arrow
返回
C

Carolien G. F. de Kovel

royal netherlands academy of arts & sciences

48H指数
121论文数
8.4K被引数
收录论文 45
发表时间
Tailoring a DMA-based cryopreservation protocol with anti-freeze (glycol)proteins for commercial and native breeds of chicken基于DMA的抗冻(乙二醇)蛋白定制鸡商业和地方品种的低温保存方案
err2026-02-01
err0
PREAI
errBernal, Berenice; Varadi, Eva; Drobnyak, Arpad; Hogervorst, Tim; Liptoi, Krisztina; Voets, Ilja K.; de Wit, Agnes; Santiago-Moreno, Julian; Hawken, Rachel; de Kovel, Carolien; Hiemstra, Sipke-Joost; Woelders, Henri; Vegi, Barbara
err分享
err收藏
Mapping brain asymmetry in health and disease through the ENIGMA consortium通过ENIGMA联盟绘制健康和疾病中的大脑不对称
err2020-05-18
err102
errOAAI
errKong, Xiang-Zhen; Postema, Merel C.; Guadalupe, Tulio; de Kovel, Carolien; Boedhoe, Premika S. W.; Hoogman, Martine; Mathias, Samuel R.; van Rooij, Daan; Schijven, Dick; Glahn, David C.; Medland, Sarah E.; Jahanshad, Neda; Thomopoulos, Sophia, I; Turner, Jessica A.; Buitelaar, Jan; van Erp, Theo G. M.; Franke, Barbara; Fisher, Simon E.; van den Heuvel, Odile A.; Schmaal, Lianne; Thompson, Paul M.; Francks, Clyde
err分享
err收藏
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries谜与全球神经科学: 40多个国家对健康和疾病中的大脑进行的十年大规模研究
err2020-03-20
err374
errOAAI
errThompson, Paul M.; Jahanshad, Neda; Ching, Christopher R. K.; Salminen, Lauren E.; Thomopoulos, Sophia I.; Bright, Joanna; Baune, Bernhard T.; Bertolin, Sara; Bralten, Janita; Bruin, Willem B.; Buelow, Robin; Chen, Jian; Chye, Yann; Dannlowski, Udo; de Kovel, Carolien G. F.; Donohoe, Gary; Eyler, Lisa T.; Faraone, Stephen V.; Favre, Pauline; Filippi, Courtney A.; Frodl, Thomas; Garijo, Daniel; Gil, Yolanda; Grabe, Hans J.; Grasby, Katrina L.; Hajek, Tomas; Han, Laura K. M.; Hatton, Sean N.; Hilbert, Kevin; Ho, Tiffany C.; Holleran, Laurena; Homuth, Georg; Hosten, Norbert; Houenou, Josselin; Ivanov, Iliyan; Jia, Tianye; Kelly, Sinead; Klein, Marieke; Kwon, Jun Soo; Laansma, Max A.; Leerssen, Jeanne; Lueken, Ulrike; Nunes, Abraham; Neill, Joseph O'; Opel, Nils; Piras, Fabrizio; Piras, Federica; Postema, Merel C.; Pozzi, Elena; Shatokhina, Natalia; Soriano-Mas, Carles; Spalletta, Gianfranco; Sun, Daqiang; Teumer, Alexander; Tilot, Amanda K.; Tozzi, Leonardo; van der Merwe, Celia; Van Someren, Eus J. W.; van Wingen, Guido A.; Voelzke, Henry; Walton, Esther; Wang, Lei; Winkler, Anderson M.; Wittfeld, Katharina; Wright, Margaret J.; Yun, Je-Yeon; Zhang, Guohao; Zhang-James, Yanli; Adhikari, Bhim M.; Agartz, Ingrid; Aghajani, Moji; Aleman, Andre; Althoff, Robert R.; Altmann, Andre; Andreassen, Ole A.; Baron, David A.; Bartnik-Olson, Brenda L.; Bas-Hoogendam, Janna; Baskin-Sommers, Arielle R.; Bearden, Carrie E.; Berner, Laura A.; Boedhoe, Premika S. W.; Brouwer, Rachel M.; Buitelaar, Jan K.; Caeyenberghs, Karen; Cecil, Charlotte A. M.; Cohen, Ronald A.; Cole, James H.; Conrod, Patricia J.; De Brito, Stephane A.; de Zwarte, Sonja M. C.; Dennis, Emily L.; Desrivieres, Sylvane; Dima, Danai; Ehrlich, Stefan; Esopenko, Carrie; Fairchild, Graeme; Fisher, Simon E.; Fouche, Jean-Paul; Francks, Clyde; Frangou, Sophia; Franke, Barbara; Garavan, Hugh P.; Glahn, David C.; Groenewold, Nynke A.; Gurholt, Tiril P.; Gutman, Boris A.; Hahn, Tim; Harding, Ian H.; Hernaus, Dennis; Hibar, Derrek P.; Hillary, Frank G.; Hoogman, Martine; Pol, Hilleke E.; Jalbrzikowski, Maria; Karkashadze, George A.; Klapwijk, Eduard T.; Knickmeyer, Rebecca C.; Kochunov, Peter; Koerte, Inga K.; Kong, Xiang-Zhen; Liew, Sook-Lei; Lin, Alexander P.; Logue, Mark W.; Luders, Eileen; Macciardi, Fabio; Mackey, Scott; Mayer, Andrew R.; McDonald, Carrie R.; McMahon, Agnes B.; Medland, Sarah E.; Modinos, Gemma; Morey, Rajendra A.; Mueller, Sven C.; Mukherjee, Pratik; Namazova-Baranova, Leyla; Nir, Talia M.; Olsen, Alexander; Paschou, Peristera; Pine, Daniel S.; Pizzagalli, Fabrizio; Renteria, Miguel E.; Rohrer, Jonathan D.; Saemann, Philipp G.; Schmaal, Lianne; Schumann, Gunter; Shiroishi, Mark S.; Sisodiya, Sanjay M.; Smit, Dirk J. A.; Sonderby, Ida E.; Stein, Dan J.; Stein, Jason L.; Tahmasian, Masoud; Tate, David F.; Turner, Jessica A.; van den Heuvel, Odile A.; van der Wee, Nic J. A.; van der Werf, Ysbrand D.; van Erp, Theo G. M.; van Haren, Neeltje E. M.; van Rooij, Daan; van Velzen, Laura S.; Veer, Ilya M.; Veltman, Dick J.; Villalon-Reina, Julio E.; Walter, Henrik; Whelan, Christopher D.; Wilde, Elisabeth A.; Zarei, Mojtaba; Zelman, Vladimir
err分享
err收藏
No Alterations of Brain Structural Asymmetry in Major Depressive Disorder: An ENIGMA Consortium Analysis
err2019-12-01
err34
errOAAI
errde Kovel, Carolien G. F.; Aftanas, Lyubomir; Aleman, Andre; Alexander-Bloch, Aaron F.; Baune, Bernhard T.; Brack, Ivan; Bulow, Robin; Busatto Filho, Geraldo; Carballedo, Angela; Connolly, Colm G.; Cullen, Kathryn R.; Dannlowski, Udo; Davey, Christopher G.; Dima, Danai; Dohm, Katharina; Erwin-Grabner, Tracy; Frodl, Thomas; Fu, Cynthia H. Y.; Hall, Geoffrey B.; Glahn, David C.; Godlewska, Beata; Gotlib, Ian H.; Goya-Maldonado, Roberto; Grabe, Hans Jorgen; Groenewold, Nynke A.; Grotegerd, Dominik; Gruber, Oliver; Harris, Mathew A.; Harrison, Ben J.; Hatton, Sean N.; Hickie, Ian B.; Ho, Tiffany C.; Jahanshad, Neda; Kircher, Tilo; Kramer, Bernd; Krug, Axel; Lagopoulos, Jim; Leehr, Elisabeth J.; Li, Meng; MacMaster, Frank P.; MacQueen, Glenda; McIntosh, Andrew M.; McLellan, Quinn; Medland, Sarah E.; Mueller, Bryon A.; Nenadic, Igor; Osipov, Evgeny; Papmeyer, Martina; Portella, Maria J.; Reneman, Liesbeth; Rosa, Pedro G. P.; Sacchet, Matthew D.; Schnell, Knut; Schrantee, Anouk; Sim, Kang; Simulionyte, Egle; Sindermann, Lisa; Van der Werff, Steven J. A.; Veer, Ilya M.; Vives-Gilabert, Yolanda; Volzke, Henry; Walter, Henrik; Walter, Martin; Schreiner, Melinda Westlund; Whalley, Heather; Winter, Nils; Wittfeld, Katharina; Yang, Tony T.; Yuksel, Dilara; Zaremba, Dario; Thompson, Paul M.; Veltman, Dick J.; Schmaal, Lianne; Francks, Clyde
err分享
err收藏
The molecular genetics of hand preference revisited
err2019-04-12
err49
errOAAI
errde Kovel, Carolien G. F.; Francks, Clyde
err分享
err收藏
A large-scale population study of early life factors influencing left-handedness
err2019-01-24
err111
errOAAI
errde Kovel, Carolien G. F.; Carrion-Castillo, Amaia; Francks, Clyde
err分享
err收藏
LEFT-RIGHT ASYMMETRY OF MATURATION RATES IN HUMAN EMBRYONIC NEURAL DEVELOPMENT
err2019-01-01
err0
errOAAI
errde Kovel, Carolien; Lisgo, Steven; Karlebach, Guy; Ju, Jia; Cheng, Gang; Fisher, Simon E.; Francks, Clyde
err分享
err收藏
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies全基因组巨型分析确定了16个基因座,并突出了常见癫痫的不同生物学机制
err2018-12-10
err293
errOAAI
errAbou-Khalil, Bassel; Auce, Pauls; Avbersek, Andreja; Bahlo, Melanie; Balding, David J.; Bast, Thomas; Baum, Larry; Becker, Albert J.; Becker, Felicitas; Berghuis, Bianca; Berkovic, Samuel F.; Boysen, Katja E.; Bradfield, Jonathan P.; Brody, Lawrence C.; Buono, Russell J.; Campbell, Ellen; Cascino, Gregory D.; Catarino, Claudia B.; Cavalleri, Gianpiero L.; Cherny, Stacey S.; Chinthapalli, Krishna; Coffey, Alison J.; Compston, Alastair; Coppola, Antonietta; Cossette, Patrick; Craig, John J.; de Haan, Gerrit-Jan; De Jonghe, Peter; de Kovel, Carolien G. F.; Delanty, Norman; Depondt, Chantal; Devinsky, Orrin; Dlugos, Dennis J.; Doherty, Colin P.; Elger, Christian E.; Eriksson, Johan G.; Ferraro, Thomas N.; Feucht, Martha; Francis, Ben; Franke, Andre; French, Jacqueline A.; Freytag, Saskia; Gaus, Verena; Geller, Eric B.; Gieger, Christian; Glauser, Tracy; Glynn, Simon; Goldstein, David B.; Gui, Hongsheng; Guo, Youling; Haas, Kevin F.; Hakonarson, Hakon; Hallmann, Kerstin; Haut, Sheryl; Heinzen, Erin L.; Helbig, Ingo; Hengsbach, Christian; Hjalgrim, Helle; Iacomino, Michele; Ingason, Andres; Jamnadas-Khoda, Jennifer; Johnson, Michael R.; Kalviainen, Reetta; Kantanen, Anne-Mari; Kasperaviciute, Dalia; Trenite, Dorothee Kasteleijn-Nolst; Kirsch, Heidi E.; Knowlton, Robert C.; Koeleman, Bobby P. C.; Krause, Roland; Krenn, Martin; Kunz, Wolfram S.; Kuzniecky, Ruben; Kwan, Patrick; Lal, Dennis; Lau, Yu-Lung; Lehesjoki, Anna-Elina; Lerche, Holger; Leu, Costin; Lieb, Wolfgang; Lindhout, Dick; Lo, Warren D.; Lopes-Cendes, Iscia; Lowenstein, Daniel H.; Malovini, Alberto; Marson, Anthony G.; Mayer, Thomas; McCormack, Mark; Mills, James L.; Mirza, Nasir; Moerzinger, Martina; Moller, Rikke S.; Molloy, Anne M.; Muhle, Hiltrud; Newton, Mark; Ng, Ping-Wing; Noethen, Markus M.; Nuernberg, Peter; O'Brien, Terence J.; Oliver, Karen L.; Palotie, Aarno; Pangilinan, Faith; Peter, Sarah; Petrovski, Slave; Poduri, Annapurna; Privitera, Michael; Radtke, Rodney; Rau, Sarah; Reif, Philipp S.; Reinthaler, Eva M.; Rosenow, Felix; Sander, Josemir W.; Sander, Thomas; Scattergood, Theresa; Schachter, Steven C.; Schankin, Christoph J.; Scheffer, Ingrid E.; Schmitz, Bettina; Schoch, Susanne; Sham, Pak C.; Shih, Jerry J.; Sills, Graeme J.; Sisodiya, Sanjay M.; Slattery, Lisa; Smith, Alexander; Smith, David F.; Smith, Michael C.; Smith, Philip E.; Sonsma, Anja C. M.; Speed, Doug; Sperling, Michael R.; Steinhoff, Bernhard J.; Stephani, Ulrich; Stevelink, Remi; Strauch, Konstantin; Striano, Pasquale; Stroink, Hans; Surges, Rainer; Tan, K. Meng; Thio, Liu Lin; Thomas, G. Neil; Todaro, Marian; Tozzi, Rossana; Vari, Maria S.; Vining, Eileen P. G.; Visscher, Frank; von Spiczak, Sarah; Walley, Nicole M.; Weber, Yvonne G.; Wei, Zhi; Weisenberg, Judith; Whelan, Christopher D.; Widdess-Walsh, Peter; Wolff, Markus; Wolking, Stefan; Yang, Wanling; Zara, Federico; Zimprich, Fritz
err分享
err收藏
Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains
err2018-09-04
err48
errOAAI
errde Kovel, Carolien G. F.; Lisgo, Steven N.; Fisher, Simon E.; Francks, Clyde
err分享
err收藏
Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development
err2017-08-01
err41
errOAAI
errde Kovel, Carolien G. F.; Lisgo, Steven; Karlebach, Guy; Ju, Jia; Cheng, Gang; Fisher, Simon E.; Francks, Clyde
err分享
err收藏
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU1q43q44微缺失综合征的遗传和表型解剖以及与ZBTB18和HNRNPU突变相关的神经发育表型
err2017-03-10
err76
errOAAI
errDepienne, Christel; Nava, Caroline; Keren, Boris; Heide, Solveig; Rastetter, AgnSs; Passemard, Sandrine; Chantot-Bastaraud, Sandra; Moutard, Marie-Laure; Agrawal, Pankaj B.; VanNoy, Grace; Stoler, Joan M.; Amor, David J.; de Villemeur, Thierry Billette; Doummar, Diane; Alby, Caroline; Cormier-Daire, Valerie; Garel, Catherine; Marzin, Pauline; Scheidecker, Sophie; de Saint-Martin, Anne; Hirsch, Edouard; Korff, Christian; Bottani, Armand; Faivre, Laurence; Verloes, Alain; Orzechowski, Christine; Burglen, Lydie; Leheup, Bruno; Roume, Joelle; Andrieux, Joris; Sheth, Frenny; Datar, Chaitanya; Parker, Michael J.; Pasquier, Laurent; Odent, Sylvie; Naudion, Sophie; Delrue, Marie-Ange; Le Caignec, Cedric; Vincent, Marie; Isidor, Bertrand; Renaldo, Florence; Stewart, Fiona; Toutain, Annick; Koehler, Udo; Hackl, Birgit; von Stulpnagel, Celina; Kluger, Gerhard; Moller, Rikke S.; Pal, Deb; Jonson, Tord; Soller, Maria; Verbeek, Nienke E.; van Haelst, Mieke M.; de Kovel, Carolien; Koeleman, Bobby; Monroe, Glen; van Haaften, Gijs; Study, D. D. D.; Attie-Bitach, Tania; Boutaud, Lucile; Heron, Delphine; Mignot, Cyril
err分享
err收藏
Erythematous nodes, urticarial rash and arthralgias in a large pedigree with NLRC4-related autoinflammatory disease, expansion of the phenotype
err2016-12-08
err57
errOAAI
errVolker-Touw, C. M. L.; de Koning, H. D.; Giltay, J. C.; de Kovel, C. G. F.; van Kempen, T. S.; Oberndorff, K. M. E. J.; Boes, M. L.; van Steensel, M. A. M.; van Well, G. T. J.; Blokx, W. A. M.; Schalkwijk, J.; Simon, A.; Frenkel, J.; van Gijn, M. E.
err分享
err收藏
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy
err2016-06-29
err52
errOAAI
errde Lange, Iris M.; Helbig, Katherine L.; Weckhuysen, Sarah; Moller, Rikke S.; Velinov, Milen; Dolzhanskaya, Natalia; Marsh, Eric; Helbig, Ingo; Devinsky, Orrin; Tang, Sha; Mefford, Heather C.; Myers, Candace T.; van Paesschen, Wim; Striano, Pasquale; van Gassen, Koen; van Kempen, Marjan; de Kovel, Carolien G. F.; Piard, Juliette; Minassian, Berge A.; Nezarati, Marjan M.; Pessoa, Andre; Jacquette, Aurelia; Maher, Bridget; Balestrini, Simona; Sisodiya, Sanjay; Warde, Marie Therese Abi; De St Martin, Anne; Chelly, Jamel; van 't Slot, Ruben; Van Maldergem, Lionel; Brilstra, Eva H.; Koeleman, Bobby P. C.
err分享
err收藏
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy
err2016-06-07
err153
errOAAI
errLemke, Johannes R.; Geider, Kirsten; Helbig, Katherine L.; Heyne, Henrike O.; Schuetz, Hannah; Hentschel, Julia; Courage, Carolina; Depienne, Christel; Nava, Caroline; Heron, Delphine; Moller, Rikke S.; Hjalgrim, Helle; Lal, Dennis; Neubauer, Bernd A.; Nuernberg, Peter; Thiele, Holger; Kurlemann, Gerhard; Arnold, Georgianne L.; Bhambhani, Vikas; Bartholdi, Deborah; Pedurupillay, Christeen Ramane J.; Misceo, Doriana; Frengen, Eirik; Stromme, Petter; Dlugos, Dennis J.; Doherty, Emily S.; Bijlsma, Emilia K.; Ruivenkamp, Claudia A.; Hoffer, Mariette J. V.; Goldstein, Amy; Rajan, Deepa S.; Narayanan, Vinodh; Ramsey, Keri; Belnap, Newell; Schrauwen, Isabelle; Richholt, Ryan; Koeleman, Bobby P. C.; Sa, Joaquim; Mendonca, Carla; de Kovel, Carolien G. F.; Weckhuysen, Sarah; Hardies, Katia; De Jonghe, Peter; De Meirleir, Linda; Milh, Mathieu; Badens, Catherine; Lebrun, Marine; Busa, Tiffany; Francannet, Christine; Piton, Amelie; Riesch, Erik; Biskup, Saskia; Vogt, Heinrich; Dorn, Thomas; Helbig, Ingo; Michaud, Jacques L.; Laube, Bodo; Syrbe, Steffen
err分享
err收藏
Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach
err2016-01-01
err121
errOAAI
errBoerma, Ragna S.; Braun, Kees P.; van de Broek, Maarten P. H.; van Berkestijn, Frederique M. C.; Swinkels, Marielle E.; Hagebeuk, Eveline O.; Lindhout, Dick; van Kempen, Marjan; Boon, Maartje; Nicolai, Joost; de Kovel, Carolien G.; Brilstra, Eva H.; Koeleman, Bobby P. C.
err分享
err收藏
Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach (vol 13, pg 192, 2016)
err2016-01-01
err5
errOAAI
errBoerma, Ragna S.; Braun, Kees P.; van den Broek, Marcel P. H.; van Berkestijn, Frederique M. C.; Swinkels, Marielle E.; Hagebeuk, Eveline O.; Lindhout, Dick; van Kempen, Marjan; Boon, Maartje; Nicolai, Joost; de Kovel, Carolien G.; Brilstra, Eva H.; Koeleman, Bobby P. C.
err分享
err收藏
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia
errBRAIN
IF11.7
err2015-09-17
err72
errOAAI
errHardies, Katia; de Kovel, Carolien G. F.; Weckhuysen, Sarah; Asselbergh, Bob; Geuens, Thomas; Deconinck, Tine; Azmi, Abdelkrim; May, Patrick; Brilstra, Eva; Becker, Felicitas; Barisic, Nina; Craiu, Dana; Braun, Kees P. J.; Lal, Dennis; Thiele, Holger; Schubert, Julian; Weber, Yvonne; van't Slot, Ruben; Nuernberg, Peter; Balling, Rudi; Timmerman, Vincent; Lerche, Holger; Maudsley, Stuart; Helbig, Ingo; Suls, Arvid; Koeleman, Bobby P. C.; De Jonghe, Peter
err分享
err收藏
Effect of vaccinations on seizure risk and disease course in Dravet syndrome
err2015-08-18
err28
PREAI
errVerbeek, Nienke E.; van der Maas, Nicoline A. T.; Sonsma, Anja C. M.; Ippel, Elly; Bondt, Patricia E. Vermeer-de; Hagebeuk, Eveline; Jansen, Floor E.; Geesink, Huibert H.; Braun, Kees P.; de Louw, Anton; Augustijn, Paul B.; Neuteboom, Rinze F.; Schieving, Jolanda H.; Stroink, Hans; Vermeulen, R. Jeroen; Nicolai, Joost; Brouwer, Oebele F.; Van Kempen, Marjan; de Kovel, Carolien G. F.; Kemmeren, Jeanet M.; Koeleman, Bobby P. C.; Knoers, Nine V.; Lindhout, Dick; Gunning, W. Boudewijn; Brilstra, Eva H.
err分享
err收藏
Genetic Factors for the Severity of ACPA-negative Rheumatoid Arthritis in 2 Cohorts of Early Disease: A Genome-wide Study
err2015-06-15
err20
errOAAI
errde Rooy, Diederik P. C.; Tsonaka, Roula; Andersson, Maria L. E.; Forslind, Kristina; Zhernakova, Alexandra; Frank-Bertoncelj, Mojca; de Kovel, Caroline G. F.; Koeleman, Bobby P. C.; van der Heijde, Desiree M. F. M.; Huizinga, Tom W. J.; Toes, Rene E. M.; Houwing-Duistermaat, Jeanine J.; Ospelt, Caroline; Svensson, Bjorn; van der Helm-van Mil, Annette H. M.
err分享
err收藏
Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies
err2015-05-07
err74
errOAAI
errLal, Dennis; Ruppert, Ann-Kathrin; Trucks, Holger; Schulz, Herbert; de Kovel, Carolien G.; Trenite, Dorothee Kasteleijn-Nolst; Sonsma, Anja C. M.; Koeleman, Bobby P.; Lindhout, Dick; Weber, Yvonne G.; Lerche, Holger; Kapser, Claudia; Schankin, Christoph J.; Kunz, Wolfram S.; Surges, Rainer; Elger, Christian E.; Gaus, Verena; Schmitz, Bettina; Helbig, Ingo; Muhle, Hiltrud; Stephani, Ulrich; Klein, Karl M.; Rosenow, Felix; Neubauer, Bernd A.; Reinthaler, Eva M.; Zimprich, Fritz; Feucht, Martha; Moller, Rikke S.; Hjalgrim, Helle; De Jonghe, Peter; Suls, Arvid; Lieb, Wolfgang; Franke, Andre; Strauch, Konstantin; Gieger, Christian; Schurmann, Claudia; Schminke, Ulf; Nuernberg, Peter; Sander, Thomas
err分享
err收藏