A citation-based method for searching scientific literature

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, Lindsey Kent, Frank Middleton, Yanli Zhang-James, Lu Liu, Jobst Meyer, Thuy Trang Nguyen, Jasmin Romanos, Marcel Romanos, Christiane Seitz, Tobias J Renner, Susanne Walitza, Andreas Warnke, Haukur Palmason, Jan Buitelaar, Nanda Rommelse, Alejandro Arias Vasquez, Ziarih Hawi, Kate Langley, Joseph Sergeant, Hans-Christoph Steinhausen, Herbert Roeyers, Joseph Biederman, Irina Zaharieva, Hakon Hakonarson, Josephine Elia, Anath C Lionel, Jennifer Crosbie, Christian R Marshall, Russell Schachar, Stephen W Scherer, Alexandre Todorov, Susan L Smalley, Sandra Loo, Stanley Nelson, Corina Shtir, Philip Asherson, Andreas Reif, Klaus-Peter Lesch, Stephen V Faraone. Am J Psychiatry 2012
Times Cited: 174







List of co-cited articles
1062 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
Nigel M Williams, Irina Zaharieva, Andrew Martin, Kate Langley, Kiran Mantripragada, Ragnheidur Fossdal, Hreinn Stefansson, Kari Stefansson, Pall Magnusson, Olafur O Gudmundsson,[...]. Lancet 2010
328
38

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
S Hong Lee, Stephan Ripke, Benjamin M Neale, Stephen V Faraone, Shaun M Purcell, Roy H Perlis, Bryan J Mowry, Anita Thapar, Michael E Goddard, John S Witte,[...]. Nat Genet 2013
30

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
26


Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.
Evangelia Stergiakouli, Marian Hamshere, Peter Holmans, Kate Langley, Irina Zaharieva, Ziarah Hawi, Lindsey Kent, Michael Gill, Nigel Williams, Michael J Owen,[...]. Am J Psychiatry 2012
128
23

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.
Li Yang, Benjamin M Neale, Lu Liu, S Hong Lee, Naomi R Wray, Ning Ji, Haimei Li, Qiujin Qian, Dongliang Wang, Jun Li,[...]. Am J Med Genet B Neuropsychiatr Genet 2013
112
23

Molecular genetics of attention-deficit/hyperactivity disorder.
Stephen V Faraone, Roy H Perlis, Alysa E Doyle, Jordan W Smoller, Jennifer J Goralnick, Meredith A Holmgren, Pamela Sklar. Biol Psychiatry 2005
22

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.
Josephine Elia, Joseph T Glessner, Kai Wang, Nagahide Takahashi, Corina J Shtir, Dexter Hadley, Patrick M A Sleiman, Haitao Zhang, Cecilia E Kim, Reid Robison,[...]. Nat Genet 2011
213
21


Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.
Benjamin M Neale, Sarah E Medland, Stephan Ripke, Philip Asherson, Barbara Franke, Klaus-Peter Lesch, Stephen V Faraone, Thuy Trang Nguyen, Helmut Schäfer, Peter Holmans,[...]. J Am Acad Child Adolesc Psychiatry 2010
298
18

Candidate gene studies of ADHD: a meta-analytic review.
Ian R Gizer, Courtney Ficks, Irwin D Waldman. Hum Genet 2009
618
18

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
18

The worldwide prevalence of ADHD: a systematic review and metaregression analysis.
Guilherme Polanczyk, Maurício Silva de Lima, Bernardo Lessa Horta, Joseph Biederman, Luis Augusto Rohde. Am J Psychiatry 2007
17


Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants.
Joanna Martin, Miriam Cooper, Marian L Hamshere, Andrew Pocklington, Stephen W Scherer, Lindsey Kent, Michael Gill, Michael J Owen, Nigel Williams, Michael C O'Donovan,[...]. J Am Acad Child Adolesc Psychiatry 2014
55
29

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
K-P Lesch, S Selch, T J Renner, C Jacob, T T Nguyen, T Hahn, M Romanos, S Walitza, S Shoichet, A Dempfle,[...]. Mol Psychiatry 2011
104
16

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Jessica Lasky-Su, Benjamin M Neale, Barbara Franke, Richard J L Anney, Kaixin Zhou, Julian B Maller, Alejandro Arias Vasquez, Wai Chen, Philip Asherson, Jan Buitelaar,[...]. Am J Med Genet B Neuropsychiatr Genet 2008
272
15

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
J Elia, X Gai, H M Xie, J C Perin, E Geiger, J T Glessner, M D'arcy, R deBerardinis, E Frackelton, C Kim,[...]. Mol Psychiatry 2010
352
15


Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
I Jarick, A-L Volckmar, C Pütter, S Pechlivanis, T T Nguyen, M R Dauvermann, S Beck, Ö Albayrak, S Scherag, S Gilsbach,[...]. Mol Psychiatry 2014
50
28

Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample.
Angelica Ronald, Emily Simonoff, Jonna Kuntsi, Philip Asherson, Robert Plomin. J Child Psychol Psychiatry 2008
255
13

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
14

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
15

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
B W M van Bon, H C Mefford, B Menten, D A Koolen, A J Sharp, W M Nillesen, J W Innis, T J L de Ravel, C L Mercer, M Fichera,[...]. J Med Genet 2009
199
13

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
D T Miller, Y Shen, L A Weiss, J Korn, I Anselm, C Bridgemohan, G F Cox, H Dickinson, J Gentile, D J Harris,[...]. J Med Genet 2009
241
13

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?
Przemyslaw Szafranski, Christian P Schaaf, Richard E Person, Ian B Gibson, Zhilian Xia, Sangeetha Mahadevan, Joanna Wiszniewska, Carlos A Bacino, Seema Lalani, Lorraine Potocki,[...]. Hum Mutat 2010
96
13

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
13

Genome-wide association studies in ADHD.
Barbara Franke, Benjamin M Neale, Stephen V Faraone. Hum Genet 2009
281
12

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
12

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak,[...]. Nat Genet 2009
394
12


Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
12

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
Klaus-Peter Lesch, Nina Timmesfeld, Tobias J Renner, Rebecca Halperin, Christoph Röser, T Trang Nguyen, David W Craig, Jasmin Romanos, Monika Heine, Jobst Meyer,[...]. J Neural Transm (Vienna) 2008
262
12

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
75
16

The human clinical phenotypes of altered CHRNA7 copy number.
Madelyn A Gillentine, Christian P Schaaf. Biochem Pharmacol 2015
55
21

The molecular genetic architecture of attention deficit hyperactivity disorder.
Z Hawi, T D R Cummins, J Tong, B Johnson, R Lau, W Samarrai, M A Bellgrove. Mol Psychiatry 2015
122
12

Genome-wide association scan of attention deficit hyperactivity disorder.
Benjamin M Neale, Jessica Lasky-Su, Richard Anney, Barbara Franke, Kaixin Zhou, Julian B Maller, Alejandro Arias Vasquez, Philip Asherson, Wai Chen, Tobias Banaschewski,[...]. Am J Med Genet B Neuropsychiatr Genet 2008
189
11


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
11

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes.
Marwan Shinawi, Christian P Schaaf, Samarth S Bhatt, Zhilian Xia, Ankita Patel, Sau Wai Cheung, Brendan Lanpher, Sandra Nagl, Heinrich Stephan Herding, Claudia Nevinny-Stickel,[...]. Nat Genet 2009
138
11

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Andrew J Sharp, Heather C Mefford, Kelly Li, Carl Baker, Cindy Skinner, Roger E Stevenson, Richard J Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone,[...]. Nat Genet 2008
403
11

Molecular genetics of attention deficit hyperactivity disorder.
Stephen V Faraone, Eric Mick. Psychiatr Clin North Am 2010
233
11

The genetics of attention deficit/hyperactivity disorder in adults, a review.
B Franke, S V Faraone, P Asherson, J Buitelaar, C H D Bau, J A Ramos-Quiroga, E Mick, E H Grevet, S Johansson, J Haavik,[...]. Mol Psychiatry 2012
211
11

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.
Eric Mick, Alexandre Todorov, Susan Smalley, Xiaolan Hu, Sandra Loo, Richard D Todd, Joseph Biederman, Deirdre Byrne, Bryan Dechairo, Allan Guiney,[...]. J Am Acad Child Adolesc Psychiatry 2010
99
11

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
11

The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function.
Melissa L Sinkus, Sharon Graw, Robert Freedman, Randal G Ross, Henry A Lester, Sherry Leonard. Neuropharmacology 2015
90
12

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder.
Kaixin Zhou, Astrid Dempfle, Mauricio Arcos-Burgos, Steven C Bakker, Tobias Banaschewski, Joseph Biederman, Jan Buitelaar, F Xavier Castellanos, Alysa Doyle, Richard P Ebstein,[...]. Am J Med Genet B Neuropsychiatr Genet 2008
120
10

Genetic architectures of psychiatric disorders: the emerging picture and its implications.
Patrick F Sullivan, Mark J Daly, Michael O'Donovan. Nat Rev Genet 2012
709
10

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
10

Case-control genome-wide association study of attention-deficit/hyperactivity disorder.
Benjamin M Neale, Sarah Medland, Stephan Ripke, Richard J L Anney, Philip Asherson, Jan Buitelaar, Barbara Franke, Michael Gill, Lindsey Kent, Peter Holmans,[...]. J Am Acad Child Adolesc Psychiatry 2010
115
10


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.