Articoli con mandati relativi all'accesso pubblico - Stan NelsonUlteriori informazioni
Non disponibile pubblicamente: 1
Controlla
PPP3CA truncating variants clustered in the regulatory domain cause early‐onset refractory epilepsy
S Panneerselvam, J Wang, W Zhu, H Dai, JG Pappas, R Rabin, KJ Low, ...
Clinical genetics 100 (2), 227-233, 2021
Mandati: US National Institutes of Health
Disponibili pubblicamente: 242
Controlla
Melanomas acquire resistance to B-RAF (V600E) inhibition by RTK or N-RAS upregulation
R Nazarian, H Shi, QI Wang, X Kong, RC Koya, H Lee, Z Chen, MK Lee, ...
Nature 468 (7326), 973-977, 2010
Mandati: US National Institutes of Health
Controlla
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning
SJ Cokus, S Feng, X Zhang, Z Chen, B Merriman, CD Haudenschild, ...
Nature 452 (7184), 215-219, 2008
Mandati: Howard Hughes Medical Institute
Controlla
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Mandati: US National Institutes of Health, Australian Research Council, National …
Controlla
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Controlla
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
T Walsh, JM McClellan, SE McCarthy, AM Addington, SB Pierce, ...
science 320 (5875), 539-543, 2008
Mandati: US National Institutes of Health, Howard Hughes Medical Institute
Controlla
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Mandati: Genome Canada, German Research Foundation
Controlla
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays
N Homer, S Szelinger, M Redman, D Duggan, W Tembe, J Muehling, ...
PLoS genetics 4 (8), e1000167, 2008
Mandati: US National Institutes of Health
Controlla
Clinical exome sequencing for genetic identification of rare Mendelian disorders
H Lee, JL Deignan, N Dorrani, SP Strom, S Kantarci, F Quintero-Rivera, ...
Jama 312 (18), 1880-1887, 2014
Mandati: US National Institutes of Health
Controlla
Melanoma whole-exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance
H Shi, G Moriceau, X Kong, MK Lee, H Lee, RC Koya, C Ng, T Chodon, ...
Nature communications 3 (1), 724, 2012
Mandati: US National Institutes of Health
Controlla
BFAST: an alignment tool for large scale genome resequencing
N Homer, B Merriman, SF Nelson
PloS one 4 (11), e7767, 2009
Mandati: US National Institutes of Health
Controlla
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
Mandati: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Controlla
Genome sequencing highlights the dynamic early history of dogs
AH Freedman, I Gronau, RM Schweizer, D Ortega-Del Vecchyo, E Han, ...
PLoS genetics 10 (1), e1004016, 2014
Mandati: US National Institutes of Health, European Commission, Government of Spain
Controlla
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
BM Neale, SE Medland, S Ripke, P Asherson, B Franke, KP Lesch, ...
Journal of the American Academy of Child & Adolescent Psychiatry 49 (9), 884-897, 2010
Mandati: US National Institutes of Health, German Research Foundation
Controlla
Targeted therapy resistance mediated by dynamic regulation of extrachromosomal mutant EGFR DNA
DA Nathanson, B Gini, J Mottahedeh, K Visnyei, T Koga, G Gomez, ...
Science 343 (6166), 72-76, 2014
Mandati: US National Institutes of Health
Controlla
Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
JF Sathirapongsasuti, H Lee, BAJ Horst, G Brunner, AJ Cochran, S Binder, ...
Bioinformatics 27 (19), 2648-2654, 2011
Mandati: US National Institutes of Health
Controlla
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
Mandati: US National Institutes of Health, National Institute for Health Research, UK
Controlla
Gene expression profile correlates with T-cell infiltration and relative survival in glioblastoma patients vaccinated with dendritic cell immunotherapy
RM Prins, H Soto, V Konkankit, SK Odesa, A Eskin, WH Yong, SF Nelson, ...
Clinical cancer research 17 (6), 1603-1615, 2011
Mandati: US National Institutes of Health
Controlla
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Controlla
Cold Urticaria, Immunodeficiency, and Autoimmunity Related to PLCG2 Deletions
MJ Ombrello, EF Remmers, G Sun, AF Freeman, S Datta, P Torabi-Parizi, ...
New England Journal of Medicine 366 (4), 330-338, 2012
Mandati: US National Institutes of Health
Le informazioni sulla pubblicazione e sul finanziamento vengono stabilite automaticamente da un software