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Laboratory Publications
Selected Papers
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Olivier, M., A. Aggarwal, J. Allen, A. A. Almendras, E. S. Bajorek,
E. M. Beasley, S. D. Brady, J. M. Bushard, V. I. Bustos, A. Chu,
T. R. Chung, A. De Witte, M. E. Denys, R. Dominguez, N. Y. Fang,
B. D. Foster, R. W. Freudenberg, D. Hadley, L. R. Hamilton, T. J.
Jeffrey, L. Kelly, L. Lazzeroni, M. R. Levy, S. C. Lewis, X. Liu,
F. J. Lopez, B. Louie, J. P. Marquis, R. A. Martinez, M. K. Matsuura,
N. S. Misherghi, J. A. Norton, A. Olshen, S. M. Perkins, A. J. Perou,
C. Piercy, M. Piercy, F. Qin, T. Reif, K. Sheppard, V. Shokoohi,
G. A. Smick, W. L. Sun, E. A. Stewart, J. Fernando, Tejeda, N. M.
Tran, T. Trejo, N. T. Vo, S. C. Yan, D. L. Zierten, S. Zhao, R.
Sachidanandam, B. J. Trask, R. M. Myers and D. R. Cox (2001). "A
high-resolution radiation hybrid map of the human genome draft sequence."
Science 291(5507): 1298-302.
- Olivier, M., V. I. Bustos, M. R. Levy, G. A. Smick, I. Moreno,
J. M. Bushard, A. A. Almendras, K. Sheppard, D. L. Zierten, A. Aggarwal,
C. S. Carlson, B. D. Foster, N. Vo, L. Kelly, X. Liu and D. R. Cox
(2001). "Complex high-resolution linkage disequilibrium and
haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb
of sequence on human chromosome 21." Genomics 78(1-2): 64-72.
- Cheung, V. G., N. Nowak, W. Jang, I. R. Kirsch, S. Zhao, X. N.
Chen, T. S. Furey, U. J. Kim, W. L. Kuo, M. Olivier, J. Conroy,
A. Kasprzyk, H. Massa, R. Yonescu, S. Sait, C. Thoreen, A. Snijders,
E. Lemyre, J. A. Bailey, A. Bruzel, W. D. Burrill, S. M. Clegg,
S. Collins, P. Dhami, C. Friedman, C. S. Han, S. Herrick, J. Lee,
A. H. Ligon, S. Lowry, M. Morley, S. Narasimhan, K. Osoegawa, Z.
Peng, I. Plajzer-Frick, B. J. Quade, D. Scott, K. Sirotkin, A. A.
Thorpe, J. W. Gray, J. Hudson, D. Pinkel, T. Ried, L. Rowen, G.
L. Shen-Ong, R. L. Strausberg, E. Birney, D. F. Callen, J. F. Cheng,
D. R. Cox, N. A. Doggett, N. P. Carter, E. E. Eichler, D. Haussler,
J. R. Korenberg, C. C. Morton, D. Albertson, G. Schuler, P. J. de
Jong and B. J. Trask (2001). "Integration of cytogenetic landmarks
into the draft sequence of the human genome." Nature 409(6822):
953-8.
- Ranade, K., W. H. Shue, Y. J. Hung, C. A. Hsuing, F. T. Chiang,
R. Pesich, J. Hebert, M. Olivier, Y. D. Chen, R. Pratt, R. Olshen,
D. Curb, D. Botstein, N. Risch and D. R. Cox (2001). "The glycine
allele of a glycine/arginine polymorphism in the beta2-adrenergic
receptor gene is associated with essential hypertension in a population
of Chinese origin." Am J Hypertens 14(12): 1196-200.
- Pennacchio, L. A., M. Olivier, J. A. Hubacek, J. C. Cohen, D. R.
Cox, J. C. Fruchart, R. M. Krauss and E. M. Rubin (2001). "An
apolipoprotein influencing triglycerides in humans and mice revealed
by comparative sequencing." Science 294(5540): 169-73.
- Ranade, K., K. D. Wu, N. Risch, M. Olivier, D. Pei, C. F. Hsiao,
L. M. Chuang, L. T. Ho, E. Jorgenson, R. Pesich, Y. D. Chen, V.
Dzau, A. Lin, R. A. Olshen, D. Curb, D. R. Cox and D. Botstein (2001).
"Genetic variation in aldosterone synthase predicts plasma
glucose levels." Proc Natl Acad Sci U S A 98(23): 13219-24.
- Ranade, K., M. S. Chang, C. T. Ting, D. Pei, C. F. Hsiao, M. Olivier,
R. Pesich, J. Hebert, Y. D. Chen, V. J. Dzau, D. Curb, R. Olshen,
N. Risch, D. R. Cox and D. Botstein (2001). "High-throughput
genotyping with single nucleotide polymorphisms." Genome Res
11(7): 1262-8.
- Olivier, M., L. M. Chuang, M. S. Chang, Y. T. Chen, D. Pei, K.
Ranade, A. de Witte, J. Allen, N. Tran, D. Curb, R. Pratt, H. Neefs,
M. de Arruda Indig, S. Law, B. Neri, L. Wang and D. R. Cox (2002).
"High-throughput genotyping of single nucleotide polymorphisms
using new biplex invader technology." Nucleic Acids Res 30(12):
e53.
- Pennacchio, L. A., M. Olivier, J. A. Hubacek, R. M. Krauss, E.
M. Rubin and J. C. Cohen (2002). "Two independent apolipoprotein
A5 haplotypes influence human plasma triglyceride levels."
Hum Mol Genet 11(24): 3031-3038.
- Talmud, P. J., E. Hawe, S. Martin, M. Olivier, G. J. Miller, E.
M. Rubin, L. A. Pennacchio and S. E. Humphries (2002). "Relative
contribution of variation within the APOC3/A4/A5 gene cluster in
determining plasma triglycerides." Hum Mol Genet 11(24): 3039-3046.
- Liang, M., B. Yuan, E. Rute, A. S. Greene, M. Olivier and A. W.
Cowley, Jr. (2003). "Insights into Dahl salt-sensitive hypertension
revealed by temporal patterns of renal medullary gene expression."
Physiol Genomics 12(3): 229-37.
- Olivier, M. (2003). "A haplotype map of the human genome."
Physiol Genomics 13(1): 3-9.
- Yuan, B., M. Liang, Z. Yang, E. Rute, N. Taylor, M. Olivier and
A. W. Cowley, Jr. (2003). "Gene expression reveals vulnerability
to oxidative stress and interstitial fibrosis of renal outer medulla
to nonhypertensive elevations of ANG II." Am J Physiol Regul
Integr Comp Physiol 284(5): R1219-30.
Posters
- Olivier M., Pennacchio L.A., Gau B., Cole R., Krauss R.M., and
Rubin E.M. (2001) Sequence Variation in Apolipoprotein AV and Association
with Triglyceride Levels in Humans. AHA Asia Pacific Scientific
Forum, April 23-26, 2002, Honolulu, HI. (add pdf file link)
- Olivier M., Pennacchio L.A, Gau B., Krauss R.M., and Rubin E.M.
(2002). Linkage disequilibrium and haplotype structure of the apolipoprotein
gene cluster region on human chromosome 11. Cold Spring Harbor Laboratories
Meeting: Genome Sequencing and Biology, May 7-11, 2002, Cold Spring
Harbor, NY. (add pdf file link)
- Olivier M., Savic D., and Brauer S. (2002). Linkage disequilibrium
and haplotype structure of the Protein Tyrosine Phosphatase 1B (PTPN1)
gene region on human chromosome 20. American Society for Human Genetics
Annual Meeting, Oct. 16-19, 2002, Baltimore, MD. (add pdf file link)
Other Publications
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