Method for manufacturing semiconductor device von YANG SIQI, DING ZHENTING, LIN SHIHAO, JIAN HENIAN, LIN JIANZHI, YE ZHIKAI, HUANG CAIYU, LI JIANZHI, LI ZONGHONG, XIAO BAIKAI

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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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Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia von Dron, Jacqueline S., Wang, Jian, Berberich, Amanda J., Iacocca, Michael A., Cao, Henian, Yang, Ping, Knoll, Joan, Tremblay, Karine, Brisson, Diane, Netzer, Christian, Gouni-Berthold, Ioanna, Gaudet, Daniel, 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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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 in monogenic dyslipidemias von Hegele, Robert A, Ban, Matthew R, Cao, Henian, McIntyre, Adam D, Robinson, John F, Wang, Jian

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A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia von Hegele, Robert A., Ban, Matthew R., Hsueh, Neil, Kennedy, Brooke A., Cao, Henian, Zou, Guang Yong, Anand, Sonia, Yusuf, Salim, Huff, Murray W., Wang, Jian

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An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia von Johansen, Christopher T, Wang, Jian, Lanktree, Matthew B, McIntyre, Adam D, Ban, Matthew R, Martins, Rebecca A, Kennedy, Brooke A, Hassell, Reina G, Visser, Maartje E, Schwartz, Stephen M, Voight, Benjamin F, Elosua, Roberto, Salomaa, Veikko, OʼDonnell, Christopher J, Dallinga-Thie, Geesje M, Anand, Sonia S, Yusuf, Salim, Huff, Murray W, Kathiresan, Sekar, Cao, Henian, Hegele, Robert A

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Complex genetic determinants of hypertriglyceridemia von Dron, Jacqueline S, Wang, Jian, Cao, Henian, McIntyre, Adam D, Hegele, Rob A

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The polygenic nature of mild-to-moderate hypertriglyceridemia von Dron, Jacqueline S., Wang, Jian, McIntyre, Adam D., Cao, Henian, Hegele, Robert A.

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Polygenic determinants of severe hypertriglyceridemia von Wang, Jian, Ban, Matthew R., Zou, Guang Yong, Cao, Henian, Lin, Tim, Kennedy, Brooke A., Anand, Sonia, Yusuf, Salim, Huff, Murray W., Pollex, Rebecca L., Hegele, Robert A.

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Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia von Hegele, Robert A, Johansen, Christopher T, Wang, Jian, Lanktree, Matthew B, Cao, Henian, McIntyre, Adam D, Ban, Matthew R, Martins, Rebecca A, Kennedy, Brooke A, Hassell, Reina G, Visser, Maartje E, Schwartz, Stephen M, Voight, Benjamin F, Elosua, Roberto, Salomaa, Veikko, O'Donnell, Christopher J, Dallinga-Thie, Geesje M, Anand, Sonia S, Yusuf, Salim, Huff, Murray W, Kathiresan, Sekar

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Genetic Confirmation Rate in Clinically Suspected Maturity-Onset Diabetes of the Young von Brahm, Amanda J., MD, FRCPC, Wang, Grace, BSc, Wang, Jian, MD, McIntyre, Adam D., BSc, Cao, Henian, MD, Ban, Matthew R., BSc, Hegele, Robert A., MD, FRCPC, FACP

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Enrichment of loss-of-function and cony number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillation von Lazarte, Julieta, Laksman, Zachary W., Wang, Jian, Robinson, John F., Dron, Jacqueline S., Leach, Emma, Liew, Janet, McIntyre, Adam D., Skanes, Allan C., Gula, Lorne J., Leong-Sit, Peter, Cao, Henian, Trost, Brett, Scherer, Stephen W., Hegele, Robert A., Roberts, Jason D.

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Use of next-generation sequencing to detect copy number variations in the molecular diagnosis of familial hypercholesterolemia von Iacocca, Michael, Wang, Jian, Dron, Jacqueline, Robinson, John, Mcintyre, Adam, Cao, Henian, Hegele, Robert

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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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Bioinformatic detection of copy number variation in HNF4A causing maturity onset diabetes of the young von Berberich, Amanda J., Mokashi, Arati, McIntyre, Adam D., Robinson, John F., Cao, Henian, Wang, Jian, Hegele, Robert A.

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Abstract 174: The Use of Next-Generation Sequencing to Detect Copy Number Variation in the Molecular Diagnosis of Familial Hypercholesterolemia von Iacocca, Michael A, Wang, Jian, Dron, Jacqueline S, Robinson, John F, McIntyre, Adam D, Ban, Matthew R, Cao, Henian, Hegele, Robert A

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Severe hypertriglyceridemia is primarily polygenic von Dron, Jacqueline S., Wang, Jian, Cao, Henian, McIntyre, Adam D., Iacocca, Michael A., Menard, Jyler R., Movsesyan, Irina, Malloy, Mary J., Pullinger, Clive R., Kane, John P., Hegele, Robert A.

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