دنبال کردن
Audrey E. Hendricks, PhD
Audrey E. Hendricks, PhD
Associate Professor of Statistics, University of Colorado - Denver
ایمیل تأیید شده در ucdenver.edu - صفحهٔ اصلی
عنوان
نقل شده توسط
نقل شده توسط
سال
The UK10K project identifies rare variants in health and disease
Statistics group Ciampi Antonio 8 Greenwood Celia MT (co-chair) 7 8 14 19 ...
Nature 526 (7571), 82-90, 2015
11222015
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
3702018
Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset
M Swami, AE Hendricks, T Gillis, T Massood, J Mysore, RH Myers, ...
Human molecular genetics 18 (16), 3039-3047, 2009
3482009
Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes
E Dragileva, A Hendricks, A Teed, T Gillis, ET Lopez, EC Friedberg, ...
Neurobiology of disease 33 (1), 37-47, 2009
2582009
KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidation
LR Pearce, N Atanassova, MC Banton, B Bottomley, AA van der Klaauw, ...
Cell 155 (4), 765-777, 2013
2072013
Whole-genome sequencing coupled to imputation discovers genetic signals for anthropometric traits
I Tachmazidou, D Süveges, JL Min, GRS Ritchie, J Steinberg, K Walter, ...
The American Journal of Human Genetics 100 (6), 865-884, 2017
1742017
Body mass index is negatively associated with telomere length: a collaborative cross-sectional meta-analysis of 87 observational studies
M Gielen, GJ Hageman, EE Antoniou, K Nordfjall, M Mangino, ...
The American journal of clinical nutrition 108 (3), 453-475, 2018
1722018
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
JE Tobin, JC Latourelle, MF Lew, C Klein, O Suchowersky, HA Shill, ...
Neurology 71 (1), 28-34, 2008
1532008
Genetic architecture of human thinness compared to severe obesity
F Riveros-McKay, V Mistry, R Bounds, A Hendricks, JM Keogh, H Thomas, ...
PLoS genetics 15 (1), e1007603, 2019
1302019
The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study
JC Latourelle, M Sun, MF Lew, O Suchowersky, C Klein, LI Golbe, ...
BMC medicine 6, 1-7, 2008
1242008
Human semaphorin 3 variants link melanocortin circuit development and energy balance
AA Van Der Klaauw, S Croizier, EM De Oliveira, LKJ Stadler, S Park, ...
Cell 176 (4), 729-742. e18, 2019
1202019
Iron in micronutrient powder promotes an unfavorable gut microbiota in Kenyan infants
M Tang, DN Frank, AE Hendricks, D Ir, F Esamai, E Liechty, ...
Nutrients 9 (7), 776, 2017
842017
Assessment of cortical and striatal involvement in 523 Huntington disease brains
TC Hadzi, AE Hendricks, JC Latourelle, KL Lunetta, LA Cupples, T Gillis, ...
Neurology 79 (16), 1708-1715, 2012
732012
Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27 …
AE Hendricks, JC Latourelle, KL Lunetta, LA Cupples, V Wheeler, ...
American Journal of Medical Genetics Part A 149 (7), 1375-1381, 2009
702009
Rare variant analysis of human and rodent obesity genes in individuals with severe childhood obesity
AE Hendricks, EG Bochukova, G Marenne, JM Keogh, N Atanassova, ...
Scientific reports 7 (1), 4394, 2017
682017
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis
Y Yang, AA van der Klaauw, L Zhu, TM Cacciottolo, Y He, LKJ Stadler, ...
Nature communications 10 (1), 1718, 2019
652019
Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes
X Zhang, AD Johnson, AE Hendricks, SJ Hwang, K Tanriverdi, ...
Human molecular genetics 23 (3), 782-795, 2014
632014
Exome sequencing identifies genes and gene sets contributing to severe childhood obesity, linking PHIP variants to repressed POMC transcription
G Marenne, AE Hendricks, A Perdikari, R Bounds, F Payne, JM Keogh, ...
Cell Metabolism 31 (6), 1107-1119. e12, 2020
572020
Correction for multiple testing in a gene region
AE Hendricks, J Dupuis, MW Logue, RH Myers, KL Lunetta
European Journal of Human Genetics 22 (3), 414-418, 2014
542014
Replication of association between ELAVL4 and Parkinson disease: the GenePD study
AL DeStefano, J Latourelle, MF Lew, O Suchowersky, C Klein, LI Golbe, ...
Human genetics 124, 95-99, 2008
532008
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مقاله‌ها 1–20