SVEP1 is an endogenous ligand for the orphan receptor PEAR1 von Elenbaas, Jared S., Pudupakkam, Upasana, Ashworth, Katrina J., Kang, Chul Joo, Patel, Ved, Santana, Katherine, Jung, In-Hyuk, Lee, Paul C., Burks, Kendall H., Amrute, Junedh M., Mecham, Robert P., Halabi, Carmen M., Alisio, Arturo, Di Paola, Jorge, Stitziel, Nathan O.

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Author Correction: SVEP1 is an endogenous ligand for the orphan receptor PEAR1 von Elenbaas, Jared S., Pudupakkam, Upasana, Ashworth, Katrina J., Kang, Chul Joo, Patel, Ved, Santana, Katherine, Jung, In-Hyuk, Lee, Paul C., Burks, Kendall H., Amrute, Junedh M., Mecham, Robert P., Halabi, Carmen M., Alisio, Arturo, Di Paola, Jorge, Stitziel, Nathan O.

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Exact coalescent simulation of new haplotype data from existing reference haplotypes von CHUL JOO KANG, MARJORAM, Paul

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Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences von Ganel, Liron, Chen, Lei, Christ, Ryan, Vangipurapu, Jagadish, Young, Erica, Das, Indraniel, Kanchi, Krishna, Larson, David, Regier, Allison, Abel, Haley, Kang, Chul Joo, Scott, Alexandra, Havulinna, Aki, Chiang, Charleston W K, Service, Susan, Freimer, Nelson, Palotie, Aarno, Ripatti, Samuli, Kuusisto, Johanna, Boehnke, Michael, Laakso, Markku, Locke, Adam, Stitziel, Nathan O, Hall, Ira M

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Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease von Lee, Paul C., Jung, In-Hyuk, Thussu, Shreeya, Patel, Ved, Wagoner, Ryan, Burks, Kendall H., Amrute, Junedh, Elenbaas, Jared S., Kang, Chul Joo, Young, Erica P., Scherer, Philipp E., Stitziel, Nathan O.

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Mapping and characterization of structural variation in 17,795 human genomes von Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.

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Exome sequencing of Finnish isolates enhances rare-variant association power von Locke, Adam E., Steinberg, Karyn Meltz, Chiang, Charleston W. K., Service, Susan K., Havulinna, Aki S., Stell, Laurel, Pirinen, Matti, Abel, Haley J., Chiang, Colby C., Fulton, Robert S., Jackson, Anne U., Kang, Chul Joo, Kanchi, Krishna L., Koboldt, Daniel C., Larson, David E., Nelson, Joanne, Nicholas, Thomas J., Pietilä, Arto, Ramensky, Vasily, Ray, Debashree, Scott, Laura J., Stringham, Heather M., Vangipurapu, Jagadish, Welch, Ryan, Yajnik, Pranav, Yin, Xianyong, Eriksson, Johan G., Ala-Korpela, Mika, Järvelin, Marjo-Riitta, Männikkö, Minna, Laivuori, Hannele, Dutcher, Susan K., Stitziel, Nathan O., Wilson, Richard K., Hall, Ira M., Sabatti, Chiara, Palotie, Aarno, Salomaa, Veikko, Laakso, Markku, Ripatti, Samuli, Boehnke, Michael, Freimer, Nelson B.

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Abstract 496: The Cardiometabolic Disease Risk Protein SVEP1 Activates AKT/mTOR By Signaling Through The Orphan Receptor PEAR1 von Elenbaas, Jared S, Pudupakkam, Upasana, Patel, Ved, Ashworth, Katrina, Kang, Chul Joo, Jung, In-Hyuk, Santana, Katherine, Alisio, Arturo, Di Paola, Jorge, Stitziel, Nathan

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Inference of population mutation rate and detection of segregating sites from next-generation sequence data von Kang, Chul Joo, Marjoram, Paul

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ANGPTL3 Deficiency and Risk of Hepatic Steatosis von D'Erasmo, Laura, Di Martino, Michele, Neufeld, Thomas, Fraum, Tyler J, Kang, Chul Joo, Burks, Kendall H, Di Costanzo, Alessia, Minicocci, Ilenia, Bini, Simone, Maranghi, Marianna, Pigna, Giovanni, Labbadia, Giancarlo, Zheng, Jie, Fierro, Davide, Montali, Anna, Ceci, Fabrizio, Catalano, Carlo, Davidson, Nicholas O, Lucisano, Giuseppe, Nicolucci, Antonio, Arca, Marcello, Stitziel, Nathan O

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A Sample Selection Strategy for Next-Generation Sequencing von Kang, Chul Joo, Marjoram, Paul

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Association of structural variation with cardiometabolic traits in Finns von Chen, Lei, Abel, Haley J., Das, Indraniel, Larson, David E., Ganel, Liron, Kanchi, Krishna L., Regier, Allison A., Young, Erica P., Kang, Chul Joo, Scott, Alexandra J., Chiang, Colby, Wang, Xinxin, Lu, Shuangjia, Christ, Ryan, Service, Susan K., Chiang, Charleston W.K., Havulinna, Aki S., Kuusisto, Johanna, Boehnke, Michael, Laakso, Markku, Palotie, Aarno, Ripatti, Samuli, Freimer, Nelson B., Locke, Adam E., Stitziel, Nathan O., Hall, Ira M.

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Corrections & amendments von Locke, Adam E, Steinberg, Karyn Meltz, K Chiang, Charleston W, Service, Susan K, Havulinna, Aki S, Stell, Laurel, Pirinen, Matti, Abel, Haley J, Chiang, Colby C, Fulton, Robert S, Jackson, Anne U, Kang, Chul Joo, Kanchi, Krishna L, Koboldt, Daniel C, Larson, David E, Nelson, Joanne, Nicholas, Thomas J, Pietilä, Arto, Ramensky, Vasily, Ray, Debashree, Scott, Laura J, Stringham, Heather M, Vangipurapu, Jagadish, Welch, Ryan, Yajnik, Pranav, Yin, Xianyong, Eriksson, Johan G, Ala-Korpela, Mika, Järvelin, Marjo-Riitta

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Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power von Locke, Adam E., Steinberg, Karyn Meltz, Chiang, Charleston W. K., Service, Susan K., Havulinna, Aki S., Stell, Laurel, Pirinen, Matti, Abel, Haley J., Chiang, Colby C., Fulton, Robert S., Jackson, Anne U., Kang, Chul Joo, Kanchi, Krishna L., Koboldt, Daniel C., Larson, David E., Nelson, Joanne, Nicholas, Thomas J., Pietilä, Arto, Ramensky, Vasily, Ray, Debashree, Scott, Laura J., Stringham, Heather M., Vangipurapu, Jagadish, Welch, Ryan, Yajnik, Pranav, Yin, Xianyong, Eriksson, Johan G., Ala-Korpela, Mika, Järvelin, Marjo-Riitta, Männikkö, Minna, Laivuori, Hannele, Dutcher, Susan K., Stitziel, Nathan O., Wilson, Richard K., Hall, Ira M., Sabatti, Chiara, Palotie, Aarno, Salomaa, Veikko, Laakso, Markku, Ripatti, Samuli, Boehnke, Michael, Freimer, Nelson B.

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P1‐055: Exome‐sequencing in a large dataset of late‐onset families with Alzheimer's disease von Kobolt, Dan, Lord, Jenny, Fernandez, Victoria, del-Aguila, Jorge, Kang, Chul Joo, Saef, Ben, Wilson, Rick, Goate, Alison, Cruchaga, Carlos

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Exome-sequencing in a large dataset of late-onset families with Alzheimer’s disease von Kobolt, Dan, Lord, Jenny, Fernandez, Victoria, del-Aguila, Jorge, Kang, Chul Joo, Saef, Ben, Wilson, Rick, Goate, Alison, Cruchaga, Carlos

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IRF6 mutation screening in nonsyndromic orofacial clefting: analysis of 1521 families von Leslie, Elizabeth J., Koboldt, Daniel C., Kang, Chul Joo, Ma, Lian, Hecht, Jacqueline T., Wehby, George L., Christensen, Kaare, Czeizel, Andrew E., Deleyiannis, Frederic W.-B., Fulton, Robert S., Wilson, Richard K., Beaty, Terri H., Schutte, Brian C., Murray, Jeffrey C., Marazita, Mary L.

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Methods for detecting associations between phenotype and aggregations of rare variants von Yang, Fan, Kang, Chul Joo, Marjoram, Paul

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Additional file 2 of Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences von Ganel, Liron, Chen, Lei, Christ, Ryan, Vangipurapu, Jagadish, Young, Erica, Das, Indraniel, Kanchi, Krishna, Larson, David, Regier, Allison, Abel, Haley, Kang, Chul Joo, Scott, Alexandra, Havulinna, Aki, Chiang, Charleston W. K., Service, Susan, Freimer, Nelson, Palotie, Aarno, Ripatti, Samuli, Kuusisto, Johanna, Boehnke, Michael, Laakso, Markku, Locke, Adam, Stitziel, Nathan O., Hall, Ira M.

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Characterization of Geranium (Pelargonium graveolens) Chloroplast EF-Tu cDNA von Kang, Chul Joo, Lee, Min Goo, Cho, Young Sil, Lee, Joong Won, Kyung, Yoon Jung, Shin, Jeong Sheop, Kim, Eun-Soo, Kim, Jeong-Kook

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