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Raheleh Rahbari

Showing results (11-20 of 42) with videos related to

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Human Mutation|December 21, 2016
Understanding the Genomic Structure of Copy-Number Variation of the Low-Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid ArthritisRaheleh Rahbari, Luciana W Zuccherato, German Tischler, et al.
Andrology|October 18, 2022
Small non-coding RNA sequencing reveals global dysregulation of piwi-interacting RNA (piRNA) expression in gonadal malignant germ cell tumoursSean Laidlaw, Luz Alonso-Crisostomo, Shivani Bailey, et al.
Genome Research|September 1, 2017
Detection of structural mosaicism from targeted and whole-genome sequencing dataDaniel A King, Alejandro Sifrim, Tomas W Fitzgerald, et al.
Nature Genetics|December 15, 2015
Timing, rates and spectra of human germline mutationRaheleh Rahbari, Arthur Wuster, Sarah J Lindsay, et al.
Nature Communications|May 15, 2025
The impact of ancestral, genetic, and environmental influences on germline de novo mutation rates and spectraO Isaac Garcia-Salinas, Seongwon Hwang, Qin Qin Huang, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Nature Communications|February 17, 2026
Author Correction: Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Nature|May 11, 2022
Genetic and chemotherapeutic influences on germline hypermutationJoanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
Frontiers in Aging|July 13, 2022
Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal ProcessesIrene Lobon, Manuel Solís-Moruno, David Juan, et al.
Nature Communications|August 23, 2017
Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processesVagheesh M Narasimhan, Raheleh Rahbari, Aylwyn Scally, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Human Mutation|December 21, 2016
Understanding the Genomic Structure of Copy-Number Variation of the Low-Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid ArthritisRaheleh Rahbari, Luciana W Zuccherato, German Tischler, et al.
Andrology|October 18, 2022
Small non-coding RNA sequencing reveals global dysregulation of piwi-interacting RNA (piRNA) expression in gonadal malignant germ cell tumoursSean Laidlaw, Luz Alonso-Crisostomo, Shivani Bailey, et al.
Genome Research|September 1, 2017
Detection of structural mosaicism from targeted and whole-genome sequencing dataDaniel A King, Alejandro Sifrim, Tomas W Fitzgerald, et al.
Nature Genetics|December 15, 2015
Timing, rates and spectra of human germline mutationRaheleh Rahbari, Arthur Wuster, Sarah J Lindsay, et al.
Nature Communications|May 15, 2025
The impact of ancestral, genetic, and environmental influences on germline de novo mutation rates and spectraO Isaac Garcia-Salinas, Seongwon Hwang, Qin Qin Huang, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Nature Communications|February 17, 2026
Author Correction: Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Nature|May 11, 2022
Genetic and chemotherapeutic influences on germline hypermutationJoanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
Frontiers in Aging|July 13, 2022
Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal ProcessesIrene Lobon, Manuel Solís-Moruno, David Juan, et al.
Nature Communications|August 23, 2017
Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processesVagheesh M Narasimhan, Raheleh Rahbari, Aylwyn Scally, et al.
Pageof 5