A citation-based method for searching scientific literature

B Glaser, P Kesavan, M Heyman, E Davis, A Cuesta, A Buchs, C A Stanley, P S Thornton, M A Permutt, F M Matschinsky, K C Herold. N Engl J Med 1998
Times Cited: 406







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



Times Cited
  Times     Co-cited
Similarity


Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene.
C A Stanley, Y K Lieu, B Y Hsu, A B Burlina, C R Greenberg, N J Hopwood, K Perlman, B H Rich, E Zammarchi, M Poncz. N Engl J Med 1998
484
31

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene.
Ewan R Pearson, Sylvia F Boj, Anna M Steele, Timothy Barrett, Karen Stals, Julian P Shield, Sian Ellard, Jorge Ferrer, Andrew T Hattersley. PLoS Med 2007
233
28

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.
Kara K Osbak, Kevin Colclough, Cecile Saint-Martin, Nicola L Beer, Christine Bellanné-Chantelot, Sian Ellard, Anna L Gloyn. Hum Mutat 2009
257
27

Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy.
P M Thomas, G J Cote, N Wohllk, B Haddad, P M Mathew, W Rabl, L Aguilar-Bryan, R F Gagel, J Bryan. Science 1995
644
25

Severe persistent hyperinsulinemic hypoglycemia due to a de novo glucokinase mutation.
Antonio L Cuesta-Muñoz, Hanna Huopio, Timo Otonkoski, Juan M Gomez-Zumaquero, Kirsti Näntö-Salonen, Jacques Rahier, Soledad López-Enriquez, Maria A García-Gimeno, Pascual Sanz, Federico C Soriguer,[...]. Diabetes 2004
129
25

Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion.
M Mar González-Barroso, Irina Giurgea, Fredéric Bouillaud, Andrea Anedda, Christine Bellanné-Chantelot, Laurence Hubert, Yves de Keyzer, Pascale de Lonlay, Daniel Ricquier. PLoS One 2008
71
33

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.
Sara E Pinney, Courtney MacMullen, Susan Becker, Yu-Wen Lin, Cheryl Hanna, Paul Thornton, Arupa Ganguly, Show-Ling Shyng, Charles A Stanley. J Clin Invest 2008
119
23

Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells.
Timo Otonkoski, Hong Jiao, Nina Kaminen-Ahola, Isabel Tapia-Paez, Mohammed S Ullah, Laura E Parton, Frans Schuit, Roel Quintens, Ilkka Sipilä, Ertan Mayatepek,[...]. Am J Hum Genet 2007
129
23

Structural basis for allosteric regulation of the monomeric allosteric enzyme human glucokinase.
Kenji Kamata, Morihiro Mitsuya, Teruyuki Nishimura, Jun-Ichi Eiki, Yasufumi Nagata. Structure 2004
329
21

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion.
P T Clayton, S Eaton, A Aynsley-Green, M Edginton, K Hussain, S Krywawych, V Datta, H E Malingre, R Berger, I E van den Berg. J Clin Invest 2001
191
20

Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.
Diana E Stanescu, Nkecha Hughes, Bernard Kaplan, Charles A Stanley, Diva D De León. J Clin Endocrinol Metab 2012
78
25

The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapy.
Henrik B T Christesen, Bendt B Jacobsen, Stella Odili, Carol Buettger, Antonio Cuesta-Munoz, Torben Hansen, Klaus Brusgaard, Ornella Massa, Mark A Magnuson, Chiyo Shiota,[...]. Diabetes 2002
112
20


Extremes of clinical and enzymatic phenotypes in children with hyperinsulinism caused by glucokinase activating mutations.
Samir Sayed, David R Langdon, Stella Odili, Pan Chen, Carol Buettger, Alisa B Schiffman, Mariko Suchi, Rebecca Taub, Joseph Grimsby, Franz M Matschinsky,[...]. Diabetes 2009
65
29

Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.
K E Snider, S Becker, L Boyajian, S-L Shyng, C MacMullen, N Hughes, K Ganapathy, T Bhatti, C A Stanley, A Ganguly. J Clin Endocrinol Metab 2013
144
19

Neonatal diabetes mellitus due to complete glucokinase deficiency.
P R Njølstad, O Søvik, A Cuesta-Muñoz, L Bjørkhaug, O Massa, F Barbetti, D E Undlien, C Shiota, M A Magnuson, A Molven,[...]. N Engl J Med 2001
275
17

Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.
H Huopio, F Reimann, R Ashfield, J Komulainen, H L Lenko, J Rahier, I Vauhkonen, J Kere, M Laakso, F Ashcroft,[...]. J Clin Invest 2000
183
17


Allosteric activators of glucokinase: potential role in diabetes therapy.
Joseph Grimsby, Ramakanth Sarabu, Wendy L Corbett, Nancy-Ellen Haynes, Fred T Bizzarro, John W Coffey, Kevin R Guertin, Darryl W Hilliard, Robert F Kester, Paige E Mahaney,[...]. Science 2003
361
16

Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release.
Timo Otonkoski, Nina Kaminen, Jarkko Ustinov, Risto Lapatto, Thomas Meissner, Ertan Mayatepek, Juha Kere, Ilkka Sipilä. Diabetes 2003
94
17

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
Ritika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, Julian P Shield, Sian Ellard, Khalid Hussain. Eur J Endocrinol 2013
119
16

Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations.
Ritika R Kapoor, Jonathan Locke, Kevin Colclough, Jerry Wales, Jennifer J Conn, Andrew T Hattersley, Sian Ellard, Khalid Hussain. Diabetes 2008
80
18


Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy.
M Wabitsch, G Lahr, M Van de Bunt, C Marchant, M Lindner, J von Puttkamer, A Fenneberg, K M Debatin, R Klein, S Ellard,[...]. Diabet Med 2007
41
34

Insights into the biochemical and genetic basis of glucokinase activation from naturally occurring hypoglycemia mutations.
Anna L Gloyn, Kees Noordam, Michèl A A P Willemsen, Sian Ellard, Wayne W K Lam, Ian W Campbell, Paula Midgley, Chyio Shiota, Carol Buettger, Mark A Magnuson,[...]. Diabetes 2003
111
14

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.
Anders Molven, Guri E Matre, Marinus Duran, Ronald J Wanders, Unni Rishaug, Pål R Njølstad, Egil Jellum, Oddmund Søvik. Diabetes 2004
127
14

Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations.
S E Flanagan, R R Kapoor, G Mali, D Cody, N Murphy, B Schwahn, T Siahanidou, I Banerjee, T Akcay, O Rubio-Cabezas,[...]. Eur J Endocrinol 2010
79
17

Effects of MK-0941, a novel glucokinase activator, on glycemic control in insulin-treated patients with type 2 diabetes.
Gary E Meininger, Russell Scott, Maria Alba, Yue Shentu, Edmund Luo, Himal Amin, Michael J Davies, Keith D Kaufman, Barry J Goldstein. Diabetes Care 2011
123
13

Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy.
P de Lonlay, J C Fournet, J Rahier, M S Gross-Morand, F Poggi-Travert, V Foussier, J P Bonnefont, M C Brusset, F Brunelle, J J Robert,[...]. J Clin Invest 1997
216
13

Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the β-cell sulfonylurea receptor SUR1.
Courtney M Macmullen, Qing Zhou, Kara E Snider, Paul H Tewson, Susan A Becker, Ali Rahim Aziz, Arupa Ganguly, Show-Ling Shyng, Charles A Stanley. Diabetes 2011
46
28

Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
Changhong Li, Pan Chen, Andrew Palladino, Srinivas Narayan, Laurie K Russell, Samir Sayed, Guoxiang Xiong, Jie Chen, David Stokes, Yasmeen M Butt,[...]. J Biol Chem 2010
107
13

Noninvasive diagnosis of focal hyperinsulinism of infancy with [18F]-DOPA positron emission tomography.
Timo Otonkoski, Kirsti Näntö-Salonen, Marko Seppänen, Riitta Veijola, Hanna Huopio, Khalid Hussain, Päivi Tapanainen, Olli Eskola, Riitta Parkkola, Klas Ekström,[...]. Diabetes 2006
165
13

Glucose metabolism in 105 children and adolescents after pancreatectomy for congenital hyperinsulinism.
Jacques Beltrand, Marylène Caquard, Jean-Baptiste Arnoux, Kathleen Laborde, Gilberto Velho, Virginie Verkarre, Jacques Rahier, Francis Brunelle, Claire Nihoul-Fékété, Jean-Marie Saudubray,[...]. Diabetes Care 2012
75
17

Practical management of hyperinsulinism in infancy.
A Aynsley-Green, K Hussain, J Hall, J M Saudubray, C Nihoul-Fékété, P De Lonlay-Debeney, F Brunelle, T Otonkoski, P Thornton, K J Lindley. Arch Dis Child Fetal Neonatal Ed 2000
171
13

Congenital hyperinsulinism: current trends in diagnosis and therapy.
Jean-Baptiste Arnoux, Virginie Verkarre, Cécile Saint-Martin, Françoise Montravers, Anaïs Brassier, Vassili Valayannopoulos, Francis Brunelle, Jean-Christophe Fournet, Jean-Jacques Robert, Yves Aigrain,[...]. Orphanet J Rare Dis 2011
145
13


Congenital hyperinsulinism caused by hexokinase I expression or glucokinase-activating mutation in a subset of β-cells.
Jean-Claude Henquin, Christine Sempoux, Joelle Marchandise, Sebastien Godecharles, Yves Guiot, Myriam Nenquin, Jacques Rahier. Diabetes 2013
37
32

The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver.
Nicola L Beer, Nicholas D Tribble, Laura J McCulloch, Charlotta Roos, Paul R V Johnson, Marju Orho-Melander, Anna L Gloyn. Hum Mol Genet 2009
232
11


Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation.
Henrik B T Christesen, Nicholas D Tribble, Anders Molven, Juveria Siddiqui, Tone Sandal, Klaus Brusgaard, Sian Ellard, Pål R Njølstad, Jan Alm, Bendt Brock Jacobsen,[...]. Eur J Endocrinol 2008
53
20

Successful treatment of congenital hyperinsulinism with long-acting release octreotide.
Kim-Hanh Le Quan Sang, Jean-Baptiste Arnoux, Asmaa Mamoune, Cécile Saint-Martin, Christine Bellanné-Chantelot, Vassili Valayannopoulos, Anais Brassier, Honorine Kayirangwa, Valérie Barbier, Christine Broissand,[...]. Eur J Endocrinol 2012
45
24



Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus.
P Froguel, M Vaxillaire, F Sun, G Velho, H Zouali, M O Butel, S Lesage, N Vionnet, K Clément, F Fougerousse. Nature 1992
512
10


Exercise induced hypoglycaemic hyperinsulinism.
T Meissner, T Otonkoski, R Feneberg, B Beinbrech, S Apostolidou, I Sipilä, F Schaefer, E Mayatepek. Arch Dis Child 2001
31
32

Treatment of congenital hyperinsulinism with lanreotide acetate (Somatuline Autogel).
Dalit Modan-Moses, Ilana Koren, Kineret Mazor-Aronovitch, Orit Pinhas-Hamiel, Heddy Landau. J Clin Endocrinol Metab 2011
37
27

Necrotizing enterocolitis in neonates receiving octreotide for the management of congenital hyperinsulinism.
Pablo Laje, Lori Halaby, N Scott Adzick, Charles A Stanley. Pediatr Diabetes 2010
62
16

Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
N Vionnet, M Stoffel, J Takeda, K Yasuda, G I Bell, H Zouali, S Lesage, G Velho, F Iris, P Passa. Nature 1992
540
10

A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene.
Kurt Højlund, Torben Hansen, Maria Lajer, Jan Erik Henriksen, Klaus Levin, Jörgen Lindholm, Oluf Pedersen, Henning Beck-Nielsen. Diabetes 2004
75
13


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.