| 31064750 | Hydroa vacciniforme-like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites. | Blood | 2019 |
| 31076557 | Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle. | Proc Natl Acad Sci U S A | 2019 |
| 29193904 | Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype. | Mol Genet Genomic Med | 2018 |
| 27920058 | A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome. | J Med Genet | 2017 |
| 26411452 | Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites. | Hum Mutat | 2016 |
| 26432246 | An integrated map of structural variation in 2,504 human genomes. | Nature | 2015 |
| 24693920 | Integrative genetic analysis of allergic inflammation in the murine lung. | Am J Respir Cell Mol Biol | 2014 |
| 25411967 | A systems genetics approach identifies CXCL14, ITGAX, and LPCAT2 as novel aggressive prostate cancer susceptibility genes. | PLoS Genet | 2014 |
| 25114278 | Genetic regulation of Zfp30, CXCL1, and neutrophilic inflammation in murine lung. | Genetics | 2014 |
| 22238593 | A genome-wide association search for type 2 diabetes genes in African Americans. | PLoS One | 2012 |
| 22479202 | Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. | PLoS Genet | 2012 |
| 22856873 | Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects. | BMC Med Genet | 2012 |
| 20185807 | Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans. | Diabetes | 2010 |
| 20081858 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. | Nat Genet | 2010 |
| 19779022 | FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. | Hum Mol Genet | 2009 |
| 19557161 | Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. | PLoS Genet | 2009 |
| 19079261 | Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. | Nat Genet | 2009 |
| 16374835 | Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database. | Genet Epidemiol | 2006 |
| 14988269 | A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. | Diabetes | 2004 |
| 11032783 | 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. | Am J Hum Genet | 2000 |
| 11032784 | The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci. | Am J Hum Genet | 2000 |
| 10051618 | Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. | Proc Natl Acad Sci U S A | 1999 |
| 9049634 | Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group. | Genome Res | 1997 |