A citation-based method for searching scientific literature

Sophie R Wang, Heather Carmichael, Shayne F Andrew, Timothy C Miller, Jennifer E Moon, Michael A Derr, Vivian Hwa, Joel N Hirschhorn, Andrew Dauber. J Clin Endocrinol Metab 2013
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


Rare copy number variants are a common cause of short stature.
Diana Zahnleiter, Steffen Uebe, Arif B Ekici, Juliane Hoyer, Antje Wiesener, Dagmar Wieczorek, Erdmute Kunstmann, André Reis, Helmuth-Guenther Doerr, Anita Rauch,[...]. PLoS Genet 2013
46
31

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
31

Whole exome sequencing to identify genetic causes of short stature.
Michael H Guo, Yiping Shen, Emily C Walvoord, Timothy C Miller, Jennifer E Moon, Joel N Hirschhorn, Andrew Dauber. Horm Res Paediatr 2014
44
29

Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.
Andrew Dauber, Yongguo Yu, Michael C Turchin, Charleston W Chiang, Yan A Meng, Ellen W Demerath, Sanjay R Patel, Stephen S Rich, Jerome I Rotter, Pamela J Schreiner,[...]. Am J Hum Genet 2011
47
26

IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation.
M Jennifer Abuzzahab, Anke Schneider, Audrey Goddard, Florin Grigorescu, Corinne Lautier, Eberhard Keller, Wieland Kiess, Jürgen Klammt, Jürgen Kratzsch, Doreen Osgood,[...]. N Engl J Med 2003
395
26

Genetic evaluation of short stature.
Andrew Dauber, Ron G Rosenfeld, Joel N Hirschhorn. J Clin Endocrinol Metab 2014
69
26

Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivity.
Alessia David, Vivian Hwa, Louise A Metherell, Irène Netchine, Cecilia Camacho-Hübner, Adrian J L Clark, Ron G Rosenfeld, Martin O Savage. Endocr Rev 2011
125
24

Copy number variants in patients with short stature.
Hermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, Wilma Oostdijk, Antoinet C J Gijsbers, Mariëtte J V Hoffer, Marcel Karperien, Marie J E Walenkamp, Cees Noordam, Paul G Voorhoeve,[...]. Eur J Hum Genet 2014
41
26



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
63
22

Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature.
Sophie R Wang, Christina M Jacobsen, Heather Carmichael, Aaron B Edmund, Jerid W Robinson, Robert C Olney, Timothy C Miller, Jennifer E Moon, Veronica Mericq, Lincoln R Potter,[...]. Hum Mutat 2015
56
22

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
22

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
20

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
20

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
28

Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 gene.
H A van Duyvenvoorde, P A van Setten, M J E Walenkamp, J van Doorn, J Koenig, L Gauguin, W Oostdijk, C A L Ruivenkamp, M Losekoot, J D Wade,[...]. J Clin Endocrinol Metab 2010
42
19

Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Hana Lango Allen, Karol Estrada, Guillaume Lettre, Sonja I Berndt, Michael N Weedon, Fernando Rivadeneira, Cristen J Willer, Anne U Jackson, Sailaja Vedantam, Soumya Raychaudhuri,[...]. Nature 2010
17

Low incidence of pathology detection and high cost of screening in the evaluation of asymptomatic short children.
Stephanie Sisley, Marcela Vargas Trujillo, Jane Khoury, Philippe Backeljauw. J Pediatr 2013
48
17

ACMG practice guideline: genetic evaluation of short stature.
Laurie H Seaver, Mira Irons. Genet Med 2009
36
22

A novel variant of FGFR3 causes proportionate short stature.
Sarina G Kant, Iveta Cervenkova, Lukas Balek, Lukas Trantirek, Gijs W E Santen, Martine C de Vries, Hermine A van Duyvenvoorde, Michiel J R van der Wielen, Annemieke J M H Verkerk, André G Uitterlinden,[...]. Eur J Endocrinol 2015
26
30

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
34

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
47
17

Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
Emma L Wakeling, Frédéric Brioude, Oluwakemi Lokulo-Sodipe, Susan M O'Connell, Jennifer Salem, Jet Bliek, Ana P M Canton, Krystyna H Chrzanowska, Justin H Davies, Renuka P Dias,[...]. Nat Rev Endocrinol 2017
181
17

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
17

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
47
15

IGF1, IGF1R and SHOX mutation analysis in short children born small for gestational age and short children with normal birth size (idiopathic short stature).
Janina Caliebe, Sander Broekman, Merel Boogaard, Cathy A J Bosch, Claudia A L Ruivenkamp, Wilma Oostdijk, S G Kant, Gerhard Binder, Michael B Ranke, Jan M Wit,[...]. Horm Res Paediatr 2012
37
18

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
17

A novel deletion of IGF1 in a patient with idiopathic short stature provides insight Into IGF1 haploinsufficiency.
Lara Batey, Jennifer E Moon, Yongguo Yu, Bingbing Wu, Joel N Hirschhorn, Yiping Shen, Andrew Dauber. J Clin Endocrinol Metab 2014
25
28

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
46

Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availability.
Andrew Dauber, María T Muñoz-Calvo, Vicente Barrios, Horacio M Domené, Soren Kloverpris, Clara Serra-Juhé, Vardhini Desikan, Jesús Pozo, Radhika Muzumdar, Gabriel Á Martos-Moreno,[...]. EMBO Mol Med 2016
91
15

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
278
15

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
13

Deficiency of the circulating insulin-like growth factor system associated with inactivation of the acid-labile subunit gene.
Horacio M Domené, Sonia V Bengolea, Alicia S Martínez, M Gabriela Ropelato, Patricia Pennisi, Paula Scaglia, Juan J Heinrich, Héctor G Jasper. N Engl J Med 2004
159
13

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
24

Growth hormone insensitivity associated with a STAT5b mutation.
Eric M Kofoed, Vivian Hwa, Brian Little, Katie A Woods, Caroline K Buckway, Junko Tsubaki, Katherine L Pratt, Liliana Bezrodnik, Hector Jasper, Alejandro Tepper,[...]. N Engl J Med 2003
342
13


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
13


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
13

Defining the role of common variation in the genomic and biological architecture of adult human height.
Andrew R Wood, Tonu Esko, Jian Yang, Sailaja Vedantam, Tune H Pers, Stefan Gustafsson, Audrey Y Chu, Karol Estrada, Jian'an Luan, Zoltán Kutalik,[...]. Nat Genet 2014
991
13

The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis.
Alexsandra C Malaquias, Renata C Scalco, Eveline G P Fontenele, Everlayny F Costalonga, Alexandre D Baldin, Adriana F Braz, Mariana F A Funari, Mirian Y Nishi, Gil Guerra-Junior, Berenice B Mendonca,[...]. Horm Res Paediatr 2013
36
16

IGF1R mutations as cause of SGA.
J Klammt, W Kiess, R Pfäffle. Best Pract Res Clin Endocrinol Metab 2011
69
13

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
18

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
13

Short and tall stature: a new paradigm emerges.
Jeffrey Baron, Lars Sävendahl, Francesco De Luca, Andrew Dauber, Moshe Phillip, Jan M Wit, Ola Nilsson. Nat Rev Endocrinol 2015
126
13

A New Homozygous IGF1R Variant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome.
Paolo Prontera, Lucia Micale, Alberto Verrotti, Valerio Napolioni, Gabriela Stangoni, Giuseppe Merla. Hum Mutat 2015
32
18

Severe short stature caused by novel compound heterozygous mutations of the insulin-like growth factor 1 receptor (IGF1R).
Peng Fang, Yoon Hi Cho, Michael A Derr, Ron G Rosenfeld, Vivian Hwa, Christopher T Cowell. J Clin Endocrinol Metab 2012
43
13

Homozygous and heterozygous expression of a novel insulin-like growth factor-I mutation.
M J E Walenkamp, M Karperien, A M Pereira, Y Hilhorst-Hofstee, J van Doorn, J W Chen, S Mohan, A Denley, B Forbes, H A van Duyvenvoorde,[...]. J Clin Endocrinol Metab 2005
216
11

Characterizing short stature by insulin-like growth factor axis status and genetic associations: results from the prospective, cross-sectional, epidemiogenetic EPIGROW study.
Peter Clayton, Mireille Bonnemaire, Pascale Dutailly, Pascal Maisonobe, Laurent Naudin, Emmanuel Pham, Zhidong Zhang, Andrew Grupe, Arunthathi Thiagalingam, Patrice Denèfle. J Clin Endocrinol Metab 2013
13
38


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.