Daniel Nilsson

Karolinska Institutet

Sweden

Research Interests

Explore related searches

Professors in Sweden Professors in Medical Science Medical Science professors in Sweden

Contact this professor

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

Articles (10)

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Collaborators (10)

Ana Beleza-Meireles

University Hospitals Bristol and Weston NHS Foundation Trust

UNITED KINGDOM

View details

Anders Jemt

KTH Royal Institute of Technology

SWEDEN

View details

Maria Johansson Soller

Karolinska Institutet

SWEDEN

View details

Anna Lindstrand

Professor

Karolinska Institutet

SWEDEN

View details

Mansoureh Shahsavani

Karolinska University Hospital

SWEDEN

View details

Magnus Nordenskjöld

Professor of Clinical Genetics

Karolinska Institutet

SWEDEN

View details

Hafdis Helgadottir

Karolinska Institutet

SWEDEN

View details

Fulya Taylan

Karolinska Institutet

SWEDEN

View details

Kristina Lagerstedt Robinson

Karolinska Institutet

SWEDEN

View details

Rolf Zetterström

Karolinska Institutet

SWEDEN

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Daniel Nilsson

Research Interests

Explore related searches

Contact this professor

Articles (10)

Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders.

Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability

PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network

Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model.

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses.

Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients

Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis

Adult-Onset Ataxia With Neuropathy and White Matter Abnormalities Due to a Novel <i>SAMD9L</i> Variant.

Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier

Collaborators (10)

Ana Beleza-Meireles

Anders Jemt

Maria Johansson Soller

Anna Lindstrand

Mansoureh Shahsavani

Magnus Nordenskjöld

Hafdis Helgadottir

Fulya Taylan

Kristina Lagerstedt Robinson

Rolf Zetterström

Make your next move.