Neil D Romberg, MD

faculty photo
Assistant Professor of Pediatrics at the Children's Hospital of Philadelphia
Department: Pediatrics
Graduate Group Affiliations

Contact information
The Children's Hospital of Philadelphia
Abramson Center
3615 Civic Center Blvd.
Suite 1216C
Philadelphia, PA 19104
Office: (267) 426-8195
Fax: 267-426-0363
Education:
B.S. (Botany)
University of Michigan, 1999.
M.D. (Medicine)
Pennsylvania State University, College of Medicine, 2004.
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Selected Publications

Lawless D, Geier CB, Farmer JR, Allen Lango H, Thwaites D, Atschekzei F, Brown M, Buchbinder D, Burns SO, Butte MJ, Csomos K, Deevi SVV, Egner W, Ehl S, Eibl MM, Fadugba O, Foldvari Z, Green DM, Henrickson SE, Holland SM, John T, Klemann C, Kuijpers TW, Moreira F, Piller A, Rayner-Matthews P, Romberg ND, Sargur R, Schmidt RE, Schröder C, Schuetz C, Sharapova SO, Smith KGC, Sogkas G, Speckmann C, Stirrups K, Thrasher AJ, Wolf HM, Notarangelo LD, Anwar R, Boyes J, Ujhazi B; NIHR BioResource–Rare Diseases Consortium, Thaventhiran J, Walter JE, Savic S: Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency. J Allergy Clin Immunol March 2018.

Le Coz C, Trofa M, Syrett CM, Martin A, Jyonouchi H, Jyonouchi S, Anguera MC, Romberg N: CD40LG duplication-associated autoimmune disease is silenced by nonrandom X-chromosome inactivation. J Allergy Clin Immunol March 2018.

Romberg N, Vogel TP, Canna SW: NLRC4 inflammasomopathies. Current Opinion in Allergy and Clinical Immunology 17(6): 398-404, Dec 2017.

Perkins T, Rosenberg JM, Le Coz C, Alaimo JT, Trofa M, Mullegama SV, Antaya RJ, Jyonouchi S, Elsea SH, Utz PJ, Meffre E, Romberg N.: Smith-Magenis syndrome patients often display antibody deficiency but not other immune pathologies. The Journal of Allergy and Clinical Immunology: In Practice. 5(5): 1344-1350, Sep 2017.

Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg ND, Meffre E, Gelfand EW, Snow AL, Milner JD.: Germline hypomorphic CARD11 mutations in severe atopic disease. Nature Genetics. 49(8): 1192-1201, Aug 2017.

Canna SW, Girard C, Malle L, de Jesus A, Romberg N, Kelsen J, Surrey LF, Russo, P, Sleight A, Schiffrin E, Gabay C, Goldbach-Mansky R, Behrens EM. : Life-threatening NLRC4-associated hyperinflammation successfully treated with IL-18 inhibition. The Journal of Allergy and Clinical Immunology 139(5): 1698-1701, May 2017 Notes: Epub ahead of print, Nov 19, 2016.

Romberg Neil, Virdee Manmeet, Chamberlain Nicolas, Oe Tyler, Schickel Jean-Nicolas, Perkins Tiffany, Cantaert Tineke, Rachid Rima, Rosengren Sally, Palazzo Regina, Geha Raif, Cunningham-Rundles Charlotte, Meffre Eric: TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development. The Journal of Allergy and Clinical Immunology 136(5): 1315-25, Nov 2015.

Pala Francesca, Morbach Henner, Castiello Maria Carmina, Schickel Jean-Nicolas, Scaramuzza Samantha, Chamberlain Nicolas, Cassani Barbara, Glauzy Salome, Romberg Neil, Candotti Fabio, Aiuti Alessandro, Bosticardo Marita, Villa Anna, Meffre Eric: Lentiviral-mediated gene therapy restores B cell tolerance in Wiskott-Aldrich syndrome patients. The Journal of clinical investigation 125(10): 3941-51, Oct 2015.

Pagovich Odelya E, Lebastchi Amir H, Romberg Neil: Peri-operative considerations in the patient with primary immune deficiency: a review. Surgical Infections 15(6): 672-8, Dec 2014.

Romberg Neil, Al Moussawi Khatoun, Nelson-Williams Carol, Stiegler Amy L, Loring Erin, Choi Murim, Overton John, Meffre Eric, Khokha Mustafa K, Huttner Anita J, West Brian, Podoltsev Nikolai A, Boggon Titus J, Kazmierczak Barbara I, Lifton Richard P: Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation. Nature Genetics 46(10): 1135-9, Oct 2014.

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Last updated: 03/30/2018
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