A citation-based method for searching scientific literature

Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp, Thomas Hansen, Klaus D Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M Matthews, Arnaldur Gylfason, Bjarni V Halldorsson, Daniel Gudbjartsson, Thorgeir E Thorgeirsson, Asgeir Sigurdsson, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Asgeir Bjornsson, Sigurborg Mattiasdottir, Thorarinn Blondal, Magnus Haraldsson, Brynja B Magnusdottir, Ina Giegling, Hans-Jürgen Möller, Annette Hartmann, Kevin V Shianna, Dongliang Ge, Anna C Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lonnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W Mühleisen, August G Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B Freimer, Jeffrey R Gulcher, Unnur Thorsteinsdottir, Augustine Kong, Ole A Andreassen, Roel A Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Petursson, David B Goldstein, Markus M Nöthen, Leena Peltonen, David A Collier, David St Clair, Kari Stefansson. Nature 2008
Times Cited: 1220







List of co-cited articles
931 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis.
Ian T Fiddes, Gerrald A Lodewijk, Meghan Mooring, Colleen M Bosworth, Adam D Ewing, Gary L Mantalas, Adam M Novak, Anouk van den Bout, Alex Bishara, Jimi L Rosenkrantz,[...]. Cell 2018
143
5


Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Michael J Gandal, Jillian R Haney, Neelroop N Parikshak, Virpi Leppa, Gokul Ramaswami, Chris Hartl, Andrew J Schork, Vivek Appadurai, Alfonso Buil, Thomas M Werge,[...]. Science 2018
381
5

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Ana I Silva, Magnus O Ulfarsson, Hreinn Stefansson, Omar Gustafsson, G Bragi Walters, David E J Linden, Lawrence S Wilkinson, Mark Drakesmith, Michael J Owen, Jeremy Hall,[...]. Biol Psychiatry 2019
16
31

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
5

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
952
5

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
474
5

Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Guillaume Huguet, Catherine Schramm, Elise Douard, Lai Jiang, Aurélie Labbe, Frédérique Tihy, Géraldine Mathonnet, Sonia Nizard, Emmanuelle Lemyre, Alexandre Mathieu,[...]. JAMA Psychiatry 2018
33
15

High rate of disease-related copy number variations in childhood onset schizophrenia.
K Ahn, N Gotay, T M Andersen, A A Anvari, P Gochman, Y Lee, S Sanders, S Guha, A Darvasi, J T Glessner,[...]. Mol Psychiatry 2014
78
5

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
375
4

Rate of de novo mutations and the importance of father's age to disease risk.
Augustine Kong, Michael L Frigge, Gisli Masson, Soren Besenbacher, Patrick Sulem, Gisli Magnusson, Sigurjon A Gudjonsson, Asgeir Sigurdsson, Aslaug Jonasdottir, Adalbjorg Jonasdottir,[...]. Nature 2012
4

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Santhosh Girirajan, Megan Y Dennis, Carl Baker, Maika Malig, Bradley P Coe, Catarina D Campbell, Kenneth Mark, Tiffany H Vu, Can Alkan, Ze Cheng,[...]. Am J Hum Genet 2013
178
4

SHANK1 Deletions in Males with Autism Spectrum Disorder.
Daisuke Sato, Anath C Lionel, Claire S Leblond, Aparna Prasad, Dalila Pinto, Susan Walker, Irene O'Connor, Carolyn Russell, Irene E Drmic, Fadi F Hamdan,[...]. Am J Hum Genet 2012
201
4

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
4

High frequency of neurexin 1beta signal peptide structural variants in patients with autism.
Jinong Feng, Richard Schroer, Jin Yan, Wenjia Song, Chunmei Yang, Anke Bockholt, Edwin H Cook, Cindy Skinner, Charles E Schwartz, Steve S Sommer. Neurosci Lett 2006
221
4

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
328
4

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Giulio Genovese, Menachem Fromer, Eli A Stahl, Douglas M Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L Moran, Shaun M Purcell, Pamela Sklar, Patrick F Sullivan,[...]. Nat Neurosci 2016
208
4


Research domain criteria (RDoC): toward a new classification framework for research on mental disorders.
Thomas Insel, Bruce Cuthbert, Marjorie Garvey, Robert Heinssen, Daniel S Pine, Kevin Quinn, Charles Sanislow, Philip Wang. Am J Psychiatry 2010
4

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
4

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
617
4

Gene expression elucidates functional impact of polygenic risk for schizophrenia.
Menachem Fromer, Panos Roussos, Solveig K Sieberts, Jessica S Johnson, David H Kavanagh, Thanneer M Perumal, Douglas M Ruderfer, Edwin C Oh, Aaron Topol, Hardik R Shah,[...]. Nat Neurosci 2016
429
4

Common vs. rare allele hypotheses for complex diseases.
Nicholas J Schork, Sarah S Murray, Kelly A Frazer, Eric J Topol. Curr Opin Genet Dev 2009
407
4

CNVs in neuropsychiatric disorders.
George Kirov. Hum Mol Genet 2015
74
5

Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register.
Rikke Hilker, Dorte Helenius, Birgitte Fagerlund, Axel Skytthe, Kaare Christensen, Thomas M Werge, Merete Nordentoft, Birte Glenthøj. Biol Psychiatry 2018
123
4

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
40
10

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.
Leanne M Dibbens, Saul Mullen, Ingo Helbig, Heather C Mefford, Marta A Bayly, Susannah Bellows, Costin Leu, Holger Trucks, Tanja Obermeier, Michael Wittig,[...]. Hum Mol Genet 2009
164
4

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.
Jacobine E Buizer-Voskamp, Jan-Willem Muntjewerff, Eric Strengman, Chiara Sabatti, Hreinn Stefansson, Jacob A S Vorstman, Roel A Ophoff. Biol Psychiatry 2011
52
7

A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations.
Kim Fejgin, Jacob Nielsen, Michelle R Birknow, Jesper F Bastlund, Vibeke Nielsen, Jes B Lauridsen, Hreinn Stefansson, Stacy Steinberg, Helge B D Sorensen, Troels E Mortensen,[...]. Biol Psychiatry 2014
65
6

A genome-wide investigation of SNPs and CNVs in schizophrenia.
Anna C Need, Dongliang Ge, Michael E Weale, Jessica Maia, Sheng Feng, Erin L Heinzen, Kevin V Shianna, Woohyun Yoon, Dalia Kasperaviciūte, Massimo Gennarelli,[...]. PLoS Genet 2009
352
4


TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, H Xie,[...]. N Engl J Med 2015
143
4

New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.
Sabiha Abekhoukh, H Bahar Sahin, Mauro Grossi, Samantha Zongaro, Thomas Maurin, Irene Madrigal, Daniele Kazue-Sugioka, Annick Raas-Rothschild, Mohamed Doulazmi, Pilar Carrera,[...]. Dis Model Mech 2017
32
12

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.
Merlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, Travis Thompson. Pediatrics 2004
169
4

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
4

Copy number variation in schizophrenia in the Japanese population.
Masashi Ikeda, Branko Aleksic, George Kirov, Yoko Kinoshita, Yoshio Yamanouchi, Tsuyoshi Kitajima, Kunihiro Kawashima, Tomo Okochi, Taro Kishi, Irina Zaharieva,[...]. Biol Psychiatry 2010
89
4

Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice.
Ozlem Bozdagi, Takeshi Sakurai, Nathan Dorr, Marion Pilorge, Nagahide Takahashi, Joseph D Buxbaum. PLoS One 2012
69
5

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
506
4

Phenotypic impact of genomic structural variation: insights from and for human disease.
Joachim Weischenfeldt, Orsolya Symmons, François Spitz, Jan O Korbel. Nat Rev Genet 2013
241
4

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
4

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature.
Chelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, Rebecca Melvin, Candice K Silversides, Danielle M Andrade, Joyce So, Hanna Faghfoury, Anath C Lionel, Christian R Marshall,[...]. Genet Med 2015
72
5

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
802
4

Rare copy number variation in treatment-resistant major depressive disorder.
Colm O'Dushlaine, Stephan Ripke, Douglas M Ruderfer, Steven P Hamilton, Maurizio Fava, Dan V Iosifescu, Isaac S Kohane, Susanne E Churchill, Victor M Castro, Caitlin C Clements,[...]. Biol Psychiatry 2014
39
10

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Karen Crawford, Matthew Bracher-Smith, David Owen, Kimberley M Kendall, Elliott Rees, Antonio F Pardiñas, Mark Einon, Valentina Escott-Price, James T R Walters, Michael C O'Donovan,[...]. J Med Genet 2019
37
10

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
Nigel M Williams, Barbara Franke, Eric Mick, Richard J L Anney, Christine M Freitag, Michael Gill, Anita Thapar, Michael C O'Donovan, Michael J Owen, Peter Holmans,[...]. Am J Psychiatry 2012
172
4

Common variants on chromosome 6p22.1 are associated with schizophrenia.
Jianxin Shi, Douglas F Levinson, Jubao Duan, Alan R Sanders, Yonglan Zheng, Itsik Pe'er, Frank Dudbridge, Peter A Holmans, Alice S Whittemore, Bryan J Mowry,[...]. Nature 2009
798
4

Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Annika Forsingdal, Trine Nygaard Jørgensen, Line Olsen, Thomas Werge, Michael Didriksen, Jacob Nielsen. Biol Psychiatry 2019
13
30

Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation.
Ikuo K Suzuki, David Gacquer, Roxane Van Heurck, Devesh Kumar, Marta Wojno, Angéline Bilheu, Adèle Herpoel, Nelle Lambert, Julian Cheron, Franck Polleux,[...]. Cell 2018
110
4

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.
Zhiqiang Li, Jianhua Chen, Yifeng Xu, Qizhong Yi, Weidong Ji, Peng Wang, Jiawei Shen, Zhijian Song, Meng Wang, Ping Yang,[...]. Biol Psychiatry 2016
34
11

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.
Derek W Morris, Richard D Pearson, Paul Cormican, Elaine M Kenny, Colm T O'Dushlaine, Louis-Philippe Lemieux Perreault, Eleni Giannoulatou, Daniela Tropea, Brion S Maher, Brandon Wormley,[...]. Hum Mol Genet 2014
24
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.