NEWS
New Feature!!!! University Subject Rankings in 12 branches
FOR SCIENTIST REGISTRATION FOR INSTITUTIONAL BULK REGISTRATION
FOR EDIT YOUR UNIVERSITY / INSTITUTION PAGE
Some differences of the AD Scientific Index
New Feature!!!! University Subject Rankings in 12 branches
List without CERN, Statistical Data etc. Only in AD Scientific Index
New Feature!!!! University Subject Rankings in 12 branches
AD
Scientific Index 2024
About Us
Methodology
Compare & Choose
Contact - FAQ
login
Login
person_add
Register
school
University Rankings
subject
University Subject Rankings
place
Country Rankings
insights
i10 Productivity Rankings
insights
Subject Rankings
format_list_numbered
Top 100 Scientists
format_list_numbered
Citation Rankings
format_quote
Top 100 Institutions
local_fire_department
Country Top Lists
Stefano Onano
AD Scientific Index 2024
Medical and Health Sciences / Medical Genetics
Institute of Genetic and Biomedical Research, CNR - / Italy
Edit Form
Registration, Add Profile,
Premium Membership
Ranking &
Analysis
Job
Experiences (0)
Education
Information (0)
Published Books (0)
Book Chapters (0)
Articles (0)
Presentations (0)
Lessons (0)
Projects (0)
Congresses (0)
Editorship, Referee &
Scientific Board (0 )
Patents /
Designs (0)
Academic Grants
& Awards (0)
Artistic
Activities (0)
Certificate / Course
/ Trainings (0)
Association &
Society Memberships (0)
Contact, Office
& Social Media
person_outline
Stefano Onano's MOST POPULAR ARTICLES
1-)
Complex genetic signatures in immune cells underlie autoimmunity and inform therapyV Orrù, M Steri, C Sidore, M Marongiu, V Serra, S Olla, G Sole, S Lai, ...Nature genetics 52 (10), 1036-1045, 20203082020
2-)
Bi-allelic mutations in KLHL7 cause a Crisponi/CISS1-like phenotype associated with early-onset retinitis pigmentosaA Angius, P Uva, I Buers, M Oppo, A Puddu, S Onano, I Persico, A Loi, ...The American Journal of Human Genetics 99 (1), 236-245, 2016452016
3-)
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case reportRM Alves, P Uva, MF Veiga, M Oppo, FCR Zschaber, G Porcu, HP Porto, ...BMC Medical Genetics 20, 1-7, 2019222019
4-)
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBPA Angius, P Uva, M Oppo, I Persico, S Onano, S Olla, V Pes, C Perria, ...American Journal of Medical Genetics Part A 179 (4), 634-638, 2019202019
5-)
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndromeA Angius, S Cossu, P Uva, M Oppo, S Onano, I Persico, G Fotia, R Atzeni, ...Clinical genetics 93 (6), 1245-1247, 2018182018
ARTICLES
Add your articles
We use cookies to personalize our website and offer you a better experience. If you accept cookies, we can offer you special services.
Cookie Policy
Accept