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2024 | OriginalPaper | Hoofdstuk

7. Genetische epidemiologie

Auteurs : L. M. Bouter, M. P. A. Zeegers, S. M. J. van Kuijk

Gepubliceerd in: Leerboek epidemiologie

Uitgeverij: Bohn Stafleu van Loghum

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Samenvatting

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Literatuur
go back to reference Chan BKC. Biostatistics for human genetic epidemiology. New York: Springer; 2018.CrossRef Chan BKC. Biostatistics for human genetic epidemiology. New York: Springer; 2018.CrossRef
go back to reference Khoury MJ, Bedrosian SR, Gwinn M, Higgins JPT, Ioannidis JPA, Little J. Human genome epidemiology: building the evidence for using genetic information to improve health and prevent disease. 2nd ed. Oxford: Oxford University Press; 2010. Khoury MJ, Bedrosian SR, Gwinn M, Higgins JPT, Ioannidis JPA, Little J. Human genome epidemiology: building the evidence for using genetic information to improve health and prevent disease. 2nd ed. Oxford: Oxford University Press; 2010.
go back to reference Araki S, Dariusz KM, Hanna L, Scott LJ, Warram JH, Krolewski AS. APOE polymorphisms and the development of diabetic nephropathy in type 1 diabetes. Diabetes. 2000;49:2190–5 (Casus 7.4 en 7.7). Araki S, Dariusz KM, Hanna L, Scott LJ, Warram JH, Krolewski AS. APOE polymorphisms and the development of diabetic nephropathy in type 1 diabetes. Diabetes. 2000;49:2190–5 (Casus 7.4 en 7.7).
go back to reference Claus EB, Risch NJ, Thompson WD. Age at onset as an indicator of familial risk in breast cancer. Am J Epidemiol. 1990;131:961–72 (Casus 7.1). Claus EB, Risch NJ, Thompson WD. Age at onset as an indicator of familial risk in breast cancer. Am J Epidemiol. 1990;131:961–72 (Casus 7.1).
go back to reference Grant SFA, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, et al. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat Genet. 2006;38:320–3 (Casus 7.5). Grant SFA, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, et al. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat Genet. 2006;38:320–3 (Casus 7.5).
go back to reference Hall JM, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, King MC. Linkage of early-onset familial breast cancer to chromosome 17q21. Science. 1990;250:1684–9 (Casus 7.3). Hall JM, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, King MC. Linkage of early-onset familial breast cancer to chromosome 17q21. Science. 1990;250:1684–9 (Casus 7.3).
go back to reference Helgason A, Pálsson S, Thorleifsson G, Grant SF, Emilsson V, Gunnarsdottir S, et al. Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution. Nat Genet. 2007;39:218–25 (Casus 7.5). Helgason A, Pálsson S, Thorleifsson G, Grant SF, Emilsson V, Gunnarsdottir S, et al. Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution. Nat Genet. 2007;39:218–25 (Casus 7.5).
go back to reference Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994;266:66–71 (Casus 7.3). Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994;266:66–71 (Casus 7.3).
go back to reference Newman B, Austin MA, Lee M, King MC. Inheritance of human breast cancer: evidence for autosomal transmission in high risk families. Proc Natl Acad Sci USA. 1988;85:3044–8 (Casus 7.3). Newman B, Austin MA, Lee M, King MC. Inheritance of human breast cancer: evidence for autosomal transmission in high risk families. Proc Natl Acad Sci USA. 1988;85:3044–8 (Casus 7.3).
go back to reference Palmer ND, Hester JM, An SS, Adeyemo A, Rotimi C, Langefeld CD et al. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes. 2011;60:662–8 (Casus 7.5). Palmer ND, Hester JM, An SS, Adeyemo A, Rotimi C, Langefeld CD et al. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes. 2011;60:662–8 (Casus 7.5).
go back to reference Polderman TJC, Benyamin B, De Leeuw CA, Sullivan PF, Van Bochoven A, Visscher PM, Posthuma D. Meta-analysis of the heritability of human traits based on fifty years of twin studies. Nat Genet. 2015;47:702–9 (Casus 7.2). Polderman TJC, Benyamin B, De Leeuw CA, Sullivan PF, Van Bochoven A, Visscher PM, Posthuma D. Meta-analysis of the heritability of human traits based on fifty years of twin studies. Nat Genet. 2015;47:702–9 (Casus 7.2).
go back to reference Scott LJ, Bonnycastle LL, Willer CJ, Sprau AG, Jackson AU, Narisu N, et al. Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. Diabetes. 2006;55:2649–53 (Casus 7.5). Scott LJ, Bonnycastle LL, Willer CJ, Sprau AG, Jackson AU, Narisu N, et al. Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. Diabetes. 2006;55:2649–53 (Casus 7.5).
go back to reference Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447:661–78 (Casus 7.6). Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447:661–78 (Casus 7.6).
Metagegevens
Titel
Genetische epidemiologie
Auteurs
L. M. Bouter
M. P. A. Zeegers
S. M. J. van Kuijk
Copyright
2024
Uitgeverij
Bohn Stafleu van Loghum
DOI
https://doi.org/10.1007/978-90-368-2952-6_7