New subtypes of allele-specific epigenetic effects: implications for brain development, function and disease von Kravitz, Stephanie N, Gregg, Christopher

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Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism von Prusiner, Stanley B., Woerman, Amanda L., Mordes, Daniel A., Watts, Joel C., Rampersaud, Ryan, Berry, David B., Patel, Smita, Oehler, Abby, Lowe, Jennifer K., Kravitz, Stephanie N., Geschwind, Daniel H., Glidden, David V., Halliday, Glenda M., Middleton, Lefkos T., Gentleman, Steve M., Grinberg, Lea T., Giles, Kurt

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Random allelic expression in the adult human body von Kravitz, Stephanie N., Ferris, Elliott, Love, Michael I., Thomas, Alun, Quinlan, Aaron R., Gregg, Christopher

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Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches von Pedersen, Brent S., Bhetariya, Preetida J., Brown, Joe, Kravitz, Stephanie N., Marth, Gabor, Jensen, Randy L., Bronner, Mary P., Underhill, Hunter R., Quinlan, Aaron R.

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Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families von Leppa, Virpi M., Kravitz, Stephanie N., Martin, Christa Lese, Andrieux, Joris, Le Caignec, Cedric, Martin-Coignard, Dominique, DyBuncio, Christina, Sanders, Stephan J., Lowe, Jennifer K., Cantor, Rita M., Geschwind, Daniel H.

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SV-plaudit: A cloud-based framework for manually curating thousands of structural variants von Belyeu, Jonathan R, Nicholas, Thomas J, Pedersen, Brent S, Sasani, Thomas A, Havrilla, James M, Kravitz, Stephanie N, Conway, Megan E, Lohman, Brian K, Quinlan, Aaron R, Layer, Ryan M

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Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy von Chen, Zhongbo, Chen, Jason A., Shatunov, Aleksey, Jones, Ashley R., Kravitz, Stephanie N., Huang, Alden Y., Lawrence, Lauren, Lowe, Jennifer K., Lewis, Cathryn M., Payan, Christine A. M., Lieb, Wolfgang, Franke, Andre, Deloukas, Panagiotis, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean‐François, Ludolph, Albert, Bensimon, Gilbert, Leigh, P. Nigel, Bronstein, Jeff M., Coppola, Giovanni, Geschwind, Daniel H., Al‐Chalabi, Ammar

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Evidence for [alpha]-synuclein prions causing multiple system atrophy in humans with parkinsonism von Prusiner, Stanley B, Woerman, Amanda L, Mordes, Daniel A, Watts, Joel C, Rampersaud, Ryan, Berry, David B, Patel, Smita, Oehler, Abby, Lowe, Jennifer K, Kravitz, Stephanie N, Geschwind, Daniel H, Glidden, David V, Halliday, Glenda M, Middleton, Lefkos T, Gentleman, Steve M, Grinberg, Lea T, Giles, Kurt

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Additional file 3 of Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches von Pedersen, Brent S., Preetida J. Bhetariya, Brown, Joe, Kravitz, Stephanie N., Gabor Marth, Jensen, Randy L., Bronner, Mary P., Underhill, Hunter R., Quinlan, Aaron R.

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Additional file 2 of Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches von Pedersen, Brent S., Preetida J. Bhetariya, Brown, Joe, Kravitz, Stephanie N., Gabor Marth, Jensen, Randy L., Bronner, Mary P., Underhill, Hunter R., Quinlan, Aaron R.

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Supporting data for "SV-plaudit: A cloud-based framework for manually curating thousands of structural variants" von Aaron, Quinlan R., Brent, Pedersen S., Brian, Lohman K., James, Havrilla M., Jonathan, Belyeu R., Megan, Conway E., Ryan, Layer M., Stephanie, Kravitz N., Thomas, Sasani A., Thomas, Nicholas J.

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Noncanonical genomic imprinting in the monoamine system determines naturalistic foraging and brain-adrenal axis functions von Bonthuis, Paul J., Steinwand, Susan, Stacher Hörndli, Cornelia N., Emery, Jared, Huang, Wei-Chao, Kravitz, Stephanie, Ferris, Elliott, Gregg, Christopher

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Climate Change and Children's Health: Building a Healthy Future for Every Child von Ahdoot, Samantha, Baum, Carl R, Cataletto, Mary Bono, Hogan, Patrick, Wu, Christina B, Bernstein, Aaron

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Climate Change and Children's Health: Building a Healthy Future for Every Child von Ahdoot, Samantha, Baum, Carl R, Cataletto, Mary Bono, Hogan, Patrick, Wu, Christina B, Bernstein, Aaron

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Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, ift27 and parvalbumin von Nissen, Stephanie, Liang, Sherri, Shehktman, Tatyana, Kelsoe, John R.

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Problems and Questions von Brooke, Maxey, Demir, Huseyin, Ivanoff, Vladimir F., Trigg, C. W., Weesakul, B., Hochster, Melvin, Thebault, Victor, Walden, Harvey, Carlitz, Leonard, Churchyard, James, Stephanie, M., Mills, C. N., Klamkin, M. S., Thomas, P. D., Frankel, Edward T., Thoro, Dmitri, Kravitz, Sidney, Christilles, William E., Alfred, Brother, Bissinger, Barney, Bankoff, Leon, Bumcrot, R., Brown, Arthur B.

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Problems and Questions von Brooke, Maxey, Demir, Huseyin, Ivanoff, Vladimir F., Trigg, C. W., Weesakul, B., Hochster, Melvin, Thebault, Victor, Walden, Harvey, Carlitz, Leonard, Churchyard, James, Joseph D. E. Konhauser, Stephanie, M., Mills, C. N., Klamkin, M. S., Thomas, P. D., Frankel, Edward T., Thoro, Dmitri, Kravitz, Sidney, Christilles, William E., Alfred, Brother, Bissinger, Barney, Bankoff, Leon, Bumcrot, R., Brown, Arthur B.

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Problems and Questions von Kravitz, Sidney, Gandhi, J. M., Thomas, P. D., Rajagopal, A. K., Gold, Ben K., Wang, Chih-yi, Bissinger, Barney, B. Keshava R. Pai, Parrish, Gene B., Calabi, Eugenio, Coffman, Raphael T., Bankoff, Leon, Court, N. A., Stephanie, M., Piza, P. A., Painter, James A., Duncan, Dewey, Eves, Howard, Demir, Huseyin, Cappel, K. L., Klamkin, M. S., Howell, John M.

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