Resultats de la cerca - Veronica J. Vieland

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  1. 1
    Bayesian Linkage Analysis, or: How I Learned to Stop Worrying and Love the Posterior Probability of Linkage

    Bayesian Linkage Analysis, or: How I Learned to Stop Worrying and Love the Posterior Probability of Linkage per Veronica J. Vieland

    Publicat 1998
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  2. 2
    Further Evidence for the Increased Power of LOD Scores Compared with Nonparametric Methods

    Further Evidence for the Increased Power of LOD Scores Compared with Nonparametric Methods per Martina Durner, Veronica J. Vieland, David A. Greenberg

    Publicat 1999
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  3. 3
    The impact of curriculum-based suicide prevention programs for teenagers: An 18-month follow-up

    The impact of curriculum-based suicide prevention programs for teenagers: An 18-month follow-up per Veronica J. Vieland, Barry Whittle, Ann F. Garland, Roger Hicks, David Shaffer

    Publicat 1991
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  4. 4
    Long‐range genomic regulators of <i>THBS1</i> and <i>LTBP4</i> modify disease severity in duchenne muscular dystrophy

    Long‐range genomic regulators of <i>THBS1</i> and <i>LTBP4</i> modify disease severity in duchenne muscular dystrophy per Robert B. Weiss, Veronica J. Vieland, Diane M. Dunn, Yuuki Kaminoh, Kevin M. Flanigan

    Publicat 2018
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  5. 5
    A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions

    A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions per Jaana Oikkonen, Yungui Huang, Päivi Onkamo, Liisa Ukkola‐Vuoti, Pirre Raijas, Kai Karma, Veronica J. Vieland, Irma Järvelä

    Publicat 2014
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  6. 6
    A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21

    A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21 per Christopher W. Bartlett, Judy F. Flax, Mark W. Logue, Veronica J. Vieland, Anne S. Bassett, Paula Tallal, Linda M. Brzustowicz

    Publicat 2002
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  7. 7
    Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment

    Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment per Christopher W. Bartlett, Judy F. Flax, Mark W. Logue, Brett J. Smith, Veronica J. Vieland, Paula Tallal, Linda M. Brzustowicz

    Publicat 2004
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  8. 8
    Incorporating language phenotypes strengthens evidence of linkage to autism

    Incorporating language phenotypes strengthens evidence of linkage to autism per Yuki Bradford, Jonathan L. Haines, Holli B. Hutcheson, Marybeth Gardiner, Terry A. Braun, Val C. Sheffield, Tom Cassavant, Wen Huang, Kai Wang, Veronica J. Vieland, Susan E. Folstein, Susan L. Santangelo, Joseph Piven

    Publicat 2001
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  9. 9
    Identification of a Schizophrenia-Associated Functional Noncoding Variant in<i>NOS1AP</i>

    Identification of a Schizophrenia-Associated Functional Noncoding Variant in<i>NOS1AP</i> per Naomi S. Wratten, Holly Memoli, Yungui Huang, Anna M. Dulencin, Paul G. Matteson, Michelle A. Cornacchia, Marco A. Azaro, Jaime S Messenger, Jared E. Hayter, Anne S. Bassett, Steven Buyske, James H. Millonig, Veronica J. Vieland, Linda M. Brzustowicz

    Publicat 2009
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  10. 10
    Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

    Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability per A. T. Pagnamenta, Hamza Khan, Susan Walker, Dianne Gerrelli, Kirsty Wing, María Clara Bonaglia, Roberto Giorda, T. P. Berney, Elisa Mani, Massimo Molteni, Dalila Pinto, Ann Le Couteur, Joachim Hallmayer, James S. Sutcliffe, Peter Szatmari, Andrew D. Paterson, Stephen W. Scherer, Veronica J. Vieland, Anthony P. Monaco

    Publicat 2010
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  11. 11
    Results of a genome-wide genetic screen for panic disorder

    Results of a genome-wide genetic screen for panic disorder per James A. Knowles, Abby J. Fyer, Veronica J. Vieland, Myrna M. Weissman, Susan E. Hodge, Gary A. Heiman, Fatemeh Haghighi, Gracielle M. de Jesus, Hilary Rassnick, X. Preud'homme-Rivelli, Travis Austin, J. Cunjak, Stephen S. Mick, Leonard Fine, K.A. Woodley, K. Das, W. Maier, Phillip Adams, Nelson B. Freimer, D F Klein, T. Conrad Gilliam

    Publicat 1998
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  12. 12
    <i>SRGAP1</i>Is a Candidate Gene for Papillary Thyroid Carcinoma Susceptibility

    <i>SRGAP1</i>Is a Candidate Gene for Papillary Thyroid Carcinoma Susceptibility per Huiling He, Agnieszka Bronisz, Sandya Liyanarachchi, Rebecca Nagy, Wei Li, Yungui Huang, Keiko Akagi, Motoyasu Saji, Dorota Kula, Anna Wójcicka, Nikhil Sebastian, Bernard Wen, Zbigniew Puch, Michał Kalemba, Elżbieta Stachlewska, Małgorzata Czetwertyńska, Joanna Długosińska, Kinga Dymecka, Rafał Płoski, Marek Krawczyk, Patrick J. Morrison, Matthew D. Ringel, Richard T. Kloos, Krystian Jażdżewski, David E. Symer, Veronica J. Vieland, Michael C. Ostrowski, Barbara Jarząb, Albert de la Chapelle

    Publicat 2013
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  13. 13
    The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

    The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism per Dexter Hadley, Zhi-liang Wu, Charlly Kao, Akshata Kini, Alisha Mohamed-Hadley, Kelly Thomas, Lyam Vazquez, Haijun Qiu, Frank Mentch, Renata Pellegrino, Cecilia Kim, John J. Connolly, Dalila Pinto, Alison Merikangas, Lambertus Klei, Jacob Vorstman, Ann Thompson, Regina Regan, Alistair T. Pagnamenta, Bárbara Oliveira, Tiago R. Magalhães, John R. Gilbert, Eftichia Duketis, Maretha Jonge, Michael L. Cuccaro, Catarina Correia, Judith Conroy, Inês C. Conceição, Andreas G. Chiocchetti, Jillian P. Casey, Nadia Bolshakova, Elena Bacchelli, Richard Anney, Lonnie Zwaigenbaum, Kerstin Wittemeyer, Simon Wallace, Hermán van Engeland, Latha Soorya, Bernadette Rogé, Wendy Roberts, Fritz Poustka, Susana Mouga, Nancy J. Minshew, Susan G. McGrew, Catherine Lord, Marion Leboyer, Ann S. Couteur, Alexander Kolevzon, Suma Jacob, Stephen J. Guter, Jonathan Green, Andrew Green, Christopher Gillberg, Bridget A. Fernandez, Frederico Duque, Richard Delorme, Géraldine Dawson, Cátia Café, S. Brennan, Thomas Bourgeron, Patrick Bolton, Sven Bölte, Raphael Bernier, Gillian Baird, Anthony Bailey, Evdokia Anagnostou, Joana Almeida, Ellen M. Wijsman, Veronica J. Vieland, Astrid M. Vicente, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Andrew D. Paterson, Jeremy Parr, Guiomar Oliveira, Joana Almeida, Cátia Café, Susana Mouga, Catarina Correia, John I. Nürnberger, Anthony P. Monaco, Elena Maestrini, Sabine M. Klauck, Hákon Hákonarson, Jonathan L. Haines, Daniel H. Geschwind, Christine M. Freitag, Susan E. Folstein, Sean Ennis, Hilary Coon, Agatino Battaglia, Peter Szatmari, James S. Sutcliffe, Joachim Hallmayer, Michael Gill, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Louise Gallagher, Catalina Betancur

    Publicat 2014
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  14. 14
    Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

    Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders per Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang, Jacob Vorstman, Ann Thompson, Regina Regan, Marion Pilorge, Giovanna Pellecchia, Alistair T. Pagnamenta, Bárbara Oliveira, Christian R. Marshall, Tiago R. Magalhães, Jennifer K. Lowe, Jennifer Howe, Anthony J. Griswold, John R. Gilbert, Eftichia Duketis, Beth A. Dombroski, Maretha Jonge, Michael L. Cuccaro, Emily L. Crawford, Catarina Correia, Judith Conroy, Inês C. Conceição, Andreas G. Chiocchetti, Jillian P. Casey, Guiqing Cai, Christelle Cabrol, Nadia Bolshakova, Elena Bacchelli, Richard Anney, Steven Gallinger, Michelle Cotterchio, Graham Casey, Lonnie Zwaigenbaum, Kerstin Wittemeyer, Kirsty Wing, Simon Wallace, Hermán van Engeland, Ana Tryfon, Susanne Thomson, Latha Soorya, Bernadette Rogé, Wendy Roberts, Fritz Poustka, Susana Mouga, Nancy J. Minshew, L. Alison McInnes, Susan G. McGrew, Catherine Lord, Marion Leboyer, Ann S. Couteur, Alexander Kolevzon, Patricia González, Suma Jacob, Richard Holt, Stephen J. Guter, Jonathan Green, Andrew Green, Christopher Gillberg, Bridget A. Fernandez, Frederico Duque, Richard Delorme, Géraldine Dawson, Pauline Chaste, Cátia Café, S. Brennan, Thomas Bourgeron, Patrick Bolton, Sven Bölte, Raphael Bernier, Gillian Baird, Anthony Bailey, Evdokia Anagnostou, Joana Almeida, Ellen M. Wijsman, Veronica J. Vieland, Astrid M. Vicente, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Andrew D. Paterson, Jeremy Parr, Guiomar Oliveira, John I. Nürnberger, Anthony P. Monaco, Elena Maestrini, Sabine M. Klauck, Hákon Hákonarson, Jonathan L. Haines, Daniel H. Geschwind, Christine M. Freitag, Susan E. Folstein, Sean Ennis

    Publicat 2014
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  15. 15
    Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Mapping autism risk loci using genetic linkage and chromosomal rearrangements per Peter Szatmari, Andrew D. Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiaoqing Liu, John B. Vincent, Jennifer Skaug, Ann Thompson, Lili Senman, Lars Feuk, Qian Cheng, Susan E. Bryson, Marshall B. Jones, Christian R. Marshall, Stephen W. Scherer, Veronica J. Vieland, Christopher W. Bartlett, La Vonne Mangin, Rhinda Goedken, Alberto M. Segre, Margaret A. Pericak‐Vance, Michael L. Cuccaro, John R. Gilbert, Harry H. Wright, Ruth K. Abramson, Catalina Betancur, Thomas Bourgeron, Christopher Gillberg, Marion Leboyer, Joseph D. Buxbaum, Kenneth L. Davis, Eric Hollander, Jeremy M. Silverman, Joachim Hallmayer, Linda Lotspeich, James S. Sutcliffe, Jonathan L. Haines, Susan E. Folstein, Joseph Piven, Thomas H. Wassink, Val C. Sheffield, Daniel H. Geschwind, Maja Bućan, W. Ted Brown, Rita M. Cantor, John N. Constantino, T. Conrad Gilliam, Martha R. Herbert, Clara Lajonchere, David H. Ledbetter, Christa Lese‐Martin, Janet Miller, Stan F. Nelson, Carol A Samango-Sprouse, Sarah Spence, Matthew W. State, Rudolph E. Tanzi, Hilary Coon, Géraldine Dawson, Bernie Devlin, Annette Estes, Pamela Flodman, Lambertus Klei, William M. McMahon, Nancy J. Minshew, Jeff Munson, Elena Korvatska, Patricia M. Rodier, Gerard D. Schellenberg, Moyra Smith, M. Anne Spence, Chris Stodgell, Ping G. Tepper, Ellen M. Wijsman, Chang-En Yu, Bernadette Rogé, Carine Mantoulan, Kerstin Wittemeyer, Annemarie Poustka, Bärbel Felder, Sabine M. Klauck, Claudia Schuster, Fritz Poustka, Sven Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, Gabi Schmötzer, John Tsiantis, Κaterina Papanikolaou, Elena Maestrini, Elena Bacchelli, Francesca Blasi, Simona Carone, Claudio Toma, Hermán van Engeland, Maretha Jonge, Chantal Kemner, Frederieke Koop, Frederike Koop

    Publicat 2007
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  16. 16
    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

    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 per Richard Anney, Stephan Ripke, Verneri Anttila, Jakob Grove, Peter Holmans, Aiden Corvin, Lambertus Klei, Phil H. Lee, Sarah E. Medland, Benjamin M. Neale, Elise Robinson, Lauren A. Weiss, Lonnie Zwaigenbaum, Timothy W. Yu, Kerstin Wittemeyer, A. Jeremy Willsey, Ellen M. Wijsman, Thomas Werge, Thomas H. Wassink, Regina Waltes, Christopher A. Walsh, Simon Wallace, Jacob Vorstman, Veronica J. Vieland, Astrid M. Vicente, Herman Vanengeland, Kathryn Tsang, Ann Thompson, Peter Szatmari, Oscar Svantesson, Stacy Steinberg, Kāri Stefánsson, Hreinn Stefánsson, Matthew W. State, Latha Soorya, Teimuraz Silagadze, Stephen W. Scherer, Gerard D. Schellenberg, Sven Sandin, Stephan Sanders, Evald Sæmundsen, Guy A. Rouleau, Bernadette Rogé, Kathryn Roeder, Wendy Roberts, Jennifer Reichert, Abraham Reichenberg, Karola Rehnström, Regina Regan, Fritz Poustka, Christopher S. Poultney, Joseph Piven, Dalila Pinto, Margaret A. Pericak‐Vance, Milica Pejović-Milovančević, Marianne Giørtz Pedersen, Carsten Bøcker Pedersen, Andrew D. Paterson, Jeremy Parr, Alistair T. Pagnamenta, Guiomar Oliveira, John I. Nürnberger, Merete Nordentoft, Michael T. Murtha, Susana Mouga, Preben Bo Mortensen, Ole Mors, Eric M. Morrow, Daniel Moreno‐De‐Luca, Anthony P. Monaco, Nancy J. Minshew, Alison Merikangas, William M. McMahon, Susan G. McGrew, Jouko Lönnqvist, Igor Martsenkovsky, Donna M. Martin, Shrikant Mane, Páll Magnússon, Tiago R. Magalhães, Elena Maestrini, Jennifer K. Lowe, Catherine Lord, Pat Levitt, Christa Lese Martin, David H. Ledbetter, Marion Leboyer, Ann S. LeCouteur, Christine Ladd‐Acosta, Alexander Kolevzon, Sabine M. Klauck, Suma Jacob, Bozenna Iliadou, Christina M. Hultman, David M. Hougaard, Irva Hertz‐Picciotto, Robert L. Hendren, Christine Søholm Hansen, Jonathan L. Haines, Stephen J. Guter

    Publicat 2017
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