A citation-based method for searching scientific literature

Qiumei Du, M Teresa de la Morena, Nicolai S C van Oers. Front Genet 2020
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


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
390
36

Rebalancing gene haploinsufficiency in vivo by targeting chromatin.
Filomena Gabriella Fulcoli, Monica Franzese, Xiangyang Liu, Zhen Zhang, Claudia Angelini, Antonio Baldini. Nat Commun 2016
34
26

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
760
21

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
60
15

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
18
16

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
15

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
23
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
524
15

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
19
15

Long-term results of bone marrow transplantation in complete DiGeorge syndrome.
Michael H Land, Maria I Garcia-Lloret, Michael S Borzy, P Nagesh Rao, Najib Aziz, Sean A McGhee, Karin Chen, Jack Gorski, E Richard Stiehm. J Allergy Clin Immunol 2007
29
15

FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans.
Qiumei Du, Larry K Huynh, Fatma Coskun, Erika Molina, Matthew A King, Prithvi Raj, Shaheen Khan, Igor Dozmorov, Christine M Seroogy, Christian A Wysocki,[...]. J Clin Invest 2019
13
23

Dynamics of thymus organogenesis and colonization in early human development.
Alison M Farley, Lucy X Morris, Eric Vroegindeweij, Marianne L G Depreter, Harsh Vaidya, Frances H Stenhouse, Simon R Tomlinson, Richard A Anderson, Tom Cupedo, Jan J Cornelissen,[...]. Development 2013
53
15

Thymus transplantation.
M Louise Markert, Blythe H Devlin, Elizabeth A McCarthy. Clin Immunol 2010
82
15

Thymic Epithelial Cells.
Jakub Abramson, Graham Anderson. Annu Rev Immunol 2017
123
15

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
19
15

Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome.
M Teresa de la Morena, Jennifer L Eitson, Igor M Dozmorov, Serkan Belkaya, Ashley R Hoover, Esperanza Anguiano, M Virginia Pascual, Nicolai S C van Oers. Clin Immunol 2013
37
15

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
15

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Yingjie Zhao, Alexander Diacou, H Richard Johnston, Fadi I Musfee, Donna M McDonald-McGinn, Daniel McGinn, T Blaine Crowley, Gabriela M Repetto, Ann Swillen, Jeroen Breckpot,[...]. Am J Hum Genet 2020
14
21


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
408
15

FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program.
Rosa Romano, Loredana Palamaro, Anna Fusco, Giuliana Giardino, Vera Gallo, Luigi Del Vecchio, Claudio Pignata. Front Immunol 2013
42
15

Mechanisms of thymus organogenesis and morphogenesis.
Julie Gordon, Nancy R Manley. Development 2011
120
15

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
15

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
15


Congenital heart disease in mice deficient for the DiGeorge syndrome region.
E A Lindsay, A Botta, V Jurecic, S Carattini-Rivera, Y C Cheah, H M Rosenblatt, A Bradley, A Baldini. Nature 1999
298
15

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
15

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
21
15

Practical guidelines for managing adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman,[...]. Genet Med 2015
113
15

Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
291
15


Low thymic output, peripheral homeostasis deregulation, and hastened regulatory T cells differentiation in children with 22q11.2 deletion syndrome.
Sara Ferrando-Martínez, Raquel Lorente, Dolores Gurbindo, Ma Isabel De José, Manuel Leal, Ma Angeles Muñoz-Fernández, Rafael Correa-Rocha. J Pediatr 2014
24
10

Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
Lauren Staple, Timothy Andrews, Donna McDonald-McGinn, Elaine Zackai, Kathleen E Sullivan. Pediatr Allergy Immunol 2005
31
10

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
77
10

Cytokines, leptin, and stress-induced thymic atrophy.
Amanda L Gruver, Gregory D Sempowski. J Leukoc Biol 2008
131
10

Thymocyte-thymocyte interaction for efficient positive selection and maturation of CD4 T cells.
Eun Young Choi, Kyeong Cheon Jung, Hyo Jin Park, Doo Hyun Chung, Jin Sook Song, Seung Don Yang, Elizabeth Simpson, Seong Hoe Park. Immunity 2005
88
10

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.
D Sanlaville, H C Etchevers, M Gonzales, J Martinovic, M Clément-Ziza, A-L Delezoide, M-C Aubry, A Pelet, S Chemouny, C Cruaud,[...]. J Med Genet 2006
156
10

Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients.
M Louise Markert, Marcella Sarzotti, Daniel A Ozaki, Gregory D Sempowski, Maria E Rhein, Laura P Hale, Francoise Le Deist, Marilyn J Alexieff, Jie Li, Elizabeth R Hauser,[...]. Blood 2003
89
10

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
95
10


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
18

The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificity.
Joseph A Newman, Hazel Aitkenhead, Angeline E Gavard, Ioanna A Rota, Adam E Handel, Georg A Hollander, Opher Gileadi. J Biol Chem 2020
5
40

Thymus: the next (re)generation.
Mohammed S Chaudhry, Enrico Velardi, Jarrod A Dudakov, Marcel R M van den Brink. Immunol Rev 2016
75
10


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
141
10

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
10

A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome.
Jorieke E H Bergman, Nicole Janssen, Almer M van der Sloot, Hermien E K de Walle, Jeroen Schoots, Nanna D Rendtorff, Lisbeth Tranebjaerg, Lies H Hoefsloot, Conny M A van Ravenswaaij-Arts, Robert M W Hofstra. Hum Mutat 2012
45
10

FOXN1 in thymus organogenesis and development.
Harsh Jayesh Vaidya, Alberto Briones Leon, C Clare Blackburn. Eur J Immunol 2016
45
10

Thymus Size and Age-related Thymic Involution: Early Programming, Sexual Dimorphism, Progenitors and Stroma.
Jingang Gui, Lisa Maria Mustachio, Dong-Ming Su, Ruth W Craig. Aging Dis 2012
109
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.