Impacts of Hurricane Michael on Watershed Hydrology: A Case Study in the Southeastern United States von Worley, Elijah, Liu, Ning, Sun, Ge, Norman, Steven P., Christie, William M., Gavazzi, Michael, Boggs, Johnny, McNulty, Steven G.

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'There were ethical dilemmas all day long!': harrowing tales of ethnographic researchers in criminology and criminal justice von Worley, Robert M., Worley, Vidisha Barua, Wood, Brittany Ann

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IVIVE: Facilitating the Use of In Vitro Toxicity Data in Risk Assessment and Decision Making von Chang, Xiaoqing, Tan, Yu-Mei, Allen, David G, Bell, Shannon, Brown, Paul C, Browning, Lauren, Ceger, Patricia, Gearhart, Jeffery, Hakkinen, Pertti J, Kabadi, Shruti V, Kleinstreuer, Nicole C, Lumen, Annie, Matheson, Joanna, Paini, Alicia, Pangburn, Heather A, Petersen, Elijah J, Reinke, Emily N, Ribeiro, Alexandre J S, Sipes, Nisha, Sweeney, Lisa M, Wambaugh, John F, Wange, Ronald, Wetmore, Barbara A, Mumtaz, Moiz

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Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract von Hwang, Daw-Yang, Kohl, Stefan, Fan, Xueping, Vivante, Asaf, Chan, Stefanie, Dworschak, Gabriel C., Schulz, Julian, van Eerde, Albertien M., Hilger, Alina C., Gee, Heon Yung, Pennimpede, Tracie, Herrmann, Bernhard G., van de Hoek, Glenn, Renkema, Kirsten Y., Schell, Christoph, Huber, Tobias B., Reutter, Heiko M., Soliman, Neveen A., Stajic, Natasa, Bogdanovic, Radovan, Kehinde, Elijah O., Lifton, Richard P., Tasic, Velibor, Lu, Weining, Hildebrandt, Friedhelm

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The Changing Correctional Mental Health Workers' Demographics and Duties von Ricks, Elijah P., Ferreira, Mark, Eno Louden, Jennifer

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Analysis of the P. lividus sea urchin genome highlights contrasting trends of genomic and regulatory evolution in deuterostomes von Marlétaz, Ferdinand, Couloux, Arnaud, Poulain, Julie, Labadie, Karine, Da Silva, Corinne, Mangenot, Sophie, Noel, Benjamin, Poustka, Albert J., Dru, Philippe, Pegueroles, Cinta, Borra, Marco, Lowe, Elijah K., Lhomond, Guy, Besnardeau, Lydia, Le Gras, Stéphanie, Ye, Tao, Gavriouchkina, Daria, Russo, Roberta, Costa, Caterina, Zito, Francesca, Anello, Letizia, Nicosia, Aldo, Ragusa, Maria Antonietta, Pascual, Marta, Molina, M. Dolores, Chessel, Aline, Di Carlo, Marta, Turon, Xavier, Copley, Richard R., Exposito, Jean-Yves, Martinez, Pedro, Cavalieri, Vincenzo, Ben Tabou de Leon, Smadar, Croce, Jenifer, Oliveri, Paola, Matranga, Valeria, Di Bernardo, Maria, Morales, Julia, Cormier, Patrick, Geneviève, Anne-Marie, Aury, Jean Marc, Barbe, Valérie, Wincker, Patrick, Arnone, Maria Ina, Gache, Christian, Lepage, Thierry

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Citrus aurantifolia (Chrism.) Swingle peel extract attenuate nephrotoxicity induced by doxorubicin von Oyinloye, Elijah O., Murtala, Abdullahi A., Oladoja, Farouk A., Aderinola, Aderonke A., Okunye, Lionel O., Saka, Sule A., Abolarinwa, Julius A., Kasumu, Olubusayo E., Osipitan, Lukman E.

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Improvements in or relating to apparatus for seasoning and colouring tobacco pipes

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Correctional officers and the use of force as an organizational behavior von Schultz, William J.

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Electrostatic particle ionization for suppressing air pollutants in cage-free layer facilities von Bist, Ramesh Bahadur, Yang, Xiao, Subedi, Sachin, Ritz, Casey W., Kim, Woo Kyun, Chai, Lilong

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Why Online Consumption Communities Brutalize von Sibai, Olivier, Luedicke, Marius K, de Valck, Kristine

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Participation in a national diagnostic research study: assessing the patient experience von Rosenfeld, Lindsay E, LeBlanc, Kimberly, Nagy, Anna, Ego, Braeden K, McCray, Alexa T

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Continuing a search for a diagnosis: the impact of adolescence and family dynamics von Miller, Ilana M, Yashar, Beverly M, Macnamara, Ellen F

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Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients von Fitzsimmons, Lane, Beaulieu-Jones, Brett, Kobren, Shilpa Nadimpalli

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Reanalysis of RNA sequencing data ends diagnostic odyssey and expands the phenotypic spectrum of congenital titinopathy von McNamee, Lucy, Huang, Alden, Wang, Lee‐kai, Buckley, Anne F., Adams, David R., Afzali, Ben, Allworth, Aimee, Alvey, Justin, Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Borja, Nicholas, Briere, Lauren C., Callaway, Kaitlin, Chanprasert, Sirisak, Coggins, Matthew, Craigen, William J., Cuddapah, Vishnu, Darr, Kahlen, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Karasozen, Yigit, Ketkar, Shamika, Kilich, Gonench, Klee, Eric, Kohler, Jennefer N., Korrick, Susan, Kravets, Elijah, Lalani, Seema R., Latchman, Kumarie, LeBlanc, Kimberly, Liu, Pengfei, Longo, Nicola, MacRae, Calum A., Maghiro, AudreyStephannie, Mahoney, Rachel, Malicdan, May Christine V., Martin, Beth A., Miller, Danny, Moretti, Paolo, Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network von Fernandes, Samuela, Adams, David R., Afzali, Ben, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Beck, Anita, Beggs, Alan H., Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Borja, Nicholas, Briere, Lauren C., Byers, Peter, Callaway, Kaitlin, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Corona, Rosario I., Craigen, William J., Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Darr, Kahlen, Dasari, Surendra, Dipple, Katrina, Dorrani, Naghmeh, Douine, Emilie D., Earl, Dawn, Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Goddard, Page C., Gropman, Andrea, Halley, Meghan C., Hanchard, Neal, High, Frances, Hing, Anne, Hisama, Fuki M., Hom, Jason, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Hurst, Anna, Introne, Wendy, Jarvik, Gail P., Kanca, Oguz, Kiley, Dana, Korf, Bruce, Krakow, Deborah, Lam, Christina, Lanpher, Brendan C., Lee, Brendan H., Liu, Pengfei, Longo, Nicola, Malicdan, May Christine V., Marth, Gabor, Martínez‐Agosto, Julian A., McCray, Alexa T., Might, Matthew, Mikati, Mohamad, Moretti, Paolo, Morimoto, Marie, Mulvihill, John J., Novacic, Donna, Oglesbee, Devin, Parker, Neil H., Petcharet, Leoyklang, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rajagopalan, Ramakrishnan, Reuter, Chloe M., Sabaii, Marla, Sheppeard, Sam, Silverman, Edwin K., Skelton, Tammi, Skraban, Cara, Sutton, Shirley, Tabor, Holly K., Tan, Queenie, Taylor, Herman, Tekin, Mustafa, Tifft, Cynthia J., Toro, Camilo, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Wambach, Jennifer, Ward, Patricia A., Hubshman, Monika Weisz, Wenger, Tara, Westerfield, Monte, Wood, Heidi

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A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseases von Furuta, Yutaka, Tinker, Rory J, Hamid, Rizwan, Cogan, Joy D, Ezell, Kimberly M, Oglesbee, Devin, DeBerardinis, Ralph J, Phillips, 3rd, John A

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Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant von Gulsevin, Alican, Hamid, Rizwan, Neumann, Serena, Phillips, John A., Adams, David R., Afzali, Ben, Andrews, Ashley, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Borja, Nicholas, Butte, Manish J., Byrd, William E., Callaway, Kaitlin, Carvalho, George, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Cogan, Joy D., Coggins, Matthew, Corner, Brian, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Kaitryn, Emerald, Kanca, Oguz, Kohler, Jennefer N., Krakow, Deborah, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Liu, Pengfei, Longo, Nicola, Mahoney, Rachel, Marth, Gabor, McCray, Alexa T., Might, Matthew, Miller, Danny, Moretti, Paolo, Mulvihill, John J., Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants von Lu, Jinfeng, Toro, Camilo, Adams, David R, Moreno, Cristiane Araujo Martins, Lee, Wan-Ping, Leung, Yuk Yee, Harms, Mathew B, Vardarajan, Badri, Heinzen, Erin L

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Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1 von Schoch, Kelly, McConkie-Rosell, Allyn, Walley, Nicole, Bhambhani, Vikas, Feyma, Timothy, Pizoli, Carolyn E, Smith, Edward C, Tan, Queenie K.-G, Shashi, Vandana

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