Targeted methylation sequencing of plasma cell-free DNA for cancer detection and classification von Liu, L., Toung, J.M., Jassowicz, A.F., Vijayaraghavan, R., Kang, H., Zhang, R., Kruglyak, K.M., Huang, H.J., Hinoue, T., Shen, H., Salathia, N.S., Hong, D.S., Naing, A., Subbiah, V., Piha-Paul, S.A., Bibikova, M., Granger, G., Barnes, B., Shen, R., Gutekunst, K., Fu, S., Tsimberidou, A.M., Lu, C., Eng, C., Moulder, S.L., Kopetz, E.S., Amaria, R.N., Meric-Bernstam, F., Laird, P.W., Fan, J.-B., Janku, F.

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Clinical Characteristics of Ovarian Cancer Classified by BRCA1, BRCA2 and RAD51C Status von Cunningham, J. M., Cicek, M. S., Larson, N. B., Davila, J., Wang, C., Larson, M. C., Song, H., Dicks, E. M., Harrington, P., Wick, M., Winterhoff, B. J., Hamidi, H., Konecny, G. E., Chien, J., Bibikova, M., Fan, J.-B., Kalli, K. R., Lindor, N. M., Fridley, B. L., Pharoah, P. P. D., Goode, E. L.

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Population genetic study of the brain-derived neurotrophic factor ( ) gene von Petryshen, T L, Sabeti, P C, Aldinger, K A, Fry, B, Fan, J B, Schaffner, S F, Waggoner, S G, Tahl, A R, Sklar, P

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Meta-analysis reveals association between serotonin transporter gene STin2 VNTR polymorphism and schizophrenia von FAN, J. B, SKLAR, P

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Identification of disease-associated DNA methylation in intestinal tissues from patients with inflammatory bowel disease von Lin, Z, Hegarty, JP, Cappel, JA, Yu, W, Chen, X, Faber, P, Wang, Y, Kelly, AA, Poritz, LS, Peterson, BZ, Schreiber, S, Fan, J-B, Koltun, WA

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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis von Chakravarti, Aravinda, Halushka, Marc K, Fan, Jian-Bing, Bentley, Kimberly, Hsie, Linda, Shen, Naiping, Weder, Alan, Cooper, Richard, Lipshutz, Robert

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Family-based association study of DTNBP1 in 6p22.3 and schizophrenia von Tang, J X, Zhou, J, Fan, J B, Li, X W, Shi, Y Y, Gu, N F, Feng, G Y, Xing, Y L, Shi, J G, He, L

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Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays von Collins, Francis S, Hacia, Joseph G, Fan, Jian-Bing, Ryder, Oliver, Jin, Li, Edgemon, Keith, Ghandour, Ghassan, Mayer, R. Aeryn, Sun, Bryan, Hsie, Linda, Robbins, Christiane M, Brody, Lawrence C, Wang, David, Lander, Eric S, Lipshutz, Robert, Fodor, Stephen P.A

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Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome von Wang, David G., Fan, Jian-Bing, Siao, Chia-Jen, Berno, Anthony, Young, Peter, Sapolsky, Ron, Ghandour, Ghassan, Perkins, Nancy, Winchester, Ellen, Spencer, Jessica, Kruglyak, Leonid, Stein, Lincoln, Hsie, Linda, Topaloglou, Thodoros, Hubbell, Earl, Robinson, Elizabeth, Mittmann, Michael, Morris, Macdonald S., Shen, Naiping, Kilburn, Dan, Rioux, John, Nusbaum, Chad, Rozen, Steve, Hudson, Thomas J., Lipshutz, Robert, Chee, Mark, Lander, Eric S.

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Characterization of the single-cell transcriptional landscape by highly multiplex RNA-seq von Islam, Saiful, Kjällquist, Una, Moliner, Annalena, Zajac, Pawel, Fan, Jian-Bing, Lönnerberg, Peter, Linnarsson, Sten

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Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse von Laviolette, Jean-Philippe, Gingeras, Thomas, Wang, David G, Hirschhorn, Joel N, Daly, Mark J, Warrington, Janet, Lindblad-Toh, Kerstin, Shah, Nila, Hudson, Thomas J, Thomas, Daryl, Reich, David E, Patil, Nila, Sklar, Pamela, Winchester, Ellen, Robinson, Elizabeth, Lander, Eric S, Ardlie, Kristin, Fan, Jian-Bing

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Highly multiplexed and strand-specific single-cell RNA 5′ end sequencing von Islam, Saiful, Kjällquist, Una, Moliner, Annalena, Zajac, Pawel, Fan, Jian-Bing, Lönnerberg, Peter, Linnarsson, Sten

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Meta-analysis reveals association between serotonin transporter gene STin2 VNTR polymorphism and schizophrenia von Fan, J B, Sklar, P

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Gene mutations in retinitis pigmentosa and their clinical implications von Wang, D.Y., Chan, W.M., Tam, P.O.S., Baum, L., Lam, D.S.C., Chong, K.K.L., Fan, B.J., Pang, C.P.

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High-throughput SNP genotyping on universal bead arrays von Shen, R, Fan, J B, Campbell, D, Chang, W, Chen, J, Doucet, D, Yeakley, J, Bibikova, M, Wickham Garcia, E, McBride, C, Steemers, F, Garcia, F, Kermani, B G, Gunderson, K, Oliphant, A

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A family-based and case-control association study of the NOTCH4 gene and schizophrenia von FAN, J. B, TANG, J. X, SUN, W. W, ZHENG, Y. L, LIU, W. Q, BREEN, G, ST CLAIR, D, HE, L, GU, N. F, FENG, G. Y, ZOU, F. G, XING, Y. L, SHI, J. G, ZHAO, S. M, ZHU, S. M, JI, L. P

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Enhanced toxicity of Cry2Ab with cantharidin and its analogues on Mythimna separata von Fan, J. B., Velde, S., Sun, W. B., Yu, H., Zhang, Y. L., Wang, D.

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A Gene Map of the Human Genome von Schuler, G. D., Boguski, M. S., Stewart, E. A., Stein, L. D., Gyapay, G., Rice, K., White, R. E., Rodriguez-Tomé, P., Aggarwal, A., Bajorek, E., Bentolila, S., Birren, B. B., Butler, A., Chiannilkulchai, N., Chu, A., Clee, C., Cowles, S., Day, P. J. R., Dibling, T., Drouot, N., Dunham, I., Duprat, S., East, C., Edwards, C., J.-B. Fan, Fang, N., Fizames, C., Garrett, C., Green, L., Hadley, D., Harris, M., Brady, S., Hicks, A., Holloway, E., Hui, L., Hussain, S., C. Louis-Dit-Sully, Ma, J., MacGilvery, A., Mader, C., Maratukulam, A., Matise, T. C., McKusick, K. B., Mungall, A., Muselet, D., Nusbaum, H. C., Page, D. C., Peck, A., Perkins, S., Piercy, M., Qin, F., Quackenbush, J., Ranby, S., Reif, T., Rozen, S., Sanders, C., She, X., Silva, J., Slonim, D. K., Soderlund, C., W.-L. Sun, Tabar, P., Thangarajah, T., Vega-Czarny, N., Vollrath, D., Voyticky, S., Wilmer, T., Wu, X., Adams, M. D., Aufiray, C., Walter, N. A. R., Brandon, R., Dehejia, A., Goodfellow, P. N., Houlgatte, R., Hudson, J. R., Ide, S. E., Iorio, K. R., Lee, W. Y., Seki, N., Nagase, T., Ishikawa, K., Nomura, N., Phillips, C., Polymeropoulos, M. H., Sandusky, M., Schmitt, K., Berry, R., Swanson, K., Torres, R., Venter, J. C., Sikela, J. M., Weissenbach, J., Myers, R. M., Cox, D. R., James, M. R., Bentley, D., Deloukas, P., Lander, E. S., Hudson, T. J.

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Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness von Desronvil, T, Logan-Wyatt, D, Abdrabou, W, Triana, M, Jones, R, Taheri, S, Del Bono, E, Pasquale, L R, Olivier, M, Haines, J L, Fan, B J, Wiggs, J L

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Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays von Fan, J B, Chen, X, Halushka, M K, Berno, A, Huang, X, Ryder, T, Lipshutz, R J, Lockhart, D J, Chakravarti, A

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