A citation-based method for searching scientific literature

Jibin John, Aditya Sharma, Prachi Kukshal, Triptish Bhatia, Vishwajit L Nimgaonkar, Smita N Deshpande, B K Thelma. Schizophr Bull 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
879
85


Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia.
Zhifan Zhou, Zhengmao Hu, Lu Zhang, Zhaoting Hu, Haihong Liu, Zhening Liu, Juan Du, Jingping Zhao, Lin Zhou, Kun Xia,[...]. Sci Rep 2016
17
57

Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.
Jibin John, Prachi Kukshal, Triptish Bhatia, K V Chowdari, V L Nimgaonkar, S N Deshpande, B K Thelma. Schizophr Res 2017
27
57

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.
Jun Egawa, Satoshi Hoya, Yuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Emiko Inoue, Shujiro Okuda, Kenji Kondo, Takeo Saito,[...]. Am J Med Genet B Neuropsychiatr Genet 2016
15
57

Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.
O R Homann, K Misura, E Lamas, R W Sandrock, P Nelson, S I McDonough, L E DeLisi. Mol Psychiatry 2016
56
57

Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
Andrew E Timms, Michael O Dorschner, Jeremy Wechsler, Kyu Yeong Choi, Robert Kirkwood, Santhosh Girirajan, Carl Baker, Evan E Eichler, Olena Korvatska, Katherine W Roche,[...]. JAMA Psychiatry 2013
95
57

De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
969
57

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
42

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Tarjinder Singh, Mitja I Kurki, David Curtis, Shaun M Purcell, Lucy Crooks, Jeremy McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen,[...]. Nat Neurosci 2016
214
42

Truncating mutations in RBM12 are associated with psychosis.
Stacy Steinberg, Steinunn Gudmundsdottir, Gardar Sveinbjornsson, Jaana Suvisaari, Tiina Paunio, Minna Torniainen-Holm, Michael L Frigge, Gudrun A Jonsdottir, Johanna Huttenlocher, Sunna Arnarsdottir,[...]. Nat Genet 2017
34
42


De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
229
28


De novo mutations from sporadic schizophrenia cases highlight important signaling genes in an independent sample.
Thorsten M Kranz, Sheila Harroch, Orly Manor, Pesach Lichtenberg, Yechiel Friedlander, Marco Seandel, Jill Harkavy-Friedman, Julie Walsh-Messinger, Igor Dolgalev, Adriana Heguy,[...]. Schizophr Res 2015
30
28

Qualimap: evaluating next-generation sequencing alignment data.
Fernando García-Alcalde, Konstantin Okonechnikov, José Carbonell, Luis M Cruz, Stefan Götz, Sonia Tarazona, Joaquín Dopazo, Thomas F Meyer, Ana Conesa. Bioinformatics 2012
377
28

Increased exonic de novo mutation rate in individuals with schizophrenia.
Simon L Girard, Julie Gauthier, Anne Noreau, Lan Xiong, Sirui Zhou, Loubna Jouan, Alexandre Dionne-Laporte, Dan Spiegelman, Edouard Henrion, Ousmane Diallo,[...]. Nat Genet 2011
272
28

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.
Po-Ru Loh, Gaurav Bhatia, Alexander Gusev, Hilary K Finucane, Brendan K Bulik-Sullivan, Samuela J Pollack, Teresa R de Candia, Sang Hong Lee, Naomi R Wray, Kenneth S Kendler,[...]. Nat Genet 2015
191
28

A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases.
Miao-Xin Li, Hong-Sheng Gui, Johnny S H Kwan, Su-Ying Bao, Pak C Sham. Nucleic Acids Res 2012
163
28

Detecting false-positive signals in exome sequencing.
Karin V Fuentes Fajardo, David Adams, Christopher E Mason, Murat Sincan, Cynthia Tifft, Camilo Toro, Cornelius F Boerkoel, William Gahl, Thomas Markello. Hum Mutat 2012
103
28

Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition.
Jibin John, Triptish Bhatia, Prachi Kukshal, Puneet Chandna, Vishwajit L Nimgaonkar, Smita N Deshpande, B K Thelma. Schizophr Res 2016
10
28

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.
Bin Xu, Iuliana Ionita-Laza, J Louw Roos, Braden Boone, Scarlet Woodrick, Yan Sun, Shawn Levy, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2012
289
28

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
28

GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders.
Tobias Hornig, Björn Grüning, Kousik Kundu, Torsten Houwaart, Rolf Backofen, Knut Biber, Claus Normann. Genet Res (Camb) 2017
9
28

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
332
28

A practical guide to filtering and prioritizing genetic variants.
Mahjoubeh Jalali Sefid Dashti, Junaid Gamieldien. Biotechniques 2017
25
28

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
28

Schizophrenia: a neurodevelopmental disorder--integrative genomic hypothesis and therapeutic implications from a transgenic mouse model.
M K Stachowiak, A Kucinski, R Curl, C Syposs, Y Yang, S Narla, C Terranova, D Prokop, I Klejbor, M Bencherif,[...]. Schizophr Res 2013
30
28


The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.
Tarjinder Singh, James T R Walters, Mandy Johnstone, David Curtis, Jaana Suvisaari, Minna Torniainen, Elliott Rees, Conrad Iyegbe, Douglas Blackwood, Andrew M McIntosh,[...]. Nat Genet 2017
86
28

Exome sequencing supports a de novo mutational paradigm for schizophrenia.
Bin Xu, J Louw Roos, Phillip Dexheimer, Braden Boone, Brooks Plummer, Shawn Levy, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2011
312
28

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.
Paul Lichtenstein, Benjamin H Yip, Camilla Björk, Yudi Pawitan, Tyrone D Cannon, Patrick F Sullivan, Christina M Hultman. Lancet 2009
28

Rare variants in neuronal excitability genes influence risk for bipolar disorder.
Seth A Ament, Szabolcs Szelinger, Gustavo Glusman, Justin Ashworth, Liping Hou, Nirmala Akula, Tatyana Shekhtman, Judith A Badner, Mary E Brunkow, Denise E Mauldin,[...]. Proc Natl Acad Sci U S A 2015
94
28

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Giulio Genovese, Menachem Fromer, Eli A Stahl, Douglas M Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L Moran, Shaun M Purcell, Pamela Sklar, Patrick F Sullivan,[...]. Nat Neurosci 2016
213
28

Rediscovering the value of families for psychiatric genetics research.
David C Glahn, Vishwajit L Nimgaonkar, Henriette Raventós, Javier Contreras, Andrew M McIntosh, Pippa A Thomson, Assen Jablensky, Nina S McCarthy, Jac C Charlesworth, Nicholas B Blackburn,[...]. Mol Psychiatry 2019
25
28

Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia.
Jinsong Tang, Yu Fan, Hong Li, Qun Xiang, Deng-Feng Zhang, Zongchang Li, Ying He, Yanhui Liao, Ya Wang, Fan He,[...]. J Genet Genomics 2017
24
28

Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways.
Edoardo Giacopuzzi, Massimo Gennarelli, Alessandra Minelli, Rita Gardella, Paolo Valsecchi, Michele Traversa, Cristian Bonvicini, Antonio Vita, Emilio Sacchetti, Chiara Magri. PLoS One 2017
9
28

De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia.
Atsushi Takata, Iuliana Ionita-Laza, Joseph A Gogos, Bin Xu, Maria Karayiorgou. Neuron 2016
71
28

Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder.
N L O'Brien, A Fiorentino, D Curtis, C Rayner, C Petrosellini, M Al Eissa, N J Bass, A McQuillin, S I Sharp. Schizophr Res 2018
5
40

Genetic linkage analysis in the age of whole-genome sequencing.
Jurg Ott, Jing Wang, Suzanne M Leal. Nat Rev Genet 2015
127
28

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
28

The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study.
T D Cannon, J Kaprio, J Lönnqvist, M Huttunen, M Koskenvuo. Arch Gen Psychiatry 1998
336
28

Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.
Satoshi Hoya, Yuichiro Watanabe, Akitoyo Hishimoto, Ayako Nunokawa, Naoshi Kaneko, Tatsuyuki Muratake, Naofumi Shinmyo, Ikuo Otsuka, Shujiro Okuda, Emiko Inoue,[...]. Psychiatry Clin Neurosci 2017
6
33

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
28

The role of cadherin genes in five major psychiatric disorders: A literature update.
Ziarih Hawi, Janette Tong, Callum Dark, Hannah Yates, Beth Johnson, Mark A Bellgrove. Am J Med Genet B Neuropsychiatr Genet 2018
20
28

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
341
14

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
Omri Teltsh, Kyra Kanyas, Osnat Karni, Adi Levi, Mira Korner, Edna Ben-Asher, Doron Lancet, Adnan Hamdan, Bernard Lerer, Yoav Kohn. Am J Med Genet B Neuropsychiatr Genet 2008
11
14

Contribution of Kv1.2 voltage-gated potassium channel to D2 autoreceptor regulation of axonal dopamine overflow.
Stephanie Fulton, Dominic Thibault, Jose A Mendez, Nicolas Lahaie, Emanuele Tirotta, Emiliana Borrelli, Michel Bouvier, Bruce L Tempel, Louis-Eric Trudeau. J Biol Chem 2011
32
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.