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Sabrina Mitchell
Sabrina Mitchell
Vanderbilt University Medical Center
Email verificata su vumc.org
Titolo
Citata da
Citata da
Anno
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained
Y Wu, LL Waite, AU Jackson, WHH Sheu, S Buyske, D Absher, DK Arnett, ...
PLoS genetics 9 (3), e1003379, 2013
1462013
Effects of meals high in carbohydrate, protein, and fat on ghrelin and peptide YY secretion in prepubertal children
JP Lomenick, MS Melguizo, SL Mitchell, ML Summar, JW Anderson
The Journal of Clinical Endocrinology & Metabolism 94 (11), 4463-4471, 2009
1112009
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study
S Buyske, Y Wu, CL Carty, I Cheng, TL Assimes, L Dumitrescu, ...
PloS one 7 (4), e35651, 2012
882012
Characterization of mitochondrial haplogroups in a large population-based sample from the United States
SL Mitchell, R Goodloe, K Brown-Gentry, SA Pendergrass, DG Murdock, ...
Human genetics 133, 861-868, 2014
802014
Arginine and carnitine metabolites are altered in diabetic retinopathy
K Sumarriva, K Uppal, C Ma, DJ Herren, Y Wang, IM Chocron, C Warden, ...
Investigative ophthalmology & visual science 60 (8), 3119-3126, 2019
692019
Genetic variation in the urea cycle: a model resource for investigating key candidate genes for common diseases
S Mitchell, C Ellingson, T Coyne, L Hall, M Neill, N Christian, C Higham, ...
Human mutation 30 (1), 56-60, 2009
512009
The carnitine shuttle pathway is altered in patients with neovascular age-related macular degeneration
SL Mitchell, K Uppal, SM Williamson, K Liu, LG Burgess, VL Tran, ...
Investigative ophthalmology & visual science 59 (12), 4978-4985, 2018
412018
Altering the mitochondrial fatty acid synthesis (mtFASII) pathway modulates cellular metabolic states and bioactive lipid profiles as revealed by metabolomic profiling
HB Clay, AK Parl, SL Mitchell, L Singh, LN Bell, DG Murdock
PloS one 11 (3), e0151171, 2016
382016
The mitochondrial fatty acid synthesis (mtFASII) pathway is capable of mediating nuclear-mitochondrial cross talk through the PPAR system of transcriptional activation
A Parl, SL Mitchell, HB Clay, S Reiss, Z Li, DG Murdock
Biochemical and biophysical research communications 441 (2), 418-424, 2013
332013
Plasma arginine and citrulline are elevated in diabetic retinopathy
KS Peters, E Rivera, C Warden, PA Harlow, SL Mitchell, MW Calcutt, ...
American Journal of Ophthalmology 235, 154-162, 2022
242022
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies
SL Mitchell, JB Hall, RJ Goodloe, J Boston, E Farber-Eger, ...
BioData Mining 7, 1-11, 2014
182014
Plasma metabolomics of intermediate and neovascular age-related macular degeneration patients
SL Mitchell, C Ma, WK Scott, A Agarwal, MA Pericak-Vance, JL Haines, ...
Cells 10 (11), 3141, 2021
152021
Mitochondrial variation and the risk of age-related macular degeneration across diverse populations
NA Restrepo, SL Mitchell, RJ Goodloe, DG Murdock, JL Haines, ...
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 243, 2015
132015
KIAA1462, A Coronary Artery Disease Associated Gene, Is a Candidate Gene for Late Onset Alzheimer Disease in APOE Carriers
DG Murdock, Y Bradford, N Schnetz-Boutaud, P Mayo, MJ Allen, ...
Plos one 8 (12), e82194, 2013
122013
Mitochondrial haplogroups modify the effect of diabetes duration and hba1c on proliferative diabetic retinopathy risk in patients with type 2 diabetes
SL Mitchell, AC Neininger, CN Bruce, IM Chocron, JA Bregman, ...
Investigative Ophthalmology & Visual Science 58 (14), 6481-6488, 2017
92017
Hyperammonemia from a urea cycle disorder presenting in adulthood
T C Priester, TK Khoo, E R Fernández-Pérez, K R Regner, J A Tracy, ...
The Open Critical Care Medicine Journal 2 (1), 2009
92009
Pharmacogenetics of hypoglycemia associated with sulfonylurea therapy in usual clinical care
SL Mitchell, DAC Leon, S Chaugai, VK Kawai, RT Levinson, WQ Wei, ...
The pharmacogenomics journal 20 (6), 831-839, 2020
82020
Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification
S Smieszek, SL Mitchell, EH Farber-Eger, OJ Veatch, NR Wheeler, ...
PeerJ 6, e5149, 2018
82018
Peptide tyrosine tyrosine levels are increased in patients with urea cycle disorders
S Mitchell, T Welch-Burke, L Dumitrescu, JP Lomenick, DG Murdock, ...
Molecular genetics and metabolism 106 (1), 39-42, 2012
52012
Plasma peptide tyrosine tyrosine (PYY) levels are increased in urea cycle disorder patients.
S Mitchell, D Murdock, M Summar
MOLECULAR GENETICS AND METABOLISM 93 (3), 258-258, 2008
32008
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
Articoli 1–20