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Gerard D Schellenberg, Ph.D.

Gerard D Schellenberg, Ph.D.

faculty photo
Professor of Pathology and Laboratory Medicine
Department: Pathology and Laboratory Medicine
Graduate Group Affiliations

Contact information
Department of Pathology and Laboratory Medicine
University of Pennsylvania School of Medicine
Room 609B, Stellar-Chance Laboratories
422 Curie Blvd.
Philadelphia, PA 19104
Education:
B.S. (Biochemistry/minor: Cell Biology)
University of California at Riverside, Riverside, California, 1973.
Ph.D. (Biochemistry/minor- Cell Biology)
University of California at Riverside, Riverside, California, 1978.
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Selected Publications

Chen-Plotkin, A.S., Martinez-Lage, M., Sleiman, P.M.A., Hu, W., Greene, R., McCarty Wood, E., Bing, S., Grossman, M., Schellenberg, G.D., Kimmo, H., Weiner, M.F., White, C.L., Brooks, W., Halliday, G.M., Kril, J.J., Gearing, M., Beach, T.G., Graff-Radford, N.R., Dickson, D.W., Rademakers, R., Boeve, B.F., Pickering-Brown, S.M., Snowden, J., van Swieten, J.C., Murrell, J.R., Ghetti, B., Spina, S., Grafman, J., Kaye, J.A., Woltjer. R.L., Mesulam, M., Lladó, A., Miller, B.L., Alzualde, A., Moreno, F., Rohrer, J.D., Mackenzie, I.R.A., Feldman, H.H., Hamilton, R.L., Cruts, M., Engelborghs, S., De Deyn, P.P., Van Broeckhoven, C., Mayeux, R.,. Vonsattel, J.P.G., Bird, T.D., Cairns, N.J., Goate, A., Frosch, M.P., Riederer, P.F., Bogdanovic, N., Lee, V. M.-Y., Trojanowski, J.Q., Van Deerlin, V.M.: Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Arch. Neurol. 68(4): 488-97, April 2011 Notes: PMID:21482928.

Huentelman MJ, Myers AJ, Barmada MM, Demirci FY, Baldwin CT, Green RC, Rogaeva E, George-Hyslop PS, Arnold SE, Barber R, Beach T, Bigio EH, Bowen JD, Boxer A, Burke JR, Cairns NJ, Carlson CS, Carney RM, Carroll SL, Chui HC, Clark DG, Corneveaux J, Cotman CW, Cummings JL, Decarli C, Dekosky ST, Diaz-Arrastia R, Dick M, Dickson DW, Ellis WG, Faber KM, Fallon KB, Farlow MR, Ferris S, Frosch MP, Galasko DR, Ganguli M, Gearing M, Geschwind DH, Ghetti B, Gilbert JR, Gilman S, Giordani B, Glass JD, Growdon JH, Hamilton RL, Harrell LE, Head E, Honig LS, Hulette CM, Hyman BT, Jicha GA, Jin LW, Johnson N, Karlawish J, Karydas A, Kaye JA, Kim R, Koo EH, Kowall NW, Lah JJ, Levey AI, Lieberman AP, Lopez OL, Mack WJ, Marson DC, Martiniuk F, Mash DC, Masliah E, McCormick WC, McCurry SM, McDavid AN, McKee AC, Mesulam M, Miller BL, Miller CA, Miller JW, Parisi JE, Perl DP, Peskind E, Petersen RC, Poon WW, Quinn JF, Rajbhandary RA, Raskind M, Reisberg B, Ringman JM, Roberson ED, Rosenberg RN, Sano M, Schneider LS, Seeley W, Shelanski ML, Slifer MA, Smith CD, Sonnen JA, Spina S, Stern RA, Tanzi RE, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Vinters HV, Vonsattel JP, Weintraub S, Welsh-Bohmer KA, Williamson J, Woltjer RL, Cantwell LB, Dombroski BA, Beekly D, Lunetta KL, Martin ER, Kamboh MI, Saykin AJ, Reiman EM, Bennett DA, Morris JC, Montine TJ, Goate AM, Blacker D, Tsuang DW, Hakonarson H, Kukull WA, Foroud TM, Haines JL, Mayeux R, Pericak-Vance MA, Farrer LA, Schellenberg GD.: Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet. April 2011 Notes: PMID:21460841.

Kohen R, Shofer JB, Korvatska O, Petrie EC, Wang LY, Schellenberg GD, Peskind ER, Wilkinson CW. : ABCB1 Genotype and CSF {beta}-Amyloid in Alzheimer Disease. J Geriatr Psychiatry Neurol April 2011 Notes: PMID:21478475.

Korvatska O, Estes A, Munson J, Dawson G, Bekris LM, Kohen R, Yu CE, Schellenberg GD, Raskind WH. : Mutations in the TSGA14 gene in families with autism spectrum disorders. Am J Med Genet B Neuropsychiatr Genet. April 2011 Notes: PMID:21438139.

Jayadev, S., Nochlin, D., Poorkaj, P., Steinbart, E.J., Mastrianni, J.A., Montine, T., Ghetti, B., Schellenberg, G.D., Bird, T.D., Leverenz, J.B.: Familial Prion Disease in a family with a rare truncating mutation in PRNP (Q160X): clinical, pathological, and biochemical features. Anal. Neurol. March 2011 Notes: PMID:21416485.

Bekris LM, Galloway NM, Millard S, Lockhart D, Li G, Galasko DR, Farlow MR, Clark CM, Quinn JF, Kaye JA, Schellenberg GD, Leverenz JB, Seubert P, Tsuang DW, Peskind ER, Yu CE. : Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease. Neurobiol Aging. 32(3): 13-23, March 2011 Notes: PMID:21196064.

Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM. : Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16. Hum Genet. 129(1): 59-70, Jan 2011 Notes: PMID:20963441.

Melrose H L, Dächsel J C, Behrouz B, Lincoln S J, Yue M, Hinkle K M, Kent C B, Korvatska E, Taylor J P, Witten L, Liang Y-Q, Beevers J E, Boules M, Dugger B N, Serna V A, Gaukhman A, Yu X, Castanedes-Casey M, Braithwaite A T, Ogholikhan S, Yu N, Bass D, Tyndall G, Schellenberg G D, Dickson D W, Janus C, Farrer M J: Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice. Neurobiology of disease Dec 2010 Notes: PMID:20659558.

Jun, G., Naj, A.C., Beecham, G.W., Wang, L.-S., Buros, J., Gallins, P.J., Buxbaum, J.D., Ertekin-Taner, N., Fallin, M.D., Friedland, R., Rivka Inzelberg, R., Kramer, P., Rogaeva, E., St George-Hyslop, P., ADGC, Cantwell, L., Dombrosk, B.A., Saykin, A.J., Reiman, E.M., Bennett, D.A., Morris, J.C., Lunetta, K.L., Martin, E.R., Montine, T.J., Goate, A.M., Blacker, D., Tsuang, D.W., Beekly, D., Cupples, A.L., Hakonarson, H., Kukull, W., Foroud, T.M., Haines, J., Mayeux, R., Farrer, L.A., Pericak-Vance, M.A., Schellenberg, G.D.,: Meta-Analysis confirms CR1, CLU, and PICALM as Alzheimer’s disease risk loci and reveals interactions with APOE genotypes. Arch. Neurol. 67: 1473-84, Dec 2010 Notes: PMID:20697030.

Lajonchere CM; AGRE Consortium. : Changing the landscape of autism research: the autism genetic resource exchange. Neuron. 68(2): 187-91, Oct 2010 Notes: PMID:20955925.

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Last updated: 05/04/2011
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