Jacinda B Sampson, MD, PhD

Zhang F, Potocki L, Sampson JB, Liu P, Sanchez-Valle A, Robbins-Furman P, Navarro AD, Wheeler PG, Spence JE, Brasington CK, Withers MA, Lupski JR.
Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS.
Am J Hum Genet. 2010;86(3):462-70. PubMed abstract / Full Text

Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Gappmaier E, Howard MT, Sampson JB, Mendell JR, Wall C, King WM, Pestronk A, Florence JM, Connolly AM, Mathews KD, Stephan CM, Laubenthal KS, Wong BL, Morehart PJ, Meyer A, Finkel RS, Bonnemann CG, Medne L, Day JW, Dalton JC, Margolis MK, Hinton VJ, Weiss RB.
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Hum Mutat. 2009;30(12):1657-66. PubMed abstract

Sampson JB, Chin SS, Clayton FC, Pestronk A, Swoboda KJ, Flanigan KM.
An unusual pathologic feature associated with dermatomyositis.
Neuromuscul Disord. 2006;16(6):391-3. PubMed abstract

Davis IC, Zhu S, Sampson JB, Crow JP, Matalon S.
Inhibition of human surfactant protein A function by oxidation intermediates of nitrite.
Free Radic Biol Med. 2002;33(12):1703-13. PubMed abstract