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Risk factors and outcomes associated with Left Ventricular Thrombus in patients with Peripartum Cardiomyopathy: An insight from National Inpatient Sample Database.
Luthra K, Avula SR, Raju M, Gangu K, Waqar Z, Doddamani R, Settipalle BH, Shah J, Ali SS, Singh H. Luthra K, et al. Among authors: waqar z. Am J Prev Cardiol. 2021 Dec 24;9:100313. doi: 10.1016/j.ajpc.2021.100313. eCollection 2022 Mar. Am J Prev Cardiol. 2021. PMID: 35059680 Free PMC article.
Cardiovascular Events in Patients with Thyroid Storm.
Waqar Z, Avula S, Shah J, Ali SS. Waqar Z, et al. J Endocr Soc. 2021 Mar 11;5(6):bvab040. doi: 10.1210/jendso/bvab040. eCollection 2021 Jun 1. J Endocr Soc. 2021. PMID: 34056498 Free PMC article.
Burden of atrial fibrillation in patients with rheumatic diseases.
Khan MZ, Patel K, Patel KA, Doshi R, Shah V, Adalja D, Waqar Z, Franklin S, Gupta N, Gul MH, Jesani S, Kutalek S, Figueredo V. Khan MZ, et al. Among authors: waqar z. World J Clin Cases. 2021 May 16;9(14):3252-3264. doi: 10.12998/wjcc.v9.i14.3252. World J Clin Cases. 2021. PMID: 34002134 Free PMC article.
Neurogenetic analysis of childhood disintegrative disorder.
Gupta AR, Westphal A, Yang DYJ, Sullivan CAW, Eilbott J, Zaidi S, Voos A, Vander Wyk BC, Ventola P, Waqar Z, Fernandez TV, Ercan-Sencicek AG, Walker MF, Choi M, Schneider A, Hedderly T, Baird G, Friedman H, Cordeaux C, Ristow A, Shic F, Volkmar FR, Pelphrey KA. Gupta AR, et al. Among authors: waqar z. Mol Autism. 2017 Apr 4;8:19. doi: 10.1186/s13229-017-0133-0. eCollection 2017. Mol Autism. 2017. PMID: 28392909 Free PMC article.
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.
Murdoch JD, Gupta AR, Sanders SJ, Walker MF, Keaney J, Fernandez TV, Murtha MT, Anyanwu S, Ober GT, Raubeson MJ, DiLullo NM, Villa N, Waqar Z, Sullivan C, Gonzalez L, Willsey AJ, Choe SY, Neale BM, Daly MJ, State MW. Murdoch JD, et al. Among authors: waqar z. PLoS Genet. 2015 Jan 26;11(1):e1004852. doi: 10.1371/journal.pgen.1004852. eCollection 2015 Jan. PLoS Genet. 2015. PMID: 25621974 Free PMC article.
The contribution of de novo coding mutations to autism spectrum disorder.
Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei L, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang Z, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma B, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M. Iossifov I, et al. Among authors: waqar z. Nature. 2014 Nov 13;515(7526):216-21. doi: 10.1038/nature13908. Epub 2014 Oct 29. Nature. 2014. PMID: 25363768 Free PMC article.
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