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European Journal of Human Genetics : EJHG
|
May 13, 2024
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort
Sophia Hammer-Hansen, Ulrik Stoltze, Emil Bartels, et al.
NAR Genomics and Bioinformatics
|
February 18, 2026
DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data
Mads Cort Nielsen, Christian Munch Hagen, Ulrik Kristoffer Stoltze, et al.
Journal of Medical Genetics
|
April 5, 2023
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort
Ulrik Kristoffer Stoltze, Mathis Hildonen, Thomas Van Overeem Hansen, et al.
Genome Medicine
|
March 15, 2023
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants
Ulrik Kristoffer Stoltze, Christian Munch Hagen, Thomas van Overeem Hansen, et al.
Neuro-Oncology
|
July 28, 2022
Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, et al.
Leukemia
|
March 25, 2025
Overt and covert genetic causes of pediatric acute lymphoblastic leukemia
Ulrik Stoltze, Stefanie V Junk, Anna Byrjalsen, et al.
Plos Genetics
|
December 17, 2020
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes
Anna Byrjalsen, Thomas V O Hansen, Ulrik K Stoltze, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 15, 2025
Childhood Cancer Predisposition and Evolutionary Constraints: Novel lessons from Germline Genomes from 1,127 Children with Cancer
Ulrik Kristoffer Stoltze, Thomas van Overeem Hansen, Jon Foss-Skiftesvik, et al.
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Search research articles
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Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
European Journal of Human Genetics : EJHG
|
May 13, 2024
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort
Sophia Hammer-Hansen, Ulrik Stoltze, Emil Bartels, et al.
NAR Genomics and Bioinformatics
|
February 18, 2026
DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data
Mads Cort Nielsen, Christian Munch Hagen, Ulrik Kristoffer Stoltze, et al.
Journal of Medical Genetics
|
April 5, 2023
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort
Ulrik Kristoffer Stoltze, Mathis Hildonen, Thomas Van Overeem Hansen, et al.
Genome Medicine
|
March 15, 2023
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants
Ulrik Kristoffer Stoltze, Christian Munch Hagen, Thomas van Overeem Hansen, et al.
Neuro-Oncology
|
July 28, 2022
Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, et al.
Leukemia
|
March 25, 2025
Overt and covert genetic causes of pediatric acute lymphoblastic leukemia
Ulrik Stoltze, Stefanie V Junk, Anna Byrjalsen, et al.
Plos Genetics
|
December 17, 2020
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes
Anna Byrjalsen, Thomas V O Hansen, Ulrik K Stoltze, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 15, 2025
Childhood Cancer Predisposition and Evolutionary Constraints: Novel lessons from Germline Genomes from 1,127 Children with Cancer
Ulrik Kristoffer Stoltze, Thomas van Overeem Hansen, Jon Foss-Skiftesvik, et al.
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of 3