Pascale Fanen

3.1k citations

93 papers · 2.1k indexed · h-index 26

Pulmonary and Respiratory Medicine top 2%
Molecular Biology top 10%
Genetics top 5%
Genetics top 10%
Physiology

Co-authors: Michel Goossens Nada Ghanem Bruno Costes Alexandre Hinzpeter Michel Vidaud Aleksander Edelman Josiane Martin François Plassa
Topics: Cystic Fibrosis Research Advances (49 papers)Neonatal Respiratory Health Research (41 papers)Amyloidosis: Diagnosis, Treatment, Outcomes (16 papers)
Cited by: Pulmonary and Respiratory Medicine Genetics Molecular Biology
Journals: Journal of Biological Chemistry Journal of Clinical InvestigationSHILAP Revista de lepidopterología
Partner nations: France United States Italy

In The Last Decade

Pascale Fanen

92 papers receiving 2.1k citations

Peers

Countries citing papers authored by Pascale Fanen

Since Specialization

Citations

This map shows the geographic impact of Pascale Fanen's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Pascale Fanen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pascale Fanen more than expected).

Fields of papers citing papers by Pascale Fanen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pascale Fanen. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Pascale Fanen. The network helps show where Pascale Fanen may publish in the future.

Co-authorship network of co-authors of Pascale Fanen

This figure shows the co-authorship network connecting the top 25 collaborators of Pascale Fanen. A scholar is included among the top collaborators of Pascale Fanen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Pascale Fanen. Pascale Fanen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	ABC transporters involved in respiratory and cholestatic diseases: From rare to very rare monogenic diseases 2024 ·Biochemical Pharmacology ·(unknown),(unknown),(unknown),Frédéric Becq,Thomas Falguières,Pascale Fanen	4
2	Idiopathic pulmonary fibrosis with benignSFTPCvariant and pathogenicMARS1mutations: can't see the forest for the trees! 2023 ·ERJ Open Research ·Alice Castaldo,Céline Delestrain,(unknown),(unknown),(unknown),Renaud Touraine,Lara Chalabreysse,Pascale Fanen,Ralph Epaud,Vincent Cottin,Alix de Becdelièvre	2
3	Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant 2023 ·Frontiers in Pediatrics ·Céline Delestrain,(unknown),Elodie Nattes,(unknown),V. Lacroze,Stéphanie Simon,Xavier Decrouy,Alix de Becdelièvre,Pascale Fanen,Ralph Epaud	5
4	Echocardiographic Patterns of Left Ventricular Diastolic Function in Cardiac Amyloidosis: An Updated Evaluation 2021 ·Journal of Clinical Medicine ·Silvia Oghina,Wulfran Bougouin,Mounira Kharoubi,(unknown),Arnault Galat,Soulef Guendouz,Mélanie Bézard,Fabien Le Bras,Jean‐François Deux,Emmanuel Itti,Anissa Moktefi,Pascale Fanen,Emmanuel Teíger,Dania Mohty,Thibaud Damy,Diane Bodez	6
5	Assessing Cardiac Amyloidosis Subtypes by Unsupervised Phenotype Clustering Analysis 2021 ·Journal of the American College of Cardiology ·(unknown),Mounira Kharoubi,Mélanie Bézard,Silvia Oghina,Fabien Le Bras,Elsa Poullot,Valérie Molinier‐Frenkel,Pascale Fanen,Jean‐François Deux,Vincent Audard,Emmanuel Itti,Thibaud Damy,Étienne Audureau	9
6	Exon identity influences splicing induced by exonic variants and in silico prediction efficacy 2020 ·Journal of Cystic Fibrosis ·Natacha Martin,Anne Bergougnoux,(unknown),B. Chevalier,(unknown),David Baux,Bruno Costes,Pascale Fanen,Caroline Raynal,Isabelle Sermet‐Gaudelus,Emmanuelle Girodon,Magali Taulan‐Cadars,Alexandre Hinzpeter	6
7	Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons 2018 ·ERJ Open Research ·Iwona Pranke,Laure Bidou,Natacha Martin,Sandra Blanchet,Aurélie Hatton,(unknown),(unknown),Bruno Costes,B. Chevalier,Danielle Tondelier,Emmanuelle Girodon,(unknown),Aleksander Edelman,Pascale Fanen,Olivier Namy,Isabelle Sermet‐Gaudelus,Alexandre Hinzpeter	36
8	The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible 2017 ·Clinical Case Reports ·Alexandre Hinzpeter,(unknown),Isabelle Callebaut,Cécile Zordan,Bruno Costes,Julie Guichoux,A. Iron,Didier Lacombe,Natacha Martin,Benoı̂t Arveiler,Pascale Fanen,Patricia Fergelot,Emmanuelle Girodon	4
9	The most frequent ABCA3 nonsense mutation -p.Tyr1515* (Y1515X) causing lethal neonatal respiratory failure in a term neonate 2017 ·Annals of Thoracic Medicine ·(unknown),Ralph Epaud,Humariya Heena,Alix de Becdelièvre,(unknown),Pascale Fanen	8
10	Pathologies respiratoires de l’enfant associées à des anomalies héréditaires du métabolisme du surfactant 2013 ·Revue de Pneumologie Clinique ·Céline Delestrain,Florence Flamein,Laurence Jonard,R. Couderc,Loïc Guillot,Pascale Fanen,Ralph Epaud	1
11	Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies 2012 ·Human Mutation ·Alexandre Hinzpeter,(unknown),Alix de Becdelièvre,Éric Bieth,Elvira Sondo,Natacha Martin,Bruno Costes,Cathérine Costa,Michel Goossens,Luis J. V. Galietta,Emmanuelle Girodon,Pascale Fanen	10
12	A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice 2011 ·Journal of Cystic Fibrosis ·Cathérine Costa,V. Prulière‐Escabasse,Alix de Becdelièvre,(unknown),Lisa Golmard,Caroline Guittard,Laurence Bassinet,Thierry Bienvenu,Marie des Georges,Ralph Epaud,Éric Bieth,Irina Giurgea,(unknown),Alexandre Hinzpeter,Bruno Costes,Pascale Fanen,Michel Goossens,Mireille Claustres,A. Coste,Emmanuelle Girodon	17
13	CSN5 binds to misfolded CFTR and promotes its degradation 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Gaëlle Tanguy,(unknown),N. Arous,(unknown),Alexandre Hinzpeter,Janine Fritsch,Michel Goossens,Pascale Fanen	11
14	Global proteomic approach unmasks involvement of keratins 8 and 18 in the delivery of cystic fibrosis transmembrane conductance regulator (CFTR)/ΔF508‐CFTR to the plasma membrane 2004 ·PROTEOMICS ·Noélie Davezac,Danielle Tondelier,Joanna Lipecka,Pascale Fanen,France Demaugre,Janusz Dȩbski,Michał Dadlez,André Schrattenholz,Michael A. Cahill,Aleksander Edelman	49
15	Altered channel gating mechanism for CFTR inhibition by a high‐affinity thiazolidinone blocker 2004 ·FEBS Letters ·Alessandro Taddei,Chiara Folli,Olga Zegarra‐Moran,Pascale Fanen,A. S. Verkman,Luis J. V. Galietta	91
16	Correction of G551D‐CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB‐07 2002 ·British Journal of Pharmacology ·Olga Zegarra‐Moran,Leila Romio,Chiara Folli,Emanuela Caci,Frédéric Becq,J.‐M. VIERFOND,Yvette Mettey,Giulio Cabrini,Pascale Fanen,Luis J. V. Galietta	49
17	Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy gene. 1994 ·Journal of Clinical Investigation ·Pascale Fanen,(unknown),Claude‐Olivier Sarde,Jean‐Louis Mandel,Michel Goossens,Patrick Aubourg	56
18	Exhaustive analysis of the P53 gene coding sequence by denaturing gradient gel electrophoresis: Application to the detection of point mutations in acute leukemias 1994 ·Human Mutation ·(unknown),Isabelle Vinatier,Pascale Fanen,Philippe Jonveaux,Olivier Tournilhac,M Imbert,H Rochant,M. Goossens	18
19	Screening for cystic fibrosis in dried blood spots of newborns 1993 ·Molecular and Cellular Probes ·M.‐P. Audrézet,Bruno Costes,N. Ghanem,Pascale Fanen,C. Verlingue,(unknown),Bernard Mercier,Michel Goossens,Claude Férec	25
20	A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A → G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene 1992 ·Genomics ·Patrizia Ronchetto,Juan José Tellería Orriols,Pascale Fanen,Laura Cremonesi,Maurizio Ferrari,Carmelina Magnani,Manuela Seia,M. Goossens,Giovanni Romeo,Marcella Devoto	17

About Pascale Fanen

Pascale Fanen is a scholar working on Pulmonary and Respiratory Medicine, Nephrology and Genetics, having authored 93 papers that have together received 2.1k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (49 papers), Neonatal Respiratory Health Research (41 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (16 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (1.3k citations), Genetics (329 citations) and Molecular Biology (764 citations). Pascale Fanen has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Michel Goossens, Nada Ghanem, Bruno Costes, Alexandre Hinzpeter, Michel Vidaud, Aleksander Edelman, Josiane Martin, François Plassa, Emmanuelle Girodon and Luis J. V. Galietta. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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