Treffer 1 - 20 von 75 für Suche 'LeBlanc, Sam A.', Suchdauer: 2,15s Treffer weiter einschränken
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    Denial of long‐term issues with agriculture on tropical peatlands will have devastating consequences von Wijedasa, Lahiru S., Lampela, Maija, Leblanc, Marie‐Claire, Yule, Catherine M., Parish, Faizal, Clements, Gopalasamy R., Aziz, Sheema Abdul, Harrison, Mark E., Cheyne, Susan, Anshari, Gusti Z., Meijaard, Erik, Goldstein, Jenny E., Waldron, Susan, Hergoualc'h, Kristell, Dommain, Rene, Evans, Christopher D., Posa, Mary Rose C., Glaser, Paul H., Suryadiputra, Nyoman, Santika, Truly, Padfield, Rory, Kurnianto, Sofyan, Hadisiswoyo, Panut, Page, Susan E., Gauci, Vincent, Van Der Meer, Peter J., Samuel, Marshall K., Choo, Liza Nuriati Lim Kim, O'Reilly, Patrick, Sumarga, Elham, Jain, Anuj, Laurance, William F., Couwenberg, John, Hooijer, Aljosja, Cochrane, Mark A., Perumal, Balu, Peh, Kelvin S.‐H., Comeau, Louis‐Pierre, Verchot, Louis, Harvey, Charles F., Wösten, Henk, Manuri, Solichin, Giesen, Wim, Phelps, Jacob, Yong, Ding Li, Silvius, Marcel, Wedeux, Béatrice M. M., Hoyt, Alison, Osaki, Mitsuru, Hirano, Takashi, Takahashi, Hidenori, Kohyama, Takashi S., Haraguchi, Akira, Nugroho, Nunung P., Coomes, David A., Quoi, Le Phat, Dohong, Alue, Gaveau, David L. A., Lim, Felix K. S., Edwards, David P., Giam, Xingli, Van Der Werf, Guido, Carmenta, Rachel, Gibson, Luke, Regalino, Jhanson, Rieley, Jack, Kettridge, Nicholas, Brown, Chloe, Pirard, Romain, Moore, Sam, Capilla, B. Ripoll, Ballhorn, Uwe, Ho, Hua Chew, Hoscilo, Agata, Lohberger, Sandra, Evans, Theodore A., Yulianti, Nina, Blackham, Grace, Onrizal, Husson, Simon, Murdiyarso, Daniel, Cole, Lydia E. S., Tacconi, Luca, Tonoto, Prayoto, Lee, Janice S. H., Schmilewski, Gerald, Putra, Erianto Indra, Cattau, Megan E., Clymo, R. S., Mujahid, Aazani, Miettinen, Jukka, Liew, Soo Chin, Valpola, Samu, D'Arcy, Laura, Gerding, Michiel, Thornton, Sara A., Kalisz, Barbara, Su, Ahmad Suhaizi Mat, Sloan, Sean, Sayok, Alexander K.

    Veröffentlicht in Global change biology

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    Advanced chronic kidney disease populations have elevated trimethylamine N-oxide levels associated with increased cardiovascular events von Kim, Richard B., Morse, Bridget L., Djurdjev, Ognjenka, Tang, Mila, Barrett, Brendan, Holmes, Daniel T., Madore, Francois, Rigatto, Claudio, Agharazii, Mohsen, Blouin, Joanne, Samson, France, Akbarii, Ayub, Cheesman, Judy, Courtney, Jennilea, Hamer, Sabrina, Delic, Edita, Cronin, Valerie, Barré, Paul, Golden, Jeffrey, Barrett, Brendan, Langille, Elizabeth, Adams, Sandra, Morgan, Janet, Clase, Catherine, Moreau, Cathy, Cooper, Susan, Forzley, Brian, Caron, Susan, Valley, Susan, Sather, Helen, Cournoyer, Serge, Roy, Michèle, Skidmore, Hélène, Beaudry, Dolores, Sahraei, Valla, Donnelly, Sandra, Dacouris, Niki, Marticorena, Rosa, Hemmelgarn, Brenda, Gulewich, Sharon, Hamilton, Troy, Keown, Paul, Zalunardo, Nadia, Rogers, Daniel, Tut, Reena, Paquette, Matthew, Yung, Rossitta, Levin, Adeera, Ferguson, Nancy, Tang, Mila, Chiu, Helen, Carlson, Kathleen, Sioson, Lina, Perry, Taylor, Sheriff, Zainab, Rozen, Naama, Lok, Charmaine, Cross, Michelle, Forrester, Cathy, Madore, François, Moist, Louise, Gallo, Kerri, Langford, Sarah, Slamen, Leah, Cram, Danielle, Muirhead, Norman, Edgar, Mary Jeanne, Edgar, Cameron, Groeneweg, Karen, McKinnon, Eileen, Blackie, Kyla, Nathoo, Bharat, Lau, Kimmy, Parmar, Malvinder, Gelinas, Sylvie, Leblanc, Martine, Lépine, Lucie, Rigatto, Claudio, Friesen, Dolores, Soroka, Steven, Fleet, Susan, Squires, Jeanette, Thanamayooran, Siva, Binder, Michael, Hines, Christine, McNeil, Brenda, McDougall, Patrice, Howard, Joy, Hines, Kathleen, Tobe, Sheldon, Chessman, Mary, Perkins, Nancy, Agelopoulos, Martha, Knox, Stacey, Richards, Tiffany, Tonelli, Marcello, Szigety, Susan, Opgenorth, Dawn, Yeates, Karen, Mahoney, Karen

    Veröffentlicht in Kidney international

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    HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder von Niggl, Eva, Elgersma, Minetta, Clayton-Smith, Jill, Jain, Mahim, Krantz, Ian, Vetrini, Francesco, Witt, Dennis, Zhou, Dihong, Arumugam, P., Boardman-Pretty, F., Brown, M.A., Chan, G.C., Henderson, S., Kayikci, M., Kousathanas, A., Lahnstein, L., Maleady-Crowe, F., McEntagart, M., Minneci, F., O‘Donovan, P., Pereira, M.B., Rahim, T., Savage, K., Sawant, K., Smith, S.C., Sosinsky, A., Tucci, A., Williams, E., Alvey, Justin, Andrews, Ashley, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Bayrak-Toydemir, Pinar, Bejerano, Gill, Bican, Anna, Bivona, Stephanie, Bonner, Devon, Burke, Elizabeth A., Chang, Ta Chen, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Clark, Gary D., Corona, Rosario, Crouse, Andrew B., Dipple, Katrina, Doss, Argenia L., Fisher, Paul G., Fu, Jiayu, Gahl, William A., Hamid, Rizwan, Hassey, Kelly, Huang, Yan, Introne, Wendy, Izumi, Kosuke, Jean-Marie, Orpa, Kaitryn, Emerald, Ketkar, Shamika, Kiley, Dana, Kilich, Gonench, Kohane, Isaac S., Krakow, Deborah, Lewis, Richard A., Loscalzo, Joseph, Maghiro, AudreyStephannie, Mahoney, Rachel, Mao, Rong, Marth, Gabor, McCauley, Jacob, McConkie-Rosell, Allyn, McCray, Alexa T., McGee, Elisabeth, Mirzaa, Ghayda, Morava, Eva, Morimoto, Marie, Nelson, Stanley F., Novacic, Donna, Posey, Jennifer E., Potocki, Lorraine, Swerdzewski, Barbara N., Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Rossignol, Francis, Schaechter, Judy, Shashi, Vandana, Shin, Jimann, Sinsheimer, Janet, Solnica-Krezel, Lilianna, Sullivan, Kathleen, Tan, Amelia L., Tarakad, Arjun, Telischi, Fred, Urv, Tiina K., Wahl, Colleen E., Wan, Jijun


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    De novo variants in DENND5B cause a neurodevelopmental disorder von Scala, Marcello, Ferla, Matteo, Fatemi, Ali, Phillips, John A., Rio, Marlene, Siquier, Karine, Musante, Ilaria, Baldassari, Simona, Iacomino, Michele, Acosta, Maria T., Allworth, Aimee, Afzali, Ben, Bademci, Guney, Beck, Anita, Berry, Gerard T., Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, HsiaoTuan, Chinn, Ivan, Clark, Gary D., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Fisher, Paul G., Fogel, Brent L., Gahl, William A., Glass, Ian, Godfrey, Rena A., Grajewski, Alana, Gropman, Andrea, Halley, Meghan C., Hanchard, Neal, Hassey, Kelly, Hayes, Nichole, Hom, Jason, Huang, Alden, Introne, Wendy, Jarvik, Jeffrey, Jobanputra, Vaidehi, Kilich, Gonench, Kohler, Jennefer N., Korrick, Susan, Krasnewich, Donna M., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Marth, Gabor, Martin, Beth A., Marwaha, Shruti, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo, Morimoto, Marie, Nakano-Okuno, Mariko, Nieves-Rodriguez, Shirley, Orengo, James P., Pace, Laura, Parker, Neil H., Quinlan, Aaron, Raper, Anna, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rossignol, Francis, Saporta, Mario, Schaechter, Judy, Seto, Elaine, Shelkowitz, Emily, Shin, Jimann, Solnica-Krezel, Lilianna, Sweetser, David A., Sybert, Virginia, Tarakad, Arjun, Velinder, Matt, Viskochil, Dave, Ward, Patricia A., Wegner, Daniel, Weisz Hubshman, Monika, Wener, Mark, Wenger, Tara, Reed, Sara, Al Saif, Hind, Walsh, Matthew B., Gustincich, Stefano, Ruggiero, Sarah M., Fitzgerald, Mark P., Helbig, Ingo, Severino, Mariasavina


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    Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly von Wan, Jijun, Adams, David R., Balasubramanyam, Ashok, Bamshad, Michael, Beck, Anita, Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bernstein, Jonathan A., Bonner, Devon, Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Cassini, Thomas, Chao, Hsiao-Tuan, Chinn, Ivan, Cogan, Joy D., Coggins, Matthew, Cole, F. Sessions, Dai, Hongzheng, Davis, Joie, Douine, Emilie D., Eckstein, David J., Emrick, Lisa T., Hadley, Don, Halley, Meghan C., Hassey, Kelly, High, Frances, Hing, Anne, Hisama, Fuki M., Hutchison, Sarah, Jean-Marie, Orpa, Kaitryn, Emerald, Kilich, Gonench, Kobren, Shilpa N., Krakow, Deborah, Krasnewich, Donna M., Kravets, Elijah, Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Loo, Sandra K., MacRae, Calum A., Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Marth, Gabor, McCauley, Jacob, McConkie-Rosell, Allyn, McCray, Alexa T., Novacic, Donna, Oglesbee, Devin, Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raper, Anna, Raskind, Wendy, Renteria, Genecee, Rives, Lynette, Rodan, Lance H., Rosenthal, Elizabeth, Rossignol, Francis, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Scott, Daryl A., Shelkowitz, Emily, Shin, Jimann, Sisco, Kathy, Smith, Edward C., Solomon, Ben, Sullivan, Kathleen, Sybert, Virginia, Tarakad, Arjun, Tekin, Mustafa, Thorson, Willa, Toro, Camilo, Tran, Alyssa A., Ungar, Rachel A., Vanderver, Adeline, Viskochil, Dave, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Worley, Kim, Xiao, Changrui, Yang, John, Saillour, Virginie, Sacharow, Stephanie, Kanca, Oguz, Bellen, Hugo J., Palmer, Christina G.S.

    Veröffentlicht in Genetics in medicine

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