S. Pinson - Concepedia

Author

S. Pinson

Also Known As

Adrien Buisson, Eric Puzenat, François Petit, Michel Vidaud, Pinson, Stéphane, S Pinson, S. Pinson, Stephane Pinson, Stéphane Pinson, Vincent des Portes

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Hôpital Edouard Herriot Inserm Hospices Civils de Lyon Sorbonne Université Assistance Publique – Hôpitaux de Paris

About

S. Pinson is an author at Hôpital Edouard Herriot specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	257
2	Engineering	1	1	18
3	Health Sciences	1	1	25
4	Public Health	1	1	16
5	Data Science	1	1	18

S. Pinson

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
<i>NF1</i> Molecular Characterization and Neurofibromatosis Type I Genotype-Phenotype Correlation: The French Experience Audrey Sabbagh, Éric Pasmant, Apolline Imbard, Human Mutation	2013	173
Molecular screening of<i>ALK1/ACVRL1</i>and<i>ENG</i>genes in hereditary hemorrhagic telangiectasia in France Gaëtan Lesca, Henri Plauchu, Florence Coulet, Human Mutation	2004	119
Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1genes Véronique Gelsi‐Boyer, Virginie Trouplin, José Adélaı̈de, BMC Cancer	2008	118
Inactivation of the<i>APC</i>Gene Is Constant in Adrenocortical Tumors from Patients with Familial Adenomatous Polyposis but Not Frequent in Sporadic Adrenocortical Cancers Sébastien Gaujoux, S. Pinson, Anne‐Paule Gimenez‐Roqueplo, Clinical Cancer Research	2010	113
Mapping QTLs for field resistance to the rice blast pathogen and evaluating their individual and combined utility in improved varieties Rodante E. Tabien, Zhongyi Li, Andrew H. Paterson, Theoretical and Applied Genetics GeneticsCrop ProtectionCombined UtilityPlant PathologyRice Blast Pathogen	2002	105
Distribution ofENG andACVRL1 (ALK1) mutations in French HHT patients Gaëtan Lesca, Nelly Burnichon, Grégory Raux, Human Mutation	2006	83
Interest of systematic screening of pheochromocytoma in patients with neurofibromatosis type 1 L. Képénékian, Thomas Mognetti, Jean‐Christophe Lifante, European Journal of Endocrinology	2016	67
Novel biallelic mutations inMSH6 andPMS2 genes: gene conversion as a likely cause ofPMS2 gene inactivation Jessie Auclair, Dominique Leroux, Françoise Desseigne, Human Mutation	2007	66
Nevus anemicus in neurofibromatosis type 1: A potential new diagnostic criterion M. Marque, Agathe Roubertie, Audrey Jaussent, Journal of the American Academy of Dermatology PathologyNeurofibromatosis Type 1NeurologyNevus AnemicusDermatology	2013	61
Utility of 18F-FDG PET with a Semi-Quantitative Index in the Detection of Sarcomatous Transformation in Patients with Neurofibromatosis Type 1 P. Combemale, L. Valeyrie‐Allanore, Francesco Giammarile, PLoS ONE	2014	59

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