Arama Sonuçları - Matthew B. Lanktree
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Advances in Genomic Analysis of Stroke Yazar: Matthew B. Lanktree, Martin Dichgans, Robert A. Hegele
Baskı/Yayın Bilgisi 2010Revisão -
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Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Yazar: Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele
Baskı/Yayın Bilgisi 2009Artigo -
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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 Yazar: Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele
Baskı/Yayın Bilgisi 2009Artigo -
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Insights into Autosomal Dominant Polycystic Kidney Disease from Genetic Studies Yazar: Matthew B. Lanktree, Amirreza Haghighi, Ighli di Bari, Xuewen Song, York Pei
Baskı/Yayın Bilgisi 2020Revisão -
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Clonal haematopoiesis, ageing and kidney disease Yazar: Caitlyn Vlasschaert, Matthew B. Lanktree, Michael J. Rauh, Tanika N. Kelly, Pradeep Natarajan
Baskı/Yayın Bilgisi 2023Revisão -
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Causal Relationship between Adiponectin and Metabolic Traits: A Mendelian Randomization Study in a Multiethnic Population Yazar: 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
Baskı/Yayın Bilgisi 2013Artigo -
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Elevated Lipoprotein(a) and Risk of Atrial Fibrillation Yazar: 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
Baskı/Yayın Bilgisi 2022Artigo -
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A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulat... Yazar: 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
Baskı/Yayın Bilgisi 2023Artigo -
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Clonal Hematopoiesis of Indeterminate Potential and Kidney Function Decline in the General Population Yazar: 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
Baskı/Yayın Bilgisi 2022Revisão -
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Intrafamilial Variability of ADPKD Yazar: 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
Baskı/Yayın Bilgisi 2019Artigo -
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A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems Yazar: 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
Baskı/Yayın Bilgisi 2009Artigo -
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Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease Yazar: 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
Baskı/Yayın Bilgisi 2022Artigo -
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A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic datasets Yazar: 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
Baskı/Yayın Bilgisi 2023Artigo -
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Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia Yazar: 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
Baskı/Yayın Bilgisi 2011Artigo -
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Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling Yazar: 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
Baskı/Yayın Bilgisi 2010Artigo -
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An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia Yazar: 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
Baskı/Yayın Bilgisi 2011Artigo -
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Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia Yazar: 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
Baskı/Yayın Bilgisi 2010Artigo
Arama Araçları:
İlgili Konular
Biology
Gene
Genetics
Medicine
Genotype
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Endocrinology
Genetic association
Population
Environmental health
Bioinformatics
Computational biology
Genetic variants
Kidney disease
Mendelian randomization
Disease
Allele
Cholesterol
Meta-analysis
Mutation
Phenotype
Quantitative trait locus
Renal function
SNP
Autosomal dominant polycystic kidney disease
Body mass index
Candidate gene
Evolutionary biology