Mark David Levin - Division of Pediatric Cardiology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA

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Bio

Mark D. Levin, MD currently works at the Cardiopulmonary Branch of the Intramural Research Program at the National Heart, Lung, and Blood Institute, NIH. He combines human cardiovacular data with animal model data to investigate arrhythmia mechanisms and conduction system disease.

Research Interests

Papers共 58 篇Author StatisticsCo-AuthorSimilar Experts

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Loss of Baz1b in Mice Causes Perinatal Lethality, Growth Failure, and Variable Multi-System Outcomes

Christopher Pai, Basil A. McIntosh,Russell H. Knutsen,Mark D. Levin,Kit Man Tsang,Beth A. Kozel,Robert O. Heuckeroth

Developmental Biology (2024): 42-57

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Identifying Individuals at Risk for Surgical Supravalvar Aortic Stenosis by Polygenic Risk Score with Graded Phenotyping

D Liu,C B Mervis,M D Levin,E Biamino,M F Bedeschi, M C Digilio,G M Squeo,R Villa, S Osgood, J A Freeman, N Raja, G Merla, A E Roberts,C A Morris,L R Osborne,B A Kozel

medRxiv the preprint server for health sciences (2024)

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Gastrointestinal Manifestations in Williams Syndrome: A Prospective Analysis of an Adult and Pediatric Cohort

Michael Boechler,Yi-Ping Fu,Neelam Raja, Emily Ruiz-Escobar, Likitha Nimmagadda,Sharon Osgood,Mark D. Levin,Colleen Hadigan,Beth A. Kozel

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2024)

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Increased Heart Rate Fragmentation in Those with Williams-Beuren Syndrome Suggests Nonautonomic Mechanistic Contributors to Sudden Death Risk

Brianna M. Cathey, Anna Bellach,James Troendle, Kevin Smith,Sharon Osgood,Neelam Raja,Beth A. Kozel,Mark D. Levin

AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGYno. 2 (2024): H521-H532

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Deep Phenotyping of Post-Infectious Myalgic Encephalomyelitis/chronic Fatigue Syndrome

Brian Walitt,Komudi Singh,Samuel R. LaMunion,Mark Hallett,Steve Jacobson,Kong Chen,Yoshimi Enose-Akahata,Richard Apps,Jennifer J. Barb,Patrick Bedard,Robert J. Brychta,Ashura Williams Buckley,Peter D. Burbelo,Brice Calco, Brianna Cathay,Li Chen,Snigdha Chigurupati,Jinguo Chen,Foo Cheung,Lisa M. K. Chin,Benjamin W. Coleman,Amber B. Courville,Madeleine S. Deming,Bart Drinkard,Li Rebekah Feng,Luigi Ferrucci,Scott A. Gabel,Angelique Gavin,David S. Goldstein,Shahin Hassanzadeh, Sean C. Horan,Silvina G. Horovitz,Kory R. Johnson,Anita Jones Govan,Kristine M. Knutson,Joy D. Kreskow,Mark Levin,Jonathan J. Lyons,Nicholas Madian,Nasir Malik,Andrew L. Mammen,John A. McCulloch,Patrick M. McGurrin, Joshua D. Milner,Ruin Moaddel,Geoffrey A. Mueller,Amrita Mukherjee,Sandra Muñoz-Braceras,Gina Norato,Katherine Pak,Iago Pinal-Fernandez,Traian Popa,Lauren B. Reoma,Michael N. Sack,Farinaz Safavi,Leorey N. Saligan,Brian A. Sellers,Stephen Sinclair,Bryan Smith,Joseph Snow, Stacey Solin,Barbara J. Stussman,Giorgio Trinchieri,Sara A. Turner,C. Stephenie Vetter,Felipe Vial,Carlotta Vizioli, Ashley Williams,Shanna B. Yang,Avindra Nath

NATURE COMMUNICATIONSno. 1 (2024)

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P212: Modifiers of arterial stenosis in Williams syndrome: Using genomics to discover drivers of vessel-specific outcomes

Ashley Golbus,Delong Liu,Mark Levin,Neelam Raja,Elisa Biamino, Maria Bedeschi, Maria Digilio,Gabriella Squeo,Roberta Villa, Joy Lynne Freeman,Sharon Osgood,Giuseppe Merla,Barbara Pober,Carolyn Mervis,Amy Roberts,Colleen Morris,Lucy Osborne,Beth Kozel

Genetics in Medicine Open (2024): 101109

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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams–Beuren Syndrome

JOURNAL OF THE AMERICAN HEART ASSOCIATIONno. 3 (2024)

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Abstract 17825: Heart Rate Fragmentation Analysis May Suggest Non-Autonomic Markers of Sudden Cardiac Death Risk in Adults with Williams-Beuren Syndrome

Brianna Cathey,Mark D. Levin,Yi-Ping Fu,Kevin Smith,Sharon Osgood,Neelam Raja,Beth Kozel

CIRCULATION (2023)

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Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome

Laryssa A. Huryn,Taylor Flaherty,Rosalie Nolen,Lev Prasov,Wadih M. Zein,Catherine A. Cukras,Sharon Osgood,Neelam Raja,Mark D. Levin,Susan Vitale, Brian P. Brooks,Robert B. Hufnagel,Beth A. Kozel

Br J Ophthalmol（2023）

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Pathway Analysis Identifies Novel Non-Synonymous Variants Contributing to Extreme Vascular Outcomes in Williams-Beuren Syndrome

D. Liu,C.J. Billington, N. Raja,Z.C. Wong,M.D. Levin, W. Resch, C. Alba,D.N. Hupalo,E. Biamino,M.F. Bedeschi,M.C. Digilio, G.M. Squeo, R. Villa,P.C.R. Parrish,R.H. Knutsen, S. Osgood, J.A. Freeman,C.L. Dalgard,G. Merla,B.R. Pober,C.B. Mervis, A.E. Roberts, C.A. Morris,L.R. Osborne,B.A. Kozel

medrxiv（2022）

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