Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically von Wang, Jian, Dron, Jacqueline S, Ban, Matthew R, Robinson, John F, McIntyre, Adam D, Alazzam, Maher, Zhao, Pei Jun, Dilliott, Allison A, Cao, Henian, Huff, Murray W, Rhainds, David, Low-Kam, Cécile, Dubé, Marie-Pierre, Lettre, Guillaume, Tardif, Jean-Claude, Hegele, Robert A

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Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia von Iacocca, Michael A., Wang, Jian, Dron, Jacqueline S., Robinson, John F., McIntyre, Adam D., Cao, Henian, Hegele, Robert A.

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Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias von Dron, Jacqueline S., Wang, Jian, McIntyre, Adam D., Iacocca, Michael A., Robinson, John F., Ban, Matthew R., Cao, Henian, Hegele, Robert A.

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LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias[S] von Johansen, Christopher T., Dubé, Joseph B., Loyzer, Melissa N., MacDonald, Austin, Carter, David E., McIntyre, Adam D., Cao, Henian, Wang, Jian, Robinson, John F., Hegele, Robert A.

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Targeted next generation sequencing as a tool for precision medicine von Gulilat, Markus, Lamb, Tyler, Teft, Wendy A, Wang, Jian, Dron, Jacqueline S, Robinson, John F, Tirona, Rommel G, Hegele, Robert A, Kim, Richard B, Schwarz, Ute I

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Polygenic determinants in extremes of high-density lipoprotein cholesterol von Dron, Jacqueline S., Wang, Jian, Low-Kam, Cécile, Khetarpal, Sumeet A., Robinson, John F., McIntyre, Adam D., Ban, Matthew R., Cao, Henian, Rhainds, David, Dubé, Marie-Pierre, Rader, Daniel J., Lettre, Guillaume, Tardif, Jean-Claude, Hegele, Robert A.

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Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia von Dron, Jacqueline S., Wang, Jian, McIntyre, Adam D., Cao, Henian, Robinson, John F., Duell, P. Barton, Manjoo, Priya, Feng, James, Movsesyan, Irina, Malloy, Mary J., Pullinger, Clive R., Kane, John P., Hegele, Robert A.

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease von Dilliott, Allison A, Farhan, Sali M K, Ghani, Mahdi, Sato, Christine, Liang, Eric, Zhang, Ming, McIntyre, Adam D, Cao, Henian, Racacho, Lemuel, Robinson, John F, Strong, Michael J, Masellis, Mario, Bulman, Dennis E, Rogaeva, Ekaterina, Lang, Anthony, Tartaglia, Carmela, Finger, Elizabeth, Zinman, Lorne, Turnbull, John, Freedman, Morris, Swartz, Rick, Black, Sandra E, Hegele, Robert A

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Scaling of GaN HEMTs and Schottky Diodes for Submillimeter-Wave MMIC Applications von Shinohara, Keisuke, Regan, Dean C., Yan Tang, Corrion, Andrea L., Brown, David F., Wong, Joel C., Robinson, John F., Fung, Helen H., Schmitz, Adele, Oh, Thomas C., Kim, Samuel Jungjin, Chen, Peter S., Nagele, Robert G., Margomenos, Alexandros D., Micovic, Miroslav

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Targeted next-generation sequencing in monogenic dyslipidemias von Hegele, Robert A, Ban, Matthew R, Cao, Henian, McIntyre, Adam D, Robinson, John F, Wang, Jian

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Clinical Utility and Practical Considerations of a Coronary Artery Disease Genetic Risk Score von Liu, Robin, Cheng, Jiahui, Muzlera, Carlos, Robinson, John F, Ban, Matthew R, Hegele, Robert A

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Exome sequencing identifies NFS1 deficiency in a novel Fe‐S cluster disease, infantile mitochondrial complex II/III deficiency von Farhan, Sali M. K., Wang, Jian, Robinson, John F., Lahiry, Piya, Siu, Victoria M., Prasad, Chitra, Kronick, Jonathan B., Ramsay, David A., Rupar, C. Anthony, Hegele, Robert A.

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Copy Number Variation in GCK in Patients With Maturity-Onset Diabetes of the Young von Berberich, Amanda J, Huot, Céline, Cao, Henian, McIntyre, Adam D, Robinson, John F, Wang, Jian, Hegele, Robert A

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Characteristics of the Ontario Neurodegenerative Disease Research Initiative cohort von Sunderland, Kelly M., Beaton, Derek, Arnott, Stephen R., Kleinstiver, Peter, Kwan, Donna, Lawrence‐Dewar, Jane M., Ramirez, Joel, Tan, Brian, Bartha, Robert, Black, Sandra E., Borrie, Michael, Brien, Donald, Casaubon, Leanne K., Coe, Brian C., Cornish, Benjamin, Dilliott, Allison A., Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne, Frank, Andrew, Fraser, Julia, Freedman, Morris, Greenberg, Barry, Grimes, David A., Hassan, Ayman, Hatch, Wendy, Hegele, Robert A., Hudson, Christopher, Jog, Mandar, Kumar, Sanjeev, Lang, Anthony, Levine, Brian, Lou, Wendy, Mandzia, Jennifer, Marras, Connie, McIlroy, William, Montero‐Odasso, Manuel, Munoz, David G., Munoz, Douglas P., Orange, Joseph B., Park, David S., Pasternak, Stephen H., Pieruccini‐Faria, Frederico, Rajji, Tarek K., Roberts, Angela C., Robinson, John F., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Scott, Christopher J.M., Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D.L., Strong, Michael J., Strother, Stephen C., Swartz, Richard H., Symons, Sean, Tang‐Wai, David F., Tartaglia, Maria Carmela, Troyer, Angela K., Turnbull, John, Zinman, Lorne, McLaughlin, Paula M., Masellis, Mario, Binns, Malcolm A., Abrahao, Agessandro, Adamo, Sabrina, Berezuk, Courtney, Black, Alanna, Breen, David P., Bulman, Dennis, Chen, Ying, El‐Defrawy, Sherif, Farhan, Sali, Ghani, Mahdi, Gonder, John, Haddad, Seyyed M. H., Holmes, Melissa, Huang, Jeff, Leontieva, Elena, Mandelcorn, Efrem, Margolin, Edward, Nanayakkara, Nuwan, Ozzoude, Miracle, Peltsch, Alicia J., Pollock, Bruce, Raamana, Pradeep, Rashkovan, Natalie, Yanina, Southwell, Alisia, Sujanthan, Sujeevini, Tayyari, Faryan, Van Ooteghem, Karen, Woulfe, John, Zamyadi, Mojdeh, Zou, Guangyong

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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy von Roberts, Jason D, Murphy, Nathaniel P, Hamilton, Robert M, Lubbers, Ellen R, James, Cynthia A, Kline, Crystal F, Gollob, Michael H, Krahn, Andrew D, Sturm, Amy C, Musa, Hassan, El-Refaey, Mona, Koenig, Sara, Aneq, Meriam Åström, Hoorntje, Edgar T, Graw, Sharon L, Davies, Robert W, Rafiq, Muhammad Arshad, Koopmann, Tamara T, Aafaqi, Shabana, Fatah, Meena, Chiasson, David A, Taylor, Matthew Rg, Simmons, Samantha L, Han, Mei, van Opbergen, Chantal Jm, Wold, Loren E, Sinagra, Gianfranco, Mittal, Kirti, Tichnell, Crystal, Murray, Brittney, Codima, Alberto, Nazer, Babak, Nguyen, Duy T, Marcus, Frank I, Sobriera, Nara, Lodder, Elisabeth M, van den Berg, Maarten P, Spears, Danna A, Robinson, John F, Ursell, Philip C, Green, Anna K, Skanes, Allan C, Tang, Anthony S, Gardner, Martin J, Hegele, Robert A, van Veen, Toon Ab, Wilde, Arthur Am, Healey, Jeff S, Janssen, Paul Ml, Mestroni, Luisa, van Tintelen, J Peter, Calkins, Hugh, Judge, Daniel P, Hund, Thomas J, Scheinman, Melvin M, Mohler, Peter J

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27-OR: Simplifying Detection of Large Scale Deletions Causing MODY5 von BERBERICH, AMANDA J., WANG, JIAN, CAO, HENIAN, MCINTYRE, ADAM D., ROBINSON, JOHN F., YANG, PING, KNOLL, JOAN, HEGELE, ROBERT

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Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial Hypercholesterolemia von Iacocca, Michael A., Wang, Jian, Sarkar, Samantha, Dron, Jacqueline S., Lagace, Thomas, McIntyre, Adam D., Lau, Paulina, Robinson, John F., Yang, Ping, Knoll, Joan H., Cao, Henian, McPherson, Ruth, Hegele, Robert A.

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Novel Asymmetric Slant Field Plate Technology for High-Speed Low-Dynamic Ron E/D-mode GaN HEMTs von Wong, Joel, Shinohara, Keisuke, Corrion, Andrea L., Brown, David F., Carlos, Zenon, Williams, Adam, Yan Tang, Robinson, John F., Khalaf, Isaac, Fung, Helen, Schmitz, Adele, Oh, Thomas, Kim, Samuel, Chen, Steven, Burnham, Shawn, Margomenos, Alex, Micovic, Miroslav

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Association of plasma biomarkers with cognition, cognitive decline, and daily function across and within neurodegenerative diseases: Results from the Ontario Neurodegenerative Dise... von Sanchez, Erlan, Wilkinson, Tim, Coughlan, Gillian, Mirza, Saira, Baril, Andrée‐Ann, Ramirez, Joel, Binns, Malcolm A., Black, Sandra E., Borrie, Michael, Dilliott, Allison A., Dixon, Roger A., Dowlatshahi, Dar, Farhan, Sali, Finger, Elizabeth, Fischer, Corinne E., Frank, Andrew, Freedman, Morris, Goncalves, Rafaella A., Grimes, David A., Hassan, Ayman, Hegele, Robert A., Kumar, Sanjeev, Lang, Anthony E., Marras, Connie, McLaughlin, Paula M., Orange, Joseph B., Pasternak, Stephen H., Pollock, Bruce G., Rajji, Tarek K., Roberts, Angela C., Robinson, John F., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Strong, Michael J., Swartz, Richard H., Tang‐Wai, David F., Tartaglia, Maria Carmela, Troyer, Angela K., Kvartsberg, Hlin, Zetterberg, Henrik, Munoz, Douglas P., Masellis, Mario

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Genetic and epigenetic study of an Alzheimer's disease family with monozygotic triplets von Zhang, Ming, Dilliott, Allison A, Khallaf, Roaa, Robinson, John F, Hegele, Robert A, Comishen, Michael, Sato, Christine, Tosto, Giuseppe, Reitz, Christiane, Mayeux, Richard, George-Hyslop, Peter St, Freedman, Morris, Rogaeva, Ekaterina

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