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Autor:
Charalambos P. Kyriacou, Caroline Hayward, C M van Duijn, Till Roenneberg, Karla V. Allebrandt, Nicole Vogelzangs, Tõnu Esko, A. C. J. W. Janssens, J. van Mill, James F. Wilson, Peter Lichtner, Harry Campbell, Igor Rudan, R. V. D. M. Azevedo, Bertram Mueller-Myhsok, Edward W. Green, Zoran Dogas, Andres Metspalu, Martha Merrow, H-E Wichmann, Scott A. Melville, Ben A. Oostra, Brenda W.J.H. Penninx, Maris Teder-Laving, Najaf Amin, Thomas Meitinger, Andrew A. Hicks, Peter P. Pramstaller
Publikováno v:
Allebrandt, K V, Amin, N, Muller-Myhsok, B, Esko, T, Teder-Laving, M, Azevedo, R V D M, Hayward, C, van Mill, J G, Vogelzangs, N, Green, E W, Melville, S A, Lichtner, P, Wichmann, H E, Oostra, B A, Janssens, A C J W, Campbell, H, Wilson, J F, Hicks, A A, Pramstaller, P P, Dogas, Z, Rudan, I, Merrow, M, Penninx, B W J H, Kyriacou, C P, Metspalu, A, van Duijn, C M, Meitinger, T & Roenneberg, T 2013, ' A K-ATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila ', Molecular Psychiatry, vol. 18, no. 1, pp. 122-132 . https://doi.org/10.1038/mp.2011.142
Molecular Psychiatry, 18(1), 122-132. Nature Publishing Group
Mol. Psychiatry 18, 122-132 (2013)
Molecular Psychiatry, 18(1), 122-132. Nature Publishing Group
Mol. Psychiatry 18, 122-132 (2013)
Humans sleep approximately a third of their lifetime. The observation that individuals with either long or short sleep duration show associations with metabolic syndrome and psychiatric disorders suggests that the length of sleep is adaptive. Althoug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53f77bb516ffc69c3c1d440a0a418ad5
https://doi.org/10.1038/mp.2011.142
https://doi.org/10.1038/mp.2011.142
Autor:
Igor Rudan, Tõnu Esko, Wilfred F. J. van IJcken, Alan F. Wright, Caroline Hayward, Nathaniel F. Watson, Ben A. Oostra, Karla V. Allebrandt, Scott A. Melville, Steven R. Cummings, Aaron Isaacs, Gonneke Willemsen, Yurii S. Aulchenko, Albert Hofman, Fran Borovečki, Maris Teder-Laving, Sina A. Gharib, Brenda W.J.H. Penninx, Cornelia M. van Duijn, Josine G. van Mill, Dorret I. Boomsma, Harry Campbell, James F. Wilson, Katie L. Stone, Rutger W W Brouwer, Philip R. Gehrman, Annemarie I. Luik, Ozren Polasek, Naresh M. Punjabi, Jouke-Jan Hottenga, Jennifer E. Huffman, Daniel S. Evans, Martina Müller-Nurasyid, Ashley van der Spek, Andrew A. Hicks, Susan Redline, Peter P. Pramstaller, Fabiola M. Del Greco, Rudolf S N Fehrmann, Bertram Müller-Myhsok, Nicole Vogelzangs, Man Li, Lude Franke, Edwin Oole, Ayse Demirkan, Lina Zgaga, Karin Hek, Mirjam C G N van den Hout, Wen Hong Linda Kao, Gregory J. Tranah, Enda M. Byrne, Bruce M. Psaty, Hamdi Mbarek, Martha Merrow, Kristin D. Marciante, Josef Coresh, Henning Tiemeier, Grant W. Montgomery, Till Roenneberg, Susan Campbell, Ivana Kolcic, Juha Karjalainen, Zoran Dogas, Andres Metspalu, Ting Hsu Chen, Najaf Amin, André G. Uitterlinden, Nicholas G. Martin, Daniel J. Gottlieb, Andrew C. Heath, Thomas Meitinger, Heinz Erich Wichmann, Jacqueline M. Vink, Evelin Mihailov
Publikováno v:
European Journal of Human Genetics, 24(10), 1488-1495. Nature Publishing Group
Amin, N, Allebrandt, K V, van der Spek, A, Mueller-Myhsok, B, Hek, K, Teder-Laving, M, Hayward, C, Esko, T, van Mill, J G, Mbarek, H, Watson, N F, Melville, S A, Del Greco, F M, Byrne, E M, Oole, E, Kolcic, I, Chen, T, Evans, D S, Coresh, J, Vogelzangs, N, Karjalainen, J, Willemsen, G, Gharib, S A, Zgaga, L, Mihailov, E, Stone, K L, Campbell, H, Brouwer, R W, Demirkan, A, Isaacs, A, Dogas, Z, Marciante, K D, Campbell, S, Borovecki, F, Luik, A I, Li, M, Hottenga, J J, Huffman, J E, van den Hout, M C G N, Cummings, S R, Aulchenko, Y S, Gehrman, P R, Uitterlinden, A G, Wichmann, H-E, Muller-Nurasyid, M, Fehrmann, R S N, Montgomery, G W, Hofman, A, Kao, W H L, Oostra, B A, Wright, A F, Vink, J M, Wilson, J F, Pramstaller, P P, Hicks, A A, Polasek, O, Punjabi, N M, Redline, S, Psaty, B M, Heath, A C, Merrow, M, Tranah, G J, Gottlieb, D J, Boomsma, D I, Martin, N G, Rudan, I, Tiemeier, H, van IJcken, W F J, Penninx, B W, Metspalu, A, Meitinger, T, Franke, L, Roenneberg, T & van Duijn, C M 2016, ' Genetic variants in RBFOX3 are associated with sleep latency ', European Journal of Human Genetics, vol. 24, no. 10, pp. 1488-1495 . https://doi.org/10.1038/ejhg.2016.31
European Journal of Human Genetics, 24, 1488-1495
European Journal of Human Genetics, 24, 10, pp. 1488-1495
EUROPEAN JOURNAL OF HUMAN GENETICS
Eur. J. Hum. Genet. 24, 1488-1495 (2016)
Amin, N, Allebrandt, K V, Spek, A, Müller-Myhsok, B, Hek, K, Teder-Laving, M, Hayward, C, Esko, T, van Mill, J G, Mbarek, H, Watson, N F, Melville, S A, Del Greco, M F, Byrne, E M, Oole, E, Kolcic, I, Chen, T, Evans, D S, Coresh, J, Vogelzangs, N, Karjalainen, J, Willemsen, G, Gharib, S A, Zgaga, L, Mihailov, E, Stone, K L, Campbell, H, Brouwer, R W W, Demirkan, A, Isaacs, A, Dogas, Z, Marciante, K, Campbell, S, Borovecki, F, Luik, A I, Li, M, Hottenga, J J, Huffman, J E, van den Hout, M C G N, Cummings, S R, Aulchenko, Y S, Gehrman, P R, Uitterlinden, A G, Wichmann, H E, Müller-Nurasyid, M, Fehrmann, R S N, Montgomery, G W, Hofman, A, Hong, W, Kao, L, Oostra, B A, Wright, A F, Vink, J M, Wilson, J F, Pramstaller, P P, Hicks, A A, Polasek, O, Punjabi, N M, Redline, S, Psaty, B M, Heath, A C, Merrow, M, Tranah, G J, Gottlieb, D J, Boomsma, D I, Martin, N G, Rudan, I, Tiemeier, H, van Ijcken, W F J, Penninx, B W J H, Metspalu, A, Meitinger, T, Franke, L, Roenneberg, T & van Duijn, C M 2016, ' Genetic variants in RBFOX3 are associated with sleep latency ', European Journal of Human Genetics, vol. 24, no. 10, pp. 1488-1495 . https://doi.org/10.1038/ejhg.2016.31
European Journal of Human Genetics
Amin, N, Allebrandt, K V, van der Spek, A, Mueller-Myhsok, B, Hek, K, Teder-Laving, M, Hayward, C, Esko, T, van Mill, J G, Mbarek, H, Watson, N F, Melville, S A, Del Greco, F M, Byrne, E M, Oole, E, Kolcic, I, Chen, T, Evans, D S, Coresh, J, Vogelzangs, N, Karjalainen, J, Willemsen, G, Gharib, S A, Zgaga, L, Mihailov, E, Stone, K L, Campbell, H, Brouwer, R W, Demirkan, A, Isaacs, A, Dogas, Z, Marciante, K D, Campbell, S, Borovecki, F, Luik, A I, Li, M, Hottenga, J J, Huffman, J E, van den Hout, M C G N, Cummings, S R, Aulchenko, Y S, Gehrman, P R, Uitterlinden, A G, Wichmann, H-E, Muller-Nurasyid, M, Fehrmann, R S N, Montgomery, G W, Hofman, A, Kao, W H L, Oostra, B A, Wright, A F, Vink, J M, Wilson, J F, Pramstaller, P P, Hicks, A A, Polasek, O, Punjabi, N M, Redline, S, Psaty, B M, Heath, A C, Merrow, M, Tranah, G J, Gottlieb, D J, Boomsma, D I, Martin, N G, Rudan, I, Tiemeier, H, van IJcken, W F J, Penninx, B W, Metspalu, A, Meitinger, T, Franke, L, Roenneberg, T & van Duijn, C M 2016, ' Genetic variants in RBFOX3 are associated with sleep latency ', European Journal of Human Genetics, vol. 24, no. 10, pp. 1488-1495 . https://doi.org/10.1038/ejhg.2016.31
European Journal of Human Genetics, 24, 1488-1495
European Journal of Human Genetics, 24, 10, pp. 1488-1495
EUROPEAN JOURNAL OF HUMAN GENETICS
Eur. J. Hum. Genet. 24, 1488-1495 (2016)
Amin, N, Allebrandt, K V, Spek, A, Müller-Myhsok, B, Hek, K, Teder-Laving, M, Hayward, C, Esko, T, van Mill, J G, Mbarek, H, Watson, N F, Melville, S A, Del Greco, M F, Byrne, E M, Oole, E, Kolcic, I, Chen, T, Evans, D S, Coresh, J, Vogelzangs, N, Karjalainen, J, Willemsen, G, Gharib, S A, Zgaga, L, Mihailov, E, Stone, K L, Campbell, H, Brouwer, R W W, Demirkan, A, Isaacs, A, Dogas, Z, Marciante, K, Campbell, S, Borovecki, F, Luik, A I, Li, M, Hottenga, J J, Huffman, J E, van den Hout, M C G N, Cummings, S R, Aulchenko, Y S, Gehrman, P R, Uitterlinden, A G, Wichmann, H E, Müller-Nurasyid, M, Fehrmann, R S N, Montgomery, G W, Hofman, A, Hong, W, Kao, L, Oostra, B A, Wright, A F, Vink, J M, Wilson, J F, Pramstaller, P P, Hicks, A A, Polasek, O, Punjabi, N M, Redline, S, Psaty, B M, Heath, A C, Merrow, M, Tranah, G J, Gottlieb, D J, Boomsma, D I, Martin, N G, Rudan, I, Tiemeier, H, van Ijcken, W F J, Penninx, B W J H, Metspalu, A, Meitinger, T, Franke, L, Roenneberg, T & van Duijn, C M 2016, ' Genetic variants in RBFOX3 are associated with sleep latency ', European Journal of Human Genetics, vol. 24, no. 10, pp. 1488-1495 . https://doi.org/10.1038/ejhg.2016.31
European Journal of Human Genetics
Time to fall asleep (sleep latency) is a major determinant of sleep quality. Chronic, long sleep latency is a major characteristic of sleep-onset insomnia and/or delayed sleep phase syndrome. In this study we aimed to discover common polymorphisms th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c15e019588fe0e67cecaae1393586b60
https://research.rug.nl/en/publications/18161e92-3b6d-4d78-92ac-a40e0b26044c
https://research.rug.nl/en/publications/18161e92-3b6d-4d78-92ac-a40e0b26044c
Autor:
Kathryn L. Lunetta, Li Shen, Shannon L. Risacher, Sungeun Kim, Andrew J. Saykin, Clinton T. Baldwin, Jacqueline L. Buros, Gyungah Jun, Badri N. Vardarajan, Mark W. Logue, Lindsay A. Farrer, Antonio R. Parrado, Scott A. Melville, Charles DeCarli
Publikováno v:
Annals of Neurology. 72:65-75
Large genome-wide association studies (GWASs) have identified many novel genes influencing Alzheimer disease (AD) risk, but most of the genetic variance remains unexplained. We conducted a 2-stage GWAS for AD-related quantitative measures of hippocam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e972459e5fe4868796c0051ae5ff71a6
https://doi.org/10.1002/ana.23644
https://doi.org/10.1002/ana.23644
Autor:
Günter Weiss, Dena G. Hernandez, Fabio Busonero, Toshiko Tanaka, Serena Sanna, Irene Pichler, Igor Theurl, Eleonora Porcu, Dan L. Longo, Peter P. Pramstaller, Cosetta Minelli, David Schlessinger, Victor J. Wroblewski, Maria Grazia Piras, Eric E. Schadt, Elmar Aigner, Carsten Gnewuch, Alessandra Zanon, Christine Schwienbacher, Silvia Naitza, Andrea Maschio, Luigi Ferrucci, Manfred Mitterer, Jack M. Guralnik, Stefania Bandinelli, Anthony T. Murphy, Manuela Uda, Cristian Pattaro, Scott A. Melville, Derrick R. Witcher, Fabio Marroni, Andrew A. Hicks
Publikováno v:
Human Molecular Genetics. 20:1232-1240
The genetic determinants of variation in iron status are actively sought, but remain incompletely understood. Meta-analysis of two genome-wide association (GWA) studies and replication in three independent cohorts was performed to identify genetic lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e7b730a6f03021541b73a75f145bcb5
https://doi.org/10.1093/hmg/ddq552
https://doi.org/10.1093/hmg/ddq552
Autor:
Scott, Ian Melville, Zhu, Hong, Schieck, Katherine, Follick, Amanda, Reynolds, L. Bruce, Menassa, Rima
Publikováno v:
Frontiers in Plant Science; 7/9/2019, p1-12, 12p
Autor:
Charles DeCarli, Li Shen, Andrew J. Saykin, Tony Parrado, Clinton T. Baldwin, Scott A. Melville, Gyungah Jun, Shannon L. Risacher, Sungeun Kim, Kathryn L. Lunetta, Lindsay A. Farrer, Badri N. Vardarajan, Jacqueline L. Buros
Publikováno v:
Alzheimer's & Dementia. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ae53935f10bdc305308c70faa485acd
https://doi.org/10.1016/j.jalz.2012.05.1984
https://doi.org/10.1016/j.jalz.2012.05.1984
Autor:
Christian Fuchsberger, Andrew A. Hicks, Irene Pichler, Scott A. Melville, Fabiola Del Greco M, Christian J. Wiedermann, Stefan Schreiber, Andreas Luchner, Iris M. Heid, Cristian Pattaro, Michael Krawczak, Peter P. Pramstaller, Cosetta Minelli, Annette Peters, Andre Franke, Thomas W. Winkler, H.-Erich Wichmann
Publikováno v:
Hum. Mol. Genet. 20, 1660-1671 (2011)
Human Molecular Genetics
Human Molecular Genetics
High blood concentration of the N-terminal cleavage product of the B-type natriuretic peptide (NT-proBNP) is strongly associated with cardiac dysfunction and is increasingly used for heart failure diagnosis. To identify genetic variants associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57a5ced2342fcf9f2aebd6448b4fa264
http://hdl.handle.net/10044/1/34671
http://hdl.handle.net/10044/1/34671
Autor:
Ozren Polasek, Stefan Schreiber, Igor Rudan, Ute Nöthlings, Lina Zgaga, Susan Campbell, Cristian Pattaro, Åsa Johansson, Yurii S. Aulchenko, Ben A. Oostra, David Ellinghaus, James F. Wilson, Michael Krawczak, Caroline Hayward, Mladen Boban, Harry Campbell, Sarah H. Wild, Cornelia M. van Duijn, Alan F. Wright, Alessandro De Grandi, Scott A. Melville, Peter Riegler, Nicholas D. Hastie, Aaron Isaacs, Andre Franke, Ulf Gyllensten, Ivana Kolcic, Thomas Meitinger, Peter P. Pramstaller, Cosetta Minelli, Tatijana Zemunik, Veronique Vitart, Carsten Gnewuch
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 41 (2010)
Pattaro, C, De Grandi, A, Vitart, V, Hayward, C, Franke, A, Aulchenko, Y S, Johansson, A, Wild, S H, Melville, S A, Isaacs, A, Polasek, O, Ellinghaus, D, Kolcic, I, Noethlings, U, Zgaga, L, Zemunik, T, Gnewuch, C, Schreiber, S, Campbell, S, Hastie, N, Boban, M, Meitinger, T, Oostra, B A, Riegler, P, Minelli, C, Wright, A F, Campbell, H, van Duijn, C M, Gyllensten, U, Wilson, J F, Krawczak, M & Rudan, I & Pramstaller, P P 2010, ' A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level ', BMC Medical Genetics, vol. 11, no. 41, pp.-. https://doi.org/10.1186/1471-2350-11-41
BMC Medical Genetics
BMC Med. Genet. 11:41 (2010)
BMC Medical Genetics, 11. BioMed Central Ltd.
Pattaro, C, De Grandi, A, Vitart, V, Hayward, C, Franke, A, Aulchenko, Y S, Johansson, A, Wild, S H, Melville, S A, Isaacs, A, Polasek, O, Ellinghaus, D, Kolcic, I, Noethlings, U, Zgaga, L, Zemunik, T, Gnewuch, C, Schreiber, S, Campbell, S, Hastie, N, Boban, M, Meitinger, T, Oostra, B A, Riegler, P, Minelli, C, Wright, A F, Campbell, H, van Duijn, C M, Gyllensten, U, Wilson, J F, Krawczak, M & Rudan, I & Pramstaller, P P 2010, ' A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level ', BMC Medical Genetics, vol. 11, no. 41, pp.-. https://doi.org/10.1186/1471-2350-11-41
BMC Medical Genetics
BMC Med. Genet. 11:41 (2010)
BMC Medical Genetics, 11. BioMed Central Ltd.
Background Serum creatinine (SCR) is the most important biomarker for a quick and non-invasive assessment of kidney function in population-based surveys. A substantial proportion of the inter-individual variability in SCR level is explicable by genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::164696b904dac4eb63e7491f35925d8e
http://hdl.handle.net/10044/1/34670
http://hdl.handle.net/10044/1/34670
Autor:
Alan N. Wilton, Scott A. Melville, V. P. Studdert, Carmen L. Wilson, Chiu S. Chiang, Frode Lingaas
Publikováno v:
Genomics. 86(3)
Neuronal ceroid lipofuscinosis (NCL) is a neurodegenerative disease found in Border collie dogs, humans, and other animals. Disease gene studies in humans and animals provided candidates for the NCL gene in Border collies. A combination of linkage an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22432ba0caddf73f23ac0ce55c8a59c7
https://pubmed.ncbi.nlm.nih.gov/16033706
https://pubmed.ncbi.nlm.nih.gov/16033706