Výsledky vyhledávání - Matthew B. Lanktree

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  1. 1
    Gene-gene and gene-environment interactions: new insights into the prevention, detection and management of coronary artery disease

    Gene-gene and gene-environment interactions: new insights into the prevention, detection and management of coronary artery disease Autor Matthew B. Lanktree, Robert A. Hegele

    Vydáno 2009
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  2. 2
    Advances in Genomic Analysis of Stroke

    Advances in Genomic Analysis of Stroke Autor Matthew B. Lanktree, Martin Dichgans, Robert A. Hegele

    Vydáno 2010
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  3. 3
    Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample

    Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Autor Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele

    Vydáno 2009
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  4. 4
    Comprehensive Analysis of Genomic Variation in the <i>LPA</i> Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians

    Comprehensive Analysis of Genomic Variation in the <i>LPA</i> Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians Autor Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele

    Vydáno 2009
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  5. 5
    Insights into Autosomal Dominant Polycystic Kidney Disease from Genetic Studies

    Insights into Autosomal Dominant Polycystic Kidney Disease from Genetic Studies Autor Matthew B. Lanktree, Amirreza Haghighi, Ighli di Bari, Xuewen Song, York Pei

    Vydáno 2020
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  6. 6
    Clonal haematopoiesis, ageing and kidney disease

    Clonal haematopoiesis, ageing and kidney disease Autor Caitlyn Vlasschaert, Matthew B. Lanktree, Michael J. Rauh, Tanika N. Kelly, Pradeep Natarajan

    Vydáno 2023
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  7. 7
    Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

    Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals Autor Yiran Guo, Matthew B. Lanktree, Kira C. Taylor, Hákon Hákonarson, Leslie A. Lange, Brendan J. Keating

    Vydáno 2012
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  8. 8
    Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing

    Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing Autor Matthew B. Lanktree, Amirreza Haghighi, Elsa Guiard, Ioan-Andrei Iliuta, Xuewen Song, Peter C. Harris, Andrew D. Paterson, York Pei

    Vydáno 2018
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  9. 9
    Causal Relationship between Adiponectin and Metabolic Traits: A Mendelian Randomization Study in a Multiethnic Population

    Causal Relationship between Adiponectin and Metabolic Traits: A Mendelian Randomization Study in a Multiethnic Population Autor Andrew Mente, David Meyre, Matthew B. Lanktree, Mahyar Heydarpour, A. Darlene Davis, Ruby Miller, Hertzel C. Gerstein, Robert A. Hegele, Salim Yusuf, Sonia S. Anand

    Vydáno 2013
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  10. 10
    Elevated Lipoprotein(a) and Risk of Atrial Fibrillation

    Elevated Lipoprotein(a) and Risk of Atrial Fibrillation Autor Pedrum Mohammadi‐Shemirani, Michael Chong, Sukrit Narula, Nicolas Perrot, David Conen, Jason D. Roberts, Sébastien Thériault, Yohan Bossé, Matthew B. Lanktree, Marie Pigeyre, Guillaume Paré

    Vydáno 2022
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  11. 11
    A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation

    A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulat... Autor Matthew B. Lanktree, Nicolas Perrot, Andrew Smyth, Michael Chong, Sukrit Narula, Meera Shanmuganathan, Zachary Kroezen, Philip Britz‐McKibbin, Mario Berger, Joan C. Krepinsky, Marie Pigeyre, Salim Yusuf, Guillaume Paré

    Vydáno 2023
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  12. 12
    Clonal Hematopoiesis of Indeterminate Potential and Kidney Function Decline in the General Population

    Clonal Hematopoiesis of Indeterminate Potential and Kidney Function Decline in the General Population Autor Bryan Kestenbaum, Alexander G. Bick, Caitlyn Vlasschaert, Michael J. Rauh, Matthew B. Lanktree, Nora Franceschini, M. Benjamin Shoemaker, Raymond C. Harris, Bruce M. Psaty, Anna Köttgen, Pradeep Natarajan, Cassianne Robinson‐Cohen

    Vydáno 2022
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  13. 13
    Intrafamilial Variability of ADPKD

    Intrafamilial Variability of ADPKD Autor Matthew B. Lanktree, Elsa Guiard, Weili Li, Pedram Akbari, Amirreza Haghighi, Ioan-Andrei Iliuta, Belili Shi, Chen Chen, Ning He, Xuewen Song, Peter J. Margetts, Alistair J. Ingram, Korosh Khalili, Andrew D. Paterson, York Pei

    Vydáno 2019
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  14. 14
    A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems

    A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems Autor Piya Lahiry, Jian Wang, John F. Robinson, Jacob P. Turowec, David W. Litchfield, Matthew B. Lanktree, Gregory B. Gloor, Erik G. Puffenberger, Kevin A. Strauss, Mildred Martens, David A. Ramsay, C. Anthony Rupar, Victoria Mok Siu, Robert A. Hegele

    Vydáno 2009
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  15. 15
    Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease

    Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease Autor Caitlyn Vlasschaert, Amy J. M. McNaughton, Michael Chong, Elina K. Cook, Wilma M. Hopman, Bryan Kestenbaum, Cassianne Robinson‐Cohen, Jocelyn S. Garland, Sarah Moran, Guillaume Paré, Catherine M. Clase, Mila Tang, Adeera Levin, Rachel M. Holden, Michael J. Rauh, Matthew B. Lanktree

    Vydáno 2022
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  16. 16
    A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic datasets

    A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic datasets Autor Caitlyn Vlasschaert, Taralynn Mack, J. Brett Heimlich, Abhishek Niroula, Md Mesbah Uddin, Joshua S. Weinstock, Brian Sharber, Alexander J. Silver, Yaomin Xu, Michael R. Savona, Christopher J. Gibson, Matthew B. Lanktree, Michael J. Rauh, Benjamin L. Ebert, Pradeep Natarajan, Siddhartha Jaiswal, Alexander G. Bick

    Vydáno 2023
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  17. 17
    Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia

    Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia Autor Christopher T. Johansen, Jian Wang, Adam D. McIntyre, Rebecca A. Martins, Matthew R. Ban, Matthew B. Lanktree, Murray W. Huff, Miklós Péterfy, Margarete Mehrabian, Aldons J. Lusis, Sekar Kathiresan, Sonia S. Anand, Salim Yusuf, Ann–Hwee Lee, Laurie H. Glimcher, Henian Cao, Robert A. Hegele

    Vydáno 2011
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  18. 18
    Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling

    Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling Autor Yun Li, Kathrin Laue, Samia A. Temtamy, Mona Aglan, Leman Damla Kotan, Gökhan Yigit, Husniye Canan, Barbara Pawlik, Gudrun Nürnberg, Emma Wakeling, Oliver Quarrell, Ingelore Baessmann, Matthew B. Lanktree, M. Yılmaz, Robert A. Hegele, Khalda Amr, Klaus W. May, Peter Nürnberg, A. Kemal Topaloğlu, Matthias Hammerschmidt, Bernd Wollnik

    Vydáno 2010
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  19. 19
    An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia

    An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia Autor Christopher T. Johansen, Jian Wang, Matthew B. Lanktree, Adam D. McIntyre, Matthew R. Ban, Rebecca A. Martins, Brooke A. Kennedy, Reina G. Hassell, Maartje E. Visser, Stephen M. Schwartz, Benjamin F. Voight, Roberto Elosúa, Veikko Salomaa, Christopher J. O’Donnell, Geesje M. Dallinga‐Thie, Sonia S. Anand, Salim Yusuf, Murray W. Huff, Sekar Kathiresan, Henian Cao, Robert A. Hegele

    Vydáno 2011
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  20. 20
    Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

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

    Vydáno 2010
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