SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap von Johnson, Andrew D., Handsaker, Robert E., Pulit, Sara L., Nizzari, Marcia M., O'Donnell, Christopher J., de Bakker, Paul I. W.

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs von Korn, Joshua M, Kuruvilla, Finny G, McCarroll, Steven A, Wysoker, Alec, Nemesh, James, Cawley, Simon, Hubbell, Earl, Veitch, Jim, Collins, Patrick J, Darvishi, Katayoon, Lee, Charles, Nizzari, Marcia M, Gabriel, Stacey B, Purcell, Shaun, Daly, Mark J, Altshuler, David

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Next-generation carrier screening von Umbarger, Mark A., Kennedy, Caleb J., Saunders, Patrick, Breton, Benjamin, Chennagiri, Niru, Emhoff, John, Greger, Valerie, Hallam, Stephanie, Maganzini, David, Micale, Cynthia, Nizzari, Marcia M., Towne, Charles F., Church, George M., Porreca, Gregory J.

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Orthogonal NGS for High Throughput Clinical Diagnostics von Chennagiri, Niru, White, Eric J., Frieden, Alexander, Lopez, Edgardo, Lieber, Daniel S., Nikiforov, Anastasia, Ross, Tristen, Batorsky, Rebecca, Hansen, Sherry, Lip, Va, Luquette, Lovelace J., Mauceli, Evan, Margulies, David, Milos, Patrice M., Napolitano, Nichole, Nizzari, Marcia M., Yu, Timothy, Thompson, John F.

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Candidate Gene Association Resource (CARe): Design, Methods, and Proof of Concept von Musunuru, Kiran, Lettre, Guillaume, Young, Taylor, Farlow, Deborah N, Pirruccello, James P, Ejebe, Kenechi G, Keating, Brendan J, Yang, Qiong, Chen, Ming-Huei, Lapchyk, Nina, Crenshaw, Andrew, Ziaugra, Liuda, Rachupka, Anthony, Benjamin, Emelia J, Cupples, L. Adrienne, Fornage, Myriam, Fox, Ervin R, Heckbert, Susan R, Hirschhorn, Joel N, Newton-Cheh, Christopher, Nizzari, Marcia M, Paltoo, Dina N, Papanicolaou, George J, Patel, Sanjay R, Psaty, Bruce M, Rader, Daniel J, Redline, Susan, Rich, Stephen S, Rotter, Jerome I, Taylor, Herman A, Tracy, Russell P, Vasan, Ramachandran S, Wilson, James G, Kathiresan, Sekar, Fabsitz, Richard R, Boerwinkle, Eric, Gabriel, Stacey B

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Orthogonal NGS for High Throughput Clinical Diagnostics von Chennagiri, Niru, White, Eric J, Frieden, Alexander, Lopez, Edgardo, Lieber, Daniel S, Nikiforov, Anastasia, Ross, Tristen, Batorsky, Rebecca, Hansen, Sherry, Lip, Va, Luquette, Lovelace J, Mauceli, Evan, Margulies, David, Milos, Patrice M, Napolitano, Nichole, Nizzari, Marcia M, Yu, Timothy, Thompson, John F

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Next-generation carrier screening von Umbarger, Mark A, Kennedy, Caleb J, Saunders, Patrick, Breton, Benjamin, Chennagiri, Niru, Emhoff, John, Greger, Valerie, Hallam, Stephanie, Maganzini, David, Micale, Cynthia, Nizzari, Marcia M, Towne, Charles F, Church, George M, Porreca, Gregory J

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Variant database von TEFFT DAVID L, HAURIE XAVIER S, NIZZARI MARCIA M, BRETON BENJAMIN H

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VARIANT DATABASE von NIZZARI, MARCIA, M, HAURIE, XAVIER, S, BRETON, BENJAMIN, H, TEFFT, DAVID, L

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VARIANT DATABASE von NIZZARI, MARCIA, M, HAURIE, XAVIER, S, BRETON, BENJAMIN, H, TEFFT, DAVID, L

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VARIANT DATABASE von TEFFT DAVID L, HAURIE XAVIER S, NIZZARI MARCIA M, BRETON BENJAMIN H

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Variant database von TEFFT DAVID L, HAURIE XAVIER S, NIZZARI MARCIA M, BRETON BENJAMIN H

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VARIANT DATABASE von NIZZARI, MARCIA, M, HAURIE, XAVIER, S, BRETON, BENJAMIN, H, TEFFT, DAVID, L

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VARIANT DATABASE von HAURIE, XAVIER S, TEFFT, DAVID L, BRETON, BENJAMIN H, NIZZARI, MARCIA M

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VARIANT DATABASE von TEFFT DAVID L, HAURIE XAVIER S, NIZZARI MARCIA M, BRETON BENJAMIN H

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Customer interaction tracking von MCNEILL, KEITH D, NIZZARI, MARCIA M

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Integrated detection and population-genetic analysis of SNPs and copy number variation von McCarroll, Steven A, Kuruvilla, Finny G, Korn, Joshua M, Cawley, Simon, Nemesh, James, Wysoker, Alec, Shapero, Michael H, de Bakker, Paul I W, Maller, Julian B, Kirby, Andrew, Elliott, Amanda L, Parkin, Melissa, Hubbell, Earl, Webster, Teresa, Mei, Rui, Veitch, James, Collins, Patrick J, Handsaker, Robert, Lincoln, Steve, Nizzari, Marcia, Blume, John, Jones, Keith W, Rava, Rich, Daly, Mark J, Gabriel, Stacey B, Altshuler, David

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