| scholarly article | Q13442814 |
| meta-analysis | Q815382 |
| P356 | DOI | 10.1159/000114164 |
| P8608 | Fatcat ID | release_yffumdil6re47mhomo6onbn3ri |
| P932 | PMC publication ID | 2855874 |
| P698 | PubMed publication ID | 18223311 |
| P5875 | ResearchGate publication ID | 5629146 |
| P50 | author | Michael Boehnke | Q6828710 |
| Adebowale A. Adeyemo | Q37390255 | ||
| Nancy J Cox | Q67954217 | ||
| P2093 | author name string | Weihua Guan | |
| Anna Pluzhnikov | |||
| International Type 2 Diabetes Linkage Analysis Consortium | |||
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes | Q24290189 | ||
| Merlin--rapid analysis of dense genetic maps using sparse gene flow trees | Q27860829 | ||
| A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 | Q28118289 | ||
| A genome-wide association study identifies novel risk loci for type 2 diabetes | Q28287727 | ||
| Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study | Q28345118 | ||
| Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes | Q28680760 | ||
| Parametric and nonparametric linkage analysis: a unified multipoint approach | Q28762162 | ||
| Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus | Q28771769 | ||
| 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 | ||
| A high-resolution recombination map of the human genome | Q29547815 | ||
| Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes | Q29614589 | ||
| A variant in CDKAL1 influences insulin response and risk of type 2 diabetes | Q29614878 | ||
| Comprehensive human genetic maps: individual and sex-specific variation in recombination | Q29618511 | ||
| Inclusion of candidate region studies in meta-analysis using the genome screen meta-analysis method: application to asthma data | Q30670284 | ||
| A Genome-Wide Search for Type 2 Diabetes Susceptibility Genes in West Africans: The Africa America Diabetes Mellitus (AADM) Study | Q33198713 | ||
| Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method | Q33283857 | ||
| Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24. | Q33963885 | ||
| A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q | Q34044595 | ||
| Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24. | Q34144320 | ||
| The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. | Q34146763 | ||
| An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians | Q34387450 | ||
| Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans | Q34389390 | ||
| Genomewide search for type 2 diabetes susceptibility genes in four American populations | Q34390662 | ||
| Allele-sharing models: LOD scores and accurate linkage tests | Q35249919 | ||
| Robust variance-components approach for assessing genetic linkage in pedigrees | Q35889010 | ||
| Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium | Q35946296 | ||
| A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians | Q37360693 | ||
| An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians | Q37381130 | ||
| Meta-analysis of genome searches | Q42622749 | ||
| Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy | Q42654901 | ||
| Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects | Q44262570 | ||
| Genome-wide search for type 2 diabetes/impaired glucose homeostasis susceptibility genes in the Chinese: significant linkage to chromosome 6q21-q23 and chromosome 1q21-q24. | Q44705010 | ||
| The GENNID Study. A resource for mapping the genes that cause NIDDM. | Q45254865 | ||
| A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q. | Q46661066 | ||
| A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes | Q47745459 | ||
| Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2. | Q51552143 | ||
| Truncated product method for combining P-values. | Q52936699 | ||
| A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. | Q53780537 | ||
| A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene | Q56893821 | ||
| A Gene Conferring Susceptibility to Type 2 Diabetes in Conjunction With Obesity Is Located on Chromosome 18p11 | Q57122175 | ||
| A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population | Q57499717 | ||
| Genome-wide Scan for Type 2 Diabetes Loci in Hong Kong Chinese and Confirmation of a Susceptibility Locus on Chromosome 1q21-q25 | Q58209883 | ||
| Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families | Q63916576 | ||
| New susceptibility locus for NIDDM is localized to human chromosome 20q | Q73303103 | ||
| A genome-wide search for type II diabetes susceptibility genes in Chinese Hans | Q73891270 | ||
| A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14 | Q76385443 | ||
| A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians | Q77759155 | ||
| Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p | Q77829278 | ||
| Genome-wide scanning for type 2 diabetes susceptibility in Canadian Oji-Cree, using 190 microsatellite markers | Q77941019 | ||
| An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese | Q81542448 | ||
| P433 | issue | 1 | |
| P921 | main subject | meta-analysis | Q815382 |
| type 2 diabetes | Q3025883 | ||
| P304 | page(s) | 35-49 | |
| P577 | publication date | 2007-01-28 | |
| P1433 | published in | Human Heredity | Q15755116 |
| P1476 | title | Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium | |
| P478 | volume | 66 |
| Q34044595 | A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q |
| Q34235548 | ABCC5 transporter is a novel type 2 diabetes susceptibility gene in European and African American populations |
| Q44798018 | Agreement among type 2 diabetes linkage studies but a poor correlation with results from genome-wide association studies |
| Q38808702 | Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes |
| Q39329664 | Evaluating empirical bounds on complex disease genetic architecture |
| Q37538006 | Finding common susceptibility variants for complex disease: past, present and future |
| Q33891719 | GWAS to Sequencing: Divergence in Study Design and Analysis |
| Q37857564 | Genome-wide association studies and type 2 diabetes |
| Q28752564 | Genome-wide association studies in type 2 diabetes |
| Q37023074 | Genome-wide linkage and admixture mapping of type 2 diabetes in African American families from the American Diabetes Association GENNID (Genetics of NIDDM) Study Cohort |
| Q28345118 | Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study |
| Q36625794 | Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes |
| Q36080938 | Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis |
| Q37573689 | Linkage of type 2 diabetes on chromosome 9p24 in Mexican Americans: additional evidence from the Veterans Administration Genetic Epidemiology Study (VAGES). |
| Q35894344 | Nuclear factor κB-inducing kinase activation as a mechanism of pancreatic β cell failure in obesity. |
| Q46240925 | Proceedings of the Eighth Annual UT-ORNL-KBRIN Bioinformatics Summit 2009. |
| Q37698685 | Progress in the genetics of common obesity and type 2 diabetes |
| Q24288830 | Replication in Genome-Wide Association Studies |
| Q37758804 | Roots, development and future directions of laboratory medicine |
| Q64066397 | The Contribution of Low-Frequency and Rare Coding Variation to Susceptibility to Type 2 Diabetes |
| Q26997813 | The complex interplay of genetic and lifestyle risk factors in type 2 diabetes: an overview |
| Q30390388 | Type 2 diabetes: genetic data sharing to advance complex disease research |
| Q37980673 | Who should we target for diabetes prevention and diabetes risk reduction? |
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