Ulrik Kristoffer Stoltze (Ulrik Stoltze, Ulrik K Stoltze)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Topics

Top Venues

European journal of human genetics : EJHG

Nature communications

Genome medicine

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Sophia Hammer-Hansen, Ulrik Kristoffer Stoltze, Emil Bartels, Thomas van Overeem Hansen, Anna Byrjalsen, Anne Tybjærg-Hansen, Klaus Juul, Kjeld Schmiegelow, Jacob Tfelt, Henning Bundgaard, Karin Wadt, Birgitte Rode Diness
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort. European journal of human genetics : EJHG 32 (7) (2024)
Sophia Hammer-Hansen, Ulrik Kristoffer Stoltze, Emil Bartels, Thomas van Overeem Hansen, Anna Byrjalsen, Anne Tybjærg-Hansen, Klaus Juul, Kjeld Schmiegelow, Jacob Tfelt, Henning Bundgaard, Karin Wadt, Birgitte Rode Diness
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort. European journal of human genetics : EJHG 32 (7) (2024)
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, Simon Rasmussen, Konrad J Karczewski, Karin A W Wadt, Kjeld Schmiegelow
The evolutionary impact of childhood cancer on the human gene pool. Nature communications 15 (1) (2024)
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, Simon Rasmussen, Konrad J Karczewski, Karin A W Wadt, Kjeld Schmiegelow
The evolutionary impact of childhood cancer on the human gene pool. Nature communications 15 (1) (2024)
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, Simon Rasmussen, Konrad J Karczewski, Karin A W Wadt, Kjeld Schmiegelow
The evolutionary impact of childhood cancer on the human gene pool. Nature communications 15 (1) (2024)
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, Simon Rasmussen, Konrad J Karczewski, Karin A W Wadt, Kjeld Schmiegelow
The evolutionary impact of childhood cancer on the human gene pool. Nature communications 15 (1) (2024)
Sophia Hammer-Hansen, Ulrik Kristoffer Stoltze, Emil Bartels, Thomas van Overeem Hansen, Anna Byrjalsen, Anne Tybjærg-Hansen, Klaus Juul, Kjeld Schmiegelow, Jacob Tfelt, Henning Bundgaard, Karin Wadt, Birgitte Rode Diness
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort. European journal of human genetics : EJHG 32 (7) (2024)
Sophia Hammer-Hansen, Ulrik Kristoffer Stoltze, Emil Bartels, Thomas van Overeem Hansen, Anna Byrjalsen, Anne Tybjærg-Hansen, Klaus Juul, Kjeld Schmiegelow, Jacob Tfelt, Henning Bundgaard, Karin Wadt, Birgitte Rode Diness
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort. European journal of human genetics : EJHG (2024)
Ulrik Kristoffer Stoltze, Mathis Hildonen, Thomas Van Overeem Hansen, Jon Foss-Skiftesvik, Anna Byrjalsen, Malene Lundsgaard, Laura Pignata, Karen Grønskov, Asuman Z Tumer, Kjeld Schmiegelow, Jesper Sune Brok, Karin A W Wadt
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort. Journal of medical genetics (2023)
Ulrik Kristoffer Stoltze, Christian Munch Hagen, Thomas van Overeem Hansen, Anna Byrjalsen, Anne-Marie Gerdes, Victor Yakimov, Simon Rasmussen, Marie Bækvad-Hansen, David Michael Hougaard, Kjeld Schmiegelow, Henrik Hjalgrim, Karin Wadt, Jonas Bybjerg-Grauholm
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants. Genome medicine 15 (1) (2023)
Ulrik Kristoffer Stoltze, Christian Munch Hagen, Thomas van Overeem Hansen, Anna Byrjalsen, Anne-Marie Gerdes, Victor Yakimov, Simon Rasmussen, Marie Bækvad-Hansen, David Michael Hougaard, Kjeld Schmiegelow, Henrik Hjalgrim, Karin Wadt, Jonas Bybjerg-Grauholm
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants. Genome medicine 15 (1) (2023)
Ulrik Kristoffer Stoltze, Thomas Van Overeem Hansen, Jesper Sune Brok, Karen Grønskov, Asuman Z Tumer, Lise Barlebo Ahlborn, Kjeld Schmiegelow, Karin A W Wadt
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes. Journal of medical genetics (2022)
Jon Foss-Skiftesvik, Ulrik Kristoffer Stoltze
Genetic predisposition to central nervous system tumors in children - what the neurosurgeon should know. Acta neurochirurgica 164 (11) (2022)
Marlene Richter Jensen, Ulrik Kristoffer Stoltze, Thomas Van Overeem Hansen, Mads Bak, Astrid Sehested, Catherine Rechnitzer, René Mathiasen, David Scheie, Karen Bonde Larsen, Tina Elisabeth Olsen, Aida Muhic, Jane Skjøth-Rasmussen, Maria Rossing, Kjeld Schmiegelow, Karin A W Wadt
9p21.3 Microdeletion involving CDKN2A/2B in a young patient with multiple primary cancers and review of the literature. Cold Spring Harbor molecular case studies 8 (4) (2022)
Anna Byrjalsen, Thomas V O Hansen, Ulrik Kristoffer Stoltze, Mana M Mehrjouy, Nanna Moeller Barnkob, Lisa Lyngsie Hjalgrim, René Mathiasen, Charlotte K Lautrup, Pernille Axel Gregersen, Henrik Hasle, Peder S Wehner, Ruta Tuckuviene, Peter Wad Sackett, Adrian O Laspiur, Maria Rossing, Rasmus Lykke Marvig, Niels Tommerup, Tina Elisabeth Olsen, David Scheie, Ramneek Gupta, Anne-Marie Gerdes, Kjeld Schmiegelow, Karin A W Wadt
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes. PLoS genetics 16 (12) (2020)
Ulrik Kristoffer Stoltze, Anne-Bine Skytte, Henriette Roed, Henrik Hasle, Bent Ejlertsen, Thomas van Overeem Hansen, Kjeld Schmiegelow, Anne-Marie Gerdes, Karin Wadt
Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark. PloS one 13 (1) (2018)