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Martin A Haagmans

Showing results (1-10 of 12) with videos related to

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Clinical Epigenetics|July 7, 2025
ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disordersFrédéric Brioude, Martin A Haagmans, Marcel Mannens, et al.
Microbiology Resource Announcements|February 8, 2020
Five Complete Genome Sequences Spanning the Dutch Streptococcus suis Serotype 2 and Serotype 9 PopulationsBoas C L van der Putten, Thomas J Roodsant, Martin A Haagmans, et al.
European Journal of Medical Genetics|April 3, 2025
A rare triplication of 16p11.2: Unravelling the genomic complexity and review of the literatureLiselot van der Laan, Lotte Kleinendorst, Martin A Haagmans, et al.
Forensic Science International. Genetics|October 14, 2025
DNA methylation-based forensic framework for age prediction and body fluid identification using nanopore sequencingIsis Beentjes, Martin A Haagmans, Desiree D S H de Bruin, et al.
Human Genetics|June 11, 2014
Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndromeMariëlle Alders, Lihadh Al-Gazali, Isabelle Cordeiro, et al.
Neurology. Genetics|November 24, 2025
Search for Additional Pathogenic Variants to Explain Variation in <i>PMP22</i>-Related NeuropathiesBarbara W van Paassen, Camiel Verhamme, Fred van Ruissen, et al.
Journal of Medical Genetics|June 21, 2013
Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnosticsOlaf R F Mook, Martin A Haagmans, Jean-François Soucy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2015
RELN rare variants in myoclonus-dystoniaJustus L Groen, Katja Ritz, Hamid Jalalzadeh, et al.
Frontiers in Genetics|January 20, 2026
Nanopore sequencing enables combined detection of <i>USP7</i> variants and a known Hao-Fountain syndrome episignatureLiselot van der Laan, Martin A Haagmans, Andrea Venema, et al.
Forensic Science International. Genetics|October 19, 2024
Exploring nanopore direct sequencing performance of forensic STRs, SNPs, InDels, and DNA methylation markers in a single assayDesiree D S H de Bruin, Martin A Haagmans, Kristiaan J van der Gaag, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Clinical Epigenetics|July 7, 2025
ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disordersFrédéric Brioude, Martin A Haagmans, Marcel Mannens, et al.
Microbiology Resource Announcements|February 8, 2020
Five Complete Genome Sequences Spanning the Dutch Streptococcus suis Serotype 2 and Serotype 9 PopulationsBoas C L van der Putten, Thomas J Roodsant, Martin A Haagmans, et al.
European Journal of Medical Genetics|April 3, 2025
A rare triplication of 16p11.2: Unravelling the genomic complexity and review of the literatureLiselot van der Laan, Lotte Kleinendorst, Martin A Haagmans, et al.
Forensic Science International. Genetics|October 14, 2025
DNA methylation-based forensic framework for age prediction and body fluid identification using nanopore sequencingIsis Beentjes, Martin A Haagmans, Desiree D S H de Bruin, et al.
Human Genetics|June 11, 2014
Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndromeMariëlle Alders, Lihadh Al-Gazali, Isabelle Cordeiro, et al.
Neurology. Genetics|November 24, 2025
Search for Additional Pathogenic Variants to Explain Variation in <i>PMP22</i>-Related NeuropathiesBarbara W van Paassen, Camiel Verhamme, Fred van Ruissen, et al.
Journal of Medical Genetics|June 21, 2013
Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnosticsOlaf R F Mook, Martin A Haagmans, Jean-François Soucy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2015
RELN rare variants in myoclonus-dystoniaJustus L Groen, Katja Ritz, Hamid Jalalzadeh, et al.
Frontiers in Genetics|January 20, 2026
Nanopore sequencing enables combined detection of <i>USP7</i> variants and a known Hao-Fountain syndrome episignatureLiselot van der Laan, Martin A Haagmans, Andrea Venema, et al.
Forensic Science International. Genetics|October 19, 2024
Exploring nanopore direct sequencing performance of forensic STRs, SNPs, InDels, and DNA methylation markers in a single assayDesiree D S H de Bruin, Martin A Haagmans, Kristiaan J van der Gaag, et al.
Pageof 2