JenniferKalishMD

PubMed

• 331 citations
  Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
  Frédéric Brioude, Jennifer M. Kalish, Alessandro Mussa, Alison Foster, Jet Bliek
  Nature Reviews. Endocrinology. 2018-01-29
• 64 citations
  Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management.
  Kelly A. Duffy, Christopher M. Cielo, Jennifer L. Cohen, Christina X Gonzalez-Gandolfi, Jessica R Griff
  American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2019-08-30
• 18 citations
  Obstructive sleep apnoea and the role of tongue reduction surgery in children with Beckwith-Wiedemann syndrome
  Christopher M. Cielo, Kelly A. Duffy, Aesha Vyas, Jesse A. Taylor, Jennifer M. Kalish
  Paediatric Respiratory Reviews. 2018-01-01

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
• Overgrowth Syndromes  
  Edmondson A and Kalish JM, J Ped Genet, 1/1/2015
• Epigenetics and Imprinting in Human Disease  
  Kalish JM, Jiang CL, Bartolomei MS, Int J Dev Biol, 1/1/2014
• Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-level Uniparental Disomy  
  Kalish JM, Conlin LK, Mostoufi-Moab S, Wilkens AB, Mulchandani S, Zelley K, Kowalski M, Bhatti T, Russo P, Mattei P, Mackenzie WG, LiVolsi V, Nichols KE, Biegel JA, Sp..., Am J Med Genet Part A, 1/1/2013
• Clinical Features of Three Girls with Mosaic Genome-Wide Paternal Uniparental Isodisomy  
  Kalish JM, Conlin LK, Bhatti T, Dubbs HA, Harris MC, Izumi K, Mostoufi-Moab S, Mulchandani S, Saitta S, States L, Swarr D, Wilkens AB, Zackai E, Zelley K, Bartolomei M..., Am J Med Genet Part A, 1/1/2013
• Triplex-Stimulated Intermolecular Recombination at a Single-Copy Genomic Target  
  Knauert MP, Kalish JM, Hegan DC, and Glazer PM, Molecular Therapy, 1/1/2006
• Triplex-Induced Recombination and Repair in the Pyrimidine Motif  
  Kalish JM, Seidman MM, Weeks DL, and Glazer PM, Nucleic Acids Research, 1/1/2005
• Targeted Genome Modification via Triple Helix Formation  
  Kalish JM and Glazer PM, Annals of the New York Academy of Science, 1/1/2005
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Books/Book Chapters

• Human Malformations and Related Anomalies 
  Chapter: Asymmetry and Hypertrophy. 
  Kalish JMEditors: Roger E. Stevenson, Judith G. Hall, David B. Everman, and Benjamin S. Soloman.Oxford University Press2015
• The Five Minute Clinical Consult 2014 
  Chapter: Immunodeficiency Diseases. 
  Nixdorff N, Goodman A, and Kalish JMEditors: Domino F. Lippincott.Williams and WilkinsEdition 22nd,2013
• Netter's Pediatrics 
  Chapter: Genetic Syndromes. 
  Kalish JM, Haldeman-Englert C, and Deardorff MAEditors: Todd A. Florin and Stephen M. Ludwig.Elsevier Press2011
• Netter's Pediatrics 
  Chapter: Disorders of Sexual Development. 
  Haldeman-Englert C, Kalish JM, and Deardorff MAEditors: Todd A. Florin and Stephen M. Ludwig.Elsevier Press2011
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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
• Increased Prevalence of Malignancy in Twins with 22q11. 2 Deletion Syndrome.
  Schott AR, Valverde KD, Kalish JM, Lambert MP, Morrissette JJD, Emanuel BS, Zackai EH, and McDonald-McGinn DM, American Society of Human Genetics, Baltimore, MD, 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
• 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
• Cardiac Features of Mosaic Beckwith-Wiedemann Syndrome.
  Kalish JM, Jiang C, Ginart P, Raj A, Goldmuntz E, Engel N, Bartolomei M, and Deardorff MA, 35th Annual David W. Smith Workshop, Madison, WI, 1/1/2014
• Adrenal Disease in Beckwith-Wiedemann Syndrome.
  Kalish JM, Wilkens AB, Mulchandani S, Bartolomei M, Conlin LK, States LJ, Bhatti TR, and Deardorff MA, 34th Annual David W. Smith Workshop, Mont Tremblant, Quebec, Canada, 1/1/2013
• The Spectrum of Hyperinsulinism in Mosaic Beckwith-Wiedemann Syndrome: Dissection of 11p15 Paternal Uniparental Isodisomy.
  Kalish JM, Snider K, Conlin LK, Bhatti T, Ganguly A, Stanley C, Deardorff MA, American College of Medical Genetics, Phoenix, AZ, 1/1/2013
• Non-reentrant Tachycardia in Dysmorphic Infants Suggests Rasopathy.
  Lin AE, Wenger T, Saitta S, Smith R, Epstein M, Alexander ME, Gripp KW, Hopkins E, Ganesh J, Kalish J, Levin M, Prada C, Hopkin R, Zackai E, The American College of Medical Genetics, Charlotte, NC, 1/1/2012
• Whole Genome Paternal Uniparental Disomy.
  Kalish JM, Wilkens AB, Mulchandani S, Zackai EH, Spinner NB, Bartolomei M, Conlin LK, and Deardorff MA, The American Society for Human Genetics Meeting, San Francisco, CA, 1/1/2012
• Whole Genome Paternal Uniparental Disomy.
  Kalish JM, Wilkens AB, Mulchandani S, Zackai EH, Spinner NB, Bartolomei M, Conlin LK, and Deardorff MA, 33rd Annual David W. Smith Workshop, Buford, GA, 1/1/2012
• Clinical and Molecular Characterization of Patients with Whole Genome Paternal Uniparental Disomy.
  Kalish JM, Conlin LK, Daber R, Wilkens AB, Spinner NB, Bartolomei M, and Deardorff MA, The American College of Medical Genetics, Charlotte, NC, 1/1/2012
• The Spectrum of Hyperinsulinism in Mosaic Beckwith-Wiedemann Syndrome: Dissection of 11p15 Paternal Uniparental Isodisomy.
  Kalish JM, Snider K, Conlin LK, Bhatti T, Ganguly A, Stanley C, Deardorff MA, Monogenic Disorders of Insulin Secretion: Congenital Hyperinsulinism and Neonatal Diabetes Meeting, Philadelphia, P., 1/1/2012
• The Role of Cohesin in Imprinting and Escape from X-inactivation.
  Kalish JM, Lin S, Bartolomei MS, The American Society for Human Genetics Meeting, Montreal, Canada, 1/1/2011
• Utility of SNP Array Analysis in Mild Hemihypertrophy to Identify Subtle Mosaicism.
  Kalish JM, Conlin LK, Wilkens AB, Mulchandani S, Nichols KE, Biegel JA, Spinner NB, and Deardorff MA, 32nd Annual David W. Smith Workshop, Lake Arrowhead, CA, 1/1/2011
• Non-reentrant Tachycardia: Expanded Rasopathy Association and Cardiac Description.
  Lin AE, Wenger T, Zackai E, Saitta S, Smith R, Epstein M, Alexander ME, Gripp KW, Ganesh J, Kalish J, Levin M, Third International Ras Pathway Syndrome Symposium, Chicago, IL, 1/1/2011
• Hemihypertrophy, Bilateral Pheochromocytomas, and Subtle Somatic Mosaicism: the Utility of SNP Array Analysis.
  Kalish JM, Conlin LK, Wilkens AB, Mulchandani S, Nichols KE, Biegel JA, Spinner NB, and Deardorff MA, The American Society for Human Genetics Meeting, Washington, DC, 1/1/2010
• Unsuspected paternal UPD14 diagnosed by whole genome array: clinical and radiological features.
  Mucha-Le Ny B, Kalish JM, Spinner NB, Zackai EH, and Conlin LK, The American Society for Human Genetics Meeting, Washington, DC, 1/1/2010
• Detection and quantification of mosaic isodisomy in Beckwith-Wiedemann patients in the clinical cytogenetics laboratory.
  Conlin LK, Thiel BD, Mulchandani S, Kalish JM, Nichols KE, Biegel JA, Stanley CA, Ernst LM, Spinner NB, and Deardorff MA, The American Society for Human Genetics Meeting, Washington, DC, 1/1/2010
• Expanding the Phenotype in a Fryns Syndrome Survivor.
  Kalish JM, Mucha-Le Ny B, Bonnemann CG, Evans JA, McDonald-McGinn D, and Zackai EH, The 30th Annual David W. Smith Workshop, Philadelphia, PA, 1/1/2009
• Gene Targeting with Triplex-Forming Oligonucleotides in the Pyrimidine Motif.
  Kalish JM, Knauert MP, Hegan DC, and Glazer PM, The American Society of Gene Therapy Annual Meeting, Baltimore, MD, 1/1/2006
• The Mechanism of Incision Repair with Triplex-Forming Oligonucleotides.
  Kalish JM, Bessho T, and Glazer PM, The American Society for Microbiology Conference on DNA Repair and Mutagenesis, Southampton, Bermuda, 1/1/2004
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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
• "The Spectrum of Hyperinsulinism in Mosaic Beckwith-Wiedemann Syndrome." 
  Philadelphia, PA - 1/1/2014
• "The Mechanism of Tumor Formation in Beckwith-Wiedemann Syndrome." 
  Philadelphia, PA - 1/1/2014
• "Symmetry and Growth, When Things are Not Even." 
  Emory University, Atlanta, GA - 1/1/2013
• "Genetics for Primary Care." 
  Pennsylvania Hospital, Philadelphia, PA - 1/1/2011
• "Genetics for Internists." 
  Mercy Fitzgerald Hospital, Philadelphia, PA - 1/1/2010
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