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by Francioli, Laurent C and Menelaou, Anoniki and Pulit, Sara L and van Dijk, Freerk and Palamara, Pier Francesco and Elbers, Clara C and Neerincx, Pieter B. T and Ye, Kai and Guryev, Victor and Kloosterman, Wigard P and Deelen, Patrick and Abdellaoui, Abdel and van Leeuwen, Elisabeth M and van Oven, Mannis and Vermaat, Martijn and Li, Mingkun and Laros, Jeroen F. J and Karssen, Lennart C and Kanterakis, Alexanos and Amin, Najaf and Hottenga, Jouke Jan and Lameijer, Eric-Wubbo and Kattenberg, Mathijs and Dijkstra, Martijn and Byelas, Heorhiy and van Setten, Jessica and van Schaik, Barbera D. C and Bot, Jan and Nijman, Isaäc J and Renkens, Ivo and Marschall, Tobias and Schönhuth, Alexander and Hehir-Kwa, Jayne Y and Handsaker, Robert E and Polak, Paz and Sohail, Mashaal and Vuzman, Dana and Hormozdiari, Fereydoun and van Enckevort, David and Mei, Hailiang and Koval, Vyacheslav and Moed, Matthijs H and van der Velde, K. Joeri and Rivadeneira, Fernando and Estrada, Karol and Medina-Gomez, Carolina and Isaacs, Aaron and McCarroll, Steven A and Beekman, Marian and de Craen, Anton J. M and Suchiman, H. Eka D and Hofman, Albert and Oostra, Ben and Uitterlinden, Ané G and Willemsen, Gonneke and Platteel, Mathieu and Veldink, Jan H and van den Berg, Leonard H and Pitts, Steven J and Potluri, Shobha and Sundar, Purnima and Cox, David R and Sunyaev, Shamil R and den Dunnen, Johan T and Stoneking, Mark and de Knijff, Peter and Kayser, Manfred and Li, Qibin and Li, Yingrui and Du, Yuanping and Chen, Ruoyan and Cao, Hongzhi and Li, Ning and Cao, Sujie and Wang, Jun and Bovenberg, Jasper A and Pe'er, Itsik and Slagboom, P. Eline and van Duijn, Cornelia M and Boomsma, Dorret I and van Ommen, Gert-Jan B and de Bakker, Paul I. W and Swertz, Morris A and Wijmenga, Cisca and LifeLines Cohort Study and Genome Netherlands Consortium and Genome of the Netherlands Consortium and The Genome of the Netherlands Consortium
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 8, pp. 818 - 825
Journal Article
by van Rheenen, Wouter and Shatunov, Aleksey and Dekker, Annelot M and McLaughlin, Russell L and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A. A and Võsa, Urmo and de Jong, Simone and Robinson, Matthew R and Yang, Jian and Fogh, Isabella and van Doormaal, Perry Tc and Tazelaar, Gijs H. P and Koppers, Max and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Schellevis, Raymond D and Brands, William J and Medic, Jelena and Menelaou, Anoniki and Vajda, Alice and Ticozzi, Nicola and Lin, Kuang and Rogelj, Boris and Vrabec, Katarina and Ravnik-Glavač, Metka and Koritnik, Blaž and Zidar, Janez and Leonardis, Lea and Grošelj, Leja Dolenc and Millecamps, Stéphanie and Salachas, François and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-García, Ricardo and Polak, Meraida and Chanan, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Anea and Topp, Simon and Petri, Susanne and Abdulla, Susanne and pper, Carsten and Sendtner, Michael and Meyer, Thomas and Ophoff, Roel A and Staats, Kim A and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, A. Nazli and Tunca, Ceren and Hamzeiy, Hamid and Parman, Yesim and Meitinger, Thomas and Lichtner, Peter and Radivojkov-Blagojevic, Milena and Anes, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A. M and Saker-Delye, Safaa and Dürr, Alexana and Wood, Nicholas W and Tittmann, Lukas and Lieb, Wolfgang and Franke, Ane and Rietschel, Marcella and Cichon, Sven and Nöthen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-François and Uitterlinden, Ane G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and Blauw, Hylke M and van der Kooi, Anneke J and ... and PARALS Registry and FALS Sequencing Consortium and SLALOM Grp and SLAGEN Consortium and NNIPPS Study Grp and SLAP Registry and SLALOM Group and NNIPPS Study Group and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Nature genetics, ISSN 1061-4036, 2016, Volume 48, Issue 9, pp. 1043 - 1048
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 02/2014, Volume 22, Issue 2, pp. 221 - 227
Journal Article
by Deelen, Patrick and Menelaou, Anoniki and van Leeuwen, Elisabeth M and Kanterakis, Alexanos and van Dijk, Freerk and Medina-Gomez, Carolina and Francioli, Laurent C and Hottenga, Jouke Jan and Karssen, Lennart C and Estrada, Karol and Kreiner-Møller, Eskil and Rivadeneira, Fernando and van Setten, Jessica and Gutierrez-Achury, Javier and Westra, Harm-Jan and Franke, Lude and van Enckevort, David and Dijkstra, Martijn and Byelas, Heorhiy and van Duijn, Cornelia M and de Bakker, Paul I. W and Wijmenga, Cisca and Swertz, Morris A and Neerincx, Pieter B. T and Pulit, Sara L and Elbers, Clara C and Palamara, Pier Francesco and Pe'er, Itsik and Abdellaoui, Abdel and Kloosterman, Wigard P and van Oven, Mannis and Vermaat, Martijn and Li, Mingkun and Laros, Jeroen F. J and Stoneking, Mark and de Knijff, Peter and Kayser, Manfred and Veldink, Jan H and van den Berg, Leonard H and den Dunnen, Johan T and Amin, Najaf and van der Velde, K. Joeri and Kattenberg, Mathijs and van Schaik, Barbera D. C and Bot, Jan and Nijman, Isaäuc J and Mei, Hailiang and Koval, Vyacheslav and Ye, Kai and Lameijer, Eric-Wubbo and Moed, Matthijs H and Hehir-Kwa, Jayne Y and Handsaker, Robert E and Sunyaev, Shamil R and Sohail, Mashaal and Hormozdiari, Fereydoun and Marschall, Tobias and Schönhuth, Alexander and Guryev, Victor and Slagboom, P. Eline and Beekman, Marian B and de Craen, Anton J. M and Suchiman, H. Eka D and Hofman, Albert and van Duijn, Cornelia and Boomsma, Dorret I and Willemsen, Gonneke and Wolffenbuttel, Bruce H and Platteel, Mathieu and Pitts, Steven J and Potluri, Shobha and Cox, David R and Li, Qibin and Li, Yingrui and Du, Yuanping and Chen, Ruoyan and Cao, Hongzhi and Li, Ning and Cao, Sujie and Wang, Jun and Bovenberg, Jasper A and van Ommen, Gertjan B and Genome Netherlands Consortium and Genome of Netherlands Consortium and Genome of the Netherlands Consortium
European journal of human genetics, ISSN 1018-4813, 2014, Volume 22, Issue 11, pp. 1321 - 1326
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2015, Volume 47, Issue 7, pp. 822 - +
Mutations create variation in the population, fuel evolution and cause genetic diseases. Current knowledge about de novo mutations is incomplete and mostly... 
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 11/2014, Volume 22, Issue 11, pp. 1321 - 1326
Although genome-wide association studies (GWAS) have identified many common variants associated with complex traits, low-frequency and rare variants have not... 
Journal Article
by van Rheenen, Wouter and Shatunov, Aleksey and Dekker, Annelot M and McLaughlin, Russell L and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A. A and Vosa, Urmo and de Jong, Simone and Robinson, Matthew R and Yang, Jian and Fogh, Isabella and van Doormaal, Perry T. C and Tazelaar, Gijs H. P and Koppers, Max and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Schellevis, Raymond D and Brands, William J and Medic, Jelena and Menelaou, Anoniki and Vajda, Alice and Ticozzi, Nicola and Lin, Kuang and Rogelj, Boris and Vrabec, Katarina and Ravnik-Glavac, Metka and Koritnik, Blazi and Zidar, Janez and Leonardis, Lea and Groselj, Leja Dolenc and Millecamps, Stephanie and Salachas, Francois and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-Garcia, Ricardo and Polak, Meraida and Chanan, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Anea and Topp, Simon and Petri, Susanne and Abdulla, Susanne and pper, Carsten and Sendtner, Michael and Meyer, Thomas and Ophoff, Roel A and Staats, Kim A and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and Van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, A. Nazli and Tunca, Ceren and Hamzeiy, Hamid and Parman, Yesim and Meitinger, Thomas and Lichtner, Peter and Radivojkov-Blagojevic, Milena and Anes, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A. M and Saker-Delye, Safaa and Duerr, Alexana and Wood, Nicholas W and Tittmann, Lukas and Lieb, Wolfgang and Franke, Ane and Rietschel, Marcella and Cichon, Sven and Noethen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-Francois and Uitterlinden, Ane G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and Blauw, Hylke M and van der Kooi, Anneke J and ...
Nature Genetics, ISSN 1061-4036, 09/2016, Volume 48, Issue 9, pp. 1043 - +
To elucidate the genetic architecture of amyotrophic lateral sclerosis (ALS) and find associated loci, we assembled a custom imputation reference panel from... 
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2014, Volume 22, Issue 11, pp. 1321 - 1326
textabstractAlthough genome-wide association studies (GWAS) have identified many common variants associated with complex traits, low-frequency and rare... 
Journal Article
Cell Reports, ISSN 2211-1247, 12/2014, Volume 9, Issue 6, pp. 2001 - 10
Genomic rearrangements are a common cause of human congenital abnormalities. However, their origin and consequences are poorly understood. We performed... 
Journal Article
by van Leeuwen, Elisabeth M and Karssen, Lennart C and Deelen, Joris and Isaacs, Aaron and Medina-Gomez, Carolina and Mbarek, Hamdi and Kanterakis, Alexanos and Trompet, Stella and Postmus, Iris and Verweij, Niek and van Enckevort, David J and Huffman, Jennifer E and White, Charles C and Feitosa, Mary F and Bartz, Traci M and Manichaikul, Ani and Joshi, Peter K and Peloso, Gina M and Deelen, Patrick and van Dijk, Freerk and Willemsen, Gonneke and de Geus, Eco J and Milaneschi, Yuri and Penninx, Brenda W. J. H and Francioli, Laurent C and Menelaou, Anoniki and Pulit, Sara L and Rivadeneira, Fernando and Hofman, Albert and Oostra, Ben A and Franco, Oscar H and Leach, Irene Mateo and Beekman, Marian and de Craen, Anton J. M and Uh, Hae-Won and Trochet, Holly and Hocking, Lynne J and Porteous, David J and Sattar, Naveed and Packard, Chris J and Buckley, Brendan M and Brody, Jennifer A and Bis, Joshua C and Rotter, Jerome I and Mychaleckyj, Josyf C and Campbell, Harry and Duan, Qing and Lange, Leslie A and Wilson, James F and Hayward, Caroline and Polasek, Ozren and Vitart, Veronique and Rudan, Igor and Wright, Alan F and Rich, Stephen S and Psaty, Bruce M and Borecki, Ingrid B and Kearney, Patricia M and Stott, David J and Cupples, L. Aienne and Jukema, J. Wouter and van der Harst, Pim and Sijbrands, Eric J and Hottenga, Jouke-Jan and Uitterlinden, Ane G and Swertz, Morris A and van Ommen, Gert-Jan B and de Bakker, Paul I. W and Slagboom, P. Eline and Boomsma, Dorret I and Wijmenga, Cisca and van Duijn, Cornelia M
Nature Communications, ISSN 2041-1723, 03/2015, Volume 6
Variants associated with blood lipid levels may be population-specific. To identify low-frequency variants associated with this phenotype, population-specific... 
Journal Article
Nature Communications, ISSN 2041-1723, 03/2015, Volume 6
textabstractVariants associated with blood lipid levels may be population-specific. To identify low-frequency variants associated with this phenotype,... 
Journal Article
by Van Leeuwen, Elisabeth M and Karssen, Lennart C and Deelen, Joris and Isaacs, Aaron and Medina-Gomez, Carolina and Mbarek, Hamdi and Kanterakis, Alexanos and Trompet, Stella and Postmus, Iris and Verweij, Niek and Van Enckevort, David J and Huffman, Jennifer E and White, Charles C and Feitosa, Mary F and Bartz, Traci M and Manichaikul, Ani and Joshi, Peter K and Peloso, Gina M and Deelen, Patrick and Van Dijk, Freerk and Willemsen, Gonneke and De Geus, Eco J and Milaneschi, Yuri and Penninx, Brenda W J H and Francioli, Laurent C and Menelaou, Anoniki and Pulit, Sara L and Rivadeneira, Fernando and Hofman, Albert and Oostra, Ben A and Franco, Oscar H and Leach, Irene Mateo and Beekman, Marian and De Craen, Anton J M and Uh, Hae Won and Trochet, Holly and Hocking, Lynne J and Porteous, David J and Sattar, Naveed and Packard, Chris J and Buckley, Brendan M and Brody, Jennifer A and Bis, Joshua C and Rotter, Jerome I and Mychaleckyj, Josyf C and Campbell, Harry and Duan, Qing and Lange, Leslie A and Wilson, James F and Hayward, Caroline and Polasek, Ozren and Vitart, Veronique and Rudan, Igor and Wright, Alan F and Rich, Stephen S and Psaty, Bruce M and Borecki, Ingrid B and Kearney, Patricia M and Stott, David J and Cupples, L. Aienne and Jukema, J. Wouter and Van Der Harst, Pim and Sijbrands, Eric J and Hottenga, Jouke Jan and Uitterlinden, Ane G and Swertz, Morris A and Van Ommen, Gert Jan B and De Bakker, Paul I W and Eline Slagboom, P and Boomsma, Dorret I and Wijmenga, Cisca and Van Duijn, Cornelia M and Neerincx, Pieter B T and Elbers, Clara C and Palamara, Pier Francesco and Peer, Itsik and Abdellaoui, Abdel and Kloosterman, Wigard P and Van Oven, Mannis and Vermaat, Martijn and Li, Mingkun and Laros, Jeroen F J and Stoneking, Mark and De Knijff, Peter and Kayser, Manfred and Veldink, Jan H and Van Den Berg, Leonard H and Byelas, Heorhiy and Den Dunnen, Johan T and Dijkstra, Martijn and Amin, Najaf and Van Der Velde, K. Joeri and Van Setten, Jessica and Kattenberg, Mathijs and Van Schaik, Barbera D C and Bot, Jan and Nijman, Isaäc J and Mei, Hailiang and Koval, Vyacheslav and Ye, Kai and ...
Nature Communications [E], ISSN 2041-1723, 03/2015, Volume 6
Variants associated with blood lipid levels may be population-specific. To identify low-frequency variants associated with this phenotype, population-specific... 
Journal Article