A citation-based method for searching scientific literature

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, Laura Pacheco-Hansen, Ariana Vajdi, Jennifer K Forsyth, Maria Jalbrzikowski, Geor Bakker, Therese van Amelsvoort, Kevin M Antshel, Wanda Fremont, Wendy R Kates, Linda E Campbell, Kathryn L McCabe, Michael C Craig, Eileen Daly, Maria Gudbrandsen, Clodagh M Murphy, Declan G Murphy, Kieran C Murphy, Ania Fiksinski, Sanne Koops, Jacob Vorstman, T Blaine Crowley, Beverly S Emanuel, Raquel E Gur, Donna M McDonald-McGinn, David R Roalf, Kosha Ruparel, J Eric Schmitt, Elaine H Zackai, Courtney A Durdle, Naomi J Goodrich-Hunsaker, Tony J Simon, Anne S Bassett, Nancy J Butcher, Eva W C Chow, Fidel Vila-Rodriguez, Adam Cunningham, Joanne Doherty, David E Linden, Hayley Moss, Michael J Owen, Marianne van den Bree, Nicolas A Crossley, Gabriela M Repetto, Paul M Thompson, Carrie E Bearden. Am J Psychiatry 2020
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


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
56
54

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
395
36

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
414
31

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
114
31

Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium.
Theo G M van Erp, Esther Walton, Derrek P Hibar, Lianne Schmaal, Wenhao Jiang, David C Glahn, Godfrey D Pearlson, Nailin Yao, Masaki Fukunaga, Ryota Hashimoto,[...]. Biol Psychiatry 2018
220
31

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
397
27

Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium.
T G M van Erp, D P Hibar, J M Rasmussen, D C Glahn, G D Pearlson, O A Andreassen, I Agartz, L T Westlye, U K Haukvik, A M Dale,[...]. Mol Psychiatry 2016
407
27

Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group.
Daan van Rooij, Evdokia Anagnostou, Celso Arango, Guillaume Auzias, Marlene Behrmann, Geraldo F Busatto, Sara Calderoni, Eileen Daly, Christine Deruelle, Adriana Di Martino,[...]. Am J Psychiatry 2018
142
27

Mapping 22q11.2 Gene Dosage Effects on Brain Morphometry.
Amy Lin, Christopher R K Ching, Ariana Vajdi, Daqiang Sun, Rachel K Jonas, Maria Jalbrzikowski, Leila Kushan-Wells, Laura Pacheco Hansen, Emma Krikorian, Boris Gutman,[...]. J Neurosci 2017
34
27

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.
Paul M Thompson, Jason L Stein, Sarah E Medland, Derrek P Hibar, Alejandro Arias Vasquez, Miguel E Renteria, Roberto Toro, Neda Jahanshad, Gunter Schumann, Barbara Franke,[...]. Brain Imaging Behav 2014
371
22

Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group.
L Schmaal, D J Veltman, T G M van Erp, P G Sämann, T Frodl, N Jahanshad, E Loehrer, H Tiemeier, A Hofman, W J Niessen,[...]. Mol Psychiatry 2016
483
22

ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries.
Paul M Thompson, Neda Jahanshad, Christopher R K Ching, Lauren E Salminen, Sophia I Thomopoulos, Joanna Bright, Bernhard T Baune, Sara Bertolín, Janita Bralten, Willem B Bruin,[...]. Transl Psychiatry 2020
97
22

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Julio E Villalón-Reina, Kenia Martínez, Xiaoping Qu, Christopher R K Ching, Talia M Nir, Deydeep Kothapalli, Conor Corbin, Daqiang Sun, Amy Lin, Jennifer K Forsyth,[...]. Mol Psychiatry 2020
23
22

Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group.
S Kelly, N Jahanshad, A Zalesky, P Kochunov, I Agartz, C Alloza, O A Andreassen, C Arango, N Banaj, S Bouix,[...]. Mol Psychiatry 2018
245
22

Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome.
J Eric Schmitt, Simon Vandekar, James Yi, Monica E Calkins, Kosha Ruparel, David R Roalf, Daneen Whinna, Margaret C Souders, Theodore D Satterwaite, Karthik Prabhakaran,[...]. Biol Psychiatry 2015
48
22

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
37
22

The Adolescent Brain Cognitive Development (ABCD) study: Imaging acquisition across 21 sites.
B J Casey, Tariq Cannonier, May I Conley, Alexandra O Cohen, Deanna M Barch, Mary M Heitzeg, Mary E Soules, Theresa Teslovich, Danielle V Dellarco, Hugh Garavan,[...]. Dev Cogn Neurosci 2018
303
18

Distinct Subcortical Volume Alterations in Pediatric and Adult OCD: A Worldwide Meta- and Mega-Analysis.
Premika S W Boedhoe, Lianne Schmaal, Yoshinari Abe, Stephanie H Ameis, Paul D Arnold, Marcelo C Batistuzzo, Francesco Benedetti, Jan C Beucke, Irene Bollettini, Anushree Bose,[...]. Am J Psychiatry 2017
150
18

Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group.
L Schmaal, D P Hibar, P G Sämann, G B Hall, B T Baune, N Jahanshad, J W Cheung, T G M van Erp, D Bos, M A Ikram,[...]. Mol Psychiatry 2017
387
18

Genetic architecture of subcortical brain structures in 38,851 individuals.
Claudia L Satizabal, Hieab H H Adams, Derrek P Hibar, Charles C White, Maria J Knol, Jason L Stein, Markus Scholz, Muralidharan Sargurupremraj, Neda Jahanshad, Gennady V Roshchupkin,[...]. Nat Genet 2019
57
18

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
414
18

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
895
18

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
676
18

Neurobiological perspective of 22q11.2 deletion syndrome.
Janneke R Zinkstok, Erik Boot, Anne S Bassett, Noboru Hiroi, Nancy J Butcher, Claudia Vingerhoets, Jacob A S Vorstman, Therese A M J van Amelsvoort. Lancet Psychiatry 2019
23
18

Dissociable Disruptions in Thalamic and Hippocampal Resting-State Functional Connectivity in Youth with 22q11.2 Deletions.
Charles Schleifer, Amy Lin, Leila Kushan, Jie Lisa Ji, Genevieve Yang, Carrie E Bearden, Alan Anticevic. J Neurosci 2019
14
28

Prodromal assessment with the structured interview for prodromal syndromes and the scale of prodromal symptoms: predictive validity, interrater reliability, and training to reliability.
Tandy J Miller, Thomas H McGlashan, Joanna L Rosen, Kristen Cadenhead, Tyrone Cannon, Joseph Ventura, William McFarlane, Diana O Perkins, Godfrey D Pearlson, Scott W Woods. Schizophr Bull 2003
18

Frontal dysconnectivity in 22q11.2 deletion syndrome: an atlas-based functional connectivity analysis.
Leah M Mattiaccio, Ioana L Coman, Carlie A Thompson, Wanda P Fremont, Kevin M Antshel, Wendy R Kates. Behav Brain Funct 2018
13
30

Abnormal Development and Dysconnectivity of Distinct Thalamic Nuclei in Patients With 22q11.2 Deletion Syndrome Experiencing Auditory Hallucinations.
Valentina Mancini, Daniela Zöller, Maude Schneider, Marie Schaer, Stephan Eliez. Biol Psychiatry Cogn Neurosci Neuroimaging 2020
9
44

Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
86
18

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Jacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, Stephan Eliez, Maude Schneider, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Vandana Shashi, Stephen R Hooper,[...]. JAMA Psychiatry 2015
115
18

Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
Sandra Martin-Brevet, Borja Rodríguez-Herreros, Jared A Nielsen, Clara Moreau, Claudia Modenato, Anne M Maillard, Aurélie Pain, Sonia Richetin, Aia E Jønch, Abid Y Qureshi,[...]. Biol Psychiatry 2018
28
18

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
28
18

Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.
Clara A Moreau, Sebastian G W Urchs, Kumar Kuldeep, Pierre Orban, Catherine Schramm, Guillaume Dumas, Aurélie Labbe, Guillaume Huguet, Elise Douard, Pierre-Olivier Quirion,[...]. Nat Commun 2020
9
44

Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium.
T G M van Erp, D P Hibar, J M Rasmussen, D C Glahn, G D Pearlson, O A Andreassen, I Agartz, L T Westlye, U K Haukvik, A M Dale,[...]. Mol Psychiatry 2016
134
13

Subcortical volumetric abnormalities in bipolar disorder.
D P Hibar, L T Westlye, T G M van Erp, J Rasmussen, C D Leonardo, J Faskowitz, U K Haukvik, C B Hartberg, N T Doan, I Agartz,[...]. Mol Psychiatry 2016
220
13

Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis.
Martine Hoogman, Janita Bralten, Derrek P Hibar, Maarten Mennes, Marcel P Zwiers, Lizanne S J Schweren, Kimm J E van Hulzen, Sarah E Medland, Elena Shumskaya, Neda Jahanshad,[...]. Lancet Psychiatry 2017
266
13

Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data.
Stephen M Smith, Mark Jenkinson, Heidi Johansen-Berg, Daniel Rueckert, Thomas E Nichols, Clare E Mackay, Kate E Watkins, Olga Ciccarelli, M Zaheer Cader, Paul M Matthews,[...]. Neuroimage 2006
13

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
461
13

Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain.
Bruce Fischl, David H Salat, Evelina Busa, Marilyn Albert, Megan Dieterich, Christian Haselgrove, Andre van der Kouwe, Ron Killiany, David Kennedy, Shuna Klaveness,[...]. Neuron 2002
13

Identification of common variants associated with human hippocampal and intracranial volumes.
Jason L Stein, Sarah E Medland, Alejandro Arias Vasquez, Derrek P Hibar, Rudy E Senstad, Anderson M Winkler, Roberto Toro, Katja Appel, Richard Bartecek, Ørjan Bergmann,[...]. Nat Genet 2012
418
13

Common genetic variants influence human subcortical brain structures.
Derrek P Hibar, Jason L Stein, Miguel E Renteria, Alejandro Arias-Vasquez, Sylvane Desrivières, Neda Jahanshad, Roberto Toro, Katharina Wittfeld, Lucija Abramovic, Micael Andersson,[...]. Nature 2015
443
13

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.
R E Gur, J J Yi, D M McDonald-McGinn, S X Tang, M E Calkins, D Whinna, M C Souders, A Savitt, E H Zackai, P J Moberg,[...]. Mol Psychiatry 2014
61
13

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
201
13


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
32
13

Abnormalities in brain white matter in adolescents with 22q11.2 deletion syndrome and psychotic symptoms.
Zora Kikinis, Kang Ik K Cho, Ioana L Coman, Petya D Radoeva, Sylvain Bouix, Yingying Tang, Ryan Eckbo, Nikos Makris, Jun Soo Kwon, Marek Kubicki,[...]. Brain Imaging Behav 2017
14
21

An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest.
Rahul S Desikan, Florent Ségonne, Bruce Fischl, Brian T Quinn, Bradford C Dickerson, Deborah Blacker, Randy L Buckner, Anders M Dale, R Paul Maguire, Bradley T Hyman,[...]. Neuroimage 2006
13

Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study.
Wendy R Kates, Kevin M Antshel, Stephen V Faraone, Wanda P Fremont, Anne Marie Higgins, Robert J Shprintzen, Jo-Anna Botti, Lauren Kelchner, Christopher McCarthy. Biol Psychiatry 2011
64
13

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.
Linda E Campbell, Eileen Daly, Fiona Toal, Angela Stevens, Rayna Azuma, Marco Catani, Virginia Ng, Therese van Amelsvoort, Xavier Chitnis, William Cutter,[...]. Brain 2006
133
13

Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study.
Daniel S Tylee, Zora Kikinis, Thomas P Quinn, Kevin M Antshel, Wanda Fremont, Muhammad A Tahir, Anni Zhu, Xue Gong, Stephen J Glatt, Ioana L Coman,[...]. Neuroimage Clin 2017
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.