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Marianna E Weener (Marianna E Ivanova, Marianna Weener)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 3

Top Topics

Dna Methylation

Ejection Fraction

Immune Response

Hodgkin Lymphoma

Top Venues

NPJ genomic medicine

Ophthalmic genetics

CRO Oftalmic

This page only lists publications with an associated author ORCID identifier.

Affiliation History

CRO Oftalmic Dec 8o 2008

Russia

CEO :: -

Publications

Neringa Jurkute, Francesca Cancellieri, Lisa Pohl, Catherina H Z Li, Robert A Heaton, Janine Reurink, James Bellingham, Mathieu Quinodoz, Georgia Yioti, Maria Stefaniotou, Marianna E Weener, Theresia Zuleger, Tobias B Haack, Katarina Stingl, null null, Carel B Hoyng, Omar A Mahroo, Iain Hargreaves, F Lucy Raymond, Michel Michaelides, Carlo Rivolta, Susanne Kohl, Susanne Roosing, Andrew R Webster, Gavin Arno
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype. NPJ genomic medicine 7 (1) (2022)
Debmalya Barh, Sandeep Tiwari, Lucas Gabriel Rodrigues Gomes, Marianna E Weener, Khalid J Alzahrani, Khalaf F Alsharif, Alaa A A Aljabali, Murtaza M Tambuwala, Kenneth Lundstrom, Sk Sarif Hassan, Ãngel Serrano-Aroca, Kazuo Takayama, Preetam Ghosh, Elrashdy Mustafa Redwan, Bruno Silva Andrade, Siomar de Castro Soares, Vasco Ariston de Carvalho Azevedo, Vladimir N Uversky
Potential Molecular Mechanisms of Rare Anti-Tumor Immune Response by SARS-CoV-2 in Isolated Cases of Lymphomas. Viruses 13 (10) (2021)
Marianna E Weener, Inna V Zolnikova, Ketevan V Gorgisheli, Dmitry S Atarshchikov, Preetam Ghosh, Debmalya Barh
Novel frameshift mutation in NYX gene in a Russian family with complete congenital stationary night blindness. Ophthalmic genetics 40 (6) (2019)