Michael Backlund - Folkhalsan Research Center

基本信息

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职业迁徙

个人简介

Researcher with a focus on RNA biology and RNA-binding proteins.

研究兴趣

论文共 19 篇作者统计合作学者相似作者

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Using Long‐read Adaptive Nanopore Sequencing to Decipher a Novel Pathogenic Duplication in the PRPH2 Gene in Patients with Macular Dystrophy

Michael Backlund,Suzie Gasparian,Pauliina Repo, Harri Kangas,Kati Donner,Sanna Seitsonen,Maarjaliis Paavo,Tero Kivelä,David Sierpina,Joni Turunen

Acta Ophthalmologica（2025）

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Genetic Variations in Human Opsin Genetics: Understanding Color Vision Phenotypes and Defects

Olivia Lilja,Michael Backlund, Jussi Tiihonen, Harri Kangas,Kati Donner,Petri Ala‐Laurila,Joni Turunen

Acta Ophthalmologicano. S284 (2025)

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Genetic Variations in Human Opsin Genetics: Understanding Color Vision Phenotypes and Defects

Olivia Lilja,Michael Backlund, Jussi Tiihonen, Harri Kangas,Kati Donner,Petri Ala‐Laurila,Joni Turunen

Acta Ophthalmologicano. S284 (2025)

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Diagnostic Errors and Delay of Keratitis Fugax Hereditaria

Annamari Immonen,Sabita Kawan,Michael Backlund, Heikki Saaren-Seppala,Tero Kivela,Joni Turunen

Acta Ophthalmologicano. S279 (2024)

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Characterisation of a LINE-1 Insertion in the RP1 Gene by Targeted Adaptive Nanopore Sequencing in a Family with Retinitis Pigmentosa

Michael P. Backlund,Pauliina Repo, Harri Kangas,Kati Donner,Eeva-Marja Sankila, Julia Krootila,Maarjaliis Paavo,Kirmo Wartiovaara,Tero T. Kivela,Joni A. Turunen

HUMAN MUTATION (2024)

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A Retrospective Longitudinal Study of 52 Finnish Patients with X-linked Retinoschisis

Mira A. Jarvinen,Rigmor C. Baraas,Anna Majander,Michael P. Backlund, Julia Krootila,Maarjaliis Paavo, Paeivi Lindahl, Kristiina Vasara,Eeva-Marja Sankila,Tero T. Kivela,Joni A. Turunen

ACTA OPHTHALMOLOGICA (2024)

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Functional Assay for Assessment of Pathogenicity of BAP1 Variants

Pauliina E. Repo,Michael P. Backlund,Tero T. Kivela,Joni A. Turunen

HUMAN MOLECULAR GENETICSno. 5 (2024): 426-434

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LINE‐1 Insertion in the RP1 Gene in a Family with Retinitis Pigmentosa

Michael Backlund,Pauliina Repo,Eeva-Marja Sankila,Maarjaliis Paavo,Kirmo Wartiovaara,Joni Turunen

Acta Ophthalmologica（2022）

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Pathogenic Variant C.61g > C in NLRP3 Lowers NLRP3 Inflammasome Activation Threshold in Patients with Keratitis Fugax Hereditaria

Sabita Kawan,Michael Backlund,Annamari Immonen,Tero Kivela,Joni Turunen

Acta Ophthalmologica（2022）

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Keratitis Fugax Hereditaria ‐ Useful to Consider when You Have a Child with Non‐specific Corneal Findings and Symptoms

Annamari Immonen,Anna Majander,Sabita Kawan,Michael Backlund, Kristiina Vasara, Pivi Lindahl,Tero Kivela,Joni Turunen

ACTA OPHTHALMOLOGICA（2022）

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