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Author Details

Lisa Baird
1989
33
18
PMIDPaper TitleJournal TitlePublished Year
35212379A tRNA modifying enzyme as a tunable regulatory nexus for bacterial stress responses and virulence.Nucleic Acids Research2022
36510265The mutational dynamics of short tandem repeats in large, multigenerational families.Genome Biol2022
33668674Acute Effects of Cheddar Cheese Consumption on Circulating Amino Acids and Human Skeletal Muscle.Nutrients2021
33705535Reduced Physical Activity Alters the Leucine-Stimulated Translatome in Aged Skeletal Muscle.2021
32561805Germline mutation rates in young adults predict longevity and reproductive lifespan.Sci Rep2020
31549960Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation.Elife2019
31575651Pedigree-based estimation of human mobile element retrotransposition rates.Genome Res2019
29570242Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia.Birth Defects Res2018
28917040Studying Selenoprotein mRNA Translation Using RNA-Seq and Ribosome Profiling.Methods in Molecular Biology2018
28250457Genome-wide analyses identify common variants associated with macular telangiectasia type 2.Nat Genet2017
28615380Leucine Differentially Regulates Gene-Specific Translation in Mouse Skeletal Muscle.Journal of Nutrition2017
29069514Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein P.Nucleic Acids Research2017
27867939A Rare Variant in <i>CACNA1D</i> Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree.Mol Neuropsychiatry2016
27603779Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome.PLoS One2016
24467814Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.Mol Autism2014
23341896Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.PLoS One2013
19855918Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations.Acta Diabetol2010
20522424Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer.J Med Genet2010
19265784The 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 Hypertens2009
18618000A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.PLoS Genet2008
18523456Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.Eur J Hum Genet2008
12624758Genetic 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 Genet2003
10577921Delineation 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 Genet1999
9054934A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.Nat Genet1997
8946299A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma.J Glaucoma1996
8533764A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.Am J Hum Genet1995
8075632Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.Nat Genet1994
8094389Sequence analysis and phenotypic characterization of groEL mutations that block lambda and T4 bacteriophage growth.Journal of Bacteriology1993
8102362Identification and transcriptional analysis of the Escherichia coli htrE operon which is homologous to pap and related pilin operons.Journal of Bacteriology1993
1847383Analysis of an Escherichia coli dnaB temperature-sensitive insertion mutation and its cold-sensitive extragenic suppressor.Journal of Biological Chemistry1991
1885549Identification of the Escherichia coli sohB gene, a multicopy suppressor of the HtrA (DegP) null phenotype.Journal of Bacteriology1991
2407727Identification, cloning, and characterization of the Escherichia coli sohA gene, a suppressor of the htrA (degP) null phenotype.Journal of Bacteriology1990
2537822Identification, characterization, and mapping of the Escherichia coli htrA gene, whose product is essential for bacterial growth only at elevated temperatures.Journal of Bacteriology1989
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