Maen Abou Ziki, MD
Clinical Fellow; Cardiology, Internal Medicine
Research & Publications
Biography
News
Coauthors
Research Interests
Arrhythmias, Cardiac; Diagnosis; Genetics, Medical; Heart Failure; Internal Medicine; Molecular Biology; Thromboembolism; Atherosclerosis
Selected Publications
- Tachyarrhythmia Onset Captured on Telemetry Deciphers the Diagnosis.Abou Ziki MD, Rosenfeld LE. Tachyarrhythmia Onset Captured on Telemetry Deciphers the Diagnosis. JAMA Internal Medicine 2017, 177: 1673-1675. PMID: 28873172, DOI: 10.1001/jamainternmed.2017.3328.
- Wnt signaling, a novel pathway regulating blood pressure? State of the art review.Abou Ziki MD, Mani A. Wnt signaling, a novel pathway regulating blood pressure? State of the art review. Atherosclerosis 2017, 262: 171-178. PMID: 28522145, PMCID: PMC5508596, DOI: 10.1016/j.atherosclerosis.2017.05.001.
- Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.Abou Ziki MD, Seidelmann SB, Smith E, Atteya G, Jiang Y, Fernandes RG, Marieb MA, Akar JG, Mani A. Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT. Clinical Genetics 2018, 93: 741-751. PMID: 28407228, PMCID: PMC5640462, DOI: 10.1111/cge.13036.
- Pulmonary Embolism and Atrial Fibrillation: Two Sides of the Same Coin? A Systematic Review.Bikdeli B, Abou Ziki MD, Lip GYH. Pulmonary Embolism and Atrial Fibrillation: Two Sides of the Same Coin? A Systematic Review. Seminars In Thrombosis And Hemostasis 2017, 43: 849-863. PMID: 28196379, DOI: 10.1055/s-0036-1598005.
- Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults.Seidelmann SB, Smith E, Subrahmanyan L, Dykas D, Abou Ziki MD, Azari B, Hannah-Shmouni F, Jiang Y, Akar JG, Marieb M, Jacoby D, Bale AE, Lifton RP, Mani A. Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults. Circulation. Cardiovascular Genetics 2017, 10 PMID: 28087566, PMCID: PMC5245580, DOI: 10.1161/CIRCGENETICS.116.001573.
- Metabolic syndrome: genetic insights into disease pathogenesis.Abou Ziki MD, Mani A. Metabolic syndrome: genetic insights into disease pathogenesis. Current Opinion In Lipidology 2016, 27: 162-71. PMID: 26825138, PMCID: PMC5141383, DOI: 10.1097/MOL.0000000000000276.
- The Value of the History and Physical Examination--Sailing Through Medicine With Modern Tools: A Teachable Moment.Abou Ziki MD, Podell DN, Schiliro DM. The Value of the History and Physical Examination--Sailing Through Medicine With Modern Tools: A Teachable Moment. JAMA Internal Medicine 2015, 175: 1901-2. PMID: 26501402, DOI: 10.1001/jamainternmed.2015.5768.
- Rare mutation in the SLC26A3 transporter causes life-long diarrhoea with metabolic alkalosis.Abou Ziki MD, Verjee MA. Rare mutation in the SLC26A3 transporter causes life-long diarrhoea with metabolic alkalosis. BMJ Case Reports 2015, 2015 PMID: 25568271, PMCID: PMC4289764, DOI: 10.1136/bcr-2014-206849.
- Prevalence of the apolipoprotein E Arg145Cys dyslipidemia at-risk polymorphism in African-derived populations.Abou Ziki MD, Strulovici-Barel Y, Hackett NR, Rodriguez-Flores JL, Mezey JG, Salit J, Radisch S, Hollmann C, Chouchane L, Malek J, Zirie MA, Jayyuosi A, Gotto AM, Crystal RG. Prevalence of the apolipoprotein E Arg145Cys dyslipidemia at-risk polymorphism in African-derived populations. The American Journal Of Cardiology 2014, 113: 302-8. PMID: 24239320, PMCID: PMC3943837, DOI: 10.1016/j.amjcard.2013.09.021.
- Beware of Limb Lead Reversal-Reply.Abou Ziki MD, Rosenfeld LE. Beware of Limb Lead Reversal-Reply. JAMA Internal Medicine 2018, 178: 435. PMID: 29507991, DOI: 10.1001/jamainternmed.2017.8639.
- The interplay of canonical and noncanonical Wnt signaling in metabolic syndrome.Abou Ziki MD, Mani A. The interplay of canonical and noncanonical Wnt signaling in metabolic syndrome. Nutrition Research (New York, N.Y.) 2019, 70: 18-25. PMID: 30049588, PMCID: PMC6320319, DOI: 10.1016/j.nutres.2018.06.009.