A citation-based method for searching scientific literature

Joseph Rosenbluh, Deepak Nijhawan, Zhao Chen, Kwok-Kin Wong, Kenkichi Masutomi, William C Hahn. PLoS One 2011
Times Cited: 34







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



Times Cited
  Times     Co-cited
Similarity


Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
Ewan Birney, John A Stamatoyannopoulos, Anindya Dutta, Roderic Guigó, Thomas R Gingeras, Elliott H Margulies, Zhiping Weng, Michael Snyder, Emmanouil T Dermitzakis, Robert E Thurman,[...]. Nature 2007
2

MicroRNA-206 acts as a tumor suppressor in bladder cancer via targeting YRDC.
Bisheng Huang, Wei Zhai, Guanghui Hu, Chi Huang, Tiancheng Xie, Jingwei Zhang, Yunfei Xu. Am J Transl Res 2016
13
7


NF-kappaB in cancer: from innocent bystander to major culprit.
Michael Karin, Yixue Cao, Florian R Greten, Zhi-Wei Li. Nat Rev Cancer 2002
2

GADD45 proteins: central players in tumorigenesis.
R E Tamura, J F de Vasconcellos, D Sarkar, T A Libermann, P B Fisher, L F Zerbini. Curr Mol Med 2012
151
2

Altered expression of long noncoding RNAs in patients with major depressive disorder.
Tomoe Seki, Hirotaka Yamagata, Shusaku Uchida, Chong Chen, Ayumi Kobayashi, Masaaki Kobayashi, Kenichiro Harada, Koji Matsuo, Yoshifumi Watanabe, Shin Nakagawa. J Psychiatr Res 2019
7
14


Non-canonical NF-κB signaling pathway.
Shao-Cong Sun. Cell Res 2011
575
2


Non-coding RNA: what is functional and what is junk?
Alexander F Palazzo, Eliza S Lee. Front Genet 2015
267
2

Long Noncoding RNA RMRP Suppresses the Tumorigenesis of Hepatocellular Carcinoma Through Targeting microRNA-766.
Cunhua Shao, Gongpan Liu, Xiaobin Zhang, Anyun Li, Xingjun Guo. Onco Targets Ther 2020
2
50

Heat Shock Proteins and Cancer.
Jianming Wu, Tuoen Liu, Zechary Rios, Qibing Mei, Xiukun Lin, Shousong Cao. Trends Pharmacol Sci 2017
192
2

lncRNA RMRP Prevents Mitochondrial Dysfunction and Cardiomyocyte Apoptosis via the miR-1-5p/hsp70 Axis in LPS-Induced Sepsis Mice.
Ying Han, Yixin Cai, Xiaoquan Lai, Zhenling Wang, Shiqing Wei, Kun Tan, Min Xu, Hongyan Xie. Inflammation 2020
10
10


Liraglutide improves atherosclerosis by regulating long non-coding RNA RMRP/miR-128-1-5P/Gadd45g axis.
J-H An, Z-Y Chen, Q-L Ma, Y-B Li, F-W Shi. Eur Rev Med Pharmacol Sci 2020
1
100

MicroRNA: Biogenesis, Function and Role in Cancer.
Leigh-Ann Macfarlane, Paul R Murphy. Curr Genomics 2010
769
2

Somatic mutations in long-non-coding RNA RMRP in acute leukemias.
Hyun Ji Son, Eun Ji Choi, Nam Jin Yoo, Sug Hyung Lee. Pathol Res Pract 2019
3
33

Vascular and pulmonary comorbidities in children with congenital EA/TEF.
Thomas S Poore, Jason P Weinman, Elyse Handley, Todd Wine, Sparrow Helland, Benjamin Corbett, Natalie Antoniolli, Stig Somme, Joel Friedlander, Jeremy D Prager,[...]. Pediatr Pulmonol 2021
1
100

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Ella M M A Martin, Annabelle Enriquez, Duncan B Sparrow, David T Humphreys, Aideen M McInerney-Leo, Paul J Leo, Emma L Duncan, Kavitha R Iyer, Joelene A Greasby, Eddie Ip,[...]. Hum Mol Genet 2020
1
100

The organizer factors Chordin and Noggin are required for mouse forebrain development.
D Bachiller, J Klingensmith, C Kemp, J A Belo, R M Anderson, S R May, J A McMahon, A P McMahon, R M Harland, J Rossant,[...]. Nature 2000
380
2

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula.
Erwin Brosens, Florian Marsch, Elisabeth M de Jong, Hitisha P Zaveri, Alina C Hilger, Vera Gisela Choinitzki, Alice Hölscher, Per Hoffmann, Stefan Herms, Thomas M Boemers,[...]. Eur J Hum Genet 2016
13
7

Genetic players in esophageal atresia and tracheoesophageal fistula.
Han G Brunner, Hans van Bokhoven. Curr Opin Genet Dev 2005
46
2


Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association.
Elisabeth M de Jong, Janine F Felix, Jacqueline A Deurloo, Marieke F van Dooren, Daniël C Aronson, Claudine P Torfs, Hugo A Heij, Dick Tibboel. Birth Defects Res A Clin Mol Teratol 2008
53
2

Mutational analysis of NOG in esophageal atresia and tracheoesophageal fistula patients.
Andrew J Murphy, Yina Li, Joshua B Pietsch, Chin Chiang, Harold N Lovvorn. Pediatr Surg Int 2012
5
20

Sonic hedgehog is essential to foregut development.
Y Litingtung, L Lei, H Westphal, C Chiang. Nat Genet 1998
502
2


Modelling human hepato-biliary-pancreatic organogenesis from the foregut-midgut boundary.
Hiroyuki Koike, Kentaro Iwasawa, Rie Ouchi, Mari Maezawa, Kirsten Giesbrecht, Norikazu Saiki, Autumn Ferguson, Masaki Kimura, Wendy L Thompson, James M Wells,[...]. Nature 2019
60
2

De novo GLI3 mutation in esophageal atresia: reproducing the phenotypic spectrum of Gli3 defects in murine models.
Lin Yang, Chun Shen, Mei Mei, Guodong Zhan, Yunke Zhao, Huijun Wang, Guoying Huang, Zilong Qiu, Weineng Lu, Wenhao Zhou. Biochim Biophys Acta 2014
6
16

The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome.
Daniel Bachiller, John Klingensmith, Natalya Shneyder, Uyen Tran, Ryan Anderson, Janet Rossant, E M De Robertis. Development 2003
114
2

Disruption of a hedgehog-foxf1-rspo2 signaling axis leads to tracheomalacia and a loss of sox9+ tracheal chondrocytes.
Talia Nasr, Andrea M Holderbaum, Praneet Chaturvedi, Kunal Agarwal, Jessica L Kinney, Keziah Daniels, Stephen L Trisno, Vladimir Ustiyan, John M Shannon, James M Wells,[...]. Dis Model Mech 2020
2
50

A Retinoic Acid-Hedgehog Cascade Coordinates Mesoderm-Inducing Signals and Endoderm Competence during Lung Specification.
Scott A Rankin, Lu Han, Kyle W McCracken, Alan P Kenny, Christopher T Anglin, Emily A Grigg, Calyn M Crawford, James M Wells, John M Shannon, Aaron M Zorn. Cell Rep 2016
50
2

Development and stem cells of the esophagus.
Yongchun Zhang, Ming Jiang, Eugene Kim, Sijie Lin, Kuancan Liu, Xiaopeng Lan, Jianwen Que. Semin Cell Dev Biol 2017
30
3

Engineered human pluripotent-stem-cell-derived intestinal tissues with a functional enteric nervous system.
Michael J Workman, Maxime M Mahe, Stephen Trisno, Holly M Poling, Carey L Watson, Nambirajan Sundaram, Ching-Fang Chang, Jacqueline Schiesser, Philippe Aubert, Edouard G Stanley,[...]. Nat Med 2017
234
2

In vitro generation of human pluripotent stem cell derived lung organoids.
Briana R Dye, David R Hill, Michael A H Ferguson, Yu-Hwai Tsai, Melinda S Nagy, Rachel Dyal, James M Wells, Christopher N Mayhew, Roy Nattiv, Ophir D Klein,[...]. Elife 2015
320
2

Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
Marie Cognet, Agnés Nougayrede, Valérie Malan, Patrick Callier, Celia Cretolle, Laurence Faivre, David Genevieve, Alice Goldenberg, Delphine Heron, Sandra Mercier,[...]. Eur J Hum Genet 2011
16
6


Signaling through BMP receptors promotes respiratory identity in the foregut via repression of Sox2.
Eric T Domyan, Elisabetta Ferretti, Kurt Throckmorton, Yuji Mishina, Silvia K Nicolis, Xin Sun. Development 2011
116
2

Single cell transcriptomics identifies a signaling network coordinating endoderm and mesoderm diversification during foregut organogenesis.
Lu Han, Praneet Chaturvedi, Keishi Kishimoto, Hiroyuki Koike, Talia Nasr, Kentaro Iwasawa, Kirsten Giesbrecht, Phillip C Witcher, Alexandra Eicher, Lauren Haines,[...]. Nat Commun 2020
16
6

De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene.
Benjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, Amelia A Keaton, Nneamaka B Agochukwu, Manu S Raam, Hannah E Carlson-Donohoe, Aparna Kamat, Settara C Chandrasekharappa. Birth Defects Res A Clin Mol Teratol 2011
19
5

Associated anomalies in cases with esophageal atresia.
Claude Stoll, Yves Alembik, Beatrice Dott, Marie-Paule Roth. Am J Med Genet A 2017
15
6

Tissue morphogenesis and vascular stability require the Frem2 protein, product of the mouse myelencephalic blebs gene.
John R Timmer, Tracy W Mak, Katia Manova, Kathryn V Anderson, Lee Niswander. Proc Natl Acad Sci U S A 2005
40
2


Specificity of sensory-motor connections encoded by Sema3e-Plxnd1 recognition.
Eline Pecho-Vrieseling, Markus Sigrist, Yutaka Yoshida, Thomas M Jessell, Silvia Arber. Nature 2009
124
2

Tracheoesophageal anomalies in oculoauriculovertebral (Goldenhar) spectrum.
R Sutphen, E Galan-Gomez, X Cortada, P N Newkirk, B G Kousseff. Clin Genet 1995
23
4

Structural and numerical changes of chromosome X in patients with esophageal atresia.
Erwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, Bert H Eussen, Barbara D'haene, Elfride De Baere, Hannah Verdin, Pino J Poddighe, Robert-Jan Galjaard, Joost Gribnau,[...]. Eur J Hum Genet 2014
10
10

Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects.
Susan McLeskey Kiefer, Kevin K Ohlemiller, Jing Yang, Bradley W McDill, Jürgen Kohlhase, Michael Rauchman. Hum Mol Genet 2003
90
2

Unexpected tracheal agenesis with prenatal diagnosis of aortic coarctation, lung hyperecogenicity and polyhydramnios: a case report.
Alessandro Perri, Maria Letizia Patti, Annamaria Sbordone, Giovanni Vento, Rita Luciano. Ital J Pediatr 2020
2
50

Barx1-mediated inhibition of Wnt signaling in the mouse thoracic foregut controls tracheo-esophageal septation and epithelial differentiation.
Janghee Woo, Isabelle Miletich, Byeong-Moo Kim, Paul T Sharpe, Ramesh A Shivdasani. PLoS One 2011
44
2

E3 ubiquitin ligase MDM2 acts through p53 to control respiratory progenitor cell number and lung size.
Pengfei Sui, Rongbo Li, Yan Zhang, Chunting Tan, Ankur Garg, Jamie M Verheyden, Xin Sun. Development 2019
3
33


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.