Sequence-based genotyping for marker discovery and co-dominant scoring in germplasm and populations von Truong, Hoa T, Ramos, A Marcos, Yalcin, Feyruz, de Ruiter, Marjo, van der Poel, Hein J A, Huvenaars, Koen H J, Hogers, René C J, van Enckevort, Leonora J G, Janssen, Antoine, van Orsouw, Nathalie J, van Eijk, Michiel J T

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Complexity reduction of polymorphic sequences (CRoPS): a novel approach for large-scale polymorphism discovery in complex genomes von van Orsouw, Nathalie J, Hogers, René C J, Janssen, Antoine, Yalcin, Feyruz, Snoeijers, Sandor, Verstege, Esther, Schneiders, Harrie, van der Poel, Hein, van Oeveren, Jan, Verstegen, Harold, van Eijk, Michiel J T

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High-throughput detection of induced mutations and natural variation using KeyPoint technology von Rigola, Diana, van Oeveren, Jan, Janssen, Antoine, Bonné, Anita, Schneiders, Harrie, van der Poel, Hein J A, van Orsouw, Nathalie J, Hogers, René C J, de Both, Michiel T J, van Eijk, Michiel J T

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Sequence‐based SNP genotyping in durum wheat von Poecke, Remco M.P., Maccaferri, Marco, Tang, Jifeng, Truong, Hoa T., Janssen, Antoine, Orsouw, Nathalie J., Salvi, Silvio, Sanguineti, Maria C., Tuberosa, Roberto, Vossen, Edwin A.G.

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SNPSelect: A scalable and flexible targeted sequence-based genotyping solution von Hogers, René C J, de Ruiter, Marjo, Huvenaars, Koen H J, van der Poel, Hein, Janssen, Antoine, van Eijk, Michiel J T, van Orsouw, Nathalie J

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Clonally Expanded mtDNA Point Mutations are Abundant in Individual Cells of Human Tissues von Nekhaeva, Ekaterina, Bodyak, Natalya D., Kraytsberg, Yevgenya, McGrath, Sean B., Van Orsouw, Nathalie J., Pluzhnikov, Anna, Wei, Jeanne Y., Vijg, Jan, Khrapko, Konstantin

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Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours von JEN JEN YEH, LUNETTA, K. L, VAN ORSOUW, N. J, MOORE, F. D, MUTTER, G. L, VIJG, J, DAHIA, P. L. M, ENG, C

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Generation of a 3D indexed Petunia insertion database for reverse genetics von Vandenbussche, Michiel, Janssen, Antoine, Zethof, Jan, Van Orsouw, Nathalie, Peters, Janny, Van Eijk, Michiel J.T., Rijpkema, Anneke S., Schneiders, Harrie, Santhanam, Parthasarathy, De Been, Mark, Van Tunen, Arjen, Gerats, Tom

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Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions von Khrapko, Konstantin, Bodyak, Natalya, Thilly, William G., van Orsouw, Nathalie J., Zhang, Xiaomin, Coller, Hilary A., Perls, Thomas T., Upton, Melissa, Vijg, Jan, Wei, Jeanne Y.

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Comparison of DNA- and RNA-Based Methods for Detection of Truncating BRCA1 Mutations von Andrulis, Irene L., Anton-Culver, Hoda, Beck, Jeanne, Bove, Betsy, Boyd, Jeff, Buys, Saundra, Godwin, Andrew K., Hopper, John L., Li, Frederick, Neuhausen, Susan L., Ozcelik, Hilmi, Peel, David, Santella, Regina M., Southey, Melissa C., van Orsouw, Nathalie J., Venter, Deon J., Vijg, Jan, Whittemore, Alice S.

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Comprehensive mutational scanning of the p53 coding region by two-dimensional gene scanning von RINES, R. D, VAN ORSOUW, N. J, SIGALAS, I, LI, F. P, ENG, C, VIJG, J

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Characterization of color mutants in lacZ plasmid-based transgenic mice, as detected by positive selection von Dollé, Martijn E.T., Martus, Hans-Jörg, Novak, Maja, van Orsouw, Nathalie J., Vijg, Jan

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Searching for genetic determinants of human aging and longevity: opportunities and challenges von Vijg, Jan, van Orsouw, Nathalie

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Complexity Reduction of Polymorphic Sequences von van Orsouw, Nathalie J, Hogers, René C. J, Janssen, Antoine, Yalcin, Feyruz, Snoeijers, Sandor, Verstege, Esther, Schneiders, Harrie, van der Poel, Hein, van Oeveren, Jan, Verstegen, Harold, van Eijk, Michiel J. T

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BRCA1 Gene Sequence Variation in Centenarians von Vijg, Jan, Perls, Thomas, Franceschi, Claudio, Van Orsouw, Nathalie J.

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Two-dimensional gene scanning: Exploring human genetic variability von Vijg, Jan, van Orsouw, Nathalie J.

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Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome von MARSH, D. J, ROTH, S, COTTRELL, S. E, DUNLOP, M. G, ECCLES, D, HODGSON, S. V, JÄRVINEN, H, KELLOKUMPU, I, MARKIE, D, NEALE, K, PHILLIPS, R, ROZEN, P, LUNETTA, K. L, SYNGAL, S, VIJG, J, TOMLINSON, I. P. M, AALTONEN, L. A, ENG, C, HEMMINKI, A, DAHIA, P. L. M, SISTONEN, P, ZHENG, Z, CARON, S, VAN ORSOUW, N. J, BODMER, W. F

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A highly accurate, low cost test for BRCA1 mutations von VAN ORSOUW, N. J, DHANDA, R. K, ELHAJI, Y, NAROD, S. A, LI, F. P, ENG, C, VIJG, J

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Spanish family study on hereditary breast and/or ovarian cancer: Analysis of the BRCA1 gene von de la Hoya, Miguel, Pérez‐Segura, Pedro, Van Orsouw, Nathalie, Díaz‐Rubio, Eduardo, Caldés, Trinidad

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Mutational Scanning of Mitochondrial DNA by Two-Dimensional Electrophoresis von van Orsouw, Nathalie J., Zhang, Xiaomin, Wei, Jeanne Y., Johns, Donald R., Vijg, Jan

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