A citation-based method for searching scientific literature

Gabriela A Vasques, Naoko Amano, Ana J Docko, Mariana F A Funari, Elisangela P S Quedas, Mirian Y Nishi, Ivo J P Arnhold, Tomonobu Hasegawa, Alexander A L Jorge. J Clin Endocrinol Metab 2013
Times Cited: 71







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



Times Cited
  Times     Co-cited
Similarity


[Acromesomelic dwarfism].
P Maroteaux, B Martinelli, E Campailla. Presse Med 1971
60
8

Nitric oxide, C-type natriuretic peptide and cGMP as regulators of endochondral ossification.
Cristina C Teixeira, Hanga Agoston, Frank Beier. Dev Biol 2008
50
10

Recent research on the growth plate: Recent insights into the regulation of the growth plate.
Julian C Lui, Ola Nilsson, Jeffrey Baron. J Mol Endocrinol 2014
48
10

The continuum of growth hormone-IGF-I axis defects causing short stature: diagnostic and therapeutic challenges.
Martin O Savage, Christine P Burren, Ron G Rosenfeld. Clin Endocrinol (Oxf) 2010
72
7

A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.
Reha M Toydemir, Anna E Brassington, Pinar Bayrak-Toydemir, Patrycja A Krakowiak, Lynn B Jorde, Frank G Whitby, Nicola Longo, David H Viskochil, John C Carey, Michael J Bamshad. Am J Hum Genet 2006
85
7

Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways.
Ana P M Canton, Sílvia S Costa, Tatiane C Rodrigues, Debora R Bertola, Alexsandra C Malaquias, Fernanda A Correa, Ivo J P Arnhold, Carla Rosenberg, Alexander A L Jorge. Eur J Endocrinol 2014
23
21


Heterozygous IGFALS gene variants in idiopathic short stature and normal children: impact on height and the IGF system.
Horacio M Domené, Paula A Scaglia, Alicia S Martínez, Ana C Keselman, Liliana M Karabatas, Viviana R Pipman, Sonia V Bengolea, María C Guida, María G Ropelato, María G Ballerini,[...]. Horm Res Paediatr 2013
28
17

Furin-mediated processing of Pro-C-type natriuretic peptide.
Chengliang Wu, Faye Wu, Junliang Pan, John Morser, Qingyu Wu. J Biol Chem 2003
141
7

The receptor guanylyl cyclase Npr2 is essential for sensory axon bifurcation within the spinal cord.
Hannes Schmidt, Agne Stonkute, René Jüttner, Susanne Schäffer, Jens Buttgereit, Robert Feil, Franz Hofmann, Fritz G Rathjen. J Cell Biol 2007
63
7

Nationwide age references for sitting height, leg length, and sitting height/height ratio, and their diagnostic value for disproportionate growth disorders.
A M Fredriks, S van Buuren, W J M van Heel, R H M Dijkman-Neerincx, S P Verloove-Vanhorick, J M Wit. Arch Dis Child 2005
140
7

Catalytically Active Guanylyl Cyclase B Requires Endoplasmic Reticulum-mediated Glycosylation, and Mutations That Inhibit This Process Cause Dwarfism.
Deborah M Dickey, Aaron B Edmund, Neil M Otto, Thomas S Chaffee, Jerid W Robinson, Lincoln R Potter. J Biol Chem 2016
11
45

A genetic approach to evaluation of short stature of undetermined cause.
Philip G Murray, Peter E Clayton, Steven D Chernausek. Lancet Diabetes Endocrinol 2018
18
27

Multigene Sequencing Analysis of Children Born Small for Gestational Age With Isolated Short Stature.
Bruna L Freire, Thais K Homma, Mariana F A Funari, Antônio M Lerario, Gabriela A Vasques, Alexsandra C Malaquias, Ivo J P Arnhold, Alexander A L Jorge. J Clin Endocrinol Metab 2019
21
23

C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia.
Ravi Savarirayan, Melita Irving, Carlos A Bacino, Bret Bostwick, Joel Charrow, Valerie Cormier-Daire, Kim-Hanh Le Quan Sang, Patricia Dickson, Paul Harmatz, John Phillips,[...]. N Engl J Med 2019
54
9

NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy.
Lukas Plachy, Petra Dusatkova, Klara Maratova, Lenka Petruzelkova, Dana Zemkova, Lenka Elblova, Petra Kucerova, Ledjona Toni, Stanislava Kolouskova, Marta Snajderova,[...]. J Clin Endocrinol Metab 2020
9
55


Identification and functional analysis of novel human growth hormone secretagogue receptor (GHSR) gene mutations in Japanese subjects with short stature.
Hiroshi Inoue, Natsumi Kangawa, Atsuko Kinouchi, Yukiko Sakamoto, Chizuko Kimura, Reiko Horikawa, Yosuke Shigematsu, Mitsuo Itakura, Tsutomu Ogata, Kenji Fujieda. J Clin Endocrinol Metab 2011
44
9


Nosology and classification of genetic skeletal disorders: 2010 revision.
Matthew L Warman, Valerie Cormier-Daire, Christine Hall, Deborah Krakow, Ralph Lachman, Martine LeMerrer, Geert Mortier, Stefan Mundlos, Gen Nishimura, David L Rimoin,[...]. Am J Med Genet A 2011
403
5

Utah Growth Study: growth standards and the prevalence of growth hormone deficiency.
R Lindsay, M Feldkamp, D Harris, J Robertson, M Rallison. J Pediatr 1994
256
5


Genetic evaluation of short stature.
J M Wit, W Kiess, P Mullis. Best Pract Res Clin Endocrinol Metab 2011
43
9

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.
Gudrun A Rappold, Maki Fukami, Beate Niesler, Simone Schiller, Walter Zumkeller, Markus Bettendorf, Udo Heinrich, Elpis Vlachopapadoupoulou, Thomas Reinehr, Kazumichi Onigata,[...]. J Clin Endocrinol Metab 2002
139
5

Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorder.
Andrew Dauber, Joan Stoler, Eliana Hechter, Jason Safer, Joel N Hirschhorn. J Pediatr 2013
25
16

Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
Louise S Bicknell, Ernie M H F Bongers, Andrea Leitch, Stephen Brown, Jeroen Schoots, Margaret E Harley, Salim Aftimos, Jumana Y Al-Aama, Michael Bober, Paul A J Brown,[...]. Nat Genet 2011
164
5

Genetic analysis of short children with apparent growth hormone insensitivity.
J M Wit, H A van Duyvenvoorde, S A Scheltinga, S de Bruin, L Hafkenscheid, S G Kant, C A L Ruivenkamp, A C J Gijsbers, J van Doorn, E Feigerlova,[...]. Horm Res Paediatr 2012
40
10

Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency.
Gudrun Rappold, Werner F Blum, Elena P Shavrikova, Brenda J Crowe, Ralph Roeth, Charmian A Quigley, Judith L Ross, Beate Niesler. J Med Genet 2007
145
5

Bloom syndrome in short children born small for gestational age: a challenging diagnosis.
Judith S Renes, Ruben H Willemsen, Anja Wagner, Martijn J J Finken, Anita C S Hokken-Koelega. J Clin Endocrinol Metab 2013
27
14

Dose-dependent effect of growth hormone on final height in children with short stature without growth hormone deficiency.
Kerstin Albertsson-Wikland, A Stefan Aronson, Jan Gustafsson, Lars Hagenäs, Sten A Ivarsson, Björn Jonsson, Berit Kriström, Claude Marcus, Karl Olof Nilsson, E Martin Ritzén,[...]. J Clin Endocrinol Metab 2008
103
5

Achondroplasia.
William A Horton, Judith G Hall, Jacqueline T Hecht. Lancet 2007
269
5

Granulosa cell ligand NPPC and its receptor NPR2 maintain meiotic arrest in mouse oocytes.
Meijia Zhang, You-Qiang Su, Koji Sugiura, Guoliang Xia, John J Eppig. Science 2010
309
5


Receptor selectivity of natriuretic peptide family, atrial natriuretic peptide, brain natriuretic peptide, and C-type natriuretic peptide.
S Suga, K Nakao, K Hosoda, M Mukoyama, Y Ogawa, G Shirakami, H Arai, Y Saito, Y Kambayashi, K Inouye. Endocrinology 1992
652
5

Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trial.
Werner F Blum, Brenda J Crowe, Charmian A Quigley, Heike Jung, Dachuang Cao, Judith L Ross, LeeAnn Braun, Gudrun Rappold. J Clin Endocrinol Metab 2007
72
5

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome).
V Belin, V Cusin, G Viot, D Girlich, A Toutain, A Moncla, M Vekemans, M Le Merrer, A Munnich, V Cormier-Daire. Nat Genet 1998
263
5

The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes.
Antonio Marchini, Tiina Marttila, Anja Winter, Sandra Caldeira, Ilaria Malanchi, Rüdiger J Blaschke, Beate Häcker, Ercole Rao, Marcel Karperien, Jan M Wit,[...]. J Biol Chem 2004
76
5

Intestinal secretory defects and dwarfism in mice lacking cGMP-dependent protein kinase II.
A Pfeifer, A Aszódi, U Seidler, P Ruth, F Hofmann, R Fässler. Science 1996
311
5

Paternally Inherited IGF2 Mutation and Growth Restriction.
Matthias Begemann, Birgit Zirn, Gijs Santen, Elisa Wirthgen, Lukas Soellner, Hans-Martin Büttel, Roland Schweizer, Wilbert van Workum, Gerhard Binder, Thomas Eggermann. N Engl J Med 2015
122
5

IGF1R mutations as cause of SGA.
J Klammt, W Kiess, R Pfäffle. Best Pract Res Clin Endocrinol Metab 2011
69
5

The growth response to GH treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects.
S H Donze, C R Meijer, S G Kant, G R J Zandwijken, A H van der Hout, R M L van Spaendonk, A M W van den Ouweland, J M Wit, M Losekoot, W Oostdijk. Eur J Endocrinol 2015
11
36

Two short children born small for gestational age with insulin-like growth factor 1 receptor haploinsufficiency illustrate the heterogeneity of its phenotype.
Wietske A Ester, Hermine A van Duyvenvoorde, Caroline C de Wit, Alexander J Broekman, Claudia A L Ruivenkamp, Lutgarde C P Govaerts, Jan M Wit, Anita C S Hokken-Koelega, Monique Losekoot. J Clin Endocrinol Metab 2009
73
5

Identification of a novel heterozygous IGF1 splicing mutation in a large kindred with familial short stature.
John S Fuqua, Michael Derr, Ron G Rosenfeld, Vivian Hwa. Horm Res Paediatr 2012
28
14

Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature.
Sara Benito-Sanz, Miriam Aza-Carmona, Amaya Rodríguez-Estevez, Ixaso Rica-Etxebarria, Ricardo Gracia, Angel Campos-Barros, Karen E Heath. Eur J Hum Genet 2012
37
10

Copy number variants in short children born small for gestational age.
Jan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, Janina Caliebe, Cathy A J Bosch, Julian C Lui, Antoinet C J Gijsbers, Egbert Bakker, Martijn H Breuning, Wilma Oostdijk,[...]. Horm Res Paediatr 2014
15
26

C-type natriuretic peptide plasma levels are elevated in subjects with achondroplasia, hypochondroplasia, and thanatophoric dysplasia.
Robert C Olney, Timothy C R Prickett, Eric A Espiner, William G Mackenzie, Angela L Duker, Colleen Ditro, Bernhard Zabel, Tomonobu Hasegawa, Hiroshi Kitoh, Arthur S Aylsworth,[...]. J Clin Endocrinol Metab 2015
19
21


Cardiac fibrosis in mice lacking brain natriuretic peptide.
N Tamura, Y Ogawa, H Chusho, K Nakamura, K Nakao, M Suda, M Kasahara, R Hashimoto, G Katsuura, M Mukoyama,[...]. Proc Natl Acad Sci U S A 2000
431
5

Neutral endopeptidase-resistant C-type natriuretic peptide variant represents a new therapeutic approach for treatment of fibroblast growth factor receptor 3-related dwarfism.
Daniel J Wendt, Melita Dvorak-Ewell, Sherry Bullens, Florence Lorget, Sean M Bell, Jeff Peng, Sianna Castillo, Mika Aoyagi-Scharber, Charles A O'Neill, Pavel Krejci,[...]. J Pharmacol Exp Ther 2015
56
7

C-type natriuretic peptide (CNP) is a bifurcation factor for sensory neurons.
Hannes Schmidt, Agne Stonkute, René Jüttner, Doris Koesling, Andreas Friebe, Fritz G Rathjen. Proc Natl Acad Sci U S A 2009
56
7


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.