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Martin J Larsen

Showing results (11-20 of 45) with videos related to

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Neurogenetics|May 14, 2018
Compound heterozygous mutations in two different domains of ALDH18A1 do not affect the amino acid levels in a patient with hereditary spastic paraplegiaMaria Steenhof, Maria Kibæk, Martin J Larsen, et al.
Frontiers in Neuroscience|April 25, 2020
A Genome-Wide Integrative Association Study of DNA Methylation and Gene Expression Data and Later Life Cognitive Functioning in Monozygotic TwinsMette Soerensen, Dominika Marzena Hozakowska-Roszkowska, Marianne Nygaard, et al.
Breast Cancer Research : BCR|April 19, 2015
Long non-coding RNA expression profiles predict metastasis in lymph node-negative breast cancer independently of traditional prognostic markersKristina P Sørensen, Mads Thomassen, Qihua Tan, et al.
Breast Cancer Research and Treatment|November 22, 2013
Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast cancerKristina P Sørensen, Mads Thomassen, Qihua Tan, et al.
Nature Communications|August 23, 2025
Deep genome sequencing reveals extensive genetic heterogeneity in early human placentasIeva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen, et al.
Scientific Reports|February 9, 2020
Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in childrenYazeid Alhaidan, Martin J Larsen, Anders Jørgen Schou, et al.
Molecular Genetics & Genomic Medicine|October 15, 2020
Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic TelangiectasiaKatrine S Aagaard, Klaus Brusgaard, Ieva Miceikaite, et al.
Clinical Genetics|September 21, 2020
Biallelic variants in GLE1 with survival beyond neonatal periodT Michael Yates, Philippe M Campeau, Jamal Ghoumid, et al.
Oncotarget|March 7, 2018
Association of miR-548c-5p, miR-7-5p, miR-210-3p, miR-128-3p with recurrence in systemically untreated breast cancerInes Block, Mark Burton, Kristina P Sørensen, et al.
Pediatric Nephrology (Berlin, Germany)|February 25, 2022
Detection of DZIP1L mutations by whole-exome sequencing in consanguineous families with polycystic kidney diseaseJens Michael Hertz, Per Svenningsen, Henrik Dimke, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Neurogenetics|May 14, 2018
Compound heterozygous mutations in two different domains of ALDH18A1 do not affect the amino acid levels in a patient with hereditary spastic paraplegiaMaria Steenhof, Maria Kibæk, Martin J Larsen, et al.
Frontiers in Neuroscience|April 25, 2020
A Genome-Wide Integrative Association Study of DNA Methylation and Gene Expression Data and Later Life Cognitive Functioning in Monozygotic TwinsMette Soerensen, Dominika Marzena Hozakowska-Roszkowska, Marianne Nygaard, et al.
Breast Cancer Research : BCR|April 19, 2015
Long non-coding RNA expression profiles predict metastasis in lymph node-negative breast cancer independently of traditional prognostic markersKristina P Sørensen, Mads Thomassen, Qihua Tan, et al.
Breast Cancer Research and Treatment|November 22, 2013
Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast cancerKristina P Sørensen, Mads Thomassen, Qihua Tan, et al.
Nature Communications|August 23, 2025
Deep genome sequencing reveals extensive genetic heterogeneity in early human placentasIeva Miceikaite, Christina Fagerberg, Charlotte Brasch-Andersen, et al.
Scientific Reports|February 9, 2020
Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in childrenYazeid Alhaidan, Martin J Larsen, Anders Jørgen Schou, et al.
Molecular Genetics & Genomic Medicine|October 15, 2020
Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic TelangiectasiaKatrine S Aagaard, Klaus Brusgaard, Ieva Miceikaite, et al.
Clinical Genetics|September 21, 2020
Biallelic variants in GLE1 with survival beyond neonatal periodT Michael Yates, Philippe M Campeau, Jamal Ghoumid, et al.
Oncotarget|March 7, 2018
Association of miR-548c-5p, miR-7-5p, miR-210-3p, miR-128-3p with recurrence in systemically untreated breast cancerInes Block, Mark Burton, Kristina P Sørensen, et al.
Pediatric Nephrology (Berlin, Germany)|February 25, 2022
Detection of DZIP1L mutations by whole-exome sequencing in consanguineous families with polycystic kidney diseaseJens Michael Hertz, Per Svenningsen, Henrik Dimke, et al.
Pageof 5