A citation-based method for searching scientific literature

Amy Lin, Ariana Vajdi, Leila Kushan-Wells, Gerhard Helleman, Laura Pacheco Hansen, Rachel K Jonas, Maria Jalbrzikowski, Lyle Kingsbury, Armin Raznahan, Carrie E Bearden. Biol Psychiatry 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
57

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
57

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, Tracy Heung, Aaron M Holleman, H Richard Johnston, Thomas Monfeuga, Donna M McDonald-McGinn, Raquel E Gur, Bernice E Morrow,[...]. Mol Psychiatry 2020
21
42

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
42

Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
32
42

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Robert W Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne S Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow,[...]. Nat Med 2020
18
42

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
42


The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Loyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, Aurélie Pain, Sandra Martin-Brevet, Carina Ferrari, Philippe Conus, Aurélien Macé, Nouchine Hadjikhani, Andres Metspalu,[...]. Biol Psychiatry 2016
49
28

Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome.
Mariela Mosheva, Virginie Pouillard, Yael Fishman, Lydia Dubourg, Dafna Sofrin-Frumer, Yaffa Serur, Abraham Weizman, Stephan Eliez, Doron Gothelf, Maude Schneider. Eur Child Adolesc Psychiatry 2019
8
28

Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.
Kelly Schoch, Waverly Harrell, Stephen R Hooper, Edward H Ip, Santiago Saldana, Thomas R Kwapil, Vandana Shashi. J Learn Disabil 2014
10
28

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS).
H A Moulding, U Bartsch, J Hall, M W Jones, D E Linden, M J Owen, M B M van den Bree. Psychol Med 2020
8
28

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
E M Moss, M L Batshaw, C B Solot, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai, P P Wang. J Pediatr 1999
217
28

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
736
28

Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis?
Maria Jalbrzikowski, Chelsea Carter, Damla Senturk, Carolyn Chow, Jessica M Hopkins, Michael F Green, Adriana Galván, Tyrone D Cannon, Carrie E Bearden. Schizophr Res 2012
51
28

Social cognition deficit and genetic vulnerability to schizophrenia in 22q11 deletion syndrome.
Marianna Frascarelli, Gaia Padovani, Antonino Buzzanca, Tommaso Accinni, Luca Carlone, Francesco Ghezzi, Guido Maria Lattanzi, Martina Fanella, Carolina Putotto, Carlo Di Bonaventura,[...]. Ann Ist Super Sanita 2020
3
66


Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness.
Christopher R K Ching, Boris A Gutman, Daqiang Sun, Julio Villalon Reina, Anjanibhargavi Ragothaman, Dmitry Isaev, Artemis Zavaliangos-Petropulu, Amy Lin, Rachel K Jonas, Leila Kushan,[...]. Am J Psychiatry 2020
19
28

Psychiatric genetics and the structure of psychopathology.
Jordan W Smoller, Ole A Andreassen, Howard J Edenberg, Stephen V Faraone, Stephen J Glatt, Kenneth S Kendler. Mol Psychiatry 2019
95
28

The genetic architecture of the human cerebral cortex.
Katrina L Grasby, Neda Jahanshad, Jodie N Painter, Lucía Colodro-Conde, Janita Bralten, Derrek P Hibar, Penelope A Lind, Fabrizio Pizzagalli, Christopher R K Ching, Mary Agnes B McMahon,[...]. Science 2020
92
28

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
28

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.
Kimberley M Kendall, Matthew Bracher-Smith, Harry Fitzpatrick, Amy Lynham, Elliott Rees, Valentina Escott-Price, Michael J Owen, Michael C O'Donovan, James T R Walters, George Kirov. Br J Psychiatry 2019
31
28

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
28

A large data resource of genomic copy number variation across neurodevelopmental disorders.
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edwin J Young, Edward J Higginbotham, Jeffrey R MacDonald, Brett Trost, Ada J S Chan, Susan Walker, Sylvia Lamoureux,[...]. NPJ Genom Med 2019
31
28

Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
622
28

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Daqiang Sun, Christopher R K Ching, Amy Lin, Jennifer K Forsyth, Leila Kushan, Ariana Vajdi, Maria Jalbrzikowski, Laura Hansen, Julio E Villalon-Reina, Xiaoping Qu,[...]. Mol Psychiatry 2020
53
28

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
386
28

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
Chelsea Lowther, Marsha Speevak, Christine M Armour, Elaine S Goh, Gail E Graham, Chumei Li, Susan Zeesman, Malgorzata J M Nowaczyk, Lee-Anne Schultz, Antonella Morra,[...]. Genet Med 2017
37
28

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
11
28

A framework for the investigation of rare genetic disorders in neuropsychiatry.
Stephan J Sanders, Mustafa Sahin, Joseph Hostyk, Audrey Thurm, Sebastien Jacquemont, Paul Avillach, Elise Douard, Christa L Martin, Meera E Modi, Andres Moreno-De-Luca,[...]. Nat Med 2019
28
28

Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
Sarah E Bergen, Alexander Ploner, Daniel Howrigan, Michael C O'Donovan, Jordan W Smoller, Patrick F Sullivan, Jonathan Sebat, Benjamin Neale, Kenneth S Kendler. Am J Psychiatry 2019
41
28

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
28

Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.
Adam C Cunningham, Sue Delport, Wendy Cumines, Monica Busse, David E J Linden, Jeremy Hall, Michael J Owen, Marianne B M van den Bree. Br J Psychiatry 2018
12
28

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
28


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
38
28

Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.
Petra Klaassen, Sasja Duijff, Henriëtte Swanenburg de Veye, Frits Beemer, Gerben Sinnema, Elemi Breetvelt, Renske Schappin, Jacob Vorstman. Am J Med Genet B Neuropsychiatr Genet 2016
17
28

Child psychiatry branch of the National Institute of Mental Health longitudinal structural magnetic resonance imaging study of human brain development.
Jay N Giedd, Armin Raznahan, Aaron Alexander-Bloch, Eric Schmitt, Nitin Gogtay, Judith L Rapoport. Neuropsychopharmacology 2015
150
14

A volumetric study of parietal lobe subregions in Turner syndrome.
Wendy E Brown, Shelli R Kesler, Stephan Eliez, Ilana S Warsofsky, Michael Haberecht, Allan L Reiss. Dev Med Child Neurol 2004
41
14

Structural brain imaging correlates of general intelligence in UK Biobank.
S R Cox, S J Ritchie, C Fawns-Ritchie, E M Tucker-Drob, I J Deary. Intelligence 2019
23
14

An Allometric Analysis of Sex and Sex Chromosome Dosage Effects on Subcortical Anatomy in Humans.
Paul Kirkpatrick Reardon, Liv Clasen, Jay N Giedd, Jonathan Blumenthal, Jason P Lerch, M Mallar Chakravarty, Armin Raznahan. J Neurosci 2016
32
14

Brain morphology in Klinefelter syndrome: extra X chromosome and testosterone supplementation.
A J Patwardhan, S Eliez, B Bender, M G Linden, A L Reiss. Neurology 2000
102
14

The Role of Human Parietal Area 7A as a Link between Sequencing in Hand Actions and in Overt Speech Production.
Stefan Heim, Katrin Amunts, Tanja Hensel, Marion Grande, Walter Huber, Ferdinand Binkofski, Simon B Eickhoff. Front Psychol 2012
18
14

Large and fast human pyramidal neurons associate with intelligence.
Natalia A Goriounova, Djai B Heyer, René Wilbers, Matthijs B Verhoog, Michele Giugliano, Christophe Verbist, Joshua Obermayer, Amber Kerkhofs, Harriët Smeding, Maaike Verberne,[...]. Elife 2018
37
14

Multiple bases of human intelligence revealed by cortical thickness and neural activation.
Yu Yong Choi, Noah A Shamosh, Sun Hee Cho, Colin G DeYoung, Min Joo Lee, Jong-Min Lee, Sun I Kim, Zang-Hee Cho, Kyungjin Kim, Jeremy R Gray,[...]. J Neurosci 2008
112
14

Brain morphological abnormalities in 49,XXXXY syndrome: A pediatric magnetic resonance imaging study.
Jonathan D Blumenthal, Eva H Baker, Nancy Raitano Lee, Benjamin Wade, Liv S Clasen, Rhoshel K Lenroot, Jay N Giedd. Neuroimage Clin 2013
14
14

Genetic contributions to human brain morphology and intelligence.
Hilleke E Hulshoff Pol, Hugo G Schnack, Danielle Posthuma, René C W Mandl, Wim F Baaré, Clarine van Oel, Neeltje E van Haren, D Louis Collins, Alan C Evans, Katrin Amunts,[...]. J Neurosci 2006
168
14

The role of area 17 in visual imagery: convergent evidence from PET and rTMS.
S M Kosslyn, A Pascual-Leone, O Felician, S Camposano, J P Keenan, W L Thompson, G Ganis, K E Sukel, N M Alpert. Science 1999
409
14

How does your cortex grow?
Armin Raznahan, Phillip Shaw, Francois Lalonde, Mike Stockman, Gregory L Wallace, Dede Greenstein, Liv Clasen, Nitin Gogtay, Jay N Giedd. J Neurosci 2011
418
14

Automatic "pipeline" analysis of 3-D MRI data for clinical trials: application to multiple sclerosis.
Alex P Zijdenbos, Reza Forghani, Alan C Evans. IEEE Trans Med Imaging 2002
501
14


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.