A citation-based method for searching scientific literature

Aitana Alonso-Gonzalez, Manuel Calaza, Cristina Rodriguez-Fontenla, Angel Carracedo. Front Genet 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
780
63


Functional mapping and annotation of genetic associations with FUMA.
Kyoko Watanabe, Erdogan Taskesen, Arjen van Bochoven, Danielle Posthuma. Nat Commun 2017
27


Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
853
27

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
18


Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.
Jon Baio, Lisa Wiggins, Deborah L Christensen, Matthew J Maenner, Julie Daniels, Zachary Warren, Margaret Kurzius-Spencer, Walter Zahorodny, Cordelia Robinson Rosenberg, Tiffany White,[...]. MMWR Surveill Summ 2018
18

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
689
18

Small-conductance Ca2+-activated K+ channel type 2 (SK2) modulates hippocampal learning, memory, and synaptic plasticity.
Rebecca S Hammond, Chris T Bond, Timothy Strassmaier, Thu Jennifer Ngo-Anh, John P Adelman, James Maylie, Robert W Stackman. J Neurosci 2006
167
18


Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels.
Marek Szatanik, Nicolas Vibert, Isabelle Vassias, Jean-Louis Guénet, Daniel Eugène, Catherine de Waele, Jean Jaubert. Neurogenetics 2008
20
18

Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome.
Christiane K Bauer, Pauline E Schneeberger, Fanny Kortüm, Janine Altmüller, Fernando Santos-Simarro, Laura Baker, Jennifer Keller-Ramey, Susan M White, Philippe M Campeau, Karen W Gripp,[...]. Am J Hum Genet 2019
27
18

KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia.
B Balint, R Guerreiro, S Carmona, N Dehghani, A Latorre, C Cordivari, K P Bhatia, J Bras. Eur J Neurol 2020
10
20

Tremor dominant Kyoto (Trdk) rats carry a missense mutation in the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channel.
Takashi Kuramoto, Mayuko Yokoe, Naofumi Kunisawa, Kana Ohashi, Takahito Miyake, Yuki Higuchi, Kazuto Yoshimi, Tomoji Mashimo, Miyuu Tanaka, Mitusru Kuwamura,[...]. Brain Res 2017
11
18

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
18

The familial co-aggregation of ASD and ADHD: a register-based cohort study.
L Ghirardi, I Brikell, R Kuja-Halkola, C M Freitag, B Franke, P Asherson, P Lichtenstein, H Larsson. Mol Psychiatry 2018
108
18

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Elise B Robinson, Beate St Pourcain, Verneri Anttila, Jack A Kosmicki, Brendan Bulik-Sullivan, Jakob Grove, Julian Maller, Kaitlin E Samocha, Stephan J Sanders, Stephan Ripke,[...]. Nat Genet 2016
231
18

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
436
18

Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
18

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
755
18

Genetic contributions to autism spectrum disorder.
A Havdahl, M Niarchou, A Starnawska, M Uddin, C van der Merwe, V Warrier. Psychol Med 2021
20
18


Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity.
Michael J Ombrello, Yohei Kirino, Paul I W de Bakker, Ahmet Gül, Daniel L Kastner, Elaine F Remmers. Proc Natl Acad Sci U S A 2014
79
9


Gene-environment interactions in human diseases.
David J Hunter. Nat Rev Genet 2005
653
9

Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray.
Jonathan R I Coleman, Jack Euesden, Hamel Patel, Amos A Folarin, Stephen Newhouse, Gerome Breen. Brief Funct Genomics 2016
44
9


zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
Jacqueline I Goldstein, Andrew Crenshaw, Jason Carey, George B Grant, Jared Maguire, Menachem Fromer, Colm O'Dushlaine, Jennifer L Moran, Kimberly Chambert, Christine Stevens,[...]. Bioinformatics 2012
141
9

Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index.
Jin Li, Jinxiu Shi, Wei Huang, Jielin Sun, Ying Wu, Qing Duan, Jingchun Luo, Leslie A Lange, Penny Gordon-Larsen, S Lilly Zheng,[...]. Am J Hypertens 2015
11
9

Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.
N R Wray, M L Pergadia, D H R Blackwood, B W J H Penninx, S D Gordon, D R Nyholt, S Ripke, D J MacIntyre, K A McGhee, A W Maclean,[...]. Mol Psychiatry 2012
323
9

Accommodating linkage disequilibrium in genetic-association analyses via ridge regression.
Nathalie Malo, Ondrej Libiger, Nicholas J Schork. Am J Hum Genet 2008
84
9



Sex-specific autosomal genetic effects across 26 human complex traits.
Wan-Yu Lin, Chang-Chuan Chan, Yu-Li Liu, Albert C Yang, Shih-Jen Tsai, Po-Hsiu Kuo. Hum Mol Genet 2020
3
33

Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children.
Tuomas O Kilpeläinen, Lu Qi, Soren Brage, Stephen J Sharp, Emily Sonestedt, Ellen Demerath, Tariq Ahmad, Samia Mora, Marika Kaakinen, Camilla Helene Sandholt,[...]. PLoS Med 2011
351
9

Regularization Paths for Generalized Linear Models via Coordinate Descent.
Jerome Friedman, Trevor Hastie, Rob Tibshirani. J Stat Softw 2010
9

Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests.
Wan-Yu Lin, Ching-Chieh Huang, Yu-Li Liu, Shih-Jen Tsai, Po-Hsiu Kuo. Front Genet 2019
11
9

Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.
Kimberly McAllister, Leah E Mechanic, Christopher Amos, Hugues Aschard, Ian A Blair, Nilanjan Chatterjee, David Conti, W James Gauderman, Li Hsu, Carolyn M Hutter,[...]. Am J Epidemiol 2017
84
9

Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry.
Shafqat Ahmad, Gull Rukh, Tibor V Varga, Ashfaq Ali, Azra Kurbasic, Dmitry Shungin, Ulrika Ericson, Robert W Koivula, Audrey Y Chu, Lynda M Rose,[...]. PLoS Genet 2013
139
9

Comparison of weighting approaches for genetic risk scores in gene-environment interaction studies.
Anke Hüls, Ursula Krämer, Christopher Carlsten, Tamara Schikowski, Katja Ickstadt, Holger Schwender. BMC Genet 2017
32
9


Physical activity attenuates the body mass index-increasing influence of genetic variation in the FTO gene.
Karani S Vimaleswaran, Shengxu Li, Jing Hua Zhao, Jian'an Luan, Sheila A Bingham, Kay-Tee Khaw, Ulf Ekelund, Nicholas J Wareham, Ruth J F Loos. Am J Clin Nutr 2009
135
9


A unified set-based test with adaptive filtering for gene-environment interaction analyses.
Qianying Liu, Lin S Chen, Dan L Nicolae, Brandon L Pierce. Biometrics 2016
8
12

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
Jennifer K Lowe, Julian B Maller, Itsik Pe'er, Benjamin M Neale, Jacqueline Salit, Eimear E Kenny, Jessica L Shea, Ralph Burkhardt, J Gustav Smith, Weizhen Ji,[...]. PLoS Genet 2009
68
9

Assessing the effect of interaction between an FTO variant (rs9939609) and physical activity on obesity in 15,925 Swedish and 2,511 Finnish adults.
A Jonsson, F Renström, V Lyssenko, E C Brito, B Isomaa, G Berglund, P M Nilsson, L Groop, P W Franks. Diabetologia 2009
64
9

The genetics of obesity: FTO leads the way.
Katherine A Fawcett, Inês Barroso. Trends Genet 2010
206
9

From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era.
Alan G Baxter, Margaret A Jordan. Rev Diabet Stud 2012
10
10

Two-stage testing procedures with independent filtering for genome-wide gene-environment interaction.
James Y Dai, Charles Kooperberg, Michael Leblanc, Ross L Prentice. Biometrika 2012
71
9


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.