Allelic Heterogeneity at the Serotonin Transporter Locus ( SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors
Sutcliffe, James S., Delahanty, Ryan J., Prasad, Harish C., McCauley, Jacob L., Han, Qiao, Jiang, Lan, Li, Chun, Folstein, Susan E., Blakely, Randy D.
Published in American journal of human genetics (01.08.2005)
Published in American journal of human genetics (01.08.2005)
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Overlap between autism and specific language impairment: comparison of Autism Diagnostic Interview and Autism Diagnostic Observation Schedule scores
Leyfer, Ovsanna T, Tager-Flusberg, Helen, Dowd, Michael, Tomblin, J Bruce, Folstein, Susan E
Published in Autism research (01.10.2008)
Published in Autism research (01.10.2008)
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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Vorstman, Jacob A.S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bacchelli, Elena, Gallinger, Steven, Cotterchio, Michelle, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, Jiménez González, Patricia, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen W.
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Weiner, Daniel J, Wigdor, Emilie M, Ripke, Stephan, Walters, Raymond K, Kosmicki, Jack A, Grove, Jakob, Samocha, Kaitlin E, Goldstein, Jacqueline I, Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J, Robinson, Elise B
Published in Nature genetics (01.07.2017)
Published in Nature genetics (01.07.2017)
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Comorbid Psychiatric Disorders in Children with Autism: Interview Development and Rates of Disorders
Leyfer, Ovsanna T, Folstein, Susan E, Bacalman, Susan, Davis, Naomi O, Dinh, Elena, Morgan, Jubel, Tager-Flusberg, Helen, Lainhart, Janet E
Published in Journal of autism and developmental disorders (01.10.2006)
Published in Journal of autism and developmental disorders (01.10.2006)
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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates
McCauley, Jacob L, Li, Chun, Jiang, Lan, Olson, Lana M, Crockett, Genea, Gainer, Kimberly, Folstein, Susan E, Haines, Jonathan L, Sutcliffe, James S
Published in BMC medical genetics (12.01.2005)
Published in BMC medical genetics (12.01.2005)
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Functional impact of global rare copy number variation in autism spectrum disorders
Gillberg, Christopher, Kolevzon, Alexander, Nelson, Stanley F, Sansom, Katherine, Casallo, Guillermo, Miller, Judith, Brennan, Sean, Leboyer, Marion, Bacchelli, Elena, Delorme, Richard, Fombonne, Eric, Hallmayer, Joachim, Green, Jonathan, Pickles, Andrew, Heron, Elizabeth A, Salt, Jeff, Battaglia, Agatino, Klauck, Sabine M, McDougle, Christopher J, Mahoney, William, Noor, Abdul, Cytrynbaum, Cheryl, Sato, Daisuke, Almeida, Joana, Korvatska, Olena, Dawson, Geraldine, Bierut, Laura J, Coon, Hilary, Rickaby, Jessica, Freitag, Christine M, Roeder, Kathryn, Bader, Gary D, Wijsman, Ellen M, Vincent, John B, Hakonarson, Hakon, Segurado, Ricardo, Paton, Tara, Roge, Bernadette, Ennis, Sean, Kim, Cecilia, Monaco, Anthony P, Paterson, Andrew D, Crossett, Andrew, McGrath, Jane, Carson, Andrew R, Le Couteur, Ann, Cook, Edwin H, Chung, Brian H.Y, Cuccaro, Michael L, Van Engeland, Herman, Conroy, Judith, Holt, Richard, Strawbridge, Christina, Kustanovich, Vlad, Migita, Ohsuke, Stoppioni, Vera, Igliozzi, Roberta, Poustka, Fritz, Stein, Olaf, Posey, David J, Sheffield, Val C, Duque, Frederico, Parrini, Barbara, Berney, Tom, Hus, Vanessa, Baird, Gillian, Duketis, Eftichia, Soorya, Latha, Corsello, Christina, Drmic, Irene, Sousa, Inês, Abrahams, Brett S, Thomson, Susanne, Lajonchere, Clara M, Tsiantis, John, Pinto, Dalila, Green, Andrew, Hughes, Gillian, Mantoulan, Carine, Betancur, Catalina, Volkmar, Fred, Poustka, Annemarie, Shah, Naisha, Bryson, Susan E, Munson, Jeff, Tancredi, Raffaella, Nygren, Gudrun, Wittemeyer, Kerstin, Merikangas, Alison, Oliveira, Guiomar, Farrar, Penny, Maestrini, Elena, Liu, Xiao-Qing, Gallagher, Louise, McConachie, Helen, Zurawiecki, Danielle, Schellenberg, Gerard D, Glessner, Joseph T, Lord, Catherine, Piven, Joseph
Published in Nature (London) (15.07.2010)
Published in Nature (London) (15.07.2010)
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Individual common variants exert weak effects on the risk for autism spectrum disorders
Anney, Richard, Klei, Lambertus, Pinto, Dalila, Almeida, Joana, Bacchelli, Elena, Baird, Gillian, Bolshakova, Nadia, Bölte, Sven, Bolton, Patrick F, Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Casey, Jillian, Conroy, Judith, Correia, Catarina, Corsello, Christina, Crawford, Emily L, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A, Folstein, Susan E, Fombonne, Eric, Gilbert, John, Gillberg, Christopher, Glessner, Joseph T, Green, Andrew, Green, Jonathan, Guter, Stephen J, Heron, Elizabeth A, Holt, Richard, Howe, Jennifer L, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Jacob, Suma, Kenny, Graham P, Kim, Cecilia, Kolevzon, Alexander, Kustanovich, Vlad, Lajonchere, Clara M, Lamb, Janine A, Law-Smith, Miriam, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L, Liu, Xiao-Qing, Lombard, Frances, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C, Magalhaes, Tiago R, Mantoulan, Carine, McDougle, Christopher J, Melhem, Nadine M, Merikangas, Alison, Minshew, Nancy J, Mirza, Ghazala K, Munson, Jeff, Noakes, Carolyn, Nygren, Gudrun, Papanikolaou, Katerina, Pagnamenta, Alistair T, Parrini, Barbara, Paton, Tara, Pickles, Andrew, Posey, David J, Poustka, Fritz, Ragoussis, Jiannis, Regan, Regina, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L, Schlitt, Sabine, Shah, Naisha, Sheffield, Val C, Soorya, Latha, Sousa, Inês, Stoppioni, Vera, Sykes, Nuala, Tancredi, Raffaella, Thompson, Ann P, Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B, Volkmar, Fred, Vorstman, J A S, Wallace, Simon, Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Bailey, Anthony J
Published in Human molecular genetics (01.11.2012)
Published in Human molecular genetics (01.11.2012)
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Early Loss of Neostriatal Striosome Neurons in Huntingtonʼs Disease
HEDREEN, JOHN C, FOLSTEIN, SUSAN E
Published in Journal of neuropathology and experimental neurology (01.01.1995)
Published in Journal of neuropathology and experimental neurology (01.01.1995)
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Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families
Nurmi, Erika L., Bradford, Yuki, Chen, Yi-hui, Hall, Jenifer, Arnone, Brenda, Gardiner, Mary Beth, Hutcheson, Holli B., Gilbert, John R., Pericak-Vance, Margaret A., Copeland-Yates, Susan A., Michaelis, Ron C., Wassink, Thomas H., Santangelo, Susan L., Sheffield, Val C., Piven, Joseph, Folstein, Susan E., Haines, Jonathan L., Sutcliffe, James S.
Published in Genomics (San Diego, Calif.) (01.09.2001)
Published in Genomics (San Diego, Calif.) (01.09.2001)
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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Casey, Jillian P., Magalhaes, Tiago, Conroy, Judith M., Regan, Regina, Shah, Naisha, Anney, Richard, Shields, Denis C., Almeida, Joana, Bacchelli, Elena, Battaglia, Agatino, Berney, Tom, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Cali, Phil, Correia, Catarina, Corsello, Christina, Coutanche, Marc, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Foley, Suzanne, Fombonne, Eric, Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Green, Jonathan, Holt, Richard, Hus, Vanessa, Klauck, Sabine M., Le Couteur, Ann, Leventhal, Bennett L., Lord, Catherine, Maestrini, Elena, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McMahon, William M., Merikangas, Alison, Minopoli, Fiorella, Mirza, Ghazala K., Munson, Jeff, Nygren, Gudrun, Oliveira, Guiomar, Pagnamenta, Alistair T., Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Pickles, Andrew, Pinto, Dalila, Piven, Joseph, Posey, David J., Poustka, Annemarie, Poustka, Fritz, Ragoussis, Jiannis, Rutter, Michael L., Soorya, Latha, Sousa, Inês, Tancredi, Raffaella, Tauber, Maïté, Thompson, Ann P., Thomson, Susanne, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Vorstman, Jacob A. S., Wang, Kai, Wassink, Thomas H., White, Kathy, Wing, Kirsty, Wittemeyer, Kerstin, Yaspan, Brian L., Zwaigenbaum, Lonnie, Betancur, Catalina, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Geschwind, Daniel H., Monaco, Anthony P., Nurnberger, John I., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Sutcliffe, James S., Szatmari, Peter, Wijsman, Ellen M., Green, Andrew, Gill, Michael, Gallagher, Louise, Vicente, Astrid, Ennis, Sean
Published in Human genetics (01.04.2012)
Published in Human genetics (01.04.2012)
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Evaluation of FOXP2 as an autism susceptibility gene
Wassink, Thomas H, Piven, Joseph, Vieland, Veronica J, Pietila, Jennifer, Goedken, Rhinda J, Folstein, Susan E, Sheffield, Val C
Published in American journal of medical genetics (08.07.2002)
Published in American journal of medical genetics (08.07.2002)
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Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes
Hutcheson, Holli B, Olson, Lana M, Bradford, Yuki, Folstein, Susan E, Santangelo, Susan L, Sutcliffe, James S, Haines, Jonathan L
Published in BMC medical genetics (05.05.2004)
Published in BMC medical genetics (05.05.2004)
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"The presentation and classification of anxiety in autism spectrum disorder": Commentary
Folstein, Susan E., Carbajal, Jessica
Published in Clinical psychology (New York, N.Y.) (01.12.2012)
Published in Clinical psychology (New York, N.Y.) (01.12.2012)
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A genome-wide scan for common alleles affecting risk for autism
Pinto, Dalila, Regan, Regina, Magalhaes, Tiago R., Abrahams, Brett S., Pagnamenta, Alistair T., Almeida, Joana, Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Bolshakova, Nadia, Bölte, Sven, Bolton, Patrick F., Brennan, Sean, Carson, Andrew R., Casallo, Guillermo, Chu, Su H., Cochrane, Lynne, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Fernandez, Bridget A., Fombonne, Eric, Freitag, Christine M., Glessner, Joseph T., Goldberg, Jeremy, Green, Jonathan, Heron, Elizabeth A., Holt, Richard, Hughes, Gillian, Hus, Vanessa, Kim, Cecilia, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M., Leboyer, Marion, Leventhal, Bennett L., Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Marshall, Christian R., McConachie, Helen, McMahon, William M., Melhem, Nadine M., Merikangas, Alison, Migita, Ohsuke, Munson, Jeff, Nelson, Stanley F., Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Papanikolaou, Katerina, Parr, Jeremy R., Poustka, Annemarie, Poustka, Fritz, Prasad, Aparna, Renshaw, Katy, Rickaby, Jessica, Roberts, Wendy, Roge, Bernadette, Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Sato, Daisuke, Segurado, Ricardo, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Stoppioni, Vera, Tancredi, Raffaella, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Van Engeland, Herman, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Wittemeyer, Kerstin, Wood, Shawn, Yaspan, Brian L., Zurawiecki, Danielle, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Haines, Jonathan L., Paterson, Andrew D., Sutcliffe, James S., Szatmari, Peter, Vicente, Astrid M., Wijsman, Ellen M., Devlin, Bernie, Hallmayer, Joachim
Published in Human molecular genetics (15.10.2010)
Published in Human molecular genetics (15.10.2010)
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Szatmari, Peter, Paterson, Andrew D, Zwaigenbaum, Lonnie, Roberts, Wendy, Brian, Jessica, Liu, Xiao-Qing, Vincent, John B, Skaug, Jennifer L, Thompson, Ann P, Senman, Lili, Feuk, Lars, Qian, Cheng, Bryson, Susan E, Jones, Marshall B, Marshall, Christian R, Scherer, Stephen W, Vieland, Veronica J, Bartlett, Christopher, Mangin, La Vonne, Goedken, Rhinda, Segre, Alberto, Pericak-Vance, Margaret A, Cuccaro, Michael L, Gilbert, John R, Wright, Harry H, Abramson, Ruth K, Betancur, Catalina, Bourgeron, Thomas, Gillberg, Christopher, Leboyer, Marion, Buxbaum, Joseph D, Davis, Kenneth L, Hollander, Eric, Silverman, Jeremy M, Hallmayer, Joachim, Lotspeich, Linda, Sutcliffe, James S, Haines, Jonathan L, Folstein, Susan E, Piven, Joseph, Wassink, Thomas H, Sheffield, Val, Geschwind, Daniel H, Bucan, Maja, Brown, W Ted, Cantor, Rita M, Constantino, John N, Gilliam, T Conrad, Herbert, Martha, Lajonchere, Clara, Ledbetter, David H, Lese-Martin, Christa, Miller, Janet, Nelson, Stan, Samango-Sprouse, Carol A, Spence, Sarah, State, Matthew, Tanzi, Rudolph E, Coon, Hilary, Dawson, Geraldine, Devlin, Bernie, Estes, Annette, Flodman, Pamela, Klei, Lambertus, McMahon, William M, Minshew, Nancy, Munson, Jeff, Korvatska, Elena, Rodier, Patricia M, Schellenberg, Gerard D, Smith, Moyra, Spence, M Anne, Stodgell, Chris, Tepper, Ping Guo, Wijsman, Ellen M, Yu, Chang-En, Rogé, Bernadette, Mantoulan, Carine, Wittemeyer, Kerstin, Poustka, Annemarie, Felder, Bärbel, Klauck, Sabine M, Schuster, Claudia, Poustka, Fritz, Bölte, Sven, Feineis-Matthews, Sabine, Herbrecht, Evelyn, Schmötzer, Gabi, Tsiantis, John, Papanikolaou, Katerina, Maestrini, Elena, Bacchelli, Elena, Blasi, Francesca, Carone, Simona, Toma, Claudio, Van Engeland, Herman, de Jonge, Maretha, Kemner, Chantal, Koop, Frederieke, Koop, Frederike
Published in Nature genetics (01.03.2007)
Published in Nature genetics (01.03.2007)
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