| 35212379 | A tRNA modifying enzyme as a tunable regulatory nexus for bacterial stress responses and virulence. | Nucleic Acids Research | 2022 |
| 36510265 | The mutational dynamics of short tandem repeats in large, multigenerational families. | Genome Biol | 2022 |
| 33668674 | Acute Effects of Cheddar Cheese Consumption on Circulating Amino Acids and Human Skeletal Muscle. | Nutrients | 2021 |
| 33705535 | Reduced Physical Activity Alters the Leucine-Stimulated Translatome in Aged Skeletal Muscle. | | 2021 |
| 32561805 | Germline mutation rates in young adults predict longevity and reproductive lifespan. | Sci Rep | 2020 |
| 31549960 | Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. | Elife | 2019 |
| 31575651 | Pedigree-based estimation of human mobile element retrotransposition rates. | Genome Res | 2019 |
| 29570242 | Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia. | Birth Defects Res | 2018 |
| 28917040 | Studying Selenoprotein mRNA Translation Using RNA-Seq and Ribosome Profiling. | Methods in Molecular Biology | 2018 |
| 28250457 | Genome-wide analyses identify common variants associated with macular telangiectasia type 2. | Nat Genet | 2017 |
| 28615380 | Leucine Differentially Regulates Gene-Specific Translation in Mouse Skeletal Muscle. | Journal of Nutrition | 2017 |
| 29069514 | Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein P. | Nucleic Acids Research | 2017 |
| 27867939 | A Rare Variant in <i>CACNA1D</i> Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree. | Mol Neuropsychiatry | 2016 |
| 27603779 | Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome. | PLoS One | 2016 |
| 24467814 | Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population. | Mol Autism | 2014 |
| 23341896 | Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population. | PLoS One | 2013 |
| 19855918 | Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations. | Acta Diabetol | 2010 |
| 20522424 | Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer. | J Med Genet | 2010 |
| 19265784 | The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. | Am J Hypertens | 2009 |
| 18618000 | A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction. | PLoS Genet | 2008 |
| 18523456 | Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program. | Eur J Hum Genet | 2008 |
| 12624758 | Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. | Hum Genet | 2003 |
| 10577921 | Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees. | Am J Hum Genet | 1999 |
| 9054934 | A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. | Nat Genet | 1997 |
| 8946299 | A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma. | J Glaucoma | 1996 |
| 8533764 | A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. | Am J Hum Genet | 1995 |
| 8075632 | Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. | Nat Genet | 1994 |
| 8094389 | Sequence analysis and phenotypic characterization of groEL mutations that block lambda and T4 bacteriophage growth. | Journal of Bacteriology | 1993 |
| 8102362 | Identification and transcriptional analysis of the Escherichia coli htrE operon which is homologous to pap and related pilin operons. | Journal of Bacteriology | 1993 |
| 1847383 | Analysis of an Escherichia coli dnaB temperature-sensitive insertion mutation and its cold-sensitive extragenic suppressor. | Journal of Biological Chemistry | 1991 |
| 1885549 | Identification of the Escherichia coli sohB gene, a multicopy suppressor of the HtrA (DegP) null phenotype. | Journal of Bacteriology | 1991 |
| 2407727 | Identification, cloning, and characterization of the Escherichia coli sohA gene, a suppressor of the htrA (degP) null phenotype. | Journal of Bacteriology | 1990 |
| 2537822 | Identification, characterization, and mapping of the Escherichia coli htrA gene, whose product is essential for bacterial growth only at elevated temperatures. | Journal of Bacteriology | 1989 |