Sean Mooney
Sean Mooney
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Citata da
Citata da
Comprehensive molecular portraits of human breast tumours
D Koboldt, R Fulton, M McLellan, H Schmidt, J Kalicki-Veizer, ...
Nature 490 (7418), 61-70, 2012
A large-scale evaluation of computational protein function prediction
P Radivojac, WT Clark, TR Oron, AM Schnoes, T Wittkop, A Sokolov, ...
Nature methods 10 (3), 221-227, 2013
Automated inference of molecular mechanisms of disease from amino acid substitutions
B Li, VG Krishnan, ME Mort, F Xin, KK Kamati, DN Cooper, SD Mooney, ...
Bioinformatics 25 (21), 2744, 2009
A community effort to assess and improve drug sensitivity prediction algorithms
JC Costello, LM Heiser, E Georgii, M Gnen, MP Menden, NJ Wang, ...
Nature biotechnology 32 (12), 1202-1212, 2014
Genetic correction of Huntington's disease phenotypes in induced pluripotent stem cells
MC An, N Zhang, G Scott, D Montoro, T Wittkop, S Mooney, S Melov, ...
Cell stem cell 11 (2), 253-263, 2012
Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways
MJ Rardin, JC Newman, JM Held, MP Cusack, DJ Sorensen, B Li, ...
Proceedings of the National Academy of Sciences 110 (16), 6601-6606, 2013
Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts
JR Sanford, X Wang, M Mort, N VanDuyn, DN Cooper, SD Mooney, ...
Genome research 19 (3), 381-394, 2009
An expanded evaluation of protein function prediction methods shows an improvement in accuracy
Y Jiang, TR Oron, WT Clark, AR Bankapur, D D’Andrea, R Lepore, ...
Genome biology 17 (1), 1-19, 2016
Late‐life rapamycin treatment reverses age‐related heart dysfunction
JM Flynn, MN O'Leary, CA Zambataro, EC Academia, MP Presley, ...
Aging cell 12 (5), 851-862, 2013
A novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosis
T Larsson, X Yu, SI Davis, MS Draman, SD Mooney, MJ Cullen, KE White
The Journal of Clinical Endocrinology & Metabolism 90 (4), 2424-2427, 2005
Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis
S Mooney
Briefings in bioinformatics 6 (1), 44-56, 2005
An integrated approach to inferring gene–disease associations in humans
P Radivojac, K Peng, WT Clark, BJ Peters, A Mohan, SM Boyle, ...
Proteins: Structure, Function, and Bioinformatics 72 (3), 1030-1037, 2008
Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine
RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ...
The American Journal of Human Genetics 98 (6), 1051-1066, 2016
Proteomic analysis of age‐dependent changes in protein solubility identifies genes that modulate lifespan
P Reis‐Rodrigues, G Czerwieniec, TW Peters, US Evani, S Alavez, ...
Aging cell, 2011
Fibroblast growth factor-23 mutants causing familial tumoral calcinosis are differentially processed
T Larsson, SI Davis, HJ Garringer, SD Mooney, MS Draman, MJ Cullen, ...
Endocrinology 146 (9), 3883-3891, 2005
Newborn sequencing in genomic medicine and public health
JS Berg, PB Agrawal, DB Bailey, AH Beggs, SE Brenner, AM Brower, ...
Pediatrics 139 (2), 2017
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
M Mort, T Sterne-Weiler, B Li, EV Ball, DN Cooper, P Radivojac, ...
Genome biology 15 (1), 1-20, 2014
High-performance web services for querying gene and variant annotation
J Xin, A Mark, C Afrasiabi, G Tsueng, M Juchler, N Gopal, GS Stupp, ...
Genome biology 17 (1), 1-7, 2016
Genome‐wide DNA methylation changes with age in disease‐free human skeletal muscle
A Zykovich, A Hubbard, JM Flynn, M Tarnopolsky, MF Fraga, C Kerksick, ...
Aging cell 13 (2), 360-366, 2014
MutPred2: inferring the molecular and phenotypic impact of amino acid variants
V Pejaver, J Urresti, J Lugo-Martinez, KA Pagel, GN Lin, HJ Nam, M Mort, ...
BioRxiv, 134981, 2017
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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