A citation-based method for searching scientific literature

Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle, Heike Tost, Oliver Grimm, Solveig Kristjansdottir, Heimir Snorrason, Solveig R Davidsdottir, Larus J Gudmundsson, Gudbjorn F Jonsson, Berglind Stefansdottir, Isafold Helgadottir, Magnus Haraldsson, Birna Jonsdottir, Johan H Thygesen, Adam J Schwarz, Michael Didriksen, Tine B Stensbøl, Michael Brammer, Shitij Kapur, Jonas G Halldorsson, Stefan Hreidarsson, Evald Saemundsen, Engilbert Sigurdsson, Kari Stefansson. Nature 2014
Times Cited: 370







List of shared articles



Times cited


Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Elmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, Ari Ahola-Olli, Tuomo Tapio Johannes Kiiskinen, Juulia Partanen, Sanni Ruotsalainen, Mitja Kurki, Lea Martta Urpa, Lei Chen,[...]. Mol Psychiatry 2021
0

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E Villalon-Reina, Ingrid Agartz, Katrin Amunts, Celso Arango, Nicola J Armstrong,[...]. Hum Brain Mapp 2021
0


Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes.
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Víctor Asensio, Bernat Ortega-Vila, Diego Marzese, Carme Vidal, Carmen Santos,[...]. Front Genet 2021
0


CYFIP1 Dosages Exhibit Divergent Behavioral Impact via Diametric Regulation of NMDA Receptor Complex Translation in Mouse Models of Psychiatric Disorders.
Nam-Shik Kim, Francisca Rojas Ringeling, Ying Zhou, Ha Nam Nguyen, Stephanie J Temme, Yu-Ting Lin, Stephen Eacker, Valina L Dawson, Ted M Dawson, Bo Xiao,[...]. Biol Psychiatry 2021
0

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank.
Anthony Warland, Kimberley M Kendall, Elliott Rees, George Kirov, Xavier Caseras. Mol Psychiatry 2020
26

The abiding relevance of mouse models of rare mutations to psychiatric neuroscience and therapeutics.
Joseph A Gogos, Gregg Crabtree, Anastasia Diamantopoulou. Schizophr Res 2020
4

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.
Alice Poisson, Nicolas Chatron, Audrey Labalme, Pierre Fourneret, Dorothée Ville, Marie Laure Mathieu, Damien Sanlaville, Caroline Demily, Gaëtan Lesca. BMC Med Genet 2020
0

Novel Approaches for Identifying the Molecular Background of Schizophrenia.
Arkadiy K Golov, Nikolay V Kondratyev, George P Kostyuk, And Vera E Golimbet. Cells 2020
6


Focus on Causality in ESC/iPSC-Based Modeling of Psychiatric Disorders.
Anke Hoffmann, Michael Ziller, Dietmar Spengler. Cells 2020
7

The Role of Genetic Variation of BMI, Body Composition, and Fat Distribution for Mental Traits and Disorders: A Look-Up and Mendelian Randomization Study.
Triinu Peters, Lena Nüllig, Jochen Antel, Roaa Naaresh, Björn-Hergen Laabs, Lisa Tegeler, Chaima Amhaouach, Lars Libuda, Anke Hinney, Johannes Hebebrand. Front Genet 2020
3

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
10

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U Ludwig, Darina Czamara, Beate St Pourcain, Ferenc Honbolygó,[...]. Mol Psychiatry 2020
10

Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-related cellular phenotypes.
Edit Hathy, Eszter Szabó, Nóra Varga, Zsuzsa Erdei, Csongor Tordai, Boróka Czehlár, Máté Baradits, Bálint Jezsó, Júlia Koller, László Nagy,[...]. Stem Cell Res Ther 2020
0