A citation-based method for searching scientific literature

Joanna Balcerek, Jing Jiang, Yang Li, Qinqin Jiang, Nicholas Holdreith, Brijendra Singh, Vemika Chandra, Kaosheng Lv, Jian-Gang Ren, Krasimira Rozenova, Weihua Li, Roger A Greenberg, Wei Tong. Nat Commun 2018
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


TSLP: A Key Regulator of Asthma Pathogenesis.
Erin E West, Mohit Kashyap, Warren J Leonard. Drug Discov Today Dis Mech 2012
32
7

Cas proteins: dodgy scaffolding in breast cancer.
Giusy Tornillo, Paola Defilippi, Sara Cabodi. Breast Cancer Res 2014
19
7

A crucial role for the ubiquitously expressed transcription factor Sp1 at early stages of hematopoietic specification.
Jane Gilmour, Salam A Assi, Ulrike Jaegle, Divine Kulu, Harmen van de Werken, Deborah Clarke, David R Westhead, Sjaak Philipsen, Constanze Bonifer. Development 2014
39
7

Atopic asthma after rhinovirus-induced wheezing is associated with DNA methylation change in the SMAD3 gene promoter.
R J Lund, M Osmala, M Malonzo, M Lukkarinen, A Leino, J Salmi, S Vuorikoski, R Turunen, T Vuorinen, C Akdis,[...]. Allergy 2018
32
7

Estrogen defines the dorsal-ventral limit of VEGF regulation to specify the location of the hemogenic endothelial niche.
Kelli J Carroll, Virginie Esain, Maija K Garnaas, Mauricio Cortes, Michael C Dovey, Sahar Nissim, Gregory M Frechette, Sarah Y Liu, Wanda Kwan, Claire C Cutting,[...]. Dev Cell 2014
28
7

TRAIL on trial: preclinical advances in cancer therapy.
Daniel W Stuckey, Khalid Shah. Trends Mol Med 2013
203
7

Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.
Azmeraw T Amare, Ahmad Vaez, Yi-Hsiang Hsu, Nese Direk, Zoha Kamali, David M Howard, Andrew M McIntosh, Henning Tiemeier, Ute Bültmann, Harold Snieder,[...]. Mol Psychiatry 2020
39
7

Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number.
Vijay G Sankaran, Leif S Ludwig, Ewa Sicinska, Jian Xu, Daniel E Bauer, Jennifer C Eng, Heide Christine Patterson, Ryan A Metcalf, Yasodha Natkunam, Stuart H Orkin,[...]. Genes Dev 2012
77
7

Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits.
Jacob C Ulirsch, Satish K Nandakumar, Li Wang, Felix C Giani, Xiaolan Zhang, Peter Rogov, Alexandre Melnikov, Patrick McDonel, Ron Do, Tarjei S Mikkelsen,[...]. Cell 2016
178
7

Identification of genetic variants associated with alternative splicing using sQTLseekeR.
Jean Monlong, Miquel Calvo, Pedro G Ferreira, Roderic Guigó. Nat Commun 2014
73
7

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Katrina M de Lange, Loukas Moutsianas, James C Lee, Christopher A Lamb, Yang Luo, Nicholas A Kennedy, Luke Jostins, Daniel L Rice, Javier Gutierrez-Achury, Sun-Gou Ji,[...]. Nat Genet 2017
497
7

Association between TCF7L2 polymorphisms and breast cancer susceptibility: a meta-analysis.
Feng Wang, Lixin Jiang, Jianlin Li, Xiao Yu, Mingchuan Li, Guochang Wu, Zhenyu Yu, Kai Zhou, Haidi Chu, Huiyuan Zhai. Int J Clin Exp Med 2015
8
12

Alternative Splicing QTLs in European and African Populations.
Halit Ongen, Emmanouil T Dermitzakis. Am J Hum Genet 2015
35
7

rs2476601 polymorphism in PTPN22 is associated with Crohn's disease but not with ulcerative colitis: a meta-analysis of 16,838 cases and 13,356 controls.
Abdellah Hedjoudje, Chérifa Cheurfa, Clément Briquez, Allen Zhang, Stéphane Koch, Lucine Vuitton. Ann Gastroenterol 2017
4
25

HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
Paul C Adams, James S Pankow, James C Barton, Ron T Acton, Cathie Leiendecker-Foster, Gordon D McLaren, Mark Speechley, John H Eckfeldt. Circ Cardiovasc Genet 2009
21
7

Hemolysis in primary lipoprotein lipase deficiency.
B Cantin, S Boudriau, M Bertrand, L D Brun, C Gagné, P A Rogers, M R Ven Murthy, P J Lupien, P Julien. Metabolism 1995
10
10


Diagnostic approaches for inherited hemolytic anemia in the genetic era.
Yonggoo Kim, Joonhong Park, Myungshin Kim. Blood Res 2017
22
7

Asthma Genetics in the Post-GWAS Era.
Carole Ober. Ann Am Thorac Soc 2016
59
7

Genetic Evidence for the Association between Schizophrenia and Breast Cancer.
Jiajun Shi, Lang Wu, Wei Zheng, Wanqing Wen, Shuyang Wang, Xiang Shu, Jirong Long, Chen-Yang Shen, Pei-Ei Wu, Emmanouil Saloustros,[...]. J Psychiatr Brain Sci 2018
7
14

The MR-Base platform supports systematic causal inference across the human phenome.
Gibran Hemani, Jie Zheng, Benjamin Elsworth, Kaitlin H Wade, Valeriia Haberland, Denis Baird, Charles Laurin, Stephen Burgess, Jack Bowden, Ryan Langdon,[...]. Elife 2018
7

C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.
Alfonso Buil, David-Alexandre Trégouët, Juan Carlos Souto, Noémie Saut, Marine Germain, Maxime Rotival, Laurence Tiret, Françcois Cambien, Mark Lathrop, Tanja Zeller,[...]. Blood 2010
51
7

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.
Lavinia Paternoster, Marie Standl, Johannes Waage, Hansjörg Baurecht, Melanie Hotze, David P Strachan, John A Curtin, Klaus Bønnelykke, Chao Tian, Atsushi Takahashi,[...]. Nat Genet 2015
328
7

Eosinophils in atopic dermatitis.
K M Leiferman. J Allergy Clin Immunol 1994
53
7

A Bayesian framework for multiple trait colocalization from summary association statistics.
Claudia Giambartolomei, Jimmy Zhenli Liu, Wen Zhang, Mads Hauberg, Huwenbo Shi, James Boocock, Joe Pickrell, Andrew E Jaffe, Bogdan Pasaniuc, Panos Roussos. Bioinformatics 2018
95
7

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Anubha Mahajan, Daniel Taliun, Matthias Thurner, Neil R Robertson, Jason M Torres, N William Rayner, Anthony J Payne, Valgerdur Steinthorsdottir, Robert A Scott, Niels Grarup,[...]. Nat Genet 2018
701
7


Checking NEKs: Overcoming a Bottleneck in Human Diseases.
Andressa Peres de Oliveira, Luidy Kazuo Issayama, Isadora Carolina Betim Pavan, Fernando Riback Silva, Talita Diniz Melo-Hanchuk, Fernando Moreira Simabuco, Jörg Kobarg. Molecules 2020
18
7


Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry.
Loic Yengo, Julia Sidorenko, Kathryn E Kemper, Zhili Zheng, Andrew R Wood, Michael N Weedon, Timothy M Frayling, Joel Hirschhorn, Jian Yang, Peter M Visscher. Hum Mol Genet 2018
735
7

NEK10 tyrosine phosphorylates p53 and controls its transcriptional activity.
Nasir Haider, Previn Dutt, Bert van de Kooij, Jason Ho, Luis Palomero, Miquel Angel Pujana, Michael Yaffe, Vuk Stambolic. Oncogene 2020
8
12

Calculating statistical power in Mendelian randomization studies.
Marie-Jo A Brion, Konstantin Shakhbazov, Peter M Visscher. Int J Epidemiol 2013
550
7

p38 Mitogen-activated protein kinase inhibition enhances in vitro erythropoiesis of Fanconi anemia, complementation group A-deficient bone marrow cells.
Johanna Svahn, Tiziana Lanza, Keaney Rathbun, Grover Bagby, Silvia Ravera, Fabio Corsolini, Angela Pistorio, Daniela Longoni, Piero Farruggia, Carlo Dufour,[...]. Exp Hematol 2015
10
10

Novel Immune Check-Point Regulators in Tolerance Maintenance.
Yanxia Guo, Adele Y Wang. Front Immunol 2015
29
7


High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors.
Stella T Chou, Tannoa Jackson, Sunitha Vege, Kim Smith-Whitley, David F Friedman, Connie M Westhoff. Blood 2013
293
7


Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesis.
Leif S Ludwig, Hyunjii Cho, Aoi Wakabayashi, Jennifer C Eng, Jacob C Ulirsch, Mark D Fleming, Harvey F Lodish, Vijay G Sankaran. Am J Hematol 2015
11
9


The Coronary Artery Disease-associated Coding Variant in Zinc Finger C3HC-type Containing 1 (ZC3HC1) Affects Cell Cycle Regulation.
Peter D Jones, Michael A Kaiser, Maryam Ghaderi Najafabadi, David G McVey, Allan J Beveridge, Christine L Schofield, Nilesh J Samani, Tom R Webb. J Biol Chem 2016
9
11

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Padhraig Gormley, Verneri Anttila, Bendik S Winsvold, Priit Palta, Tonu Esko, Tune H Pers, Kai-How Farh, Ester Cuenca-Leon, Mikko Muona, Nicholas A Furlotte,[...]. Nat Genet 2016
331
7

Relative contributions of stromal interaction molecule 1 and CalDAG-GEFI to calcium-dependent platelet activation and thrombosis.
F Ahmad, Y Boulaftali, T K Greene, T D Ouellette, M Poncz, S Feske, W Bergmeier. J Thromb Haemost 2011
37
7

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
Mats Nagel, Philip R Jansen, Sven Stringer, Kyoko Watanabe, Christiaan A de Leeuw, Julien Bryois, Jeanne E Savage, Anke R Hammerschlag, Nathan G Skene, Ana B Muñoz-Manchado,[...]. Nat Genet 2018
254
7


Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
Derek Klarin, Scott M Damrauer, Kelly Cho, Yan V Sun, Tanya M Teslovich, Jacqueline Honerlaw, David R Gagnon, Scott L DuVall, Jin Li, Gina M Peloso,[...]. Nat Genet 2018
281
7

Only one independent genetic association with rheumatoid arthritis within the KIAA1109-TENR-IL2-IL21 locus in Caucasian sample sets: confirmation of association of rs6822844 with rheumatoid arthritis at a genome-wide level of significance.
Jade E Hollis-Moffatt, Michael Chen-Xu, Ruth Topless, Nicola Dalbeth, Peter J Gow, Andrew A Harrison, John Highton, Peter B B Jones, Michael Nissen, Malcolm D Smith,[...]. Arthritis Res Ther 2010
32
7


Discovery and refinement of loci associated with lipid levels.
Cristen J Willer, Ellen M Schmidt, Sebanti Sengupta, Gina M Peloso, Stefan Gustafsson, Stavroula Kanoni, Andrea Ganna, Jin Chen, Martin L Buchkovich, Samia Mora,[...]. Nat Genet 2013
7

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
7

Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
Irina Pleines, Joanne Woods, Stephane Chappaz, Verity Kew, Nicola Foad, José Ballester-Beltrán, Katja Aurbach, Chiara Lincetto, Rachael M Lane, Galina Schevzov,[...]. J Clin Invest 2017
41
7


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.