Note on the Pt and Hg mass-197 isomers von Haverfield, A.J., Easterday, H.T., Hollander, J.M.

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An internal conversion coefficient spectrometer utilizing semi-conductor detectors von Easterday, H.T., Haverfield, A.J., Hollander, J.M.

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Study of interaction of low dose power source radiation fields with selected space scientific instruments Quarterly progress report von Endres, G. W. R., Haverfield, A. J.

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A Proportional Counter for Space and High Altitude Dosimetry Applications von Endres, G. W. R., Glass, W. A., Haverfield, A. J.

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HIGH RESOLUTION STUDIES IN THE DECAY OF BA133 WITH SEMICONDUCTOR COUNTERS von Bosch, H. E, Haverfield, A. J, Szichman, E, Abecasis, S. M

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New transitions and precise energy and intensity determinations in the decay of 177mLu von Haverfield, A.J., Bernthal, F.M., Hollander, J.M.

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High-resolution studies in the decay of 133Ba with semiconductor counters von Bosch, H.E., Haverfield, A.J., Szichman, E., Abecasis, S.M.

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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Exp... von Kelly, Melissa A, Caleshu, Colleen, Morales, Ana, Buchan, Jillian, Wolf, Zena, Harrison, Steven M, Cook, Stuart, Dillon, Mitchell W, Garcia, John, Haverfield, Eden, Jongbloed, Jan D H, Macaya, Daniela, Manrai, Arjun, Orland, Kate, Richard, Gabriele, Spoonamore, Katherine, Thomas, Matthew, Thomson, Kate, Vincent, Lisa M, Walsh, Roddy, Watkins, Hugh, Whiffin, Nicola, Ingles, Jodie, van Tintelen, J Peter, Semsarian, Christopher, Ware, James S, Hershberger, Ray, Funke, Birgit

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Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study von Haverfield, Eden V, Esplin, Edward D, Aguilar, Sienna J, Hatchell, Kathryn E, Ormond, Kelly E, Hanson-Kahn, Andrea, Atwal, Paldeep S, Macklin-Mantia, Sarah, Hines, Stephanie, Sak, Caron W.-M, Tucker, Steven, Bleyl, Steven B, Hulick, Peter J, Gordon, Ora K, Velsher, Lea, Gu, Jessica Y. J, Weissman, Scott M, Kruisselbrink, Teresa, Abel, Christopher, Kettles, Michele, Slavotinek, Anne, Mendelsohn, Bryce A, Green, Robert C, Aradhya, Swaroop, Nussbaum, Robert L

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The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives von Schmidlen, Tara J, Bristow, Sara L, Hatchell, Kathryn E, Esplin, Edward D, Nussbaum, Robert L, Haverfield, Eden V

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Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study von Haverfield, Eden V, Esplin, Edward D, Aguilar, Sienna J, Hatchell, Kathryn E, Ormond, Kelly E, Hanson-Kahn, Andrea, Atwal, Paldeep S, Macklin-Mantia, Sarah, Hines, Stephanie, Sak, Caron W.-M, Tucker, Steven, Bleyl, Steven B, Hulick, Peter J, Gordon, Ora K, Velsher, Lea, Gu, Jessica Y. J, Weissman, Scott M, Kruisselbrink, Teresa, Abel, Christopher, Kettles, Michele, Slavotinek, Anne, Mendelsohn, Bryce A, Green, Robert C, Aradhya, Swaroop, Nussbaum, Robert L

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Differential Permeability of the Blood-Testis Barrier During Reinitiation of Spermatogenesis in Adult Male Rats von Haverfield, Jenna T, Meachem, Sarah J, Nicholls, Peter K, Rainczuk, Katarzyna E, Simpson, Evan R, Stanton, Peter G

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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling von Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske

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Returning integrated genomic risk and clinical recommendations: The eMERGE study von Chisholm, Rex L., Clayton, Ellen Wright, DiVietro, Alanna, Green, Richard, Harden, Maegan V., Limdi, Nita A., Rasmussen, Luke V., Schmidlen, Tara, Cimino, James J., Guiducci, Candace, Harr, Margaret, Larkin, Katie, Mooney, Sean D., Mutai, Brenda, Namjou, Bahram, Perez, Emma F., Saadatagah, Seyedmohammad, Seabolt, Lynn, Shaibi, Gabriel Q., Sharp, Richard R., Sterling, Rene, Tiwari, Hemant K., Allworth, Aimee, DiVietro, Alanna, Khera, Amit, Kontorovich, Amy, Prince, Anya, Iverson, Ayuko, Khales, Bahram Namjou, Benoit, Barbara, Satterfield, Benjamin, Devine, Beth, Grundmeier, Bob, Piening, Brian, Korf, Bruce, Hammack, Catherine, Gascoigne, Caytie, Lange, Christoph, Liu, Cong, Shimbo, Daichi, Singh, Davinder, Edwards, Digna Velez, Morales, Eduardo, Cohn, Elizabeth, Karlson, Elizabeth, DeFranco, Emily, Perez, Emma, Cash, Erin, Berner, Eta, Wang, Fei, Mentch, Frank, Wiesner, Georgia, Belbin, Gillian, Hakonarson, Hakon, Tiwari, Hemant, Thomas, Hope, Hellwege, Jacklyn, Snyder, James, Olson, Janet, Glessner, Joe, Alsip, Jorge, Kannry, Joseph, Peterson, Josh, Galasso, Julia, Starren, Justin, Mittendorf, Kate, Anderson, Katherine, Bonini, Katherine, Rasmussen-Torvik, Laura, Gomez, Lizbeth, Petukhova, Lynn, Beasley, Mark, Horike, Martha, Hamed, Marwan, Davis, Matthew, Preuss, Michael, Shi, Mingjian, Perera, Minoli, Elkind, Mitch, Saadatagah, Mohammad, Netherly, Neil, Lennon, Niall, Limdi, Nita, Robinson, Nora, Elsekaily, Omar, Kovatch, Patricia, O’Reilly, Paul, Murali, Priyanka, Sharp, Richard, Peters, Riki, Rowley, Robb, Freimuth, Robert, Green, Robert, Winter, Robert, Irvin, Ryan, Knerr, Sarah, Bland, S.T., Booth, Stuart James, Desai, Vimi, Luo, Yuan

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Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia von Haverfield, Eden V, Whited, Amanda J, Petras, Kristin S, Dobyns, William B, Das, Soma

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The Presence 5 for Racial Justice Framework for anti‐racist communication with Black patients von Brown‐Johnson, Cati, Cox, Joy, Shankar, Megha, Baratta, Juliana, De Leon, Gisselle, Garcia, Raquel, Hollis, Taylor, Verano, Mae, Henderson, Kelsey, Upchurch, Mauranda, Safaeinili, Nadia, Shaw, Jonathan Glazer, Fortuna, Robert J., Beverly, Clyde, Walsh, Meredith, Somerville, Carlie Stein, Haverfield, Marie, Israni, Sonoo Thadaney, Verghese, Abraham, Zulman, Donna M.

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UGT1A1 variation and gallstone formation in sickle cell disease von Haverfield, Eden V., McKenzie, Colin A., Forrester, Terrence, Bouzekri, Nourdine, Harding, Rosalind, Serjeant, Graham, Walker, Thomas, Peto, Tim E.A., Ward, Ryk, Weatherall, David J.

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Genetic evidence in support of a shared Eurasian-North African dairying origin von MYLES, Sean, BOUZEKRI, Nourdine, HAVERFIELD, Eden, CHERKAOUI, Mohamed, DUGOUJON, Jean-Michel, WARD, Ryk

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SMC1A expression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndrome von Liu, Jinglan, Feldman, Rachel, Zhang, Zhe, Deardorff, Matthew A, Haverfield, Eden V, Kaur, Maninder, Li, Jennifer R, Clark, Dinah, Kline, Antonie D, Waggoner, Darrel J, Das, Soma, Jackson, Laird G, Krantz, Ian D

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Neuregulin1 (NRG1) Signaling through Fyn Modulates NMDA Receptor Phosphorylation: Differential Synaptic Function in NRG1+/- Knock-Outs Compared with Wild-Type Mice von Bjarnadottir, Maria, Misner, Dinah L, Haverfield-Gross, Sascha, Bruun, Silas, Helgason, Vignir G, Stefansson, Hreinn, Sigmundsson, Arnar, Firth, David R, Nielsen, Berit, Stefansdottir, Ragnheidur, Novak, Thomas J, Stefansson, Kari, Gurney, Mark E, Andresson, Thorkell

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