Hufsah Ashraf

Düsseldorf University Hospital — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

8h-index1.1kcitations17works22.52yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genomic variations and chromosomal abnormalities(12), Genomics and Phylogenetic Studies(7), Genomics and Rare Diseases(7), Chromosomal and Genetic Variations(6), RNA and protein synthesis mechanisms(5)

Publications17 total

Structural and transduction patterns of human-specific polymorphic SVA insertions
Mobile DNA·2025Open Access
Author Correction: Complex genetic variation in nearly complete human genomes
Nature·2025· 1 citedOpen Access
Complex genetic variation in nearly complete human genomes
Nature·2025· 43 citedOpen Access
Structural variation in 1,019 diverse humans based on long-read sequencing
Nature·2025· 29 citedOpen Access
Complex genetic variation in nearly complete human genomes
2024· 26 citedOpen Access
Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project
2024· 36 citedOpen Access
Inversion polymorphism in a complete human genome assembly
Genome biology·2023· 32 citedOpen Access
Inversion polymorphism in a complete human genome assembly
2023Open Access
Inversion polymorphism in a complete human genome assembly
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Inversion polymorphism in a complete human genome assembly
2023Open Access
Allele detection using <i>k</i>-mer-based sequencing error profiles
Bioinformatics Advances·2023· 1 citedOpen Access
Additional file 2 of Inversion polymorphism in a complete human genome assembly
Figshare·2023Open Access
Inversion polymorphism in a complete human genome assembly
2022· 5 citedOpen Access
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders
Cell·2022· 176 citedOpen Access
Haplotype-resolved inversion landscape reveals hotspots of mutational recurrence associated with genomic disorders
2021· 11 citedOpen Access
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
Science·2021· 754 citedOpen Access
<i>De novo</i> assembly of 64 haplotype-resolved human genomes of diverse ancestry and integrated analysis of structural variation
2020· 5 citedOpen Access

Frequent Co-authors

Jana Ebler(17), Tobias Marschall(17), Evan E. Eichler(17), Jan O. Korbel(16), Patrick Hasenfeld(14), Wolfram Höps(12), David Porubský(11), Ashley D. Sanders(11), Benedict Paten(9), Peter Ebert(8), Peter A. Audano(8), Feyza Yilmaz(8), Tobias Rausch(8), Charles Lee(8), William T. Harvey(8), Bernardo Rodríguez–Martín(7), Qihui Zhu(6), Marc Jan Bonder(6), Arvis Sulovari(6), Weichen Zhou(6)