Improved IBD detection using incomplete haplotype information by Pollak Martin R, Leibon Gregory, Genovese Giulio, Rockmore Daniel N

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SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity by Carrasquillo Robert, Tian Dequan, Krishna Sneha, Pollak Martin R, Greka Anna, Schlöndorff Johannes

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Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data by Smith Richard JH, Pollak Martin R, Meyer Nicole, Cheng Junsheng, Hao Ke, Leykin Igor, Wong Wing, Rosenow Carsten, Li Cheng

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<it>NPHS2 </it>variation in focal and segmental glomerulosclerosis by Savige Judy, Jerums George, Kaplan Bernard S, Al-Waheeb Salah, Katz Avi, Falk Ronald J, Appel Gerald B, Uscinski Andrea, Polu Krishna, Needham Alexander, Tonna Stephen J, Harmon Jennifer, Zhang Kang, Curhan Gary C, Pollak Martin R

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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing by Kirby, Andrew, Gnirke, Andreas, Jaffe, David B., Baresova, Veronika, Pochet, Nathalie, Blumenstiel, Brendan, Ye, Chun, Aird, Daniel, Stevens, Christine, Robinson, James T., Cabili, Moran N., Gat-Viks, Irit, Kelliher, Edward, Daza, Riza, DeFelice, Matthew, Hulkova, Helena, Sovova, Jana, Vylet'al, Petr, Antignac, Corinne, Guttman, Mitchell, Handsaker, Robert E., Perrin, Danielle, Steelman, Scott, Sigurdsson, Snaevar, Scheinman, Steven J., Sougnez, Carrie, Cibulskis, Kristian, Parkin, Melissa, Green, Todd, Rossin, Elizabeth, Zody, Michael C., Xavier, Ramnik J., Pollak, Martin R., Alper, Seth L., Lindblad-Toh, Kerstin, Gabriel, Stacey B., Hart, P. Suzanne, Regev, Aviv, Nusbaum, Chad, Kmoch, Stanislav, Bleyer, Anthony J., Daly, Mark J., Lander, Eric Steven

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