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



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, Sara Benito-Sanz, Alexander A Jorge, Angel Campos-Barros, Karen E Heath. J Clin Endocrinol Metab 2015
Times Cited: 43




List of shared articles



Times cited

The Biology of Stature.
Youn Hee Jee, Jeffrey Baron. J Pediatr 2016
14

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
5

Heterozygous NPR2 Mutation in Two Family Members with Short Stature and Skeletal Dysplasia.
Marianne Jacob, Surabhi Menon, Christina Botti, Ian Marshall. Case Rep Endocrinol 2018
5

Clinical Characteristics of Short-Stature Patients With an NPR2 Mutation and the Therapeutic Response to rhGH.
Xiaoan Ke, Hanting Liang, Hui Miao, Hongbo Yang, Linjie Wang, Fengying Gong, Hui Pan, Huijuan Zhu. J Clin Endocrinol Metab 2021
2

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

Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy
Jan M. Wit, Asma Deeb, Bassam Bin-Abbas, Angham Al Mutair, Ekaterina Koledova, Martin O. Savage. J Clin Res Pediatr Endocrinol 2019
6


Biallelic cGMP-dependent type II protein kinase gene (PRKG2) variants cause a novel acromesomelic dysplasia.
Francisca Díaz-González, Saruchi Wadhwa, Maria Rodriguez-Zabala, Somesh Kumar, Miriam Aza-Carmona, Lucia Sentchordi-Montané, Milagros Alonso, Istaq Ahmad, Sana Zahra, Deepak Kumar,[...]. J Med Genet 2020
3

Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature.
Gilyazetdinov Kamil, Ju Young Yoon, Sukdong Yoo, Chong Kun Cheon. Orphanet J Rare Dis 2021
0

Regulation of the Natriuretic Peptide Receptor 2 (Npr2) by Phosphorylation of Juxtamembrane Serine and Threonine Residues Is Essential for Bifurcation of Sensory Axons.
Hannes Schmidt, Deborah M Dickey, Alexandre Dumoulin, Marie Octave, Jerid W Robinson, Ralf Kühn, Robert Feil, Lincoln R Potter, Fritz G Rathjen. J Neurosci 2018
8

Growth failure: 'idiopathic' only after a detailed diagnostic evaluation.
Robert Rapaport, Jan M Wit, Martin O Savage. Endocr Connect 2021
2

Genetic Techniques in the Evaluation of Short Stature.
Christopher J Romero, Lakshmi Mehta, Robert Rapaport. Endocrinol Metab Clin North Am 2016
4

A Track Record on SHOX: From Basic Research to Complex Models and Therapy.
Antonio Marchini, Tsutomu Ogata, Gudrun A Rappold. Endocr Rev 2016
44

Novel genetic cause of idiopathic short stature.
Min Jae Kang. Ann Pediatr Endocrinol Metab 2017
15

A novel NPR2 mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type Maroteaux.
Naoko Amano, Hiroshi Kitoh, Satoshi Narumi, Gen Nishimura, Tomonobu Hasegawa. Clin Pediatr Endocrinol 2020
1

Acromesomelic dysplasia Maroteaux-type in patients from Vietnam.
Thinh Huy Tran, My Ha Cao, Long Hoang Luong, Phuong Thi Le, Dung Chi Vu, Thanh Dat Ta, The-Hung Bui, Duc Hinh Nguyen, Thanh Van Ta, Van Khanh Tran. Am J Med Genet A 2019
5


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

Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type Maroteaux.
Irfanullah, Amir Zeb, Naila Shinwari, Khadim Shah, Syed Zohaib Tayyab Gilani, Saadullah Khan, Keun Woo Lee, Syed Irfan Raza, Shabir Hussain, Khurram Liaqat,[...]. Int J Biochem Cell Biol 2018
6

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

NPR2 gene variants in familial short stature: a single-center study.
Ke Yuan, Jiao Chen, Qingqing Chen, Hong Chen, Jianfang Zhu, Yanlan Fang, Chunlin Wang. J Pediatr Endocrinol Metab 2021
0

Role of NPR2 mutation in idiopathic short stature: Identification of two novel mutations.
Il Tae Hwang, Yusuke Mizuno, Naoko Amano, Hye Jin Lee, Young Suk Shim, Hyo-Kyoung Nam, Young-Jun Rhie, Seung Yang, Kee-Hyoung Lee, Tomonobu Hasegawa,[...]. Mol Genet Genomic Med 2020
8

Hormone resistance and short stature: A journey through the pathways of hormone signaling.
Renata C Scalco, Fernanda A Correa, Naiara C B Dantas, Gabriela A Vasques, Alexander A L Jorge. Mol Cell Endocrinol 2021
0

Circulating osteocrin stimulates bone growth by limiting C-type natriuretic peptide clearance.
Yugo Kanai, Akihiro Yasoda, Keita P Mori, Haruko Watanabe-Takano, Chiaki Nagai-Okatani, Yui Yamashita, Keisho Hirota, Yohei Ueda, Ichiro Yamauchi, Eri Kondo,[...]. J Clin Invest 2017
18

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

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

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
80

Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature.
Nadine N Hauer, Bernt Popp, Eva Schoeller, Sarah Schuhmann, Karen E Heath, Alfonso Hisado-Oliva, Patricia Klinger, Cornelia Kraus, Udo Trautmann, Martin Zenker,[...]. Genet Med 2018
51

The Absence of Sensory Axon Bifurcation Affects Nociception and Termination Fields of Afferents in the Spinal Cord.
Philip Tröster, Julia Haseleu, Jonas Petersen, Oliver Drees, Achim Schmidtko, Frederick Schwaller, Gary R Lewin, Gohar Ter-Avetisyan, York Winter, Stefanie Peters,[...]. Front Mol Neurosci 2018
12

Rats deficient C-type natriuretic peptide suffer from impaired skeletal growth without early death.
Toshihito Fujii, Keisho Hirota, Akihiro Yasoda, Akiko Takizawa, Naomi Morozumi, Ryuichi Nakamura, Takafumi Yotsumoto, Eri Kondo, Yui Yamashita, Yoriko Sakane,[...]. PLoS One 2018
8