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Characteristics, Outcomes, and Trends of Patients With COVID-19-Related Critical Illness at a Learning Health System in the United States.
Ann Intern Med. 2021 May;174(5):613-621. doi: 10.7326/M20-5327. Epub 2021 Jan 19.
Ann Intern Med. 2021.
PMID: 33460330
Free PMC article.
Post-Acute Coronary Syndrome Disparities in Guideline-Directed Lipid Therapy and Insufficient Achievement of Optimal Low-Density Lipoprotein.
Ambrosino M, Emerson S, Catalano L, Hossain E, Julien HM, Jacoby DS.
Ambrosino M, et al.
Am J Cardiol. 2023 Mar 1;190:8-16. doi: 10.1016/j.amjcard.2022.11.039. Epub 2022 Dec 19.
Am J Cardiol. 2023.
PMID: 36543078
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Role of Vitamin-D Receptor (VDR) single nucleotide polymorphisms in gestational hypertension development: A case-control study.
Caccamo D, Cannata A, Ricca S, Catalano LM, Montalto AF, Alibrandi A, Ercoli A, Granese R.
Caccamo D, et al. Among authors: catalano lm.
PLoS One. 2020 Nov 13;15(11):e0239407. doi: 10.1371/journal.pone.0239407. eCollection 2020.
PLoS One. 2020.
PMID: 33186385
Free PMC article.
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Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
Riley KN, Catalano LM, Bernat JA, Adams SD, Martin DM, Lalani SR, Patel A, Burnside RD, Innis JW, Rudd MK.
Riley KN, et al. Among authors: catalano lm.
Am J Med Genet A. 2015 Nov;167A(11):2664-73. doi: 10.1002/ajmg.a.37269. Epub 2015 Jul 31.
Am J Med Genet A. 2015.
PMID: 26227573
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Mouse model implicates GNB3 duplication in a childhood obesity syndrome.
Goldlust IS, Hermetz KE, Catalano LM, Barfield RT, Cozad R, Wynn G, Ozdemir AC, Conneely KN, Mulle JG, Dharamrup S, Hegde MR, Kim KH, Angle B, Colley A, Webb AE, Thorland EC, Ellison JW, Rosenfeld JA, Ballif BC, Shaffer LG, Demmer LA; Unique Rare Chromosome Disorder Support Group; Rudd MK.
Goldlust IS, et al. Among authors: catalano lm.
Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):14990-4. doi: 10.1073/pnas.1305999110. Epub 2013 Aug 26.
Proc Natl Acad Sci U S A. 2013.
PMID: 23980137
Free PMC article.
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