A citation-based method for searching scientific literature

Alan F Rope, Deborah L Cragun, Howard M Saal, Robert J Hopkin. J Pediatr 2009
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
38

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
22

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
22

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
22

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.
Antonia Kwan, Roshini S Abraham, Robert Currier, Amy Brower, Karen Andruszewski, Jordan K Abbott, Mei Baker, Mark Ballow, Louis E Bartoshesky, Francisco A Bonilla,[...]. JAMA 2014
344
22

The DiGeorge anomaly.
R Hong. Clin Rev Allergy Immunol 2001
14
21

Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation.
C Pignata, L Gaetaniello, A M Masci, J Frank, A Christiano, E Matrecano, L Racioppi. Blood 2001
44
16

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
16

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
16

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
16

The cutaneous manifestations of atypical complete DiGeorge syndrome: a histopathologic and immunohistochemical study.
Maria Angelica Selim, Mary L Markert, James L Burchette, Christopher M Herman, John W Turner. J Cutan Pathol 2008
20
16

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
16

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
16

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
16

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
16

Statewide newborn screening for severe T-cell lymphopenia.
John M Routes, William J Grossman, James Verbsky, Ronald H Laessig, Gary L Hoffman, Charles D Brokopp, Mei W Baker. JAMA 2009
141
16


DiGeorge anomaly with renal agenesis in infants of mothers with diabetes.
T A Wilson, S L Blethen, A Vallone, D S Alenick, P Nolan, A Katz, T P Amorillo, E Goldmuntz, B S Emanuel, D A Driscoll. Am J Med Genet 1993
40
16

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

Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
194
16

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
16


Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience.
William T Shearer, Elizabeth Dunn, Luigi D Notarangelo, Christopher C Dvorak, Jennifer M Puck, Brent R Logan, Linda M Griffith, Donald B Kohn, Richard J O'Reilly, Thomas A Fleisher,[...]. J Allergy Clin Immunol 2014
164
16

Successful cord blood transplantation for a CHARGE syndrome with CHD7 mutation showing DiGeorge sequence including hypoparathyroidism.
Hirosuke Inoue, Hidetoshi Takada, Takeshi Kusuda, Takako Goto, Masayuki Ochiai, Tadamune Kinjo, Jun Muneuchi, Yasushi Takahata, Naomi Takahashi, Tomohiro Morio,[...]. Eur J Pediatr 2010
15
20

Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts.
William T Shearer, Thomas A Fleisher, Rebecca H Buckley, Zuhair Ballas, Mark Ballow, R Michael Blaese, Francisco A Bonilla, Mary Ellen Conley, Charlotte Cunningham-Rundles, Alexandra H Filipovich,[...]. J Allergy Clin Immunol 2014
73
16


The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
326
11

Use of allograft biopsies to assess thymopoiesis after thymus transplantation.
M Louise Markert, Jie Li, Blythe H Devlin, Jeffrey C Hoehner, Henry E Rice, Michael A Skinner, Yi-Ju Li, Laura P Hale. J Immunol 2008
18
11

Factors affecting success of thymus transplantation for complete DiGeorge anomaly.
M L Markert, B H Devlin, I K Chinn, E A McCarthy, Y J Li. Am J Transplant 2008
25
11

Exposing the human nude phenotype.
J Frank, C Pignata, A A Panteleyev, D M Prowse, H Baden, L Weiner, L Gaetaniello, W Ahmad, N Pozzi, P B Cserhalmi-Friedman,[...]. Nature 1999
185
11

Thymic transplantation for complete DiGeorge syndrome: medical and surgical considerations.
Henry E Rice, Michael A Skinner, Samuel M Mahaffey, Keith T Oldham, Richard J Ing, Laura P Hale, M Louise Markert. J Pediatr Surg 2004
39
11

Thymus transplantation in complete DiGeorge anomaly.
M Louise Markert, Blythe H Devlin, Ivan K Chinn, Elizabeth A McCarthy. Immunol Res 2009
32
11


Maldescent of the thymus.
A M DiGeorge. Pediatr Pathol 1994
3
66

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
288
11



Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Kathleen E Sullivan. Immunol Allergy Clin North Am 2008
61
11

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
11


Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
F Greenberg, F F Elder, P Haffner, H Northrup, D H Ledbetter. Am J Hum Genet 1988
157
11

Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly.
F Greenberg, K B Courtney, R A Wessels, J Huhta, R J Carpenter, D C Rich, D H Ledbetter. Am J Med Genet 1988
45
11

Thymus transplantation.
M Louise Markert, Blythe H Devlin, Elizabeth A McCarthy. Clin Immunol 2010
82
11

Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome.
Jodi-Ann M Swaby, Candice K Silversides, Sean C Bekeschus, Sara Piran, Erwin N Oechslin, Eva W C Chow, Anne S Bassett. Am J Cardiol 2011
15
13

VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study.
Juan Francisco Calderón, Alonso R Puga, M Luisa Guzmán, Carmen Paz Astete, Marta Arriaza, Mariana Aracena, Teresa Aravena, Patricia Sanz, Gabriela M Repetto. Biol Res 2009
4
50


A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans.
Lanying Li, Despina Moshous, Yungui Zhou, Junhua Wang, Gang Xie, Eduardo Salido, Diana Hu, Jean-Pierre de Villartay, Morton J Cowan. J Immunol 2002
120
11

4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.
Goran Cuturilo, Björn Menten, Aleksandar Krstic, Danijela Drakulic, Ida Jovanovic, Vojislav Parezanovic, Milena Stevanovic. Eur J Pediatr 2011
14
14

Progressive deficiencies in blood T cells associated with a 10p12-13 interstitial deletion.
C Pignata, A D'Agostino, P Finelli, M Fiore, I Scotese, E Cosentini, C Cuomo, S Venuta. Clin Immunol Immunopathol 1996
10
20

Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: entering a new century, do we do better?
Andrew R Gennery, Mary A Slatter, Laure Grandin, Pierre Taupin, Andrew J Cant, Paul Veys, Persis J Amrolia, H Bobby Gaspar, E Graham Davies, Wilhelm Friedrich,[...]. J Allergy Clin Immunol 2010
269
11


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.