Investigating parent of origin effects in studies of type 2 diabetes and obesity.
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[1] Susan C. Brown,et al. Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies. , 2007, Brain : a journal of neurology.
[2] M. Jarvelin,et al. Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals. , 2007, American journal of human genetics.
[3] J. Dudenhausen,et al. Birth weight and subsequent risk of type 2 diabetes: a meta-analysis. , 2007, American journal of epidemiology.
[4] S. Ho,et al. Techniques used in studies of epigenome dysregulation due to aberrant DNA methylation: an emphasis on fetal-based adult diseases. , 2007, Reproductive toxicology.
[5] C. Weinberg,et al. Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent‐of‐origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available , 2007, Genetic epidemiology.
[6] D. Melzer,et al. A common haplotype of the glucokinase gene alters fasting glucose and birth weight: association in six studies and population-genetics analyses. , 2006, American journal of human genetics.
[7] Hui Shen,et al. Assessment of genetic linkage and parent-of-origin effects on obesity. , 2006, The Journal of clinical endocrinology and metabolism.
[8] A. Molven,et al. A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry. , 2006, Diabetes.
[9] S. Apostolidou,et al. Imprinted genes and their role in human fetal growth , 2006, Cytogenetic and Genome Research.
[10] D. Haig,et al. An earlier formulation of the genetic conflict hypothesis of genomic imprinting , 2006, Nature Genetics.
[11] C. Weinberg,et al. A method for using incomplete triads to test maternally mediated genetic effects and parent-of-origin effects in relation to a quantitative trait. , 2006, American journal of epidemiology.
[12] Jonathan D. Wren,et al. Data-Mining Analysis Suggests an Epigenetic Pathogenesis for Type 2 Diabetes , 2005, Journal of biomedicine & biotechnology.
[13] S. Shete,et al. Parametric Approach to Genomic Imprinting Analysis with Applications to Angelman’s Syndrome , 2005, Human Heredity.
[14] C. Amos,et al. Possible genomic imprinting of three human obesity-related genetic loci. , 2005, American journal of human genetics.
[15] I. Temple,et al. Bisulphite sequencing of the transient neonatal diabetes mellitus DMR facilitates a novel diagnostic test but reveals no methylation anomalies in patients of unknown aetiology , 2005, Human Genetics.
[16] S. Shete,et al. Linkage Analysis of Affected Sib Pairs Allowing for Parent‐of‐Origin Effects , 2005, Annals of human genetics.
[17] A. Feinberg,et al. Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome. , 2004, American journal of human genetics.
[18] Heather J Cordell,et al. Properties of case/pseudocontrol analysis for genetic association studies: Effects of recombination, ascertainment, and multiple affected offspring , 2004, Genetic epidemiology.
[19] Heather J Cordell,et al. Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene‐gene and gene‐environment interactions, and parent‐of‐origin effects , 2004, Genetic epidemiology.
[20] A. Plagemann. ‘Fetal programming’ and ‘functional teratogenesis’: on epigenetic mechanisms and prevention of perinatally acquired lasting health risks , 2004, Journal of perinatal medicine.
[21] S. Shete,et al. Genomic imprinting and linkage test for quantitative-trait Loci in extended pedigrees. , 2003, American journal of human genetics.
[22] J. Gulcher,et al. Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. , 2003, American journal of human genetics.
[23] E. Boerwinkle,et al. Genetic linkage and imprinting effects on body mass index in children and young adults , 2003, European Journal of Human Genetics.
[24] S. Murphy,et al. Imprinting evolution and the price of silence. , 2003, BioEssays : news and reviews in molecular, cellular and developmental biology.
[25] A. Bird,et al. Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals , 2003, Nature Genetics.
[26] Janet S Sinsheimer,et al. Detecting genotype combinations that increase risk for disease: Maternal‐Fetal genotype incompatibility test , 2003, Genetic epidemiology.
[27] P. Heckerling. Paternal inheritance of mitochondrial DNA. , 2002 .
[28] S. Rich,et al. Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect. , 2002, Diabetes care.
[29] J. Shield,et al. Transient neonatal diabetes, a disorder of imprinting , 2002, Journal of medical genetics.
[30] C. Polychronakos,et al. Parental genomic imprinting in endocrinopathies. , 2002, European journal of endocrinology.
[31] R. Oakey,et al. Imprinted genes: identification by chromosome rearrangements and post-genomic strategies. , 2002, Trends in genetics : TIG.
[32] M. Hitchins,et al. Genomic imprinting in fetal growth and development , 2002, Expert Reviews in Molecular Medicine.
[33] Sanjay Shete,et al. Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting. , 2002, American journal of human genetics.
[34] J. Kere,et al. Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause. , 2002, Pediatrics.
[35] V. Sutija,et al. Effect of amino acids on glucose tolerance and hyperkalemia in very low birth weight infants , 2002, Journal of perinatal medicine.
[36] L. Weinstein. The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease , 2001, Biological Psychiatry.
[37] R. Hanson,et al. Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians. , 2001, Diabetes.
[38] G I Bell,et al. Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. , 2001, The New England journal of medicine.
[39] C. Fischbacher,et al. Maternal transmission of type 2 diabetes varies by ethnic group: cross-sectional survey of Europeans and South Asians. , 2001, Diabetes care.
[40] A. Hattersley,et al. Influence of maternal and fetal glucokinase mutations in gestational diabetes. , 2001, American journal of obstetrics and gynecology.
[41] H. Gin,et al. Maternally Inherited Diabetes and Deafness: A Multicenter Study , 2001, Annals of Internal Medicine.
[42] R. Hanson,et al. Assessment of parent-of-origin effects in linkage analysis of quantitative traits. , 2001, American journal of human genetics.
[43] M. Oshimura,et al. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome , 2000, Journal of medical genetics.
[44] E. Zouros,et al. The exceptional mitochondrial DNA system of the mussel family Mytilidae. , 2000, Genes & genetic systems.
[45] P. Wilson,et al. Parental transmission of type 2 diabetes: the Framingham Offspring Study. , 2000, Diabetes.
[46] K. Liestøl,et al. Type 2 diabetes and maternal family history: an impact beyond slow glucose removal rate and fasting hyperglycemia in low-risk individuals? Results from 22.5 years of follow-up of healthy nondiabetic men. , 2000, Diabetes care.
[47] G. Schatten,et al. Ubiquitinated Sperm Mitochondria, Selective Proteolysis, and the Regulation of Mitochondrial Inheritance in Mammalian Embryos1 , 2000, Biology of reproduction.
[48] R. A. Drewell,et al. A novel imprinted gene, HYMAI, is located within an imprinted domain on human chromosome 6 containing ZAC. , 2000, Genomics.
[49] Nicolas Produit,et al. Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization. , 2000, American journal of human genetics.
[50] D. Gudbjartsson,et al. Erratum to “MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans” , 2000, Nature Genetics.
[51] R. Siebert,et al. An imprinted locus associated with transient neonatal diabetes mellitus. , 2000, Human molecular genetics.
[52] C R Weinberg,et al. Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. , 1999, American journal of human genetics.
[53] A. Karter,et al. Excess maternal transmission of type 2 diabetes. The Northern California Kaiser Permanente Diabetes Registry. , 1999, Diabetes care.
[54] Y. Momiyama,et al. Maternally transmitted susceptibility to non-insulin-dependent diabetes mellitus and left ventricular hypertrophy. , 1999, Journal of the American College of Cardiology.
[55] Sian Ellard,et al. Mutations in the glucokinase gene of the fetus result in reduced birth weight , 1998, Nature Genetics.
[56] S. Saitoh,et al. Imprinting in Prader-Willi and Angelman syndromes. , 1998, Trends in genetics : TIG.
[57] C R Weinberg,et al. A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. , 1998, American journal of human genetics.
[58] R. Klein,et al. Parental History of Diabetes in a Population-Based Study , 1996, Diabetes Care.
[59] A. Boulton,et al. Excess maternal history of diabetes in Caucasian and Afro-origin non-insulin-dependent diabetic patients suggests dominant maternal factors in disease transmission. , 1995, Diabetes research and clinical practice.
[60] J. D. Baum,et al. An imprinted gene(s) for diabetes? , 1995, Nature Genetics.
[61] M. Andrien,et al. Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus. , 1994, The Journal of clinical investigation.
[62] S. Haffner,et al. Differences in the Prevalence of Diabetes and Impaired Glucose Tolerance According to Maternal or Paternal History of Diabetes , 1993, Diabetes Care.
[63] C. Polychronakos,et al. Parental genomic imprinting of the human IGF2 gene , 1993, Nature Genetics.
[64] J. Maassen,et al. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness , 1992, Nature Genetics.
[65] D. Wallace,et al. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion , 1992, Nature Genetics.
[66] J. Alcolado,et al. Importance of maternal history of non-insulin dependent diabetic patients. , 1991, BMJ.
[67] Y. Hirao,et al. Fate of sperm tail components after incorporation into the hamster egg. , 1988, Gamete research.
[68] P. Savage,et al. Diabetes incidence in Pima indians: contributions of obesity and parental diabetes. , 1981, American journal of epidemiology.
[69] D. Szőllősi. The fate of sperm middle-piece mitochondria in the rat egg. , 1965, The Journal of experimental zoology.
[70] H. Crouse. The Controlling Element in Sex Chromosome Behavior in Sciara. , 1960, Genetics.
[71] Manuel Mattheisen,et al. Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE , 2007, Bioinform..
[72] Thomas Lengauer,et al. Computational epigenetics , 2008, Bioinform..
[73] T. Hudson,et al. A genome-wide approach to identifying novel-imprinted genes , 2007, Human Genetics.
[74] C. Osmond,et al. Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth , 2004, Diabetologia.
[75] C. Yajnik. Early life origins of insulin resistance and type 2 diabetes in India and other Asian countries. , 2004, The Journal of nutrition.
[76] D. Gudbjartsson,et al. A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting. , 2003, American journal of human genetics.
[77] I M Morison,et al. The imprinted gene and parent-of-origin effect database , 2001, Nucleic Acids Res..
[78] C. W. Birky,et al. The inheritance of genes in mitochondria and chloroplasts: laws, mechanisms, and models. , 2001, Annual review of genetics.
[79] M. McCarthy,et al. Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles. , 2000, Diabetes.
[80] E. Denamur,et al. Refinement of the 6q chromosomal region implicated in transient neonatal diabetes. , 2000, Diabetes.
[81] S. Zaina,et al. Insulin-like growth factor-2 regulation of conceptus composition: effects of the trophectoderm and inner cell mass genotypes in the mouse. , 1999, Biology of reproduction.
[82] K. Strauch,et al. Linkage analysis with adequate modeling of a parent‐of‐origin effect , 1999, Genetic epidemiology.
[83] S. Smalley. Sex-specific recombination frequencies: a consequence of imprinting? , 1993, American journal of human genetics.