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Publications of Dr. M. Olivier


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Peer-reviewed Journal Publications/Original Papers: (* co-first authorships)

  1. Loria R., Bukhalid R.A., Creath R.A., Leiner R.H., Olivier M., and Steffens J.C. (1995). Dfferential Production of Thaxtomins by Pathogenic Streptomyces Species In Vitro. Phytopathology 85(5):537-541.
  2. Olivier M. and Lust G. (1998). Two DNA Sequences Characteristic of the Canine Y Chromosome. Animal Genetics 29(2): 146-149.
  3. Olivier M., Meehl M.A., and Lust G. (1999). Random Amplified Polymorphic DNA (RAPD) Sequences as Markers for Canine Genetic Studies. Journal of Heredity 90(1): 78-82.
  4. Todhunter R.J., Acland G.M., Olivier M., Williams A.J., Vernier-Singer M., Burton-Wurster N., Farese J.P., Grohn Y.T., Gilbert R.O., Dykes N.L., and Lust G. (1999). Development of an Outcrossed Canine Pedigree for Linkage Analysis of Hip Dysplasia. Journal of Heredity 90(1): 83-92.
  5. Olivier M., Breen M., Binns M.M., and Lust G. (1999). Localization and characterization of nucleotide sequences from the canine Y chromosome. Chromosome Research 7(3): 223-233.
  6. Olivier M., Aggarwal A., Allen J.R., Almendras A.A., Bajorek E.S., Beasley E.M., Brady S.D., Bushard J.M., Bustos V.I., Chu A., Chung T.R., De Witte A., Denys M.E., Dominguez R., Fang N., Foster B.D., Freudenberg R.W., Hadley D., Hamilton L.R., Jeffrey T.J., Kelly L., Lazzeroni L., Levy M., Lewis S.C., Liu X., Lopez F.J., Louie B., Marquis J.P., Martinez R.A., Matsuura M.K., Misherghi N.S., Norton J.A., Olshen A., Perkins S.M., Perou A.J., Piercy C., Piercy M., Qin F., Reif T., Sheppard K., Shokoohi V., Smick G.A., Sun W.-L., Stewart E.A., Tejeda J.F., Tran N.M., Trejo T., Vo N.T., Yan S.C.M., Zierten D.L., Zhao S., Sachidanandam R., Trask B.J., Myers R.M., and Cox D.R. (2001). A High Resolution Radiation Hybrid Map of the Human Genome Draft Sequence. Science 291: 1298-1302.
  7. Cheung V.G., Nowak N., Jang W., Kirsch I.R., Zhao S., Chen X.-N., Furey T.S., Kim U.-J., Kuo W.-L., Olivier M., Conroy J., Kasprzyk A., Massa H., Yonescu R., Sait S., Thoreen C., Snijders A., Lemyre E., Bailey J.A., Bruzel A., Burrill W.D., Clegg S.M., Collins S., Dhami P., Friedman C., Han C.S., Herrick S., Lee J., Ligon A.H., Lowry S., Morley M., Narasimhan S., Osoegawa K., Peng Z., Plajzer-Frick I., Quade B.J., Scott D., Sirotkin K., Thorpe A.A., Gray J.W., Hudson J., Pinkel D., Reid T., Rowen L., Shen-Ong G.L., Strausberg R.L., Birney E., Callen D.F., Cheng J.-F., Cox D.R., Doggett N.A., Carter N.P., Eichler E.E., Haussler D., Korenberg J.R., Morton C.C., Albertson D., Schuler G., de Jong P.J., and Trask B.J. (2001). Integration of Cytogenetic Landmarks into the Draft Sequence of the Human Genome. Nature 409: 953-958.
  8. Ranade K., Chang M.S., Ting C.T., Pei D., Hsiao C.F., Olivier M., Pesich R., Hebert J., Chen Y.D., Dzau V.J., Curb D., Olshen R., Risch N., Cox D.R., and Botstein D. (2001). High-throughput Genotyping with Single Nucleotide Polymorphisms. Genome Research 11: 62-1268.
  9. Sundqvist A.K., Ellegren H., Olivier M., and Vila C. (2001). Y Chromosome Haplotyping in Scandinavian Wolves (Canis lupus) Based on Microsatellite Markers. Molecular Ecology 10: 1959-1966.
  10. Pennacchio L.A., Olivier M., Hubacek J.A., Cohen J.C., Cox D.R., Fruchart J.C., Krauss R.M., and Rubin E.M. (2001). An Apolipoprotein Influencing Triglyerides in Humans and Mice Revealed by Comparative Sequencing. Science 294: 169-173.
  11. Ranade K., Wu K.D., Risch N., Olivier M., Pei D., Hsiao C.F., Chuang L.M., Ho L.T., Jorgenson E., Pesich R., Chen Y.D., Dzau V., Lin A., Olshen R.A., Curb D., Cox D.R., and Botstein D. (2001). Genetics Variation in Aldosterone Synthase Predicts Plasma Glucose Levels. Proceedings of the National Academy of Sciences U S A 98: 13219-13224.
  12. Olivier M., Bustos V.I., Levy M.R., Smick G.A., Moreno I., Bushard J.M., Almendras A.A., Sheppard K., Zierten D.L., Aggarwal A., Carlson C.S., Foster B.D., Vo N., Kelly L., Liu X., and Cox D.R. (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: 64-72.
  13. Ranade K., Shue W.H., Hung Y.J., Hsiung C.A., Chiang F.T., Pesich R., Hebert J., Olivier M., Chen Y.D., Pratt R., Olshen R., Curb D., Botstein D., Risch N., Cox D.R. (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. American Journal of Hypertension 14:1196-200.
  14. Olivier M., Chuang L.M., Chang M.S., Chen Y.T., Pei D., Ranade K., de Witte A., Allen J., Tran N., Curb D., Pratt R., Neefs ., de Arruda Indig M., Law S., Neri B., Wang L., and Cox D.R. (2002). High-throughput Genotyping of Single Nucleotide Polymorphisms Using New Invader Technology. Nucleic Acids Research 30(12): e53.
  15. Pennacchio L.A.*, Olivier M.*, Hubacek J.A.*, Krauss R.M., Rubin E.M., and Cohen J.C. (2002). Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels. Human Molecular Genetics 11(24): 3031-3038.
  16. Talmud P.J., Hawe E., Martin S., Nicaud V., Olivier M., Miller G.J., Rubin E.M., Pennacchio L.A., and Humphries S. (2002). Relative contribution of variation within the APOC3-A4-A5 gene cluster in determining plasma triglycerides. Human Molecular Genetics 11(24): 3039-3046.
  17. Liang M., Yuan B., Rute E., Greene A.S., Olivier M., and Cowley A.W. Jr. (2003). Insights into Dahl salt-sensitive hypertension revealed by temporal patterns of renal medullary gene expression. Physiological Genomics 12(3): 229-237.
  18. Yuan B., Liang M., Yang Z., Rute E., Olivier M., and Cowley A.W. Jr. (2003). Gene expression reveals vulnerability to oxidative stess and interstitial fibrosis of the renal outer medulla to non-hypertensive elevations of angiotensin II. American Journal of Physiology - Regulatory, Integrative and Comparative Physiology 284(5): R1219-1230.
  19. Olivier M. (2003). A haplotype map of the human genome. Physiological Genomics 13(1):3-9.
  20. Kerns J.A., Olivier M., Lust G., and Barsh G. (2003). Exclusion of melanocortin 1 receptor (Mc1r) and agouti as candidates for dominant black in dogs. Journal of Heredity 94(1): 75-79.
  21. Eichenbaum-Voline S.*, Olivier M.*, Jones E.L., Naoumova R.P., Jones B., Gau B., Patel H.N., Seed M., Betteridge D.J., Galton D.J., Rubin E.M., Scott J., Shoulders C.C., Pennacchio L.A. (2004). Linkage and Association Between Distinct Variants of the APOA1/C3/A4/A5 Gene Cluster and Familial Combined Hyperlipidemia. Arteriosclerosis, Thrombosis, and Vascular Biology 24(1):167-174.
  22. Olivier M., Wang X., Cole R., Gau B., Kim J., Rubin E.M., and Pennacchio L.A. (2004). Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11. Genomics 83:912-923.
  23. Sonnenberg G.E., Krakower G.R., Martin L.J., Olivier M., Kwitek A.E.., Comuzzie A.G., Blangero J., and Kissebah A.H. (2004). Genetic determinants of obesity-related lipid traits. Journal of Lipid Research 45(4):610-615.
  24. Olivier M., Hsiung C.A., Chuang L.-M., Ho L.-T., Ting C.-T., Bustos V.I., Lee T.M., de Witte A., Chen I., Rodriguez B., Wen C.-C., and Cox D.R. (2004). Single nucleotide polymorphisms in protein tyrosine phosphatase 1 (PTPN1) are associated with essential hypertension and obesity in Japanese and Chinese. Human Molecular Genetics 13(17):1885-1892.
  25. Huang J., Lin A., Narasimhan B., Quertermous T., Hsiung A.C., Ho L.-T., Grove J.S., Olivier M., Ranade K., Risch N.J., and Olshen R.A. (2004). Tree-structured supervised learning and the genetics of hypertension. Proceedings of the National Academy of Sciences U S A 101(29):10529-34.
  26. Baessler A., Hasinoff M., Fischer M., Reinhard W., Sonnenberg G., Olivier M., Erdmann J., Schunkert H., Doering A., Jacob H.J., Comuzzie A.G., Kissebah A.H., and Kwitek A.E. (2005). Genetic linkage and association of the Growth Hormone Sectretagogue Receptor (GHSR, Ghrelin Receptor) gene in human obesity. Diabetes 54(1):259-267.
  27. Halligan B.D., Slyper R.Y., Twigger S.N., Hicks W.A., Olivier M., and Greene A.S. (2005). ZoomQuant: An application for the quantitation of stable isotope labeled peptides. Journal of the American Society for Mass Spectrometry 16(3):302-306.
  28. Chen Y., Shortreed M.R., Olivier M., and Smith L.M. (2005). Direct SNP genotyping on surface invasive cleavage arrays. Analytical Chemistry 77(8):2400-5.
  29. Olivier M. (2005). SNP genotyping using Invader technology. Mutation Research 573(1-2):103-10.
  30. Hicks W.A., Halligan B.D., Slyper R.Y., Twigger S.N., Greene A.S., and Olivier M. (2005). Simultaneous Quantification and Identification using 18O Labeling with an Ion Trap Mass Spectrometer and the Analysis Software Application "ZoomQuant". Journal of the American Society for Mass Spectrometry 16(6):916-25.

Book Chapters:

  1. Olivier M., Brady S., and Cox D.R. (2003). Radiation Hybrid Mapping of BAC End Sequences. In: Bacterial Artificial Chromosomes Vol. 1 (S. Zhao and M. Stodolsky, ed.), 163-169, Humana Press, Totowa, NJ.

Editorials, Letters To Editor:

  1. Olivier M. (2003). From SNPs to function: the effect of sequence variation on gene expression. Physiological Genomics 16(2):182-183.

Published Abstracts:

  1. Olivier M. and Lust G. (1997). Two new nucleotide sequences specific for the canine Y chromosome. FASEB Journal 11(9): 513.
  2. Olivier M., Wang D.-J., Hsiao C.-F., Tai T.-Y., Ho L.-T., Ranade K., Chen Y.-D.I., Olshen R., Curb D., Pratt R., Jarvis N., De Arruda Indig M., Risch N., and Cox D.R. (1999). Analysis of single nucleotide polymorphisms in candidate genes for hypertension and insulin resistance. American Journal of Human Genetics 65(4 Suppl): A438 (Abstract 2484).
  3. Olivier M., Aggarwal A., Bustos V.I., Foster B.D., Levy M.R., Moreno I., Smick G.A., and Cox D.R. (2000). Long-range haplotypes and linkage disequilibrium of single nucleotide polymorphisms extend over more than 120 Kb in the sequence of human chromosome 21. American Journal of Human Genetics 67(4 Suppl 2): 22 (Abstract 71).
  4. 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 Journal of Human Genetics 71(4 Suppl): 358 (Abstract 1091).
  5. Olivier M., Martin L.J., Blangero J., Comuzzie A.G., Rainwater D.L., Sonnenberg G.E., and Kissebah A.H. (2003). Two new loci linked to altered lipoprotein particle size in obese individuals. American Journal of Human Genetics 73(5 Suppl): 182 (Abstract 103).