A citation-based method for searching scientific literature

Niti Sardana Agarwal, Lesley Northrop, Kwame Anyane-Yeboa, Vimla S Aggarwal, Peter L Nagy, Yesim Yilmaz Demirdag. J Clin Immunol 2014
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


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
94

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
89

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
89

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
84

Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency.
W Yang, P P W Lee, M-K Thong, T M Ramanujam, A Shanmugam, M-T Koh, K-W Chan, D Ying, Y Wang, J J Shen,[...]. Clin Genet 2015
17
58

Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency.
Roxane Lemoine, Jana Pachlopnik-Schmid, Henner F Farin, Amélie Bigorgne, Marianne Debré, Fernando Sepulveda, Sébastien Héritier, Julie Lemale, Cécile Talbotec, Frédéric Rieux-Laucat,[...]. J Allergy Clin Immunol 2014
37
47

Hypomorphic mutation in TTC7A causes combined immunodeficiency with mild structural intestinal defects.
Stavroula Woutsas, Caner Aytekin, Elisabeth Salzer, Cecilia Domínguez Conde, Sema Apaydin, Herbert Pichler, Nima Memaran-Dadgar, Ferda Ozbay Hosnut, Elisabeth Förster-Waldl, Susanne Matthes,[...]. Blood 2015
12
66

Donor immune reconstitution after liver-small bowel transplantation for multiple intestinal atresia with immunodeficiency.
Richard K Gilroy, Peter F Coccia, James E Talmadge, Lori I Hatcher, Samuel J Pirruccello, Byers W Shaw, Ronald J Rubocki, Debra L Sudan, Alan N Langnas, Simon P Horslen. Blood 2004
30
36


Multiple intestinal atresia with combined immune deficiency related to TTC7A defect is a multiorgan pathology: study of a French-Canadian-based cohort.
Isabel Fernandez, Natalie Patey, Valérie Marchand, Mirela Birlea, Bruno Maranda, Elie Haddad, Hélène Decaluwe, Françoise Le Deist. Medicine (Baltimore) 2014
20
36

The complex surgical management of the first case of severe combined immunodeficiency and multiple intestinal atresias surviving after the fourth year of life.
Riccardo Guanà, Salvatore Garofano, Elisabetta Teruzzi, Simona Vinardi, Giulia Carbonaro, Alessia Cerrina, Isabella Morra, Davide Montin, Alessandro Mussa, Jürgen Schleef. Pediatr Gastroenterol Hepatol Nutr 2014
8
87

Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family.
L A Moreno, F Gottrand, D Turck, S Manouvrier-Hanu, F Mazingue, C Morisot, F Le Deist, C Ricour, C Nihoul-Feketé, P Debeugny. Am J Med Genet 1990
44
31

Ichthyosis as the dermatological phenotype associated with TTC7A mutations.
S Leclerc-Mercier, R Lemoine, A E Bigorgne, F Sepulveda, C Leveau, A Fischer, N Mahlaoui, S Hadj-Rabia, G de Saint Basile. Br J Dermatol 2016
9
66

Stem cell transplantation for tetratricopeptide repeat domain 7A deficiency: long-term follow-up.
Jochen Kammermeier, Giovanna Lucchini, Sung-Yun Pai, Austen Worth, Dyanne Rampling, Persis Amrolia, Juliana Silva, Robert Chiesa, Kanchan Rao, Gabriele Noble-Jamieson,[...]. Blood 2016
19
31

Assembly of the PtdIns 4-kinase Stt4 complex at the plasma membrane requires Ypp1 and Efr3.
Dan Baird, Chris Stefan, Anjon Audhya, Sabine Weys, Scott D Emr. J Cell Biol 2008
95
26

Intestinal transplantation in children with multiple intestinal atresias and immunodeficiency.
Ryan T Fischer, Brian Friend, Geoffrey A Talmon, Wendy J Grant, Ruben E Quiros-Tejeira, Alan N Langnas, Peter F Coccia. Pediatr Transplant 2014
16
31


The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane.
Jeremy M Baskin, Xudong Wu, Romain Christiano, Michael S Oh, Curtis M Schauder, Elisabetta Gazzerro, Mirko Messa, Simona Baldassari, Stefania Assereto, Roberta Biancheri,[...]. Nat Cell Biol 2016
54
26

Multiple atresias and a new syndrome of hereditary multiple atresias involving the gastrointestinal tract from stomach to rectum.
F M Guttman, P Braun, P H Garance, H Blanchard, P P Collin, L Dallaire, J G Desjardins, G Perreault. J Pediatr Surg 1973
106
21

Hereditary multiple intestinal atresias: 2 new cases and review of the literature.
Conrad Cole, Alessandrina Freitas, Matthew S Clifton, Megan M Durham. J Pediatr Surg 2010
13
30

Evaluation of phosphatidylinositol-4-kinase IIIα as a hepatitis C virus drug target.
Frédéric H Vaillancourt, Martine Brault, Louise Pilote, Nathalie Uyttersprot, Elias T Gaillard, James H Stoltz, Brian L Knight, Lynn Pantages, Mary McFarland, Steffen Breitfelder,[...]. J Virol 2012
44
21

Multiple intestinal atresia with combined immune deficiency.
Luigi D Notarangelo. Curr Opin Pediatr 2014
10
40

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy.
Dylan Lawless, Anoop Mistry, Philip M Wood, Jens Stahlschmidt, Gururaj Arumugakani, Mark Hull, David Parry, Rashida Anwar, Clive Carter, Sinisa Savic. J Clin Immunol 2017
7
57

Novel Mutations of the Tetratricopeptide Repeat Domain 7A Gene and Phenotype/Genotype Comparison.
Reyin Lien, Yung-Feng Lin, Min-Wei Lai, Hui-Ying Weng, Ren-Chin Wu, Tang-Her Jaing, Jing-Long Huang, Shih-Feng Tsai, Wen-I Lee. Front Immunol 2017
16
25

Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel disease.
João Farela Neves, Isabel Afonso, Luis Borrego, Catarina Martins, Ana Isabel Cordeiro, Conceição Neves, Caroline Lacoste, Catherine Badens, Alexandre Fabre. Eur J Med Genet 2018
7
57

A syndrome involving immunodeficiency and multiple intestinal atresias.
M E Rothenberg, F V White, B Chilmonczyk, T Chatila. Immunodeficiency 1995
20
15


PtdIns4P synthesis by PI4KIIIα at the plasma membrane and its impact on plasma membrane identity.
Fubito Nakatsu, Jeremy M Baskin, Jeeyun Chung, Lukas B Tanner, Guanghou Shui, Sang Yoon Lee, Michelle Pirruccello, Mingming Hao, Nicholas T Ingolia, Markus R Wenk,[...]. J Cell Biol 2012
162
15

The Tetratricopeptide repeat domain 7 gene is mutated in flaky skin mice: a model for psoriasis, autoimmunity, and anemia.
Cynthia Helms, Stephen Pelsue, Li Cao, Erika Lamb, Brett Loffredo, Patricia Taillon-Miller, Brooke Herrin, Lisa M Burzenski, Bruce Gott, Bonnie L Lyons,[...]. Exp Biol Med (Maywood) 2005
22
15

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
15

Phenotypic and Genotypic Characterisation of Inflammatory Bowel Disease Presenting Before the Age of 2 years.
Jochen Kammermeier, Robert Dziubak, Matilde Pescarin, Suzanne Drury, Heather Godwin, Kate Reeve, Sibongile Chadokufa, Bonita Huggett, Sara Sider, Chela James,[...]. J Crohns Colitis 2017
68
15

Architecture of the human PI4KIIIα lipid kinase complex.
Joshua A Lees, Yixiao Zhang, Michael S Oh, Curtis M Schauder, Xiaoling Yu, Jeremy M Baskin, Kerry Dobbs, Luigi D Notarangelo, Pietro De Camilli, Thomas Walz,[...]. Proc Natl Acad Sci U S A 2017
27
15

Hyperactivation and proliferation of lymphocytes from the spleens of flaky skin (fsn) mutant mice.
Robert Welner, William Hastings, Beth L Hill, Stephen C Pelsue. Autoimmunity 2004
10
20

The peripheral lymphoid compartment is disrupted in flaky skin mice.
N J Abernethy, C Hagan, P L Tan, N M Birchall, J D Watson. Immunol Cell Biol 2000
12
16

Pharmacological and genetic targeting of the PI4KA enzyme reveals its important role in maintaining plasma membrane phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate levels.
Naveen Bojjireddy, Janos Botyanszki, Gerald Hammond, Donald Creech, Richard Peterson, Daniel C Kemp, Mark Snead, Randy Brown, Alastair Morrison, Steve Wilson,[...]. J Biol Chem 2014
82
10

Positional cloning of the Ttc7 gene required for normal iron homeostasis and mutated in hea and fsn anemia mice.
Robert A White, Steven G McNulty, Ndona N Nsumu, Leigh A Boydston, Brandon P Brewer, Koji Shimizu. Genomics 2005
26
10


Developmental abnormalities of the thymus in hea/hea mutant mice.
Yuki Kasahara, Koji Shimizu, Koichi Kuribayashi. Exp Anim 2008
3
66


Hereditary multiple intestinal atresia.
L Dallaire, G Perreault. Birth Defects Orig Artic Ser 1974
18
11

Familial intestinal polyatresia syndrome.
N Güngör, S Balci, F C Tanyel, S Göğüş. Clin Genet 1995
14
14

Hereditary erythroblastic anaemia in the laboratory mouse.
K Shimizu, H Keino, N Ogasawara, K Esaki. Lab Anim 1983
13
15


Immune deficiency in familial duodenal atresia.
S W Moore, G de Jongh, P Bouic, R A Brown, G Kirsten. J Pediatr Surg 1996
11
18

The novel tetratricopeptide repeat domain 7 mutation, Ttc7fsn-Jic, with deletion of the TPR-2B repeat causes severe flaky skin phenotype.
Shuji Takabayashi, Shuichi Iwashita, Tsukasa Hirashima, Hideki Katoh. Exp Biol Med (Maywood) 2007
8
25

Myosin light chain kinase: pulling the strings of epithelial tight junction function.
Kevin E Cunningham, Jerrold R Turner. Ann N Y Acad Sci 2012
179
10

Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium.
Toshiro Sato, Daniel E Stange, Marc Ferrante, Robert G J Vries, Johan H Van Es, Stieneke Van den Brink, Winan J Van Houdt, Apollo Pronk, Joost Van Gorp, Peter D Siersema,[...]. Gastroenterology 2011
10

Development and progression of psoriasiform dermatitis and systemic lesions in the flaky skin (fsn) mouse mutant.
J P Sundberg, M France, D Boggess, B A Sundberg, A B Jenson, W G Beamer, L D Shultz. Pathobiology 1997
37
10

The flaky skin (fsn) mutation in mice: map location and description of the anemia.
W G Beamer, S C Pelsue, L D Shultz, J P Sundberg, J E Barker. Blood 1995
32
10

CUSHAW: a CUDA compatible short read aligner to large genomes based on the Burrows-Wheeler transform.
Yongchao Liu, Bertil Schmidt, Douglas L Maskell. Bioinformatics 2012
60
10


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.