Construction of a 5000ᵣₐd whole-genome radiation hybrid panel in the horse and generation of a comprehensive and comparative map for ECA11 von Chowdhary, Bhanu P, Raudsepp, Terje, Honeycutt, Dee, Owens, Elaine K, Piumi, François, Guérin, Gérard, Matise, Tara C, Kata, Srinivas R, Womack, James E, Skow, Loren C

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A whole-genome radiation hybrid panel for bovine gene mapping von Womack, J E, Johnson, J S, Owens, E K, Rexroad, 3rd, C E, Schläpfer, J, Yang, Y P

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Construction of a 5000(rad) whole-genome radiation hybrid panel in the horse and generation of a comprehensive and comparative map for ECA11 von Chowdhary, Bhanu P, Raudsepp, Terje, Honeycutt, Dee, Owens, Elaine K, Piumi, François, Guérin, Gérard, Matise, Tara C, Kata, Srinivas R, Womack, James E, Skow, Loren C

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EFFECT OF CHROMOSOMAL ABNORMALITIES ON G6PD ACTIVITY IN CULTURED HUMAN FIBROBLASTS von Steele, Mark W, Owens, K Elaine

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SKIN-BIOPSY SITE AND SUCCESSFUL FIBROBLAST CULTURE von Steele, MarkW, Owens, K.Elaine, Ward, Carol

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Developmental, tissue-specific, and sex differences in activity among three enzymes from human erythrocytes and cultured fibroblasts von Steele, M W, Owens, K E

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Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes von Soh, Y Q Shirleen, Alföldi, Jessica, Pyntikova, Tatyana, Brown, Laura G, Graves, Tina, Minx, Patrick J, Fulton, Robert S, Kremitzki, Colin, Koutseva, Natalia, Mueller, Jacob L, Rozen, Steve, Hughes, Jennifer F, Owens, Elaine, Womack, James E, Murphy, William J, Cao, Qing, de Jong, Pieter, Warren, Wesley C, Wilson, Richard K, Skaletsky, Helen, Page, David C

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Neuropsychology of COVID-19: Anticipated Cognitive and Mental Health Outcomes von Bailey, Erin K., Steward, Kayla A., VandenBussche Jantz, Alicia B., Kamper, Joel E., Mahoney, Elaine J., Duchnick, Jennifer J.

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Visuospatial Working Memory in Attention-Deficit/Hyperactivity Disorder: Characterizing Path Length and Path Crossings as Mechanisms of Impairment von Arrington, Elaine F., Alderson, R. Matt, Tarle, Stephanie J., Roberts, Delanie K., Sarver, Dustin E., Sullivan, Maureen A., Gette, Jordan A.

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Smooth Muscle Cell Plasticity: Fact or Fiction? von Nguyen, Anh T, Gomez, Delphine, Bell, Robert D, Campbell, Julie H, Clowes, Alexander W, Gabbiani, Giulio, Giachelli, Cecilia M, Parmacek, Michael S, Raines, Elaine W, Rusch, Nancy J, Speer, Mei Y, Sturek, Michael, Thyberg, Johan, Towler, Dwight A, Weiser-Evans, Mary C, Yan, Chen, Miano, Joseph M, Owens, Gary K

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Sequence analysis in Bos taurus reveals pervasiveness of X-Y arms races in mammalian lineages von Hughes, Jennifer F, Skaletsky, Helen, Pyntikova, Tatyana, Koutseva, Natalia, Raudsepp, Terje, Brown, Laura G, Bellott, Daniel W, Cho, Ting-Jan, Dugan-Rocha, Shannon, Khan, Ziad, Kremitzki, Colin, Fronick, Catrina, Graves-Lindsay, Tina A, Fulton, Lucinda, Warren, Wesley C, Wilson, Richard K, Owens, Elaine, Womack, James E, Murphy, William J, Muzny, Donna M, Worley, Kim C, Chowdhary, Bhanu P, Gibbs, Richard A, Page, David C

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Magneto-optical measurement of magnetic field and electrical current on a short pulse high energy pulsed power accelerator von Owens, Israel, Coffey, Sean, Ulmen, Ben, Harrison, Richard K., Trujillo, Alex, Rhoades, Elaine, McCutcheon, Brandon, Grabowski, Chris

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Determination of dopamine, serotonin, and their metabolites in pediatric cerebrospinal fluid by isocratic high performance liquid chromatography coupled with electrochemical detect... von Hubbard, K. Elaine, Wells, Amy, Owens, Thandranese S., Tagen, Michael, Fraga, Charles H., Stewart, Clinton F.

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Stability of mismatch negativity event‐related potentials in a multisite study von Roach, Brian J., Hamilton, Holly K., Bachman, Peter, Belger, Aysenil, Carrión, Ricardo E., Duncan, Erica, Johannesen, Jason, Kenney, Joshua G., Light, Gregory, Niznikiewicz, Margaret, Addington, Jean, Bearden, Carrie E., Owens, Emily M., Cadenhead, Kristin S., Cannon, Tyrone D., Cornblatt, Barbara A., McGlashan, Thomas H., Perkins, Diana O., Seidman, Larry, Tsuang, Ming, Walker, Elaine F., Woods, Scott W., Mathalon, Daniel H.

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Increasing medication error reporting rates while reducing harm through simultaneous cultural and system-level interventions in an intensive care unit von Abstoss, Katherine M, Shaw, Brenda E, Owens, Tonie A, Juno, Julie L, Commiskey, Elaine L, Niedner, Matthew F

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Rare chromosomal deletions and duplications increase risk of schizophrenia von Stone, Jennifer L., O'Donovan, Michael C., Gurling, Hugh, Kirov, George K., Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nick J., Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael J., St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M.

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs von Meer, Dennis, Agartz, Ingrid, Arango, Celso, Ayesa‐Arriola, Rosa, Bakker, Geor, Boomsma, Dorret I., Bülow, Robin, Butcher, Nancy J., Caspers, Svenja, Crespo‐Facorro, Benedicto, Dale, Anders M., Dazzan, Paola, Zubicaray, Greig I., Donohoe, Gary, Espeseth, Thomas, Fisher, Simon E., Ge, Tian, Glahn, David C., Grabe, Hans J., Gur, Raquel E., Håberg, Asta K., Hashimoto, Ryota, Hibar, Derrek P., Holmes, Avram J., Hulshoff Pol, Hilleke E., Kushan, Leila, Liu, Jingyu, Martin‐Brevet, Sandra, Martínez, Kenia, Mather, Karen A., Mathias, Samuel R., Medland, Sarah E., Modenato, Claudia, Mühleisen, Thomas W., Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S., Reis Marques, Tiago, Repetto, Gabriela M., Reymond, Alexandre, Sachdev, Perminder S., Schmitt, James E., Schofield, Peter R., Silva, Ana I., Stefansson, Hreinn, Stein, Dan J., Tamnes, Christian K., Ulfarsson, Magnus O., Vajdi, Ariana, Ent, Dennis, Bree, Marianne B. M., Vassos, Evangelos, Vázquez‐Bourgon, Javier, Vila‐Rodriguez, Fidel, Walters, G. Bragi, Wen, Wei, Zackai, Elaine H., Thompson, Paul M., Bearden, Carrie E., Blackburn, Nicholas B., Bøen, Rune, Zwarte, Sonja M. C., Forti, Marta Di, Frei, Oleksandr, Fukunaga, Masaki, Hehir‐Kwa, Jayne Y., Hoffmann, Per, Homuth, Georg, Jahanshad, Neda, Koops, Sanne, Kumar, Kuldeep, Kikuchi, Masataka, Le Hellard, Stephanie, Leu, Costin, Murray, Robin M, Nyberg, Lars, Shumskaya, Elena, Sisodiya, Sanjay M., Steen, Vidar M., Teumer, Alexander, Uhlmann, Anne, Wright, Margaret J., Campbell, Linda E., Crossley, Nicolas A., Crowley, T. Blaine, Daly, Eileen, Fiksinski, Ania M., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Jonas, Rachel K., Kates, Wendy R., Lin, Amy, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J., Simon, Tony. J., Amelsvoort, Therese, Vorstman, Jacob A. S.

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Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics von Forsyth, Jennifer K, Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R K, Villalon-Reina, Julio E, Thompson, Paul M, Bearden, Carrie E

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CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290 von Gorden, Nicholas T., Arts, Heleen H., Parisi, Melissa A., Coene, Karlien L.M., Letteboer, Stef J.F., van Beersum, Sylvia E.C., Mans, Dorus A., Hikida, Abigail, Eckert, Melissa, Knutzen, Dana, Alswaid, Abdulrahman F., Özyurek, Hamit, Dibooglu, Sel, Otto, Edgar A., Liu, Yangfan, Davis, Erica E., Hutter, Carolyn M., Bammler, Theo K., Farin, Frederico M., Dorschner, Michael, Topçu, Meral, Zackai, Elaine H., Rosenthal, Phillip, Owens, Kelly N., Katsanis, Nicholas, Vincent, John B., Hildebrandt, Friedhelm, Rubel, Edwin W., Raible, David W., Knoers, Nine V.A.M., Chance, Phillip F., Roepman, Ronald, Moens, Cecilia B., Glass, Ian A., Doherty, Dan

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