Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

O. Xerri · SciRah

Researcher profile · Semantic Scholar

O. Xerri

Share profile

O. Xerri — researcher profile on SciRah

h-index: 4
Works: 10
Citations: 192

Most-cited papers

Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy
I. Perrault, S. Hanein, X. Zanlonghi, V. Serre +19 more
2012Nature Genetics139 citations
Semantic Scholar
Untreated Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE): a case series
O. Xerri, S. Salah, D. Monnet, A. Brézin
2018BMC Ophthalmology29 citations Open access
Semantic Scholar
[Ocular manifestations in Ehlers-Danlos Syndromes: Clinical study of 21 patients].
S. Perez-Roustit, Diem Trang Nguyen, O. Xerri, M. Robert +4 more
2019Journal Francais d'Ophtalmologie16 citations
Semantic Scholar
Choroidal and peripapillary changes in high myopic eyes with Stickler syndrome
O. Xerri, F. Bernabei, E. Philippakis, Cyril Burin-des-Roziers +8 more
2021BMC Ophthalmology8 citations Open access
Semantic Scholar
Sostdc1, a secreted dual BMP and WNT antagonist, is differentially expressed in RCS rdy+ and rdy- rat retinal pigment epithelial cells
M. Abitbol, O. Xerri, Maud Valensi, Virginie Dinet +8 more
20170 citations
Semantic Scholar
Acute Posterior Multifocal Pigment Epitheliopathy : visual outcome in untreated patients
O. Xerri, S. Salah, D. Monnet, A. Brézin
20160 citations
Semantic Scholar
Ciliome resequencing: A lifeline for molecular diagnosis in LCA
I. Perrault, S. Hanein, M. Nicouleau, S. Saunier +7 more
2015Cilia0 citations Open access
Semantic Scholar
Comprehensive molecular diagnosis of 160 Leber congenital amaurosis or Early Onset Severe Retinal Dystrophy by targeted next generation sequencing.
I. Perrault, S. Hanein, C. Bole, P. Nitschké +5 more
20150 citations
Semantic Scholar
Leber congenital amaurosis with early-onset severe macular atrophy and optic atrophy is likely pathognomonic of NMNAT1 mutations
O. Xerri, I. Perrault, S. Hanein, N. Delphin +6 more
20150 citations
Semantic Scholar
[Bilateral retinal folds and familial high hyperopia: a case report].
O. Xerri, C. Orssaud, M. Kaluszyner, J. Dufier +1 more
2013Journal Francais d'Ophtalmologie0 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

I. Perrault×4
Invite
I. Perrault — researcher profile on SciRah
S. Hanein×4
Invite
S. Hanein — researcher profile on SciRah
N. Delphin×4
Invite
N. Delphin — researcher profile on SciRah
A. Munnich×4
Invite
A. Munnich — researcher profile on SciRah

×3

Invite

P. Nitschké — researcher profile on SciRah

Invite

O. Roche — researcher profile on SciRah

Invite

J. Kaplan — researcher profile on SciRah

Invite

J. Rozet — researcher profile on SciRah

Invite

A. Brézin — researcher profile on SciRah

M. Nicouleau×2

Invite

M. Nicouleau — researcher profile on SciRah

L. Fares-Taie×2

Invite

L. Fares-Taie — researcher profile on SciRah

Invite

S. Gerber — researcher profile on SciRah