Miroslava Hancarova

Charles University

Czech Republic

Research Interests

Explore related searches

Professors in Medical Science

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (7)

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Collaborators (5)

Bradley Coe

Clinical Assistant Professor

The University of British Columbia

CANADA

View details

Arvis Sulovari

Principal Scientist

UNITED STATES

View details

Magnus Nordenskjöld

Professor of Clinical Genetics

Karolinska Institutet

SWEDEN

View details

Cristina Dias

King’s College London

UNITED KINGDOM

View details

Alexandre Reymond

University of Lausanne

SWITZERLAND

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Miroslava Hancarova

Research Interests

Explore related searches

Contact this professor

Articles (7)

Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities

Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier

Collaborators (5)

Bradley Coe

Arvis Sulovari

Magnus Nordenskjöld

Cristina Dias

Alexandre Reymond

Make your next move.