Delphine Fradin - Concepedia

Author

Delphine Fradin

Inserm ORCID

Also Known As

D Fradin, D. Fradin, Daniella Fradin, Delphine D Fradin, Delphine Fradin, Fradin, Delphine

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Inserm Université Paris-Sud Nantes Université Bicêtre Hospital Centre National de la Recherche Scientifique

About

Delphine Fradin is an author at Inserm specializing in medicine, genetics, and chromatin.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	227
2	Natural Sciences	2	2	25
3	Cell Biology	2	2	125
4	Engineering	1	1	15
5	Biostatistics	1	1	10

Delphine Fradin

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Personalized Epigenomic Signatures That Are Stable Over Time and Covary with Body Mass Index Andrew P. Feinberg, Rafael A. Irizarry, Delphine Fradin, Science Translational Medicine	2010	333
MicroRNAs in Tumor Exosomes Drive Immune Escape in Melanoma Virginie Vignard, Maureen Labbé, Nadège Marec, Cancer Immunology Research	2019	149
XPG and XPF Endonucleases Trigger Chromatin Looping and DNA Demethylation for Accurate Expression of Activated Genes Nicolas Le May, Delphine Fradin, Izarn Iltis, Molecular Cell Histone ModificationsChromatinChromatin RemodelingMedicineGenetics	2012	107
Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes Delphine Fradin, Sophie Le Fur, Clémence Mille, PLoS ONE	2012	94
Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children Delphine Fradin, Pierre‐Yves Boëlle, Marie‐Pierre Belot, Scientific Reports	2017	69
Frequent Homozygous Deletions of Type I Interferon Genes in Pleural Mesothelioma Confer Sensitivity to Oncolytic Measles Virus Tiphaine Delaunay, Carole Achard, Nicolas Boisgerault, Journal of Thoracic Oncology Frequent Homozygous DeletionsPathogenesisViral PathogenesisImmunologyPathology	2020	59
Parent-Of-Origin Effects in Autism Identified through Genome-Wide Linkage Analysis of 16,000 SNPs Delphine Fradin, Keely Cheslack‐Postava, Christine Ladd‐Acosta, PLoS ONE	2010	57
The GH receptor exon 3 deletion is a marker of male-specific exceptional longevity associated with increased GH sensitivity and taller stature Danny Ben‐Avraham, Diddahally R. Govindaraju, Temuri Budagov, Science Advances	2017	57
CpG Methylation Changes within the IL2RA Promoter in Type 1 Diabetes of Childhood Onset Marie‐Pierre Belot, Delphine Fradin, Nga Mai, PLoS ONE	2013	49
The IGF1 P2 promoter is an epigenetic QTL for circulating IGF1 and human growth Meriem Ouni, Yasemin Güneş, Marie‐Pierre Belot, Clinical Epigenetics	2015	47

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