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Genetic variants in RBFOX3 are associated with sleep latency

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

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

Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels

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

O5‐03‐04: Genome‐wide association study of Alzheimer's‐related brain MRI traits identifies several loci influencing degeneration of the hippocampus

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

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level

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.

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