| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00125-011-2267-5 |
| P698 | PubMed publication ID | 21826484 |
| P50 | author | Marja-Riitta Taskinen | Q18246437 |
| Leif Groop | Q27214742 | ||
| Tiinamaija Tuomi | Q29839491 | ||
| Valeriya Lyssenko | Q29839540 | ||
| Bo Isomaa | Q29839548 | ||
| Peter Almgren | Q87790487 | ||
| P2093 | author name string | L. Sarelin | |
| M. Lehtovirta | |||
| P2860 | cites work | Analysis of genetic inheritance in a family quartet by whole-genome sequencing | Q22065898 |
| Finding the missing heritability of complex diseases | Q22122198 | ||
| Genome-wide meta-analyses identify multiple loci associated with smoking behavior | Q24597886 | ||
| Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis | Q24609915 | ||
| Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man | Q26776977 | ||
| Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes | Q28680760 | ||
| Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes | Q29417138 | ||
| A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants | Q29547210 | ||
| Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels | Q29547214 | ||
| Multipoint quantitative-trait linkage analysis in general pedigrees | Q29614967 | ||
| Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy | Q30156928 | ||
| Familial risks for type 2 diabetes in Sweden | Q33602186 | ||
| Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study | Q33903845 | ||
| Heritabilities of the metabolic syndrome and its components in the Northern Manhattan Family Study. | Q34147834 | ||
| Genetic factors in determining bone mass | Q34513372 | ||
| Genetic determinants of bone mass in adults. A twin study | Q35578513 | ||
| Parental origin of sequence variants associated with complex diseases | Q37102209 | ||
| A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia study | Q43068410 | ||
| Ethnic Variability in Glucose Tolerance and Insulin Secretion | Q44950778 | ||
| Heritability estimates for beta cell function and features of the insulin resistance syndrome in UK families with an increased susceptibility to type 2 diabetes. | Q45009717 | ||
| Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes | Q45199153 | ||
| Heritability of insulin secretion, peripheral and hepatic insulin action, and intracellular glucose partitioning in young and old Danish twins | Q45199185 | ||
| HDL subspecies in young adult twins: heritability and impact of overweight. | Q45936247 | ||
| Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland | Q46088274 | ||
| Heritability of multivariate factors of the metabolic syndrome in nondiabetic Japanese americans | Q47871843 | ||
| Metabolic consequences of a family history of NIDDM (the Botnia study): evidence for sex-specific parental effects | Q51000283 | ||
| Immigrants from the Middle-East have a different form of Type 2 diabetes compared with Swedish patients. | Q51452949 | ||
| A longitudinal study on genetic and environmental influences on leisure time physical activity in the Finnish Twin Cohort. | Q51540429 | ||
| Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp. | Q51561183 | ||
| Postprandial hypertriglyceridemia and insulin resistance in normoglycemic first-degree relatives of patients with type 2 diabetes. | Q51562526 | ||
| Ascertainment bias in the estimation of sibling genetic risk parameters. | Q52920165 | ||
| Insulin sensitivity and insulin secretion in monozygotic and dizygotic twins. | Q54055230 | ||
| Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance--a population-based twin study. | Q54103713 | ||
| Concordance for type 2 (non-insulin-dependent) diabetes mellitus in male twins | Q68535734 | ||
| Heritability of albumin excretion rate in families of patients with Type II diabetes | Q73153929 | ||
| A variance component approach to dichotomous trait linkage analysis using a threshold model | Q74059402 | ||
| Heritability of pancreatic beta-cell function among nondiabetic members of Caucasian familial type 2 diabetic kindreds | Q77312676 | ||
| P433 | issue | 11 | |
| P921 | main subject | heritability | Q1503548 |
| type 2 diabetes | Q3025883 | ||
| quantitative trait | Q112670498 | ||
| P304 | page(s) | 2811-2819 | |
| P577 | publication date | 2011-08-09 | |
| P1433 | published in | Diabetologia | Q5270140 |
| P1476 | title | Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia Study | |
| P478 | volume | 54 |
| Q48561722 | A Decade of Genetic and Metabolomic Contributions to Type 2 Diabetes Risk Prediction |
| Q47409799 | A Qualitative Study of Anticipated Decision Making around Type 2 Diabetes Genetic Testing: the Role of Scientifically Concordant and Discordant Expectations |
| Q21563356 | A six months exercise intervention influences the genome-wide DNA methylation pattern in human adipose tissue |
| Q35753282 | Adaptive Immunity and Antigen-Specific Activation in Obesity-Associated Insulin Resistance |
| Q57115763 | Additional common variants associated with type 2 diabetes and coronary artery disease detected using a pleiotropic cFDR method |
| Q92972342 | Age-related late-onset disease heritability patterns and implications for genome-wide association studies |
| Q37044783 | Association between IGF2BP2 Polymorphisms and Type 2 Diabetes Mellitus: A Case-Control Study and Meta-Analysis |
| Q35695980 | Association between major depression and type 2 diabetes in midlife: findings from the Screening Across the Lifespan Twin Study |
| Q90727344 | Association of genetic and behavioral characteristics with the onset of diabetes |
| Q44921278 | Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis |
| Q36035631 | Childhood cognitive ability moderates later-life manifestation of type 2 diabetes genetic risk |
| Q38808702 | Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes |
| Q34478063 | Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait |
| Q36085678 | Do personality traits moderate the manifestation of type 2 diabetes genetic risk? |
| Q57273688 | Epigenetic mechanisms underlying type 2 diabetes mellitus |
| Q33779170 | Epipolymorphisms within lipoprotein genes contribute independently to plasma lipid levels in familial hypercholesterolemia |
| Q39329664 | Evaluating empirical bounds on complex disease genetic architecture |
| Q47116334 | Evaluation of glutathione S-transferase P1 (GSTP1) Ile105Val polymorphism and susceptibility to type 2 diabetes mellitus, a meta-analysis |
| Q47382488 | Evidence of selection at insulin receptor substrate-1 gene loci. |
| Q91386045 | Evidence that genes involved in hedgehog signaling are associated with both bipolar disorder and high BMI |
| Q39786100 | Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes |
| Q38847542 | Family history and perceived risk of diabetes, cardiovascular disease, cancer, and depression |
| Q51360798 | Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traits. |
| Q36528807 | Finding genetic risk factors of gestational diabetes |
| Q33914292 | Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C |
| Q50148610 | Genes associated with Type 2 Diabetes and vascular complications |
| Q57077043 | Genetic Overlap Between Depression and Cardiometabolic Disorders |
| Q58122539 | Genetic Variants Related to Cardiometabolic Traits Are Associated to B Cell Function, Insulin Resistance, and Diabetes Among AmeriCan Indians: The Strong Heart Family Study |
| Q35919437 | Genetic and Environmental Regulation on Longitudinal Change of Metabolic Phenotypes in Danish and Chinese Adult Twins. |
| Q51012029 | Genetic and baseline metabolic factors for incident diabetes and HbA(1c) at follow-up: the healthy twin study |
| Q90884911 | Genetic contributions to NAFLD: leveraging shared genetics to uncover systems biology |
| Q33709055 | Genetic correlation of the plasma lipidome with type 2 diabetes, prediabetes and insulin resistance in Mexican American families |
| Q26822607 | Genetic prediction of common diseases. Still no help for the clinical diabetologist! |
| Q45094290 | Genetic risk scores ascertained in early adulthood and the prediction of type 2 diabetes later in life |
| Q38214522 | Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond |
| Q35808509 | Genetics of Type 2 Diabetes and Clinical Utility. |
| Q38816589 | Genetics of Type 2 Diabetes: It Matters From Which Parent We Inherit the Risk |
| Q51372835 | Genetics of type 2 diabetes. |
| Q26742051 | Genome-edited human stem cell-derived beta cells: a powerful tool for drilling down on type 2 diabetes GWAS biology |
| Q45305959 | Global aetiology and epidemiology of type 2 diabetes mellitus and its complications |
| Q89827214 | Heritability of Curve Patterns in Oral Glucose Tolerance Test |
| Q90523207 | High-Throughput Approaches onto Uncover (Epi)Genomic Architecture of Type 2 Diabetes |
| Q47108340 | Identification of five genetic variants as novel determinants of type 2 diabetes mellitus in Japanese by exome-wide association studies |
| Q55303000 | Identification of four genes as novel susceptibility loci for early-onset type 2 diabetes mellitus, metabolic syndrome, or hyperuricemia. |
| Q42697328 | Improved detection of genetic loci in estimated glomerular filtration rate and type 2 diabetes using a pleiotropic cFDR method |
| Q64103249 | Influence of obesity, parental history of diabetes, and genes in type 2 diabetes: A case-control study |
| Q26781353 | Insights into the Genetic Susceptibility to Type 2 Diabetes from Genome-Wide Association Studies of Obesity-Related Traits |
| Q48133244 | Integrative analysis of super enhancer SNPs for type 2 diabetes |
| Q35092657 | Joint effects of known type 2 diabetes susceptibility loci in genome-wide association study of Singapore Chinese: the Singapore Chinese health study |
| Q36043360 | Lack of association between type 2 diabetes and major depression: epidemiologic and genetic evidence in a multiethnic population |
| Q36129897 | Longitudinal Investigation into Genetics in the Conservation of Metabolic Phenotypes in Danish and Chinese Twins |
| Q91973409 | Mitochondrial Dysfunctions: A Thread Sewing Together Alzheimer's Disease, Diabetes, and Obesity |
| Q39117309 | Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts |
| Q43111069 | Mouse-human experimental epigenetic analysis unmasks dietary targets and genetic liability for diabetic phenotypes |
| Q89522669 | Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology |
| Q47150554 | Novel Common Variants Associated with Obesity and Type 2 Diabetes Detected Using a cFDR Method |
| Q43187196 | On the simple and the complex in psychiatry, with reference to DSM 5 and research domain criteria |
| Q41706055 | Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores |
| Q28391758 | Population ancestry and genetic risk for diabetes and kidney, cardiovascular, and bone disease: modifiable environmental factors may produce the cures |
| Q28607995 | Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals |
| Q36008752 | Reduced CD300LG mRNA tissue expression, increased intramyocellular lipid content and impaired glucose metabolism in healthy male carriers of Arg82Cys in CD300LG: a novel genometabolic cross-link between CD300LG and common metabolic phenotypes |
| Q47667669 | Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study |
| Q35532317 | Sixty-five common genetic variants and prediction of type 2 diabetes |
| Q90274128 | Sociodemographic and lifestyle-related risk factors for identifying vulnerable groups for type 2 diabetes: a narrative review with emphasis on data from Europe |
| Q37511821 | Spousal diabetes as a diabetes risk factor: a systematic review and meta-analysis |
| Q34587130 | Study design of DIACORE (DIAbetes COhoRtE) - a cohort study of patients with diabetes mellitus type 2. |
| Q90047790 | Systematic Review of Polygenic Risk Scores for Type 1 and Type 2 Diabetes |
| Q40201240 | The Concordance and Heritability of Type 2 Diabetes in 34,166 Twin Pairs From International Twin Registers: The Discordant Twin (DISCOTWIN) Consortium |
| Q33898977 | The Genetic Architecture of Diabetes in Pregnancy: Implications for Clinical Practice. |
| Q39100917 | The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies |
| Q38061186 | The genetics of type 2 diabetes and its clinical relevance |
| Q34499691 | The pancreatic β cell: recent insights from human genetics |
| Q40041955 | Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium |
| Q36726180 | Type 2 Diabetes Genetic Predisposition, Obesity, and All-Cause Mortality Risk in the U.S.: A Multiethnic Analysis |
| Q91777758 | Type 2 Diabetes: Multiple Genes, Multiple Diseases |
| Q30390388 | Type 2 diabetes: genetic data sharing to advance complex disease research |
| Q37702457 | Untangling the interplay of genetic and metabolic influences on beta-cell function: Examples of potential therapeutic implications involving TCF7L2 and FFAR1. |
| Q36066989 | Untargeted mass spectrometric approach in metabolic healthy offspring of patients with type 2 diabetes reveals medium-chain acylcarnitine as potential biomarker for lipid induced glucose intolerance (LGIT). |
| Q37283671 | Validation of Type 2 Diabetes Risk Variants Identified by Genome-Wide Association Studies in Northern Han Chinese. |
| Q35149473 | Validation of type 2 diabetes risk variants identified by genome-wide association studies in Han Chinese population: a replication study and meta-analysis |
| Q37367893 | Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes |
Search more.