ScholarIQanswers from OpenAlex & ORCID
Pascale de Lonlay
ResearcherPublications, citations & collaboration network
Pascale de Lonlay is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Pascale de Lonlay have?
ScholarIQindexed works
Pascale de Lonlay has 132 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Pascale de Lonlay have?
ScholarIQcitation count
Pascale de Lonlay has 3,646 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Pascale de Lonlay?
ScholarIQh-index
Pascale de Lonlay has an h-index of 33 in OpenAlex.
What is the i10-index of Pascale de Lonlay?
ScholarIQi10-index
Pascale de Lonlay has an i10-index of 59 in OpenAlex.
What is the ORCID of Pascale de Lonlay?
ScholarIQorcid
The ORCID for Pascale de Lonlay is on the source record.
What is the OpenAlex record for Pascale de Lonlay?
ScholarIQopenalex
The OpenAlex for Pascale de Lonlay is on the source record.
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
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
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
Clinical approach to inherited metabolic disorders in neonates: an overview
Jean‐Marie Saudubray, Marie‐Cécile Nassogne, Pascale de Lonlay, Guy Touati
<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