Konstantinos Nikopoulos

Author

University of Lausanne ORCID

Also Known As

K. Nikopoulos, KONSTANTINOS NIKOPOULOS, Konstantinos Nikopoulos, Kostas Nikopoulos, Nikopoulos, Konstantinos

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University of Lausanne Radboud University Nijmegen Radboud University Medical Center University of Leicester Lund University

About

Konstantinos Nikopoulos is an author at University of Lausanne specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	524
2	Pathology	5	5	524
3	Molecular Genetics	3	3	288
4	Public Health	2	2	57
5	Biology	2	2	57

Konstantinos Nikopoulos

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy Konstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen, The American Journal of Human Genetics Mendelian DisorderFamilial Exudative VitreoretinopathyGenetic DisorderNext-generation SequencingGenetics	2010	231
L1 retrotransposition can occur early in human embryonic development José A. J. M. van den Hurk, Iwan C. Meij, Maria del Carmen Seleme, Human Molecular Genetics	2007	187
<i>ZNF408</i> is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature Rob W.J. Collin, Konstantinos Nikopoulos, Margo Dona, Proceedings of the National Academy of Sciences Ocular DiseasePeripheral RetinaExome SequencingGeneticsPathology	2013	179
Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP Konstantinos Nikopoulos, Hanka Venselaar, Rob W.J. Collin, Human Mutation	2010	148
Erosive Vitreoretinopathy and Wagner Disease Are Caused by Intronic Mutations in<i>CSPG2</i>/<i>Versican</i>That Result in an Imbalance of Splice Variants Arijit Mukhopadhyay, Konstantinos Nikopoulos, Alessandra Maugeri, Investigative Ophthalmology & Visual Science	2006	89
Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis Marta Cortón, Koji M. Nishiguchi, Almudena Ávila‐Fernández, PLoS ONE	2013	77
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects Konstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, The American Journal of Human Genetics Primary-cilia DefectsGenetic DisorderGeneticsHearing Loss AssociatedPathology	2016	57
Autosomal Recessive Stickler Syndrome in Two Families Is Caused by Mutations in the<i>COL9A1</i>Gene Konstantinos Nikopoulos, Isabelle Schrauwen, Marleen Simon, Investigative Ophthalmology & Visual Science	2011	49
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1 , a Gene Implicated in Ubiquitination Frauke Coppieters, Giulia Ascari, Katharina Dannhausen, The American Journal of Human Genetics	2016	49
CEP78 functions downstream of CEP350 to control biogenesis of primary cilia by negatively regulating CP110 levels André Brás Gonçalves, Sarah Kirstine Hasselbalch, Beinta Biskopstø Joensen, eLife	2021	42

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