SGTC Publications

Following is a list of publications starting in 1993, when the Stanford Genome Technology Center was founded.

The references below are hyper-linked to their abstract in PubMed or, whenever possible, directly to the journal. (Access to journals may require membership or subscription).

For some papers supplemental web sites provide additional information.

Detailed information about patents can be found under Stanford References (Office of Technology Licensing at Stanford University) or at the United States Patent and Trademark Office (USPTO).

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Original Articles

Reviews

Yeast chemical genomics and drug discovery: an update.
Hoon S, St Onge RP, Giaever G, Nislow C. Trends Pharmacol Sci. (2008). [PubMed]
Genetic variation analyses by Pyrosequencing.
Langaee, T., Ronaghi, M. Mutat Res 573 (2005): 96-102. [PubMed], [Publisher Full Text]
Maximizing the potential of functional genomics.
Steimetz, L.M., Davis, R.W. Nature Reviews Genetics 5 (2004): 190 –201. doi:10.1038/nrg1293. [PubMed], [Publisher Full Text]
Progress in maize gene discovery: a project update.
Lunde, C. F., Morrow, D. J., Roy, L. M., Walbot, V. Funct Integr Genomics. 3.1-2 (2003):25-32. Epub 2002. [PubMed]
Denaturing high performance liquid chromatography in the molecular diagnosis of genetic disorders.
Sivakumaran T.A., Kucheria, K., Oefner, P.J. Current Science 84 (2003): 101-106.
Gene mutation analysis by denaturing high performance liquid chromatography.
Premstaller, A., Oefner, P.J. PharmaGenomics 3.2 (2003):20-37.
Denaturing high performance liquid chromatography of nucleic acids.
Premstaller, A., Oefner, P.J. LC&GC 15.7 (2002): 410-422.
Technologische Neuentwicklungen in der Genomwissenschaft - Von Mutation zu Funktion mittels DHPLC und DNS Chips; 2. Teil
Steinmetz L., Oefner P.J. Lebensmittel- und Biotechnologie 19.3 (2002): 93-96.
Technologische Neuentwicklungen in der Genomwissenschaft - Von Mutation zu Funktion mittels DHPLC und DNS Chips; 1. Teil
Steinmetz L., Oefner P.J. Lebensmittel- und Biotechnologie 19.2 (2002): 60-64.
Gene function on a genomic scale.
Steinmetz L.M., Deutschbauer A.M. J Chromatogr B Analyt Technol Biomed Life Sci Dec 25.782 (2002): 151-63. [PubMed Abstract], [Publisher Full Text]
New trends in DHPLC.
Premstaller, A., Oefner, P.J., American Genomic/Proteomic Technology 2.1 (2002): 27-29.
A decade of high-resolution liquid chromatography of nucleic acids on styrene-divinylbenzene copolymers.
Oefner, P.J., Huber, C.G. J. Chromatogr. B Analyt Technol Biomed Life Sci Dec 25.782 (2002): 3-25.
Progress in Maize Gene Discovery: a project update.
Lunde, C.F., Morrow, D. R., Roy L.M., Walbot V. Funct Integr Genomics 3.1-2 (2002): 25-32. [PubMed]
Pyrosequencing™: an accurate detection platform for single nucleotide polymorphisms.
Fakhrai-Rad, H., Pourmand, N., Ronaghi, M. Hum Mutat 19.5 (2002): 479-485. [Publisher Abstract].
Comparative genomics of Arabidopsis and maize: prospects and limitations.
Brendel, V., Kurtz, S., Walbot, V. Genome Biol 3.3 (2002): REVIEWS1005. [PubMed Abstract].
Denaturing high-performance liquid chromatography: A review.
Xiao, W., Oefner, P.J. Jun, Hum Mutat 17.6 (2001): 439-474. [PubMed Abstract].
3rd International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis: SNPs: 'some notable progress'.
White, P.S., Kwok, P.Y., Oefner, P., Brookes, A.J. Apr, Eur J Hum Genet 9.4 (2001): 316-318. [Publisher Abstract].
Pyrosequencing sheds light on DNA sequencing.
Ronaghi, M. Jan Genome Res 11.1 (2001):3-11. [Publisher Full Text].
Expression monitoring using cDNA microarrays. A general protocol.
Lou, X.J., Schena, M., Horrigan, F.T., Lawn, R.M., Davis, R.W. Methods Mol Biol 175 (2001): 323-340.
Computational methods for gene annotation: the Arabidopsis genome.
Cho, Y., Walbot, V. Apr, Curr Opin Biotechnol 12.2 (2001): 126-130. [PubMed Abstract].
SNiPpets from the Third International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis.
Brookes, A.J., Kwok, P.Y., White, P.S., Oefner, J.P. September 8-11, 2000, Taos, New Mexico, USA, Hum. Mutat, 17 (2001): 241-242.
Combining genome sequences and new technologies for dissecting the genetics of complex phenotypes.
Steinmetz, L.M., Mindrinos, M., Oefner, P.J. Trends Plant Sci 5.9 (2000): 397-401.
High-density arrays and insights into genome function.
Steinmetz, L.M., Davis, R.W. Biotechnol Genet Eng Rev 17 (2000): 109-146.
Fluorescence-based expression monitoring using microarrays.
Winzeler, E.A., Schena, M., Davis, R.W. Methods Enzymol 306 (1999): 3-18.
Microarrays: biotechnology's discovery platform for functional genomics.
Schena, M., Heller, R.A., Theriault, T.P., Konrad, K., Lachenmeier, E., Davis, R.W. Trends Biotechnol 16.7 (1988): 301-306. [PubMed Abstract].
Quantitative analysis of gene expression by ion-pair high-performance liquid chromatography.
Doris, P.A., Oefner, P.J., Chilton, B.S., Hayward-Lester, A. J. Chromatogr A 806.1 (1988): 47-60. [PubMed Abstract].
Functional analysis of the yeast genome.
Winzeler, E.A., Davis, R.W. Curr Opin Genet Dev 7.6 (1997): 771-776. [PubMed Abstract].
Life with 6000 genes.
Goffeau, A., Barrell, B.G., Bussey, H., Davis, R.W., Dujon, B., Feldmann, H., Galibert, F., Hoheisel, J.D., Jacq, C., Johnston, M., Louis, E.J., Mewes, H.W., Murakami, Y., Philippsen, P., Tettelin, H., Oliver, S.G. Science, 274.5287 (1996): 546, 563-547. [Publisher Full Text].

Short Communications

Analysis of eight exons of the CFTR gene in 65 Iranian cystic fibrosis patients by DHPLC and sequencing.
Elahi, E., Alinasab, B., Esson, G., Ghassemi, F., Houshmand, M., Khodadad, A., Oefner, P., Reihani-Sabet, F., Ronaghi, M., Shahabi, M., Thorstenson, Y. Am. J. Hum. Genet. 71 (2002): 546.
Interspecies comparisons of the ATM gene.
Wayne, T.L., Thorstenson, Y.R., Oefner, P.J. Am. J. Hum. Genet. 69.5 (2001): 42.
Parallels and contrasts in female and male human evolutionary history.
Shen, P., Tang, H., Passarino, P., Do, B., Sung, R., Davis, K., Scharfe, C., Cavalli-Sforza, L.L., Feldman, M.W., Oefner, P.J. Am. J. Hum. Genet. 69 (2001): 423.
BRCA1 and BRCA2 analysis in 523 Austrian HPOC and HBC families.
Kroiss, R., Wagner, T., Muhr, D., Fleischmann, E., Korn, V., Helbich, T., Zielinski, C., Kubista, E., Oefner, P. Am. J. Hum. Genet. 69 (2001): 252.
Interspecies comparisons of the ATM gene.
Wayne, T.L., Thorstenson, Y.R., Oefner, P.J. Am. J. Hum. Genet 69 (2001): 42.
Germline carriers of ATM mutations are prevalent among Austrian hereditary breast and ovarian cancer (HBOC) patients.
Thorstenson, Y.R., Roxas, A., Kroiss, R., Wagner, T., Oefner, P.J. Am. J. Hum. Genet 69 (2001): 205.
Estimation of time to the most recent common ancestor by tree-partition.
Tang, H., Siegmund, D., Shen, P., Oefner, P., Feldman, M. Am. J. Hum. Genet 69 (2001): 394.
Mapping genes in Saccharomyces cerevisiae and arabidopsis thaliana using high-density DNA arrays and denaturing high-performance liquid chromatography.
Steinmetz, L., Mindrinos, M., Spiegelman, J., Richards, D., Xiao, W., Fankhauser, C., McCusker, J., Chory, J., Davis, R., Oefner, P. Hum. Mutat 17 (2001): 323.
Parallels and contrasts in female and male human evolutionary history.
Shen, P., Passarino, G., Sung, R., Song, S., Do, B., Roxas, A., Hurlbut, A., Lin, A., Sherry, S., Feldman, M., Cavalli-Sforza, L., Underhill, P., Oefner, P. Hum. Mutat 17 (2001): 341.
Parallels and contrasts in female and male human evolutionary history.
Shen, P., Tang, H., Passarino, P., Do, B., Sung, R., Davis, K., Scharfe, C., Cavalli-Sforza, L.L., Feldman, M.W., Oefner, P.J. Am. J. Hum. Genet 69 (2001): 423.
BRCA1 and BRCA2 analysis in 523 Austrian HPOC and HBC families.
Kroiss, R., Wagner, T., Muhr, D., Fleischmann, E., Korn, V., Helbich, T., Zielinski, C., Kubista, E., Oefner, P. Am. J. Hum. Genet 69 (2001): 252.
BRCA1 and BRCA2 analysis of 268 HBOC and HBC families by DHPLC.
Wagner, T., Moeslinger, R., Muhr, D., Richards, D., Schreiber, M., Fleischmann, E. Am. J. Hum. Genet 67.2 (2000): 87.
Comprehensive mutational analysis of the ATM gene by denaturing HPLC.
Thorstenson, Y.R., Oefner, P.J., Goss, V., Davis, R.W., Gatti, R.A., Chu, G. Am. J. Hum. Genet 67.2 (2000): 100.
Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer.
Shiri-Sverdlov, R., Oefner, P., Gershoni-Baruch, R., Green, L., Hofstra, R.M.W., Wagner, T., Friedman, E. Am. J. Hum. Genet 67.2 (2000): 88.
Attitude towards prophylactic surgery and effects of genetic counselling in families with BRCA mutations. denaturing HPLC.
Moeslinger, R., Wagner, T., Langbauer, G., Austrian HBOC Group, Fleischmann, E., Autherith, A., Friedmann, A., Helbich, T., Oefner, P. Am. J. Hum. Genet 67.2 (2000): 202.
BRCA1 Analysis by DHPLC in 272 Austrian Breast Cancer only and Breast and Ovarian Cancer Families.
Wagner, T., Moeslinger, R., Fleischmann, E., Muhr, D., Hareter, M., Kofler, P., Austrian HBOC Group, Helbich, T., Zielinski, C., Oefner, P. Am. J. Hum. Genet 65 (1999): A328.
Denaturing High Performance Liquid Chromatography (DHPLC) Detects BRCA1 and BRCA2 Mutations with High Sensitivity.
Oefner, P., Stoppa-Lyonnet, D., Fleischmann, E., Muhr, D., Pages, S., Sandberg, T., Caux, V., Moeslinger, R., Langbauer, G., Borg, A., Wagner, T., Am. J. Hum. Genet 65 (1999): A416.
Attitude towards prophylactic surgery and effects of genetic counselling in families with BRCA mutations.
Moeslinger, R., Wagner, T., Langbauer, G., Austrian HBOC Group, Autherith, A., Friedmann, A., Zielinski, C., Seifert, M., Oefner, P. Am. J. Hum. Genet 65 (1999): A386.
Molecular reconstruction of the genealogy of the isolated population of the Costa Rican Central Valley.
Freimer, N.B., R. Ophoff, R., Meshi1, D., Poon, W., Oefner, P., Service, S. Am. J. Hum. Genet 65 (1999): A203.
Polynesian origins: new insights from the Y-chromosome.
Deka, R., Su, B., Underhill, P., Saha, N., McGarvey, S.T., Chou, J., Oefner, P., Shriver, M.D., Chakraborty, R., Martinson, J. Jin, L. Am. J. Hum. Genet 65 (1999): A83.
High frequency of simple sequence variation in BRCA2: Analysis of 70 breast cancer families and 95 control individuals of world wide populations.
Wagner, T., Hirtenlehner, K., Shen, P., Moeslinger, R., Muhr, D., Fleischmann, E., Concin, H., Doeller, W., Haid, A., Lang, A.H., Mayer, P., Petru, E., Ropp, E., Kubista, E., Scheiner, O., Underhill, P., Stierer, M., Zielinski, C., Oefner, P. Am. J. Hum. Genet 63 (1998): A90.
Panorama of Y chromosome SNP haplotype diversity in Pakistan.
Underhill, P.A., Mehdi, S.Q., Cavalli-Sforza, L.L., Davis, R.W., Oefner, P.J. Am. J. Hum. Genet 63 (1998): A223.
Blind Analysis of denaturing high-performance liquid chromatography as a tool for mutation detection.
O'Donovan, M.C., Oefner, P.J., Roberts, S.C., Austin, J., Hoogendoorn, B., Guy, C., Speight, G., Upadhyaya, M., Sommer, S.S., McGuffin, P. Am. J. Hum. Genet 63 (1998): A238.
Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography.
Hoogendoorn, B., Owen, M.J., Oefner, P.J., Williams, N., Austin, J., O’Donovan, M.C. Am. J. Hum. Genet 63 (1998): A232.
Founding BRCA1 and 2 mutations in Austrian HBOC families and individuals of the 5 continents.
Wagner, T., Muhr, D., Hirtenlehner, K., Möslinger, R., Underhill, P., Scheiner, O., Kubista, E., Oefner, P.J. Am. J. Hum. Genet 61 (1997): A86.
An African origin of human Y chromosomes.
Underhill, P.A., Jin, L., Lin, A., Chan, C., Shen, P., Kauffman, E., Choi, L., Hurlbut, A., Cavalli-Sforza, L.L., Mehdi, S.Q., Jenkins, T., Seielstad, M.T., Wells, R.S., Ibrahim, M., Vollrath, D., Hyman, R., Davis, R., Oefner, P.J. Am. J. Hum. Genet 61 (1997): A18.
Hepatitis G virus infection in hemodialysis patients and the effects of interferon.
Umlauft, F., Wong, D.T., Underhill, P.A., Oefner, P.J., Jin, L., Urbanek, M., Grünewald, K., Greenberg, H.B. Gastroenterology 112 (1997): A1406.
Denaturing HPLC identified novel FBN1 mutations, polymorphisms and sequence variants in Marfan syndrome patients.
Liu, W., Oefner, P., Qian, C., Odom, R., Francke, U. Am. J. Hum. Genet 61 (1997): A223.
Autosomal DNA haplotypes distinguish ancient human migrations.
Jin, L., Underhill, P.A., Doctor, V., Cavalli-Sforza, L.L., Davis, R., Oefner, P.J. Am. J. Hum. Genet 61 (1997): A201
Amassing a wealth of Y chromosome polymorphisms for evolutionary studies.
Underhill, P.A., Jin, L., Cavalli-Sforza, L.L., Davis, R., Oefner, P.J. Am. J. Hum. Genet 59 (1996): A30. [Abstract].
The terminal 3' non-coding region of hepatitis C virus: A new target for PCR detection.
Umlauft, F., Wong, D.T., Oefner, P.J., Cheung, R.C., Wright, T.L., Kolykhalov, A.A., Grünewald, K., Greenberg, H.B. Hepatology 24 (1996): 251A.
Rapid quantification of HCV RNA by competitive RT-PCR and ion-pair reversed-phase HPLC.
Umlauft, F., Oefner, P.J., Wong, D.T., Grill, E., Greenberg, H.B. Gastroenterology 110 (1996): A1349.
High-Throughput Differential Genome Analysis by Denaturing HPLC.
Oefner, P.J., Underhill, P.A., Grill, E.A., Cho, R.J., Jin, L., Cavalli-Sforza, L.L., Davis, R.W. Microbial & Comparative Genomics 1 (1996): 245.
Sequencing the Chlamydia trachomatis Genome.
Kalman, S.S., Araujo, R., Chung, E., Dietrich, F., Komp, C., Otto, G., Lew, H., Lin, D., Marathe, R., Mirthipati, S., Namath, A., Oefner, P., Davis, R.W., Stephens, R. Microbial & Comparative Genomics 1 (1996): 236.
Kidney and nephron calcineurin (CaN) expression in spontaneously hypertensive rats (SHR) by competitive RT-PCR and IP-RP-HPLC.
Hinojos, C.A., Hayward-Lester, A., Sabatini, S., Oefner, P.J., Doris, P.A. Mol. Biol. Cell 7 (1996).
Analysis of multiple sodium pump genes expressed in nephrons from spontaneously hypertensive rats (SHR) by competitive RT-PCR and IP-RP-HPLC.
Hayward-Lester, A., Lonis, B., Sabatini, S., Lee, A.M., Oefner, P.J., Doris, P.A. Mol. Biol. Cell 7 (1996): 470A.
Mapping and Sequencing of the Arabidopsis Genome.
Dewar, K., Dunn, P.J., Li, Y.-P., Kim, C.J., Ecker, J.R., Federspiel, N.A., Dietrich, F., Marziali, A., Oefner, P., Norgren, R., Davis, R.W., Vysotskaia, V., Yu, Q., Theologis, A. Microbial & Comparative Genomics 1 (1996): 204.
Identification and characterization of pre-Columbian human Y chromo-some specific allele.
Zemans, R., Jin, L., Underhill, P.J., Oefner, P.J., Cavalli-Sforza, L.L. Am. J. Hum. Genet 57 (1995): A174.
Y-chromosomal variation and recent conquests in deciphering human origins
Underhill, P.A., Jin, L., Oefner, P.J., Cavalli-Sforza, L.L. Am. J. Hum. Genet 57 (1995): A43.
Comparative DNA sequencing by denaturing high-performance liquid chromatography (DHPLC).
Oefner, P.J., Underhill, P.A. Am. J. Hum. Genet 57 (1995): A266.
Accurate and absolute quantification of gene expression by single tube RT-PCR and HPLC.
Hayward-Lester, A., Oefner, P.J., Doris, P. Mol. Biol. Cell 6 (1995): 444A.
Systematic search for polymorphisms in the human genome using denaturing high-performance liquid chromatography (DHPLC).
Jin, L., Underhill, P.A., Oefner, P.J., Cavalli-Sforza, L.L. Am. J. Hum. Genet 57 (1995): A26.

Books & Book Chapters

High-Throughput Creation of a Whole-Genome Collection of Yeast Knockout Strains.
Chu, A.M., Davis, R.W. In: Osterman, A., Gerdes, S.(Eds.), Microbial Gene Essentiality: Protocols and Bioinformatics, Methods in Molecular Biology, Volume 416, Humana Press, Inc., Totowa, New Jersey, (2008): 205-220. [PubMed], [Publisher]
Denaturing high-performance liquid chromatography.
Premstaller, A., Oefner, P.J. (2003). In: P.-Y. Kwok (Ed), Single Nucleotide Polymorphisms: Methods and Protocols, Methods in Molecular Biology, Volume 212, Humana Press Inc., Totowa, New Jersey, (2003): 15-35.
Pyrosequencing: A tool for DNA sequence analysis.
Elahi, E., Ronaghi, M., (2002). Humana Press.
Pyrosequencing for SNP genotyping.
Ronaghi, M. in Methods in molecular Biology Volume 212 Single Nucleotide Polymorphisms: Methods and Protocols. Humana press. (2002): 189-196.
Pyrosequencing a bioluminometric method of DNA sequencing.
Ronaghi, M., Pourmand, N., Stolc. V. in Advances in luminescence biotechnology. CRS press. (2001): 247-253.
Parallel analysis with Biological Chips.
Schena, M., Davis, R.W. in PCR Applications. Academic Press. (1999): 445-456.
Genes, Genomes and Chips.
Schena, M., Davis, R.W. in DNA Microarrays: A Practical Approach; Schena, M., Editor. Oxford University Press: Oxford, United Kingdom. (1999): 1-16.
Kinetics of competitive RT PCR.
Hayward, A.L., Oefner, P.J., Kainer, D., Hinojos, C.A., Doris, P.A. in PCR Methods Manual, Academic Press, San Diego, M. Innis, D. Gelfand, J. Sninsky, Editor. Academic Press: San Diego. (1999): 231-261.
DNA mutation detection using denaturing high-performance liquid chromatography (DHPLC).
Oefner, P.J., Underhill, P.A. in Current Protocols in Human Genetics. Wiley & Sons: New York. (1989): 7.10.11-17.10.12.
Y Chromosome Variation and Human Evolution.
Underhill, P.A., Jin, L., Oefner, P.J., Cavalli-Sforza, L.L. in Advances in Research on DNA Polymorphisms, Proceedings of ISFH Hakone Symposium on DNA Polymorphisms 1996, Katsumata, Y., et al., Editor: Toyoshoten, Tokyo, Japan. (1997): 24-32.
Rapid quantification of gene expression by competitive RT-PCR and ion-pair reversed-phase HPLC.
Hayward-Lester, A., Oefner, P.J., Doris, P.A. in The PCR Technique: Quantitative PCR, Larrick, J.W., Editor. Eaton Publishing: Natick, MA. (1997): 125-139.
Quantification of specific nucleic acids, regulated RNA processing and genomic polymorphisms using reversed-phase HPLC.
Hayward-Lester, A., Chilton, B.S., Underhill, P.A., Oefner, P.J., Doris, P.A. in Gene Quantification, Ferré, F., Editor. Birkhäuser Verlag. (1997): 44-77.
Yeast Artificial Chromosome (YAC) construction and applications.
Loehrlein, C., Davis, Ronald W. in Encyclopedia of Molecular Biology and Molecular Medicine, Meyers, Robert A., Editor. VCH Publishers: Weinheim. (1996): 291-302.
Analysis of carbohydrates and oligo-saccharides.
Chiesa, C., O`Neill, R., Horváth, Cs., Oefner, P.J. in: Capillary Electrophoresis: An Analytical Tool in Biotechnology. Righetti, P.G., Editor. CRC Press, Boca Raton, (1995): 277-430.
Capillary electrophoresis of carbohydrates.
Oefner, P., Bonn, G., Chiesa, C. in: Encyclopedia of Analytical Science. Academic Press, London. (1995): 1135-1152.

Proceedings

High-throughput Pyrosequencing for analysis Single Nucleotide Polymorphisms Genomics, Proteomics and Related Technologies for Biomedical Applications.
Ronaghi, M. in Proceedings of SPIE's International Symposium on Biomedical Optics. (2001): 4626-4660.
A novel bioluminometric approach for DNA sequencing.
Nyrén, P., Ronaghi, M., Karamohammed, S., Nordström, T., Nourizad, K. in Proceedings of 10th International Symposium on Bioluminescence & Chemiluminescence. (1998).
Automation of a novel DNA sequencing method.
Nordström, T., Ronaghi, M., Nyrén, P. in Proceedings of 10th International Symposium on Bioluminescence & Chemiluminescence. (1998).
A method for real-time detection of the effect of different inhibitors on reverse transciptase activity.
Karamohammed, S., Ronaghi, M., Nyrén, P. in Proceedings of 9th International Symposium on Bioluminescence & Chemiluminescence. (1996).
Real-time sequence-based DNA analyses using bioluminscence.
Nyrén, P., Karamohammed, S., Ronaghi, M. in Proceedings of 9th International Symposium on Bioluminescence & Chemiluminescence. (1996).

Letters

Functional genomics of genes with small open reading frames (sORFs) in S. cerevisiae.
Kastenmayer, JP, Ni, L Chu, A, Kitchen, LE, Au, W-C, Yang, H, Carter, CD, Wheeler, D, Davis, RW, Boeke, JD, Snyder, MA and Basrai MA Genome Res 16.3 (2006):365-373.
A network-based analysis of systemic inflammation in humans.
Calvano, S.E., Xiao, W., Richards, D.R., Felciano, R.M., Baker, H.V., Cho, R.J., Chen, R.O., Brownstein, B.H., Cobb, J.P., Tschoeke, S.K., Miller-Graziano, C., Moldawer, L.L., Mindrinos, M.N., Davis, R.W., Tompkins, R.G. & Lowry, S.F. and Inflamm and Host Response to Injury Large Scale Collab. Res. Program. Nature 437 (2005): 1032-7. [PubMed], [Publisher]
Re: genetic analysis of the beta-tubulin gene, TUBB, in non-small-cell lung cancer.
Sale, S., Oefner, P.J., Sikic, B.I. J Natl Cancer Inst 94.10 (2002): 776-777; discussion 777.
Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Horvath, R., Scharfe, C., Hoeltzenbein, M., Do, B.H., Schroder, C., Warzok, R., Vogelgesang, S., Lochmuller, Genet (2002): 812-6.
Sequence data: posted vs. published.
Hyman, R.W., Science 291.5505 (2001): 827.
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography.
Underhill, P.A., Jin, L., Lin, A.A., Mehdi, S.Q., Jenkins, T., Vollrath, D., Davis, R.W., Cavalli-Sforza, L.L., Oefner, P.J. Genome Res 7.10 (1997): 996-1005. [Publisher Full Text].

Submissions to GenBank

Saccharomyces cerevisiae strain YJM789, full genome. Genbank: accession number AAFW00000000 (for nuclear genome); EU004203 (for mitochondrial genome). Wei, W., McCusker, J.H., Hyman, R.H., Jones, T., Ning, Y., Cao, Z., Gu, Z., Bruno, D., Miranda, M., Nguyen, M., Wilhelmy, J., Komp, C., Tamse, R., Wang, X., Jia, P., Luedi, P., Oefner P.J., David, L., Dietrich, F.S., Li, Y., Davis, R.W., Steinmetz, L.M. (2005).
Escherichia coli chromosome minutes 9-12. Genbank: accession number U82598
Chung, E., Allen, E., Araujo,R., Aparicio, A., Davis, K., Duncan, M., Federspiel, N., Hyman, R.W., Kalman, S., Komp, C., Kurdi, O., Lew, H., Lin, D., Namath, A., Oefner, P., Schramm, S., Davis, R.W., (1997).
Human chromosome 1 BAC 89N6 genomic sequence.GenBank: accession number AC003118.
Chung, E., Babb, V., Hyman, R.W., Kurdi, O., Rexan, M., Vollrath, D., Davis, Ronald W., (1997).
Human chromosome 1 BAC 308G1 genomic sequence. GenBank: accession number AC003117.
Fan, J., Babb, V., Hyman, R.W., Kalman, S., Kurdi, O., Marathe, R., Rexan, M., Vollrath, D., Davis, R.W. (1997).
Human chromosome Y cosmid 16E4 genomic sequence. GenBank: accession number AC003094.
Hyman, R.W., Chung, E., Kurdi, O., Roberts, D., Schramm, S., Vollrath, D., Davis, R.W., (1997).
Human chromosome Y cosmid 54E8 genomic sequence. GenBank: accession number AC003095.
Hyman, R.W., Vollrath, D., Davis, R.W., (1997).
Human chromosome 1 BAC 13512 genomic sequence. GenBank: accession number AC003115.
Hyman, R.W., Babb, V., Chung, E., Kurdi, O., Rexan, M., Vollrath, D., Davis, R.W., (1997).
Human chromosome Y cosmid 56B5 genomic sequence. GenBank: accession number AC003097.
Lin, D., Chung, E., Hyman, R.W., Schramm, S., Vollrath, D., Davis, R.W., (1997).
Escherichia coli chromosome minutes 9-11. Genbank: accession number U82598. Chung, E., Allen, E., Araujo,R., Aparicio, A., Davis, K., Duncan, M., Federspiel, N., Hyman, R. W., Kalman, S., Komp, C., Kurdi, O., Lew, H., Lin, D., Namath, A., Oefner, P., Schramm, S. and Davis, Ronald W. (1997).
Human chromosome Y cosmid 30H9 genomic sequence. GenBank: accession number AC003031.
Shen, P., Chung, E., Hyman, R.W., Roberts, D., Schramm, S., Vollrath, D., Davis, R.W., (1997).
Human chromosome Y cosmid 7A1 genomic sequence. GenBank: accession number AC003032.
Thorstenson, Y., Au, M., Chung, E., Hyman, R., Schramm, S., Vollrath, D., Davis, R.W., (1997).
Plasmodium falciparum 3D7 chromosome 12, complete sequence. GenBank: accession number AE014188.
Hyman, R.W., Fung, E., Conway, A., Kurdi, O., Mao, J., Miranda, M., Nakao, B., Rowley, D., Tamaki, T., Wang, F. and Davis, R.W.
Saccharomyces cerevisiae chromosome XVI left arm from MMN to PH085. Genbank: accession number U44030.
Dietrich, F.S., Allen, E., Araujo, R., Aparicio, A., Carpenter, J., Cherry, J.M., Chung, E., E., Davis, K., Duncan, M., Hunicke-Smith, S., Hyman, R.W., Kalman, S., Komp, C., Kurdi, O., Lashkari, D., Lew, H., Lin, A., Lin, D., Marathe, R., Mirtipati, S., Namath, A., Oefner, P., Petel, F., Roberts, D., Schramm, S., Schroeder, M., Botstein, D., Davis, Ronald W., (1996).
Escherichia coli chromosome minutes 6-8. Genbank: accession number U73857
Duncan, M., Allen, E., Araujo, R., Aparicio, A., Chung, E., Davis, K., Federspiel, N., Hyman, R.W., Kalman, S., Komp, C., Kurdi, O., Lew, H., Lin, D., Namath, A., Oefner, P., Roberts, D., Schramm, S., Davis, Ronald W., (1996).
Escherichia coli chromosome minutes 4-6. Genbank: accession number U70214
Schramm, S., Duncan, M., Allen, E., Araujo, R., Aparicio, A., Chung, E., Davis, K., Federspiel, N., Hyman, R.W., Kalman, S., Komp, C., Kurdi, O., Lashkari, D., Lew, H., Lin, D., Namath, A., Oefner, P., Roberts, D., Davis, Ronald W., (1996).

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