Nejla Erkilic

492 citations

18 papers · 328 indexed · h-index 10

Co-authors: Vasiliki Kalatzis Isabelle Meunier Anne‐Françoise Roux Christian P. Hamel Daria Mamaeva David Baux Francisco Espinoza Valérie Faugère
Topics: Retinal Development and Disorders (12 papers)CRISPR and Genetic Engineering (7 papers)Pluripotent Stem Cells Research (5 papers)
Cited by: Ophthalmology Sensory Systems Molecular Biology
Journals: Scientific Reports The FASEB Journal International Journal of Molecular Sciences
Partner nations: France United States Germany

In The Last Decade

Nejla Erkilic

18 papers receiving 326 citations

Peers

Countries citing papers authored by Nejla Erkilic

Since Specialization

Citations

This map shows the geographic impact of Nejla Erkilic's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Nejla Erkilic with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nejla Erkilic more than expected).

Fields of papers citing papers by Nejla Erkilic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nejla Erkilic. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Nejla Erkilic. The network helps show where Nejla Erkilic may publish in the future.

Co-authorship network of co-authors of Nejla Erkilic

This figure shows the co-authorship network connecting the top 25 collaborators of Nejla Erkilic. A scholar is included among the top collaborators of Nejla Erkilic based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nejla Erkilic. Nejla Erkilic is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

#	Work	Indexed citations
1	Dual CRALBP isoforms unveiled: iPSC-derived retinal modeling and AAV2/5-RLBP1 gene transfer raise considerations for effective therapy 2024 ·Molecular Therapy ·(unknown),(unknown),(unknown),Daria Mamaeva,Marie O. Péquignot,Nejla Erkilic,(unknown),Hassan Boukhaddaoui,Florence Bernex,Béatrice Bocquet,Jérôme Vialaret,Yvan Arsenijévic,T. Michael Redmond,(unknown),Isabelle Meunier,Philippe Brabet,Vasiliki Kalatzis	1
2	USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids 2023 ·Human Genetics and Genomics Advances ·(unknown),(unknown),Nejla Erkilic,(unknown),(unknown),Kerstin Nagel‐Wolfrum,Uwe Wolfrum,Erwin van Wijk,Anne‐Françoise Roux,Isabelle Meunier,Vasiliki Kalatzis	12
3	Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid 2022 ·Stem Cell Research & Therapy ·(unknown),Nejla Erkilic,(unknown),Hassan Boukhaddaoui,(unknown),Marcela Garita‐Hernandez,Daria Mamaeva,(unknown),(unknown),(unknown),Olivier Goureau,Isabelle Meunier,Vasiliki Kalatzis	19
4	Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa 2022 ·Stem Cell Research ·(unknown),Nejla Erkilic,Christel Vaché,(unknown),Anne‐Françoise Roux,Isabelle Meunier,Vasiliki Kalatzis	4
5	CRISPR/Cas9-Mediated Genome Editing to Generate Clonal iPSC Lines 2021 ·Methods in molecular biology ·(unknown),Nejla Erkilic,Daria Mamaeva,Vasiliki Kalatzis	7
6	Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3 2021 ·International Journal of Molecular Sciences ·(unknown),(unknown),Nejla Erkilic,(unknown),Isabelle Meunier,Vasiliki Kalatzis	31
7	Novel roles for voltage‐gated T‐type Ca ²⁺ and ClC‐2 channels in phagocytosis and angiogenic factor balance identified in human iPSC‐derived RPE 2021 ·The FASEB Journal ·Daria Mamaeva,(unknown),Mattia L. DiFrancesco,Nejla Erkilic,(unknown),Cécile Hilaire,Isabelle Meunier,Hassan Boukhaddaoui,Vasiliki Kalatzis	4
8	Study of Usutu virus neuropathogenicity in mice and human cellular models 2020 ·PLoS neglected tropical diseases ·Marion Clé,Jonathan Barthelemy,Caroline Desmetz,Vincent Foulongne,(unknown),Karine Bolloré,Édouard Tuaillon,Nejla Erkilic,Vasiliki Kalatzis,Sylvie Lecollinet,Cécile Beck,Nelly Pirot,(unknown),Fabien Gosselet,(unknown),Philippe Van de Perre,Sara Salinas,Yannick Simonin	31
9	Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy 2019 ·Stem Cell Research ·Nejla Erkilic,(unknown),(unknown),Gaël Manès,(unknown),Christian P. Hamel,Isabelle Meunier,Vasiliki Kalatzis	5
10	Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles 2019 ·Molecular Therapy — Methods & Clinical Development ·(unknown),Nejla Erkilic,David Baux,Daria Mamaeva,Christian P. Hamel,Isabelle Meunier,Anne‐Françoise Roux,Vasiliki Kalatzis	59
11	Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis 2019 ·Stem Cell Research ·Nejla Erkilic,(unknown),Gaël Manès,(unknown),Christian P. Hamel,Isabelle Meunier,Vasiliki Kalatzis	5
12	Zika virus induces strong inflammatory responses and impairs homeostasis and function of the human retinal pigment epithelium 2018 ·EBioMedicine ·Yannick Simonin,Nejla Erkilic,(unknown),Marion Clé,Caroline Desmetz,Karine Bolloré,(unknown),(unknown),Jonathan Barthelemy,(unknown),(unknown),Vincent Foulongne,Édouard Tuaillon,Philippe Van de Perre,Vasiliki Kalatzis,Sara Salinas	27
13	The effect of PTC124 on choroideremia fibroblasts and iPSC-derived RPE raises considerations for therapy 2018 ·Scientific Reports ·(unknown),Nejla Erkilic,David Baux,(unknown),(unknown),Isabelle Meunier,(unknown),Anne‐Françoise Roux,Christian Hamel,Vasiliki Kalatzis	26
14	Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa 2018 ·Stem Cell Research ·(unknown),Nejla Erkilic,Gaël Manès,(unknown),Christian P. Hamel,Isabelle Meunier,Vasiliki Kalatzis	9
15	Injection of Adipose-Derived Stromal Cells in the Knee of Patients with Severe Osteoarthritis has a Systemic Effect and Promotes an Anti-Inflammatory Phenotype of Circulating Immune Cells 2018 ·Theranostics ·Yves‐Marie Pers,(unknown),(unknown),Francisco Espinoza,Naoill Abdellaoui,Nejla Erkilic,Maïlys Cren,(unknown),Oliver Pullig,Ulrich Nöth,Christian Jørgensen,Pascale Louis‐Plence	52
16	Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2 2018 ·Stem Cell Research ·(unknown),Nejla Erkilic,Gaël Manès,(unknown),Christian P. Hamel,Isabelle Meunier,Vasiliki Kalatzis	8
17	Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analyses 2018 ·Human Mutation ·Christel Vaché,(unknown),Valérie Faugère,Nejla Erkilic,David Baux,Gema García‐García,Christian P. Hamel,Isabelle Meunier,Xavier Zanlonghi,M. Kœnig,Vasiliki Kalatzis,Anne‐Françoise Roux	7
18	Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapy 2017 ·Human Molecular Genetics ·(unknown),Nejla Erkilic,Valérie Faugère,(unknown),Christian P. Hamel,Anne‐Françoise Roux,Vasiliki Kalatzis	21

About Nejla Erkilic

Nejla Erkilic is a scholar working on Aging, Ophthalmology and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 328 indexed citations. Recurring topics across this work include Retinal Development and Disorders (12 papers), CRISPR and Genetic Engineering (7 papers) and Pluripotent Stem Cells Research (5 papers). The work is most often cited by research in Ophthalmology (56 citations), Sensory Systems (21 citations) and Molecular Biology (223 citations). Nejla Erkilic has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Vasiliki Kalatzis, Isabelle Meunier, Anne‐Françoise Roux, Christian P. Hamel, Daria Mamaeva, David Baux, Francisco Espinoza, Valérie Faugère, Ulrich Nöth and Maïlys Cren. Their work appears in journals such as Scientific Reports, The FASEB Journal and International Journal of Molecular Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact