A citation-based method for searching scientific literature

Patrick Riley, Dennis S Weiner, Bonnie Leighley, David Jonah, D Holmes Morton, Kevin A Strauss, Michael B Bober, Martin S Dicintio. J Child Orthop 2015
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia.
M Ridanpää, H van Eenennaam, K Pelin, R Chadwick, C Johnson, B Yuan, W vanVenrooij, G Pruijn, R Salmela, S Rockas,[...]. Cell 2001
304
60

Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator.
Christian T Thiel, Denise Horn, Bernhard Zabel, Arif B Ekici, Kelly Salinas, Erich Gebhart, Franz Rüschendorf, Heinrich Sticht, Jürgen Spranger, Dietmar Müller,[...]. Am J Hum Genet 2005
91
40

DWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIA.
V A MCKUSICK, R ELDRIDGE, J A HOSTETLER, U RUANGWIT, J A EGELAND. Bull Johns Hopkins Hosp 1965
266
40

RNase MRP RNA and human genetic diseases.
Allison N Martin, Yong Li. Cell Res 2007
51
40

Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia.
Pia Hermanns, Alison A Bertuch, Terry K Bertin, Brian Dawson, Mark E Schmitt, Chad Shaw, Bernhard Zabel, Brendan Lee. Hum Mol Genet 2005
75
40


Skeletal growth in cartilage-hair hypoplasia. A radiological study of 82 patients.
O Mäkitie, E Marttinen, I Kaitila. Pediatr Radiol 1992
24
40

Marked variability in the radiographic features of cartilage-hair hypoplasia: case report and review of the literature.
Andrea Kwan, M A Manning, Linda K Zollars, H Eugene Hoyme. Am J Med Genet A 2012
11
40


Evolutionary comparison provides evidence for pathogenicity of RMRP mutations.
Luisa Bonafé, Emmanouil T Dermitzakis, Sheila Unger, Cheryl R Greenberg, Belinda A Campos-Xavier, Andreas Zankl, Catherine Ucla, Stylianos E Antonarakis, Andrea Superti-Furga, Alexandre Reymond. PLoS Genet 2005
48
40

Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP.
Maaret Ridanpää, Pertti Sistonen, Susanna Rockas, David L Rimoin, Outi Mäkitie, Ilkka Kaitila. Eur J Hum Genet 2002
66
40

Mutual interactions between subunits of the human RNase MRP ribonucleoprotein complex.
Tim J M Welting, Walther J van Venrooij, Ger J M Pruijn. Nucleic Acids Res 2004
71
20

Impaired spermatogenesis: an unrecognized feature of cartilage-hair hypoplasia.
O M Mäkitie, P J Tapanainen, L Dunkel, M A Siimes. Ann Med 2001
18
20

Mechanisms Underlying Testicular Damage and Dysfunction in Mice With Partial IGF-1 Deficiency and the Effectiveness of IGF-1 Replacement Therapy.
Inma Castilla-Cortázar, Alberto Gago, Úrsula Muñoz, Elena Ávila-Gallego, Lucía Guerra-Menéndez, María Cruz Sádaba, Mariano García-Magariño, María Olleros Santos-Ruiz, G A Aguirre, Juan Enrique Puche. Urology 2015
11
20



Regulation of the growth hormone receptor/binding protein, insulin-like growth factor ternary complex system in human cirrhosis.
Anthony J Donaghy, Patric J D Delhanty, Ken K Ho, Roger Williams, Robert C Baxter. J Hepatol 2002
45
20

Insulin-like growth factor I stimulates erythropoiesis in hypophysectomized rats.
A Kurtz, J Zapf, K U Eckardt, G Clemons, E R Froesch, C Bauer. Proc Natl Acad Sci U S A 1988
118
20

Altered intestinal transport of amino acids in cirrhotic rats: the effect of insulin-like growth factor-I.
M Pascual, I Castilla-Cortazar, E Urdaneta, J Quiroga, M Garcia, A Picardi, J Prieto. Am J Physiol Gastrointest Liver Physiol 2000
27
20

Schmorl Nodes Mimicking Osteolytic Bone Metastases.
Naoya Niwa, Toru Nishiyama, Choichiro Ozu, Yasuto Yagi, Shiro Saito. Urology 2015
3
33

Clinical and molecular diagnosis of a cartilage-hair hypoplasia with IGF-1 deficiency.
Inma Castilla-Cortázar, Julieta Rodríguez De Ita, Irene Martín-Estal, Fabiola Castorena, Gabriel A Aguirre, Rocío García de la Garza, Martha I Elizondo. Am J Med Genet A 2017
2
50

Hepatoprotection and neuroprotection induced by low doses of IGF-II in aging rats.
Inma Castilla-Cortázar, María García-Fernández, Gloria Delgado, Juan E Puche, Inma Sierra, Rima Barhoum, Salvador González-Barón. J Transl Med 2011
27
20

Hirschsprung's disease in cartilage-hair hypoplasia has poor prognosis.
Outi Mäkitie, Marja Heikkinen, Ilkka Kaitila, Risto Rintala. J Pediatr Surg 2002
21
20

Deficiency of humoral immunity in cartilage-hair hypoplasia.
O Mäkitie, I Kaitila, E Savilahti. J Pediatr 2000
41
20


Effect of IGF-I on total serum antioxidant status in cirrhotic rats.
M García-Fernández, I Castilla-Cortázar, M Díaz-Sánchez, F Díez Caballero, A Castilla, A Díaz Casares, I Varela-Nieto, S González-Barón. J Physiol Biochem 2003
16
20



The role of growth hormone and insulin-like growth factors in the immune system.
S C van Buul-Offers, R Kooijman. Cell Mol Life Sci 1998
49
20

Low doses of insulin-like growth factor-I induce mitochondrial protection in aging rats.
Juan E Puche, María García-Fernández, Jordi Muntané, José Rioja, Salvador González-Barón, Inma Castilla Cortazar. Endocrinology 2008
83
20

Insulin-like growth factor I stimulates human erythroid colony formation in vitro.
M Claustres, P Chatelain, C Sultan. J Clin Endocrinol Metab 1987
99
20

Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasia.
Alireza Baradaran-Heravi, Christian Thiel, Anita Rauch, Martin Zenker, Cornelius F Boerkoel, Ilkka Kaitila. Am J Med Genet A 2008
14
20


Anemia in children with cartilage-hair hypoplasia is related to body growth and to the insulin-like growth factor system.
O Mäkitie, E Juvonen, L Dunkel, I Kaitila, M A Siimes. J Clin Endocrinol Metab 2000
20
20

Human conditions of insulin-like growth factor-I (IGF-I) deficiency.
Juan E Puche, Inma Castilla-Cortázar. J Transl Med 2012
129
20

Insulin-like growth factor-1 deficiency and metabolic syndrome.
G A Aguirre, J Rodríguez De Ita, R G de la Garza, I Castilla-Cortazar. J Transl Med 2016
121
20

Insulin-like growth factor I (IGF-I) replacement therapy increases albumin concentration in liver cirrhosis: results of a pilot randomized controlled clinical trial.
Mariam Conchillo, Robert J de Knegt, Marina Payeras, Jorge Quiroga, Bruno Sangro, Jose-Ignacio Herrero, Inma Castilla-Cortazar, Jan Frystyk, Allan Flyvbjerg, Carl Yoshizawa,[...]. J Hepatol 2005
75
20

Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015.
Capucine Picard, Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, Talal Chatila, Mary Ellen Conley, Charlotte Cunningham-Rundles, Amos Etzioni, Steven M Holland, Christoph Klein,[...]. J Clin Immunol 2015
393
20

The diversity of mutations and clinical outcomes for ELANE-associated neutropenia.
Vahagn Makaryan, Cornelia Zeidler, Audrey Anna Bolyard, Julia Skokowa, Elin Rodger, Merideth L Kelley, Laurence A Boxer, Mary Ann Bonilla, Peter E Newburger, Akiko Shimamura,[...]. Curr Opin Hematol 2015
69
20

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency.
Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, Talal Chatila, Mary Ellen Conley, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco, H Bobby Gaspar, Steven M Holland,[...]. Front Immunol 2014
291
20


Secondary immunodeficiencies, including HIV infection.
Javier Chinen, William T Shearer. J Allergy Clin Immunol 2010
82
20

Severe combined immunodeficiency--an update.
Emilia Cirillo, Giuliana Giardino, Vera Gallo, Roberta D'Assante, Fiorentino Grasso, Roberta Romano, Cristina Di Lillo, Giovanni Galasso, Claudio Pignata. Ann N Y Acad Sci 2015
44
20

Innate immunity defects in Hermansky-Pudlak type 2 syndrome.
Stefania Fontana, Silvia Parolini, William Vermi, Sarah Booth, Federico Gallo, Marta Donini, Marzia Benassi, Francesca Gentili, Daniela Ferrari, Lucia D Notarangelo,[...]. Blood 2006
94
20

Hyper-IgE syndrome update.
Kathryn J Sowerwine, Steven M Holland, Alexandra F Freeman. Ann N Y Acad Sci 2012
86
20

Severe combined immunodeficiencies and related disorders.
Alain Fischer, Luigi D Notarangelo, Bénédicte Neven, Marina Cavazzana, Jennifer M Puck. Nat Rev Dis Primers 2015
89
20

Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1.
Vahid Reza Yassaee, Feyzollah Hashemi-Gorji, Sara Boosaliki, Nima Parvaneh. Hum Immunol 2016
11
20

Laboratory evaluation of primary immunodeficiencies.
João B Oliveira, Thomas A Fleisher. J Allergy Clin Immunol 2010
47
20

Monogenic autoinflammatory diseases: concept and clinical manifestations.
Adriana Almeida de Jesus, Raphaela Goldbach-Mansky. Clin Immunol 2013
108
20

Ribosomopathies: mechanisms of disease.
Hani Nakhoul, Jiangwei Ke, Xiang Zhou, Wenjuan Liao, Shelya X Zeng, Hua Lu. Clin Med Insights Blood Disord 2014
46
20


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.