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Laurakay Bruhn
Laurakay Bruhn
Verified email at agilent.com
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Year
Functional interaction of β-catenin with the transcription factor LEF-1
J Behrens, JP Von Kries, M Kühl, L Bruhn, D Wedlich, R Grosschedl, ...
Nature 382 (6592), 638-642, 1996
39061996
lincRNAs act in the circuitry controlling pluripotency and differentiation
M Guttman, J Donaghey, BW Carey, M Garber, JK Grenier, G Munson, ...
Nature 477 (7364), 295-300, 2011
21572011
Mapping and sequencing of structural variation from eight human genomes
JM Kidd, GM Cooper, WF Donahue, HS Hayden, N Sampas, T Graves, ...
Nature 453 (7191), 56-64, 2008
14252008
Promiscuous mutations activate the noncanonical NF-κB pathway in multiple myeloma
JJ Keats, R Fonseca, M Chesi, R Schop, A Baker, WJ Chng, S Van Wier, ...
Cancer cell 12 (2), 131-144, 2007
12112007
Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice.
C van Genderen, RM Okamura, I Farinas, RG Quo, TG Parslow, L Bruhn, ...
Genes & development 8 (22), 2691-2703, 1994
12031994
Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells
A Hendel, RO Bak, JT Clark, AB Kennedy, DE Ryan, S Roy, I Steinfeld, ...
Nature biotechnology 33 (9), 985-989, 2015
11632015
Tissue classification with gene expression profiles
A Ben-Dor, L Bruhn, N Friedman, I Nachman, M Schummer, Z Yakhini
Proceedings of the fourth annual international conference on Computational …, 2000
10982000
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
7842010
PIASy, a nuclear matrix–associated SUMO E3 ligase, represses LEF1 activity by sequestration into nuclear bodies
S Sachdev, L Bruhn, H Sieber, A Pichler, F Melchior, R Grosschedl
Genes & development 15 (23), 3088-3103, 2001
6802001
Novel role for the potent endogenous inotrope apelin in human cardiac dysfunction
MM Chen, EA Ashley, DXF Deng, A Tsalenko, A Deng, R Tabibiazar, ...
Circulation 108 (12), 1432-1439, 2003
5162003
The fine-scale and complex architecture of human copy-number variation
GH Perry, A Ben-Dor, A Tsalenko, N Sampas, L Rodriguez-Revenga, ...
The American Journal of Human Genetics 82 (3), 685-695, 2008
5032008
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
MT Barrett, A Scheffer, A Ben-Dor, N Sampas, D Lipson, R Kincaid, ...
Proceedings of the National Academy of Sciences 101 (51), 17765-17770, 2004
4542004
ALY, a context-dependent coactivator of LEF-1 and AML-1, is required for TCRalpha enhancer function.
L Bruhn, A Munnerlyn, R Grosschedl
Genes & development 11 (5), 640-653, 1997
3891997
Improving CRISPR–Cas specificity with chemical modifications in single-guide RNAs
DE Ryan, D Taussig, I Steinfeld, SM Phadnis, BD Lunstad, M Singh, ...
Nucleic acids research 46 (2), 792-803, 2018
2592018
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases
AJ de Smith, A Tsalenko, N Sampas, A Scheffer, NA Yamada, P Tsang, ...
Human molecular genetics 16 (23), 2783-2794, 2007
2552007
Pathway analysis of coronary atherosclerosis
JY King, R Ferrara, R Tabibiazar, JM Spin, MM Chen, A Kuchinsky, ...
Physiological genomics 23 (1), 103-118, 2005
1982005
Characterization of missing human genome sequences and copy-number polymorphic insertions
JM Kidd, N Sampas, F Antonacci, T Graves, R Fulton, HS Hayden, ...
Nature methods 7 (5), 365-371, 2010
1832010
Method of adaptor-dimer subtraction using a CRISPR CAS6 protein
G Zeiner, L Bruhn
US Patent 9,102,936, 2015
1632015
Identification of endothelial cell genes by combined database mining and microarray analysis
M Ho, E Yang, G Matcuk, D Deng, N Sampas, A Tsalenko, R Tabibiazar, ...
Physiological genomics 13 (3), 249-262, 2003
1532003
Population-genetic properties of differentiated human copy-number polymorphisms
CD Campbell, N Sampas, A Tsalenko, PH Sudmant, JM Kidd, M Malig, ...
The American Journal of Human Genetics 88 (3), 317-332, 2011
1202011
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