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Human Genetics|April 13, 2010
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL familiesEllen M Wijsman, Joseph H Rothstein, Robert P Igo, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|May 17, 2003
Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemiaAmir F Ayyobi, Sandra H McGladdery, Marguerite J McNeely, et al.Molecular Nutrition & Food Research|March 5, 2013
Response of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: results from a crossover trialCheryl A M Anderson, Shirley A A Beresford, Dale McLerran, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|August 28, 2004
Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scanMichael D Badzioch, Robert P Igo, France Gagnon, et al.Journal of Lipid Research|August 19, 2003
Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemiaMelissa A Austin, Karen L Edwards, Stephanie A Monks, et al.American Journal of Human Genetics|November 26, 2013
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemiaElisabeth A Rosenthal, Jane Ranchalis, David R Crosslin, et al.Journal of Genetic Counseling|July 5, 2015
Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic CounselorsRobin L Bennett, Arno G Motulsky, Alan Bittles, et al.Journal of Lipid Research|December 8, 2009
Genetic and nongenetic sources of variation in phospholipid transfer protein activityGail P Jarvik, Ramakrishnan Rajagopalan, Elisabeth A Rosenthal, et al.Proceedings of the National Academy of Sciences of the United States of America|November 2, 2011
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuriaSarah B Pierce, Cailyn H Spurrell, Jessica B Mandell, et al.Journal of Lipid Research|July 16, 2011
Linkage and association of phospholipid transfer protein activity to LASS4Elisabeth A Rosenthal, James Ronald, Joseph Rothstein, et al.Pageof 3