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Kendall H. Burks, Debapriya Basu, Ira J. Goldberg, Nathan O. Stitziel. Angiopoietin-like 3: An important protein in regulating lipoprotein levels. Best Pract Res Clin Endocrinol Metab. 2023 May;37(3):101688.
Samantha K. Barrick, Ankit Garg, Lina Greenberg, Shanshan Zhang, Chieh Yu Lin, Nathan O. Stitziel, Michael Greenberg. Functional Assays Reveal the Pathogenic Mechanism of a De Novo Tropomyosin Variant Identified In Patient With Dilated Cardiomyopathy. J Mol Cell Cardiol. 2023 Mar;176:58-67.
Jared S. Elenbaas, Upasana Pudupakkam, Katrina J. Ashworth, Chul Joo Kang, Ved Patel, Katherine Santana, In Hyuk Jung, Paul C. Lee, Kendall H. Burks, Junedh M. Amrute, Robert P. Mecham, Carmen M. Halabi, Arturo Aliso, Jorge Di Paola, Nathan O. Stitziel. SVEP1 is an Endogenous Ligand for the Orphan Receptor PEAR1. Nat Commun. 2023 Feb 15;14(1):850.
Jung IH, Elenbaas JS, Alisio A, Santana K, Young EP, Kang CJ, Kachroo P, Lavine KJ, Razani B, Mecham RP, Stitziel NO. SVEP1 is a Human Coronary Artery Disease Locus that Promotes Atherosclerosis. Sci Transl Med. 2021 Mar 24;13(586):eabe0357. Stitziel NO, Kanter JE, Bornfeldt KE. Emerging Targets for Cardiovascular Disease Prevention in Diabetes. Trends Mol Med. 2020 Aug;26(8):744-757. Evans TD, Zhang X, Clark RE, Alisio A, Song E, Zhang H, Reilly MP, Stitziel NO, Razani B. Functional Characterization of LIPA (Lysosomal Acid Lipase) Variants Associated With Coronary Artery Disease. Arterioscler Thromb Vasc Biol. 2019 Dec;39(12):2480-2491. Young EP, Stitziel NO. Capitalizing on insights from human genetics to identify novel therapeutic targets for coronary artery disease. Annu Rev Med.
Stitziel NO, Khera AV, Wang X, Bierhals AJ, Vourakis AC, Sperry AE, Natarajan P, Klarin D, Emdin CA, Zekavat SM, Nomura A, Erdmann J, Schunkert H, Samani NJ, Kraus WE, Shah SH, Yu B, Boerwinkle E, Rader DJ, Gupta N, Frossard PM, Rasheed A, Danesh J, Lander ES, Gabriel S, Saleheen D, Musunuru K, Kathiresan S; PROMIS and Myocardial Infarction Genetics Consortium Investigators. ANGPTL3 deficiency and protection against coronary artery disease. J Am Coll Cardiol. 2017 Apr 25;69(16):2054-2063.
Lee VS, Halabi CM, Hoffman EP, Carmichael N, Leshchiner I, Lian CG, Bierhals AJ, Vuzman D; Brigham Genomic Medicine, Mecham RP, Frank NY, Stitziel NO. Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans. Proc Natl Acad Sci U S A.
Stitziel NO, Stirrups KE, Masca NGD, Erdmann J, et al. Coding variation in ANGPTL4 , LPL , and SVEP1 and the risk of coronary disease. N Engl J Med. 2016 March 24th; 374:1134-1144
View a complete list of Stitziel lab Publications