A citation-based method for searching scientific literature

Jibin John, Prachi Kukshal, Aditya Sharma, Triptish Bhatia, V L Nimgaonkar, S N Deshpande, B K Thelma. Schizophr Res 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Schizophrenia genetics in the genome-wide era: a review of Japanese studies.
Tetsufumi Kanazawa, Chad A Bousman, Chenxing Liu, Ian P Everall. NPJ Schizophr 2017
8
100

Psychiatric Genomics: An Update and an Agenda.
Patrick F Sullivan, Arpana Agrawal, Cynthia M Bulik, Ole A Andreassen, Anders D Børglum, Gerome Breen, Sven Cichon, Howard J Edenberg, Stephen V Faraone, Joel Gelernter,[...]. Am J Psychiatry 2018
211
100

Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.
Satoshi Hoya, Yuichiro Watanabe, Akitoyo Hishimoto, Ayako Nunokawa, Emiko Inoue, Hirofumi Igeta, Ikuo Otsuka, Masako Shibuya, Jun Egawa, Ichiro Sora,[...]. Psychiatry Clin Neurosci 2017
1
100

Trimmomatic: a flexible trimmer for Illumina sequence data.
Anthony M Bolger, Marc Lohse, Bjoern Usadel. Bioinformatics 2014
100

Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese.
Yukinori Okada, Yukihide Momozawa, Saori Sakaue, Masahiro Kanai, Kazuyoshi Ishigaki, Masato Akiyama, Toshihiro Kishikawa, Yasumichi Arai, Takashi Sasaki, Kenjiro Kosaki,[...]. Nat Commun 2018
59
100


Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.
Donna S Mackay, Louise A Ocaka, Arundhati Dev Borman, Panagiotis I Sergouniotis, Robert H Henderson, Phillip Moradi, Anthony G Robson, Dorothy A Thompson, Andrew R Webster, Anthony T Moore. Invest Ophthalmol Vis Sci 2011
28
100

Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.
Hui Wang, Anneke I den Hollander, Yalda Moayedi, Abuduaini Abulimiti, Yumei Li, Rob W J Collin, Carel B Hoyng, Irma Lopez, Emad B Abboud, Ali A Al-Rajhi,[...]. Am J Hum Genet 2009
83
100

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia.
Douglas M Ruderfer, Elaine T Lim, Giulio Genovese, Jennifer L Moran, Christina M Hultman, Patrick F Sullivan, Steven A McCarroll, Peter Holmans, Pamela Sklar, Shaun M Purcell. Eur J Hum Genet 2015
17
100

A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme.
Chiara Magri, Edoardo Giacopuzzi, Luca La Via, Daniela Bonini, Viola Ravasio, Mohammed E A Elhussiny, Flavia Orizio, Fabrizio Gangemi, Paolo Valsecchi, Roberto Bresciani,[...]. Sci Rep 2018
10
100

Human genetic variation database, a reference database of genetic variations in the Japanese population.
Koichiro Higasa, Noriko Miyake, Jun Yoshimura, Kohji Okamura, Tetsuya Niihori, Hirotomo Saitsu, Koichiro Doi, Masakazu Shimizu, Kazuhiko Nakabayashi, Yoko Aoki,[...]. J Hum Genet 2016
178
100

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
100

SZDB: A Database for Schizophrenia Genetic Research.
Yong Wu, Yong-Gang Yao, Xiong-Jian Luo. Schizophr Bull 2017
61
100

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
100

No association between the brain-derived neurotrophic factor gene and schizophrenia in a Japanese population.
Yuichiro Watanabe, Tatsuyuki Muratake, Naoshi Kaneko, Ayako Nunokawa, Toshiyuki Someya. Schizophr Res 2006
57
100

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
100

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
100

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.
Zhiqiang Li, Jianhua Chen, Yifeng Xu, Qizhong Yi, Weidong Ji, Peng Wang, Jiawei Shen, Zhijian Song, Meng Wang, Ping Yang,[...]. Biol Psychiatry 2016
36
100

Schizophrenia.
Michael J Owen, Akira Sawa, Preben B Mortensen. Lancet 2016
610
100

Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.
Yuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Akitoyo Hishimoto, Kenji Kondo, Jun Egawa, Naoshi Kaneko, Tatsuyuki Muratake, Takeo Saito,[...]. Psychiatry Res 2016
5
100

Uncovering the roles of rare variants in common disease through whole-genome sequencing.
Elizabeth T Cirulli, David B Goldstein. Nat Rev Genet 2010
763
100

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
100

The variant call format and VCFtools.
Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A Albers, Eric Banks, Mark A DePristo, Robert E Handsaker, Gerton Lunter, Gabor T Marth, Stephen T Sherry,[...]. Bioinformatics 2011
100

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.
Ina Giegling, Ladislav Hosak, Rainald Mössner, Alessandro Serretti, Frank Bellivier, Stephan Claes, David A Collier, Alejo Corrales, Lynn E DeLisi, Carla Gallo,[...]. World J Biol Psychiatry 2017
29
100

Exome Sequencing Identifies TENM4 as a Novel Candidate Gene for Schizophrenia in the SCZD2 Locus at 11q14-21.
Chao-Biao Xue, Zhou-Heng Xu, Jun Zhu, Yu Wu, Xi-Hang Zhuang, Qu-Liang Chen, Cai-Ru Wu, Jin-Tao Hu, Hou-Shi Zhou, Wei-Hang Xie,[...]. Front Genet 2019
5
100

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
100

Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina.
Aiden Eblimit, Thanh-Minh T Nguyen, Yiyun Chen, Julian Esteve-Rudd, Hua Zhong, Stef Letteboer, Jeroen Van Reeuwijk, David L Simons, Qian Ding, Ka Man Wu,[...]. Hum Mol Genet 2015
35
100


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
405
100

High-resolution copy number variation analysis of schizophrenia in Japan.
I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Shiino, A Yoshimi, H Kimura, Y Takasaki, C Wang, J Xing,[...]. Mol Psychiatry 2017
56
100

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
100

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
100

Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population.
Ikuo Otsuka, Yuichiro Watanabe, Akitoyo Hishimoto, Shuken Boku, Kentaro Mouri, Kyoichi Shiroiwa, Satoshi Okazaki, Ayako Nunokawa, Osamu Shirakawa, Toshiyuki Someya,[...]. Neuropsychiatr Dis Treat 2015
16
100

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
100

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
100

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
100

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.
S Riazuddin, M Hussain, A Razzaq, Z Iqbal, M Shahzad, D L Polla, Y Song, E van Beusekom, A A Khan, L Tomas-Roca,[...]. Mol Psychiatry 2017
61
100

Predicting the functional effect of amino acid substitutions and indels.
Yongwook Choi, Gregory E Sims, Sean Murphy, Jason R Miller, Agnes P Chan. PLoS One 2012
100

Genetic linkage analysis in the age of whole-genome sequencing.
Jurg Ott, Jing Wang, Suzanne M Leal. Nat Rev Genet 2015
127
100

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Denise Harold, Siobhan Connolly, Brien P Riley, Kenneth S Kendler, Shane E McCarthy, William R McCombie, Alex Richards, Michael J Owen, Michael C O'Donovan, James Walters,[...]. Am J Med Genet B Neuropsychiatr Genet 2019
2
100

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Masashi Ikeda, Atsushi Takahashi, Yoichiro Kamatani, Yukihide Momozawa, Takeo Saito, Kenji Kondo, Ayu Shimasaki, Kohei Kawase, Takaya Sakusabe, Yoshimi Iwayama,[...]. Schizophr Bull 2019
35
100

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
100

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
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,[...]. Nat Genet 2018
521
100

Gene expression elucidates functional impact of polygenic risk for schizophrenia.
Menachem Fromer, Panos Roussos, Solveig K Sieberts, Jessica S Johnson, David H Kavanagh, Thanneer M Perumal, Douglas M Ruderfer, Edwin C Oh, Aaron Topol, Hardik R Shah,[...]. Nat Neurosci 2016
456
100

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
100

The dopamine D3 receptor (DRD3) gene and risk of schizophrenia: case-control studies and an updated meta-analysis.
Ayako Nunokawa, Yuichiro Watanabe, Naoshi Kaneko, Takuro Sugai, Saori Yazaki, Tadao Arinami, Hiroshi Ujike, Toshiya Inada, Nakao Iwata, Hiroshi Kunugi,[...]. Schizophr Res 2010
34
100


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
100

Schizophrenia risk from complex variation of complement component 4.
Aswin Sekar, Allison R Bialas, Heather de Rivera, Avery Davis, Timothy R Hammond, Nolan Kamitaki, Katherine Tooley, Jessy Presumey, Matthew Baum, Vanessa Van Doren,[...]. Nature 2016
100

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
100


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.