Canlyniadau Chwilio - Moyra Smith

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  1. 1
    Developmental changes and polymorphism in human alcohol dehydrogenase

    Developmental changes and polymorphism in human alcohol dehydrogenase gan Moyra Smith, D. A. HOPKINSON, Harry Harris

    Cyhoeddwyd 1971
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  2. 2
    Nuclear and Mitochondrial Genome Defects in Autisms

    Nuclear and Mitochondrial Genome Defects in Autisms gan Moyra Smith, M. Anne Spence, Pamela Flodman

    Cyhoeddwyd 2008
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  3. 3
    Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients

    Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients gan Andrew Green, Moyra Smith, John R.W. Yates

    Cyhoeddwyd 1994
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  4. 4
    Autism and tuberous sclerosis

    Autism and tuberous sclerosis gan Susan L. Smalley, Peter E. Tanguay, Moyra Smith, Griselda Gutierrez

    Cyhoeddwyd 1992
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  5. 5
    Meta-analysis of genotype-phenotype analysis of OPA1 mutations in autosomal dominant optic atrophy

    Meta-analysis of genotype-phenotype analysis of OPA1 mutations in autosomal dominant optic atrophy gan Michelle Ham, Julia Han, Kathryn Osann, Moyra Smith, Virginia Kimonis

    Cyhoeddwyd 2018
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  6. 6
    Report of the Diagnostic Criteria Committee of the National Tuberous Sclerosis Association

    Report of the Diagnostic Criteria Committee of the National Tuberous Sclerosis Association gan E. Steve Roach, Moyra Smith, Peter R. Huttenlocher, Mohandes Bhat, Deborah Alcorn, Louise A. Hawley

    Cyhoeddwyd 1992
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  7. 7
    Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1–p34

    Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1–p34 gan Moyra Smith, Mitchell J. Weiss, Constance A. Griffin, Jeffrey C. Murray, Kenneth H. Buetow, Beverly S. Emanuel, Paula S. Henthorn, Harry Harris

    Cyhoeddwyd 1988
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  8. 8
    A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R

    A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB)... gan Subhadra Ramanathan, Abigail Woodroffe, Pamela Flodman, Lee Z. Mays, Mona Hanouni, Charlotte Modahl, Robin Steinberg-Epstein, Maureen Bocian, M. Anne Spence, Moyra Smith

    Cyhoeddwyd 2004
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  9. 9
    Mitochondrial and ion channel gene alterations in autism

    Mitochondrial and ion channel gene alterations in autism gan Moyra Smith, Pamela Flodman, J. Jay Gargus, Mariella Simon, Kimberley Verrell, Richard Haas, Gail Reiner, Robert K. Naviaux, K. Osann, M. Anne Spence, Douglas C. Wallace

    Cyhoeddwyd 2012
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  10. 10
    Dopamine genes and ADHD

    Dopamine genes and ADHD gan James M. Swanson, Pamela Flodman, Kristen M. Kennedy, M. Anne Spence, Robert K. Moyzis, Sabrina Schuck, Michael Murias, Joan Moriarity, Cathy L. Barr, Moyra Smith, Michael I. Posner

    Cyhoeddwyd 2000
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  11. 11
    Mitochondrial dysfunction in autistic patients with 15q inverted duplication

    Mitochondrial dysfunction in autistic patients with 15q inverted duplication gan Pauline A. Filipek, Jenifer Juranek, Moyra Smith, Lee Z. Mays, Erica R. Ramos, Maureen Bocian, Diane Masser‐Frye, Tracy M. Laulhere, Charlotte Modahl, M. Anne Spence, J. Jay Gargus

    Cyhoeddwyd 2003
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  12. 12
    Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome

    Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome gan Nancy Braverman, Paul Lin, Fabian F. Moebius, Cassandra Obie, Ann B. Moser, Hartmut Glossmann, William R. Wilcox, David L. Rimoin, Moyra Smith, Lisa E. Kratz, Richard I. Kelley, David Valle

    Cyhoeddwyd 1999
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  13. 13
    Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

    Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network gan Bernie Devlin, Pamela J. Bennett, Géraldine Dawson, Denise A. Figlewicz, Elena L. Grigorenko, William McMahon, Nancy J. Minshew, David L. Pauls, Moyra Smith, M. Anne Spence, Patricia M. Rodier, Chris Stodgell, Daniela Berg

    Cyhoeddwyd 2004
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  14. 14
    Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

    Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23 gan Moyra Smith, Susan L. Smalley, R M Cantor, Massimo Pandolfo, Maximiliano Gómez, Russell E Baumann, Pamela Flodman, Kazuhiro Yoshiyama, Yusuke Nakamura, Cécile Julier, K. Dumars, J. L. Haines, James A. Trofatter, M.A. Spence, Daniel E. Weeks, M Conneally

    Cyhoeddwyd 1990
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  15. 15
    Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention

    Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychologica... gan James M. Swanson, Jaap Oosterlaan, Michael Murias, Sabrina Schuck, Pamela Flodman, M. Anne Spence, Michael Wasdell, Yuan-Chun Ding, Han-Chang Chi, Moyra Smith, Miranda Mann, Caryn L. Carlson, James L. Kennedy, Joseph A. Sergeant, Patrick W. L. Leung, Ya-Ping Zhang, Avi Sadeh, Chuansheng Chen, Carol K. Whalen, Kimberley A. Babb, Robert K. Moyzis, Michael I. Posner

    Cyhoeddwyd 2000
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  16. 16
    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism gan Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Lambertus Klei, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Alfredo Brusco, Brian Hon‐Yin Chung, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina Girard, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Evelise Riberi, Rebecca J. Schmidt, Moyra Smith, Claudia I.C. Souza, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski

    Cyhoeddwyd 2021
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  17. 17
    Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Mapping autism risk loci using genetic linkage and chromosomal rearrangements gan 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

    Cyhoeddwyd 2007
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  18. 18
    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Rare coding variation provides insight into the genetic architecture and phenotypic context of autism gan Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montserrat Fernández Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt

    Cyhoeddwyd 2022
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