A citation-based method for searching scientific literature

Joanna Martin, Kristiina Tammimies, Robert Karlsson, Yi Lu, Henrik Larsson, Paul Lichtenstein, Patrik K E Magnusson. Am J Med Genet B Neuropsychiatr Genet 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Assessing the evidence for shared genetic risks across psychiatric disorders and traits.
Joanna Martin, Mark J Taylor, Paul Lichtenstein. Psychol Med 2018
47
36

Association of copy number variation across the genome with neuropsychiatric traits in the general population.
Anna L Guyatt, Evie Stergiakouli, Joanna Martin, James Walters, Michael O'Donovan, Michael Owen, Anita Thapar, George Kirov, Santiago Rodriguez, Dheeraj Rai,[...]. Am J Med Genet B Neuropsychiatr Genet 2018
14
36

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
174
36

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.
Paul Lichtenstein, Eva Carlström, Maria Råstam, Christopher Gillberg, Henrik Anckarsäter. Am J Psychiatry 2010
388
27

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder.
Joanna Martin, Raymond K Walters, Ditte Demontis, Manuel Mattheisen, S Hong Lee, Elise Robinson, Isabell Brikell, Laura Ghirardi, Henrik Larsson, Paul Lichtenstein,[...]. Biol Psychiatry 2018
74
27

Sex-specific manifestation of genetic risk for attention deficit hyperactivity disorder in the general population.
Joanna Martin, Mark J Taylor, Mina Rydell, Lucy Riglin, Olga Eyre, Yi Lu, Sebastian Lundström, Henrik Larsson, Anita Thapar, Paul Lichtenstein. J Child Psychol Psychiatry 2018
16
27

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
204
27

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
516
27

Anxiety disorders.
Michelle G Craske, Murray B Stein, Thalia C Eley, Mohammed R Milad, Andrew Holmes, Ronald M Rapee, Hans-Ulrich Wittchen. Nat Rev Dis Primers 2017
143
27

Attention-deficit/hyperactivity disorder.
Stephen V Faraone, Philip Asherson, Tobias Banaschewski, Joseph Biederman, Jan K Buitelaar, Josep Antoni Ramos-Quiroga, Luis Augusto Rohde, Edmund J S Sonuga-Barke, Rosemary Tannock, Barbara Franke. Nat Rev Dis Primers 2015
456
27

Is There a Female Protective Effect Against Attention-Deficit/Hyperactivity Disorder? Evidence From Two Representative Twin Samples.
Mark J Taylor, Paul Lichtenstein, Henrik Larsson, Henrik Anckarsäter, Corina U Greven, Angelica Ronald. J Am Acad Child Adolesc Psychiatry 2016
34
27

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
847
27

Genetics of attention deficit hyperactivity disorder.
Stephen V Faraone, Henrik Larsson. Mol Psychiatry 2019
180
27

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
514
27

Family study of girls with attention deficit hyperactivity disorder.
S V Faraone, J Biederman, E Mick, S Williamson, T Wilens, T Spencer, W Weber, J Jetton, I Kraus, J Pert,[...]. Am J Psychiatry 2000
96
18


Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
71
18

Neurodevelopmental disorders.
Anita Thapar, Miriam Cooper, Michael Rutter. Lancet Psychiatry 2017
143
18

High loading of polygenic risk for ADHD in children with comorbid aggression.
Marian L Hamshere, Kate Langley, Joanna Martin, Sharifah Shameem Agha, Evangelia Stergiakouli, Richard J L Anney, Jan Buitelaar, Stephen V Faraone, Klaus-Peter Lesch, Benjamin M Neale,[...]. Am J Psychiatry 2013
85
18

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
18

Childhood attention-deficit hyperactivity disorder as an extreme of a continuous trait: a quantitative genetic study of 8,500 twin pairs.
Henrik Larsson, Henrik Anckarsater, Maria Råstam, Zheng Chang, Paul Lichtenstein. J Child Psychol Psychiatry 2012
122
18

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
74
18

Familial aggregation of attention-deficit/hyperactivity disorder.
Qi Chen, Isabell Brikell, Paul Lichtenstein, Eva Serlachius, Ralf Kuja-Halkola, Sven Sandin, Henrik Larsson. J Child Psychol Psychiatry 2017
33
18

Genetic risk for attention-deficit/hyperactivity disorder contributes to neurodevelopmental traits in the general population.
Joanna Martin, Marian L Hamshere, Evangelia Stergiakouli, Michael C O'Donovan, Anita Thapar. Biol Psychiatry 2014
91
18

Cross-national epidemiology of major depression and bipolar disorder.
M M Weissman, R C Bland, G J Canino, C Faravelli, S Greenwald, H G Hwu, P R Joyce, E G Karam, C K Lee, J Lellouch,[...]. JAMA 1996
18

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
18

The genetics of Tourette syndrome: a review.
Julia A O'Rourke, Jeremiah M Scharf, Dongmei Yu, David L Pauls. J Psychosom Res 2009
102
18

Copy number variations and cognitive phenotypes in unselected populations.
Katrin Männik, Reedik Mägi, Aurélien Macé, Ben Cole, Anna L Guyatt, Hashem A Shihab, Anne M Maillard, Helene Alavere, Anneli Kolk, Anu Reigo,[...]. JAMA 2015
86
18

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
323
18

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
18

The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology.
Isabell Brikell, Henrik Larsson, Yi Lu, Erik Pettersson, Qi Chen, Ralf Kuja-Halkola, Robert Karlsson, Benjamin B Lahey, Paul Lichtenstein, Joanna Martin. Mol Psychiatry 2020
47
18


Copy number variants and therapeutic response to antidepressant medication in major depressive disorder.
K E Tansey, J J H Rucker, D H Kavanagh, M Guipponi, N Perroud, G Bondolfi, E Domenici, D M Evans, J Hauser, N Henigsberg,[...]. Pharmacogenomics J 2014
13
18

Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.
David M Howard, Mark J Adams, Masoud Shirali, Toni-Kim Clarke, Riccardo E Marioni, Gail Davies, Jonathan R I Coleman, Clara Alloza, Xueyi Shen, Miruna C Barbu,[...]. Nat Commun 2018
144
18

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle A Baribeau, Anne S Bassett. Curr Psychiatry Rep 2017
18
18

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Anath C Lionel, Jennifer Crosbie, Nicole Barbosa, Tara Goodale, Bhooma Thiruvahindrapuram, Jessica Rickaby, Matthew Gazzellone, Andrew R Carson, Jennifer L Howe, Zhuozhi Wang,[...]. Sci Transl Med 2011
221
18

Characterizing Developmental Trajectories and the Role of Neuropsychiatric Genetic Risk Variants in Early-Onset Depression.
Frances Rice, Lucy Riglin, Ajay K Thapar, Jon Heron, Richard Anney, Michael C O'Donovan, Anita Thapar. JAMA Psychiatry 2019
41
18


Genetic epidemiology of major depression: review and meta-analysis.
P F Sullivan, M C Neale, K S Kendler. Am J Psychiatry 2000
18

Association of Rare Copy Number Variants With Risk of Depression.
Kimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, Sophie Legge, Lucy Riglin, Stanley Zammit, Michael Conlon O'Donovan, Michael John Owen, Ian Jones, George Kirov,[...]. JAMA Psychiatry 2019
24
18


Association of Polygenic Risk for Attention-Deficit/Hyperactivity Disorder With Co-occurring Traits and Disorders.
Ebba Du Rietz, Jonathan Coleman, Kylie Glanville, Shing Wan Choi, Paul F O'Reilly, Jonna Kuntsi. Biol Psychiatry Cogn Neurosci Neuroimaging 2018
40
18

Meta-analysis of the heritability of human traits based on fifty years of twin studies.
Tinca J C Polderman, Beben Benyamin, Christiaan A de Leeuw, Patrick F Sullivan, Arjen van Bochoven, Peter M Visscher, Danielle Posthuma. Nat Genet 2015
648
18

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
18

Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Vassily Trubetskoy, Manuel Mattheisen, Yunpeng Wang, Jonathan R I Coleman, Héléna A Gaspar,[...]. Nat Genet 2019
408
18

Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan.
Barbara Franke, Giorgia Michelini, Philip Asherson, Tobias Banaschewski, Andrea Bilbow, Jan K Buitelaar, Bru Cormand, Stephen V Faraone, Ylva Ginsberg, Jan Haavik,[...]. Eur Neuropsychopharmacol 2018
131
18

ADHD and depression: investigating a causal explanation.
Lucy Riglin, Beate Leppert, Christina Dardani, Ajay K Thapar, Frances Rice, Michael C O'Donovan, George Davey Smith, Evie Stergiakouli, Kate Tilling, Anita Thapar. Psychol Med 2021
8
25

Investigating the genetic underpinnings of early-life irritability.
L Riglin, O Eyre, M Cooper, S Collishaw, J Martin, K Langley, E Leibenluft, A Stringaris, A K Thapar, B Maughan,[...]. Transl Psychiatry 2017
24
18


Evaluating chronic emotional dysregulation and irritability in relation to ADHD and depression genetic risk in children with ADHD.
Joel T Nigg, Sarah L Karalunas, Hanna C Gustafsson, Priya Bhatt, Peter Ryabinin, Michael A Mooney, Stephen V Faraone, Damien A Fair, Beth Wilmot. J Child Psychol Psychiatry 2020
16
18


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.