Len A. Pennacchio
Len A. Pennacchio
Email verificata su lbl.gov
Citata da
Citata da
An integrated encyclopedia of DNA elements in the human genome.
BE Bernstein, E Birney, I Dunham, ED Green, C Gunter, M Snyder
Nature 489 (7414), 57, 2012
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium
Nature, 2012
Finishing the euchromatic sequence of the human genome
International Human Genome Sequencing Consortium
Nature 431 (7011), 931, 2004
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease
S Romeo, J Kozlitina, C Xing, A Pertsemlidis, D Cox, LA Pennacchio, ...
Nature genetics 40 (12), 1461-1465, 2008
A common allele on chromosome 9 associated with coronary heart disease
R McPherson, A Pertsemlidis, N Kavaslar, A Stewart, R Roberts, DR Cox, ...
Science 316 (5830), 1488-1491, 2007
ChIP-seq accurately predicts tissue-specific activity of enhancers
A Visel, MJ Blow, Z Li, T Zhang, JA Akiyama, A Holt, I Plajzer-Frick, ...
Nature 457 (7231), 854-858, 2009
The amphioxus genome and the evolution of the chordate karyotype
NH Putnam, T Butts, DEK Ferrier, RF Furlong, U Hellsten, T Kawashima, ...
Nature 453 (7198), 1064-1071, 2008
An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing
LA Pennacchio, M Olivier, JA Hubacek, JC Cohen, DR Cox, JC Fruchart, ...
Science 294 (5540), 169-173, 2001
In vivo enhancer analysis of human conserved non-coding sequences
LA Pennacchio, N Ahituv, AM Moses, S Prabhakar, MA Nobrega, ...
Nature 444 (7118), 499-502, 2006
Metagenomic discovery of biomass-degrading genes and genomes from cow rumen
M Hess, A Sczyrba, R Egan, TW Kim, H Chokhawala, G Schroth, S Luo, ...
Science 331 (6016), 463-467, 2011
Guidelines for investigating causality of sequence variants in human disease
DG MacArthur, TA Manolio, DP Dimmock, HL Rehm, J Shendure, ...
Nature 508 (7497), 469-476, 2014
VISTA Enhancer Browser—a database of tissue-specific human enhancers
A Visel, S Minovitsky, I Dubchak, LA Pennacchio
Nucleic acids research 35 (suppl_1), D88-D92, 2007
Dicer, Drosha, and outcomes in patients with ovarian cancer
WM Merritt, YG Lin, LY Han, AA Kamat, WA Spannuth, R Schmandt, ...
New England Journal of Medicine 359 (25), 2641-2650, 2008
Genomic views of distant-acting enhancers
A Visel, EM Rubin, LA Pennacchio
Nature 461 (7261), 199-205, 2009
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
B Pandit, A Sarkozy, LA Pennacchio, C Carta, K Oishi, S Martinelli, ...
Nature genetics 39 (8), 1007-1012, 2007
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
LA Pennacchio, AE Lehesjoki, NE Stone, VL Willour, K Virtaneva, J Miao, ...
Science 271 (5256), 1731-1734, 1996
Most rare missense alleles are deleterious in humans: implications for complex disease and association studies
GV Kryukov, LA Pennacchio, SR Sunyaev
The American Journal of Human Genetics 80 (4), 727-739, 2007
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome
M Tartaglia, LA Pennacchio, C Zhao, KK Yadav, V Fodale, A Sarkozy, ...
Nature genetics 39 (1), 75-79, 2007
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL
S Romeo, LA Pennacchio, Y Fu, E Boerwinkle, A Tybjaerg-Hansen, ...
Nature genetics 39 (4), 513-516, 2007
Genomic strategies to identify mammalian regulatory sequences
LA Pennacchio, EM Rubin
Nature reviews genetics 2 (2), 100-109, 2001
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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