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Jennifer Kalish, MD, Pediatrics, Philadelphia, PA, Children's Hospital of Philadelphia

JenniferKalishMD

Pediatrics Philadelphia, PA

Medical Genetics

Assistant Professor of Pediatrics and Genetics

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  • Office

    3401 Civic Center Blvd
    Children's Hospital Of Philadelphia - Genetics
    Philadelphia, PA 19104
    Phone+1 215-590-2920
    Fax+1 215-590-3298
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Education & Training

  • Children's Hospital of Philadelphia
    Children's Hospital of PhiladelphiaResidency, Pediatrics/Medical Genetics and Genomics, 2007 - 2012
  • Yale School of Medicine
    Yale School of MedicineClass of 2007
  • Yale University
    Yale UniversityPhD, Genetics, 2006
  • Harvard University
    Harvard UniversityBA, Chemistry & Physics, Cum Laude, 1998

Certifications & Licensure

  • FL State Medical License
    FL State Medical License 2021 - Present
  • NY State Medical License
    NY State Medical License 2020 - 2026
  • VA State Medical License
    VA State Medical License 2020 - 2026
  • DE State Medical License
    DE State Medical License 2021 - 2025
  • NJ State Medical License
    NJ State Medical License 2023 - 2025
  • PA State Medical License
    PA State Medical License 2007 - 2024
  • American Board of Pediatrics Pediatrics
  • American Board of Medical Genetics and Genomics Clinical Genetics and Genomics

Awards, Honors, & Recognition

  • Distinguished Trainee Award The Children's Hospital of Philadelphia, 2014
  • John M. Opitz Young Investigator Award 2014
  • Research Day Poster Award The Children's Hospital of Philadelphia, 2013
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Publications & Presentations

PubMed

Journal Articles

  • Nonreentrant Atrial Tachycardia Occurs Independently of Hypertrophic Cardiomyopathy in RASopathy Patients  
    Karen W Gripp, Rosemarie Smith, Stephanie M Ware, Paula Goldenberg, Kathryn C Chatfield, Mark D Levin, Richard J Czosek, Elaine H Zackai, Angela E Lin, Tara L Wenger, ..., American Journal of Medical Genetics Part A
  • Congenital Hyperinsulinism in Children with Paternal 11p Uniparental Isodisomy and Beckwith- Wiedemann Syndrome  
    Kalish JM, Boodhansingh KE, Bhatti TR, Ganguly A, Conlin LK, Becker SA, Givler S, Mighion L, Palladino AA, Adzick NS, De Leon DD, Stanley CA, and Deardorff MA, J Med Genet, 1/1/2016
  • Visualizing allele-specific expression in single cells reveals epigenetic mosaicism in an H19 loss-of-imprinting mutant  
    Ginart P, Kalish JM, Jiang C, Yu A, Bartolomei M, and Raj A, Genes Dev, 1/1/2016
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Books/Book Chapters

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Abstracts/Posters

  • Placental pathology in IMAGe syndrome associated with gain-of-function mutations in CDKN1C.
    McKay E, Ruchelli E, Ganguly A, Ebrahimzadeh J, Richards-Yutz J, Seaver L, Bober M, Duker A, Deardorff MA, and Kalish JM, Society for Pediatric Pathology, Seattle, WA, 1/1/2016
  • Single cell analysis uncovers heritable monoallelic and biallelic expressing cell subpopulations in H19 loss of imprinting mutants.
    Ginart P, Kalish JM, Jiang C, Bartolomei M, and Raj A, Stochastic Physics in Biology Gordon Research Conference, Ventura, CA, 1/1/2015
  • Prenatal findings in Beckwith-Wiedemann Syndrome.
    Kalish JM, Ebrahimzadeh J, Purrazzella J, Reichert S, Richards-Yutz J, Treece A, Khalek N, McKay E, Ganguly A, and Deardorff MA, 36th Annual David W. Smith Workshop, St. Michael's, MD, 1/1/2015
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Lectures

  • "Beckwith-Wiedemann Syndrome and Congenital Hyperinsulinism." 
    Philadelphia, PA - 1/1/2016
  • "Mosaicism, Symmetry, and Growth: Balance is Key." 
    St. Jude Children's Research Hospital, Memphis, TN - 1/1/2015
  • "Dissecting the Spectrum of Beckwith-Wiedemann Syndrome." 
    The First European Imprinting School, Mery-Sur-Oise, France - 1/1/2014
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Authored Content

  • Beckwith-Wiedemann Syndrome: Partnership in the Diagnostic Journey of a Rare DisorderMarch 2018
  • Beckwith-Wiedemann Syndrome: Partnership in the Diagnostic Journey of a Rare DisorderMarch 2018

Press Mentions

  • The Society for Pediatric Research Announces New Members
    The Society for Pediatric Research Announces New MembersJanuary 16th, 2020
  • Oncology: Emerging Clinical Investigators Stars Receive Damon Runyan Awards
    Oncology: Emerging Clinical Investigators Stars Receive Damon Runyan AwardsJuly 23rd, 2019
  • Beckwith-Wiedemann Syndrome: Partnership in the Diagnostic Journey of a Rare Disorder
    Beckwith-Wiedemann Syndrome: Partnership in the Diagnostic Journey of a Rare DisorderMarch 1st, 2018
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Hospital Affiliations