Total number of reads affects the accuracy of fetal fraction estimates in NIPT

por Miceikaitė, Ieva, Brasch‐Andersen, Charlotte, Fagerberg, Christina, Larsen, Martin Jakob
Publicado 2021

Evaluation of Nine Somatic Variant Callers for Detection of Somatic Mutations in Exome and Targeted Deep Sequencing Data

por Krøigård, Anne Bruun, Thomassen, Mads, Lænkholm, Anne-Vibeke, Kruse, Torben A., Larsen, Martin Jakob
Publicado 2016

Prenatal cases with rare RIT1 variants causing severe fetal hydrops and death

por Miceikaite, Ieva, Bak, Geske Sidsel, Larsen, Martin Jakob, Kristiansen, Britta Schlott, Torring, Pernille Mathiesen
Publicado 2021

Long Non-Coding RNA Expression Profiles in Hereditary Haemorrhagic Telangiectasia

por Tørring, Pernille M., Larsen, Martin Jakob, Kjeldsen, Anette D., Ousager, Lilian Bomme, Tan, Qihua, Brusgaard, Klaus
Publicado 2014

Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip

por Dembic, Maja, van Brakel Andersen, Lars, Larsen, Martin Jakob, Mechlenburg, Inger, Søballe, Kjeld, Hertz, Jens Michael
Publicado 2022

DamX Controls Reversible Cell Morphology Switching in Uropathogenic Escherichia coli

por Khandige, Surabhi, Asferg, Cecilie Antoinette, Rasmussen, Karina Juhl, Larsen, Martin Jakob, Overgaard, Martin, Andersen, Thomas Emil, Møller-Jensen, Jakob
Publicado 2016

Clonal expansion and linear genome evolution through breast cancer progression from pre-invasive stages to asynchronous metastasis

por Krøigård, Anne Bruun, Larsen, Martin Jakob, Lænkholm, Anne-Vibeke, Knoop, Ann S., Jensen, Jeanette D., Bak, Martin, Mollenhauer, Jan, Kruse, Torben A., Thomassen, Mads
Publicado 2015

Identification of metastasis driver genes by massive parallel sequencing of successive steps of breast cancer progression

por Krøigård, Anne Bruun, Larsen, Martin Jakob, Lænkholm, Anne-Vibeke, Knoop, Ann S., Jensen, Jeanette Dupont, Bak, Martin, Mollenhauer, Jan, Thomassen, Mads, Kruse, Torben A.
Publicado 2018

Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients

por Tan, Ming, Brusgaard, Klaus, Gerdes, Anne‐Marie, Larsen, Martin Jakob, Mortensen, Michael Bau, Detlefsen, Sönke, de Muckadell, Ove B. Schaffalitzky, Joergensen, Maiken Thyregod
Publicado 2022

Genomic Analyses of Breast Cancer Progression Reveal Distinct Routes of Metastasis Emergence

por Krøigård, Anne Bruun, Larsen, Martin Jakob, Brasch-Andersen, Charlotte, Lænkholm, Anne-Vibeke, Knoop, Ann S., Jensen, Jeanette Dupont, Bak, Martin, Mollenhauer, Jan, Thomassen, Mads, Kruse, Torben A.
Publicado 2017

OTEH-4. Deeper insight into intratumoral heterogeneity by MRI and PET-guided stereotactic biopsies from glioblastoma patients

por Anand, Atul, Petersen, Jeanette Krogh, Burton, Mark, Larsen, Martin Jakob, Andersen, Lars van Brakel, Harwood, Dylan Scott Lykke, Pedersen, Christian Bonde, Poulsen, Frantz Rom, Grupe, Peter, Kruse, Torben A, Thomassen, Mads, Kristensen, Bjarne Winther
Publicado 2021