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How has Pascale de Lonlay's publication output changed over time?
ScholarIQpublication output · 1998–2024
Output declined50% over the shown period — from 2 works in 1998 to 1 in 2024.
2
1
1
1
2
1
1
1
1
199820022008201020112012202020212024
What are the most-cited papers on Pascale de Lonlay?
ScholarIQmost cited works
Congenital hyperinsulinism: current trends in diagnosis and therapy
Jean-Baptiste Arnoux, Virginie Verkarre, Cécile Saint‐Martin, Françoise Montravers, Anaïs Brassier, Vassili Valayannopoulos, Françis Brunelle, Jean‐Christophe Fournet, Jean-Jacques Robert, Y. Aigrain, Christine Bellanné‐Chantelot, Pascale de Lonlay
Orphanet Journal of Rare Diseases. 2011360 CitationsOPEN ACCESS
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.
Virginie Verkarre, Jean‐Christophe Fournet, Pascale de Lonlay, M S Gross-Morand, Martine Devillers, Jacques Rahier, Françis Brunelle, J.J. Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien
S114430552. 1998290 CitationsOPEN ACCESS
Update of mutations in the genes encoding the pancreatic beta-cell K<sub>ATP</sub>channel subunits Kir6.2 (<i>KCNJ11</i>) and sulfonylurea receptor 1 (<i>ABCC8</i>) in diabetes mellitus and hyperinsulinism
Sarah E. Flanagan, Séverine Clauin, Christine Bellanné‐Chantelot, Pascale de Lonlay, Lorna W. Harries, Anna L. Gloyn, Sian Ellard
S98809561. 2008243 CitationsOPEN ACCESS
Clinical approach to inherited metabolic disorders in neonates: an overview
Jean‐Marie Saudubray, Marie‐Cécile Nassogne, Pascale de Lonlay, Guy Touati
S168253193. 2002144 Citations
<i>ABCC8</i> and <i>KCNJ11</i> molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism
Christine Bellanné‐Chantelot, Cécile Saint‐Martin, M-J Ribeiro, Chantal Vaury, Virginie Verkarre, J-B Arnoux, Vassili Valayannopoulos, Sandrine Gobrecht, Christine Sempoux, Jacques Rahier, J-C Fournet, Francis Jaubert, Y. Aigrain, Claire Nihoul‐Feketé, Pascale de Lonlay
S112540174. 2010118 Citations
Related on ScholarIQ
Délégation Paris 5
Institution
Congenital hyperinsulinism: current trends in diagnosis and therapy
Paper
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.
Paper
Update of mutations in the genes encoding the pancreatic beta-cell K<sub>ATP</sub>channel subunits Kir6.2 (<i>KCNJ11</i>) and sulfonylurea receptor 1 (<i>ABCC8</i>) in diabetes mellitus and hyperinsulinism
Paper
Clinical approach to inherited metabolic disorders in neonates: an overview
Paper
<i>ABCC8</i> and <i>KCNJ11</i> molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism
Paper