Progress in Genomic Medicine: From Research to Clinical Application von Smith, Moyra

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MRNA Transcription, Translation, and Defects in Developmental Cognitive and Behavioral Disorders von Smith, Moyra

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DNA Sequence Analysis in Clinical Medicine, Proceeding Cautiously von Smith, Moyra

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Gene Environment Interactions: Nature and Nurture in the Twenty-First Century von Smith, Moyra

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

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The Regulatory Genome in Adaptation, Evolution, Development, and Disease von Smith, Moyra

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Expanded Insights Into Mechanisms of Gene Expression and Disease Related Disruptions von Smith, Moyra, Flodman, Pamela L

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Gene control von Smith, Moyra

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Circulating biomarkers of kidney angiomyolipoma and cysts in tuberous sclerosis complex patients von Rubtsova, Varvara I., Chun, Yujin, Kim, Joohwan, Ramirez, Cuauhtemoc B., Jung, Sunhee, Choi, Wonsuk, Kelly, Miranda E., Lopez, Miranda L., Cassidy, Elizabeth, Rushing, Gabrielle, Aguiar, Dean J., Lau, Wei Ling, Ahdoot, Rebecca S., Smith, Moyra, Edinger, Aimee L., Lee, Sang-Guk, Jang, Cholsoon, Lee, Gina

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Investigating the Human Genome: Insights into Human Variation and Disease Susceptibility von Smith, Moyra

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

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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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... von Swanson, James, Oosterlaan, Jaap, Murias, Michael, Schuck, Sabrina, Flodman, Pamela, Spence, M. Anne, Wasdell, Michael, Ding, Yuanchun, Chi, Han-Chang, Smith, Moyra, Mann, Miranda, Carlson, Caryn, Kennedy, James L., Sergeant, Joseph A., Leung, Patrick, Zhang, Ya-Ping, Sadeh, Avi, Chen, Chuansheng, Whalen, Carol K., Babb, Kimberley A., Moyzis, Robert, Posner, Michael I.

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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The year in human and medical genetics. Highlights of 2007-2008 von Smith, Moyra

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Ethnic disparities in the frequency of cancer reported in family histories von Maves, Heather, Flodman, Pamela, Nathan, Deepika, Smith, Moyra

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Preface von Smith, Moyra

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Preface von Smith, Moyra

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Preface von Smith, Moyra

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The Year in Human and Medical Genetics von Smith, Moyra

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