खोज परिणाम - Stacy Steinberg

परिणाम को परिष्कृत करें
  1. 1
    Genomewide Significant Linkage to Stuttering on Chromosome 12

    Genomewide Significant Linkage to Stuttering on Chromosome 12 द्वारा Naveeda Riaz, Stacy Steinberg, Jamil Ahmad, Anna Pluzhnikov, Sheikh Riazuddin, Nancy J. Cox, Dennis Drayna

    प्रकाशित 2005
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  2. 2
    Heterozygote carriers for CNVs in<i>PARK2</i>are at increased risk of Parkinson's disease

    Heterozygote carriers for CNVs in<i>PARK2</i>are at increased risk of Parkinson's disease द्वारा Johanna Huttenlocher, Hreinn Stefánsson, Stacy Steinberg, Hafdís T. Helgadóttir, Sigurlaug Sveinbjörnsdóttir, Olaf Rieß, Peter Bauer, Kāri Stefánsson

    प्रकाशित 2015
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    Revisão
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  3. 3
    Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction

    Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction द्वारा Gunnar W. Reginsson, Andrés Ingason, Jack Euesden, Gyða Björnsdóttir, Sigurgeir Ólafsson, Engilbert Sigurðsson, Högni Óskarsson, Þórarinn Tyrfingsson, Valgerður Rúnarsdóttir, Ingunn Hansdóttir, Stacy Steinberg, Hreinn Stefánsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Kāri Stefánsson

    प्रकाशित 2017
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  4. 4
    Detection of sharing by descent, long-range phasing and haplotype imputation

    Detection of sharing by descent, long-range phasing and haplotype imputation द्वारा Augustine Kong, Gísli Másson, Michael L. Frigge, Arnaldur Gylfason, Pasha Zusmanovich, Guðmar Þorleifsson, Pall I. Olason, Andrés Ingason, Stacy Steinberg, Þórunn Rafnar, Patrick Sulem, Magali Mouy, Frosti Jónsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hreinn Stefánsson, Kāri Stefánsson

    प्रकाशित 2008
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  5. 5
    Rate of de novo mutations and the importance of father’s age to disease risk

    Rate of de novo mutations and the importance of father’s age to disease risk द्वारा Augustine Kong, Michael L. Frigge, Gísli Másson, Søren Besenbacher, Patrick Sulem, Gísli Magnússon, Sigurjón A. Guðjónsson, Ásgeir Sigurðsson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Wendy S.W. Wong, Gunnar Sigurðsson, G. Bragi Walters, Stacy Steinberg, Hannes Helgason, Guðmar Þorleifsson, Daníel F. Guðbjartsson, Agnar Helgason, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Kāri Stefánsson

    प्रकाशित 2012
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  6. 6
    Variant of<i>TREM2</i>Associated with the Risk of Alzheimer's Disease

    Variant of<i>TREM2</i>Associated with the Risk of Alzheimer's Disease द्वारा Thorlákur Jónsson, Hreinn Stefánsson, Stacy Steinberg, Ingileif Jónsdóttir, Pálmi V. Jónsson, Jón Snædal, Sigurbjörn Björnsson, Johanna Huttenlocher, Allan I. Levey, James J. Lah, Dan Rujescu, Harald Hampel, Ina Giegling, Ole A. Andreassen, Knut Engedal, Ingun Ulstein, Srdjan Djurovic, Carla A. Ibrahim‐Verbaas, Albert Hofman, M. Arfan Ikram, Cornelia M. van Duijn, Unnur Þorsteinsdóttir, Augustine Kong, Kāri Stefánsson

    प्रकाशित 2012
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  7. 7
    A polygenic resilience score moderates the genetic risk for schizophrenia

    A polygenic resilience score moderates the genetic risk for schizophrenia द्वारा Jonathan Hess, Sang Lee, Manuel Mattheisen, Anders D. Børglum, Thomas D. Als, Jakob Grove, Thomas Werge, Preben Bo Mortensen, Ole Mors, Merete Nordentoft, David M. Hougaard, Jonas Byberg-Grauholm, Marie Bækvad‐Hansen, Tiffany A. Greenwood, Ming T. Tsuang, David Curtis, Stacy Steinberg, Engilbert Sigurðsson, Hreinn Stefánsson, Hreinn Stefánsson, Howard J. Edenberg, Peter Holmans, Stephen V. Faraone, Stephen J. Glatt

    प्रकाशित 2019
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  8. 8
    Variant in the sequence of the LINGO1 gene confers risk of essential tremor

    Variant in the sequence of the LINGO1 gene confers risk of essential tremor द्वारा Hreinn Stefánsson, Stacy Steinberg, Hjörvar Pétursson, Ómar Gústafsson, Iris H Gudjonsdottir, Guðrún A. Jónsdóttir, Stefan Palsson, Thorlákur Jónsson, Jona Saemundsdottir, Gyða Björnsdóttir, Yvonne Böttcher, Theodora Thorlacius, Dietrich Haubenberger, Alexander Zimprich, Eduard Auff, Christoph Hotzy, Claudia Testa, Lisa A Miyatake, Ami Rosen, Kristleifur Kristleifsson, David B. Rye, Friedrich Asmus, Lüdger Schöls, Martin Dichgans, Finnbogi Jakobsson, John Benedikz, Unnur Þorsteinsdóttir, Jeffrey R. Gulcher, Augustine Kong, Kāri Stefánsson

    प्रकाशित 2009
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  9. 9
    Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci

    Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci द्वारा Aree Witoelar, Arvid Rongve, Ina S. Almdahl, Ingun Ulstein, Andreas Engvig, Linda R. White, Geir Selbæk, Eystein Stordal, Fred Andersen, Anne Brækhus, Ingvild Saltvedt, Knut Engedal, Timothy Hughes, Sverre Bergh, Geir Bråthen, Nenad Bogdanović, Francesco Bettella, Yunpeng Wang, Lavinia Athanasiu, Shahram Bahrami, Stéphanie Le Hellard, Sudheer Giddaluru, Anders M. Dale, Sigrid Botne Sando, Stacy Steinberg, Hreinn Stefánsson, Jón Snædal, Rahul S. Desikan, Kāri Stefánsson, Dag Aarsland, Srdjan Djurovic, Tormod Fladby, Ole A. Andreassen

    प्रकाशित 2018
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    Revisão
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  10. 10
    15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

    15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia द्वारा Magnús Ö. Úlfarsson, G. Bragi Walters, Ómar Gústafsson, Stacy Steinberg, Ana Isabel Silva, Orla Doyle, Michael Brammer, Daníel F. Guðbjartsson, Sunna Arnarsdóttir, Guðrún A. Jónsdóttir, Rósa S. Gísladóttir, Gyða Björnsdóttir, Hannes Helgason, Lotta M. Ellingsen, Jónas G. Halldórsson, Evald Sæmundsen, Berglind Stefánsdóttir, Lina Jönsson, Valgerdur Kristin Eiriksdottir, Guðný Eiríksdóttir, G H Johannesdottir, Unnur Unnsteinsdóttir, Birna Jónsdóttir, Brynja B. Magnúsdóttir, Patrick Sulem, U. Thorsteinsdottir, Engilbert Sigurðsson, Daniel Brandeis, Andreas Meyer‐Lindenberg, Hreinn Stefánsson, Hreinn Stefánsson

    प्रकाशित 2017
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  11. 11
    Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

    Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort द्वारा Birgitte Bertelsen, Hreinn Stefánsson, Lars R. Jensen, Linea Melchior, Nanette Mol Debes, Camilla Groth, Liselotte Skov, Thomas Werge, Iordanis Karagiannidis, Zsanett Tárnok, Csaba Barta, Péter Nagy, Luca Farkas, Karen Brøndum‐Nielsen, Renata Rizzo, Mariangela Gulisano, Dan Rujescu, Lambertus A. Kiemeney, Sarah Tosato, Muhammad Sulaman Nawaz, Andrés Ingason, Unnur Unnsteinsdóttir, Stacy Steinberg, Pétur Lúðvígsson, Kāri Stefánsson, Andreas W. Kuß, Peristera Paschou, Daniëlle C. Cath, Pieter J. Hoekstra, Kirsten Müller‐Vahl, Manfred Stuhrmann, Asli Silahtaroglu, Rolph Pfundt, Zeynep Tümer

    प्रकाशित 2015
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  12. 12
    Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

    Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease द्वारा Stacy Steinberg, Hreinn Stefánsson, Thorlákur Jónsson, Hrefna Johannsdottir, Andrés Ingason, Hannes Helgason, Patrick Sulem, Ólafur Þ. Magnússon, Sigurjón A. Guðjónsson, Unnur Unnsteinsdóttir, Augustine Kong, Seppo Helisalmi, Hilkka Soininen, James J. Lah, DemGene, Dag Aarsland, Tormod Fladby, Ingun Ulstein, Srdjan Djurovic, Sigrid Botne Sando, Linda R White, Gun-Peggy Knudsen, Lars T. Westlye, Geir Selbæk, Ina Giegling, Harald Hampel, Mikko Hiltunen, Allan I. Levey, Ole A Andreassen, Dan Rujescu, Pálmi V. Jónsson, Sigurbjörn Björnsson, Jón Snædal, Hreinn Stefánsson

    प्रकाशित 2015
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  13. 13
    Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

    Common variants on 8p12 and 1q24.2 confer risk of schizophrenia द्वारा Yongyong Shi, Zhiqiang Li, Qi Xu, Ti Wang, Tao Li, Jiawei Shen, Fengyu Zhang, Jianhua Chen, Guoquan Zhou, Weidong Ji, Baojie Li, Yifeng Xu, Dengtang Liu, Peng Wang, Ping Yang, Benxiu Liu, Wensheng Sun, Chunling Wan, Shengying Qin, Guang He, Stacy Steinberg, Sven Cichon, Thomas Werge, Engilbert Sigurðsson, Sarah Tosato, Aarno Palotie, Markus M. Nöthen, Marcella Rietschel, Roel A. Ophoff, David Collier, Dan Rujescu, David St Clair, Hreinn Stefánsson, Hreinn Stefánsson, Jue Ji, Qingzhong Wang, Wenjin Li, Linqing Zheng, Hairong Zhang, Guoyin Feng, Lin He

    प्रकाशित 2011
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  14. 14
    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene

    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene द्वारा X-j Luo, Mei LI, Liang Huang, Stacy Steinberg, Manuel Mattheisen, Guoqing Liang, Gary Donohoe, Yongyong Shi, Chuansheng Chen, Weihua Yue, Anna Alkelai, Bernard Lerer, Zhiqiang Li, Qizhong Yi, Marcella Rietschel, Sven Cichon, David Collier, Sarah Tosato, Jaana Suvisaari, Dan Rujescu, В. Е. Голимбет, Teimuraz Silagadze, Naser Durmishi, Miloš Milovančević, Hreinn Stefánsson, Thomas G. Schulze, Markus M. Nöthen, Chao Chen, Rachel Lyne, Derek W. Morris, Michael Gill, Aiden Corvin, D Zhang, Qian Dong, Robert K. Moyzis, Kāri Stefánsson, Engilbert Sigurðsson, Fang Hu, Bing Su, Lin Gan

    प्रकाशित 2013
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  15. 15
    Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

    Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence द्वारा Dana B. Hancock, Gunnar W. Reginsson, Nathan Gaddis, X Chen, Nancy L. Saccone, Sharon M. Lutz, Beenish Qaiser, Richard Sherva, Stacy Steinberg, Florian Zink, Simon Stacey, Cristie Glasheen, Jingchun Chen, Fangyi Gu, Brittni N. Frederiksen, Anu Loukola, Daníel F. Guðbjartsson, Irene Brüske, M. T. Landi, Heike Bickeböller, Pamela A. F. Madden, Lindsay A. Farrer, Jaakko Kaprio, Henry R. Kranzler, Joel Gelernter, Timothy B. Baker, Peter Kraft, Christopher I. Amos, Neil E. Caporaso, John E. Hokanson, Laura J. Bierut, Thorgeir E. Thorgeirsson, Eric O. Johnson, Kāri Stefánsson

    प्रकाशित 2015
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  16. 16
    Rare and Common Variants Conferring Risk of Tooth Agenesis

    Rare and Common Variants Conferring Risk of Tooth Agenesis द्वारा Lina Jönsson, Þórður Eydal Magnússon, Arni Thordarson, Teitur Jónsson, Frank Geller, Bjarke Feenstra, Mads Melbye, Ellen A. Nøhr, Strahinja Vučić, Brunilda Dhamo, Fernando Rivadeneira, Edwin M. Ongkosuwito, Eppo B. Wolvius, Elizabeth J. Leslie, Mary L. Marazita, Brian J. Howe, Lina M. Moreno Uribe, Isabel Alonso, Mariana Santos, Teresa Pinho, Rafn Jónsson, Gunnar Auðólfsson, Lárus J. Gudmundsson, Muhammad Sulaman Nawaz, Sigurgeir Ólafsson, Ómar Gústafsson, Andrés Ingason, Unnur Unnsteinsdóttir, Gyða Björnsdóttir, G. Bragi Walters, Mark Zervas, Ásmundur Oddsson, Daníel F. Guðbjartsson, Stacy Steinberg, Hreinn Stefánsson, Kāri Stefánsson

    प्रकाशित 2018
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  17. 17
    Copy number variations of chromosome 16p13.1 region associated with schizophrenia

    Copy number variations of chromosome 16p13.1 region associated with schizophrenia द्वारा Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, L. Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair

    प्रकाशित 2009
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  18. 18
    Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility

    Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility द्वारा Hamdi Mbarek, Stacy Steinberg, Dale R. Nyholt, Scott D. Gordon, Michael Miller, Allan F. McRae, Jouke‐Jan Hottenga, Felix R. Day, Gonneke Willemsen, Eco J. C. de Geus, Gareth E. Davies, Hilary C. Martin, Brenda W.J.H. Penninx, Rick Jansen, Kerrie McAloney, Jacqueline M. Vink, Jaakko Kaprio, Robert Plomin, Tim D. Spector, Patrik K. E. Magnusson, Bruno Reversade, R. Alan Harris, Kjersti M. Aagaard, Ragnar P. Kristjansson, Ísleifur Ólafsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, William G. Iacono, Cornelis B. Lambalk, Grant W. Montgomery, Matt McGue, Ken K. Ong, John R. B. Perry, Nicholas G. Martin, Hreinn Stefánsson, Kāri Stefánsson, Dorret I. Boomsma

    प्रकाशित 2016
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  19. 19
    Disruption of the neurexin 1 gene is associated with schizophrenia

    Disruption of the neurexin 1 gene is associated with schizophrenia द्वारा Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier

    प्रकाशित 2008
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  20. 20
    Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer’s disease risk

    Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer’s disease risk द्वारा Iris E. Jansen, Jeanne E. Savage, Kyoko Watanabe, Julien Bryois, Dylan M. Williams, Stacy Steinberg, Julia Sealock, Ida Karlsson, Sara Hägg, Lavinia Athanasiu, Nicola Voyle, Petroula Proitsi, Aree Witoelar, Sven Stringer, Dag Aarsland, Ina S. Almdahl, Fred Andersen, Sverre Bergh, Francesco Bettella, Sigurbjörn Björnsson, Anne Brækhus, Geir Bråthen, Christiaan de Leeuw, Rahul S. Desikan, Srdjan Djurovic, Logan Dumitrescu, Tormod Fladby, Timothy Homan, Pálmi V. Jónsson, Steven J. Kiddle, K Arvid Rongve, Ingvild Saltvedt, Sigrid Botne Sando, Geir Selbæk, Nathan Skenne, Jón Snædal, Eystein Stordal, Ingun Ulstein, Yunpeng Wang, Linda R. White, Jens Hjerling‐Leffler, Patrick F. Sullivan, Wiesje M. van der Flier, Richard Dobson, Lea K. Davis, Hreinn Stefánsson, Kāri Stefánsson, Nancy L. Pedersen, Stephan Ripke, Ole A. Andreassen, Daniëlle Posthuma

    प्रकाशित 2018
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