Integrating functional genomics to investigate the genomic architecture of rare inherited neurological disorders

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Identifier

139010

Type

Principal investigator

Molnár, Mária Judit

Title in Hungarian

Funkcionális genomikai kutatások a ritka örökletes neurológiai betegségek genomikai architektúrájának vizsgálatára

Title in English

Integrating functional genomics to investigate the genomic architecture of rare inherited neurological disorders

Keywords in Hungarian

ritka neurológiai betegség, RNS szekvenálás, funkcionális genomika, multi-omika

Keywords in English

rare neurological,disease, RNA sequencing, transcriptome, functional genomics multi-omics

Discipline

Biological basis of neurological and psychiatric disorders (Council of Medical and Biological Sciences)	80 %
Ortelius classification: Neurology
Molecular biology (Council of Medical and Biological Sciences)	10 %
Ortelius classification: Molecular markers and recognition
Genomics, comparative genomics, functional genomics (Council of Medical and Biological Sciences)	10 %

Panel

Clinical Medicine

Department or equivalent

Genomikai Medicina és Ritka Betegségek Intézete (Semmelweis University)

Participants

Balicza, Péter
Gál, Anikó
Gézsi, András
Molnár, Viktor
Szlepák, Tamás

Starting date

2021-11-01

Closing date

2025-10-31

Funding (in million HUF)

48.000