Frauke Coppieters - Concepedia

Author

Frauke Coppieters

Also Known As

Bart P. Leroy, COPPIETERS F, Chris Guerin, Coppieters, Frauke, F COPPIETERS, F Coppieters, F. Coppieters, Frauke Coppieters, Philippe Kestelyn

142

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

Ghent University Hospital Ghent University Children's Hospital of Philadelphia Queen Fabiola Children's University Hospital VIB-UGent Center for Inflammation Research

About

Frauke Coppieters is an author at Ghent University Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	1.5K
2	Public Health	2	2	88
3	Engineering	1	1	51
4	Natural Sciences	1	1	12
5	Biochemistry	1	1	12

Frauke Coppieters

Publications

Citations

H-Index

Page 1

	Year	Citations
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial Albert M. Maguire, Katherine A. High, Alberto Auricchio, The Lancet Gene TherapiesGenetic DisorderGeneticsClinical TrialsTranslational Research	2009	849
Vaccination with early ferroptotic cancer cells induces efficient antitumor immunity Iuliia Efimova, Elena Catanzaro, Louis Van der Meeren, Journal for ImmunoTherapy of Cancer	2020	437
A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia Susanne Kohl, Frauke Coppieters, Françoise Meire, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMolecular Genetics	2012	179
Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes Frauke Coppieters, Ingele Casteels, Françoise Meire, Human Mutation	2010	146
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development Dorien Baetens, Hans Stoop, Frank Peelman, Genetics in Medicine	2016	139
Recurrent Mutation in the First Zinc Finger of the Orphan Nuclear Receptor NR2E3 Causes Autosomal Dominant Retinitis Pigmentosa Frauke Coppieters, Bart P. Leroy, Diane Beysen, The American Journal of Human Genetics Recurrent MutationFirst Zinc FingerGenetic DisorderGeneticsMolecular Genetics	2007	125
<i>IQCB1</i>Mutations in Patients with Leber Congenital Amaurosis Alejandro Estrada‐Cuzcano, Robert K. Koenekoop, Frauke Coppieters, Investigative Ophthalmology & Visual Science	2010	113
Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy Susanne Roosing, Ideke J.C. Lamers, Erik de Vrieze, The American Journal of Human Genetics	2014	81
An Augmented<i>ABCA4</i>Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients Miriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, Human Mutation	2014	67
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations Kristof Van Schil, Sarah Naessens, Stijn Van de Sompele, Genetics in Medicine Copy-number VariationsGeneticsComplex CnvsMolecular GeneticsDisease Gene Identification	2017	66

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