Alexander E Katz (Alexander Katz)

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 4

Top Topics

Genome Wide Association Study

Abdominal Aortic

Top Venues

Circulation. Genomic and precision medicine

Proceedings of the National Academy of Sciences of the United States of America

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Alexander E Katz, Min-Lee Yang, Michael G Levin, Catherine Tcheandjieu, Michael R Mathis, Kristina L Hunker, Susan Blackburn, Jonathan L Eliason, Dawn M Coleman, Natalia Fendrikova-Mahlay, Heather L Gornik, Monita Karmakar, Hannah Hill, Chang Xu, Matthew Zawistowski, Chad M Brummett, Sebastian Zöllner, Xiang Zhou, Christopher J O'Donnell, Julie A Douglas, Themistocles L Assimes, Phillip S Tsao, Jun Z Li, Scott M Damrauer, James C Stanley, Santhi K Ganesh, null null
Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture. Circulation. Genomic and precision medicine (2022)
Jacqueline Saw, Min-Lee Yang, Mark Trinder, Catherine Tcheandjieu, Chang Xu, Andrew Starovoytov, Isabelle Birt, Michael R Mathis, Kristina L Hunker, Ellen M Schmidt, Linda Jackson, Natalia Fendrikova-Mahlay, Matthew Zawistowski, Chad M Brummett, Sebastian Zoellner, Alexander E Katz, Dawn M Coleman, Kirby Swan, Christopher J O'Donnell, null null, Xiang Zhou, Jun Z Li, Heather L Gornik, Themistocles L Assimes, James C Stanley, Liam R Brunham, Santhi K Ganesh
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. Nature communications 11 (1) (2020)
Kalpana Manthiram, Silvia Preite, Fatma Dedeoglu, Selcan Demir, Seher Sener, Kathryn M Edwards, Sivia K Lapidus, Alexander E Katz, null null, Henry M Feder, Maranda Lawton, Greg R Licameli, Peter F Wright, Julie Le, Karyl S Barron, Amanda K Ombrello, Beverly Barham, Tina Romeo, Anne Jones, Hemalatha Srinivasalu, Pamela A Mudd, Roberta L DeBiasi, Ahmet Gül, Gary S Marshall, Olcay Y Jones, Settara C Chandrasekharappa, Yuriy Stepanovskiy, Polly J Ferguson, Pamela L Schwartzberg, Elaine F Remmers, Daniel L Kastner
Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis. Proceedings of the National Academy of Sciences of the United States of America 117 (25) (2020)
Sarah J Garnai, Michelle L Brinkmeier, Ben Emery, Tomas S Aleman, Louise C Pyle, Biliana Veleva-Rotse, Robert A Sisk, Frank W Rozsa, Ayse Bilge Ozel, Jun Z Li, Sayoko E Moroi, Steven M Archer, Cheng-Mao Lin, Sarah Sheskey, Laurel Wiinikka-Buesser, James Eadie, Jill E Urquhart, Graeme C M Black, Mohammad I Othman, Michael Boehnke, Scot A Sullivan, Gregory L Skuta, Hemant S Pawar, Alexander E Katz, Laryssa A Huryn, Robert B Hufnagel, null null, Sally Ann Camper, Julia E Richards, Lev Prasov
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. PLoS genetics 15 (5) (2019)