A citation-based method for searching scientific literature

Jane Louise Hartley, Nicholas C Zachos, Ban Dawood, Mark Donowitz, Julia Forman, Rodney J Pollitt, Neil V Morgan, Louise Tee, Paul Gissen, Walter H A Kahr, Alex S Knisely, Steve Watson, David Chitayat, Ian W Booth, Sue Protheroe, Stephen Murphy, Esther de Vries, Deirdre A Kelly, Eamonn R Maher. Gastroenterology 2010
Times Cited: 78







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



Times Cited
  Times     Co-cited
Similarity


SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.
Alexandre Fabre, Bernard Charroux, Christine Martinez-Vinson, Bertrand Roquelaure, Egritas Odul, Ersin Sayar, Hilary Smith, Virginie Colomb, Nicolas Andre, Jean-Pierre Hugot,[...]. Am J Hum Genet 2012
87
65

Novel mutations in TTC37 associated with tricho-hepato-enteric syndrome.
Alexandre Fabre, Christine Martinez-Vinson, Bertrand Roquelaure, Chantal Missirian, Nicolas André, Anne Breton, Alain Lachaux, Egritas Odul, Virginie Colomb, Julie Lemale,[...]. Hum Mutat 2011
33
78

Syndromic diarrhea/Tricho-hepato-enteric syndrome.
Alexandre Fabre, Christine Martinez-Vinson, Olivier Goulet, Catherine Badens. Orphanet J Rare Dis 2013
35
68

Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency.
D Girault, O Goulet, F Le Deist, N Brousse, V Colomb, J P Césarini, S de Potter, D Canioni, C Griscelli, A Fischer. J Pediatr 1994
62
33

Tricho-hepato-enteric syndrome: further delineation of a distinct syndrome with neonatal hemochromatosis phenotype, intractable diarrhea, and hair anomalies.
A Verloes, J Lombet, Y Lambert, A F Hubert, M Deprez, V Fridman, S Gosseye, J Rigo, E Sokal. Am J Med Genet 1997
43
41


Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome.
Alexandre Fabre, Anne Breton, Marie-Edith Coste, Virginie Colomb, Beatrice Dubern, Alain Lachaux, Julie Lemale, Julien Mancini, Evelyne Marinier, Christine Martinez-Vinson,[...]. Arch Dis Child 2014
30
56

Syndromic (phenotypic) diarrhea in early infancy.
Olivier Goulet, Christine Vinson, Bertrand Roquelaure, Nicole Brousse, Christine Bodemer, Jean-Pierre Cézard. Orphanet J Rare Dis 2008
26
57

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.
Yaron Avitzur, Conghui Guo, Lucas A Mastropaolo, Ehsan Bahrami, Hannah Chen, Zhen Zhao, Abdul Elkadri, Sandeep Dhillon, Ryan Murchie, Ramzi Fattouh,[...]. Gastroenterology 2014
112
19

Tricho-hepato-enteric syndrome presenting with mild colitis.
Odul Egritas, Buket Dalgic, Meltem Onder. Eur J Pediatr 2009
16
81

The diagnostic approach to monogenic very early onset inflammatory bowel disease.
Holm H Uhlig, Tobias Schwerd, Sibylle Koletzko, Neil Shah, Jochen Kammermeier, Abdul Elkadri, Jodie Ouahed, David C Wilson, Simon P Travis, Dan Turner,[...]. Gastroenterology 2014
326
16

Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder.
Alexandre Fabre, Nicolas André, Anne Breton, Pierre Broué, Catherine Badens, Bertrand Roquelaure. Am J Med Genet A 2007
19
63

Threading the barrel of the RNA exosome.
Claudia Schneider, David Tollervey. Trends Biochem Sci 2013
82
14

Targeted gene panel sequencing in children with very early onset inflammatory bowel disease--evaluation and prospective analysis.
Jochen Kammermeier, Suzanne Drury, Chela T James, Robert Dziubak, Louise Ocaka, Mamoun Elawad, Philip Beales, Nicholas Lench, Holm H Uhlig, Chiara Bacchelli,[...]. J Med Genet 2014
58
18

Inflammatory skin and bowel disease linked to ADAM17 deletion.
Diana C Blaydon, Paolo Biancheri, Wei-Li Di, Vincent Plagnol, Rita M Cabral, Matthew A Brooke, David A van Heel, Franz Ruschendorf, Mark Toynbee, Amanda Walne,[...]. N Engl J Med 2011
211
12


TTC7A mutations disrupt intestinal epithelial apicobasal polarity.
Amélie E Bigorgne, Henner F Farin, Roxane Lemoine, Nizar Mahlaoui, Nathalie Lambert, Marine Gil, Ansgar Schulz, Pierre Philippet, Patrick Schlesser, Tore G Abrahamsen,[...]. J Clin Invest 2014
99
12

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.
Erik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, E Michael Gertz, Alejandro A Schäffer, Fatih Noyan, Mario Perro, Jana Diestelhorst, Anna Allroth, Dhaarini Murugan,[...]. N Engl J Med 2009
908
12

Expanding phenotypic and allelic heterogeneity of tricho-hepato-enteric syndrome.
Dorota M Monies, Zuhair Rahbeeni, Mohamed Abouelhoda, Ewa A Naim, Banan Al-Younes, Brian F Meyer, Ali Al-Mehaidib. J Pediatr Gastroenterol Nutr 2015
13
76

The SKIV2L RNA exosome limits activation of the RIG-I-like receptors.
Sterling C Eckard, Gillian I Rice, Alexandre Fabre, Catherine Badens, Elizabeth E Gray, Jane L Hartley, Yanick J Crow, Daniel B Stetson. Nat Immunol 2014
121
12

Tricho-Hepato-Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospects.
Patrice Bourgeois, Clothilde Esteve, Charlène Chaix, Christophe Béroud, Nicolas Lévy, Alexandre Fabre, Catherine Badens. Hum Mutat 2018
16
62

Tricho-hepato-enteric syndrome: a case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality.
Imad Dweikat, Mutaz Sultan, Nizar Maraqa, Tareq Hindi, Sara Abu-Rmeileh, Bassam Abu-Libdeh. Am J Med Genet A 2007
11
81

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
C L Bennett, J Christie, F Ramsdell, M E Brunkow, P J Ferguson, L Whitesell, T E Kelly, F T Saulsbury, P F Chance, H D Ochs. Nat Genet 2001
11

Trichohepatoenteric syndrome: founder mutation in asian indians.
U H Kotecha, S Movva, R D Puri, I C Verma. Mol Syndromol 2012
12
75

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.
Jijun Wan, Michael Yourshaw, Hafsa Mamsa, Sabine Rudnik-Schöneborn, Manoj P Menezes, Ji Eun Hong, Derek W Leong, Jan Senderek, Michael S Salman, David Chitayat,[...]. Nat Genet 2012
155
11


Crystal structure of an RNA-bound 11-subunit eukaryotic exosome complex.
Debora Lika Makino, Marc Baumgärtner, Elena Conti. Nature 2013
157
11


Novel mutations in SKIV2L and TTC37 genes in Malaysian children with trichohepatoenteric syndrome.
Way Seah Lee, Kai Ming Teo, Ruey Terng Ng, Sze Yee Chong, Boon Pin Kee, Kek Heng Chua. Gene 2016
11
81

Mutant neurogenin-3 in congenital malabsorptive diarrhea.
Jiafang Wang, Galen Cortina, S Vincent Wu, Robert Tran, Jang-Hyeon Cho, Ming-Jer Tsai, Travis J Bailey, Milan Jamrich, Marvin E Ament, William R Treem,[...]. N Engl J Med 2006
203
10

Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.
Rui Chen, Silvia Giliani, Gaetana Lanzi, George I Mias, Silvia Lonardi, Kerry Dobbs, John Manis, Hogune Im, Jennifer E Gallagher, Douglas H Phanstiel,[...]. J Allergy Clin Immunol 2013
79
10

Familial diarrhea syndrome caused by an activating GUCY2C mutation.
Torunn Fiskerstrand, Najla Arshad, Bjørn Ivar Haukanes, Rune Rose Tronstad, Khanh Do-Cong Pham, Stefan Johansson, Bjarte Håvik, Siv L Tønder, Shawn E Levy, Damien Brackman,[...]. N Engl J Med 2012
125
10

EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia.
Veronika Boczonadi, Juliane S Müller, Angela Pyle, Jennifer Munkley, Talya Dor, Jade Quartararo, Ileana Ferrero, Veronika Karcagi, Michele Giunta, Tuomo Polvikoski,[...]. Nat Commun 2014
75
10

Reconstitution, activities, and structure of the eukaryotic RNA exosome.
Quansheng Liu, Jaclyn C Greimann, Christopher D Lima. Cell 2006
399
10

The yeast ski complex: crystal structure and RNA channeling to the exosome complex.
Felix Halbach, Peter Reichelt, Michaela Rode, Elena Conti. Cell 2013
107
10

Functions of the cytoplasmic exosome.
Daneen Schaeffer, Amanda Clark, A Alejandra Klauer, Borislava Tsanova, Ambro van Hoof. Adv Exp Med Biol 2011
34
20


Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea.
Peter Heinz-Erian, Thomas Müller, Birgit Krabichler, Melanie Schranz, Christian Becker, Franz Rüschendorf, Peter Nürnberg, Bernard Rossier, Mihailo Vujic, Ian W Booth,[...]. Am J Hum Genet 2009
67
10

Identification of EpCAM as the gene for congenital tufting enteropathy.
Mamata Sivagnanam, James L Mueller, Hane Lee, Zugen Chen, Stanley F Nelson, Dan Turner, Stanley H Zlotkin, Paul B Pencharz, Bo-Yee Ngan, Ondrej Libiger,[...]. Gastroenterology 2008
123
8


Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.
Mark E Samuels, Jacek Majewski, Najmeh Alirezaie, Isabel Fernandez, Ferran Casals, Natalie Patey, Hélène Decaluwe, Isabelle Gosselin, Elie Haddad, Alan Hodgkinson,[...]. J Med Genet 2013
68
10

Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantation.
Karin R Engelhardt, Neil Shah, Intan Faizura-Yeop, Dilara F Kocacik Uygun, Natalie Frede, Aleixo M Muise, Eyal Shteyer, Serkan Filiz, Ronnie Chee, Mamoun Elawad,[...]. J Allergy Clin Immunol 2013
158
8

Persistent defective membrane trafficking in epithelial cells of patients with familial hemophagocytic lymphohistiocytosis type 5 due to STXBP2/MUNC18-2 mutations.
Polina Stepensky, Jack Bartram, Thomas F Barth, Kai Lehmberg, Paul Walther, Kerstin Amann, Alan D Philips, Ortraud Beringer, Udo Zur Stadt, Ansgar Schulz,[...]. Pediatr Blood Cancer 2013
42
16

Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies.
Roberto Berni Canani, Giuseppe Castaldo, Rosa Bacchetta, Martín G Martín, Olivier Goulet. Nat Rev Gastroenterol Hepatol 2015
44
15

Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt.
Nataliya Di Donato, Teresa Neuhann, Anne-Karin Kahlert, Barbara Klink, Karl Hackmann, Irmingard Neuhann, Barbora Novotna, Jens Schallner, Claudia Krause, Ian A Glass,[...]. J Med Genet 2016
40
17

Structure of an Rrp6-RNA exosome complex bound to poly(A) RNA.
Elizabeth V Wasmuth, Kurt Januszyk, Christopher D Lima. Nature 2014
94
8

Management of syndromic diarrhea/tricho-hepato-enteric syndrome: A review of the literature.
Alexandre Fabre, Patrice Bourgeois, Marie-Edith Coste, Céline Roman, Vincent Barlogis, Catherine Badens. Intractable Rare Dis Res 2017
12
58

Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome.
Frédéric Vély, Vincent Barlogis, Evelyne Marinier, Marie-Edith Coste, Béatrice Dubern, Emmanuelle Dugelay, Julie Lemale, Christine Martinez-Vinson, Noël Peretti, Ariane Perry,[...]. Front Immunol 2018
17
41

Exosome-mediated recognition and degradation of mRNAs lacking a termination codon.
Ambro van Hoof, Pamela A Frischmeyer, Harry C Dietz, Roy Parker. Science 2002
396
7

Function of the ski4p (Csl4p) and Ski7p proteins in 3'-to-5' degradation of mRNA.
A van Hoof, R R Staples, R E Baker, R Parker. Mol Cell Biol 2000
141
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.