Bevacizumab and chemotherapy for recurrent glioblastoma : A single-institution experience von NGHIEMPHU, P. L, LIU, W, NELSON, S. F, ELASHOFF, R, CLOUGHESY, T. F, LEE, Y, THAN, T, GRAHAM, C, LAI, A, GREEN, R. M, POPE, W. B, LIAU, L. M, MISCHEL, P. S

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Analysis of Oncogenic Signaling Networks in Glioblastoma Identifies ASPM as a Molecular Target von Horvath, S., Zhang, B., Carlson, M., Lu, K. V., Zhu, S., Felciano, R. M., Laurance, M. F., Zhao, W., Qi, S., Chen, Z., Lee, Y., Scheck, A. C., Liau, L. M., Wu, H., Geschwind, D. H., Febbo, P. G., Kornblum, H. I., Cloughesy, T. F., Nelson, S. F., Mischel, P. S.

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Targeted massively parallel sequencing provides comprehensive genetic diagnosis for patients with disorders of sex development von Arboleda, VA, Lee, H, Sánchez, FJ, Délot, EC, Sandberg, DE, Grody, WW, Nelson, SF, Vilain, E

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Insulin growth factor-binding protein 2 is a candidate biomarker for PTEN status and PI3K/Akt pathway activation in glioblastoma and prostate cancer von Mehrian-Shai, R, Chen, C.D, Shi, T, Horvath, S, Nelson, S.F, Reichardt, J.K.V, Sawyers, C.L

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Differential Gene Expression in Glioblastoma Defined by ADC Histogram Analysis: Relationship to Extracellular Matrix Molecules and Survival von POPE, W. B, MIRSADRAEI, L, NELSON, S. F, YONG, W, PHILLIPS, H. S, CLOUGHESY, T. F, LAI, A, ESKIN, A, QIAO, J, KIM, H. J, ELLINGSON, B, NGHIEMPHU, P. L, KHARBANDA, S, SORIANO, R. H

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High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene von Strom, S P, Stone, J L, ten Bosch, J R, Merriman, B, Cantor, R M, Geschwind, D H, Nelson, S F

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Biased paternal transmission of SNAP-25 risk alleles in attention-deficit hyperactivity disorder von Kustanovich, V, Merriman, B, McGough, J, McCracken, J T, Smalley, S L, Nelson, S F

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Transmission disequilibrium testing of dopamine-related candidate gene polymorphisms in ADHD: confirmation of association of ADHD with DRD4 and DRD5 von Kustanovich, V, Ishii, J, Crawford, L, Yang, M, McGough, J J, McCracken, J T, Smalley, S L, Nelson, S F

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Temperature-independent transport in high-mobility pentacene transistors von Nelson, S. F., Lin, Y.-Y., Gundlach, D. J., Jackson, T. N.

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Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD) von MCCRACKEN, J. T, SMALLEY, S. L, MCGOUGH, J. J, CRAWFORD, L, DEL'HOMME, M, CANTOR, R. M, LIU, A, NELSON, S. F

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Stacked pentacene layer organic thin-film transistors with improved characteristics von Lin, Y.-Y., Gundlach, D.J., Nelson, S.F., Jackson, T.N.

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Solvent-induced phase transition in thermally evaporated pentacene films von Gundlach, D. J., Jackson, T. N., Schlom, D. G., Nelson, S. F.

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Pentacene organic thin-film transistors-molecular ordering and mobility von Gundlach, D.J., Lin, Y.Y., Jackson, T.N., Nelson, S.F., Schlom, D.G.

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Evidence that the dopamine D4 receptor is a susceptibility gene in attention deficit hyperactivity disorder von Smalley, S L, Bailey, J N, Palmer, C G, Cantwell, D P, McGough, J J, Del'Homme, M A, Asarnow, J R, Woodward, J A, Ramsey, C, Nelson, S F

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Rare deleterious mutations are associated with disease in bipolar disorder families von Rao, A R, Yourshaw, M, Christensen, B, Nelson, S F, Kerner, B

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Detection of differentially expressed genes in primary tumor tissues using representational differences analysis coupled to microarray hybridization von Welford, Scott M, Gregg, Jeff, Chen, Emily, Garrison, Darryl, Sorensen, Poul H, Denny, Christopher T, Nelson, Stanley F

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A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia von JEN, J, YUE, Q, NELSON, S. F, YU, H, LITT, M, NUTT, J, BALOH, R. W

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Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy von JEN, J. C, WANG, H, LEE, H, SABATTI, C, TRENT, R, HANNIGAN, I, BRANTBERG, K, HALMAGYI, G. M, NELSON, S. F, BALOH, R. W

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Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25 von JEN, J, COULIN, C. J, BOSLEY, T. M, SALIH, M. A. M, SABATTI, C, NELSON, S. F, BALOH, R. W

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Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia von JEN, J. C, LEE, H, CHA, Y. H, NELSON, S. F, BALOH, R. W

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