Daniel Nilsson

10PUBLICATIONS
29CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Medical molecular engineering of nucleic acids and proteinsCell and nuclear divisionCancer genetics
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Publications (10)

|Sep 25, 2026
Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age-Dependent Clinical Trajectory.

|Jul 28, 2023
Transposable element insertions in 1000 Swedish individuals.

Kristine Bilgrav Saether, Daniel Nilsson, Håkan Thonberg

|Feb 22, 2022
PatientMatcher: A customizable Python-based open-source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network.

Chiara Rasi, Daniel Nilsson, Måns Magnusson

|Oct 29, 2021
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.

Karin Wallander, Håkan Thonberg, Daniel Nilsson

|Dec 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier.

Jesper Eisfeldt, Maria Pettersson, Anna Petri

|Apr 05, 2020
pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing.

Jessada Thutkawkorapin, Jesper Eisfeldt, Emma Tham

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Frequent Collaborators

5 joint publications

Anna Lindstrand

4 joint publications

Jesper Eisfeldt

2 joint publications

Maria Pettersson

2 joint publications

Valtteri Wirta