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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A Note on Exact Tests of Hardy-Weinberg Equilibrium von Wigginton, Janis E., Cutler, David J., Abecasis, Gonçalo R.

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The roles of vasoactive intestinal polypeptide in the mammalian circadian clock von Piggins, HD, Cutler, DJ

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Genomic alterations in cultured human embryonic stem cells von Rao, Mahendra, Chakravarti, Aravinda, Maitra, Anirban, Arking, Dan E, Shivapurkar, Narayan, Ikeda, Morna, Stastny, Victor, Kassauei, Keyaunoosh, Sui, Guoping, Cutler, David J, Liu, Ying, Brimble, Sandii N, Noaksson, Karin, Hyllner, Johan, Schulz, Thomas C, Zeng, Xianmin, Freed, William J, Crook, Jeremy, Abraham, Suman, Colman, Alan, Sartipy, Peter, Matsui, Sei-Ichi, Carpenter, Melissa, Gazdar, Adi F

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A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk von Chakravarti, Aravinda, Emison, Eileen Sproat, McCallion, Andrew S, Kashuk, Carl S, Bush, Richard T, Grice, Elizabeth, Lin, Shin, Portnoy, Matthew E, Cutler, David J, Green, Eric D

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Family-based association of FKBP5 in bipolar disorder von Willour, V L, Chen, H, Toolan, J, Belmonte, P, Cutler, D J, Goes, F S, Zandi, P P, Lee, R S, MacKinnon, D F, Mondimore, F M, Schweizer, B, DePaulo, J R, Gershon, E S, McMahon, F J, Potash, J B

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Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies von Cutler, David J, Lin, Shin, Chakravarti, Aravinda

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Haplotype Inference in Random Population Samples von Lin, Shin, Cutler, David J., Zwick, Michael E., Chakravarti, Aravinda

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Undetected Genotyping Errors Cause Apparent Overtransmission of Common Alleles in the Transmission/Disequilibrium Test von Mitchell, Adele A., Cutler, David J., Chakravarti, Aravinda

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Comparative analyses of multi-species sequences from targeted genomic regions von Green, E. D, Thomas, J. W, Touchman, J. W, Blakesley, R. W, Bouffard, G. G, Beckstrom-Sternberg, S. M, Margulies, E. H, Blanchette, M, Siepel, A. C, Thomas, P. J, McDowell, J. C, Maskeri, B, Hansen, N. F, Schwartz, M. S, Weber, R. J, Kent, W. J, Karolchik, D, Bruen, T. C, Bevan, R, Cutler, D. J, Schwartz, S, Elnitski, L, Idol, J. R, Prasad, A. B, Lee-Lin, S.-Q, Maduro, V. V. B, Summers, T. J, Portnoy, M. E, Dietrich, N. L, Akhter, N, Ayele, K, Benjamin, B, Cariaga, K, Brinkley, C. P, Brooks, S. Y, Granite, S, Guan, X, Gupta, J, Haghighi, P, Ho, S.-L, Huang, M. C, Karlins, E, Laric, P. L, Legaspi, R, Lim, M. J, Maduro, Q. L, Masiello, C. A, Mastrian, S. D, McCloskey, J. C, Pearson, R, Stantripop, S, Tiongson, E. E, Tran, J. T, Tsurgeon, C, Vogt, J. L, Walker, M. A, Wetherby, K. D, Wiggins, L. S, Young, A. C, Zhang, L.-H, Osoegawa, K, Zhu, B, Zhao, B, Shu, C. L, De Jong, P. J, Lawrence, C. E, Smit, A. F, Chakravarti, A, Haussler, D, Green, P, Miller, W

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High-throughput variation detection and genotyping using microarrays von Cutler, D J, Zwick, M E, Carrasquillo, M M, Yohn, C T, Tobin, K P, Kashuk, C, Mathews, D J, Shah, N A, Eichler, E E, Warrington, J A, Chakravarti, A

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Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet–Biedl patients with two mutations at a second BBS locus von Badano, Jose L., Kim, Jun Chul, Hoskins, Bethan E., Lewis, Richard Alan, Ansley, Stephen J., Cutler, David J., Castellan, Claudio, Beales, Philip L., Leroux, Michel R., Katsanis, Nicholas

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Estimating divergence times in the presence of an overdispersed molecular clock von Cutler, D J

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Pharmacokinetic parameter prediction from drug structure using artificial neural networks von Turner, Joseph V, Maddalena, Desmond J, Cutler, David J

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Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arrays von Wong, Christopher W, Albert, Thomas J, Vega, Vinsensius B, Norton, Jason E, Cutler, David J, Richmond, Todd A, Stanton, Lawrence W, Liu, Edison T, Miller, Lance D

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The potential role of lysosomes in tissue distribution of weak bases von Macintyre, Anna C., Cutler, David J.

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Haplotype and missing data inference in nuclear families von Lin, Shin, Chakravarti, Aravinda, Cutler, David J

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Vasoactive intestinal polypeptide (VIP) phase-shifts the rat suprachiasmatic nucleus clock in vitro von Reed, Helen E., Meyer-Spasche, Alert, Cutler, David J., Coen, Clive W., Piggins, Hugh D.

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Understanding the Overdispersed Molecular Clock von Cutler, David J

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Differential distribution of orexin-A and orexin-B immunoreactivity in the rat brain and spinal cord von Cutler, David J, Morris, Richard, Sheridhar, Vimal, Wattam, Trevor A.K, Holmes, Stephen, Patel, Sara, Arch, Jonathan R.S, Wilson, Shelagh, Buckingham, Robin E, Evans, Martyn L, Leslie, Ron A, Williams, Gareth

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