Raheleh Rahbari
Hinxton, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 42 publications
Author Correction: Complex de novo structural variants are an underestimated cause of rare disorders.
Journal: Nature communications
Published: February 17, 2026
Ultra-deep duplex sequencing reveals unique features of somatic evolution in the normal tissues of a family with Li-Fraumeni syndrome.
Journal: bioRxiv : the preprint server for biology
Published: February 06, 2026
Polyclonal selection of immune checkpoint mutations in thyroid autoimmunity.
Journal: Nature
Published: October 07, 2025
Landscape of parental postzygotic mutations across >11,000 rare disease trios.
Journal: American journal of human genetics
Published: September 16, 2025
Author Correction: The long-term effects of chemotherapy on normal blood cells.
Journal: Nature genetics
Published: July 31, 2025
Hotspots of human mutation point to clonal expansions in spermatogonia.
Journal: medRxiv : the preprint server for health sciences
Published: June 30, 2025
Hotspots of human mutation point to clonal expansions in spermatogonia.
Journal: Nature
Published: January 04, 2025
Sperm sequencing reveals extensive positive selection in the male germline.
Journal: Nature
Published: October 18, 2024
The long-term effects of chemotherapy on normal blood cells.
Journal: Nature genetics
Published: September 11, 2024
Complex de novo structural variants are an underestimated cause of rare disorders.
Journal: Nature communications
Published: August 05, 2024
The genomic and clinical consequences of replacing procarbazine with dacarbazine in escalated BEACOPP for Hodgkin lymphoma: a retrospective, observational study.
Journal: The Lancet. Oncology
Published: July 18, 2024
Last Updated: 09/26/2026