Frederic Depreux - Concepedia

Concepedia

Author

Frederic Depreux

Rosalind Franklin University of Medicine and Science

Also Known As

F. F. S. Depreux, F.F.S Depreux, F.F.S. Depreux, Frederic Depreux, Frederic F S Depreux, Frederic F. Depreux, Frederic F.S. Depreux

29

Publications

1.4K

Citations

18

H-Index

63

Concepts

All Affiliations

Rosalind Franklin University of Medicine and Science Harvard University Purdue University West Lafayette Howard Hughes Medical Institute Louisiana State University Health Sciences Center New Orleans

FD

About

Frederic Depreux is an author at Rosalind Franklin University of Medicine and Science specializing in medicine, physiology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	865
2	Health Sciences	3	3	158
3	Arts	1	1	101
4	Natural Sciences	1	1	54
5	Public Health	1	1	79

Frederic Depreux

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18

Publications

1.4K

Citations

18

H-Index

	Year	Citations
Myostatin expression in porcine tissues: tissue specificity and developmental and postnatal regulation Shaoquan Ji, R. L. Losinski, S. G. Cornelius, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology Muscle FunctionTissue SpecificityOrgan DevelopmentCellular PhysiologyEmbryology	1998	241
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss Jost Schönberger, Libin Wang, Jordan T. Shin, Nature Genetics Transcriptional RegulationSystems BiologySensorineural Hearing LossCardiomyopathyMedicine	2005	196
Nesprin-1 mutations in human and murine cardiomyopathy Megan J. Puckelwartz, Eric Kessler, Gene Kim, Journal of Molecular and Cellular Cardiology Nesprin-1 MutationsCardiomyopathyHeart FailureCardiac MuscleGenetics	2009	142
Eya4-deficient mice are a model for heritable otitis media Frederic Depreux, Keith N. Darrow, David A. Conner, Journal of Clinical Investigation GeneticsOtorhinolaryngologyEya4-deficient MiceImmunogeneticsKnockout Mouse	2008	101
Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates Martín L. Basch, Rogers M. Brown, Hsin-I Jen, eLife	2016	94
An <i>Ryr1</i> <sup> <i>I4895T</i> </sup> mutation abolishes Ca <sup>2+</sup> release channel function and delays development in homozygous offspring of a mutant mouse line Elena Zvaritch, Frederic Depreux, Natasha Kraeva, Proceedings of the National Academy of Sciences	2007	80
Myosin heavy chain isoforms account for variation in pork quality J. M. Eggert, Frederic Depreux, A. P. Schinckel, Meat Science Animal PhysiologyAnimal SciencePhysiologyBiostatisticsPork Quality	2002	79
Ca <sup>2+</sup> dysregulation in <i> Ryr1 <sup>I4895T/wt</sup> </i> mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods Elena Zvaritch, Natasha Kraeva, Éric Bombardier, Proceedings of the National Academy of Sciences	2009	72
Lunatic fringe-mediated Notch signaling regulates adult hippocampal neural stem cell maintenance Fatih Semerci, William T. Choi, Aleksandar Bajić, eLife	2017	57
Gene expression, chromosome position and lamin A/C mutations Megan J. Puckelwartz, Frederic Depreux, Elizabeth M. McNally Nucleus GeneticsNuclear LaminaMolecular BiologyMolecular GeneticsEpigenetics	2011	54

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