Faculty

Alanna Strong, MD, PhD

Assistant Professor of Pediatrics (Human Genetics)

Department: Pediatrics

Graduate Group Affiliations

Cell and Molecular Biology

Contact information

Children's Hospital of Philadelphia
Division of Human Genetics
3615 Civic Center Blvd
Abramson Research Center, Room 1016D
Philadelphia, PA 19104

Office: 267-582-0429

Email:
strong.alanna@gmail.com

Education:
BS (Biology)
University of Pennsylvania, 2005.
PhD (Cellular and Molecular Biology)
University of Pennsylvania School of Medicine, 2012.
MD
University of Pennsylvania School of Medicine, 2014.

Permanent link

> Perelman School of Medicine > Faculty > Details

Description of Clinical Expertise

Genetics, genetic liver diseases, genetic kidney diseases, ciliopathy

Description of Research Expertise

Ciliopathy, cilium, hepatobiliary disease, kidney disease

Selected Publications

Watson D, Mentch F, Billings J, Ostberg K, March ME, Kalish JM, Li D, Cannon I, Guay-Woodford LM, Hartung E, Strong, A. : Elucidating the Molecular Landscape of Cystic Kidney Disease: Old Friends, New Friends and Some Surprises. Am J Med Genet A 197(6): e64011, Jun 2025.

Grady LO, Zoltick ES, Zouk H, He W, Perez E, Clarke L, Gold J, Strong A, Sahai I, Yeo J, Green RC, Karaa A, Gold NB : Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I. American Journal Med Genet A 197(4): e63940, Apr 2025.

Weaver N, Shikany A, Vieta E, Russell B, Lerman B, Strong A, Li D: Variants in MED12 are associated with left ventricular non-compaction and arrhythmia. American College of Medical Genetics Conference, Salt Lake City, UT Mar 2025 Notes: Poster.

Curtis D, Scott D, Lalani S, Azamian M, Keller K, Strong A, Shen J, DeFilippo C, Goel H, Schmalz B, Chaudhari B, Joss S, Gucsavas-Calikoglu M, Shiloh-Malawsky S, Perilla-Young Y, Thompson O, Champaigne N, Chiratti L, Ferilli M, Tartaglia M, Priolo M, Clementina R, Achkar C, Koen Gassen, van den Boogard M, Roscioli T, McBride K, Lauzon J, Syryn H, Cools M, De Baere E, Faundes V, Repetto G, Josephi-Taylor S, Bournazos A, Cooper S, Owen N, Zhao X: Identifying new genotype/phenotype correlations for individuals carrying deleterious RERE variants. American College of Medical Genetics Conference, Los Angeles, CA Mar 2025 Notes: Poster.

Crane H; Giardine R; Pilchman L; Wright R; Gianforcaro K; Eisenberg G; Strong A; Wild KT; Zackai E; Dugoff L; Sparks T; Coleman B; Moldenhauer J: Prenatally Diagnosed Beare-Stevenson Cutis Gyrata Syndrome with a Novel Variant. American College of Medical Genetics Conference, Los Angeles, CA Mar 2025 Notes: Poster.

Rippert A, Strong A, Ahrens-Nicklas R: Characterization of Liver Disease in RASopathies. American College of Medical Genetics Conference, Los Angeles, CA Mar 2025 Notes: Platform.

Marshall RF, Landau-Prat D, Strong A, Katowitz JA, Katowitz WR. : Ocular and Systemic Abnormalities in Punctal Agenesis. Ophthalmic Plast Reconstr Surg 41(2): 209-212, Mar-Apr 2025.

Cardinale CJ, Liu Y, Kevadia A, Strong A, Watts VJ, Hakonarson H: The ulcerative colitis risk gene adenylyl cyclase 7 restrains the T helper 2 phenotype and Class II antigen presentation. J Crohns Colitis 19(3): jjaf030, Mar 2025.

Pingault V, Neiva-Vaz C, de Oliveira J, Martínez-Gil N, Lasa-Aranzasti A, Campos B, Lakeman IMM, Nibbeling EAR, Stoeva R, Jayakar P, Dabir T, Elloumi HZ, Strong A, Hanein S, Picard A, Ochsenbein F, Blanc P, Amiel J : Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum. European Journal of Human Genetics 33(1): 131-136, Jan 2025.

Gold JI, Strong A, Gold NB, Yudkoff M, Szalda D, Jan S, Schwartz LA, Ganetzky R: Executive and adaptive function impacts long-term outcomes for adults with maple syrup urine disease. Journal of Inherited Metabolic Disease 48(1): e12827, Jan 2025.