A citation-based method for searching scientific literature

Peter Lauffer, Erick Miranda-Laferte, Hermine A van Duyvenvoorde, Arie van Haeringen, Franziska Werner, Eveline Boudin, Hannes Schmidt, Thomas D Mueller, Michaela Kuhn, Daniëlle C M van der Kaay. J Clin Endocrinol Metab 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux.
Noor Ul Ain, Muddassar Iqbal, Helena Valta, Christopher A Emerling, Sufian Ahmed, Outi Makitie, Sadaf Naz. Eur J Med Genet 2019
7
100

Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.
Kohji Miura, Ok-Hwa Kim, Hey Ran Lee, Noriyuki Namba, Toshimi Michigami, Won Joon Yoo, In Ho Choi, Keiichi Ozono, Tae-Joon Cho. Am J Med Genet A 2014
46
100

An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene.
Kohji Miura, Noriyuki Namba, Makoto Fujiwara, Yasuhisa Ohata, Hidekazu Ishida, Taichi Kitaoka, Takuo Kubota, Haruhiko Hirai, Chikahisa Higuchi, Noriyuki Tsumaki,[...]. PLoS One 2012
71
100

An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformities.
Sabine E Hannema, Hermine A van Duyvenvoorde, Thomas Premsler, Ruey-Bing Yang, Thomas D Mueller, Birgit Gassner, Heike Oberwinkler, Ferdinand Roelfsema, Gijs W E Santen, Timothy Prickett,[...]. J Clin Endocrinol Metab 2013
50
100

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
50

Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway.
Akihiro Yasoda, Yasato Komatsu, Hideki Chusho, Takashi Miyazawa, Ami Ozasa, Masako Miura, Tatsuya Kurihara, Tomohiro Rogi, Shoji Tanaka, Michio Suda,[...]. Nat Med 2004
262
50

Short Stature is Progressive in Patients with Heterozygous NPR2 Mutations.
Patrick C Hanley, Harsh S Kanwar, Corine Martineau, Michael A Levine. J Clin Endocrinol Metab 2020
6
50

Sitting Height to Standing Height Ratio Reference Charts for Children in the United States.
Colin Patrick Hawkes, Sogol Mostoufi-Moab, Shana E McCormack, Adda Grimberg, Babette S Zemel. J Pediatr 2020
4
50

BNP is a transcriptional target of the short stature homeobox gene SHOX.
Antonio Marchini, Beate Häcker, Tiina Marttila, Volker Hesse, Joyce Emons, Birgit Weiss, Marcel Karperien, Gudrun Rappold. Hum Mol Genet 2007
41
50

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
55
50

Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2.
Gabriela A Vasques, Alfonso Hisado-Oliva, Mariana F A Funari, Antonio M Lerario, Elisangela P S Quedas, Paulo Solberg, Karen E Heath, Alexander A L Jorge. J Pediatr Endocrinol Metab 2017
9
50

Complementary antagonistic actions between C-type natriuretic peptide and the MAPK pathway through FGFR-3 in ATDC5 cells.
Ami Ozasa, Yasato Komatsu, Akihiro Yasoda, Masako Miura, Yoko Sakuma, Yuko Nakatsuru, Hiroshi Arai, Nobuyuki Itoh, Kazuwa Nakao. Bone 2005
43
50

Identification and functional characterization of two novel NPR2 mutations in Japanese patients with short stature.
Naoko Amano, Tokuo Mukai, Yoshiya Ito, Satoshi Narumi, Toshiaki Tanaka, Susumu Yokoya, Tsutomu Ogata, Tomonobu Hasegawa. J Clin Endocrinol Metab 2014
48
50

Heterozygous mutations in natriuretic peptide receptor-B (NPR2) are associated with short stature.
Robert C Olney, Hülya Bükülmez, Cynthia F Bartels, Timothy C R Prickett, Eric A Espiner, Lincoln R Potter, Matthew L Warman. J Clin Endocrinol Metab 2006
115
50

Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts.
Aline Jelenkovic, Reijo Sund, Yoon-Mi Hur, Yoshie Yokoyama, Jacob V B Hjelmborg, Sören Möller, Chika Honda, Patrik K E Magnusson, Nancy L Pedersen, Syuichi Ooki,[...]. Sci Rep 2016
61
50

Heterozygous NPR2 Mutations Cause Disproportionate Short Stature, Similar to Léri-Weill Dyschondrosteosis.
Alfonso Hisado-Oliva, Ana I Garre-Vázquez, Fabiola Santaolalla-Caballero, Alberta Belinchón, Ana C Barreda-Bonis, Gabriela A Vasques, Joaquin Ramirez, Cristina Luzuriaga, Gianni Carlone, Isabel González-Casado,[...]. J Clin Endocrinol Metab 2015
43
50

Variations in pattern of pubertal changes in girls.
W A Marshall, J M Tanner. Arch Dis Child 1969
50

Dwarfism and early death in mice lacking C-type natriuretic peptide.
H Chusho, N Tamura, Y Ogawa, A Yasoda, M Suda, T Miyazawa, K Nakamura, K Nakao, T Kurihara, Y Komatsu,[...]. Proc Natl Acad Sci U S A 2001
328
50

Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux.
Cynthia F Bartels, Hulya Bükülmez, Pius Padayatti, David K Rhee, Conny van Ravenswaaij-Arts, Richard M Pauli, Stefan Mundlos, David Chitayat, Ling-Yu Shih, Lihadh I Al-Gazali,[...]. Am J Hum Genet 2004
227
50

Variations in the pattern of pubertal changes in boys.
W A Marshall, J M Tanner. Arch Dis Child 1970
50

Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations.
Ola Nilsson, Michael H Guo, Nancy Dunbar, Jadranka Popovic, Daniel Flynn, Christina Jacobsen, Julian C Lui, Joel N Hirschhorn, Jeffrey Baron, Andrew Dauber. J Clin Endocrinol Metab 2014
65
50

Rare and low-frequency coding variants alter human adult height.
Eirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, Ken Sin Lo, Andrew R Wood, Troels R Kjaer, Rebecca S Fine, Yingchang Lu, Claudia Schurmann, Heather M Highland,[...]. Nature 2017
282
50

Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature in patients initially classified as idiopathic short stature.
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
71
50

Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations.
Alexandra Gkourogianni, Melissa Andrew, Leah Tyzinski, Melissa Crocker, Jessica Douglas, Nancy Dunbar, Jan Fairchild, Mariana F A Funari, Karen E Heath, Alexander A L Jorge,[...]. J Clin Endocrinol Metab 2017
49
50

Genomic insights into growth and its disorders: an update.
Christiaan de Bruin, Andrew Dauber. Curr Opin Endocrinol Diabetes Obes 2016
5
50

Intact kinase homology domain of natriuretic peptide receptor-B is essential for skeletal development.
Rumi Hachiya, Yuko Ohashi, Yasutomi Kamei, Takayoshi Suganami, Hiroshi Mochizuki, Norimasa Mitsui, Masaaki Saitoh, Masako Sakuragi, Gen Nishimura, Hirofumi Ohashi,[...]. J Clin Endocrinol Metab 2007
48
50

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry.
Loic Yengo, Julia Sidorenko, Kathryn E Kemper, Zhili Zheng, Andrew R Wood, Michael N Weedon, Timothy M Frayling, Joel Hirschhorn, Jian Yang, Peter M Visscher. Hum Mol Genet 2018
488
50

Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature.
Alfonso Hisado-Oliva, Alba Ruzafa-Martin, Lucia Sentchordi, Mariana F A Funari, Carolina Bezanilla-López, Marta Alonso-Bernáldez, Jimena Barraza-García, Maria Rodriguez-Zabala, Antonio M Lerario, Sara Benito-Sanz,[...]. Genet Med 2018
31
50

New developments in the management of achondroplasia.
Wolfgang Högler, Leanne M Ward. Wien Med Wochenschr 2020
4
50

Pharmacokinetics and safety after once and twice a day doses of meclizine hydrochloride administered to children with achondroplasia.
Hiroshi Kitoh, Masaki Matsushita, Kenichi Mishima, Tadashi Nagata, Yasunari Kamiya, Kohei Ueda, Yachiyo Kuwatsuka, Hiroshi Morikawa, Yasuhiro Nakai, Naoki Ishiguro. PLoS One 2020
2
50

Synthesizing genome-wide association studies and expression microarray reveals novel genes that act in the human growth plate to modulate height.
Julian C Lui, Ola Nilsson, Yingleong Chan, Cameron D Palmer, Anenisia C Andrade, Joel N Hirschhorn, Jeffrey Baron. Hum Mol Genet 2012
47
50

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
50


Role of the natriuretic peptide system in normal growth and growth disorders.
Gabriela A Vasques, Ivo J P Arnhold, Alexander A L Jorge. Horm Res Paediatr 2014
33
50

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
50

Genotypes and phenotypes of children with SHOX deficiency in France.
Myriam Rosilio, Céline Huber-Lequesne, Hélène Sapin, Jean-Claude Carel, Werner F Blum, Valérie Cormier-Daire. J Clin Endocrinol Metab 2012
43
50

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

2000 CDC Growth Charts for the United States: methods and development.
Robert J Kuczmarski, Cynthia L Ogden, Shumei S Guo, Laurence M Grummer-Strawn, Katherine M Flegal, Zuguo Mei, Rong Wei, Lester R Curtin, Alex F Roche, Clifford L Johnson. Vital Health Stat 11 2002
50


Interaction of fibroblast growth factor and C-natriuretic peptide signaling in regulation of chondrocyte proliferation and extracellular matrix homeostasis.
Pavel Krejci, Bernard Masri, Vincent Fontaine, Pertchoui B Mekikian, Maryann Weis, Herve Prats, William R Wilcox. J Cell Sci 2005
104
50



Critical roles of the guanylyl cyclase B receptor in endochondral ossification and development of female reproductive organs.
Naohisa Tamura, Lynda K Doolittle, Robert E Hammer, John M Shelton, James A Richardson, David L Garbers. Proc Natl Acad Sci U S A 2004
201
50

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
146
50

MECHANISMS IN ENDOCRINOLOGY: Novel genetic causes of short stature.
Jan M Wit, Wilma Oostdijk, Monique Losekoot, Hermine A van Duyvenvoorde, Claudia A L Ruivenkamp, Sarina G Kant. Eur J Endocrinol 2016
81
50

Regulation of fetal rat bone growth by C-type natriuretic peptide and cGMP.
V Mericq, J A Uyeda, K M Barnes, F De Luca, J Baron. Pediatr Res 2000
47
50

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
50

Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteaux.
Saadullah Khan, Raja Hussain Ali, Sanaullah Abbasi, Muhammad Nawaz, Noor Muhammad, Wasim Ahmad. BMC Med Genet 2012
25
50

Circulatory CNP Rescues Craniofacial Hypoplasia in Achondroplasia.
S Yamanaka, Kazumasa Nakao, N Koyama, Y Isobe, Y Ueda, Y Kanai, E Kondo, T Fujii, M Miura, A Yasoda,[...]. J Dent Res 2017
9
50

FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway.
Takehiko Matsushita, William R Wilcox, Yuk Yu Chan, Aya Kawanami, Hülya Bükülmez, Gener Balmes, Pavel Krejci, Pertchoui B Mekikian, Kazuyuki Otani, Isakichi Yamaura,[...]. Hum Mol Genet 2009
73
50


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.