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Kerstin Becker

Showing results (81-90 of 101) with videos related to

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Blood|February 9, 2026
MRD-2 in the GHSG HD21 trial assessed by a validated circulating tumor DNA sequencing assayJan-Michel Heger, Julia Mattlener, Helen Kaul, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2024
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotoniaMaria Asif, Arwa Ishaq A Khayyat, Salem Alawbathani, et al.
Blood|November 10, 2023
Entirely noninvasive outcome prediction in central nervous system lymphomas using circulating tumor DNAJan-Michel Heger, Julia Mattlener, Jessica Schneider, et al.
Nature Communications|March 10, 2026
Single-cell genomics highlight MYC-associated metabolic activation and altered cell interactions in T-prolymphocytic leukemia progressionLinus Wahnschaffe, Dennis Jungherz, Tony A Müller, et al.
Breast (Edinburgh, Scotland)|January 24, 2025
Joint analysis of germline genetic data from over 29,000 cases with suspected hereditary breast and ovarian cancer (HBOC) as part of the NASGE initiativeJan Henkel, Andreas Laner, Melanie Locher, et al.
Brain : a Journal of Neurology|October 13, 2022
The genomic landscape across 474 surgically accessible epileptogenic human brain lesionsJavier A López-Rivera, Costin Leu, Marie Macnee, et al.
Nature Communications|October 14, 2018
Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopeniaSharissa L Latham, Nadja Ehmke, Patrick Y A Reinke, et al.
Nature Communications|September 3, 2024
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansionsLars Mohren, Friedrich Erdlenbruch, Elsa Leitão, et al.
Nature Communications|November 20, 2018
Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopeniaSharissa L Latham, Nadja Ehmke, Patrick Y A Reinke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2019
The genomic and clinical landscape of fetal akinesiaMatthias Pergande, Susanne Motameny, Özkan Özdemir, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Blood|February 9, 2026
MRD-2 in the GHSG HD21 trial assessed by a validated circulating tumor DNA sequencing assayJan-Michel Heger, Julia Mattlener, Helen Kaul, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2024
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotoniaMaria Asif, Arwa Ishaq A Khayyat, Salem Alawbathani, et al.
Blood|November 10, 2023
Entirely noninvasive outcome prediction in central nervous system lymphomas using circulating tumor DNAJan-Michel Heger, Julia Mattlener, Jessica Schneider, et al.
Nature Communications|March 10, 2026
Single-cell genomics highlight MYC-associated metabolic activation and altered cell interactions in T-prolymphocytic leukemia progressionLinus Wahnschaffe, Dennis Jungherz, Tony A Müller, et al.
Breast (Edinburgh, Scotland)|January 24, 2025
Joint analysis of germline genetic data from over 29,000 cases with suspected hereditary breast and ovarian cancer (HBOC) as part of the NASGE initiativeJan Henkel, Andreas Laner, Melanie Locher, et al.
Brain : a Journal of Neurology|October 13, 2022
The genomic landscape across 474 surgically accessible epileptogenic human brain lesionsJavier A López-Rivera, Costin Leu, Marie Macnee, et al.
Nature Communications|October 14, 2018
Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopeniaSharissa L Latham, Nadja Ehmke, Patrick Y A Reinke, et al.
Nature Communications|September 3, 2024
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansionsLars Mohren, Friedrich Erdlenbruch, Elsa Leitão, et al.
Nature Communications|November 20, 2018
Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopeniaSharissa L Latham, Nadja Ehmke, Patrick Y A Reinke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2019
The genomic and clinical landscape of fetal akinesiaMatthias Pergande, Susanne Motameny, Özkan Özdemir, et al.
Pageof 11