Tara Lynn Wenger, MD, PhD
Vascular Anomalies, Clinical Genetics, Craniofacial Genetics Clinic
On staff since July 2014
Children's Title: Associate Medical Director, Inpatient Service
Academic Title: Assistant Professor
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Patient Testimonials
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Awards and Honors
Award Name Award Description Awarded By Award Date Travel Award Teratology Society 2014 Robert Gorlin Award Best poster presentation by a fellow David W. Smith Workshop on Malformations and Morphogenesis 2013 Senior Resident Teaching Award Children's Hospital of Philadelphia 2012 Seymour Hoffman Distinguished First year Resident Award Children's Hospital of Philadelphia 2009 American Medical Women's Association Award Awarded to a woman medical student for graduating with class rank #1 in her medical school class University of Rochester School of Medicine and Dentistry 2008 Class of 1996 Community Service Award University of Rochester School of Medicine and Dentistry 2007 - 2008 Alpha Omega Alpha membership University of Rochester School of Medicine and Dentistry 2007 Gilbert B. Forbes Prize in Pediatrics University of Rochester School of Medicine and Dentistry 2003 Mary and Robert Sproull Fellowship University of Rochester School of Medicine and Dentistry 2002 -
Publications
Manuscripts in Refereed Journals
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Tara Lynn Wenger, MD, PhD, Arndt TL, Stodgell CJ, Rodier PMThe teratology of autism
International Journal of Developmental Neuroscience , 2005 : 23(2-3)189-199 -
Tara Lynn Wenger, MD, PhD, 3. Cole TB, Jampsa RL, Walter BJ, Arndt TL, Richter RJ, Shih DM, Tward A, Lusis A, Jack RM, Costa LG, Furlong CEExpression of human paraoxonase (PON1) during development
12777966 Pharmacogenetics , 2003 : 13(6)357-364 -
Tara Lynn Wenger, MD, PhD, 2. Knopp EA, Arndt TL, Eng KL, Caldwell M, LeBoeuf RC, Deeb SS, OBrien KDMurine phospholipid hydroperoxide glutathione peroxidase: cDNA sequence, tissue expression, and mapping
Mammalian Genome , 1999 : 10(6)601-605 -
Tara Lynn Wenger, MD, PhD, 1. Noble KD, Arndt TL, Nicholson TM, Sletten T, Zamora ADDifferent strokes: Perceptions of social and emotional development among early college entrants
Journal of Secondary Gifted Education , 1999 : 10(2)77-84
Other Publications
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Wenger TL, Earl D, Chow P, Sanchez-Lara PARole of Pediatric Geneticists in Craniofacial Teams: The Identification of Craniofacial Conditions with Cancer Predisposition.
27289500 The Journal of pediatrics, 2016 Jun 8 -
Wenger TL, Dahl J, Bhoj EJ, Rosen A, McDonald-McGinn D, Zackai E, Jacobs I, Heike CL, Hing A, Santani A, Inglis AF, Sie KC, Cunningham M, Perkins JTracheal cartilaginous sleeves in children with syndromic craniosynostosis.
27228464 Genetics in medicine : official journal of the American College of Medical Genetics, 2016 May 26 -
Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EH"CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases" American Journal of Medical Genetics Part A. 164:2557-2566, 2014.
26097173 American journal of medical genetics. Part A, 2015 July : 167(7)1682-3 -
Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EHCHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.
25123255 American journal of medical genetics. Part A, 2014 Oct. : 164A(10)2557-66
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Overview
- Board Certification(s)
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Pediatrics
Clinical Genetics and Genomics (MD)
- Medical/Professional School
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University of Rochester School of Medicine/Dentistry, Rochester, NY
- Residency
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Children's Hospital of Philadelphia, Philadelphia, PA
- Clinical Interests
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Birth defects and neurodevelopmental disabilities; genetic syndromes; prenatal exposures