Examination of AVPR1a as an autism susceptibility gene von Wassink, T H, Piven, J, Vieland, V J, Pietila, J, Goedken, R J, Folstein, S E, Sheffield, V C

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Analysis of the RELN gene as a genetic risk factor for autism von Skaar, D A, Shao, Y, Haines, J L, Stenger, J E, Jaworski, J, Martin, E R, DeLong, G R, Moore, J H, McCauley, J L, Sutcliffe, J S, Ashley-Koch, A E, Cuccaro, M L, Folstein, S E, Gilbert, J R, Pericak-Vance, M A

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Genetics of autism: complex aetiology for a heterogeneous disorder von Folstein, S E, Rosen-Sheidley, B

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Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism von McCauley, J.L., Olson, L.M., Dowd, M., Amin, T., Steele, A., Blakely, R.D., Folstein, S.E., Haines, J.L., Sutcliffe, J.S.

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Macrocephaly in Children and Adults With Autism von LAINHART, JANET E., PIVEN, JOSEPH, WZOREK, MARYANN, LANDA, REBECCA, SANTANGELO, SUSAN L., COON, HILARY, FOLSTEIN, SUSAN E.

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Predictors of Cognitive Test Patterns in Autism Families von Folstein, S. E., Santangelo, S. L., Gilman, S. E., Piven, J., Landa, R., Lainhart, J., Hein, J., Wzorek, M.

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Chromosome 7q: Where Autism Meets Language Disorder? von Folstein, Susan E., Mankoski, Raymond E.

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Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12 von McInnis, M G, Lan, T-H, Willour, V L, McMahon, F J, Simpson, S G, Addington, A M, MacKinnon, D F, Potash, J B, Mahoney, A T, Chellis, J, Huo, Y, Swift-Scanlan, T, Chen, H, Koskela, R, Colin Stine, O, Jamison, K R, Holmans, P, Folstein, S E, Ranade, K, Friddle, C, Botstein, D, Marr, T, Beaty, T H, Zandi, P, Raymond DePaulo, J

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Early Loss of Neostriatal Striosome Neurons in Huntingtonʼs Disease von HEDREEN, JOHN C, FOLSTEIN, SUSAN E

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Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism von Nurmi, E L, Amin, T, Olson, L M, Jacobs, M M, McCauley, J L, Lam, A Y, Organ, E L, Folstein, S E, Haines, J L, Sutcliffe, J S

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Trial of d-alpha-tocopherol in Huntington's disease von PEYSER, C. E, FOLSTEIN, M, CHASE, G. A, STARKSTEIN, S, BRANDT, J, COCKRELL, J. R, BYLSMA, F, COYLE, J. T, MCHUGH, P. R, FOLSTEIN, S. E

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Affective Disorders in People with Autism: A Review of Published Cases von Lainhart, Janet E, Folstein, Susan E

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A controlled trial of idebenone in Huntington's disease von Ranen, Neal G., Peyser, Carol E., Coyle, Joseph T., Bylsma, Frederick W., Sherr, Meeia, Day, Leslie, Folstein, Marshal F., Brandt, Jason, Ross, Christopher A., Folstein, Susan E.

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Trinucleotide repeat length instability and age of onset in Huntington's disease von Duyao, M, Ambrose, C, Myers, R, Novelletto, A, Persichetti, F, Frontali, M, Folstein, S, Ross, C, Franz, M, Abbott, M, Gray, J, Conneally, P, Young, A, Penney, J, Hollingsworth, Z, Shoulson, I, Lazzarini, A, Falek, A, Koroshetz, W, Sax, D, Bird, E, Vonsattel, J, Bonilla, E, Alvir, J, Bickham Conde, J, Cha, J.-H, Dure, L, Gomez, F, Ramos, M, Sanchez-Ramos, J, Snodgrass, S, de Young, M, Wexler, N, Moscowitz, C, Penchaszadeh, G, MacFarlane, H, Anderson, M, Jenkins, B, Srinidhi, J, Barnes, G, Gusella, J, MacDonald, M

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Etiology of autism : genetic influences von FOLSTEIN, S. E, PIVEN, J

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Huntington's disease gene (IT15) is widely expressed in human and rat tissues von Li, S.-H., Schilling, G., Young, W.S., Li, X.-., Margolis, R.L., Stine, O.C., Wagster, M.V., Abbott, M.H., Franz, M.L., Ranen, N.G., Folstein, S.E., Hedreen, J.C., Ross, C.A.

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Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease von Hedreen, John C., Peyser, Carol E., Folstein, Susan E., Ross, Christopher A.

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Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15 von Stine, O.Collin, Pleasant, Nicole, Franz, Mary L., Abbott, Margaret H., Folstein, Susan E., Ross, Christopher A.

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Defining the autism minimum candidate gene region on chromosome 7 von Hutcheson, Holli B., Bradford, Y., Folstein, S.E., Gardiner, M.B., Santangelo, S.L., Sutcliffe, J.S., Haines, J.L.

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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia von The Psychiatric Genomics Consortium, The Autism Spectrum Disorders Working Group Of, Anney, Richard J L, Ripke, Stephan, Anttila, Verneri, Grove, Jakob, Holmans, Peter, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Robinson, Elise, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, a Jeremy, Wijsman, Ellen M, Werge, Thomas, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob a S, Vieland, Veronica J, Vicente, Astrid M, Vanengeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Sanders, Stephan J, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne Giørtz, Pedersen, Carsten Bøcker, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mortensen, Preben Bo, Mors, Ole, Morrow, Eric M, Moreno-De-Luca, Daniel, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, Mcmahon, William M, Mcgrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Lecouteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hougaard, David M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine Søholm, Haines, Jonathan L

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