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Sam Behjati

Showing results (41-50 of 126) with videos related to

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American Journal of Human Genetics|November 23, 2024
Primary cartilage transcriptional signatures reflect cell-type-specific molecular pathways underpinning osteoarthritisGeorgia Katsoula, John E G Lawrence, Ana Luiza Arruda, et al.
Communications Biology|September 7, 2022
Precise identification of cancer cells from allelic imbalances in single cell transcriptomesMi K Trinh, Clarissa N Pacyna, Gerda Kildisiute, et al.
Plos One|May 10, 2014
A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencingSam Behjati, Mariana Maschietto, Richard D Williams, et al.
Nature Genetics|March 6, 2019
Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangementsPeter Ly, Simon F Brunner, Ofer Shoshani, et al.
Elife|August 17, 2021
An in vitro stem cell model of human epiblast and yolk sac interactionKirsty Ml Mackinlay, Bailey At Weatherbee, Viviane Souza Rosa, et al.
Nature Reviews. Disease Primers|October 15, 2021
Wilms tumourFilippo Spreafico, Conrad V Fernandez, Jesper Brok, et al.
Histopathology|April 14, 2025
Lingual hamartoma-like lipoblastoma: the diagnostic value of routine whole-genome sequencingSheng-Yuan Kan, Ashley Ferro, James A Watkins, et al.
British Journal of Cancer|April 22, 2022
The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancerJamie Trotman, Ruth Armstrong, Helen Firth, et al.
Genome Medicine|January 9, 2024
Transcriptional signals of transformation in human cancerGerda Kildisiute, Maria Kalyva, Rasa Elmentaite, et al.
BMC Medical Education|November 7, 2024
Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practiceMichelle Bishop, Aditi Vedi, Sarah Bowdin, et al.
Pageof 13

Showing results (41-50 of 126) with videos related to

Sort By:
Pageof 13
American Journal of Human Genetics|November 23, 2024
Primary cartilage transcriptional signatures reflect cell-type-specific molecular pathways underpinning osteoarthritisGeorgia Katsoula, John E G Lawrence, Ana Luiza Arruda, et al.
Communications Biology|September 7, 2022
Precise identification of cancer cells from allelic imbalances in single cell transcriptomesMi K Trinh, Clarissa N Pacyna, Gerda Kildisiute, et al.
Plos One|May 10, 2014
A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencingSam Behjati, Mariana Maschietto, Richard D Williams, et al.
Nature Genetics|March 6, 2019
Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangementsPeter Ly, Simon F Brunner, Ofer Shoshani, et al.
Elife|August 17, 2021
An in vitro stem cell model of human epiblast and yolk sac interactionKirsty Ml Mackinlay, Bailey At Weatherbee, Viviane Souza Rosa, et al.
Nature Reviews. Disease Primers|October 15, 2021
Wilms tumourFilippo Spreafico, Conrad V Fernandez, Jesper Brok, et al.
Histopathology|April 14, 2025
Lingual hamartoma-like lipoblastoma: the diagnostic value of routine whole-genome sequencingSheng-Yuan Kan, Ashley Ferro, James A Watkins, et al.
British Journal of Cancer|April 22, 2022
The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancerJamie Trotman, Ruth Armstrong, Helen Firth, et al.
Genome Medicine|January 9, 2024
Transcriptional signals of transformation in human cancerGerda Kildisiute, Maria Kalyva, Rasa Elmentaite, et al.
BMC Medical Education|November 7, 2024
Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practiceMichelle Bishop, Aditi Vedi, Sarah Bowdin, et al.
Pageof 13