A molecular rheostat: Kv2.1 currents maintain or suppress repetitive firing in motoneurons by Romer, Shannon H., Deardorff, Adam S., Fyffe, Robert E. W.

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Swimming against the tide: investigations of the C-bouton synapse by Deardorff, Adam S, Romer, Shannon H, Sonner, Patrick M, Fyffe, Robert E W

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Another novel non-conducting functional role for Kv2 channels – regulation of calcium signaling by Fyffe, Robert EW, Deardorff, Adam S

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Location, location, location: the organization and roles of potassium channels in mammalian motoneurons by Deardorff, Adam S., Romer, Shannon H., Fyffe, Robert E.W.

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Muscle proprioceptors in adult rat: mechanosensory signaling and synapse distribution in spinal cord by Vincent, Jacob A, Gabriel, Hanna M, Deardorff, Adam S, Nardelli, Paul, Fyffe, Robert E W, Burkholder, Thomas, Cope, Timothy C

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Incentive structure in team-based learning: graded versus ungraded Group Application exercises by Deardorff, Adam S, Moore, Jeremy A, McCormick, Colleen, Koles, Paul G, Borges, Nicole J

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Expression of postsynaptic Ca2+‐activated K+ (SK) channels at C‐bouton synapses in mammalian lumbar α‐motoneurons by Deardorff, Adam S., Romer, Shannon H., Deng, Zhihui, Bullinger, Katie L., Nardelli, Paul, Cope, Timothy C., Fyffe, Robert E. W.

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Development of emotional intelligence in a team-based learning internal medicine clerkship by Borges, Nicole J., Kirkham, Karen, Deardorff, Adam S., Moore, Jeremy A.

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Complex impairment of IA muscle proprioceptors following traumatic or neurotoxic injury by Vincent, Jacob A., Nardelli, Paul, Gabriel, Hanna M., Deardorff, Adam S., Cope, Timothy C.

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Redistribution of Kv2.1 ion channels on spinal motoneurons following peripheral nerve injury by Romer, Shannon H, Dominguez, Kathleen M, Gelpi, Marc W, Deardorff, Adam S, Tracy, Robert C, Fyffe, Robert. E.W

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Activity‐dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons by Romer, Shannon H., Deardorff, Adam S., Fyffe, Robert E. W.

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Sound stimulation modulates high-threshold K+ currents in mouse auditory brainstem neurons by Leão, Katarina E., Leão, Richardson N., Deardorff, Adam S., Garrett, Andrew, Fyffe, Robert, Walmsley, Bruce

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Lateral superior olive function in congenital deafness by Couchman, Kiri, Garrett, Andrew, Deardorff, Adam S., Rattay, Frank, Resatz, Susanne, Fyffe, Robert, Walmsley, Bruce, Leão, Richardson N.

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Expression of postsynaptic Ca2+-activated K+ (SK) channels at C-bouton synapses in mammalian lumbar -motoneurons by Deardorff, Adam S, Romer, Shannon H, Deng, Zhihui, Bullinger, Katie L, Nardelli, Paul, Cope, Timothy C, Fyffe, Robert E W

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Expression of postsynaptic Ca 2+ ‐activated K + (SK) channels at C‐bouton synapses in mammalian lumbar α‐motoneurons by Deardorff, Adam S., Romer, Shannon H., Deng, Zhihui, Bullinger, Katie L., Nardelli, Paul, Cope, Timothy C., Fyffe, Robert E. W.

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Remote Characterization of Dominant Wavelengths From Surface Folding on Lava Flows Using Lidar and Discrete Fourier Transform Analyses by Deardorff, Nicholas, Booth, Adam, Cashman, Katharine

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Segmental congenital hemangiomas: Three cases of a rare entity by Smith, Robert J., Metry, Denise, Deardorff, Matthew A., Heller, Elizabeth, Grand, Katheryn L., Iacobas, Ionela, Rubin, Adam I., Phung, Thuy L., Lopez‐Terrada, Dolores, Steicher, Jenna, Cahill, Anne Marie, Low, David, Treat, James R.

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A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay by Schoch, Kelly, Meng, Linyan, Szelinger, Szabolcs, Liston, Eriskay, Scaglia, Fernando, Rosenfeld, Jill A., Deardorff, Matthew A., Akdemir, Zeynep Coban, Jasien, Joan, Kansagra, Sujay, Freedman, Sharon, Bale, Sherri, Nelson, Stanley F., Lee, Hane, Dorrani, Naghmeh, Nelson, Stanley F., Lee, Hane, Vilain, Eric, Kantarci, Sibel, Dorrani, Naghmeh, Mullegama, Sureni, Kang, Sung-Hae, Bacino, Carlos A., Balasubramanyam, Ashok, Craigen, William J., Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Lewis, Richard A., Moretti, Paolo M., Orange, Jordan S., Potocki, Lorraine, Rosenfeld, Jill A., Wangler, Michael F., Yamamoto, Shinya, Muzny, Donna M., Yang, Yaping, Gropman, Andrea L., Goldstein, David B., Schoch, Kelly, Walley, Nicole M., Beggs, Alan H., Krier, Joel B., Loscalzo, Joseph, Walsh, Chris A., Esteves, Cecilia, Holm, Ingrid A., Kohane, Isaac S., Mazur, Paul, McCray, Alexa T., Might, Matthew, Splinter, Kimberly, Brown, Donna M., Dorset, Dan C., Jones, Angela L., Lazar, Jozef, Newberry, J. Scott, Schroeder, Molly C., Strong, Kimberly A., Dayal, Jyoti G., Loomis, Carson R., Mulvihill, John J., Wise, Anastasia L., Haendel, Melissa, Kyle, Jennifer E., Webb-Robertson, Bobbie-Jo M., Kohler, Jennefer N., Herzog, Matthew R., Nelson, Stan F., Palmer, Christina G.S., Papp, Jeanette C., Adams, Christopher J., Burke, Elizabeth A., Chao, Katherine R., Davids, Mariska, Frost, Kate, Gartner, Valerie, Gordon, Mary “Gracie” G., Groden, Catherine A., Hardee, Isabel, Johnston, Jean M., Latham, Lea, Lau, C. Christopher, Maduro, Valerie V., Pusey, Barbara N., Sadozai, Sarah, Schaffer, Katherine E., Sharma, Prashant, Thomas, Sara P., Valivullah, Zaheer M., Wahl, Colleen E., Weech, Alec A., Westerfield, Monte, Bican, Anna, Phillips, John A., Robertson, Amy K., Xiao, Rui, Posey, Jennifer E., Wangler, Michael F., Shashi, Vandana

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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine by Goddard, Katrina A.B., Bernhardt, Barbara A., Biswas, Sawona, Bowling, Kevin M., Caga-anan, Charlisse F., Chinnaiyan, Arul M., Clayton, Ellen W., East, Kelly, Garraway, Levi A., Garrett, Jeremy R., Gray, Stacy W., Hindorff, Lucia A., Lewis, Michelle Huckaby, Hutter, Carolyn M., Janne, Pasi A., Knoppers, Bartha M., Krantz, Ian D., Manolio, Teri A., Nickerson, Deborah A., Ou, Jeffrey, Parsons, Donald W., Petersen, Gloria M., Plon, Sharon E., Rehm, Heidi L., Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Shirts, Brian, Tabor, Holly K., Tarczy-Hornoch, Peter, Appelbaum, Paul S., Arora, Shubhangi, Brothers, Kyle B., Brown, Brian L., Caga-anan, Charlisse F., Calikoglu, Muge G., Christensen, Kurt D., Cirino, Allison L., Conlin, Laura K., Crosslin, David R., Davis, James V., Dorschner, Michael O., Dugan, Noreen P., Exe, Nicole, Fishler, Kristen, Ghrundmeier, Bob, Gordon, Adam S., Gray, David E., Gray, Stacy W., Gutierrez, Amanda M., Hensman, Naomi, Hiatt, Susan M., Himes, Patricia, Horike-Pyne, Martha J., Hull, Sara, Jensen, Brian C., Joffe, Steve, Kaufman, Dave, Kim, Jerry H., Klein, William, Lambert, Michele P., Leo, Michael C., Lewis, Katie, Lonigro, Bob, Machini, Kalotina, Manolio, Teri A., McCullough, Laurence, McMullen, Carmit, Mooney, Sean D., Moore, Elizabeth G., Muzny, Donna, Ng, David, Nickerson, Deborah A., Oliver, Nelly M., Parsons, Will, Plon, Sharon, Powell, Bradford C., Raesz-Martinez, Robin A., Raskind, Wendy H., Rehm, Heidi L., Reiss, Jacob A., Robertson, Peggy D., Robinson, Dan, Salama, Joseph, Scarano, Maria I., Sholl, Lynette M., Silverman, Elian, Simmons, Shirley, Spinner, Nancy B., Stoffel, Elena, Tilley, Christian R., Trinidad, Susan, Ubel, Peter, Vassy, Jason L., Vries, Raymond D., Weck, Karen, Wolf, Susan M., Wynn, Julia, Yu, Joon-Ho, Zikmund-Fisher, Brian J.

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Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder by Schneeberger, Pauline E, Kortüm, Fanny, Korenke, Georg Christoph, Alawi, Malik, Santer, René, Woidy, Mathias, Buhas, Daniela, Fox, Stephanie, Juusola, Jane, Alfadhel, Majid, Webb, Bryn D, Coci, Emanuele G, Abou Jamra, Rami, Siekmeyer, Manuela, Biskup, Saskia, Heller, Corina, Maier, Esther M, Javaher-Haghighi, Poupak, Bedeschi, Maria F, Ajmone, Paola F, Iascone, Maria, Peeters, Hilde, Ballon, Katleen, Jaeken, Jaak, Rodríguez Alonso, Aroa, Palomares-Bralo, María, Santos-Simarro, Fernando, Meuwissen, Marije E C, Beysen, Diane, Kooy, R Frank, Houlden, Henry, Murphy, David, Doosti, Mohammad, Karimiani, Ehsan G, Mojarrad, Majid, Maroofian, Reza, Noskova, Lenka, Kmoch, Stanislav, Honzik, Tomas, Cope, Heidi, Sanchez-Valle, Amarilis, Gelb, Bruce D, Kurth, Ingo, Hempel, Maja, Kutsche, Kerstin

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