A citation-based method for searching scientific literature

Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto, Madhusudan Gujral, William M Brandler, Dheeraj Malhotra, Zhouzhi Wang, Karin V Fuentes Fajarado, Michelle S Maile, Stephan Ripke, Ingrid Agartz, Margot Albus, Madeline Alexander, Farooq Amin, Joshua Atkins, Silviu A Bacanu, Richard A Belliveau, Sarah E Bergen, Marcelo Bertalan, Elizabeth Bevilacqua, Tim B Bigdeli, Donald W Black, Richard Bruggeman, Nancy G Buccola, Randy L Buckner, Brendan Bulik-Sullivan, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J Cairns, Dominique Campion, Rita M Cantor, Vaughan J Carr, Noa Carrera, Stanley V Catts, Kimberley D Chambert, Wei Cheng, C Robert Cloninger, David Cohen, Paul Cormican, Nick Craddock, Benedicto Crespo-Facorro, James J Crowley, David Curtis, Michael Davidson, Kenneth L Davis, Franziska Degenhardt, Jurgen Del Favero, Lynn E DeLisi, Dimitris Dikeos, Timothy Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Peter Eichhammer, Johan Eriksson, Valentina Escott-Price, Laurent Essioux, Ayman H Fanous, Kai-How Farh, Martilias S Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B Freimer, Joseph I Friedman, Andreas J Forstner, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Elliot S Gershon, Ina Giegling, Paola Giusti-Rodríguez, Stephanie Godard, Jacqueline I Goldstein, Jacob Gratten, Lieuwe de Haan, Marian L Hamshere, Mark Hansen, Thomas Hansen, Vahram Haroutunian, Annette M Hartmann, Frans A Henskens, Stefan Herms, Joel N Hirschhorn, Per Hoffmann, Andrea Hofman, Hailiang Huang, Masashi Ikeda, Inge Joa, Anna K Kähler, René S Kahn, Luba Kalaydjieva, Juha Karjalainen, David Kavanagh, Matthew C Keller, Brian J Kelly, James L Kennedy, Yunjung Kim, James A Knowles, Bettina Konte, Claudine Laurent, Phil Lee, S Hong Lee, Sophie E Legge, Bernard Lerer, Deborah L Levy, Kung-Yee Liang, Jeffrey Lieberman, Jouko Lönnqvist, Carmel M Loughland, Patrik K E Magnusson, Brion S Maher, Wolfgang Maier, Jacques Mallet, Manuel Mattheisen, Morten Mattingsdal, Robert W McCarley, Colm McDonald, Andrew M McIntosh, Sandra Meier, Carin J Meijer, Ingrid Melle, Raquelle I Mesholam-Gately, Andres Metspalu, Patricia T Michie, Lili Milani, Vihra Milanova, Younes Mokrab, Derek W Morris, Bertram Müller-Myhsok, Kieran C Murphy, Robin M Murray, Inez Myin-Germeys, Igor Nenadic, Deborah A Nertney, Gerald Nestadt, Kristin K Nicodemus, Laura Nisenbaum, Annelie Nordin, Eadbhard O'Callaghan, Colm O'Dushlaine, Sang-Yun Oh, Ann Olincy, Line Olsen, F Anthony O'Neill, Jim Van Os, Christos Pantelis, George N Papadimitriou, Elena Parkhomenko, Michele T Pato, Tiina Paunio, Diana O Perkins, Tune H Pers, Olli Pietiläinen, Jonathan Pimm, Andrew J Pocklington, John Powell, Alkes Price, Ann E Pulver, Shaun M Purcell, Digby Quested, Henrik B Rasmussen, Abraham Reichenberg, Mark A Reimers, Alexander L Richards, Joshua L Roffman, Panos Roussos, Douglas M Ruderfer, Veikko Salomaa, Alan R Sanders, Adam Savitz, Ulrich Schall, Thomas G Schulze, Sibylle G Schwab, Edward M Scolnick, Rodney J Scott, Larry J Seidman, Jianxin Shi, Jeremy M Silverman, Jordan W Smoller, Erik Söderman, Chris C A Spencer, Eli A Stahl, Eric Strengman, Jana Strohmaier, T Scott Stroup, Jaana Suvisaari, Dragan M Svrakic, Jin P Szatkiewicz, Srinivas Thirumalai, Paul A Tooney, Juha Veijola, Peter M Visscher, John Waddington, Dermot Walsh, Bradley T Webb, Mark Weiser, Dieter B Wildenauer, Nigel M Williams, Stephanie Williams, Stephanie H Witt, Aaron R Wolen, Brandon K Wormley, Naomi R Wray, Jing Qin Wu, Clement C Zai, Rolf Adolfsson, Ole A Andreassen, Douglas H R Blackwood, Elvira Bramon, Joseph D Buxbaum, Sven Cichon, David A Collier, Aiden Corvin, Mark J Daly, Ariel Darvasi, Enrico Domenici, Tõnu Esko, Pablo V Gejman, Michael Gill, Hugh Gurling, Christina M Hultman, Nakao Iwata, Assen V Jablensky, Erik G Jönsson, Kenneth S Kendler, George Kirov, Jo Knight, Douglas F Levinson, Qingqin S Li, Steven A McCarroll, Andrew McQuillin, Jennifer L Moran, Bryan J Mowry, Markus M Nöthen, Roel A Ophoff, Michael J Owen, Aarno Palotie, Carlos N Pato, Tracey L Petryshen, Danielle Posthuma, Marcella Rietschel, Brien P Riley, Dan Rujescu, Pamela Sklar, David St Clair, James T R Walters, Thomas Werge, Patrick F Sullivan, Michael C O'Donovan, Stephen W Scherer, Benjamin M Neale, Jonathan Sebat. Nat Genet 2017
Times Cited: 386







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



Times Cited
  Times     Co-cited
Similarity


A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report.
Anna Winczewska-Wiktor, Magdalena Badura-Stronka, Anna Monies-Nowicka, Michal Maciej Nowicki, Barbara Steinborn, Anna Latos-Bieleńska, Dorota Monies. BMC Neurol 2016
13
7

Wnt-3a overcomes beta-amyloid toxicity in rat hippocampal neurons.
Alejandra R Alvarez, Juan A Godoy, Karin Mullendorff, Gonzalo H Olivares, Miguel Bronfman, Nibaldo C Inestrosa. Exp Cell Res 2004
170
1

The Neurochemistry of Autism.
Rosa Marotta, Maria C Risoleo, Giovanni Messina, Lucia Parisi, Marco Carotenuto, Luigi Vetri, Michele Roccella. Brain Sci 2020
27
3

Wnt-mediated activation of NeuroD1 and retro-elements during adult neurogenesis.
Tomoko Kuwabara, Jenny Hsieh, Alysson Muotri, Gene Yeo, Masaki Warashina, Dieter Chichung Lie, Lynne Moore, Kinichi Nakashima, Makoto Asashima, Fred H Gage. Nat Neurosci 2009
404
1

hSKCa3: a candidate gene for schizophrenia?
B Meissner, S Purmann, M Schürmann, C Zühlke, R Lencer, V Arolt, B Müller-Myhsok, D J Morris-Rosendahl, E Schwinger. Psychiatr Genet 1999
12
8

Maternal thyroid autoimmunity associated with acute-onset neuropsychiatric disorders and global regression in offspring.
Hannah F Jones, Alvin C C Ho, Suvasini Sharma, Shekeeb S Mohammad, Kavitha Kothur, Shrujna Patel, Fabienne Brilot, Adam J Guastella, Russell C Dale. Dev Med Child Neurol 2019
5
20

beta-Catenin signals regulate cell growth and the balance between progenitor cell expansion and differentiation in the nervous system.
Dietmar Zechner, Yasuyuki Fujita, Jörg Hülsken, Thomas Müller, Ingrid Walther, Makoto M Taketo, E Bryan Crenshaw, Walter Birchmeier, Carmen Birchmeier. Dev Biol 2003
370
1


Positional pathway screen of wnt signaling genes in schizophrenia: association with DKK4.
Petroula Proitsi, Tao Li, Gillian Hamilton, Marta Di Forti, David Collier, Richard Killick, Ronald Chen, Pak Sham, Robin Murray, John Powell,[...]. Biol Psychiatry 2008
32
3

An assessment of sex bias in neurodevelopmental disorders.
Andrew Polyak, Jill A Rosenfeld, Santhosh Girirajan. Genome Med 2015
40
2

Development of patient-specific neurons in schizophrenia using induced pluripotent stem cells.
Erika Pedrosa, Vladislav Sandler, Abhishek Shah, Reed Carroll, Chanjung Chang, Shira Rockowitz, Xingyi Guo, Deyou Zheng, Herbert M Lachman. J Neurogenet 2011
96
1

Substance use and schizophrenia: adverse correlates in the CATIE study sample.
Karin E Kerfoot, Robert A Rosenheck, Ismene L Petrakis, Marvin S Swartz, Richard S E Keefe, Joseph P McEvoy, T Scott Stroup. Schizophr Res 2011
39
2

Adenomatous polyposis coli protein deletion leads to cognitive and autism-like disabilities.
J L Mohn, J Alexander, A Pirone, C D Palka, S-Y Lee, L Mebane, P G Haydon, M H Jacob. Mol Psychiatry 2014
44
2

An eight-case 1q21 region series: novel aberrations and clinical variability with new features.
A C Ceylan, I Sahin, H B Erdem, G Kayhan, P O Simsek-Kiper, G E Utine, F Percin, K Boduroglu, M Alikasifoglu. J Intellect Disabil Res 2019
2
50

Deletion of CTNNB1 in inhibitory circuitry contributes to autism-associated behavioral defects.
Fengping Dong, Joanna Jiang, Colleen McSweeney, Donghua Zou, Long Liu, Yingwei Mao. Hum Mol Genet 2016
35
2

Rbm8a haploinsufficiency disrupts embryonic cortical development resulting in microcephaly.
Hanqian Mao, Louis-Jan Pilaz, John J McMahon, Christelle Golzio, Danwei Wu, Lei Shi, Nicholas Katsanis, Debra L Silver. J Neurosci 2015
46
2

Connexin 50 gene on human chromosome 1q21 is associated with schizophrenia in matched case control and family-based studies.
Xingqun Ni, Jose Valente, Maria H Azevedo, Michelle T Pato, Carlos N Pato, James L Kennedy. J Med Genet 2007
22
4

Wnt signalling regulates adult hippocampal neurogenesis.
Dieter-Chichung Lie, Sophia A Colamarino, Hong-Jun Song, Laurent Désiré, Helena Mira, Antonella Consiglio, Edward S Lein, Sebastian Jessberger, Heather Lansford, Alejandro R Dearie,[...]. Nature 2005
1

hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21.
V Dror, E Shamir, S Ghanshani, R Kimhi, M Swartz, Y Barak, R Weizman, L Avivi, T Litmanovitch, E Fantino,[...]. Mol Psychiatry 1999
64
1

De novo rates and selection of schizophrenia-associated copy number variants.
Elliott Rees, Valentina Moskvina, Michael J Owen, Michael C O'Donovan, George Kirov. Biol Psychiatry 2011
60
1

Increase in GSK3beta gene copy number variation in bipolar disorder.
Herbert M Lachman, Erika Pedrosa, Oriana A Petruolo, Melissa Cockerham, Alexander Papolos, Tomas Novak, Demitri F Papolos, Pavla Stopkova. Am J Med Genet B Neuropsychiatr Genet 2007
97
1

A critical role of RBM8a in proliferation and differentiation of embryonic neural progenitors.
Donghua Zou, Colleen McSweeney, Aswathy Sebastian, Derrick James Reynolds, Fengping Dong, Yijing Zhou, Dazhi Deng, Yonggang Wang, Long Liu, Jun Zhu,[...]. Neural Dev 2015
25
4

De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
Alma Kuechler, Marjolein H Willemsen, Beate Albrecht, Carlos A Bacino, Dennis W Bartholomew, Hans van Bokhoven, Marie Jose H van den Boogaard, Nuria Bramswig, Christian Büttner, Kirsten Cremer,[...]. Hum Genet 2015
46
2

Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
Mira Kharbanda, Daniela T Pilz, Susan Tomkins, Kate Chandler, Anand Saggar, Alan Fryer, Victoria McKay, Pedro Louro, Jill Clayton Smith, John Burn,[...]. Eur J Med Genet 2017
17
5

Modulating Neuroinflammation to Treat Neuropsychiatric Disorders.
Franziska A Radtke, Gareth Chapman, Jeremy Hall, Yasir A Syed. Biomed Res Int 2017
21
4


Wnt/beta-catenin signaling is required for CNS, but not non-CNS, angiogenesis.
Richard Daneman, Dritan Agalliu, Lu Zhou, Frank Kuhnert, Calvin J Kuo, Ben A Barres. Proc Natl Acad Sci U S A 2009
402
1

Schizophrenia after prenatal exposure to 1957 A2 influenza epidemic.
E O'Callaghan, P Sham, N Takei, G Glover, R M Murray. Lancet 1991
304
1

TSPAN12 regulates retinal vascular development by promoting Norrin- but not Wnt-induced FZD4/beta-catenin signaling.
Harald J Junge, Stacey Yang, Jeremy B Burton, Kim Paes, Xiao Shu, Dorothy M French, Mike Costa, Dennis S Rice, Weilan Ye. Cell 2009
222
1

Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism.
Jacob Ellegood, Jacqueline N Crawley. Neurotherapeutics 2015
54
1

The profile of memory function in children with autism.
Diane L Williams, Gerald Goldstein, Nancy J Minshew. Neuropsychology 2006
132
1

Association between prenatal exposure to poliovirus infection and adult schizophrenia.
J Suvisaari, J Haukka, A Tanskanen, T Hovi, J Lönnqvist. Am J Psychiatry 1999
115
1

Full function of exon junction complex factor, Rbm8a, is critical for interneuron development.
Colleen McSweeney, Fengping Dong, Miranda Chen, Jessica Vitale, Li Xu, Nicole Crowley, Bernhard Luscher, Donghua Zou, Yingwei Mao. Transl Psychiatry 2020
1
100

Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasound.
Sara Jane Webb, Michelle M Garrison, Raphael Bernier, Abbi M McClintic, Bryan H King, Pierre D Mourad. Autism Res 2017
10
10

Potential Value of Genomic Copy Number Variations in Schizophrenia.
Chuanjun Zhuo, Weihong Hou, Chongguang Lin, Lirong Hu, Jie Li. Front Mol Neurosci 2017
10
10


BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.
Chun Xu, Nagesh Aragam, Xia Li, Erika Cynthia Villla, Liang Wang, David Briones, Leonora Petty, Yolanda Posada, Tania Bedard Arana, Grace Cruz,[...]. PLoS One 2013
27
3

Neurodevelopmental disorders and prenatal residential proximity to agricultural pesticides: the CHARGE study.
Janie F Shelton, Estella M Geraghty, Daniel J Tancredi, Lora D Delwiche, Rebecca J Schmidt, Beate Ritz, Robin L Hansen, Irva Hertz-Picciotto. Environ Health Perspect 2014
216
1


Pre-natal brain development as a target for urban air pollution.
Jordi Sunyer, Payam Dadvand. Basic Clin Pharmacol Toxicol 2019
10
10

AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance.
Stanislav Nagy, Gianna W Maurer, Julie L Hentze, Morten Rose, Thomas M Werge, Kim Rewitz. PLoS Genet 2018
5
20

Nrarp coordinates endothelial Notch and Wnt signaling to control vessel density in angiogenesis.
Li-Kun Phng, Michael Potente, Jonathan D Leslie, Jane Babbage, Daniel Nyqvist, Ivan Lobov, Jennifer K Ondr, Sujata Rao, Richard A Lang, Gavin Thurston,[...]. Dev Cell 2009
237
1

Cannabis use and the course of schizophrenia: 10-year follow-up after first hospitalization.
Daniel J Foti, Roman Kotov, Lin T Guey, Evelyn J Bromet. Am J Psychiatry 2010
121
1

Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication.
Roberta Milone, Angelo Valetto, Roberta Battini, Veronica Bertini, Giulia Valvo, Giovanni Cioni, Federico Sicca. Eur J Med Genet 2016
8
12

Emerging biomarkers in autism spectrum disorder: a systematic review.
Richard E Frye, Sarah Vassall, Gurjot Kaur, Christina Lewis, Mohammand Karim, Daniel Rossignol. Ann Transl Med 2019
19
5

Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1.
Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
1
100

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1.
N Lijam, R Paylor, M P McDonald, J N Crawley, C X Deng, K Herrup, K E Stevens, G Maccaferri, C J McBain, D J Sussman,[...]. Cell 1997
358
1

Molecular and cellular approaches for diversifying and extending optogenetics.
Viviana Gradinaru, Feng Zhang, Charu Ramakrishnan, Joanna Mattis, Rohit Prakash, Ilka Diester, Inbal Goshen, Kimberly R Thompson, Karl Deisseroth. Cell 2010
566
1

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
1

Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.
P Copet, J Jauregi, V Laurier, V Ehlinger, C Arnaud, A-M Cobo, C Molinas, M Tauber, D Thuilleaux. J Intellect Disabil Res 2010
39
2


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.