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Jesper Eisfeldt

Showing results (11-20 of 68) with videos related to

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Mutation Research|November 2, 2018
Flanking complex copy number variants in the same family formed through unequal crossing-over during meiosisMaria Pettersson, Jesper Eisfeldt, Elisabeth Syk Lundberg, et al.
Human Genetics|December 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrierJesper Eisfeldt, Maria Pettersson, Anna Petri, et al.
Plos One|July 28, 2023
Transposable element insertions in 1000 Swedish individualsKristine Bilgrav Saether, Daniel Nilsson, Håkan Thonberg, et al.
Human Mutation|December 30, 2017
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafishWolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, et al.
BMC Bioinformatics|July 3, 2020
Loqusdb: added value of an observations database of local genomic variationMåns Magnusson, Jesper Eisfeldt, Daniel Nilsson, et al.
Human Mutation|July 17, 2022
Multi-omics analysis reveals multiple mechanisms causing Prader-Willi like syndrome in a family with a X;15 translocationJesper Eisfeldt, Fatemah Rezayee, Maria Pettersson, et al.
International Journal of Molecular Sciences|August 26, 2022
Multi-Omic Investigations of a 17-19 Translocation Links <i>MINK1</i> Disruption to Autism, Epilepsy and OsteoporosisJesper Eisfeldt, Jakob Schuy, Eva-Lena Stattin, et al.
BJU International|August 10, 2021
Genomic profile - a possible diagnostic and prognostic marker in upper tract urothelial carcinomaAlexandra Grahn, Jesper Eisfeldt, Camilla Malm, et al.
Blood Advances|January 4, 2022
A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twinsBenedicte Bang, Jesper Eisfeldt, Gisela Barbany, et al.
Scientific Reports|August 21, 2023
Insights into cellular behavior and micromolecular communication in urothelial micrograftsNikolai Juul, Oliver Willacy, Doste R Mamand, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Mutation Research|November 2, 2018
Flanking complex copy number variants in the same family formed through unequal crossing-over during meiosisMaria Pettersson, Jesper Eisfeldt, Elisabeth Syk Lundberg, et al.
Human Genetics|December 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrierJesper Eisfeldt, Maria Pettersson, Anna Petri, et al.
Plos One|July 28, 2023
Transposable element insertions in 1000 Swedish individualsKristine Bilgrav Saether, Daniel Nilsson, Håkan Thonberg, et al.
Human Mutation|December 30, 2017
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafishWolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, et al.
BMC Bioinformatics|July 3, 2020
Loqusdb: added value of an observations database of local genomic variationMåns Magnusson, Jesper Eisfeldt, Daniel Nilsson, et al.
Human Mutation|July 17, 2022
Multi-omics analysis reveals multiple mechanisms causing Prader-Willi like syndrome in a family with a X;15 translocationJesper Eisfeldt, Fatemah Rezayee, Maria Pettersson, et al.
International Journal of Molecular Sciences|August 26, 2022
Multi-Omic Investigations of a 17-19 Translocation Links <i>MINK1</i> Disruption to Autism, Epilepsy and OsteoporosisJesper Eisfeldt, Jakob Schuy, Eva-Lena Stattin, et al.
BJU International|August 10, 2021
Genomic profile - a possible diagnostic and prognostic marker in upper tract urothelial carcinomaAlexandra Grahn, Jesper Eisfeldt, Camilla Malm, et al.
Blood Advances|January 4, 2022
A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twinsBenedicte Bang, Jesper Eisfeldt, Gisela Barbany, et al.
Scientific Reports|August 21, 2023
Insights into cellular behavior and micromolecular communication in urothelial micrograftsNikolai Juul, Oliver Willacy, Doste R Mamand, et al.
Pageof 7