Результаты поиска - Ditte Demontis

Отмена результатов
  1. 1
    GENOME-WIDE ANALYSES OF ADHD IDENTIFY 27 RISK LOCI, REFINE THE GENETIC ARCHITECTURE AND IMPLICATE SEVERAL COGNITIVE DOMAINS

    GENOME-WIDE ANALYSES OF ADHD IDENTIFY 27 RISK LOCI, REFINE THE GENETIC ARCHITECTURE AND IMPLICATE SEVERAL COGNITIVE DOMAINS по Ditte Demontis

    Опубликовано 2022
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    Artigo
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  2. 2
    Genetic risk factors for cancer-related cognitive impairment: a systematic review

    Genetic risk factors for cancer-related cognitive impairment: a systematic review по Cecilie D. R. Buskbjerg, Ali Amidi, Ditte Demontis, Eva Rames Nissen, Robert Zachariae

    Опубликовано 2019
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  3. 3
    Attention-Deficit/Hyperactivity Disorder and Major Depressive Disorder: Evidence From Multiple Genetically Informed Designs

    Attention-Deficit/Hyperactivity Disorder and Major Depressive Disorder: Evidence From Multiple Genetically Informed Designs по Miguel Garcia‐Argibay, Isabell Brikell, Anita Thapar, Paul Lichtenstein, Sebastian Lundström, Ditte Demontis, Henrik Larsson

    Опубликовано 2023
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    Artigo
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  4. 4
    Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF

    Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF по Henriette N. Buttenschøn, Ditte Demontis, Mathias Kaas, Betina Elfving, Simon Mølgaard, Camilla Gustafsen, Linda Kærlev, C. M. Petersen, Anders D. Børglum, Ole Mors, Simon Glerup

    Опубликовано 2015
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    Artigo
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  5. 5
    Changes in cognitive functions and cerebral grey matter and their associations with inflammatory markers, endocrine markers, and APOE genotypes in testicular cancer patients undergoing treatment

    Changes in cognitive functions and cerebral grey matter and their associations with inflammatory markers, endocrine markers, and APOE genotypes in testicular cancer patients underg... по Ali Amidi, Mads Agerbæk, Lisa M. Wu, Anders Degn Pedersen, Mimi Yung Mehlsen, Cecilie R. Clausen, Ditte Demontis, Anders D. Børglum, Anja Harbøll, Robert Zachariae

    Опубликовано 2016
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    Artigo
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  6. 6
    Investigating causality between liability to ADHD and substance use, and liability to substance use and ADHD risk, using Mendelian randomization

    Investigating causality between liability to ADHD and substance use, and liability to substance use and ADHD risk, using Mendelian randomization по Jorien L. Treur, Ditte Demontis, George Davey Smith, Hannah Sallis, Tom G. Richardson, Reínout W. Wiers, Anders D. Børglum, Karin J. H. Verweij, Marcus R. Munafò

    Опубликовано 2019
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    Artigo
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  7. 7
    Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes

    Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes по Marta Ribasés, Marina Mitjans, C.A. Hartman, María Soler Artigas, Ditte Demontis, Henrik Larsson, Josep Antoni Ramos‐Quiroga, Jonna Kuntsi, Stephen V. Faraone, Børglum Ad, Andreas Reif, Barbara Franke, Bru Cormand

    Опубликовано 2023
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  8. 8
    CACNA1C (rs1006737) is associated with schizophrenia

    CACNA1C (rs1006737) is associated with schizophrenia по Mette Nyegaard, Ditte Demontis, Leslie Foldager, Anne Hedemand, Tracey Flint, Karina M. Sørensen, Paal Skytt Andersen, Merete Nordentoft, Thomas Werge, Carsten Bøcker Pedersen, David M. Hougaard, Preben Bo Mortensen, Ole Mors, Anders D. Børglum

    Опубликовано 2010
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    Carta
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  9. 9
    CACNA1C hypermethylation is associated with bipolar disorder

    CACNA1C hypermethylation is associated with bipolar disorder по Anna Starnawska, Ditte Demontis, Anja E. Pen, Anne Hedemand, Anders Lade Nielsen, Nicklas Heine Staunstrup, Jakob Grove, Thomas D. Als, A Jarram, Niamh L. O’Brien, Ole Mors, Andrew McQuillin, Anders D. Børglum, Mette Nyegaard

    Опубликовано 2016
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    Artigo
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  10. 10
    Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality

    Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality по María Soler Artigas, Cristina Sánchez‐Mora, Paula Rovira, Vanesa Richarte, Iris Garcia‐Martínez, Mireia Pagerols, Ditte Demontis, Sven Stringer, Jacqueline M. Vink, Anders D. Børglum, Benjamin M. Neale, Barbara Franke, Stephen V. Faraone, Miguel Casas, Josep Antoni Ramos‐Quiroga, Marta Ribasés

    Опубликовано 2019
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    Artigo
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  11. 11
    Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers

    Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers по Beatríz Marcheco Teruel, Esteban J. Parra, Evelyn Fuentes-Smith, Antonio Salas, Henriette N. Buttenschøn, Ditte Demontis, María Torres, Lilia C. Marín-Padrón, Enrique Javier Gómez-Cabezas, Vanesa Álvarez-Iglesias, Ana Mosquera‐Miguel, Antonio J. Martínez‐Fuentes, Ángel Carracedo, Anders D. Børglum, Ole Mors

    Опубликовано 2014
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    Artigo
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  12. 12
    Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

    Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source по Mads V. Hollegaard, Jakob Grove, Jonas Bybjerg‐Grauholm, Eskil Kreiner‐Møller, Klaus Bønnelykke, Mette Nørgaard, Thomas Benfield, Bent Nørgaard‐Pedersen, Preben Bo Mortensen, Ole Mors, Henrik Toft Sørensen, Zitta Barrella Harboe, Anders D. Børglum, Ditte Demontis, Torben F. Ørntoft, Hans Bisgaard, David M. Hougaard

    Опубликовано 2011
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    Artigo
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  13. 13
    Genetic liability to ADHD and substance use disorders in individuals with ADHD

    Genetic liability to ADHD and substance use disorders in individuals with ADHD по Theresa Wimberley, Esben Agerbo, Henriette Thisted Horsdal, Cæcilie Ottosen, Isabell Brikell, Thomas D. Als, Ditte Demontis, Anders D. Børglum, Merete Nordentoft, Ole Mors, Thomas Werge, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Preben Bo Mortensen, Anita Thapar, Lucy Riglin, K. Langley, Søren Dalsgaard

    Опубликовано 2019
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    Artigo
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  14. 14
    Genetic Markers of ADHD-Related Variations in Intracranial Volume

    Genetic Markers of ADHD-Related Variations in Intracranial Volume по Marieke Klein, Raymond K. Walters, Ditte Demontis, Jason L. Stein, Derrek P. Hibar, Hieab H.H. Adams, Janita Bralten, Nina Roth Mota, Russell Schachar, Edmund Sonuga‐Barke, Manuel Mattheisen, Benjamin M. Neale, Paul M. Thompson, Sarah E. Medland, Anders D. Børglum, Stephen V. Faraone, Alejandro Arias Vásquez, Barbara Franke

    Опубликовано 2019
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  15. 15
    Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

    Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci по Anders D. Børglum, Ditte Demontis, Jakob Grove, Jonatan Pallesen, Mads V. Hollegaard, Carsten Bøcker Pedersen, Anne Hedemand, Manuel Mattheisen, André G. Uitterlinden, Mette Nyegaard, Torben Ørntoft, Carsten Wiuf, Michael Didriksen, Merete Nordentoft, Markus M. Nöthen, Marcella Rietschel, Roel A. Ophoff, Sven Cichon, Robert H. Yolken, David M. Hougaard, Preben Bo Mortensen, Ole Mors

    Опубликовано 2013
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    Artigo
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  16. 16
    Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

    Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk... по Joseph D. Deak, Hang Zhou, Marco Galimberti, Daniel F. Levey, Frank R. Wendt, Sandra Sanchez‐Roige, Alexander S. Hatoum, Emma C. Johnson, Yaira Z. Nuñez, Ditte Demontis, Anders D. Børglum, Veera M. Rajagopal, Mariela Jennings, Rachel L. Kember, Amy C. Justice, Howard J. Edenberg, Arpana Agrawal, Renato Polimanti, Henry R. Kranzler, Joel Gelernter

    Опубликовано 2022
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  17. 17
    Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

    Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls по Erik Pettersson, Paul Lichtenstein, Henrik Larsson, Jie Song, Arpana Agrawal, Anders D. Børglum, Cynthia M. Bulik, Mark J. Daly, Lea K. Davis, Ditte Demontis, Howard J. Edenberg, Jakob Grove, Joel Gelernter, Benjamin M. Neale, Antonio F. Pardiñas, Eli A. Stahl, James Walters, Raymond K. Walters, Patrick F. Sullivan, Daniëlle Posthuma, Tinca J. C. Polderman

    Опубликовано 2018
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    Artigo
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  18. 18
    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants по F. Kyle Satterstrom, Raymond K. Walters, Tarjinder Singh, Emilie M. Wigdor, Francesco Lescai, Ditte Demontis, Jack A. Kosmicki, Jakob Grove, Christine Stevens, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Duncan S. Palmer, Julian Maller, Merete Nordentoft, Ole Mors, Elise Robinson, David M. Hougaard, Thomas Werge, Preben Bo Mortensen, Benjamin M. Neale, Anders D. Børglum, Mark J. Daly

    Опубликовано 2019
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    Artigo
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  19. 19
    High loading of polygenic risk in cases with chronic schizophrenia

    High loading of polygenic risk in cases with chronic schizophrenia по Sandra Meier, Esben Agerbo, Robert Maier, Carsten Bøcker Pedersen, Maren Lang, Jakob Grove, Mads V. Hollegaard, Ditte Demontis, Betina B. Trabjerg, Carsten Hjorthøj, Stephan Ripke, Franziska Degenhardt, Markus M. Nöthen, Dan Rujescu, Wolfgang Maier, Thomas Werge, Ole Mors, David M. Hougaard, Anders D. Børglum, Naomi R. Wray, Marcella Rietschel, Merete Nordentoft, Preben Bo Mortensen, Manuel Mattheisen

    Опубликовано 2015
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    Artigo
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  20. 20
    Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder

    Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder по Veera M. Rajagopal, Jinjie Duan, Laura Vilar‐Ribó, Jakob Grove, Tetyana Zayats, Josep Antoni Ramos‐Quiroga, F. Kyle Satterstrom, María Soler Artigas, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Thomas D. Als, Anders Rosengren, Mark J. Daly, Benjamin M. Neale, Merete Nordentoft, Thomas Werge, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Marta Ribasés, Anders D. Børglum, Ditte Demontis

    Опубликовано 2022
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    Artigo
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