A citation-based method for searching scientific literature

Raad A Haddad, Gregory A Clines, Jennifer A Wyckoff. Clin Diabetes Endocrinol 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
692
100

Histone demethylation mediated by the nuclear amine oxidase homolog LSD1.
Yujiang Shi, Fei Lan, Caitlin Matson, Peter Mulligan, Johnathan R Whetstine, Philip A Cole, Robert A Casero, Yang Shi. Cell 2004
100

Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome.
Gabriella Lania, Alberto Bresciani, Monica Bisbocci, Alessandra Francone, Vincenza Colonna, Sergio Altamura, Antonio Baldini. Hum Mol Genet 2016
10
100

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Richard Paylor, Beate Glaser, Annalisa Mupo, Paris Ataliotis, Corinne Spencer, Angela Sobotka, Chelsey Sparks, Chul-Hee Choi, John Oghalai, Sarah Curran,[...]. Proc Natl Acad Sci U S A 2006
199
100

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm.
Amélie Calmont, Sarah Ivins, Kelly Lammerts Van Bueren, Irinna Papangeli, Vanessa Kyriakopoulou, William D Andrews, James F Martin, Anne M Moon, Elizabeth A Illingworth, M Albert Basson,[...]. Development 2009
88
100

Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis.
Evan M Braunstein, Dennis C Monks, Vimla S Aggarwal, Jelena S Arnold, Bernice E Morrow. BMC Dev Biol 2009
29
100

Rebalancing gene haploinsufficiency in vivo by targeting chromatin.
Filomena Gabriella Fulcoli, Monica Franzese, Xiangyang Liu, Zhen Zhang, Claudia Angelini, Antonio Baldini. Nat Commun 2016
36
100

Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment.
Alejandra Fernandez, Daniel W Meechan, Beverly A Karpinski, Elizabeth M Paronett, Corey A Bryan, Hanna L Rutz, Eric A Radin, Noah Lubin, Erin R Bonner, Anastas Popratiloff,[...]. Neuron 2019
52
100

Long-Lasting Rescue of Network and Cognitive Dysfunction in a Genetic Schizophrenia Model.
Arghya Mukherjee, Fernando Carvalho, Stephan Eliez, Pico Caroni. Cell 2019
52
100


Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
Sarah E Prasad, Sarah Howley, Kieran C Murphy. Dev Disabil Res Rev 2008
51
100

The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.
H Fagman, J Liao, J Westerlund, L Andersson, B E Morrow, M Nilsson. Hum Mol Genet 2007
43
100

Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation.
Laura Torres-Juan, Jordi Rosell, Montse Morla, Catalina Vidal-Pou, Fernando García-Algas, Maria-Angeles de la Fuente, Miguel Juan, Albert Tubau, Daniel Bachiller, Marta Bernues,[...]. Eur J Hum Genet 2007
51
100

LSD1/KDM1A inhibitors in clinical trials: advances and prospects.
Yuan Fang, Guochao Liao, Bin Yu. J Hematol Oncol 2019
120
100

Continuous performance test impairment in a 22q11.2 microdeletion mouse model: improvement by amphetamine.
Simon R O Nilsson, Christopher J Heath, Samir Takillah, Steve Didienne, Kim Fejgin, Vibeke Nielsen, Jacob Nielsen, Lisa M Saksida, Jean Mariani, Philippe Faure,[...]. Transl Psychiatry 2018
10
100


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
100

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
Zahra Motahari, Sally Ann Moody, Thomas Michael Maynard, Anthony-Samuel LaMantia. J Neurodev Disord 2019
27
100

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Zhen Zhang, Fabiana Cerrato, Huansheng Xu, Francesca Vitelli, Masae Morishima, Joshua Vincentz, Yasuhide Furuta, Lijiang Ma, James F Martin, Antonio Baldini,[...]. Development 2005
98
100

Vitamin B12 deficiency.
Ralph Green, Lindsay H Allen, Anne-Lise Bjørke-Monsen, Alex Brito, Jean-Louis Guéant, Joshua W Miller, Anne M Molloy, Ebba Nexo, Sally Stabler, Ban-Hock Toh,[...]. Nat Rev Dis Primers 2017
248
100

Histone demethylation catalysed by LSD1 is a flavin-dependent oxidative process.
Federico Forneris, Claudia Binda, Maria Antonietta Vanoni, Andrea Mattevi, Elena Battaglioli. FEBS Lett 2005
198
100

Favorable effects of omega-3 polyunsaturated fatty acids in attentional control and conversion rate to psychosis in 22q11.2 deletion syndrome.
Marco Armando, Mariasole Ciampoli, Maria Carmela Padula, Paul Amminger, Franco De Crescenzo, Johanna Maeder, Maude Schneider, Marie Schaer, Francesca Managò, Stephan Eliez,[...]. Neuropharmacology 2020
7
100

Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.
Gemma Flore, Sara Cioffi, Marchesa Bilio, Elizabeth Illingworth. Cereb Cortex 2017
8
100



Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.
Silvia E Racedo, Erica Hasten, Mingyan Lin, Gnanapackiam Sheela Devakanmalai, Tingwei Guo, Ertugrul M Ozbudak, Chen-Leng Cai, Deyou Zheng, Bernice E Morrow. PLoS Genet 2017
16
100

Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.
Eleonora Napoli, Flora Tassone, Sarah Wong, Kathleen Angkustsiri, Tony J Simon, Gyu Song, Cecilia Giulivi. J Biol Chem 2015
31
100

Early thyroid development requires a Tbx1-Fgf8 pathway.
Gabriella Lania, Zhen Zhang, Tuong Huynh, Cinzia Caprio, Anne M Moon, Francesca Vitelli, Antonio Baldini. Dev Biol 2009
30
100

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
Huansheng Xu, Masae Morishima, John N Wylie, Robert J Schwartz, Benoit G Bruneau, Elizabeth A Lindsay, Antonio Baldini. Development 2004
274
100

TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Tsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, Masahiko Kawai, Takeshi Nagashima, Ryo Funayama, Keiko Nakayama, Shinichi Nakashima, Fumiko Kato, Maki Fukami,[...]. PLoS One 2014
30
100

Mouse models of 22q11 deletion syndrome.
Richard Paylor, Elizabeth Lindsay. Biol Psychiatry 2006
47
100

Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8.
Francesca Vitelli, Gabriella Lania, Tuong Huynh, Antonio Baldini. J Mol Cell Cardiol 2010
18
100


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.