Oxide Electronics by Spatial Atomic Layer Deposition von Levy, D.H., Nelson, S.F., Freeman, D.

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Pentacene-based organic thin-film transistors von Yen-Yi Lin, Gundlach, D.I., Nelson, S.F., Jackson, T.N.

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ZnO Thin-Film Transistor Ring Oscillators with 31-ns Propagation Delay von Jie Sun, Mourey, D.A., Dalong Zhao, Sung Kyu Park, Nelson, S.F., Levy, D.H., Freeman, D., Cowdery-Corvan, P., Tutt, L., Jackson, T.N.

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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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EE204 All-Cause Healthcare Costs By Race Among Medicaid-Insured Males with Duchenne Muscular Dystrophy Using U.S. Real-World Data von Posner, N., Manjelievskaia, J., Talaga, A.K., Richards, M., Lew, C., Merla, V., Alvir, J., Nelson, S.F.

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D.I.4 Patient fibroblast functional complementation studies: A valuable tool in the identification of novel Walker–Warburg syndrome disease genes von Willer, T, Lee, H, Lommel, M, Yoshida-Moriguchi, T, Beltran Valero de Bernabe, D, Venzke, D, Cirak, S, Schachter, H, Vajsar, J, Voit, T, Muntoni, F, Strahl, S, Mathews, K.D, Nelson, S.F, Moore, S.A, Campbell, K.P

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Mutations in Pycr1 cause progeroid changes in skin and bone due to reduced mitochondrial stress resistance von Reversade, B, Escande-Beillard, N, Dimopoulou, A, Fischer, B, Li, Y, Kayserili, H, Al-Gazali, L, Brancati, F, Lee, H, O'Connor, B, Kornak, U, Schmidt-von Kegler, M, Merriman, B, Nelson, S.F, Masri, A, Guerra, D, nanda, A, Rajab, A, Grix, A, Sommer, A, Janecke, A.R, Steichen, E, Nürnberg, P, Seemann, P, Zambruno, G, Dallapiccola, B, Schuelke, M, Robertson, S, Hamamy, H, Wollnik, B, Van Maldergem, L, Mundlos, S

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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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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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CREB regulates Meis1 expression in normal and malignant hematopoietic cells von Esparza, S D, Chang, J, Shankar, D B, Zhang, B, Nelson, S F, Sakamoto, K M

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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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Sex chromosome anomalies in childhood onset schizophrenia: an update von Eckstrand, K, Addington, A M, Stromberg, T, Merriman, B, Miller, R, Gochman, P, Long, R, Dutra, A, Chen, Z, Meltzer, P, Nelson, S F, Rapoport, J L

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P97. Loss of CHSY1, a novel FRINGE enzyme, causes syndromic brachydactyly via increased NOTCH signaling von Tian, A.J., Ling, L., Shboul, M., Lee, H., O'Connor, B., Merriman, B., Nelson, S.F., Cool, S., Ababneh, O.H., Al-Hadidy, A., Masri, A., Hamamy, H., Reversade, B.

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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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Genomic mismatch scanning: a new approach to genetic linkage mapping von Nelson, S.F.

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Genomic mismatch scanning: a new approach to genetic linkage mapping von Nelson, S.F. (Stanford University Medical Center, Stanford, CT), McCusker, J.H, Sander, M.A, Kee, Y, Modrich, P, Brown, P.O

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Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes von HU, G, MODREK, B, RIISE STENSLAND, H. M. F, SAARELA, J, PAJUKANTA, P, KUSTANOVICH, V, PELTONEN, L, NELSON, S. F, LEE, C

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KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants (vol 21, 10.1038/s41436-018-0259-2, 2019) von Kennedy, J., Goudie, D., Blair, E., Chandler, K., Joss, S., McKay, V., Green, A., Armstrong, R., Lees, M., Kamien, B., Hopper, B., Tan, T.Y., Yap, P., Stark, Z., Okamoto, N., Miyake, N., Matsumoto, N., Macnamara, E., Murphy, J.L., McCormick, E., Hakonarson, H., Falk, M.J., Li, D., Blackburn, P., Klee, E., Babovic-Vuksanovic, D., Schelley, S., Hudgins, L., Kant, S., Isidor, B., Cogne, B., Bradbury, K., Williams, M., Patel, C., Heussler, H., Duff-Farrier, C., Lakeman, P., Scurr, I., Kini, U., Elting, M., Reijnders, M., Schuurs-Hoeijmakers, J., Wafik, M., Blomhoff, A., Ruivenkamp, C.A.L., Nibbeling, E., Dingemans, A.J.M., Douine, E.D., Nelson, S.F., Hempel, M., Bierhals, T., Lessel, D., Johannsen, J., Arboleda, V.A., Newbury-Ecob, R.

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