A citation-based method for searching scientific literature

James J Ashton, Enrico Mossotto, Imogen S Stafford, Rachel Haggarty, Tracy A F Coelho, Akshay Batra, Nadeem A Afzal, Matthew Mort, David Bunyan, Robert Mark Beattie, Sarah Ennis. Clin Transl Gastroenterol 2020
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity



Dissecting the role of the gut microbiota and diet on visceral fat mass accumulation.
Caroline I Le Roy, Ruth C E Bowyer, Juan E Castillo-Fernandez, Tess Pallister, Cristina Menni, Claire J Steves, Sarah E Berry, Tim D Spector, Jordana T Bell. Sci Rep 2019
27
6

The human gene damage index as a gene-level approach to prioritizing exome variants.
Yuval Itan, Lei Shang, Bertrand Boisson, Etienne Patin, Alexandre Bolze, Marcela Moncada-Vélez, Eric Scott, Michael J Ciancanelli, Fabien G Lafaille, Janet G Markle,[...]. Proc Natl Acad Sci U S A 2015
150
6

NF-kappaB in inflammatory bowel disease.
I Atreya, R Atreya, M F Neurath. J Intern Med 2008
499
6

g:Profiler: a web server for functional enrichment analysis and conversions of gene lists (2019 update).
Uku Raudvere, Liis Kolberg, Ivan Kuzmin, Tambet Arak, Priit Adler, Hedi Peterson, Jaak Vilo. Nucleic Acids Res 2019
6

Inflammatory glycoproteins in cardiometabolic disorders, autoimmune diseases and cancer.
Margery A Connelly, Eke G Gruppen, James D Otvos, Robin P F Dullaart. Clin Chim Acta 2016
49
6

Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases.
Mathias Chamaillard, Dana Philpott, Stephen E Girardin, Habib Zouali, Suzanne Lesage, Fabrice Chareyre, The Hung Bui, Marco Giovannini, Ulrich Zaehringer, Virginie Penard-Lacronique,[...]. Proc Natl Acad Sci U S A 2003
249
6

Differential effects of NOD2 variants on Crohn's disease risk and phenotype in diverse populations: a metaanalysis.
Michael Economou, Thomas A Trikalinos, Konstantinos T Loizou, Epameinondas V Tsianos, John P A Ioannidis. Am J Gastroenterol 2004
335
6


Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
Jeffrey C Barrett, Sarah Hansoul, Dan L Nicolae, Judy H Cho, Richard H Duerr, John D Rioux, Steven R Brant, Mark S Silverberg, Kent D Taylor, M Michael Barmada,[...]. Nat Genet 2008
6

CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.
T Heliö, L Halme, M Lappalainen, H Fodstad, P Paavola-Sakki, U Turunen, M Färkkilä, T Krusius, K Kontula. Gut 2003
187
6

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.
Steven R Brant, David T Okou, Claire L Simpson, David J Cutler, Talin Haritunians, Jonathan P Bradfield, Pankaj Chopra, Jarod Prince, Ferdouse Begum, Archana Kumar,[...]. Gastroenterology 2017
87
6

The importance of phase information for human genomics.
Ryan Tewhey, Vikas Bansal, Ali Torkamani, Eric J Topol, Nicholas J Schork. Nat Rev Genet 2011
162
6

The prognostic power of the NOD2 genotype for complicated Crohn's disease: a meta-analysis.
Jeremy Adler, Sujal C Rangwalla, Ben A Dwamena, Peter D R Higgins. Am J Gastroenterol 2011
123
6

Crohn's Disease Susceptibility and Onset Are Strongly Related to Three NOD2 Gene Haplotypes.
Marta Kaczmarek-Ryś, Szymon Tytus Hryhorowicz, Emilia Lis, Tomasz Banasiewicz, Jacek Paszkowski, Maciej Borejsza-Wysocki, Jarosław Walkowiak, Wojciech Cichy, Piotr Krokowicz, Elżbieta Czkwianianc,[...]. J Clin Med 2021
4
25

Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract.
Koichi S Kobayashi, Mathias Chamaillard, Yasunori Ogura, Octavian Henegariu, Naohiro Inohara, Gabriel Nuñez, Richard A Flavell. Science 2005
6

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Andre Franke, Dermot P B McGovern, Jeffrey C Barrett, Kai Wang, Graham L Radford-Smith, Tariq Ahmad, Charlie W Lees, Tobias Balschun, James Lee, Rebecca Roberts,[...]. Nat Genet 2010
6

NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population.
R W L Leong, A Armuzzi, T Ahmad, M L Wong, P Tse, D P Jewell, J J Y Sung. Aliment Pharmacol Ther 2003
184
6

Monocyte-derived dendritic cells from Crohn patients show differential NOD2/CARD15-dependent immune responses to bacteria.
Valentina Salucci, Monica Rimoldi, Chiara Penati, Gianluca M Sampietro, Marjan Maria van Duist, Gianluca Matteoli, Simone Saibeni, Maurizio Vecchi, Sandro Ardizzone, Gabriele Bianchi Porro,[...]. Inflamm Bowel Dis 2008
28
6

Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype.
Martina Girardelli, Claudia Loganes, Alessia Pin, Elisabetta Stacul, Eva Decleva, Diego Vozzi, Gabriele Baj, Costantino De Giacomo, Alberto Tommasini, Anna Monica Bianco. Inflamm Bowel Dis 2018
10
10

NOD2 and Crohn's disease: loss or gain of function?
Lars Eckmann, Michael Karin. Immunity 2005
146
6

A catalog of GWAS fine-mapping efforts in autoimmune disease.
Minal Caliskan, Christopher D Brown, Joseph C Maranville. Am J Hum Genet 2021
12
8


Regulation of IL-8 and IL-1beta expression in Crohn's disease associated NOD2/CARD15 mutations.
Jing Li, Thomas Moran, Eric Swanson, Christina Julian, Jeremy Harris, Denise K Bonen, Matija Hedl, Dan L Nicolae, Clara Abraham, Judy H Cho. Hum Mol Genet 2004
220
6

Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognition.
Tsuyoshi Tanabe, Mathias Chamaillard, Yasunori Ogura, Li Zhu, Su Qiu, Junya Masumoto, Partho Ghosh, Anthony Moran, Martina M Predergast, Gerard Tromp,[...]. EMBO J 2004
277
6

Highly accurate protein structure prediction with AlphaFold.
John Jumper, Richard Evans, Alexander Pritzel, Tim Green, Michael Figurnov, Olaf Ronneberger, Kathryn Tunyasuvunakool, Russ Bates, Augustin Žídek, Anna Potapenko,[...]. Nature 2021
6

Mapping of a susceptibility locus for Crohn's disease on chromosome 16.
J P Hugot, P Laurent-Puig, C Gower-Rousseau, J M Olson, J C Lee, L Beaugerie, I Naom, J L Dupas, A Van Gossum, M Orholm,[...]. Nature 1996
765
6

Lack of common NOD2 variants in Japanese patients with Crohn's disease.
Nagamu Inoue, Kazuo Tamura, Yoshitaka Kinouchi, Yoshihiro Fukuda, Seiichi Takahashi, Yasunori Ogura, Naohiro Inohara, Gabriel Núñez, Yusuke Kishi, Yuji Koike,[...]. Gastroenterology 2002
370
6

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Jochen Hampe, Andre Franke, Philip Rosenstiel, Andreas Till, Markus Teuber, Klaus Huse, Mario Albrecht, Gabriele Mayr, Francisco M De La Vega, Jason Briggs,[...]. Nat Genet 2007
6

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.
Jean-Pierre Hugot, Isabelle Zaccaria, Juleen Cavanaugh, Huiying Yang, Séverine Vermeire, Maarit Lappalainen, Stefan Schreiber, Vito Annese, Derek P Jewell, Elizabeth V Fowler,[...]. Am J Gastroenterol 2007
104
6

Heritability in inflammatory bowel disease: from the first twin study to genome-wide association studies.
Hannah Gordon, Frederik Trier Moller, Vibeke Andersen, Marcus Harbord. Inflamm Bowel Dis 2015
53
6

ClinVar: public archive of interpretations of clinically relevant variants.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover,[...]. Nucleic Acids Res 2016
6

Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease.
Heather Elding, Winston Lau, Dallas M Swallow, Nikolas Maniatis. Am J Hum Genet 2011
24
6

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
Guillem de Valles-Ibáñez, Ana Esteve-Solé, Mònica Piquer, E Azucena González-Navarro, Jessica Hernandez-Rodriguez, Hafid Laayouni, Eva González-Roca, Ana María Plaza-Martin, Ángela Deyà-Martínez, Andrea Martín-Nalda,[...]. Front Immunol 2018
91
6

Explainable deep neural networks for novel viral genome prediction.
Chandra Mohan Dasari, Raju Bhukya. Appl Intell (Dordr) 2022
6
16

EL_LSTM: Prediction of DNA-Binding Residue from Protein Sequence by Combining Long Short-Term Memory and Ensemble Learning.
Jiyun Zhou, Qin Lu, Ruifeng Xu, Lin Gui, Hongpeng Wang. IEEE/ACM Trans Comput Biol Bioinform 2020
8
12

Monogenic Lupus: A Developing Paradigm of Disease.
Jessie M Alperin, Lourdes Ortiz-Fernández, Amr H Sawalha. Front Immunol 2018
60
6

A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia.
Xingkun Yang, Qinghua Zhou, Wanjun Zhou, Mei Zhong, Xiaoling Guo, Xiaofeng Wang, Xin Fan, Shanhuo Yan, Liyan Li, Yunli Lai,[...]. Adv Sci (Weinh) 2019
16
6

cfDNA screening and diagnosis of monogenic disorders - where are we heading?
Eunice Ka Long Chiu, Winnie Wai In Hui, Rossa Wai Kwun Chiu. Prenat Diagn 2018
31
6

Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2.
S Butscheidt, A Delsmann, T Rolvien, F Barvencik, M Al-Bughaili, S Mundlos, T Schinke, M Amling, U Kornak, R Oheim. Osteoporos Int 2018
27
6

A systematic review of monogenic etiologies of nonimmune hydrops fetalis.
Andrea M Quinn, Breanna N Valcarcel, Mona M Makhamreh, Huda B Al-Kouatly, Seth I Berger. Genet Med 2021
15
6

Sickle cell disease: a review for the internist.
Valeria Maria Pinto, Manuela Balocco, Sabrina Quintino, Gian Luca Forni. Intern Emerg Med 2019
23
6

Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus.
Jonas Carlsson Almlöf, Sara Nystedt, Dag Leonard, Maija-Leena Eloranta, Giorgia Grosso, Christopher Sjöwall, Anders A Bengtsson, Andreas Jönsen, Iva Gunnarsson, Elisabet Svenungsson,[...]. Hum Genet 2019
34
6

Molecular Basis and Genetic Modifiers of Thalassemia.
Sachith Mettananda, Douglas R Higgs. Hematol Oncol Clin North Am 2018
60
6

Monogenetic disorders of the cholesterol metabolism and premature cardiovascular disease.
Marianne C van Schie, Sjaam Jainandunsing, Jeanine E Roeters van Lennep. Eur J Pharmacol 2017
6
16

Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Mari E K Niemi, Hilary C Martin, Daniel L Rice, Giuseppe Gallone, Scott Gordon, Martin Kelemen, Kerrie McAloney, Jeremy McRae, Elizabeth J Radford, Sui Yu,[...]. Nature 2018
142
6

Monogenic variants in dystonia: an exome-wide sequencing study.
Michael Zech, Robert Jech, Sylvia Boesch, Matej Škorvánek, Sandrina Weber, Matias Wagner, Chen Zhao, Angela Jochim, Ján Necpál, Yasemin Dincer,[...]. Lancet Neurol 2020
70
6

A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants.
Javier A López-Rivera, Eduardo Pérez-Palma, Joseph Symonds, Amanda S Lindy, Dianalee A McKnight, Costin Leu, Sameer Zuberi, Andreas Brunklaus, Rikke S Møller, Dennis Lal. Brain 2020
25
6

Gene therapy for sickle cell disease: An update.
Selami Demirci, Naoya Uchida, John F Tisdale. Cytotherapy 2018
54
6

Application of full-genome analysis to diagnose rare monogenic disorders.
Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, Michal Levy-Sakin, Michelle Verghese, Anne Slavotinek, Renata C Gallagher, Bryce A Mendelsohn, Jessica Tenney, Daniah Beleford,[...]. NPJ Genom Med 2021
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.