A citation-based method for searching scientific literature

Shan Gao, Xiao Li, Brad A Amendt. Curr Allergy Asthma Rep 2013
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity



A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
414
20

Immunological aspects of 22q11.2 deletion syndrome.
A R Gennery. Cell Mol Life Sci 2012
66
15

The diverse clinical features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome).
Solrun Melkorka Maggadottir, Kathleen E Sullivan. J Allergy Clin Immunol Pract 2013
26
15

Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.
A Rauch, S Zink, C Zweier, C T Thiel, A Koch, R Rauch, J Lascorz, U Hüffmeier, M Weyand, H Singer,[...]. J Med Genet 2005
109
15


22q11 deletion syndrome: current perspective.
Bülent Hacıhamdioğlu, Duygu Hacıhamdioğlu, Kenan Delil. Appl Clin Genet 2015
40
15

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
526
15


Rescue of embryonic lethality in Mdm2-deficient mice by absence of p53.
S N Jones, A E Roe, L A Donehower, A Bradley. Nature 1995
10

Rescue of early embryonic lethality in mdm2-deficient mice by deletion of p53.
R Montes de Oca Luna, D S Wagner, G Lozano. Nature 1995
10

Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells.
Shilpee Dutt, Anupama Narla, Katherine Lin, Ann Mullally, Nirmalee Abayasekara, Christine Megerdichian, Frederick H Wilson, Treeve Currie, Arati Khanna-Gupta, Nancy Berliner,[...]. Blood 2011
271
10

p53 coordinates cranial neural crest cell growth and epithelial-mesenchymal transition/delamination processes.
Ariel Rinon, Alina Molchadsky, Elisha Nathan, Gili Yovel, Varda Rotter, Rachel Sarig, Eldad Tzahor. Development 2011
69
10

p53 deficiency rescues the adverse effects of telomere loss and cooperates with telomere dysfunction to accelerate carcinogenesis.
L Chin, S E Artandi, Q Shen, A Tam, S L Lee, G J Gottlieb, C W Greider, R A DePinho. Cell 1999
738
10

mdm2 Is critical for inhibition of p53 during lymphopoiesis and the response to ionizing irradiation.
Susan M Mendrysa, Matthew K McElwee, Jennifer Michalowski, Kathleen A O'Leary, Karen M Young, Mary Ellen Perry. Mol Cell Biol 2003
195
10

The p53QS transactivation-deficient mutant shows stress-specific apoptotic activity and induces embryonic lethality.
Thomas M Johnson, Ester M Hammond, Amato Giaccia, Laura D Attardi. Nat Genet 2005
102
10

A subset of p53-deficient embryos exhibit exencephaly.
V P Sah, L D Attardi, G J Mulligan, B O Williams, R T Bronson, T Jacks. Nat Genet 1995
492
10

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
Natalie C Jones, Megan L Lynn, Karin Gaudenz, Daisuke Sakai, Kazushi Aoto, Jean-Phillipe Rey, Earl F Glynn, Lacey Ellington, Chunying Du, Jill Dixon,[...]. Nat Med 2008
283
10

Tumor suppression and normal aging in mice with constitutively high p53 activity.
Susan M Mendrysa, Kathleen A O'Leary, Matthew K McElwee, Jennifer Michalowski, Robert N Eisenman, Douglas A Powell, Mary Ellen Perry. Genes Dev 2006
177
10

Inappropriate p53 activation during development induces features of CHARGE syndrome.
Jeanine L Van Nostrand, Colleen A Brady, Heiyoun Jung, Daniel R Fuentes, Margaret M Kozak, Thomas M Johnson, Chieh-Yu Lin, Chien-Jung Lin, Donald L Swiderski, Hannes Vogel,[...]. Nature 2014
92
10

Synergistic regulation of p53 by Mdm2 and Mdm4 is critical in cardiac endocardial cushion morphogenesis during heart development.
Qin Zhang, Xueyan He, Lai Chen, Chenxi Zhang, Xiang Gao, Zhongzhou Yang, Geng Liu. J Pathol 2012
18
11


Cardiac outflow tract septation failure in Pax3-deficient embryos is due to p53-dependent regulation of migrating cardiac neural crest.
Sarah C Morgan, Hyung-Yul Lee, Frédéric Relaix, Lisa L Sandell, John M Levorse, Mary R Loeken. Mech Dev 2008
43
10

Rescue of embryonic lethality in Mdm4-null mice by loss of Trp53 suggests a nonoverlapping pathway with MDM2 to regulate p53.
J Parant, A Chavez-Reyes, N A Little, W Yan, V Reinke, A G Jochemsen, G Lozano. Nat Genet 2001
393
10

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
Kelly A McGowan, Jun Z Li, Christopher Y Park, Veronica Beaudry, Holly K Tabor, Amit J Sabnis, Weibin Zhang, Helmut Fuchs, Martin Hrabé de Angelis, Richard M Myers,[...]. Nat Genet 2008
261
10

Haploinsufficiency of Mdm2 and Mdm4 in tumorigenesis and development.
Tamara Terzian, Yongxing Wang, Carolyn S Van Pelt, Neil F Box, Elisabeth L Travis, Guillermina Lozano. Mol Cell Biol 2007
90
10


A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome.
Jillian L Barlow, Lesley F Drynan, Duncan R Hewett, Luke R Holmes, Silvia Lorenzo-Abalde, Alison L Lane, Helen E Jolin, Richard Pannell, Angela J Middleton, See Heng Wong,[...]. Nat Med 2010
249
10

Pax3 stimulates p53 ubiquitination and degradation independent of transcription.
Xiao Dan Wang, Sarah C Morgan, Mary R Loeken. PLoS One 2011
36
10

"Super p53" mice exhibit enhanced DNA damage response, are tumor resistant and age normally.
Isabel García-Cao, Marta García-Cao, Juan Martín-Caballero, Luis M Criado, Peter Klatt, Juana M Flores, Jean-Claude Weill, María A Blasco, Manuel Serrano. EMBO J 2002
363
10

Induction of p53 and up-regulation of the p53 pathway in the human 5q- syndrome.
Andrea Pellagatti, Teresa Marafioti, Jennifer C Paterson, Jillian L Barlow, Lesley F Drynan, Aristoteles Giagounidis, Stefano A Pileri, Mario Cazzola, Andrew N J McKenzie, James S Wainscoat,[...]. Blood 2010
53
10

High-frequency developmental abnormalities in p53-deficient mice.
J F Armstrong, M H Kaufman, D J Harrison, A R Clarke. Curr Biol 1995
389
10

Puma is required for p53-induced depletion of adult stem cells.
Dongping Liu, Linda Ou, Gregory D Clemenson, Connie Chao, Marshall Eli Lutske, Gerard P Zambetti, Fred H Gage, Yang Xu. Nat Cell Biol 2010
80
10

The C terminus of p53 regulates gene expression by multiple mechanisms in a target- and tissue-specific manner in vivo.
Pierre-Jacques Hamard, Nicolas Barthelery, Brandon Hogstad, Sathish Kumar Mungamuri, Crystal A Tonnessen, Luis A Carvajal, Emir Senturk, Virginia Gillespie, Stuart A Aaronson, Miriam Merad,[...]. Genes Dev 2013
46
10

Modulation of mammalian life span by the short isoform of p53.
Bernhard Maier, Wendy Gluba, Brian Bernier, Terry Turner, Khalid Mohammad, Theresa Guise, Ann Sutherland, Michael Thorner, Heidi Scrable. Genes Dev 2004
446
10

p53 mutant mice that display early ageing-associated phenotypes.
Stuart D Tyner, Sundaresan Venkatachalam, Jene Choi, Stephen Jones, Nader Ghebranious, Herbert Igelmann, Xiongbin Lu, Gabrielle Soron, Benjamin Cooper, Cory Brayton,[...]. Nature 2002
10

The p53-Mdm2 network in progenitor cell expansion during mouse postnatal development.
G Liu, T Terzian, S Xiong, C S Van Pelt, A Audiffred, N F Box, G Lozano. J Pathol 2007
42
10

Switching mechanisms of cell death in mdm2- and mdm4-null mice by deletion of p53 downstream targets.
Arturo Chavez-Reyes, John M Parant, Lisa L Amelse, Roberto Montes de Oca Luna, Stanley J Korsmeyer, Guillermina Lozano. Cancer Res 2003
64
10

Mutant mice lacking the p53 C-terminal domain model telomere syndromes.
Iva Simeonova, Sara Jaber, Irena Draskovic, Boris Bardot, Ming Fang, Rachida Bouarich-Bourimi, Vincent Lejour, Laure Charbonnier, Claire Soudais, Jean-Christophe Bourdon,[...]. Cell Rep 2013
49
10

p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome.
Cinzia Caprio, Antonio Baldini. Proc Natl Acad Sci U S A 2014
21
10

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
10


Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations.
Jelena S Arnold, Uwe Werling, Evan M Braunstein, Jun Liao, Sonja Nowotschin, Winfried Edelmann, Jean M Hebert, Bernice E Morrow. Development 2006
106
10

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs,[...]. Genet Couns 1999
311
10

Head and neck manifestations of 22q11.2 deletion syndromes.
Tal Marom, Yehudah Roth, Abraham Goldfarb, Udi Cinamon. Eur Arch Otorhinolaryngol 2012
17
11

Presenting symptoms in adults with the 22q11 deletion syndrome.
Annick Vogels, Sara Schevenels, Richard Cayenberghs, Eddy Weyts, Griet Van Buggenhout, Ann Swillen, Hilde Van Esch, Thomy de Ravel, Pieter Corveleyn, Koen Devriendt. Eur J Med Genet 2014
11
18

Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times.
Alex Habel, Richard Herriot, Dinakantha Kumararatne, Jeremy Allgrove, Kate Baker, Helen Baxendale, Frances Bu'Lock, Helen Firth, Andrew Gennery, Anthony Holland,[...]. Eur J Pediatr 2014
28
10

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Maria Delio, Tingwei Guo, Donna M McDonald-McGinn, Elaine Zackai, Sean Herman, Mark Kaminetzky, Anne Marie Higgins, Karlene Coleman, Carolyn Chow, Maria Jalbrzikowski,[...]. Am J Hum Genet 2013
32
10

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Grégory Raux, Emilie Bumsel, Bernadette Hecketsweiler, Therese van Amelsvoort, Janneke Zinkstok, Sylvie Manouvrier-Hanu, Carole Fantini, Georges-Marie M Brévière, Gabriella Di Rosa, Giuseppina Pustorino,[...]. Hum Mol Genet 2007
109
10

Tbx1 coordinates addition of posterior second heart field progenitor cells to the arterial and venous poles of the heart.
M Sameer Rana, Magali Théveniau-Ruissy, Christopher De Bono, Karim Mesbah, Alexandre Francou, Mayyasa Rammah, Jorge N Domínguez, Marine Roux, Brigitte Laforest, Robert H Anderson,[...]. Circ Res 2014
59
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.