Doron Lancet
Doron Lancet
Professor, Dept. Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel
Verified email at - Homepage
TitleCited byYear
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium
nature 409 (6822), 860, 2001
Executive summary: heart disease and stroke statistics—2013 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, WB Borden, ...
Circulation 127 (1), 143-152, 2013
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence.
PI Mackenzie, IS Owens, B Burchell, KW Bock, A Bairoch, A Belanger, ...
Pharmacogenetics 7 (4), 255-269, 1997
The complete human olfactory subgenome
G Glusman, I Yanai, I Rubin, D Lancet
Genome research 11 (5), 685-702, 2001
The genome of a songbird
WC Warren, DF Clayton, H Ellegren, AP Arnold, LDW Hillier, A Künstner, ...
Nature 464 (7289), 757, 2010
Genome analysis of the platypus reveals unique signatures of evolution
WC Warren, LDW Hillier, JAM Graves, E Birney, CP Ponting, F Grützner, ...
Nature 453 (7192), 175, 2008
GeneCards Version 3: the human gene integrator
M Safran, I Dalah, J Alexander, N Rosen, T Iny Stein, M Shmoish, N Nativ, ...
Database 2010, 2010
Odorant-sensitive adenylate cyclase may mediate olfactory reception
U Pace, E Hanski, Y Salomon, D Lancet
Nature 316 (6025), 255, 1985
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families …
H Lahat, E Pras, T Olender, N Avidan, E Ben-Asher, O Man, ...
The American Journal of Human Genetics 69 (6), 1378-1384, 2001
Genome-wide midrange transcription profiles reveal expression level relationships in human tissue specification
I Yanai, H Benjamin, M Shmoish, V Chalifa-Caspi, M Shklar, R Ophir, ...
Bioinformatics 21 (5), 650-659, 2004
The lipid world
D Segré, D Ben-Eli, DW Deamer, D Lancet
Origins of Life and Evolution of the Biosphere 31 (1-2), 119-145, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
I Eisenberg, N Avidan, T Potikha, H Hochner, M Chen, T Olender, ...
Nature genetics 29 (1), 83, 2001
Vertebrate olfactory reception
D Lancet
Annual review of neuroscience 9 (1), 329-355, 1986
Loss of olfactory receptor genes coincides with the acquisition of full trichromatic vision in primates
Y Gilad, V Wiebe, M Przeworski, D Lancet, S Pääbo
PLoS biology 2 (1), e5, 2004
GeneCards: integrating information about genes, proteins and diseases
M Rebhan, V Chalifa-Caspi, J Prilusky, D Lancet
Trends in Genetics 13 (4), 163, 1997
GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support.
M Rebhan, V Chalifa-Caspi, J Prilusky, D Lancet
Bioinformatics (Oxford, England) 14 (8), 656-664, 1998
The UDP glucuronosyltransferase gene super family: Suggested nomenclature based on evolutionary divergence
B Burchell, DW Nebert, DR Nelson, KW Bock, T Iyanagi, PL Jansen, ...
DNA and cell biology 10 (7), 487-494, 1991
Human specific loss of olfactory receptor genes
Y Gilad, O Man, S Pääbo, D Lancet
Proceedings of the National Academy of Sciences 100 (6), 3324-3327, 2003
The RUNX3 gene–sequence, structure and regulated expression
C Bangsow, N Rubins, G Glusman, Y Bernstein, V Negreanu, ...
Gene 279 (2), 221-232, 2001
Identification of the gene causing mucolipidosis type IV
R Bargal, N Avidan, E Ben-Asher, Z Olender, M Zeigler, A Frumkin, ...
Nature genetics 26 (1), 118, 2000
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