A citation-based method for searching scientific literature

Leanna M Hernandez, Minsoo Kim, Gil D Hoftman, Jillian R Haney, Luis de la Torre-Ubieta, Bogdan Pasaniuc, Michael J Gandal. Biol Psychiatry 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
Michael J Gandal, Pan Zhang, Evi Hadjimichael, Rebecca L Walker, Chao Chen, Shuang Liu, Hyejung Won, Harm van Bakel, Merina Varghese, Yongjun Wang,[...]. Science 2018
298
40

Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
622
40

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.
Donna M Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An, Brooke Sheppard, Minshi Peng, Zhen Li, Claudia Dastmalchi, Gabriel Santpere, André M M Sousa,[...]. Cell Rep 2020
18
40

Adult mouse cortical cell taxonomy revealed by single cell transcriptomics.
Bosiljka Tasic, Vilas Menon, Thuc Nghi Nguyen, Tae Kyung Kim, Tim Jarsky, Zizhen Yao, Boaz Levi, Lucas T Gray, Staci A Sorensen, Tim Dolbeare,[...]. Nat Neurosci 2016
687
40

Parsing the Functional Impact of Noncoding Genetic Variants in the Brain Epigenome.
Samuel K Powell, Callan O'Shea, Kristen J Brennand, Schahram Akbarian. Biol Psychiatry 2021
2
100

Integrative analysis of 111 reference human epigenomes.
Anshul Kundaje, Wouter Meuleman, Jason Ernst, Misha Bilenky, Angela Yen, Alireza Heravi-Moussavi, Pouya Kheradpour, Zhizhuo Zhang, Jianrong Wang, Michael J Ziller,[...]. Nature 2015
20

Comprehensive functional genomic resource and integrative model for the human brain.
Daifeng Wang, Shuang Liu, Jonathan Warrell, Hyejung Won, Xu Shi, Fabio C P Navarro, Declan Clarke, Mengting Gu, Prashant Emani, Yucheng T Yang,[...]. Science 2018
214
20

Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure.
Christiaan A de Leeuw, Sven Stringer, Ilona A Dekkers, Tom Heskes, Danielle Posthuma. Nat Commun 2018
13
20


ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
20


The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
20

MINT, the molecular interaction database: 2012 update.
Luana Licata, Leonardo Briganti, Daniele Peluso, Livia Perfetto, Marta Iannuccelli, Eugenia Galeota, Francesca Sacco, Anita Palma, Aurelio Pio Nardozza, Elena Santonico,[...]. Nucleic Acids Res 2012
567
20

Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression.
Benjamin J Schmiedel, Divya Singh, Ariel Madrigal, Alan G Valdovino-Gonzalez, Brandie M White, Jose Zapardiel-Gonzalo, Brendan Ha, Gokmen Altay, Jason A Greenbaum, Graham McVicker,[...]. Cell 2018
148
20


Alternative splicing in disease and therapy.
Mariano A Garcia-Blanco, Andrew P Baraniak, Erika L Lasda. Nat Biotechnol 2004
388
20

Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics.
Wenan Chen, Beth R Larrabee, Inna G Ovsyannikova, Richard B Kennedy, Iana H Haralambieva, Gregory A Poland, Daniel J Schaid. Genetics 2015
87
20

Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes.
Inti Pedroso, Anbarasu Lourdusamy, Marcella Rietschel, Markus M Nöthen, Sven Cichon, Peter McGuffin, Ammar Al-Chalabi, Michael R Barnes, Gerome Breen. Biol Psychiatry 2012
44
20

Mapping the Mouse Cell Atlas by Microwell-Seq.
Xiaoping Han, Renying Wang, Yincong Zhou, Lijiang Fei, Huiyu Sun, Shujing Lai, Assieh Saadatpour, Ziming Zhou, Haide Chen, Fang Ye,[...]. Cell 2018
377
20

FINEMAP: efficient variable selection using summary data from genome-wide association studies.
Christian Benner, Chris C A Spencer, Aki S Havulinna, Veikko Salomaa, Samuli Ripatti, Matti Pirinen. Bioinformatics 2016
170
20


The statistical properties of gene-set analysis.
Christiaan A de Leeuw, Benjamin M Neale, Tom Heskes, Danielle Posthuma. Nat Rev Genet 2016
110
20

Spatio-temporal transcriptome of the human brain.
Hyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, Ying Zhu, Xuming Xu, Mingfeng Li, André M M Sousa, Mihovil Pletikos, Kyle A Meyer, Goran Sedmak,[...]. Nature 2011
20

Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits.
Ayellet V Segrè, Leif Groop, Vamsi K Mootha, Mark J Daly, David Altshuler. PLoS Genet 2010
325
20

Analysing biological pathways in genome-wide association studies.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nat Rev Genet 2010
554
20

Pathguide: a pathway resource list.
Gary D Bader, Michael P Cary, Chris Sander. Nucleic Acids Res 2006
241
20

Functional mapping and annotation of genetic associations with FUMA.
Kyoko Watanabe, Erdogan Taskesen, Arjen van Bochoven, Danielle Posthuma. Nat Commun 2017
635
20

The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
20



DrugBank: a comprehensive resource for in silico drug discovery and exploration.
David S Wishart, Craig Knox, An Chi Guo, Savita Shrivastava, Murtaza Hassanali, Paul Stothard, Zhan Chang, Jennifer Woolsey. Nucleic Acids Res 2006
20

Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.
Alexis Battle, Sara Mostafavi, Xiaowei Zhu, James B Potash, Myrna M Weissman, Courtney McCormick, Christian D Haudenschild, Kenneth B Beckman, Jianxin Shi, Rui Mei,[...]. Genome Res 2014
293
20

Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder.
Peter Holmans, Elaine K Green, Jaspreet Singh Pahwa, Manuel A R Ferreira, Shaun M Purcell, Pamela Sklar, Michael J Owen, Michael C O'Donovan, Nick Craddock. Am J Hum Genet 2009
301
20

Using genome-wide pathway analysis to unravel the etiology of complex diseases.
Clara C Elbers, Kristel R van Eijk, Lude Franke, Flip Mulder, Yvonne T van der Schouw, Cisca Wijmenga, N Charlotte Onland-Moret. Genet Epidemiol 2009
147
20

GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm.
Leonardo Bottolo, Marc Chadeau-Hyam, David I Hastie, Tanja Zeller, Benoit Liquet, Paul Newcombe, Loic Yengo, Philipp S Wild, Arne Schillert, Andreas Ziegler,[...]. PLoS Genet 2013
37
20

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Masahiro Kanai, Masato Akiyama, Atsushi Takahashi, Nana Matoba, Yukihide Momozawa, Masashi Ikeda, Nakao Iwata, Shiro Ikegawa, Makoto Hirata, Koichi Matsuda,[...]. Nat Genet 2018
206
20

Partitioning heritability by functional annotation using genome-wide association summary statistics.
Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh,[...]. Nat Genet 2015
712
20

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
20


TIGAR: An Improved Bayesian Tool for Transcriptomic Data Imputation Enhances Gene Mapping of Complex Traits.
Sini Nagpal, Xiaoran Meng, Michael P Epstein, Lam C Tsoi, Matthew Patrick, Greg Gibson, Philip L De Jager, David A Bennett, Aliza P Wingo, Thomas S Wingo,[...]. Am J Hum Genet 2019
20
20

Identifying a high fraction of the human genome to be under selective constraint using GERP++.
Eugene V Davydov, David L Goode, Marina Sirota, Gregory M Cooper, Arend Sidow, Serafim Batzoglou. PLoS Comput Biol 2010
848
20

A Compendium of Chromatin Contact Maps Reveals Spatially Active Regions in the Human Genome.
Anthony D Schmitt, Ming Hu, Inkyung Jung, Zheng Xu, Yunjiang Qiu, Catherine L Tan, Yun Li, Shin Lin, Yiing Lin, Cathy L Barr,[...]. Cell Rep 2016
311
20

Prioritizing GWAS results: A review of statistical methods and recommendations for their application.
Rita M Cantor, Kenneth Lange, Janet S Sinsheimer. Am J Hum Genet 2010
367
20

A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation.
Damon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman, Andrew G Elkins, Xu Shi, Jason L Stein, Celine K Vuong, Susanne Nichterwitz, Melinda Gevorgian, Carli K Opland,[...]. Neuron 2019
85
20

Mapping cis- and trans-regulatory effects across multiple tissues in twins.
Elin Grundberg, Kerrin S Small, Åsa K Hedman, Alexandra C Nica, Alfonso Buil, Sarah Keildson, Jordana T Bell, Tsun-Po Yang, Eshwar Meduri, Amy Barrett,[...]. Nat Genet 2012
504
20

A statistical framework for cross-tissue transcriptome-wide association analysis.
Yiming Hu, Mo Li, Qiongshi Lu, Haoyi Weng, Jiawei Wang, Seyedeh M Zekavat, Zhaolong Yu, Boyang Li, Jianlei Gu, Sydney Muchnik,[...]. Nat Genet 2019
67
20

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
Jie Zheng, A Mesut Erzurumluoglu, Benjamin L Elsworth, John P Kemp, Laurence Howe, Philip C Haycock, Gibran Hemani, Katherine Tansey, Charles Laurin, Beate St Pourcain,[...]. Bioinformatics 2017
373
20

New classification for neurodevelopmental disorders in DSM-5.
James C Harris. Curr Opin Psychiatry 2014
16
20

Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, Oleg V Evgrafov, Forrest O Gulden, Sirisha Pochareddy, Susan M Sunkin, Zhen Li, Yurae Shin, Ying Zhu,[...]. Science 2018
178
20

Genetic mapping of cell type specificity for complex traits.
Kyoko Watanabe, Maša Umićević Mirkov, Christiaan A de Leeuw, Martijn P van den Heuvel, Danielle Posthuma. Nat Commun 2019
31
20


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.