Systems and methods for creating variable length clips from a media stream von Lucas, Brian, Rao, Padmanabha R, Curtis, Sean, Hirschhorn, Jason, Conway, Frank, Griffin, Brian J

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SYSTEMS AND METHODS FOR CREATING VARIABLE LENGTH CLIPS FROM A MEDIA STREAM von Lucas, Brian, Rao, Padmanabha R, Curtis, Sean, Hirschhorn, Jason, Conway, Frank, Griffin, Brian J

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Systems and methods for creating variable length clips from a media stream von Lucas, Brian, Rao, Padmanabha R, Curtis, Sean, Conway, Frank, Hirschhorn, Jason, Griffin, Brian J

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SYSTEMS AND METHODS FOR CREATING VARIABLE LENGTH CLIPS FROM A MEDIA STREAM von RAO, PADMANABHA R, HIRSCHHORN, JASON, CONWAY, FRANK, LUCAS, BRIAN, CURTIS, SEAN, GRIFFIN, BRIAN J

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SYSTEMS AND METHODS FOR CREATING VARIABLE LENGTH CLIPS FROM A MEDIA STREAM von CONWAY FRANK, GRIFFIN BRIAN J, HIRSCHHORN JASON, LUCAS BRIAN, CURTIS SEAN, RAO PADMANABHA R

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Systems and methods for creating variable length clips from a media stream von RAO, PADMANABHA R, HIRSCHHORN, JASON, CONWAY, FRANK, LUCAS, BRIAN, CURTIS, SEAN, GRIFFIN, BRIAN J

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Systems and methods for creating variable length clips from a media stream von RAO, PADMANABHA R, HIRSCHHORN, JASON, CONWAY, FRANK, LUCAS, BRIAN, CURTIS, SEAN, GRIFFIN, BRIAN J

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Hepatic NADH reductive stress underlies common variation in metabolic traits von Goodman, Russell P., Markhard, Andrew L., Shah, Hardik, Sharma, Rohit, Skinner, Owen S., Clish, Clary B., Deik, Amy, Patgiri, Anupam, Hsu, Yu-Han H., Masia, Ricard, Noh, Hye Lim, Suk, Sujin, Goldberger, Olga, Hirschhorn, Joel N., Yellen, Gary, Kim, Jason K., Mootha, Vamsi K.

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Interrogation of human hematopoiesis at single-cell and single-variant resolution von Ulirsch, Jacob C., Lareau, Caleb A., Bao, Erik L., Ludwig, Leif S., Guo, Michael H., Benner, Christian, Satpathy, Ansuman T., Kartha, Vinay K., Salem, Rany M., Hirschhorn, Joel N., Finucane, Hilary K., Aryee, Martin J., Buenrostro, Jason D., Sankaran, Vijay G.

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Distribution and medical impact of loss-of-function variants in the Finnish founder population von Lim, Elaine T, Würtz, Peter, Havulinna, Aki S, Palta, Priit, Tukiainen, Taru, Rehnström, Karola, Esko, Tõnu, Mägi, Reedik, Inouye, Michael, Lappalainen, Tuuli, Chan, Yingleong, Salem, Rany M, Lek, Monkol, Flannick, Jason, Sim, Xueling, Manning, Alisa, Ladenvall, Claes, Bumpstead, Suzannah, Hämäläinen, Eija, Aalto, Kristiina, Maksimow, Mikael, Salmi, Marko, Blankenberg, Stefan, Ardissino, Diego, Shah, Svati, Horne, Benjamin, McPherson, Ruth, Hovingh, Gerald K, Reilly, Muredach P, Watkins, Hugh, Goel, Anuj, Farrall, Martin, Girelli, Domenico, Reiner, Alex P, Stitziel, Nathan O, Kathiresan, Sekar, Gabriel, Stacey, Barrett, Jeffrey C, Lehtimäki, Terho, Laakso, Markku, Groop, Leif, Kaprio, Jaakko, Perola, Markus, McCarthy, Mark I, Boehnke, Michael, Altshuler, David M, Lindgren, Cecilia M, Hirschhorn, Joel N, Metspalu, Andres, Freimer, Nelson B, Zeller, Tanja, Jalkanen, Sirpa, Koskinen, Seppo, Raitakari, Olli, Durbin, Richard, MacArthur, Daniel G, Salomaa, Veikko, Ripatti, Samuli, Daly, Mark J, Palotie, Aarno

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Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes von Flannick, Jason, Beer, Nicola L, Bick, Alexander G, Agarwala, Vineeta, Molnes, Janne, Gupta, Namrata, Burtt, Noël P, Florez, Jose C, Meigs, James B, Taylor, Herman, Lyssenko, Valeriya, Irgens, Henrik, Fox, Ervin, Burslem, Frank, Johansson, Stefan, Brosnan, M Julia, Trimmer, Jeff K, Newton-Cheh, Christopher, Tuomi, Tiinamaija, Molven, Anders, Wilson, James G, O'Donnell, Christopher J, Kathiresan, Sekar, Hirschhorn, Joel N, Njølstad, Pål R, Rolph, Tim, Seidman, J G, Gabriel, Stacey, Cox, David R, Seidman, Christine E, Groop, Leif, Altshuler, David

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Burden of Rare Sarcomere Gene Variants in the Framingham and Jackson Heart Study Cohorts von Bick, Alexander G., Flannick, Jason, Ito, Kaoru, Cheng, Susan, Vasan, Ramachandran S., Parfenov, Michael G., Herman, Daniel S., DePalma, Steven R., Gupta, Namrata, Gabriel, Stacey B., Funke, Birgit H., Rehm, Heidi L., Benjamin, Emelia J., Aragam, Jayashri, Taylor, Herman A., Fox, Ervin R., Newton-Cheh, Christopher, Kathiresan, Sekar, O’Donnell, Christopher J., Wilson, James G., Altshuler, David M., Hirschhorn, Joel N., Seidman, J.G., Seidman, Christine

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The Genetic Landscape of Renal Complications in Type 1 Diabetes von Sandholm, Niina, Van Zuydam, Natalie, Ahlqvist, Emma, Juliusdottir, Thorhildur, Deshmukh, Harshal A, Rayner, N William, Di Camillo, Barbara, Forsblom, Carol, Fadista, Joao, Ziemek, Daniel, Salem, Rany M, Hiraki, Linda T, Pezzolesi, Marcus, Trégouët, David, Dahlström, Emma, Valo, Erkka, Oskolkov, Nikolay, Ladenvall, Claes, Marcovecchio, M Loredana, Cooper, Jason, Sambo, Francesco, Malovini, Alberto, Manfrini, Marco, McKnight, Amy Jayne, Lajer, Maria, Harjutsalo, Valma, Gordin, Daniel, Parkkonen, Maija, Tuomilehto, Jaakko, Lyssenko, Valeriya, McKeigue, Paul M, Rich, Stephen S, Brosnan, Mary Julia, Fauman, Eric, Bellazzi, Riccardo, Rossing, Peter, Hadjadj, Samy, Krolewski, Andrzej, Paterson, Andrew D, Florez, Jose C, Hirschhorn, Joel N, Maxwell, Alexander P, Dunger, David, Cobelli, Claudio, Colhoun, Helen M, Groop, Leif, McCarthy, Mark I, Groop, Per-Henrik

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Increased Burden of Cardiovascular Disease in Carriers of APOL1 Genetic Variants von Ito, Kaoru, Bick, Alexander G, Flannick, Jason, Friedman, David J, Genovese, Giulio, Parfenov, Michael G, DePalma, Steven R, Gupta, Namrata, Gabriel, Stacey B, Taylor, Herman A, Fox, Ervin R, Newton-Cheh, Christopher, Kathiresan, Sekar, Hirschhorn, Joel N, Altshuler, David M, Pollak, Martin R, Wilson, James G, Seidman, J.G, Seidman, Christine

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A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity von Lim, Elaine T., Liu, Yangfan P., Chan, Yingleong, Tiinamaija, Tuomi, Käräjämäki, AnnMari, Madsen, Erik, Altshuler, David M., Raychaudhuri, Soumya, Groop, Leif, Flannick, Jason, Hirschhorn, Joel N., Katsanis, Nicholas, Daly, Mark J.

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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms von Guo, Michael H., Nandakumar, Satish K., Ulirsch, Jacob C., Zekavat, Seyedeh M., Buenrostro, Jason D., Natarajan, Pradeep, Salem, Rany M., Chiarle, Roberto, Mitt, Mario, Kals, Mart, Pärn, Kalle, Fischer, Krista, Milani, Lili, Mägi, Reedik, Palta, Priit, Gabriel, Stacey B., Metspalu, Andres, Lander, Eric S., Kathiresan, Sekar, Hirschhorn, Joel N., Esko, Tõnu, Sankaran, Vijay G.

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The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system von Mandl, Kenneth D., Glauser, Tracy, Krantz, Ian D., Avillach, Paul, Bartels, Anna, Beggs, Alan H., Biswas, Sawona, Bourgeois, Florence T., Corsmo, Jeremy, Dauber, Andrew, Devkota, Batsal, Fleisher, Gary R., Heath, Allison P., Helbig, Ingo, Hirschhorn, Joel N., Kilbourn, Judson, Kong, Sek Won, Kornetsky, Susan, Majzoub, Joseph A., Marsolo, Keith, Martin, Lisa J., Nix, Jeremy, Schwarzhoff, Amy, Stedman, Jason, Strauss, Arnold, Sund, Kristen L., Taylor, Deanne M., White, Peter S., Marsh, Eric, Grimberg, Adda, Hawkes, Colin

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Whole Exome Sequencing Reveals a Novel Mutation in CUL7 in a Patient with an Undiagnosed Growth Disorder von Dauber, Andrew, MD, MMSc, Stoler, Joan, MD, Hechter, Eliana, PhD, Safer, Jason, BS, Hirschhorn, Joel N., MD, PhD

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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes von Majithia, Amit R., Flannick, Jason, Shahinian, Peter, Guo, Michael, Bray, Mark-Anthony, Fontanillas, Pierre, Gabriel, Stacey B., Rosen, Evan D., Altshuler, David

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Blood biomarkers of trans-fatty acid intake among Nigerian adults in the Federal Capital Territory: a cross-sectional study von Marklund, Matti, Billyrose, Soji, Orji, Ikechukwu A, Ikechukwu-Orji, Mercy U, Okoro, Clementina, Obagha, Chijioke, Iyer, Guhan, Jamro, Erica L, Ojo, Adedayo, Harris, William S, Wu, Jason HY, Hirschhorn, Lisa R, Van Horn, Linda, Huffman, Mark D, Ojji, Dike B

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