Polydiscamide A: a new bioactive depsipeptide from the marine sponge Discodermia sp von Gulavita, Nanda K, Gunasekera, Sarath P, Pomponi, Shirley A, Robinson, Elise V

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Species differentiation in the marine sponge genus Discodermia (demospongiae: lithistida): the utility of ethanol extract profiles as species-specific chemotaxonomic markers von Kelly-Borges, Michelle, Robinson, Elise V., Gunasekera, Sarath P., Gunasekera, Malika, Gulavita, Nanda K., Pomponi, Shirley A.

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population von Robinson, Elise B, St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J

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The GTEx Consortium atlas of genetic regulatory effects across human tissues von Aguet, François, Anand, Shankara, Ardlie, Kristin G., Gabriel, Stacey, Getz, Gad A., Graubert, Aaron, Hadley, Kane, Handsaker, Robert E., Huang, Katherine H., Kashin, Seva, Li, Xiao, MacArthur, Daniel G., Meier, Samuel R., Nedzel, Jared L., Nguyen, Duyen T., Segrè, Ayellet V., Todres, Ellen, Balliu, Brunilda, Barbeira, Alvaro N., Battle, Alexis, Bonazzola, Rodrigo, Brown, Andrew, Brown, Christopher D., Castel, Stephane E., Conrad, Donald F., Cotter, Daniel J., Cox, Nancy, Das, Sayantan, de Goede, Olivia M., Dermitzakis, Emmanouil T., Einson, Jonah, Engelhardt, Barbara E., Eskin, Eleazar, Eulalio, Tiffany Y., Ferraro, Nicole M., Flynn, Elise D., Fresard, Laure, Gamazon, Eric R., Garrido-Martín, Diego, Gay, Nicole R., Gloudemans, Michael J., Guigó, Roderic, Hame, Andrew R., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Hou, Lei, Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kellis, Manolis, Kim-Hellmuth, Sarah, Kwong, Alan, Lappalainen, Tuuli, Li, Xin, Liang, Yanyu, Mangul, Serghei, Mohammadi, Pejman, Montgomery, Stephen B., Muñoz-Aguirre, Manuel, Nachun, Daniel C., Nobel, Andrew B., Oliva, Meritxell, Park, YoSon, Park, Yongjin, Parsana, Princy, Rao, Abhiram S., Reverter, Ferran, Rouhana, John M., Sabatti, Chiara, Saha, Ashis, Stephens, Matthew, Stranger, Barbara E., Strober, Benjamin J., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wen, Xiaoquan, Wright, Fred, Wucher, Valentin, Zou, Yuxin, Ferreira, Pedro G., Li, Gen, Melé, Marta, Yeger-Lotem, Esti, Barcus, Mary E., Bradbury, Debra, Krubit, Tanya, McLean, Jeffrey A., Qi, Liqun, Robinson, Karna, Roche, Nancy V., Smith, Anna M., Sobin, Leslie, Tabor, David E., Undale, Anita, Bridge, Jason, Brigham, Lori E., Foster, Barbara A., Gillard, Bryan M.

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Community testing practices for autism within the autism and developmental disabilities monitoring network von Robinson Williams, Ashley, Amoakohene, Esther, Maenner, Matthew J., Zahorodny, Walter, DiRienzo, Monica, Grzybowski, Andrea, Hall‐Lande, Jennifer, Pas, Elise T., Bakian, Amanda V., Lopez, Maya, Patrick, Mary, Shenouda, Josephine, Shaw, Kelly A.

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The impact of sex on gene expression across human tissues von Oliva, Meritxell, Muñoz-Aguirre, Manuel, Kim-Hellmuth, Sarah, Wucher, Valentin, Gewirtz, Ariel D H, Cotter, Daniel J, Parsana, Princy, Kasela, Silva, Balliu, Brunilda, Viñuela, Ana, Castel, Stephane E, Mohammadi, Pejman, Aguet, François, Zou, Yuxin, Khramtsova, Ekaterina A, Skol, Andrew D, Garrido-Martín, Diego, Reverter, Ferran, Brown, Andrew, Evans, Patrick, Gamazon, Eric R, Payne, Anthony, Bonazzola, Rodrigo, Barbeira, Alvaro N, Hamel, Andrew R, Martinez-Perez, Angel, Soria, José Manuel, Pierce, Brandon L, Stephens, Matthew, Eskin, Eleazar, Dermitzakis, Emmanouil T, Segrè, Ayellet V, Im, Hae Kyung, Engelhardt, Barbara E, Ardlie, Kristin G, Montgomery, Stephen B, Battle, Alexis J, Lappalainen, Tuuli, Guigó, Roderic, Stranger, Barbara E

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Determinants of telomere length across human tissues von Demanelis, Kathryn, Jasmine, Farzana, Chen, Lin S, Chernoff, Meytal, Tong, Lin, Delgado, Dayana, Zhang, Chenan, Shinkle, Justin, Sabarinathan, Mekala, Lin, Hannah, Ramirez, Eduardo, Oliva, Meritxell, Kim-Hellmuth, Sarah, Stranger, Barbara E, Lai, Tsung-Po, Aviv, Abraham, Ardlie, Kristin G, Aguet, François, Ahsan, Habibul, Doherty, Jennifer A, Kibriya, Muhammad G, Pierce, Brandon L

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Prenatal antidepressant exposure is associated with risk for attention-deficit hyperactivity disorder but not autism spectrum disorder in a large health system von Clements, C C, Castro, V M, Blumenthal, S R, Rosenfield, H R, Murphy, S N, Fava, M, Erb, J L, Churchill, S E, Kaimal, A J, Doyle, A E, Robinson, E B, Smoller, J W, Kohane, I S, Perlis, R H

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A Quantitative Proteome Map of the Human Body von Jiang, Lihua, Chan, Joanne, Fang, Huaying, Anand, Shankara, Gabriel, Stacey, Graubert, Aaron, Hadley, Kane, Huang, Katherine H., MacArthur, Daniel G., Meier, Samuel R., Segrè, Ayellet V., Balliu, Brunilda, Barbeira, Alvaro N., Battle, Alexis, Brown, Andrew, Brown, Christopher D., Castel, Stephane E., Conrad, Don, Cotter, Daniel J., Das, Sayantan, de Goede, Olivia M., Dermitzakis, Emmanouil T., Eskin, Eleazar, Eulalio, Tiffany Y., Garrido-Martín, Diego, Guigó, Roderic, He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Im, Hae Kyung, Jo, Brian, Kasela, Silva, Kellis, Manolis, Kim-Hellmuth, Sarah, Li, Xin, Mohammadi, Pejman, Montgomery, Stephen B., Muñoz-Aguirre, Manuel, Nachun, Daniel C., Oliva, Meritxell, Parsana, Princy, Sabatti, Chiara, Skol, Andrew D., Stephens, Matthew, Strober, Benjamin J., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wucher, Valentin, Zou, Yuxin, Ferreira, Pedro G., Yeger-Lotem, Esti, Barcus, Mary E., Bradbury, Debra, Krubit, Tanya, McLean, Jeffrey A., Smith, Anna M., Sobin, Leslie, Tabor, David E., Brigham, Lori E., Gillard, Bryan M., Hasz, Richard, Johnson, Mark, Kopen, Gene, Moser, Michael T., Myer, Kevin, Shad, Saboor, Thomas, Jeffrey A., Washington, Michael, Rohrer, Daniel C., Valley, Dana R., Davis, David A., Mash, Deborah C., Mosavel, Maghboeba, Siminoff, Laura A., Flicek, Paul, Juettemann, Thomas, Powell, Conner C., Rosenbloom, Kate R., Ruffier, Magali, Sheppard, Dan, Taylor, Kieron, Akey, Joshua, Demanelis, Kathryn, Feinberg, Andrew P., Hansen, Kasper D., Kibriya, Muhammad G., Li, Jin Billy, Li, Qin, Linder, Sandra E., Pierce, Brandon L., Smith, Kevin S., Tang, Hua, Carithers, Latarsha J., Koester, Susan E., Little, A. Roger, Moore, Helen M., Rao, Abhi K., Vaught, Jimmie B., Volpi, Simona

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Cell type-specific genetic regulation of gene expression across human tissues von Kim-Hellmuth, Sarah, Aguet, François, Oliva, Meritxell, Muñoz-Aguirre, Manuel, Kasela, Silva, Wucher, Valentin, Castel, Stephane E, Hamel, Andrew R, Viñuela, Ana, Roberts, Amy L, Mangul, Serghei, Wen, Xiaoquan, Wang, Gao, Barbeira, Alvaro N, Garrido-Martín, Diego, Nadel, Brian B, Zou, Yuxin, Bonazzola, Rodrigo, Quan, Jie, Brown, Andrew, Martinez-Perez, Angel, Soria, José Manuel, Getz, Gad, Dermitzakis, Emmanouil T, Small, Kerrin S, Stephens, Matthew, Xi, Hualin S, Im, Hae Kyung, Guigó, Roderic, Segrè, Ayellet V, Stranger, Barbara E, Ardlie, Kristin G, Lappalainen, Tuuli

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Health Conditions, Education Services, and Transition Planning for Adolescents With Autism von Hughes, Michelle M, Pas, Elise T, Durkin, Maureen S, DaWalt, Leann S, Bilder, Deborah A, Bakian, Amanda V, Amoakohene, Esther, Shaw, Kelly A, Patrick, Mary E, Salinas, Angelica, DiRienzo, Monica, Lopez, Maya, Williams, Susan, McArthur, Dedria, Hudson, Allison, Ladd-Acosta, Christine M, Schwenk, Yvette D, Baroud, Thaer M, Robinson Williams, Ashley, Washington, Anita, Maenner, Matthew J

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Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits von Martin, Joanna, Khramtsova, Ekaterina A., Goleva, Slavina B., Blokland, Gabriëlla A.M., Traglia, Michela, Walters, Raymond K., Hübel, Christopher, Coleman, Jonathan R.I., Breen, Gerome, Børglum, Anders D., Demontis, Ditte, Grove, Jakob, Werge, Thomas, Bralten, Janita, Bulik, Cynthia M., Lee, Phil H., Mathews, Carol A., Peterson, Roseann E., Winham, Stacey J., Wray, Naomi, Edenberg, Howard J., Guo, Wei, Yao, Yin, Neale, Benjamin M., Faraone, Stephen V., Petryshen, Tracey L., Weiss, Lauren A., Duncan, Laramie E., Goldstein, Jill M., Smoller, Jordan W., Stranger, Barbara E., Davis, Lea K., Alda, Martin, Bortolato, Marco, Burton, Christie L., Byrne, Enda, Carey, Caitlin E., Erdman, Lauren, Huckins, Laura M., Mattheisen, Manuel, Robinson, Elise, Stahl, Eli

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Post-landing major element quantification using SuperCam laser induced breakdown spectroscopy von Anderson, Ryan B., Forni, Olivier, Cousin, Agnes, Wiens, Roger C., Clegg, Samuel M., Frydenvang, Jens, Gabriel, Travis S.J., Ollila, Ann, Schröder, Susanne, Beyssac, Olivier, Gibbons, Erin, Vogt, David S., Clavé, Elise, Manrique, Jose-Antonio, Legett, Carey, Pilleri, Paolo, Newell, Raymond T., Sarrao, Joseph, Maurice, Sylvestre, Arana, Gorka, Benzerara, Karim, Bernardi, Pernelle, Bernard, Sylvain, Bousquet, Bruno, Brown, Adrian J., Alvarez-Llamas, César, Chide, Baptiste, Cloutis, Edward, Comellas, Jade, Connell, Stephanie, Dehouck, Erwin, Delapp, Dorothea M., Essunfeld, Ari, Fabre, Cecile, Fouchet, Thierry, Garcia-Florentino, Cristina, García-Gómez, Laura, Gasda, Patrick, Gasnault, Olivier, Hausrath, Elisabeth M., Lanza, Nina L., Laserna, Javier, Lasue, Jeremie, Lopez, Guillermo, Madariaga, Juan Manuel, Mandon, Lucia, Mangold, Nicolas, Meslin, Pierre-Yves, Nelson, Anthony E., Newsom, Horton, Reyes-Newell, Adriana L., Robinson, Scott, Rull, Fernando, Sharma, Shiv, Simon, Justin I., Sobron, Pablo, Fernandez, Imanol Torre, Udry, Arya, Venhaus, Dawn, McLennan, Scott M., Morris, Richard V., Ehlmann, Bethany

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The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease von Groza, Tudor, Köhler, Sebastian, Moldenhauer, Dawid, Vasilevsky, Nicole, Baynam, Gareth, Zemojtel, Tomasz, Schriml, Lynn Marie, Kibbe, Warren Alden, Schofield, Paul N., Beck, Tim, Vasant, Drashtti, Brookes, Anthony J., Zankl, Andreas, Washington, Nicole L., Mungall, Christopher J., Lewis, Suzanna E., Haendel, Melissa A., Parkinson, Helen, Robinson, Peter N.

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Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease von Gloudemans, Michael J., Smail, Craig, Eulalio, Tiffany Y., Aguet, François, Xu, Jishu, Kim-Hellmuth, Sarah, Park, YoSon, Scott, Alexandra J., Strober, Benjamin J., Gabriel, Stacey, Meier, Samuel R., Nguyen, Duyen T., Segrè, Ayellet V., Brown, Andrew, Cotter, Daniel J., Cox, Nancy, Dermitzakis, Emmanouil T., Einson, Jonah, Flynn, Elise D., Fresard, Laure, Gamazon, Eric R., Gay, Nicole R., Guigó, Roderic, Hamel, Andrew R., He, Yuan, Hoffman, Paul J., Hormozdiari, Farhad, Hou, Lei, Jo, Brian, Kashin, Seva, Mohammadi, Pejman, Oliva, Meritxell, Parsana, Princy, Sabatti, Chiara, Stranger, Barbara E., Teran, Nicole A., Viñuela, Ana, Wang, Gao, Wright, Fred, Ferreira, Pedro G., Li, Gen, Yeger-Lotem, Esti, Bradbury, Debra, Qi, Liqun, Robinson, Karna, Roche, Nancy V., Tabor, David E., Bridge, Jason, Gillard, Bryan M., Hasz, Richard, Hunter, Marcus, Kopen, Gene, Leinweber, William F., Moser, Michael T., Myer, Kevin, Washington, Michael, Wheeler, Joseph, Rohrer, Daniel C., Valley, Dana R., Branton, Philip A., Sobin, Leslie, Gardiner, Heather M., Mosavel, Maghboeba, Siminoff, Laura A., Flicek, Paul, Haeussler, Maximilian, Juettemann, Thomas, Ruffier, Magali, Sheppard, Dan, Taylor, Kieron, Abell, Nathan S., Akey, Joshua, Chen, Lin, Feinberg, Andrew P., Hansen, Kasper D., Jasmine, Farzana, Jiang, Lihua, Kaul, Rajinder, Kibriya, Muhammad G., Li, Jin Billy, Li, Qin, Lin, Shin, Pierce, Brandon L., Skol, Andrew D., Smith, Kevin S., Snyder, Michael, Stamatoyannopoulos, John, Tang, Hua, Guan, Ping, Little, A. Roger, Nierras, Concepcion R., Rao, Abhi K., Volpi, Simona, Brown, Christopher D., Wen, Xiaoquan, Hall, Ira M., Lappalainen, Tuuli, Im, Hae Kyung, Quertermous, Thomas, Kirkegaard, Karla

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Genetic correlates of phenotypic heterogeneity in autism von Warrier, Varun, Zhang, Xinhe, Reed, Patrick, Havdahl, Alexandra, Moore, Tyler M., Cliquet, Freddy, Leblond, Claire S., Rolland, Thomas, Rosengren, Anders, Rowitch, David H., Hurles, Matthew E., Geschwind, Daniel H., Børglum, Anders D., Robinson, Elise B., Grove, Jakob, Martin, Hilary C., Bourgeron, Thomas, Baron-Cohen, Simon

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Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups von Mattheisen, Manuel, Grove, Jakob, Als, Thomas D., Martin, Joanna, Voloudakis, Georgios, Meier, Sandra, Demontis, Ditte, Bendl, Jaroslav, Walters, Raymond, Carey, Caitlin E., Rosengren, Anders, Strom, Nora I., Hauberg, Mads Engel, Zeng, Biao, Hoffman, Gabriel, Zhang, Wen, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Agerbo, Esben, Cormand, Bru, Nordentoft, Merete, Werge, Thomas, Mors, Ole, Hougaard, David M., Buxbaum, Joseph D., Faraone, Stephen V., Franke, Barbara, Dalsgaard, Søren, Mortensen, Preben B., Robinson, Elise B., Roussos, Panos, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Transcriptomic signatures across human tissues identify functional rare genetic variation von Ferraro, Nicole M, Strober, Benjamin J, Einson, Jonah, Abell, Nathan S, Aguet, Francois, Barbeira, Alvaro N, Brandt, Margot, Bucan, Maja, Castel, Stephane E, Davis, Joe R, Greenwald, Emily, Hess, Gaelen T, Hilliard, Austin T, Kember, Rachel L, Kotis, Bence, Park, YoSon, Peloso, Gina, Ramdas, Shweta, Scott, Alexandra J, Smail, Craig, Tsang, Emily K, Zekavat, Seyedeh M, Ziosi, Marcello, Aradhana, Ardlie, Kristin G, Assimes, Themistocles L, Bassik, Michael C, Brown, Christopher D, Correa, Adolfo, Hall, Ira, Im, Hae Kyung, Li, Xin, Natarajan, Pradeep, Lappalainen, Tuuli, Mohammadi, Pejman, Montgomery, Stephen B, Battle, Alexis

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A vast resource of allelic expression data spanning human tissues von Castel, Stephane E, Aguet, François, Mohammadi, Pejman, Ardlie, Kristin G, Lappalainen, Tuuli

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The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort von Robinson, E B, Kirby, A, Ruparel, K, Yang, J, McGrath, L, Anttila, V, Neale, B M, Merikangas, K, Lehner, T, Sleiman, P M A, Daly, M J, Gur, R, Hakonarson, H

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