Catherine Leiendecker-Foster
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Explore the profile of Catherine Leiendecker-Foster including associated specialties, affiliations and a list of published articles.
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887
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Recent Articles
1.
Honig L, Kang M, Cheng R, Eckfeldt J, Thyagarajan B, Leiendecker-Foster C, et al.
Neurobiol Aging
. 2015 Aug;
36(10):2785-90.
PMID: 26239175
Chromosomal telomere length shortens with repeated cell divisions. Human leukocyte DNA telomere length (LTL) has been shown to shorten during aging. LTL shortening has correlated with decreased longevity, dementia, and...
2.
Huxley R, Lopez F, MacLehose R, Eckfeldt J, Couper D, Leiendecker-Foster C, et al.
PLoS One
. 2013 Apr;
8(3):e59052.
PMID: 23554968
Background: Previous cross-sectional studies have suggested that biomarkers of extracellular matrix remodelling are associated with atrial fibrillation (AF), but no prospective data have yet been published. Hence, we examine whether...
3.
Murray J, McLachlan S, Adams P, Eckfeldt J, Garner C, Vulpe C, et al.
Clin Gastroenterol Hepatol
. 2013 Feb;
11(7):808-14.
PMID: 23416278
Background & Aims: Celiac disease is an increasingly recognized disorder in Caucasian populations of European origin. Little is known about its prevalence in non-Caucasians. Although it is thought to be...
4.
McLaren C, McLachlan S, Garner C, Vulpe C, Gordeuk V, Eckfeldt J, et al.
PLoS One
. 2012 Jul;
7(6):e38339.
PMID: 22761678
The existence of multiple inherited disorders of iron metabolism suggests genetic contributions to iron deficiency. We previously performed a genome-wide association study of iron-related single nucleotide polymorphisms (SNPs) using DNA...
5.
Zhang X, Lynch A, Davis B, Ford C, Boerwinkle E, Eckfeldt J, et al.
PLoS One
. 2012 Apr;
7(3):e34217.
PMID: 22470539
Nitric oxide synthase 3 (NOS3) catalyzes production of NO in the endothelium and may play a role in cardiovascular disease (CVD). We assessed the pharmacogenetic associations of three NOS3 polymorphisms...
6.
Lynch A, Eckfeldt J, Davis B, Ford C, Boerwinkle E, Leiendecker-Foster C, et al.
Pharmacogenet Genomics
. 2012 Mar;
22(5):355-66.
PMID: 22388798
Objective: To identify panels of genetic variants that predict treatment-related coronary heart disease (CHD) outcomes in hypertensive patients on one of four different classes of initial antihypertensive treatment. The goal...
7.
Inker L, Eckfeldt J, Levey A, Leiendecker-Foster C, Rynders G, Manzi J, et al.
Am J Kidney Dis
. 2011 Aug;
58(4):682-4.
PMID: 21855190
No abstract available.
8.
McLaren C, Garner C, Constantine C, McLachlan S, Vulpe C, Snively B, et al.
PLoS One
. 2011 Apr;
6(3):e17390.
PMID: 21483845
The existence of multiple inherited disorders of iron metabolism in man, rodents and other vertebrates suggests genetic contributions to iron deficiency. To identify new genomic locations associated with iron deficiency,...
9.
Acton R, Barton J, Leiendecker-Foster C, Zaun C, McLaren C, Eckfeldt J
Blood Cells Mol Dis
. 2010 Feb;
44(4):252-6.
PMID: 20178892
We sought to determine if TNF promoter variants could explain iron phenotype heterogeneity in adults with previous HFE genotyping. HEIRS Study participants genotyped for C282Y and H63D were designated as...
10.
Adams P, Barton J, McLaren G, Acton R, Speechley M, McLaren C, et al.
Can J Gastroenterol
. 2009 Nov;
23(11):769-72.
PMID: 19893773
Background: The HEmochromatosis and IRon Overload Screening (HEIRS) Study provided data on a racially, ethnically and geographically diverse cohort of participants in North America screened from primary care populations. Methods:...