A citation-based method for searching scientific literature

Lisa M Piliero, Amy N Sanford, Donna M McDonald-McGinn, Elaine H Zackai, Kathleen E Sullivan. Blood 2004
Times Cited: 87







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



Times Cited
  Times     Co-cited
Similarity



Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
A R Gennery, D Barge, J J O'Sullivan, T J Flood, M Abinun, A J Cant. Arch Dis Child 2002
103
37

Long-term assessment of T-cell populations in DiGeorge syndrome.
Javier Chinen, Howard M Rosenblatt, E O'Brian Smith, William T Shearer, Lenora M Noroski. J Allergy Clin Immunol 2003
55
58

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
819
31

Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome).
A Finocchi, S Di Cesare, M L Romiti, C Capponi, P Rossi, R Carsetti, C Cancrini. Pediatr Allergy Immunol 2006
52
46


Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
M Pierdominici, F Mazzetta, E Caprini, M Marziali, M C Digilio, B Marino, A Aiuti, F Amati, G Russo, G Novelli,[...]. Clin Exp Immunol 2003
42
54

Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
R Zemble, E Luning Prak, K McDonald, D McDonald-McGinn, E Zackai, K Sullivan. Clin Immunol 2010
53
43

CD4(+) CD25(+) T-cell production in healthy humans and in patients with thymic hypoplasia.
Kathleen E Sullivan, Donna McDonald-McGinn, Elaine H Zackai. Clin Diagn Lab Immunol 2002
64
34

Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
C A Smith, D A Driscoll, B S Emanuel, D M McDonald-McGinn, E H Zackai, K E Sullivan. Clin Diagn Lab Immunol 1998
53
39

Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes.
K E Sullivan, A F Jawad, P Randall, D A Driscoll, B S Emanuel, D M McDonald-McGinn, E H Zackai. Clin Immunol Immunopathol 1998
75
26

Prediction of persistent immunodeficiency in the DiGeorge anomaly.
J Bastian, S Law, L Vogler, A Lawton, H Herrod, S Anderson, S Horowitz, R Hong. J Pediatr 1989
93
21

Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases.
M Louise Markert, Marilyn J Alexieff, Jie Li, Marcella Sarzotti, Daniel A Ozaki, Blythe H Devlin, Gregory D Sempowski, Maria E Rhein, Paul Szabolcs, Laura P Hale,[...]. J Allergy Clin Immunol 2004
97
21

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
21


Humoral immunity in DiGeorge syndrome.
A K Junker, D A Driscoll. J Pediatr 1995
54
31

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
18

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
17

Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Elena E Perez, Aleksandra Bokszczanin, Donna McDonald-McGinn, Elaine H Zackai, Kathleen E Sullivan. Pediatrics 2003
50
28

Clinical and immunologic spectrum of the DiGeorge syndrome.
D J Barrett, A J Ammann, D W Wara, M J Cowan, T J Fisher, E R Stiehm. J Clin Lab Immunol 1981
69
20

The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
16

A population study of chromosome 22q11 deletions in infancy.
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
180
16

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
45

Post-natal ontogenesis of the T-cell receptor CD4 and CD8 Vbeta repertoire and immune function in children with DiGeorge syndrome.
Caterina Cancrini, Maria Luisa Romiti, Andrea Finocchi, Silvia Di Cesare, Patrizia Ciaffi, Claudia Capponi, Savita Pahwa, Paolo Rossi. J Clin Immunol 2005
26
53


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
16

Immunologic defects in 22q11.2 deletion syndrome.
Andrew McLean-Tooke, Dawn Barge, Gavin P Spickett, Andrew R Gennery. J Allergy Clin Immunol 2008
53
26

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
14

Transplantation of thymus tissue in complete DiGeorge syndrome.
M L Markert, A Boeck, L P Hale, A L Kloster, T M McLaughlin, M N Batchvarova, D C Douek, R A Koup, D D Kostyu, F E Ward,[...]. N Engl J Med 1999
175
14

Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
193
14

Early development of immunity in diGeorge syndrome.
Anna Sedivá, Jiøina Bartůnková, Radana Zachová, Andrea Poloucková, Ondrej Hrusák, Ales Janda, Eduard Kocárek, Drahuse Novotná, Kamila Novotná, Tibor Klein. Med Sci Monit 2005
24
54

Maturational alterations of peripheral T cell subsets and cytokine gene expression in 22q11.2 deletion syndrome.
Y Kanaya, S Ohga, K Ikeda, K Furuno, T Ohno, H Takada, N Kinukawa, T Hara. Clin Exp Immunol 2006
22
59

Complete DiGeorge syndrome: persistence of profound immunodeficiency.
M L Markert, D S Hummell, H M Rosenblatt, S E Schiff, T O Harville, L W Williams, R I Schiff, R H Buckley. J Pediatr 1998
82
14

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome).
K E Sullivan, D M McDonald-McGinn, D A Driscoll, C M Zmijewski, A S Ellabban, L Reed, B S Emanuel, E H Zackai, B H Athreya, G Keenan. Arthritis Rheum 1997
76
15

Live viral vaccines in patients with partial DiGeorge syndrome: clinical experience and cellular immunity.
Edina H Moylett, Anita N Wasan, Lenora M Noroski, William T Shearer. Clin Immunol 2004
33
36

Autoimmune cytopenias in the 22q11.2 deletion syndrome.
J K Davies, P Telfer, J D Cavenagh, N Foot, M Neat. Clin Lab Haematol 2003
34
35


Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome.
Scott Lawrence, Donna M McDonald-McGinn, Elaine Zackai, Kathleen E Sullivan. J Pediatr 2003
51
23

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
679
13


Clinical features of 78 adults with 22q11 Deletion Syndrome.
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
285
13

Changes in thymic function with age and during the treatment of HIV infection.
D C Douek, R D McFarland, P H Keiser, E A Gage, J M Massey, B F Haynes, M A Polis, A T Haase, M B Feinberg, J L Sullivan,[...]. Nature 1998
12

Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).
Elena Perez, Kathleen E Sullivan. Curr Opin Pediatr 2002
85
11

Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: a case report.
Christian P Kratz, Tim Niehues, Sigrid Lyding, Andreas Heusch, Gisela Janssen, Ulrich Göbel. Pediatr Hematol Oncol 2003
28
35

Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome.
M Louise Markert, Marilyn J Alexieff, Jie Li, Marcella Sarzotti, Daniel A Ozaki, Blythe H Devlin, Debra A Sedlak, Gregory D Sempowski, Laura P Hale, Henry E Rice,[...]. Blood 2004
66
15


Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Sólveig Oskarsdóttir, Christina Persson, Bengt O Eriksson, Anders Fasth. Eur J Pediatr 2005
114
11

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
229
11

Immunoglobulin deficiencies: the B-lymphocyte side of DiGeorge Syndrome.
Kiran Patel, Javeed Akhter, Lisa Kobrynski, M A Benjamin Gathmann, Onika Davis, Kathleen E Sullivan. J Pediatr 2012
38
26

A prospective study of influenza vaccination and a comparison of immunologic parameters in children and adults with chromosome 22q11.2 deletion syndrome (digeorge syndrome/velocardiofacial syndrome).
Abbas F Jawad, Eline Luning Prak, Jean Boyer, Donna M McDonald-McGinn, Elaine Zackai, Kenyetta McDonald, Kathleen E Sullivan. J Clin Immunol 2011
24
41


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.