Adam Ameur

36PUBLICATIONS
191CO-AUTHORS
Sequence analysisGenomicsGene expression (incl. microarray and other genome-wide approaches)Cancer therapy (excl. chemotherapy and radiation therapy)Patient safety
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Publications (36)

|May 28, 2026
Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases.

|Nov 20, 2025
Single cell long read whole genome sequencing reveals somatic transposon activity in human brain.

Michal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner

|Sep 16, 2025
T2T-CHM13 improves read mapping and detection of clinically relevant genetic variation in the Swedish population.

Daniel Schmitz, Adam Ameur, Åsa Johansson

|May 09, 2025
UYSD: a novel data repository accessible via public website for worldwide population frequencies of Y-SNP haplogroups.

Arwin Ralf, Dion Zandstra, Bram van Wersch

|Apr 14, 2025
The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots.

Grégory Lazarian, Bernard Leroy, Floriane Theves

|Apr 04, 2025
Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare.

Anders Kämpe, Sanna Gudmundsson, Colum P Walsh

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Frequent Collaborators

5 joint publications

Ida Höijer

4 joint publications

Patrik K E Magnusson

4 joint publications

Lars Feuk

4 joint publications

Anna Lindstrand