hum. Genet. 2004, 49:424-432.
    • (2004) J. Hum. Genet. , vol.49 , pp. 424-432
    • Brouillette, C.1    Bosse, Y.2    Perusse, L.3    Gaudet, D.4    Vohl, M.C.5
  • 5
    • 79957534316 scopus 로고    scopus 로고
    • Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in Whites
    • Chen Y., et al. Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in Whites. Obesity (Silver Spring) 2011, 19:1229-1234.
    • (2011) Obesity (Silver Spring) , vol.19 , pp. 1229-1234
    • Chen, Y.1
  • 6
    • 0000067107 scopus 로고    scopus 로고
    • Genetics and pathophysiology of human obesity
    • Cummings D.E., Schwartz M.W. Genetics and pathophysiology of human obesity. Annu. Rev. Med. 2003, 54:453-471.
    • (2003) Annu. Rev. Med. , vol.54 , pp. 453-471
    • Cummings, D.E.1    Schwartz, M.W.2
  • 7
    • 77952557918 scopus 로고    scopus 로고
    • VIEWPOINT Missing heritability and strategies for finding the underlying causes of complex disease
    • Eichler E.E., et al. VIEWPOINT Missing heritability and strategies for finding the underlying causes of complex disease. Nat. Rev. Genet. 2010, 11:446-450.
    • (2010) Nat. Rev. Genet. , vol.11 , pp. 446-450
    • Eichler, E.E.1
  • 8
    • 34249720994 scopus 로고    scopus 로고
    • L-FABP T94A is associated with fasting triglycerides and LDL-cholesterol in women
    • Fisher E., et al. L-FABP T94A is associated with fasting triglycerides and LDL-cholesterol in women. Mol. Genet. Metab. 2007, 91:278-284.
    • (2007) Mol. Genet. Metab. , vol.91 , pp. 278-284
    • Fisher, E.1
  • 9
    • 34248594090 scopus 로고    scopus 로고
    • A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
    • Frayling T.M., et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science 2007, 316:889-894.
    • (2007) Science , vol.316 , pp. 889-894
    • Frayling, T.M.1
  • 10
    • 78249239776 scopus 로고    scopus 로고
    • A genome-wide study reveals copy number variants exclusive to childhood obesity cases
    • Glessner J.T., et al. A genome-wide study reveals copy number variants exclusive to childhood obesity cases. Am. J. Hum. Genet. 2010, 87:661-666.
    • (2010) Am. J. Hum. Genet. , vol.87 , pp. 661-666
    • Glessner, J.T.1
  • 11
    • 84859394262 scopus 로고    scopus 로고
    • Association of copy number variation in the AHI1 gene with risk of obesity in the Chinese population
    • Huang L., Teng D., Wang H., Sheng G., Liu T. Association of copy number variation in the AHI1 gene with risk of obesity in the Chinese population. Eur. J. Endocrinol. 2012, 166:727-734.
    • (2012) Eur. J. Endocrinol. , vol.166 , pp. 727-734
    • Huang, L.1    Teng, D.2    Wang, H.3    Sheng, G.4    Liu, T.5
  • 12
    • 78751700313 scopus 로고    scopus 로고
    • Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
    • Jarick I., et al. Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis. Hum. Mol. Genet. 2011, 20:840-852.
    • (2011) Hum. Mol. Genet. , vol.20 , pp. 840-852
    • Jarick, I.1
  • 13
    • 41049091716 scopus 로고    scopus 로고
    • Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region
    • Jiang Y.H., et al. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region. BMC Genomics 2008, 9:50.
    • (2008) BMC Genomics , vol.9 , pp. 50
    • Jiang, Y.H.1
  • 14
    • 44849086097 scopus 로고    scopus 로고
    • Genome-wide association scans identified CTNNBL1 as a novel gene for obesity
    • Liu Y.J., et al. Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. Hum. Mol. Genet. 2008, 17:1803-1813.
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 1803-1813
    • Liu, Y.J.1
  • 15
    • 42249110521 scopus 로고    scopus 로고
    • FTO: the first gene contributing to common forms of human obesity
    • Loos R.J., Bouchard C. FTO: the first gene contributing to common forms of human obesity. Obes. Rev. 2008, 9:246-250.
    • (2008) Obes. Rev. , vol.9 , pp. 246-250
    • Loos, R.J.1    Bouchard, C.2
  • 16
    • 70549083243 scopus 로고    scopus 로고
    • Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease
    • McCarroll S.A., et al. Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease. Nat. Genet. 2009, 41:1341-1344.
    • (2009) Nat. Genet. , vol.41 , pp. 1341-1344
    • McCarroll, S.A.1
  • 17
    • 59149097625 scopus 로고    scopus 로고
    • Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
    • Meyre D., et al. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nat. Genet. 2009, 41:157-159.
    • (2009) Nat. Genet. , vol.41 , pp. 157-159
    • Meyre, D.1
  • 18
    • 0033793921 scopus 로고    scopus 로고
    • Embryonic development is disrupted by modest increases in vascular endothelial growth factor gene expression
    • Miquerol L., Langille B.L., Nagy A. Embryonic development is disrupted by modest increases in vascular endothelial growth factor gene expression. Development 2000, 127:3941-3946.
    • (2000) Development , vol.127 , pp. 3941-3946
    • Miquerol, L.1    Langille, B.L.2    Nagy, A.3
  • 19
    • 33751329250 scopus 로고    scopus 로고
    • Global variation in copy number in the human genome
    • Redon R., et al. Global variation in copy number in the human genome. Nature 2006, 444:444-454.
    • (2006) Nature , vol.444 , pp. 444-454
    • Redon, R.1
  • 20
    • 66249144682 scopus 로고    scopus 로고
    • Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population
    • Sha B.Y., et al. Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population. J. Hum. Genet. 2009, 54:199-202.
    • (2009) J. Hum. Genet. , vol.54 , pp. 199-202
    • Sha, B.Y.1
  • 21
    • 84920321315 scopus 로고    scopus 로고
    • Cloning and characterization of BAI2 and BAI3, novel genes homologous to brain-specific angiogenesis inhibitor 1 (BAI1)
    • Shiratsuchi T., Nishimori H., Ichise H., Nakamura Y., Tokino T. Cloning and characterization of BAI2 and BAI3, novel genes homologous to brain-specific angiogenesis inhibitor 1 (BAI1). Cytogenet. Cell Genet. 1997, 79:103-108.
    • (1997) Cytogenet. Cell Genet. , vol.79 , pp. 103-108
    • Shiratsuchi, T.1    Nishimori, H.2    Ichise, H.3    Nakamura, Y.4    Tokino, T.5
  • 22
    • 0032577870 scopus 로고    scopus 로고
    • Cloning and characterization of BAI-associated protein 1: a PDZ domain-containing protein that interacts with BAI1
    • Shiratsuchi T., Futamura M., Oda K., Nishimori H., Nakamura Y., Tokino T. Cloning and characterization of BAI-associated protein 1: a PDZ domain-containing protein that interacts with BAI1. Biochem. Biophys. Res. Commun. 1998, 247:597-604.
    • (1998) Biochem. Biophys. Res. Commun. , vol.247 , pp. 597-604
    • Shiratsuchi, T.1    Futamura, M.2    Oda, K.3    Nishimori, H.4    Nakamura, Y.5    Tokino, T.6
  • 23
    • 74249088988 scopus 로고    scopus 로고
    • The genetic and environmental influences on childhood obesity: a systematic review of twin and adoption studies
    • Silventoinen K., Rokholm B., Kaprio J., Sorensen T.I. The genetic and environmental influences on childhood obesity: a systematic review of twin and adoption studies. Int. J. Obes. (Lond.) 2010, 34:29-40.
    • (2010) Int. J. Obes. (Lond.) , vol.34 , pp. 29-40
    • Silventoinen, K.1    Rokholm, B.2    Kaprio, J.3    Sorensen, T.I.4
  • 24
    • 33846978695 scopus 로고    scopus 로고
    • Relative impact of nucleotide and copy number variation on gene expression phenotypes
    • Stranger B.E., et al. Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science 2007, 315:848-853.
    • (2007) Science , vol.315 , pp. 848-853
    • Stranger, B.E.1
  • 25
    • 58149163141 scopus 로고    scopus 로고
    • Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
    • Thorleifsson G., et al. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. Nat. Genet. 2009, 41:18-24.
    • (2009) Nat. Genet. , vol.41 , pp. 18-24
    • Thorleifsson, G.1
  • 26
    • 84860406838 scopus 로고    scopus 로고
    • Programming towards childhood obesity
    • Tounian P. Programming towards childhood obesity. Ann. Nutr. Metab. 2011, 58(Suppl. 2):30-41.
    • (2011) Ann. Nutr. Metab. , vol.58 , Issue.SUPPL. 2 , pp. 30-41
    • Tounian, P.1
  • 27
    • 22844451617 scopus 로고    scopus 로고
    • Fine-scale structural variation of the human genome
    • Tuzun E., et al. Fine-scale structural variation of the human genome. Nat. Genet. 2005, 37:727-732.
    • (2005) Nat. Genet. , vol.37 , pp. 727-732
    • Tuzun, E.1
  • 29
    • 67649793700 scopus 로고    scopus 로고
    • The genetic contribution to non-syndromic human obesity
    • Walley A.J., Asher J.E., Froguel P. The genetic contribution to non-syndromic human obesity. Nat. Rev. Genet. 2009, 10:431-442.
    • (2009) Nat. Rev. Genet. , vol.10 , pp. 431-442
    • Walley, A.J.1    Asher, J.E.2    Froguel, P.3
  • 30
    • 76249116215 scopus 로고    scopus 로고
    • A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
    • Walters R.G., et al. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. Nature 2010, 463:671-675.
    • (2010) Nature , vol.463 , pp. 671-675
    • Walters, R.G.1
  • 31
    • 77957606877 scopus 로고    scopus 로고
    • Large copy-number variations are enriched in cases with moderate to extreme obesity
    • Wang K., Li W.D., Glessner J.T., Grant S.F., Hakonarson H., Price R.A. Large copy-number variations are enriched in cases with moderate to extreme obesity. Diabetes 2010, 59:2690-2694.
    • (2010) Diabetes , vol.59 , pp. 2690-2694
    • Wang, K.1    Li, W.D.2    Glessner, J.T.3    Grant, S.F.4    Hakonarson, H.5    Price, R.A.6
  • 32
    • 35148853628 scopus 로고    scopus 로고
    • A Thr94Ala mutation in human liver fatty acid-binding protein contributes to reduced hepatic glycogenolysis and blunted elevation of plasma glucose levels in lipid-exposed subjects
    • Weickert M.O., et al. A Thr94Ala mutation in human liver fatty acid-binding protein contributes to reduced hepatic glycogenolysis and blunted elevation of plasma glucose levels in lipid-exposed subjects. Am. J. Physiol. Endocrinol. Metab. 2007, 293:E1078-E1084.
    • (2007) Am. J. Physiol. Endocrinol. Metab. , vol.293
    • Weickert, M.O.1
  • 33
    • 58149163142 scopus 로고    scopus 로고
    • Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
    • Willer C.J., et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat. Genet. 2009, 41:25-34.
    • (2009) Nat. Genet. , vol.41 , pp. 25-34
    • Willer, C.J.1
  • 35
    • 37049019661 scopus 로고    scopus 로고
    • Gain of 5p15.33 is associated with progression of bladder cancer
    • Yamamoto Y., et al. Gain of 5p15.33 is associated with progression of bladder cancer. Oncology 2007, 72:132-138.
    • (2007) Oncology , vol.72 , pp. 132-138
    • Yamamoto, Y.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.