Hubert de Verneuil

6.8k citations

145 papers · 5.1k indexed · h-index 43

Pediatrics, Perinatology and Child Health top 0.5%
- Neonatal Health and Biochemistry 62
Molecular Biology top 2%
- Porphyrin Metabolism and Disorders 94
- Heme Oxygenase-1 and Carbon Monoxide 50
- CRISPR and Genetic Engineering 10
Hematology top 2%
Rheumatology top 1%
- Folate and B Vitamins Research 16
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 18
Genetics
- Virus-based gene therapy research 18
Pulmonary and Respiratory Medicine
- Methemoglobinemia and Tumor Lysis Syndrome 8

Co-authors: Y Nordmann Bernard Grandchamp Cécile Ged Frédéric Mazurier François Moreau‐Gaudry Jean‐Charles Deybach Sylvie Mader Pierre Chambon
Cited by: Pediatrics, Perinatology and Child Health Molecular Biology Hematology
Journals: Nature (1 paper)Science (1 paper)Proceedings of the National Academy of Sciences (3 papers)
Partner nations: France United States Spain

In The Last Decade

Hubert de Verneuil

142 papers receiving 5.0k citations

Peers

Countries citing papers authored by Hubert de Verneuil

Since Specialization

Citations

This map shows the geographic impact of Hubert de Verneuil'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 Hubert de Verneuil with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hubert de Verneuil more than expected).

Fields of papers citing papers by Hubert de Verneuil

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hubert de Verneuil. 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 Hubert de Verneuil. The network helps show where Hubert de Verneuil may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hubert de Verneuil, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hubert de Verneuil Line = papers co-authored together Hubert de Verneuil links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Missense UROS mutations causing congenital erythropoietic porphyria reduce UROS homeostasis that can be rescued by proteasome inhibition Human Molecular Genetics ·Jean‐Marc Blouin,Ganeko Bernardo‐Seisdedos,Emma Sasso,Julie Estève,Cécile Ged,Magalie Lalanne,Arantza Sanz-Parra,Pedro Urquiza,Hubert de Verneuil,Óscar Millet,Emmanuel Richard	2017	19
2	Effect of tyrosine kinase inhibitors on stemness in normal and chronic myeloid leukemia cells Leukemia ·Lucie Charaf,F-X Mahon,Isabelle Lamrissi‐Garcia,Isabelle Moranvillier,François Béliveau,Bruno Cardinaud,Sandrine Dabernat,Hubert de Verneuil,François Moreau‐Gaudry,Aurélie Bedel	2016	11
3	Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients Folia Biologica ·M. S. Farrag,Ivan Mikula,Eva Richard,Vladimı́r Saudek,Hubert de Verneuil,Pavel Martásek	2015	3
4	In vivo gene transfer targeting in pancreatic adenocarcinoma with cell surface antigens Molecular Cancer ·M. Lafitte,Benoı̂t Rousseau,Isabelle Moranvillier,Miguel Taillepierre,Evelyne Peuchant,Veronique Guyonnet‐Dupérat,Aurélie Bedel,Pierre Dubus,Hubert de Verneuil,François Moreau‐Gaudry,Sandrine Dabernat	2012	16
5	XPC silencing in normal human keratinocytes triggers metabolic alterations through NOX-1 activation-mediated reactive oxygen species Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Hamid Rezvani,Rodrigue Rossignol,Nsrein Ali,Giovanni Bénard,Xiuwei Tang,Hee Seung Yang,Thomas Jouary,Hubert de Verneuil,Alain Taı̈eb,Arianna L. Kim,Frédéric Mazurier	2010	45
6	XPC silencing in normal human keratinocytes triggers metabolic alterations that drive the formation of squamous cell carcinomas Journal of Clinical Investigation ·Hamid Rezvani,Arianna L. Kim,Rodrigue Rossignol,Nsrein Ali,Meaghan Daly,Walid Mahfouf,Nadège Bellancé,Alain Taı̈eb,Hubert de Verneuil,Frédéric Mazurier,David R. Bickers	2010	67
7	Modeling of congenital erythropoietic porphyria by RNA interference: a new tool for preclinical gene therapy evaluation The Journal of Gene Medicine ·Élodie Richard,Magalie Lalanne,Isabelle Lamrissi‐Garcia,Veronique Guyonnet‐Dupérat,Emmanuel Richard,Vincent Pitard,Frédéric Mazurier,François Moreau‐Gaudry,Cécile Ged,Hubert de Verneuil	2010	6
8	Hypoxia-inducible factor-1α regulates the expression of nucleotide excision repair proteins in keratinocytes Nucleic Acids Research ·Hamid Rezvani,Walid Mahfouf,Nsrein Ali,Cécile Chemin,Cécile Ged,Arianna L. Kim,Hubert de Verneuil,Alain Taı̈eb,David R. Bickers,Frédéric Mazurier	2009	51
9	Effective Gene Therapy of Mice with Congenital Erythropoietic Porphyria Is Facilitated by a Survival Advantage of Corrected Erythroid Cells The American Journal of Human Genetics ·Élodie Richard,François Moreau‐Gaudry,Magalie Lalanne,Isabelle Lamrissi‐Garcia,Muriel Cario,Veronique Guyonnet‐Dupérat,Laurence Taine,Cécile Ged,Hubert de Verneuil	2008	37
10	Retroviral Coexpression of IFN-α and IFN-γ Genes and Inhibitory Effects in Chronic Myeloid Leukemia Cells Journal of Interferon & Cytokine Research ·Cécile Ged,Hubert de Verneuil,Josy Reiffers,Françeois-Xavier Mahon,Stéphanie Salesse,Valélerie Lagarde	2000	2
11	Increased incidence of HFE C282Y mutations in patients with iron overload and hepatocellular carcinoma developed in non-cirrhotic liver Journal of Hepatology ·Jean‐Frédéric Blanc,Victor de Lédinghen,Pierre–Henri Bernard,Hubert de Verneuil,María Winnock,Brigitte Le Bail,Jacques Carles,Jean Saric,Charles Balabaud,Paulette Bioulac‐Sage	2000	55
12	A Novel Immunodeficient Mouse Model-RAG2 gamma Cytokine Receptor Chain Double Mutants-Requiring Exogenous Cytokine Administration for Human Hematopoietic Stem Cell Engraftment Common Journal of Interferon & Cytokine Research ·Frédéric Mazurier,Antonio Fontanellas,Stéphanie Salesse,Laurence Taine,S Landriau,François Moreau‐Gaudry,Josy Reiffers,Bruno Péault,James P. Di Santo,Hubert de Verneuil	1999	94
13	Rapid analysis and efficient selection of human transduced primitive hematopoietic cells using the humanized S65T green fluorescent protein Gene Therapy ·Frédéric Mazurier,François Moreau‐Gaudry,Véronique Maguer‐Satta,Stéphanie Salesse,V Pigeonnier-Lagarde,Cécile Ged,Françis Belloc,Francis Lacombe,F-X Mahon,Josy Reiffers,Hubert de Verneuil	1998	15
14	Hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda patients: The influence of virus C infection Hepatology ·(unknown),Antonio Fontanellas,E. Brudieux,Isabelle Hombrados,Victor de Lédinghen,Patrice Couzigou,Hubert de Verneuil,Rafael Enrı́quez de Salamanca	1998	45
15	Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males. PubMed ·Valérie Biancalana,Laurence Taine,J. Bouix,Sonja Finck,Alain Chauvin,Hubert de Verneuil,Samantha J.L. Knight,Claude Stoll,Didier Lacombe,Jean‐Louis Mandel	1996	24
16	Identification of Two NewMutations in CongenitalErythropoietic Porphyria European Journal of Human Genetics ·M. Bemidhoum,Cécile Ged,Isabelle Hombrados,François Moreau‐Gaudry,RJ Hift,P.N. Meissner,Edward D. Sturrock,Hubert de Verneuil	1995	19
17	Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria Human Genetics ·Samia Boulechfar,Vasco Da Silva,Jean‐Charles Deybach,Y Nordmann,Bernard Grandchamp,Hubert de Verneuil	1992	42
18	Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene Biochemical and Biophysical Research Communications ·J. Lamoril,Samia Boulechfar,Hubert de Verneuil,Bernard Grandchamp,Y Nordmann,Jean‐Charles Deybach	1991	102
19	Sequential activation of genes for heme pathway enzymes during erythroid differentiation of mouse Friend virus-transformed erythroleukemia cells Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Hiroyoshi Fujita,Masayuki Yamamoto,Takashi Yamagami,Norio Hayashi,Terry Rogers Bishop,Hubert de Verneuil,Takeo Yoshinaga,Shigeki Shibahara,Richard I. Morimoto,Shigeru Sassa	1991	52
20	Porphyria cutanea tarda and HLA-linked hemochromatosis Gastroenterology ·Carole Beaumont,R Fauchet,Liem Nhu Phung,Hubert de Verneuil,M. Guéguen,Y Nordmann	1987	2

About Hubert de Verneuil

Hubert de Verneuil is a scholar working on Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Molecular Biology, having authored 145 papers that have together received 5.1k indexed citations. Recurring topics across this work include Porphyrin Metabolism and Disorders (94 papers), Neonatal Health and Biochemistry (62 papers), Heme Oxygenase-1 and Carbon Monoxide (50 papers), Virus-based gene therapy research (18 papers), Metabolism and Genetic Disorders (18 papers), Folate and B Vitamins Research (16 papers), CRISPR and Genetic Engineering (10 papers) and Methemoglobinemia and Tumor Lysis Syndrome (8 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.3k citations), Molecular Biology (3.8k citations) and Hematology (480 citations). Hubert de Verneuil has collaborated with scholars based in France, United States and Spain. Frequent co-authors include Y Nordmann, Bernard Grandchamp, Cécile Ged, Frédéric Mazurier, François Moreau‐Gaudry, Jean‐Charles Deybach, Sylvie Mader, Pierre Chambon, Vijay Kumar and Alain Taı̈eb. Their work appears in journals such as Nature, Science and Proceedings of the National Academy of Sciences.

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