Výsledky vyhledávání - Kate Baker

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  1. 1
    Adolescents and young adults with 22qll deletion syndrome: psychopathology in an at-risk group

    Adolescents and young adults with 22qll deletion syndrome: psychopathology in an at-risk group Autor Kate Baker, David Skuse

    Vydáno 2005
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  2. 2
    Making sense of cilia in disease: The human ciliopathies

    Making sense of cilia in disease: The human ciliopathies Autor Kate Baker, Philip L. Beales

    Vydáno 2009
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  3. 3
    The neurodevelopmental spectrum of synaptic vesicle cycling disorders

    The neurodevelopmental spectrum of synaptic vesicle cycling disorders Autor Abinayah John, Elise Ng‐Cordell, Nancy Hanna, Diandra Brkić, Kate Baker

    Vydáno 2020
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  4. 4
    Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences

    Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences Autor Kate Baker, Rory T. Devine, Elise Ng‐Cordell, F. Lucy Raymond, Claire Hughes

    Vydáno 2020
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  5. 5
    Cognitive Training Enhances Intrinsic Brain Connectivity in Childhood

    Cognitive Training Enhances Intrinsic Brain Connectivity in Childhood Autor Duncan E. Astle, Jessica Barnes, Kate Baker, Giles L. Colclough, Mark W. Woolrich

    Vydáno 2015
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  6. 6
    A High-Density EEG Investigation into Steady State Binaural Beat Stimulation

    A High-Density EEG Investigation into Steady State Binaural Beat Stimulation Autor Peter Goodin, Joseph Ciorciari, Kate Baker, Anne-Marie Carrey, Michelle Harper, Jordy Kaufman

    Vydáno 2012
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  7. 7
    Training Working Memory in Childhood Enhances Coupling between Frontoparietal Control Network and Task-Related Regions

    Training Working Memory in Childhood Enhances Coupling between Frontoparietal Control Network and Task-Related Regions Autor Jessica Barnes, Anna C. Nobre, Mark W. Woolrich, Kate Baker, Duncan E. Astle

    Vydáno 2016
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  8. 8
    Allo-Reactivity of Mesenchymal Stem Cells in Rhesus Macaques Is Dose and Haplotype Dependent and Limits Durable Cell Engraftment In Vivo

    Allo-Reactivity of Mesenchymal Stem Cells in Rhesus Macaques Is Dose and Haplotype Dependent and Limits Durable Cell Engraftment In Vivo Autor Iryna A. Isakova, Calvin Lanclos, Julie Bruhn, Marcelo J. Kuroda, Kate Baker, Veena Krishnappa, Donald G. Phinney

    Vydáno 2014
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  9. 9
    Evaluating a Measure of Tanning Abuse and Dependence

    Evaluating a Measure of Tanning Abuse and Dependence Autor Joel Hillhouse, Mary Kate Baker, Rob Turrisi, Alan L. Shields, Jerod L. Stapleton, Shashank Jain, Ian Longacre

    Vydáno 2012
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  10. 10
    Epilepsy, cognitive deficits and neuroanatomy in males with <i><scp>ZDHHC</scp>9</i> mutations

    Epilepsy, cognitive deficits and neuroanatomy in males with <i><scp>ZDHHC</scp>9</i> mutations Autor Kate Baker, Duncan E. Astle, Gaia Scerif, Jessica Barnes, JENNIE SMITH, Georgina Moffat, Jonathan H. Gillard, Torsten Baldeweg, F. Lucy Raymond

    Vydáno 2015
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  11. 11
    Standardization of canine meningioma grading: validation of new guidelines for reproducible histopathologic criteria

    Standardization of canine meningioma grading: validation of new guidelines for reproducible histopathologic criteria Autor Sara Belluco, Giuseppe Marano, Giancarlo Avallone, Chiara Brachelente, Stefano Di Palma, R. Rasotto, Kate Baker, Andreas Beineke, Anna Oevermann, Frauke Seehusen, Patrizia Boracchi, Martı́ Pumarola, Maria Teresa Mandara

    Vydáno 2023
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  12. 12
    Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling

    Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling Autor Kate Baker, Sarah L. Gordon, Detelina Grozeva, Margriet van Kogelenberg, Nicola Roberts, Michael Pike, Edward Blair, Matthew E. Hurles, W.K. Chong, Torsten Baldeweg, Manju A. Kurian, Stewart Boyd, Michael A. Cousin, F. Lucy Raymond

    Vydáno 2015
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  13. 13
    Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times

    Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times Autor Alex Habel, Richard Herriot, Dinakantha Kumararatne, Jeremy Allgrove, Kate Baker, Helen Baxendale, Frances Bu’Lock, Helen V. Firth, Andrew R. Gennery, Anthony Holland, C Illingworth, Nigel Mercer, Merel M. Pannebakker, Andrew Parry, Anne C. Roberts, Beverly Tsai‐Goodman

    Vydáno 2014
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  14. 14
    Maternal antibodies provide partial protection from postnatal Zika viremia in nonhuman primates

    Maternal antibodies provide partial protection from postnatal Zika viremia in nonhuman primates Autor Nicholas J. Maness, Blake Schouest, Anil Singapuri, Maria Dennis, Margaret H. Gilbert, Rudolf P. Bohm, Faith Schiro, Pyone P. Aye, Kate Baker, Koen K. A. Van Rompay, Andrew A. Lackner, Myrna C. Bonaldo, Robert V. Blair, Sallie R. Permar, Lark L. Coffey, Antonito T. Panganiban, Diogo M. Magnani

    Vydáno 2019
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  15. 15
    Postnatal Zika virus infection of nonhuman primate infants born to mothers infected with homologous Brazilian Zika virus

    Postnatal Zika virus infection of nonhuman primate infants born to mothers infected with homologous Brazilian Zika virus Autor Nicholas J. Maness, Blake Schouest, Anil Singapuri, Maria Dennis, Margaret H. Gilbert, Rudolf P. Bohm, Faith Schiro, Pyone P. Aye, Kate Baker, Koen K. A. Van Rompay, Andrew A. Lackner, Myrna C. Bonaldo, Robert V. Blair, Sallie R. Permar, Lark L. Coffey, Antonito T. Panganiban, Diogo M. Magnani

    Vydáno 2019
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  16. 16
    Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation

    Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation Autor Elizabeth J. Radford, Hong-Kee Tan, Malin H. L. Andersson, James Stephenson, Eugene J. Gardner, Holly Ironfield, Andrew Waters, Daniel P. Gitterman, Sarah Lindsay, Federico Abascal, Iñigo Martincorena, Anna Kolesnik, Elise Ng‐Cordell, Helen V. Firth, Kate Baker, John R. B. Perry, David J. Adams, Sebastian S. Gerety, Matthew E. Hurles

    Vydáno 2023
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  17. 17
    SYT1-associated neurodevelopmental disorder: a case series

    SYT1-associated neurodevelopmental disorder: a case series Autor Kate Baker, Sarah L. Gordon, Holly Melland, Fabian Bumbak, Daniel J. Scott, Tess J Jiang, David J. Owen, Bradley J. Turner, Stewart Boyd, Mari Rossi, Mohammed Al‐Raqad, Orly Elpeleg, Dawn Peck, Grazia M.S. Mancini, Martina Wilke, Marcella Zollino, Giuseppe Marangi, Heike Weigand, Ingo Borggraefe, Tobias B. Haack, Zornitza Stark, Simon Sadedin, Tiong Yang Tan, Yunyun Jiang, Richard A. Gibbs, Sara Ellingwood, Michelle D. Amaral, Whitley V. Kelley, Manju A. Kurian, Michael A. Cousin, F. Lucy Raymond

    Vydáno 2018
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  18. 18
    Comparison of autism domains across thirty rare variant genotypes

    Comparison of autism domains across thirty rare variant genotypes Autor Nabila M.H. Ali, Samuel J. R. A. Chawner, Leila Kushan, Carrie E. Bearden, Jennifer G. Mullé, Rebecca M. Pollak, Raquel E. Gur, Wendy K. Chung, Harriet Housby, Irene Lee, David Skuse, Jeanne Wolstencroft, William Mandy, Spiros Denaxas, Kate Baker, Lucy Raymond, Marianne B. M. van den Bree, Samuel J. R. A. Chawner, Jérémy Hall, Peter Holmans, Josh Hope-Bell, Danielle Le Roux, Sally Morrin, Michael J. Owen, Shreeya Sivakumar, Michael J. Owen, Marianne B. M. van den Bree

    Vydáno 2025
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  19. 19
    Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study

    Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study Autor Jeanne Wolstencroft, Francesca Wicks, Ramya Srinivasan, Sarah Wynn, Tamsin Ford, Kate Baker, Samuel J. R. A. Chawner, Jérémy Hall, Marianne B. M. van den Bree, Michael J. Owen, Jeanne Wolstencroft, Francesca Wicks, Ramya Srinivasan, Marie Erwood, David Lafont, Husne Timur, Zheng Ye, Susan Walker, Frida Printzlau, Manoj Juj, Sarah Davies, Hayley Denyer, Alice Watkins, Eleanor Kerry, Nadia Coscini, Nasrtullah Fatih, Anna Lucock, Spiros Denaxas, William Mandy, Neil Walker, Sarah B. Wallwork, Eleanor Dewhurst, Andrew Cuthbert, Aimée Challenger, Sophie C. Andrews, Peter Holmans, Samantha Bowen, Karen Bradley, Philippa Birch, Molly Tong, Nicola S. Lewis, Sinead Ray, Matthew Sopp, Hayley Moss, Sarah Wynn, Beverley A. Searle, Lisa Robertson, Jonathan Berg, Anne Lampe, Shelagh Joss, Paul Brennan, Alison Kraus, Nayana Lahiri, Astrid Weber, Myfanwy Rawson, Diana Johnson, Pradeep Vasudevan, Rachel Harrison, Denise Williams, Eamonn R. Maher, Usha Kini, Fleur van Dijk, Virginia Clowes, Jana Gurasashvilli, Sahar Mansour, Muriel Holder-Espinasse, Amy Watford, Julia Rankin, Diana Baralle, Annie Procter, Tamsin Ford, Kate Baker, Samuel J. R. A. Chawner, Jérémy Hall, Marianne B. M. van den Bree, Michael J. Owen, David Skuse, F. Lucy Raymond, David Skuse, F. Lucy Raymond

    Vydáno 2022
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  20. 20
    A generative network model of neurodevelopmental diversity in structural brain organization

    A generative network model of neurodevelopmental diversity in structural brain organization Autor Danyal Akarca, Petra E. Vértes, Edward T. Bullmore, Kate Baker, Susan E. Gathercole, Joni Holmes, Rogier Kievit, Tom Manly, Joe Bathelt, Marc Bennett, Giacomo Bignardi, Sarah Bishop, Erica Bottacin, Lara Bridge, Diandra Brkić, Annie Bryant, Sally Butterfield, Elizabeth M. Byrne, Gemma Crickmore, Edwin S. Dalmaijer, Fánchea Daly, Tina Emery, Laura Forde, Grace Franckel, Delia Fuhrmann, Andrew Gadie, Sara Gharooni, Jacalyn Guy, Erin Hawkins, Agnieszka Jaroslawska, Sara Joeghan, Amy R. Johnson, Jonathan Spencer Jones, Silvana Mareva, Elise Ng‐Cordell, Sinéad O’Brien, Cliodhna O’Leary, Joseph P. Rennie, Ivan L. Simpson-Kent, Roma Šiugždaitė, Tess A. Smith, Stephani Uh, Maria Vedechkina, Francesca Woolgar, Natalia Zdorovtsova, Mengya Zhang, Duncan E. Astle

    Vydáno 2021
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