A citation-based method for searching scientific literature

S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban, E Antoniou, E Kelleher, C O'Brien, G Donohoe, M Gill, D W Morris, W R McCombie, A Corvin. Mol Psychiatry 2014
Times Cited: 226



Michel Guipponi, Federico A Santoni, Vincent Setola, Corinne Gehrig, Maud Rotharmel, Macarena Cuenca, Olivier Guillin, Dimitris Dikeos, Georgios Georgantopoulos, George Papadimitriou, Logos Curtis, Alexandre Méary, Franck Schürhoff, Stéphane Jamain, Dimitri Avramopoulos, Marion Leboyer, Dan Rujescu, Ann Pulver, Dominique Campion, David P Siderovski, Stylianos E Antonarakis. PLoS One 2014
Times Cited: 50




List of shared articles



Times cited

Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.
Joost Kummeling, Diante E Stremmelaar, Nicholas Raun, Margot R F Reijnders, Marjolein H Willemsen, Martina Ruiterkamp-Versteeg, Marga Schepens, Calvin C O Man, Christian Gilissen, Megan T Cho,[...]. Mol Psychiatry 2021
4

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
12

Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.
Guihu Zhao, Kuokuo Li, Bin Li, Zheng Wang, Zhenghuan Fang, Xiaomeng Wang, Yi Zhang, Tengfei Luo, Qiao Zhou, Lin Wang,[...]. Nucleic Acids Res 2020
16

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.
Daniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, Menachem Fromer, Felecia Cerrato, Wei J Chen, Claire Churchhouse, Kimberly Chambert, Sharon D Chandler, Mark J Daly,[...]. Nat Neurosci 2020
31

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.
Andreas J Forstner, Sascha B Fischer, Lorena M Schenk, Jana Strohmaier, Anna Maaser-Hecker, Céline S Reinbold, Sugirthan Sivalingam, Julian Hecker, Fabian Streit, Franziska Degenhardt,[...]. Transl Psychiatry 2020
5

A Caenorhabditis elegans Model for Integrating the Functions of Neuropsychiatric Risk Genes Identifies Components Required for Normal Dendritic Morphology.
Cristina Aguirre-Chen, Natalia Stec, Olivia Mendivil Ramos, Nuri Kim, Melissa Kramer, Shane McCarthy, Jesse Gillis, W Richard McCombie, Christopher M Hammell. G3 (Bethesda) 2020
4

Genetic association of FMRP targets with psychiatric disorders.
Nicholas E Clifton, Elliott Rees, Peter A Holmans, Antonio F Pardiñas, Janet C Harwood, Arianna Di Florio, George Kirov, James T R Walters, Michael C O'Donovan, Michael J Owen,[...]. Mol Psychiatry 2020
1

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.
Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez, Kymberleigh A Pagel, Guan Ning Lin, Hyun-Jun Nam, Matthew Mort, David N Cooper, Jonathan Sebat, Lilia M Iakoucheva,[...]. Nat Commun 2020
23

Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.
Jibin John, Aditya Sharma, Prachi Kukshal, Triptish Bhatia, Vishwajit L Nimgaonkar, Smita N Deshpande, B K Thelma. Schizophr Bull 2019
7

Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis.
Elliott Rees, Noa Carrera, Joanne Morgan, Kirsty Hambridge, Valentina Escott-Price, Andrew J Pocklington, Alexander L Richards, Antonio F Pardiñas, Colm McDonald, Gary Donohoe,[...]. Biol Psychiatry 2019
12

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study.
Jibin John, Prachi Kukshal, Aditya Sharma, Triptish Bhatia, V L Nimgaonkar, S N Deshpande, B K Thelma. Schizophr Res 2019
1


Essential genetic findings in neurodevelopmental disorders.
Ana R Cardoso, Mónica Lopes-Marques, Raquel M Silva, Catarina Serrano, António Amorim, Maria J Prata, Luísa Azevedo. Hum Genomics 2019
10

Paternal-age-related de novo mutations and risk for five disorders.
Jacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, Emilie M Wigdor, Henrike O Heyne, Dennis Lal, Daniel P Howrigan, Alex Bloemendal, Janne T Larsen, Jack A Kosmicki,[...]. Nat Commun 2019
18

Recent Advances in the Genetics of Schizophrenia.
Dimitrios Avramopoulos. Mol Neuropsychiatry 2018
33