Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Eriksson, Nicholas"'
Autor:
Cuellar-Partida, Gabriel, Tung, Joyce Y, Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A, Barroso, Inês, Beckmann, Jacques S, Boks, Marco P, Boomsma, Dorret I, Boyd, Heather A, Breteler, Monique MB, Campbell, Harry, Chasman, Daniel I, Cherkas, Lynn F, Davies, Gail, de Geus, Eco JC, Deary, Ian J, Deloukas, Panos, Dick, Danielle M, Duffy, David L, Eriksson, Johan G, Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D, Han, Jiali, Hansen, Thomas F, Hartmann, Annette M, Hayward, Caroline, Heikkilä, Kauko, Hicks, Andrew A, Hirschhorn, Joel N, Hottenga, Jouke-Jan, Huffman, Jennifer E, Hwang, Liang-Dar, Ikram, M Arfan, Kaprio, Jaakko, Kemp, John P, Khaw, Kay-Tee, Klopp, Norman, Konte, Bettina, Kutalik, Zoltan, Lahti, Jari, Li, Xin, Loos, Ruth JF, Luciano, Michelle, Magnusson, Sigurdur H, Mangino, Massimo, Marques-Vidal, Pedro, Martin, Nicholas G, McArdle, Wendy L, McCarthy, Mark I, Medina-Gomez, Carolina, Melbye, Mads, Melville, Scott A, Metspalu, Andres, Milani, Lili, Mooser, Vincent, Nelis, Mari, Nyholt, Dale R, O'Connell, Kevin S, Ophoff, Roel A, Palmer, Cameron, Palotie, Aarno, Palviainen, Teemu, Pare, Guillaume, Paternoster, Lavinia, Peltonen, Leena, Penninx, Brenda WJH, Polasek, Ozren, Pramstaller, Peter P, Prokopenko, Inga, Raikkonen, Katri, Ripatti, Samuli, Rivadeneira, Fernando, Rudan, Igor, Rujescu, Dan, Smit, Johannes H, Smith, George Davey, Smoller, Jordan W, Soranzo, Nicole, Spector, Tim D, Pourcain, Beate St, Starr, John M, Stefánsson, Hreinn, Steinberg, Stacy, Teder-Laving, Maris, Thorleifsson, Gudmar, Stefánsson, Kári, Timpson, Nicholas J, Uitterlinden, André G, van Duijn, Cornelia M, van Rooij, Frank JA, Vink, Jaqueline M, Vollenweider, Peter, Vuoksimaa, Eero
Publikováno v:
Nature human behaviour, vol 5, iss 1
Handedness has been extensively studied because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank, 23andMe and the International Handedness Consortium, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6be7b0d06e3986152ff24339faaff2fd
https://escholarship.org/uc/item/0ng2j3b3
https://escholarship.org/uc/item/0ng2j3b3
Autor:
Eriksson Nicholas, Benton Geoffrey M, Do Chuong B, Kiefer Amy K, Mountain Joanna L, Hinds David A, Francke Uta, Tung Joyce Y
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 53 (2012)
Abstract Background While some factors of breast morphology, such as density, are directly implicated in breast cancer, the relationship between breast size and cancer is less clear. Breast size is moderately heritable, yet the genetic variants leadi
Externí odkaz:
https://doaj.org/article/66ab525fe7204fd0b3a4a4b505d56a20
Autor:
Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I, Smith, George Davey, Esko, Tonu, Hansen, Thomas Folkmann, Ikram, M. Arfan, Paraskevi, Christofidou, Strachan, David P., Wessman, Maija, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A., Buring, Julie E., Schürks, Markus, Ridker, Paul M., Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke-Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W, Kurki, Mitja I, Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda M., Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Lili, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Werge, Thomas, Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Ferrari, Michel D., Belin, Andrea C., Dichgans, Martin, Zwart, John-Anker, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno, van den Maagdenberg, Arn M. J. M., Terwindt, Gisela M.
Publikováno v:
European Journal of Human Genetics
Boomsma, D I, Ligthart, L, Hottenga, J J, Penninx, B W J H & The International Headache Genetics Consortium 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2
The International Headache Genetics Consortium 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2
the International Headache Genetics Consortium, Yang, Y, Zhao, H, Boomsma, D I, Ligthart, L, Belin, A C, Smith, G D, Esko, T, Freilinger, T M, Hansen, T F, Ikram, M A, Kallela, M, Kubisch, C, Paraskevi, C, Strachan, D P, Wessman, M, Gormley, P, Anttila, V, Winsvold, B S, Palta, P, Esko, T, Pers, T H, Farh, K H, Cuenca-Leon, E, Muona, M, Furlotte, N A, Kurth, T, Ingason, A, McMahon, G, Ligthart, L, Terwindt, G M, Kallela, M, Freilinger, T M, Ran, C, Gordon, S G, Stam, A H, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, H H H, Lehtimäki, T, Sarin, A P, Wedenoja, J, Hinds, D A, Buring, J E, Schürks, M, Ridker, P M, Ring, S M, Stergiakouli, E & Smith, G D 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2
European Journal of Human Genetics, 26(8), 1202-1216. Nature Publishing Group
Boomsma, D I, Ligthart, L, Hottenga, J J, Penninx, B W J H & The International Headache Genetics Consortium 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2
The International Headache Genetics Consortium 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2
the International Headache Genetics Consortium, Yang, Y, Zhao, H, Boomsma, D I, Ligthart, L, Belin, A C, Smith, G D, Esko, T, Freilinger, T M, Hansen, T F, Ikram, M A, Kallela, M, Kubisch, C, Paraskevi, C, Strachan, D P, Wessman, M, Gormley, P, Anttila, V, Winsvold, B S, Palta, P, Esko, T, Pers, T H, Farh, K H, Cuenca-Leon, E, Muona, M, Furlotte, N A, Kurth, T, Ingason, A, McMahon, G, Ligthart, L, Terwindt, G M, Kallela, M, Freilinger, T M, Ran, C, Gordon, S G, Stam, A H, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, H H H, Lehtimäki, T, Sarin, A P, Wedenoja, J, Hinds, D A, Buring, J E, Schürks, M, Ridker, P M, Ring, S M, Stergiakouli, E & Smith, G D 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2
European Journal of Human Genetics, 26(8), 1202-1216. Nature Publishing Group
Migraine and major depressive disorder (MDD) are common brain disorders that frequently co-occur. Despite epidemiological evidence that migraine and MDD share a genetic basis, their overlap at the molecular genetic level has not been thoroughly inves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::950ea06bbd691cb84376056bc246b2d3
https://europepmc.org/articles/PMC6057914/
https://europepmc.org/articles/PMC6057914/
Autor:
Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline, Grove, Jakob, Hansen, Christine S., Hauberg, Mads E., Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian, Martin, Alicia R., Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S., Pedersen, Carsten B., Pedersen, Marianne G., Poterba, Timothy, Poulsen, Jesper B., Ripke, Stephan, Robinson, Elise B., Satterstrom, Kyle F., Stevens, Christine, Turley, Patrick, Won, Hyejung, Andreassen, Ole A., Burton, Christie, Boomsma, Dorret, Cormand, Bru, Dalsgaard, Søren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry, Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis A., Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund, Sullivan, Patrick F., Thapar, Anita, Tung, Joyce, Waldman, Irwin, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben B., Daly, Mark J., Faraone, Stephen V., Børglum, Anders D., Neale, Benjamin M.
Attention-Deficit/Hyperactivity Disorder (ADHD) is a highly heritable childhood behavioral disorder affecting 5% of school-age children and 2.5% of adults. Common genetic variants contribute substantially to ADHD susceptibility, but no individual var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5070c6ad6181041076aef7b402d21c99
Autor:
Eriksson, Nicholas1 nick@23andme.com, Tung, Joyce Y.1, Kiefer, Amy K.1, Hinds, David A.1, Francke, Uta1, Mountain, Joanna L.1, Do, Chuong B.1
Publikováno v:
PLoS ONE. Apr2012, Vol. 7 Issue 4, p1-8. 8p.
Autor:
Tesler, Glenn, Eriksson, Nicholas, Pachter, Lior, Mitsuya, Yumi, Rhee, Soo-Yon, Wang, Chunlin, Gharizadeh, Baback, Ronaghi, Mostafa, Shafer, Robert W., Beerenwinkel, Niko
Publikováno v:
PLoS Computational Biology
PLoS Computational Biology, 4 (5)
PLoS Computational Biology, Vol 4, Iss 4, p e1000074 (2008)
PLoS Computational Biology, 4 (5)
PLoS Computational Biology, Vol 4, Iss 4, p e1000074 (2008)
The diversity of virus populations within single infected hosts presents a major difficulty for the natural immune response as well as for vaccine design and antiviral drug therapy. Recently developed pyrophosphate-based sequencing technologies (pyro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c68830683bbe7727081ca8b2e4d8e40
http://arxiv.org/abs/0707.0114
http://arxiv.org/abs/0707.0114
Akademický článek
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Autor:
Hinds, David A, McMahon, George, Kiefer, Amy K, Do, Chuong B, Eriksson, Nicholas, Evans, David M, St Pourcain, Beate, Ring, Susan M, Mountain, Joanna L, Francke, Uta, Davey-Smith, George, Timpson, Nicholas J, Tung, Joyce Y
Publikováno v:
Nature Genetics; Aug2013, Vol. 45 Issue 8, p907-911, 5p, 3 Charts, 3 Graphs
Autor:
M. Lill, Christina, Roehr, Johannes T., McQueen, Matthew B., Kavvoura, Fotini K., Bagade, Sachin, Schjeide, Brit-Maren M., Schjeide, Leif M., Meissner, Esther, Zauft, Ute, Allen, Nicole C., Liu, Tian, Schilling, Marcel, Anderson, Kari J., Beecham, Gary, Berg, Daniela, Biernacka, Joanna M., Brice, Alexis, DeStefano, Anita L., Do, Chuong B., Eriksson, Nicholas
Publikováno v:
PLoS Genetics; Mar2012, Vol. 8 Issue 3, Special section p1-10, 10p, 1 Diagram, 2 Charts, 2 Graphs
Autor:
Martin, Joanna1,2,3,4 martinjm1@cardiff.ac.uk, Walters, Raymond K.2,3, Demontis, Ditte5,6,7, Mattheisen, Manuel5,6,7,8,9, Lee, S. Hong10,11,12, Robinson, Elise2,3, Brikell, Isabell1, Ghirardi, Laura1, Larsson, Henrik1,13, Lichtenstein, Paul1, Eriksson, Nicholas14, Werge, Thomas5,15,16, Mortensen, Preben Bo5,6,17,18, Pedersen, Marianne Giørtz5,17,18, Mors, Ole5,19, Nordentoft, Merete5,20, Hougaard, David M.5,21, Bybjerg-Grauholm, Jonas5,21, Wray, Naomi R.10, Franke, Barbara22
Publikováno v:
Biological Psychiatry. Jun2018, Vol. 83 Issue 12, p1044-1053. 10p.