Advanced Health Information Technologies to Engage Parents, Clinicians, and Community Nutritionists in Coordinating Responsive Parenting Care: Descriptive Case Series of the Women,... by Kling, Samantha Mr, Harris, Holly A, Marini, Michele, Cook, Adam, Hess, Lindsey B, Lutcher, Shawnee, Mowery, Jacob, Bell, Scott, Hassink, Sandra, Hayward, Shannon B, Johnson, Greg, Franceschelli Hosterman, Jennifer, Paul, Ian M, Seiler, Christopher, Sword, Shirley, Savage, Jennifer S, Bailey-Davis, Lisa

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U.S. state policy contexts and mortality of working-age adults by Montez, Jennifer Karas, Mehri, Nader, Monnat, Shannon M, Beckfield, Jason, Chapman, Derek, Grumbach, Jacob M, Hayward, Mark D, Woolf, Steven H, Zajacova, Anna

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Complex disease and phenotype mapping in the domestic dog by Hayward, Jessica J., Castelhano, Marta G., Oliveira, Kyle C., Corey, Elizabeth, Balkman, Cheryl, Baxter, Tara L., Casal, Margret L., Center, Sharon A., Fang, Meiying, Garrison, Susan J., Kalla, Sara E., Korniliev, Pavel, Kotlikoff, Michael I., Moise, N. S., Shannon, Laura M., Simpson, Kenneth W., Sutter, Nathan B., Todhunter, Rory J., Boyko, Adam R.

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Genetic structure in village dogs reveals a Central Asian domestication origin by Shannon, Laura M., Boyko, Ryan H., Castelhano, Marta, Corey, Elizabeth, Hayward, Jessica J., McLean, Corin, White, Michelle E., Said, Mounir Abi, Anita, Baddley A., Bondjengo, Nono Ikombe, Calero, Jorge, Galov, Ana, Hedimbi, Marius, Imam, Bulu, Khalap, Rajashree, Lally, Douglas, Masta, Andrew, Oliveira, Kyle C., Pérez, Lucía, Randall, Julia, Tam, Nguyen Minh, Trujillo-Cornejo, Francisco J., Valeriano, Carlos, Sutter, Nathan B., Todhunter, Rory J., Bustamante, Carlos D., Boyko, Adam R.

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Imputation of canine genotype array data using 365 whole-genome sequences improves power of genome-wide association studies by Hayward, Jessica J, White, Michelle E, Boyle, Michael, Shannon, Laura M, Casal, Margret L, Castelhano, Marta G, Center, Sharon A, Meyers-Wallen, Vicki N, Simpson, Kenneth W, Sutter, Nathan B, Todhunter, Rory J, Boyko, Adam R

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Multiplex melanoma families are enriched for polygenic risk by Law, Matthew H, Aoude, Lauren G, Duffy, David L, Long, Georgina V, Johansson, Peter A, Pritchard, Antonia L, Khosrotehrani, Kiarash, Mann, Graham J, Montgomery, Grant W, Iles, Mark M, Cust, Anne E, Palmer, Jane M, Shannon, Kerwin F, Spillane, Andrew J, Stretch, Jonathan R, Thompson, John F, Saw, Robyn P M, Scolyer, Richard A, Martin, Nicholas G, Hayward, Nicholas K, MacGregor, Stuart

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Diverse genetic causes of polymicrogyria with epilepsy by Allen, Andrew S, Aggarwal, Vimla, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Guerrini, Renzo, Glauser, Tracy, Heinzen, Erin L, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Poduri, Annapurna, Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Abou‐Khalil, Bassel, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Cascino, Greg, Consalvo, Damian, Crumrine, Pat, Devinsky, Orrin, Dlugos, Dennis, Fountain, Nathan, Freyer, Catharine, Friedman, Dan, Geller, Eric, Glynn, Simon, Haas, Kevin, Haut, Sheryl, Joshi, Sucheta, Kirsch, Heidi, Knowlton, Robert, Kossoff, Eric, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Poduri, Annapurna, Scheffer, Ingrid, Shellhaas, Renée A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sperling, Michael, Smith, Michael C., Sullivan, Joseph, Vining, Eileen P. G., Von Allmen, Gretchen K., Widdess‐Walsh, Peter, Winawer, Melodie R., Bautista, Jocelyn, Fiol, Miguel, Glauser, Tracy, Hayward, Jean, Helmers, Sandra, Park, Kristen, Sirven, Joseph, Lin Thio, Liu, Venkat, Anu, Weisenberg, Judith, Kuperman, Rachel, McGuire, Shannon, Novotny, Edward, Sadleir, Lynette

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Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy by Allen, Andrew S., Berkovic, Samuel F., Coe, Bradley P., Cook, Joseph, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Goldstein, David B., Heinzen, Erin L., Johnson, Michael R., Krumm, Nik, Kuzniecky, Ruben, Lowenstein, Daniel H., Marson, Anthony G., Mefford, Heather C., Nelson, Ben, Esmaeeli Nieh, Sahar, O'Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Petrovski, Slavé, Poduri, Annapurna, Raja, Archana, Ruzzo, Elizabeth K., Scheffer, Ingrid E., Sherr, Elliott, Abou‐Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Boro, Alex, Cascino, Gregory, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E., Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., McGuire, Shannon M., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Poduri, Annapurna, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Shih, Jerry J., Singh, Rani, Sirven, Joseph, Smith, Michael C., Sullivan, Joe, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Widdess‐Walsh, Peter, Winawer, Melodie R.

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Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31 by Shen, Howard C., Velkova, Aneliya, Chen, Zhihua, Lin, Hui-Yi, Ann Chen, Y, Qu, Xiaotao, Ramus, Susan J., Lee, Janet, Lee, Nathan, Larson, Melissa C., Anton-Culver, Hoda, Antoniou, Antonis C., Armasu, Sebastian M., Bacot, François, Baglietto, Laura, Bandera, Elisa V., Bogdanova, Natalia, Brooks-Wilson, Angela, Butzow, Ralf, Cai, Qiuyin, Campbell, Ian, Chang-Claude, Jenny, Chanock, Stephen, Cheng, Jin Q., Cook, Linda S., Couch, Fergus J., Cunningham, Julie M., Dansonka-Mieszkowska, Agnieszka, Doherty, Jennifer A., Easton, Douglas F., Fasching, Peter A., Flanagan, James M., Giles, Graham G., Gonzalez-Bosquet, Jesus, Gore, Martin, Halle, Mari K., Harter, Philipp, Hillemanns, Peter, Hoatlin, Maureen, Høgdall, Claus K., Høgdall, Estrid, Hosono, Satoyo, Jensen, Allan, Jim, Heather, Karlan, Beth Y., Kaye, Stanley B., Kiemeney, Lambertus A., Kikkawa, Fumitaka, Konecny, Gottfried E., Krüger Kjaer, Susanne, Lambrechts, Sandrina, Lancaster, Johnathan M., Leminen, Arto, Levine, Douglas A., Liang, Dong, Kiong Lim, Boon, Lissowska, Jolanta, Lubiński, Jan, McLaughlin, John R., Moysich, Kirsten B., Nakanishi, Toru, Narod, Steven A., Ness, Roberta B., Nickels, Stefan, Noushmehr, Houtan, Odunsi, Kunle, Olson, Sara H., Orlow, Irene, Paul, James, Pelttari, Liisa M., Pike, Malcolm C., Poole, Elizabeth M., Renner, Stefan P., Risch, Harvey A., Rodriguez-Rodriguez, Lorna, Anne Rossing, Mary, Rudolph, Anja, Rzepecka, Iwona K., Salvesen, Helga B., Shu, Xiao-Ou, Shvetsov, Yurii B., Southey, Melissa C., Spiewankiewicz, Beata, Sutphen, Rebecca, van Altena, Anne M., Vincent, Daniel, Vitonis, Allison F., Wentzensen, Nicolas, Wik, Elisabeth, Winterhoff, Boris, Ling Woo, Yin, Yang, Hannah P., Zulkifli, Famida, Schildkraut, Joellen M., Berchuck, Andrew, Goode, Ellen L., Pharoah, Paul D.P., Monteiro, Alvaro N.A., Sellers, Thomas A., Gayther, Simon A.

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REPLY TO WANG ET AL: Sequencing datasets do not refute Central Asian domestication origin of dogs by Shannon, Laura M., Boyko, Ryan H., Castelhano, Marta, Corey, Elizabeth, Hayward, Jessica J., McLean, Corin, White, Michelle E., Said, Mounir R. Abi, Anita, Baddley A., Bondjengo, Nono Ikombe, Calero, Jorge, Galov, Ana, Hedimbi, Marius, Imam, Bulu, Khalap, Rajashree, Lally, Douglas, Masta, Andrew, Oliveira, Kyle C., Pérez, Lucía, Randall, Julia, Tam, Nguyen Minh, Trujillo-Cornejo, Francisco J., Valeriano, Carlos, Sutter, Nathan B., Todhunter, Rory J., Bustamante, Carlos D., Boyko, Adam R.

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Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data by Allen, Andrew S, Berkovic, Samuel F, Bridgers, Joshua, Cossette, Patrick, Dlugos, Dennis, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Heinzen, Erin L, Jiang, Yu, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slave, Poduri, Annapurna, Ren, Zhong, Scheffer, Ingrid E, Sherr, Elliott, Wang, Quanli, Balling, Rudi, Barisic, Nina, Baulac, Stephanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jaehn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R, Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Moeller, Rikke S, Muhle, Hiltrud, Pal, Deb, et. al

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Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains by Heath, H, Odelberg, S, Jackson, C E, Teh, B T, Hayward, N, Larsson, C, Buist, N R, Krapcho, K J, Hung, B C, Capuano, I V, Garrett, J E, Leppert, M F

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