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



Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere, Jun Han, Leon Hubbard, Amy Lynham, Kiran Mantripragada, Elliott Rees, James H MacCabe, Steven A McCarroll, Bernhard T Baune, Gerome Breen, Enda M Byrne, Udo Dannlowski, Thalia C Eley, Caroline Hayward, Nicholas G Martin, Andrew M McIntosh, Robert Plomin, David J Porteous, Naomi R Wray, Armando Caballero, Daniel H Geschwind, Laura M Huckins, Douglas M Ruderfer, Enrique Santiago, Pamela Sklar, Eli A Stahl, Hyejung Won, Esben Agerbo, Thomas D Als, Ole A Andreassen, Marie Bækvad-Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D Børglum, Jonas Bybjerg-Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, Vera Golimbet, Jakob Grove, David M Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejovic-Milovancevic, Engilbert Sigurdsson, Teimuraz Silagadze, Christine Søholm Hansen, Kari Stefansson, Hreinn Stefansson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David A Collier, Dan Rujescu, George Kirov, Michael J Owen, Michael C O'Donovan, James T R Walters. Nat Genet 2018
Times Cited: 474




List of shared articles



Times cited

Combined cellomics and proteomics analysis reveals shared neuronal morphology and molecular pathway phenotypes for multiple schizophrenia risk genes.
Martina Rosato, Sven Stringer, Titia Gebuis, Iryna Paliukhovich, Ka Wan Li, Danielle Posthuma, Patrick F Sullivan, August B Smit, Ronald E van Kesteren. Mol Psychiatry 2021
6

Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations.
Aaron Gordon, Annika Forsingdal, Ib Vestergaard Klewe, Jacob Nielsen, Michael Didriksen, Thomas Werge, Daniel H Geschwind. Mol Psychiatry 2021
11


Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank.
Xavier Caseras, George Kirov, Kimberley M Kendall, Elliott Rees, Sophie E Legge, Matthew Bracher-Smith, Valentina Escott-Price, Kevin Murphy. Br J Psychiatry 2021
0

Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders.
Phil H Lee, Yen-Chen A Feng, Jordan W Smoller. Biol Psychiatry 2021
3

A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia.
Tariq Mahmood, Mohammed E El-Asrag, James A Poulter, Alastair G Cardno, Anneka Tomlinson, Sophia Ahmed, Ahmed Al-Amri, Jamshid Nazari, Joanna Neill, Rifka S Chamali,[...]. Schizophr Bull 2021
0

Functional Genomics Identify a Regulatory Risk Variation rs4420550 in the 16p11.2 Schizophrenia-Associated Locus.
Hong Chang, Xin Cai, Hui-Juan Li, Wei-Peng Liu, Li-Juan Zhao, Chu-Yi Zhang, Jun-Yang Wang, Jie-Wei Liu, Xiao-Lei Ma, Lu Wang,[...]. Biol Psychiatry 2021
2


Genetic architecture of schizophrenia: a review of major advancements.
Sophie E Legge, Marcos L Santoro, Sathish Periyasamy, Adeniran Okewole, Arsalan Arsalan, Kaarina Kowalec. Psychol Med 2021
1

RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes.
Catherine A Brownstein, Richard S Smith, Lance H Rodan, Mark P Gorman, Margaret A Hojlo, Emily A Garvey, Jianqiao Li, Kristin Cabral, Joshua J Bowen, Abhijit S Rao,[...]. Mol Psychiatry 2021
1

Functional brain defects in a mouse model of a chromosomal t(1;11) translocation that disrupts DISC1 and confers increased risk of psychiatric illness.
Marion Bonneau, Shane T O' Sullivan, Miguel A Gonzalez-Lozano, Paul Baxter, Phillippe Gautier, Elena Marchisella, Neil R Hardingham, Robert A Chesters, Helen Torrance, David M Howard,[...]. Transl Psychiatry 2021
0

A Neurodevelopment Approach for a Transitional Model of Early Onset Schizophrenia.
Domenico De Berardis, Sergio De Filippis, Gabriele Masi, Stefano Vicari, Alessandro Zuddas. Brain Sci 2021
1

Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia.
Leon Hubbard, Elliott Rees, Derek W Morris, Amy J Lynham, Alex L Richards, Antonio F Pardiñas, Sophie E Legge, Denise Harold, Stanley Zammit, Aiden C Corvin,[...]. Biol Psychiatry 2021
0

Tissue-specific enhancer functional networks for associating distal regulatory regions to disease.
Xi Chen, Jian Zhou, Ran Zhang, Aaron K Wong, Christopher Y Park, Chandra L Theesfeld, Olga G Troyanskaya. Cell Syst 2021
1

Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia.
Todd Lencz, Jin Yu, Raiyan Rashid Khan, Erin Flaherty, Shai Carmi, Max Lam, Danny Ben-Avraham, Nir Barzilai, Susan Bressman, Ariel Darvasi,[...]. Neuron 2021
1


Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia.
Minsoo Kim, Jillian R Haney, Pan Zhang, Leanna M Hernandez, Lee-Kai Wang, Laura Perez-Cano, Loes M Olde Loohuis, Luis de la Torre-Ubieta, Michael J Gandal. Nat Neurosci 2021
0

Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons.
ChangHui Pak, Tamas Danko, Vincent R Mirabella, Jinzhao Wang, Yingfei Liu, Madhuri Vangipuram, Sarah Grieder, Xianglong Zhang, Thomas Ward, Yu-Wen Alvin Huang,[...]. Proc Natl Acad Sci U S A 2021
1


The abiding relevance of mouse models of rare mutations to psychiatric neuroscience and therapeutics.
Joseph A Gogos, Gregg Crabtree, Anastasia Diamantopoulou. Schizophr Res 2020
4

The association between schizophrenia and the immune system: Review of the evidence from unbiased 'omic-studies'.
Hans C van Mierlo, Aron Schot, Marco P M Boks, Lot D de Witte. Schizophr Res 2020
10

CRISPR-based functional evaluation of schizophrenia risk variants.
Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, Kristen J Brennand. Schizophr Res 2020
2

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
Jennifer K Forsyth, Daniel Nachun, Michael J Gandal, Daniel H Geschwind, Ariana E Anderson, Giovanni Coppola, Carrie E Bearden. Biol Psychiatry 2020
11

Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
Tim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, Jacquelyn L Meyers, Roseann E Peterson, Conrad O Iyegbe, Helena Medeiros, Jorge Valderrama, Eric D Achtyes, Roman Kotov,[...]. Mol Psychiatry 2020
20

Genetics of Childhood-onset Schizophrenia 2019 Update.
Jennifer K Forsyth, Robert F Asarnow. Child Adolesc Psychiatr Clin N Am 2020
6

The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine.
Zhihui Yang, Danyang Zhou, Huijuan Li, Xin Cai, Weipeng Liu, Lu Wang, Hong Chang, Ming Li, Xiao Xiao. Mol Psychiatry 2020
17

Twin studies of brain structure and cognition in schizophrenia.
Bianca Besteher, Paolo Brambilla, Igor Nenadić. Neurosci Biobehav Rev 2020
2