A citation-based method for searching scientific literature

Qing Fang, Akima S George, Michelle L Brinkmeier, Amanda H Mortensen, Peter Gergics, Leonard Y M Cheung, Alexandre Z Daly, Adnan Ajmal, María Ines Pérez Millán, A Bilge Ozel, Jacob O Kitzman, Ryan E Mills, Jun Z Li, Sally A Camper. Endocr Rev 2016
Times Cited: 87







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



Times Cited
  Times     Co-cited
Similarity


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
24

Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
Francesca De Rienzo, Simona Mellone, Simonetta Bellone, Deepak Babu, Ileana Fusco, Flavia Prodam, Antonella Petri, Ranjith Muniswamy, Filippo De Luca, Mariacarolina Salerno,[...]. Clin Endocrinol (Oxf) 2015
51
41

Genetic regulation of pituitary gland development in human and mouse.
Daniel Kelberman, Karine Rizzoti, Robin Lovell-Badge, Iain C A F Robinson, Mehul T Dattani. Endocr Rev 2009
251
21

Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
Ulrich Boehm, Pierre-Marc Bouloux, Mehul T Dattani, Nicolas de Roux, Catherine Dodé, Leo Dunkel, Andrew A Dwyer, Paolo Giacobini, Jean-Pierre Hardelin, Anders Juul,[...]. Nat Rev Endocrinol 2015
401
16

Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.
Taneli Raivio, Magdalena Avbelj, Mark J McCabe, Christopher J Romero, Andrew A Dwyer, Johanna Tommiska, Gerasimos P Sykiotis, Louise C Gregory, Daniel Diaczok, Vaitsa Tziaferi,[...]. J Clin Endocrinol Metab 2012
89
16

Role of GLI2 in hypopituitarism phenotype.
Ivo J P Arnhold, Marcela M França, Luciani R Carvalho, Berenice B Mendonca, Alexander A L Jorge. J Mol Endocrinol 2015
39
35

Clues for Polygenic Inheritance of Pituitary Stalk Interruption Syndrome From Exome Sequencing in 20 Patients.
Nitash Zwaveling-Soonawala, Marielle Alders, Aldo Jongejan, Lidija Kovacic, Floor A Duijkers, Saskia M Maas, Eric Fliers, A S Paul van Trotsenburg, Raoul C Hennekam. J Clin Endocrinol Metab 2018
31
41

Mutations in PROP1 cause familial combined pituitary hormone deficiency.
W Wu, J D Cogan, R W Pfäffle, J S Dasen, H Frisch, S M O'Connell, S E Flynn, M R Brown, P E Mullis, J S Parks,[...]. Nat Genet 1998
367
12

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene.
K Tatsumi, K Miyai, T Notomi, K Kaibe, N Amino, Y Mizuno, H Kohno. Nat Genet 1992
260
12

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.
M T Dattani, J P Martinez-Barbera, P Q Thomas, J M Brickman, R Gupta, I L Mårtensson, H Toresson, M Fox, J K Wales, P C Hindmarsh,[...]. Nat Genet 1998
500
12

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.
S Li, E B Crenshaw, E J Rawson, D M Simmons, L W Swanson, M G Rosenfeld. Nature 1990
12

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism.
Kathryn S Woods, Maria Cundall, James Turton, Karine Rizotti, Ameeta Mehta, Rodger Palmer, Jacqueline Wong, W K Chong, Mahmoud Al-Zyoud, Maryam El-Ali,[...]. Am J Hum Genet 2005
165
12

MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency.
Frederic Castinetti, Rachel Reynaud, Alexandru Saveanu, Nicolas Jullien, Marie Helene Quentien, Claire Rochette, Anne Barlier, Alain Enjalbert, Thierry Brue. Eur J Endocrinol 2016
32
34

PROKR2 variants in multiple hypopituitarism with pituitary stalk interruption.
Rachel Reynaud, Sujatha A Jayakody, Carine Monnier, Alexandru Saveanu, Jérome Bouligand, Anne-Marie Guedj, Gilbert Simonin, Pierre Lecomte, Anne Barlier, Philippe Rondard,[...]. J Clin Endocrinol Metab 2012
50
20

Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes.
Christina Tatsi, Amalia Sertedaki, Antonis Voutetakis, Eleni Valavani, Maria-Alexandra Magiakou, Christina Kanaka-Gantenbein, George P Chrousos, Catherine Dacou-Voutetakis. J Clin Endocrinol Metab 2013
35
28

Septo-optic dysplasia.
Emma A Webb, Mehul T Dattani. Eur J Hum Genet 2010
126
11

Genetic causes and treatment of isolated growth hormone deficiency-an update.
Kyriaki S Alatzoglou, Mehul T Dattani. Nat Rev Endocrinol 2010
67
14

Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.
Petra Dusatkova, Roland Pfäffle, Milton R Brown, Natallia Akulevich, Ivo J P Arnhold, Maria A Kalina, Karolina Kot, Ciril Krzisnik, Manuel C Lemos, Jana Malikova,[...]. Eur J Hum Genet 2016
21
47

Genetic causes of isolated and combined pituitary hormone deficiency.
Mara Giordano. Best Pract Res Clin Endocrinol Metab 2016
30
33

Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.
James P G Turton, Rachel Reynaud, Ameeta Mehta, John Torpiano, Alexandru Saveanu, Kathryn S Woods, Anatoly Tiulpakov, Vera Zdravkovic, Jill Hamilton, Simon Attard-Montalto,[...]. J Clin Endocrinol Metab 2005
73
13

The Molecular Basis of Congenital Hypopituitarism and Related Disorders.
Louise Cheryl Gregory, Mehul Tulsidas Dattani. J Clin Endocrinol Metab 2020
17
58

Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephaly.
Marcela M França, Alexander A L Jorge, Luciani R S Carvalho, Everlayny F Costalonga, Gabriela A Vasques, Claudia C Leite, Berenice B Mendonca, Ivo J P Arnhold. J Clin Endocrinol Metab 2010
73
12

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.
Eleonore Bertko, Jürgen Klammt, Petra Dusatkova, Mithat Bahceci, Nazli Gonc, Louise Ten Have, Nurgun Kandemir, Georg Mansmann, Barbora Obermannova, Wilma Oostdijk,[...]. J Hum Genet 2017
14
64

Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency.
Franziska Simm, Anne Griesbeck, Daniela Choukair, Birgit Weiß, Nagarajan Paramasivam, Jürgen Klammt, Matthias Schlesner, Stefan Wiemann, Cristina Martinez, Georg F Hoffmann,[...]. Genet Med 2018
14
64

Contribution of LHX4 Mutations to Pituitary Deficits in a Cohort of 417 Unrelated Patients.
Enzo Cohen, Mohamad Maghnie, Nathalie Collot, Juliane Leger, Florence Dastot, Michel Polak, Sophie Rose, Philippe Touraine, Philippe Duquesnoy, Maïté Tauber,[...]. J Clin Endocrinol Metab 2017
15
60

Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms.
R Reynaud, F Albarel, A Saveanu, N Kaffel, F Castinetti, P Lecomte, R Brauner, G Simonin, J Gaudart, E Carmona,[...]. Eur J Endocrinol 2011
56
14

Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation.
Céline Bar, Charline Zadro, Gwenaelle Diene, Isabelle Oliver, Catherine Pienkowski, Béatrice Jouret, Audrey Cartault, Zeina Ajaltouni, Jean-Pierre Salles, Annick Sevely,[...]. PLoS One 2015
28
28

A Nonsense Mutation in the Hedgehog Receptor CDON Associated With Pituitary Stalk Interruption Syndrome.
A Bashamboo, J Bignon-Topalovic, H Rouba, K McElreavey, R Brauner. J Clin Endocrinol Metab 2016
31
25

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
James P G Turton, Ameeta Mehta, Jamal Raza, Kathryn S Woods, Anatoly Tiulpakov, Joseph Cassar, Kling Chong, Paul Q Thomas, Marumudi Eunice, Ariachery C Ammini,[...]. Clin Endocrinol (Oxf) 2005
67
11

Deletion of OTX2 in neural ectoderm delays anterior pituitary development.
Amanda H Mortensen, Vanessa Schade, Thomas Lamonerie, Sally A Camper. Hum Mol Genet 2015
31
25

Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism.
M W Sornson, W Wu, J S Dasen, S E Flynn, D J Norman, S M O'Connell, I Gukovsky, C Carrière, A K Ryan, A P Miller,[...]. Nature 1996
579
9

OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary.
Toshihiro Tajima, Akira Ohtake, Masaya Hoshino, Shin Amemiya, Nozomu Sasaki, Katsura Ishizu, Kenji Fujieda. J Clin Endocrinol Metab 2009
64
12

Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center.
Aline P Otto, Marcela M França, Fernanda A Correa, Everlayny F Costalonga, Claudia C Leite, Berenice B Mendonca, Ivo J P Arnhold, Luciani R S Carvalho, Alexander A L Jorge. Pituitary 2015
22
36


Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
Mark J McCabe, Carles Gaston-Massuet, Vaitsa Tziaferi, Louise C Gregory, Kyriaki S Alatzoglou, Massimo Signore, Eduardo Puelles, Dianne Gerrelli, I Sadaf Farooqi, Jamal Raza,[...]. J Clin Endocrinol Metab 2011
80
10

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.
K Machinis, J Pantel, I Netchine, J Léger, O J Camand, M L Sobrier, F Dastot-Le Moal, P Duquesnoy, M Abitbol, P Czernichow,[...]. Am J Hum Genet 2001
174
9

ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.
Emma A Webb, Angham AlMutair, Daniel Kelberman, Chiara Bacchelli, Estelle Chanudet, Francesco Lescai, Cynthia L Andoniadou, Abdul Banyan, Al Alsawaid, Muhammad T Alrifai,[...]. Brain 2013
40
20

Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies.
Roland W Pfaeffle, Chad S Hunter, Jesse J Savage, Mario Duran-Prado, Rachel D Mullen, Zachary P Neeb, Urs Eiholzer, Volker Hesse, Nadine G Haddad, Heike M Stobbe,[...]. J Clin Endocrinol Metab 2008
71
11

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.
Fernanda A Correa, Ericka B Trarbach, Cintia Tusset, Ana Claudia Latronico, Luciana R Montenegro, Luciani R Carvalho, Marcela M Franca, Aline P Otto, Everlayny F Costalonga, Vinicius N Brito,[...]. Endocr Connect 2015
26
26

PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells.
María Inés Pérez Millán, Michelle L Brinkmeier, Amanda H Mortensen, Sally A Camper. Elife 2016
39
17

Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiency.
G M C Flemming, J Klammt, G Ambler, Y Bao, W F Blum, C Cowell, K Donaghue, N Howard, A Kumar, J Sanchez,[...]. J Clin Endocrinol Metab 2013
26
26

Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
Rachel Reynaud, Magali Gueydan, Alexandru Saveanu, Sophie Vallette-Kasic, Alain Enjalbert, Thierry Brue, Anne Barlier. J Clin Endocrinol Metab 2006
98
8

Development of additional pituitary hormone deficiencies in pediatric patients originally diagnosed with idiopathic isolated GH deficiency.
Werner F Blum, Cheri Deal, Alan G Zimmermann, Elena P Shavrikova, Christopher J Child, Charmian A Quigley, Stenvert L S Drop, Gordon B Cutler, Ron G Rosenfeld. Eur J Endocrinol 2013
24
29

Classical and non-classical causes of GH deficiency in the paediatric age.
Natascia Di Iorgi, Giovanni Morana, Anna Elsa Maria Allegri, Flavia Napoli, Roberto Gastaldi, Annalisa Calcagno, Giuseppa Patti, Sandro Loche, Mohamad Maghnie. Best Pract Res Clin Endocrinol Metab 2016
23
30

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
238
8

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.
J Deladoëy, C Flück, A Büyükgebiz, B V Kuhlmann, A Eblé, P C Hindmarsh, W Wu, P E Mullis. J Clin Endocrinol Metab 1999
137
8

High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.
Ruta Navardauskaite, Petra Dusatkova, Barbora Obermannova, Roland W Pfaeffle, Werner F Blum, Dalia Adukauskiene, Natalija Smetanina, Ondrej Cinek, Rasa Verkauskiene, Jan Lebl. J Clin Endocrinol Metab 2014
23
30

Genetic screening of regulatory regions of pituitary transcription factors in patients with idiopathic pituitary hormone deficiencies.
Melitza Elizabeth, Anita C S Hokken-Koelega, Joyce Schuilwerve, Robin P Peeters, Theo J Visser, Laura C G de Graaff. Pituitary 2018
12
58

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans.
Daniel Kelberman, Karine Rizzoti, Ariel Avilion, Maria Bitner-Glindzicz, Stefano Cianfarani, Julie Collins, W Kling Chong, Jeremy M W Kirk, John C Achermann, Richard Ross,[...]. J Clin Invest 2006
216
8

Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion.
Sumito Dateki, Maki Fukami, Ayumi Uematsu, Masayuki Kaji, Manami Iso, Makoto Ono, Michiyo Mizota, Susumu Yokoya, Katsuaki Motomura, Eiichi Kinoshita,[...]. J Clin Endocrinol Metab 2010
40
17


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.