Resultats de la cerca - Ron Nudel

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  1. 1
    MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search

    MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search per Noa Rappaport, Michal Twik, Inbar Plaschkes, Ron Nudel, Tsippi Iny Stein, J. Levitt, Moran Gershoni, C. Paul Morrey, Marilyn Safran, Doron Lancet

    Publicat 2016
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  2. 2
    Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect

    Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect per Noa Rappaport, Simon Fishilevich, Ron Nudel, Michal Twik, Frida Belinky, Inbar Plaschkes, Tsippi Iny Stein, Dana Cohen, Danit Oz-Levi, Marilyn Safran, Doron Lancet

    Publicat 2017
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  3. 3
    GeneHancer: genome-wide integration of enhancers and target genes in GeneCards

    GeneHancer: genome-wide integration of enhancers and target genes in GeneCards per Simon Fishilevich, Ron Nudel, Noa Rappaport, Rotem Hadar, Inbar Plaschkes, Tsippi Iny Stein, Naomi Rosen, Asher Kohn, Michal Twik, Marilyn Safran, Doron Lancet, Dana Cohen

    Publicat 2017
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  4. 4
    Developmental language disorder – a comprehensive study of more than 46,000 individuals

    Developmental language disorder – a comprehensive study of more than 46,000 individuals per Ron Nudel, Rikke Vang Christensen, Nelli Kalnak, Michael Schwinn, Karina Banasik, Khoa Manh Dinh, Christian Erikstrup, Ole Birger Pedersen, Kristoffer Sølvsten Burgdorf, Henrik Ullum, Sisse Rye Ostrowski, Thomas Hansen, Thomas Werge

    Publicat 2023
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  5. 5
    Associations of HLA alleles with specific language impairment

    Associations of HLA alleles with specific language impairment per Ron Nudel, Nuala H. Simpson, Gillian Baird, Anne O’Hare, Gina Conti‐Ramsden, Patrick Bolton, Elizabeth R Hennessy, Anthony P. Monaco, Julian C. Knight, Bruce Winney, Simon E. Fisher, Dianne F. Newbury

    Publicat 2014
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  6. 6
    Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment

    Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment per Ron Nudel, Nuala H. Simpson, G. Baird, Anne O’Hare, Gina Conti‐Ramsden, Patrick Bolton, Elizabeth R Hennessy, Susan M. Ring, George Davey Smith, Clyde Francks, Silvia Paracchini, Anthony P. Monaco, Simon E. Fisher, Dianne F. Newbury

    Publicat 2014
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  7. 7
    Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

    Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study per Annette Erlangsen, Vivek Appadurai, Yunpeng Wang, Gustavo Turecki, Ole Mors, Thomas Werge, Preben Bo Mortensen, Anna Starnawska, Anders D. Børglum, Andrew J. Schork, Ron Nudel, Marie Bækvad‐Hansen, Jonas Bybjerg‐Grauholm, David M. Hougaard, Wesley K. Thompson, Merete Nordentoft, Esben Agerbo

    Publicat 2018
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  8. 8
    A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population

    A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population per Ron Nudel, Yunpeng Wang, Vivek Appadurai, Andrew J. Schork, Alfonso Buil, Esben Agerbo, Jonas Bybjerg‐Grauholm, Anders D. Børglum, Mark J. Daly, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Thomas Werge, Merete Nordentoft, Wesley K. Thompson, Michael E. Benros

    Publicat 2019
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  9. 9
    Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders

    Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders per Ron Nudel, Michael E. Benros, Morten Dybdahl Krebs, Rosa Lundbye Allesøe, Camilla K. Lemvigh, Jonas Bybjerg‐Grauholm, Anders D. Børglum, Mark J. Daly, Merete Nordentoft, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Alfonso Buil, Thomas Werge, Simon Rasmussen, Wesley K. Thompson

    Publicat 2019
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  10. 10
    VarElect: the phenotype-based variation prioritizer of the GeneCards Suite

    VarElect: the phenotype-based variation prioritizer of the GeneCards Suite per Gil Stelzer, Inbar Plaschkes, Danit Oz-Levi, Anna Alkelai, Tsviya Olender, Shahar Zimmerman, Michal Twik, Frida Belinky, Simon Fishilevich, Ron Nudel, Yaron Guan‐Golan, David Warshawsky, Dvir Dahary, Asher Kohn, Yaron Mazor, Sergey Kaplan, Tsippi Iny Stein, Hagit Baris, Noa Rappaport, Marilyn Safran, Doron Lancet

    Publicat 2016
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  11. 11
    Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

    Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment per Pía Villanueva, Ron Nudel, Alexander Hoischen, María Angélica Fernández, Nuala H. Simpson, Christian Gilissen, Rose H. Reader, Lillian Jara, María Magdalena Echeverry, Clyde Francks, Gillian Baird, Gina Conti‐Ramsden, Anne O’Hare, Patrick Bolton, Elizabeth R Hennessy, Hernán Palomino, Luis G. Carvajal‐Carmona, Joris A. Veltman, Jean‐Baptiste Cazier, Zulema De Barbieri, Simon E. Fisher, Dianne F. Newbury

    Publicat 2015
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  12. 12
    A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

    A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment per Andrew J. Schork, Hyejung Won, Vivek Appadurai, Ron Nudel, Michael J. Gandal, Olivier Delaneau, Malene Revsbech Christiansen, David M. Hougaard, Marie Bækved-Hansen, Jonas Bybjerg‐Grauholm, Marianne Giørtz Pedersen, Esben Agerbo, Carsten Bøcker Pedersen, Benjamin M. Neale, Mark J. Daly, Naomi R. Wray, Merete Nordentoft, Ole Mors, Anders D. Børglum, Preben Bo Mortensen, Alfonso Buil, Wesley K. Thompson, Daniel H. Geschwind, Thomas Werge

    Publicat 2019
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  13. 13
    Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

    Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration per Xueping Liu, Dorte Helenius, Line Skotte, Robin N. Beaumont, Matthias Wielscher, Frank Geller, Julius Juodakis, Anubha Mahajan, Jonathan P. Bradfield, Frederick T. J. Lin, Suzanne Vogelezang, Mariona Bustamante, Tarunveer S. Ahluwalia, Niina Pitkänen, Carol A. Wang, Jonas Bacelis, Maria Carolina Borges, Ge Zhang, Bruce Bedell, Robert M. Rossi, Kristin Skogstrand, Shouneng Peng, Wesley K. Thompson, Vivek Appadurai, Debbie A. Lawlor, Ilkka Kalliala, Christine Power, Mark I. McCarthy, Heather A. Boyd, Mary L. Marazita, Hákon Hákonarson, M. Geoffrey Hayes, Denise Scholtens, Fernando Rivadeneira, Vincent W. V. Jaddoe, Rebecca Vinding, Hans Bisgaard, Bridget Knight, Katja Pahkala, Olli T. Raitakari, Øyvind Helgeland, Stefan Johansson, Pål R. Njølstad, João Fadista, Andrew J. Schork, Ron Nudel, Daniel E. Miller, Xiaoting Chen, Matthew T. Weirauch, Preben Bo Mortensen, Anders D. Børglum, Merete Nordentoft, Ole Mors, Ke Hao, Kelli K. Ryckman, David M. Hougaard, Leah C. Kottyan, Craig E. Pennell, Leo‐Pekka Lyytikäinen, Klaus Bønnelykke, Martine Vrijheid, Janine F. Felix, William L. Lowe, Struan F.A. Grant, Elina Hyppönen, Bo Jacobsson, Marjo‐Riitta Järvelin, Louis J. Muglia, Jeffrey C. Murray, Rachel M. Freathy, Thomas Werge, Mads Melbye, Alfonso Buil, Bjarke Feenstra

    Publicat 2019
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