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



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  Times     Co-cited
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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
687
70

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
60

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
272
50

Retinoic acid down-regulates Tbx1 expression in vivo and in vitro.
Catherine Roberts, Sarah M Ivins, Chela T James, Peter J Scambler. Dev Dyn 2005
77
50

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
40

Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
Marita Bosticardo, Yasuhiro Yamazaki, Jennifer Cowan, Giuliana Giardino, Cristina Corsino, Giulia Scalia, Rosaria Prencipe, Melanie Ruffner, David A Hill, Inga Sakovich,[...]. Am J Hum Genet 2019
24
40

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
411
40

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
40

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
662
40

Pax1 is expressed during development of the thymus epithelium and is required for normal T-cell maturation.
J Wallin, H Eibel, A Neubüser, J Wilting, H Koseki, R Balling. Development 1996
160
40

Mechanisms of thymus organogenesis and morphogenesis.
Julie Gordon, Nancy R Manley. Development 2011
125
40


Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion.
Elisa Tassano, Vidhya Jagannathan, Cord Drögemüller, Massimiliano Leoni, Marjo K Hytönen, Mariasavina Severino, Stefania Gimelli, Cristina Cuoco, Maja Di Rocco, Kirsi Sanio,[...]. Am J Med Genet A 2015
16
30

Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
Ning Liu, Kelly Schoch, Xi Luo, Loren D M Pena, Venkata Hemanjani Bhavana, Mary K Kukolich, Sarah Stringer, Zöe Powis, Kelly Radtke, Cameron Mroske,[...]. Hum Mol Genet 2018
24
30

Thymus transplantation.
M Louise Markert, Blythe H Devlin, Elizabeth A McCarthy. Clin Immunol 2010
82
30

Tbx1: Transcriptional and Developmental Functions.
A Baldini, F G Fulcoli, E Illingworth. Curr Top Dev Biol 2017
29
30

The mouse Foxi3 transcription factor is necessary for the development of posterior placodes.
Onur Birol, Takahiro Ohyama, Renée K Edlund, Katerina Drakou, Pantelis Georgiades, Andrew K Groves. Dev Biol 2016
20
30


Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
Francesca Vitelli, Masae Morishima, Ilaria Taddei, Elizabeth A Lindsay, Antonio Baldini. Hum Mol Genet 2002
244
30

Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
Lucile Ryckebüsch, Nicolas Bertrand, Karim Mesbah, Fanny Bajolle, Karen Niederreither, Robert G Kelly, Stéphane Zaffran. Circ Res 2010
55
30

Rebalancing gene haploinsufficiency in vivo by targeting chromatin.
Filomena Gabriella Fulcoli, Monica Franzese, Xiangyang Liu, Zhen Zhang, Claudia Angelini, Antonio Baldini. Nat Commun 2016
35
30


Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.
Christiane Zweier, Heinrich Sticht, Inci Aydin-Yaylagül, Christine E Campbell, Anita Rauch. Am J Hum Genet 2007
142
30

Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis.
Abigail Jackson, Sahrunizam Kasah, Suzanne L Mansour, Bernice Morrow, M Albert Basson. Dev Dyn 2014
17
30

The role of the endoderm in the development and evolution of the pharyngeal arches.
Anthony Graham, Masataka Okabe, Robyn Quinlan. J Anat 2005
74
30


Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.
Victoria Randall, Karen McCue, Catherine Roberts, Vanessa Kyriakopoulou, Sarah Beddow, Angela N Barrett, Francesca Vitelli, Katrina Prescott, Charles Shaw-Smith, Koen Devriendt,[...]. J Clin Invest 2009
97
30

The nu gene acts cell-autonomously and is required for differentiation of thymic epithelial progenitors.
C C Blackburn, C L Augustine, R Li, R P Harvey, M A Malin, R L Boyd, J F Miller, G Morahan. Proc Natl Acad Sci U S A 1996
154
30

Nail dystrophy associated with a heterozygous mutation of the nude/SCID human FOXN1 (WHN) gene.
Luigi Auricchio, Marsilio Adriani, Jorge Frank, Rosanna Busiello, Angela Christiano, Claudio Pignata. Arch Dermatol 2005
22
30

Ectopic TBX1 suppresses thymic epithelial cell differentiation and proliferation during thymus organogenesis.
Kaitlin A G Reeh, Kim T Cardenas, Virginia E Bain, Zhijie Liu, Micheline Laurent, Nancy R Manley, Ellen R Richie. Development 2014
17
30


Pax1 and Pax9 synergistically regulate vertebral column development.
H Peters, B Wilm, N Sakai, K Imai, R Maas, R Balling. Development 1999
172
30

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
99
30

A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency.
I Paganini, R Sestini, G L Capone, A L Putignano, E Contini, I Giotti, F Gensini, A Marozza, A Barilaro, B Porfirio,[...]. Clin Genet 2017
20
30

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
821
30

PAX1 is essential for development and function of the human thymus.
Yasuhiro Yamazaki, Raul Urrutia, Luis M Franco, Silvia Giliani, Kejian Zhang, Anas M Alazami, A Kerry Dobbs, Stefania Masneri, Avni Joshi, Francisco Otaizo-Carrasquero,[...]. Sci Immunol 2020
21
30

First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases.
M Louise Markert, José G Marques, Bénédicte Neven, Blythe H Devlin, Elizabeth A McCarthy, Ivan K Chinn, Adriana S Albuquerque, Susana L Silva, Claudio Pignata, Geneviève de Saint Basile,[...]. Blood 2011
62
30

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants.
M Louise Markert, Blythe H Devlin, Marilyn J Alexieff, Jie Li, Elizabeth A McCarthy, Stephanie E Gupton, Ivan K Chinn, Laura P Hale, Thomas B Kepler, Min He,[...]. Blood 2007
137
30

Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly.
Ales Janda, Petr Sedlacek, Manfred Hönig, Wilhelm Friedrich, Martin Champagne, Tadashi Matsumoto, Alain Fischer, Benedicte Neven, Audrey Contet, Danielle Bensoussan,[...]. Blood 2010
42
30

Recurrent microdeletions at chromosome 2p11.2 are associated with thymic hypoplasia and features resembling DiGeorge syndrome.
Joshua D Bernstock, Arthur H Totten, Abdel G Elkahloun, Kory R Johnson, Anna C Hurst, Frederick Goldman, Andrew K Groves, Fady M Mikhail, T Prescott Atkinson. J Allergy Clin Immunol 2020
8
37

A novel mutation in FOXN1 resulting in SCID: a case report and literature review.
Janet Chou, Michel J Massaad, Rima Hanna Wakim, Wayne Bainter, Ghassan Dbaibo, Raif S Geha. Clin Immunol 2014
20
30

Foxn1 regulates key target genes essential for T cell development in postnatal thymic epithelial cells.
Saulius Žuklys, Adam Handel, Saule Zhanybekova, Fatima Govani, Marcel Keller, Stefano Maio, Carlos E Mayer, Hong Ying Teh, Katrin Hafen, Giuseppe Gallone,[...]. Nat Immunol 2016
81
30

CHARGE syndrome: a review of the immunological aspects.
Monica T Y Wong, Elisabeth H Schölvinck, Annechien J A Lambeck, Conny M A van Ravenswaaij-Arts. Eur J Hum Genet 2015
24
30

Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.
A R Gennery, M A Slatter, J Rice, L H Hoefsloot, D Barge, A McLean-Tooke, T Montgomery, J A Goodship, A D Burt, T J Flood,[...]. Clin Exp Immunol 2008
68
30

Chd7 Is Critical for Early T-Cell Development and Thymus Organogenesis in Zebrafish.
Zhi-Zhi Liu, Zi-Long Wang, Tae-Ik Choi, Wen-Ting Huang, Han-Tsing Wang, Ying-Ying Han, Lou-Yin Zhu, Hyun-Taek Kim, Jung-Hwa Choi, Jin-Soo Lee,[...]. Am J Pathol 2018
11
30

Thymus transplantation for complete DiGeorge syndrome: European experience.
E Graham Davies, Melissa Cheung, Kimberly Gilmour, Jesmeen Maimaris, Joe Curry, Anna Furmanski, Neil Sebire, Neil Halliday, Konstantinos Mengrelis, Stuart Adams,[...]. J Allergy Clin Immunol 2017
51
30


Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs.
C Pignata, M Fiore, V Guzzetta, A Castaldo, G Sebastio, F Porta, A Guarino. Am J Med Genet 1996
67
30

Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.
M Adriani, A Martinez-Mir, F Fusco, R Busiello, J Frank, S Telese, E Matrecano, M V Ursini, A M Christiano, C Pignata. Ann Hum Genet 2004
56
30


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.