Adding muscle where you need it: non‐uniform hypertrophy patterns in elite sprinters by Handsfield, G. G., Knaus, K. R., Fiorentino, N. M., Meyer, C. H., Hart, J. M., Blemker, S. S.

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Cover Image Volume 27, Issue 10 by Handsfield, G. G., Knaus, K. R., Fiorentino, N. M., Meyer, C. H., Hart, J. M., Blemker, S. S.

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Immune dysfunction signatures predict outcomes and define checkpoint blockade-unresponsive microenvironments in acute myeloid leukemia by Rutella, Sergio, Vadakekolathu, Jayakumar, Mazziotta, Francesco, Reeder, Stephen, Yau, Tung-On, Mukhopadhyay, Rupkatha, Dickins, Benjamin, Altmann, Heidi, Kramer, Michael, Knaus, Hanna A, Blazar, Bruce R, Radojcic, Vedran, Zeidner, Joshua F, Arruda, Andrea, Wang, Bofei, Abbas, Hussein A, Minden, Mark D, Tasian, Sarah K, Bornhäuser, Martin, Gojo, Ivana, Luznik, Leo

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Elevated blood pressure linked to primary hyperaldosteronism and impaired vasodilation in BK channel-deficient mice by SAUSBIER, Matthias, AMTZ, Claudia, ABDULLAH, Usamah, KRIPPEIT-DREWS, Peter, FEIL, Robert, HOFMANN, Franz, KNAUS, Hans-Günier, KENYON, Chris, SHIPSTON, Michael J, STORM, Johan F, NEUHUBER, Winfried, KORTH, Michael, BUCURENCIU, Iancu, SCHUBERT, Rudolf, GOLLASCH, Maik, RUTH, Peter, HONG ZHAO, ZHOU, Xiao-Bo, SAUSBIER, Ulrike, FEIL, Susanne, KAMM, Simone, ESSIN, Kyrill, SAILER, Claudia A

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Conformational diversity in prion protein variants influences intermolecular β-sheet formation by Lee, Seungjoo, Antony, Lizamma, Hartmann, Rune, Knaus, Karen J, Surewicz, Krystyna, Surewicz, Witold K, Yee, Vivien C

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Kv1.3 Channels Are a Therapeutic Target for T Cell-Mediated Autoimmune Diseases by Beeton, Christine, Wulff, Heike, Standifer, Nathan E., Azam, Philippe, Mullen, Katherine M., Pennington, Michael W., Kolski-Andreaco, Aaron, Wei, Eric, Grino, Alexandra, Counts, Debra R., Wang, Ping H., LeeHealey, Christine J., Andrews, Brian S., Sankaranarayanan, Ananthakrishnan, Homerick, Daniel, Roeck, Werner W., Tehranzadeh, Jamshid, Stanhope, Kimber L., Zimin, Pavel, Havel, Peter J., Griffey, Stephen, Knaus, Hans-Guenther, Nepom, Gerald T., Gutman, George A., Calabresi, Peter A., Chandy, K. George

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Genetic Variation within Clonal Lineages of Phytophthora infestans Revealed through Genotyping-By-Sequencing, and Implications for Late Blight Epidemiology by Hansen, Zachariah R, Everts, Kathryne L, Fry, William E, Gevens, Amanda J, Grünwald, Niklaus J, Gugino, Beth K, Johnson, Dennis A, Johnson, Steven B, Judelson, Howard S, Knaus, Brian J, McGrath, Margaret T, Myers, Kevin L, Ristaino, Jean B, Roberts, Pamela D, Secor, Gary A, Smart, Christine D

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Estimating Uncertainties from Dual-Doppler Radar Measurements of Onshore Wind Plants Using LES by Brown, K., Cheung, L., Develder, N., Herges, T., Hsieh, A., Blaylock, M., Yalla, G., Knaus, R., Maniaci, D., Hirth, B.

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Outcomes From Colonic Pull-Through for Cloacal Exstrophy Differ by Colon Length: A Multi-Institutional Study by Srinivas, Shruthi, Knaus, Maria E, Avansino, Jeffrey R, Badillo, Andrea, Calkins, Casey M, Dickie, Belinda H, Durham, Megan M, Fuller, Megan K, Ralls, Matthew W, Reeder, Ron W, Rentea, Rebecca M, Rollins, Michael D, van Leeuwen, Kathleen, Wood, Richard J

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The Voltage-Gated Potassium Channel Kv1.3 Is Highly Expressed on Inflammatory Infiltrates in Multiple Sclerosis Brain by Rus, Horea, Pardo, Carlos A., Hu, Lina, Darrah, Erika, Cudrici, Cornelia, Niculescu, Teodora, Niculescu, Florin, Mullen, Katharine M., Allie, Rameeza, Guo, Liping, Wulff, Heike, Beeton, Christine, Susan I. V. Judge, Kerr, Douglas A., Knaus, Hans-Gunther, Chandy, K. George, Calabresi, Peter A., Latorre, Ramon

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Laparoscopy versus laparotomy for pediatric ovarian dermoids by Knaus, Maria E., Onwuka, Amanda J., Afrazi, Amin, Breech, Lesley, Corkum, Kristine S., Dillon, Patrick A., Ehrlich, Peter F., Fallat, Mary E., Fraser, Jason D., Gadepalli, Samir K., Grabowski, Julia E., Hertweck, S. Paige, Kabre, Rashmi, Lal, Dave R., Landman, Matthew P., Lawrence, Amy E., Leys, Charles M., Mak, Grace Z., Markel, Troy A., Merchant, Naila, Elliott Overman, R., Rademacher, Brooks L., Raiji, Manish T., Rymeski, Beth, Sato, Thomas T., Scannell, Madeline, Schikler, Allegra G., Sujka, Joseph A., Wright, Tiffany, Aldrink, Jennifer H., Hewitt, Geri D., Minneci, Peter C., Deans, Katherine J.

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Disparities in the Management of Pediatric Breast Masses by Knaus, Maria E., Onwuka, Amanda J., Bowder, Alexis, Courtney, Cathleen, Deans, Katherine J., Downard, Cynthia D., Duran, Yara K., Fallat, Mary E., Fraser, Jason D., Gadepalli, Samir K., Kabre, Rashmi, Kalbfell, Elle L., Kohler, Jonathan, Lal, Dave R., Landman, Matthew P., Lawrence, Amy E., Leys, Charles M., Lu, Patricia, Mak, Grace Z., Markel, Troy A., Merchant, Naila, Nguyen, Tina, Pilkington, Mercedes, Port, Elissa, Rymeski, Beth, Saito, Jacqueline, Sato, Thomas T., St Peter, Shawn D., Wright, Tiffany, Minneci, Peter C., Grabowski, Julia E.

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The challenges of research data management in cardiovascular science: a DGK and DZHK position paper—executive summary by Steffens, Sabine, Schröder, Katrin, Krüger, Martina, Maack, Christoph, Streckfuss-Bömeke, Katrin, Backs, Johannes, Backofen, Rolf, Baeßler, Bettina, Devaux, Yvan, Gilsbach, Ralf, Heijman, Jordi, Knaus, Jochen, Kramann, Rafael, Linz, Dominik, Lister, Allyson L., Maatz, Henrike, Maegdefessel, Lars, Mayr, Manuel, Meder, Benjamin, Nussbeck, Sara Y., Rog-Zielinska, Eva A., Schulz, Marcel H., Sickmann, Albert, Yigit, Gökhan, Kohl, Peter

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Diagnostic Performance of Magnetic Resonance Imaging for Pediatric Ovarian Neoplasms: A Multi-Institutional Review by Bergus, Katherine C., Knaus, Maria E., Onwuka, Amanda J., Afrazi, Amin, Breech, Lesley, Corkum, Kristine S., Dillon, Patrick A., Ehrlich, Peter F., Fallat, Mary E., Fraser, Jason D., Gadepalli, Samir K., Grabowski, Julia E., Hertweck, S. Paige, Kabre, Rashmi, Lal, Dave R., Landman, Matthew P., Leys, Charles M., Mak, Grace Z., Markel, Troy A., Merchant, Naila, Overman, R. Elliott, Rademacher, Brooks L., Raiji, Manish T., Rymeski, Beth, Sato, Thomas T., Wright, Tiffany, Aldrink, Jennifer H., Hewitt, Geri D., Minneci, Peter C., Deans, Katherine J.

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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease by Schwerd, T, Bryant, R V, Pandey, S, Capitani, M, Meran, L, Cazier, J-B, Jung, J, Mondal, K, Parkes, M, Mathew, C G, Fiedler, K, McCarthy, D J, Sullivan, P B, Rodrigues, A, Travis, S P L, Moore, C, Sambrook, J, Ouwehand, W H, Roberts, D J, Danesh, J, Russell, R K, Wilson, D C, Kelsen, J R, Cornall, R, Denson, L A, Kugathasan, S, Knaus, U G, Serra, E G, Anderson, C A, Duerr, R H, McGovern, D Pb, Cho, J, Powrie, F, Li, V Sw, Muise, A M, Uhlig, H H

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Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study by May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline, Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Baulac, Stéphanie, Marini, Carla, Thiele, Holger, Jabbari, Kamel, Ruppert, Ann-Kathrin, Lal, Dennis, Cestèle, Sandrine, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, Sisodiya, Sanjay M, Nabbout, Rima, Coppola, Antonietta, Vari, Maria S, Kasteleijn-Nolst Trenité, Dorothée, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, François, Carmant, Lionel, Desbiens, Richard, Cieuta-Walti, Cécile, Sills, Graeme J, Auce, Pauls, Johnson, Michael R, Marson, Anthony G, Berghuis, Bianca, Avbersek, Andreja, McCormack, Mark, Delanty, Norman, Depondt, Chantal, Zimprich, Fritz, Peter, Sarah, van Rooij, Jeroen, Ikram, M Arfan, Avanzini, Giuliano, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby P C, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nürnberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland, Lerche, Holger, May, Patrick, Girard, Simon, Bobbili, Dheeraj R, Schubert, Julian, Arfan Ikram, M, Maljevic, Snezana, Cossette, Patrick, Lerche, Holger, Ferlazzo, Edoardo, La Neve, Angela, Vignoli, Aglaia, Crichiutti, Giovanni, Gambardella, Antonio, Belcastro, Vincenzo, Bianchi, Amedeo, Yalçın, Destina, Dizdarer, Gulsen, Arslan, Kezban, Yapıcı, Zuhal, Kuşcu, Demet, Leu, Costin, Heggeli, Kristin, Willis, Joseph, Jorgensen, Andrea, Srivastava, Prashant, Rau, Sarah

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Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2 by Seemann, Petra, Schwappacher, Raphaela, Kjaer, Klaus W, Krakow, Deborah, Lehmann, Katarina, Dawson, Katherine, Stricker, Sigmar, Pohl, Jens, Plöger, Frank, Staub, Eike, Nickel, Joachim, Sebald, Walter, Knaus, Petra, Mundlos, Stefan

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Rare coding variants in genes encoding GABA A receptors in genetic generalised epilepsies: an exome-based case-control study by May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline, Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-López, Rosa, Baulac, Stéphanie, Marini, Carla, Thiele, Holger, Altmüller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestèle, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Møller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, Jonghe, Peter De, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Kasteleijn-Nolst Trenité, Dorothée, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, François, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clément, Jean-François, Cieuta-Walti, Cécile, Sills, Graeme J, Auce, Pauls, Francis, Ben, Johnson, Michael R, Marson, Anthony G, Berghuis, Bianca, Sander, Josemir W, Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Krenn, Martin, Zimprich, Fritz, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi, Ikram, M Arfan, Uitterlinden, André G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby P C, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nürnberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland, Lerche, Holger

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Multi-Institutional Review of the Preoperative Diagnostic Accuracy for Pediatric Ovarian Mature Cystic Teratomas by Knaus, Maria E., Onwuka, Amanda J., Afrazi, Amin, Breech, Lesley, Corkum, Kristine S., Dillon, Patrick A., Ehrlich, Peter F., Fallat, Mary E., Fraser, Jason D., Gadepalli, Samir K., Grabowski, Julia E., Hertweck, S. Paige, Kabre, Rashmi, Lal, Dave R., Landman, Matthew P., Lawrence, Amy E., Leys, Charles M., Mak, Grace Z., Markel, Troy A., Merchan, Naila, Overman, R. Elliott, Rademacher, Brooks L., Raiji, Manish T., Rymeski, Beth, Sato, Thomas T., Scannel, Madeline, Schikler, Allegra G., Sujka, Joseph A., Wright, Tiffany, Aldrink, Jennifer H., Hewitt, Geri D., Minneci, Peter C., Deans, Katherine J.

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Health Heritage©, a Web-Based Tool for the Collection and Assessment of Family Health History: Initial User Experience and Analytic Validity by Cohn, W.F., Ropka, M.E., Pelletier, S.L., Barrett, J.R., Kinzie, M.B., Harrison, M.B., Liu, Z., Miesfeldt, S., Tucker, A.L., Worrall, B.B., Gibson, J., Mullins, I.M., Elward, K.S., Franko, J., Guterbock, T.M., Knaus, W.A.

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