نتائج البحث - Unda Todt
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1
Severe mental retardation with breathing abnormalities (Pitt–Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4 حسب Antje Brockschmidt, Unda Todt, Soojin Ryu, Alexander Hoischen, Christina Landwehr, Stefanie Birnbaum, Wilhelm Frenck, Bernhard Radlwimmer, Peter Lichter, Hartmut Engels, Wolfgang Driever, Christian Kubisch, Ruthild G. Weber
منشور في 2007Artigo -
2
Rare missense variants inATP1A2 in families with clustering of common forms of migraine حسب Unda Todt, Martin Dichgans, Karin Jurkat‐Rott, Axel Heinze, Giovanni Zifarelli, Jan J. Koenderink, Ingrid Goebel, Vera Zumbroich, Anne Stiller, Alfredo Ramı́rez, Thomas Friedrich, Hartmut Göbel, Christian Kubisch
منشور في 2005Artigo -
3
A high-density association screen of 155 ion transport genes for involvement with common migraine حسب Dale R. Nyholt, K. Steven LaForge, Mikko Kallela, Kirsi Alakurtti, Verneri Anttila, Martti Färkkilâ, Eija Hämäläinen, Jaakko Kaprio, Mari Kaunisto, Andrew C. Heath, Grant W. Montgomery, Hartmut Göbel, Unda Todt, Michel D. Ferrari, Lenore J. Launer, Rune R. Frants, Gisela M. Terwindt, Boukje de Vries, W. M. Monique Verschuren, Jan A.J.G. van den Brand, Tobias Freilinger, V. Pfaffenrath, Andreas Straube, Dennis G. Ballinger, Yiping Zhan, Mark J. Daly, David R. Cox, Martin Dichgans, Arn M. J. M. van den Maagdenberg, Christian Kubisch, Nicholas G. Martin, Maija Wessman, Leena Peltonen, Aarno Palotie
منشور في 2008Artigo -
4
Genome-wide association analysis identifies susceptibility loci for migraine without aura حسب Tobias Freilinger, Verneri Anttila, Boukje de Vries, Rainer Malik, Mikko Kallela, Gisela M. Terwindt, Patricia Pozo‐Rosich, Bendik S. Winsvold, Dale R. Nyholt, Willebrordus P. J. van Oosterhout, Ville Artto, Unda Todt, Eija Hämäläinen, Jessica Fernández‐Morales, Mark A. Louter, Mari Kaunisto, Jean Schoenen, Olli T. Raitakari, Terho Lehtimäki, Marta Vila‐Pueyo, Hartmut Göbel, Erich Wichmann, Cèlia Sintas, André G. Uitterlinden, Albert Hofman, Fernando Rivadeneira, Axel Heinze, Erling Tronvik, Cornelia M. van Duijn, Jaakko Kaprio, Bru Cormand, Maija Wessman, Rune R. Frants, Thomas Meitinger, Bertram Müller‐Myhsok, John‐Anker Zwart, Martti Färkkilâ, Alfons Macaya, Michel D. Ferrari, Christian Kubisch, Aarno Palotie, Martin Dichgans, Arn M. J. M. van den Maagdenberg
منشور في 2012Artigo -
5
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1 حسب Verneri Anttila, Hreinn Stefánsson, Mikko Kallela, Unda Todt, Gisela M. Terwindt, M Calafato, Dale R. Nyholt, Antigone S. Dimas, Tobias Freilinger, Bertram Müller‐Myhsok, Ville Artto, Michael Inouye, Kirsi Alakurtti, Mari Kaunisto, Eija Hämäläinen, Boukje de Vries, Anine H Stam, Claudia M Weller, Axel Heinze, Katja Heinze‐Kuhn, Ingrid Goebel, Guntram Borck, Hartmut Göbel, Stacy Steinberg, Christiane Wolf, Ásgeir Björnsson, Grétar Guðmundsson, Malene Kirchmann, Anne Werner Hauge, Thomas Werge, Jean Schoenen, Johan G. Eriksson, Knut Hagen, Lars Jacob Stovner, H-Erich Wichmann, Thomas Meitinger, Michael P. Alexander, Susanne Moebus, Stefan Schreiber, Yurii S. Aulchenko, Monique M.B. Breteler, André G. Uitterlinden, Albert Hofman, Cornelia M. van Duijn, Päivi Tikka-Kleemola, Salli Vepsäläinen, Susanne Lucae, Federica Tozzi, Pierandrea Muglia, Jeffrey C. Barrett, Jaakko Kaprio, Martti Färkkilâ, Leena Peltonen, Kāri Stefánsson, John‐Anker Zwart, Michel D. Ferrari, Jes Olesen, Mark J. Daly, Maija Wessman, Arn M. J. M. van den Maagdenberg, Martin Dichgans, Christian Kubisch, Emmanouil T. Dermitzakis, Rune R. Frants, Aarno Palotie
منشور في 2010Artigo -
6
Genome-wide meta-analysis identifies new susceptibility loci for migraine حسب Verneri Anttila, Bendik S. Winsvold, Padhraig Gormley, Tobias Kurth, Francesco Bettella, George McMahon, Mikko Kallela, Rainer Malik, Boukje de Vries, Gisela M. Terwindt, Sarah E. Medland, Unda Todt, Wendy L. McArdle, Lydia Quaye, Markku Koiranen, M. Arfan Ikram, Terho Lehtimäki, Anine H Stam, Lannie Ligthart, Juho Wedenoja, Ian Dunham, Benjamin M. Neale, Priit Palta, Eija Hämäläinen, Markus Schürks, Lynda M. Rose, Julie E. Buring, Paul M. Ridker, Stacy Steinberg, Hreinn Stefánsson, Finnbogi Jakobsson, Debbie A. Lawlor, David M. Evans, Susan M. Ring, Martti Färkkilâ, Ville Artto, Mari Kaunisto, Tobias Freilinger, Jean Schoenen, Rune R. Frants, Nadine Pelzer, Claudia M Weller, Ronald Zielman, Andrew C. Heath, Pamela A. F. Madden, Grant W. Montgomery, Nicholas G. Martin, Guntram Borck, Hartmut Göbel, Axel Heinze, Katja Heinze‐Kuhn, Frances M. K. Williams, Anna‐Liisa Hartikainen, Anneli Pouta, Joyce van den Ende, André G. Uitterlinden, Albert Hofman, Najaf Amin, Jouke‐Jan Hottenga, Jacqueline M. Vink, Kauko Heikkilä, Michael P. Alexander, Bertram Müller‐Myhsok, Stefan Schreiber, Thomas Meitinger, Heinz Erich Wichmann, Arpo Aromaa, Johan G. Eriksson, Bryan J. Traynor, Daniah Trabzuni, Elizabeth J. Rossin, Kasper Lage, Suzanne B.R. Jacobs, J. Raphael Gibbs, Ewan Birney, Jaakko Kaprio, Brenda W.J.H. Penninx, Dorret I. Boomsma, Cornelia M. van Duijn, Olli T. Raitakari, Marjo‐Riitta Järvelin, John‐Anker Zwart, Lynn Cherkas, David P. Strachan, Christian Kubisch, Michel D. Ferrari, Arn M. J. M. van den Maagdenberg, Martin Dichgans, Maija Wessman, George Davey Smith, Kāri Stefánsson, Mark J. Daly
منشور في 2013Revisão
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Internal medicine
Medicine
Genotype
Migraine
Single-nucleotide polymorphism
Aura
Genome-wide association study
Migraine with aura
Computational biology
Familial hemiplegic migraine
Genetic association
Genome
Philosophy
Anatomy
Association (psychology)
Bioinformatics
Breathing
Cortical spreading depression
Enhancer
Environmental health
Epistemology
Evolutionary biology
Haploinsufficiency
Linguistics
Meta-analysis
Missense mutation
Mutation