Molecular Psychiatry, 1359-4184

Tidskrift

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  1. 2020
  2. Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

    Frida Renström, Tibor V. Varga, Paul Franks, D.J. Liu, J.M.M. Howson & Understanding Society Scientific Group Understanding Society Scientific Group, 2020 okt, I : Molecular Psychiatry. 25, 10, s. 2392-2409 18 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Prediction of clinical diagnosis of Alzheimer’s disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years

    H Stocker, L Perna, K Weigl, T Möllers, B Schöttker, Hauke Thomsen, B Holleczek, D Rujescu & H Brenner, 2020 maj 13, I : Molecular Psychiatry.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

    Lisa de las Fuentes, Alaitz Poveda, Paul Franks, Myriam Fornage & et al. et al., 2020 maj 5, I : Molecular Psychiatry.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 2019
  6. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

    Jordi Merino, Hassan S. Dashti, Sherly X. Li, Chloé Sarnowski, Anne E. Justice, Misa Graff, Constantina Papoutsakis, Caren E. Smith, George V. Dedoussis, Rozenn N. Lemaitre, Mary K. Wojczynski, Satu Männistö, Julius S. Ngwa, Minjung Kho, Tarunveer S. Ahluwalia, Natalia Pervjakova, Denise K. Houston, Claude Bouchard, Tao Huang, Marju Orho-Melander & 30 andra, Alexis C. Frazier-Wood, Dennis O. Mook-Kanamori, Louis Pérusse, Craig E. Pennell, Paul S. de Vries, Trudy Voortman, Olivia Li, Stavroula Kanoni, Lynda M. Rose, Terho Lehtimäki, Jing Hua Zhao, Mary F. Feitosa, Jian’an Luan, Nicola M. McKeown, Jennifer A. Smith, Torben Hansen, Niina Eklund, Mike A. Nalls, Tuomo Rankinen, Jinyan Huang, Dena G. Hernandez, Christina Alexandra Schulz, Ani Manichaikul, Ruifang Li-Gao, Marie Claude Vohl, Carol A. Wang, Frank J.A. van Rooij, Jean Shin, Ulrika Ericson & Markus Perola, 2019 dec, I : Molecular Psychiatry. 24, 12, s. 1920-1932 13 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Multi-omic biomarker identification and validation for diagnosing warzone-related post-traumatic stress disorder

    Kelsey R. Dean, Rasha Hammamieh, Synthia H. Mellon, Duna Abu-Amara, Janine D. Flory, Guia Guffanti, Kai Wang, Bernie J. Daigle, Aarti Gautam, Inyoul Lee, Ruoting Yang, Lynn M. Almli, F. Saverio Bersani, Nabarun Chakraborty, Duncan Donohue, Kimberly Kerley, Taek Kyun Kim, Eugene Laska, Min Young Lee, Daniel Lindqvist & 20 andra, Adriana Lori, Liangqun Lu, Burook Misganaw, Seid Muhie, Jennifer Newman, Nathan D. Price, Shizhen Qin, Victor I. Reus, Carole Siegel, Pramod R. Somvanshi, Gunjan S. Thakur, Yong Zhou, The PTSD Systems Biology Consortium The PTSD Systems Biology Consortium, Leroy Hood, Kerry J. Ressler, Owen M. Wolkowitz, Rachel Yehuda, Marti Jett, Francis J. Doyle III & Charles Marmar, 2019 sep 10, I : Molecular Psychiatry.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. 2018
  9. 2017
  10. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

    O Mercati, G Huguet, A Danckaert, G André-Leroux, A Maruani, M Bellinzoni, T Rolland, L Gouder, A Mathieu, J Buratti, F Amsellem, M Benabou, J Van-Gils, A Beggiato, M Konyukh, J-P Bourgeois, M J Gazzellone, R K C Yuen, S Walker, M Delépine & 16 andra, A Boland, B Régnault, M Francois, T Van Den Abbeele, A L Mosca-Boidron, L Faivre, Y Shimoda, K Watanabe, D Bonneau, Maria Råstam, M Leboyer, S W Scherer, C Gillberg, R Delorme, I Cloëz-Tayarani & T Bourgeron, 2017, I : Molecular Psychiatry. 16, 1, s. 230-252 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. 2016
  12. Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism

    Marion Pilorge, Coralie Fassier, Hervé Le Corronc, Anaïs Potey, Jing Bai, S De Gois, Elsa Delaby, Brigitte Assouline, Vincent Guinchat, Francoise Devillard, Richard Delorme, Gudrun Nygren, Maria Råstam, Jochen Meier, Satoru Otani, Hélène Cheval, Victoria James, Maya Topf, Neil Dear, Christopher Gillberg & 7 andra, Marion Leboyer, Bruno Giros, Sophie Gautron, Jamilé Hazan, Robert Harvey, Pascal Legendre & Catalina Betancur, 2016, I : Molecular Psychiatry. 21, s. 936-945

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. 2015
  14. Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma

    J. J. Luykx, S. C. Bakker, W. F. Visser, N. Verhoeven-Duif, J. E. Buizer-Voskamp, J. M. Den Heijer, M. P.M. Boks, J. H. Sul, E. Eskin, A. P. Ori, R. M. Cantor, J. Vorstman, E. Strengman, J. Deyoung, T. H. Kappen, E. Pariama, E. P.A. Van Dongen, P. Borgdorff, P. Bruins, T. J. De Koning & 2 andra, R. S. Kahn & R. A. Ophoff, 2015 dec 1, I : Molecular Psychiatry. 20, 12, s. 1557-1564 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.

    M C Cornelis, E M Byrne, T Esko, M A Nalls, A Ganna, N Paynter, K L Monda, N Amin, K Fischer, Frida Renström, J S Ngwa, V Huikari, A Cavadino, I M Nolte, A Teumer, K Yu, P Marques-Vidal, R Rawal, A Manichaikul, M K Wojczynski & 134 andra, J M Vink, J H Zhao, G Burlutsky, J Lahti, V Mikkilä, R N Lemaitre, J Eriksson, S K Musani, T Tanaka, F Geller, J Luan, J Hui, R Mägi, M Dimitriou, M E Garcia, W-K Ho, M J Wright, L M Rose, P K E Magnusson, N L Pedersen, D Couper, B A Oostra, A Hofman, M A Ikram, H W Tiemeier, A G Uitterlinden, F J A van Rooij, I Barroso, I Johansson, L Xue, M Kaakinen, L Milani, C Power, H Snieder, R P Stolk, S E Baumeister, R Biffar, F Gu, F Bastardot, Z Kutalik, D R Jacobs, N G Forouhi, E Mihailov, L Lind, C Lindgren, K Michaëlsson, A Morris, M Jensen, K-T Khaw, R N Luben, J J Wang, S Männistö, M-M Perälä, M Kähönen, T Lehtimäki, J Viikari, D Mozaffarian, K Mukamal, B M Psaty, A Döring, A C Heath, G W Montgomery, N Dahmen, T Carithers, K L Tucker, L Ferrucci, H A Boyd, M Melbye, J L Treur, D Mellström, J J Hottenga, I Prokopenko, A Tönjes, P Deloukas, S Kanoni, M Lorentzon, D K Houston, Y Liu, J Danesh, A Rasheed, M A Mason, A B Zonderman, L Franke, B S Kristal, J Karjalainen, D R Reed, H-J Westra, M K Evans, D Saleheen, T B Harris, G Dedoussis, G Curhan, M Stumvoll, J Beilby, L R Pasquale, B Feenstra, S Bandinelli, J M Ordovas, A T Chan, U Peters, C Ohlsson, C Gieger, N G Martin, M Waldenberger, D S Siscovick, O Raitakari, J G Eriksson, P Mitchell, D J Hunter, P Kraft, E B Rimm, D I Boomsma, I B Borecki, R J F Loos, N J Wareham, P Vollenweider, N Caporaso, H J Grabe, M L Neuhouser, B H R Wolffenbuttel, F B Hu, E Hyppönen, M-R Järvelin, L A Cupples, Paul Franks, P M Ridker, C M van Duijn, G Heiss, A Metspalu, K E North, E Ingelsson, J A Nettleton, R M van Dam & D I Chasman, 2015, I : Molecular Psychiatry. 20, 5, s. 647-656

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  16. 2014
  17. The KMO allele encoding Arg(452) is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression

    C. Lavebratt, S. Olsson, L. Backlund, L. Frisen, C. Sellgren, L. Priebe, P. Nikamo, Lil Träskman Bendz, S. Cichon, M. P. Vawter, U. Osby, G. Engberg, M. Landen, S. Erhardt & M. Schalling, 2014, I : Molecular Psychiatry. 19, 3, s. 334-341

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  18. 2008
  19. Abnormal melatonin synthesis in autism spectrum disorders

    Jonas Melke, Hany Goubran-Botros, Pauline Chaste, Catalina Betancur, Guddrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, I Carina Gillberg, Richard D3elorme, Nadia Chabane, Marie-Christine Mouren-Simeoni, Fabien Fauchereau, Christelle M Durand, Fabien Chevalier, Xavier Drouot, Corinne Collet, Jean-Marie Launay, Marion Leboyer, Crhstopher Gilblerg & 2 andra, Thomas Bourgeron & The Paris Study and, 2008, I : Molecular Psychiatry. 13, 1, s. 90-98

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. 2005
  21. Support for the association between the rare functional variant 1425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

    Richard Delorme, Catalina Betancur, Michael Wagner, Marie-Odile Krebs, Philip Gorwood, Philip Pearl, Gudrun Nygren, Christelle M Durand, Friederike Buhtz, P Pickering, Jonas Melke, Stephan Ruhrmann, Henrik Anckarsäter, Nadia Chabane, Amélie Kipman, Claudia Reck, Bruno Millet, Isabelle Roy, Marie-Christine Mouren-Simeoni, Wolfgang Maier & 4 andra, Maria Råstam, Christopher Gillberg, Marion Leboyer & Thomas Bourgeron, 2005, I : Molecular Psychiatry. 10, 12, s. 1059-61

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift