Len A. Pennacchio
Len A. Pennacchio
Verified email at lbl.gov
TitleCited byYear
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
9039*2012
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium
Nature, 2012
90392012
Finishing the euchromatic sequence of the human genome
International Human Genome Sequencing Consortium
Nature 431 (7011), 931, 2004
36722004
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, 2008
18672008
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
17542007
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, 2009
14432009
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, 2008
13392008
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
11012001
In vivo enhancer analysis of human conserved non-coding sequences
LA Pennacchio, N Ahituv, AM Moses, S Prabhakar, MA Nobrega, ...
Nature 444 (7118), 499, 2006
10522006
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
9932011
Guidelines for investigating causality of sequence variants in human disease
DG MacArthur, TA Manolio, DP Dimmock, HL Rehm, J Shendure, ...
Nature 508 (7497), 469, 2014
9012014
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
7072008
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, 2006
6752006
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
5761996
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, 2007
5642007
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
5542007
Genomic views of distant-acting enhancers
A Visel, EM Rubin, LA Pennacchio
Nature 461 (7261), 199, 2009
5302009
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, 2007
5172007
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, 2007
5102007
Genomic strategies to identify mammalian regulatory sequences
LA Pennacchio, EM Rubin
Nature reviews genetics 2 (2), 100, 2001
4952001
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Articles 1–20