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Steven McGinn

Showing results (1-10 of 11) with videos related to

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New Biotechnology|November 21, 2012
DNA sequencing - spanning the generationsSteven McGinn, Ivo Glynne Gut
Current HIV Research|February 15, 2012
Identification of IL7RA risk alleles for rapid progression during HIV-1 infection: a comprehensive study in the GRIV cohortSophie Limou, Giovanna Melica, Cédric Coulonges, et al.
The Journal of Investigative Dermatology|June 26, 2009
An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disordersTiphaine Oudot, Fabienne Lesueur, Mickaël Guedj, et al.
Scientific Reports|July 1, 2026
A comprehensive urine workflow enables robust methylation and fragmentation analysis of cell-free DNAFlorence Mauger, Nouara Oussada, Caroline Horgues, et al.
Diabetes|July 18, 2008
G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetesDavid-Alexandre Trégouet, Per-Henrik Groop, Steven McGinn, et al.
BMC Genomics|July 29, 2025
Interlaboratory evaluation of high molecular weight DNA extraction methods for long-read sequencing and structural variant analysisAlison S Devonshire, Jordi Morata, Claire Jubin, et al.
Human Mutation|April 25, 2018
Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140Véronique Geoffroy, Corinne Stoetzel, Sophie Scheidecker, et al.
EMBO Molecular Medicine|June 6, 2020
Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stressAriane Kröll-Hermi, Frédéric Ebstein, Corinne Stoetzel, et al.
New Biotechnology|October 31, 2015
New technologies for DNA analysis--a review of the READNA ProjectSteven McGinn, David Bauer, Thomas Brefort, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
New Biotechnology|November 21, 2012
DNA sequencing - spanning the generationsSteven McGinn, Ivo Glynne Gut
Current HIV Research|February 15, 2012
Identification of IL7RA risk alleles for rapid progression during HIV-1 infection: a comprehensive study in the GRIV cohortSophie Limou, Giovanna Melica, Cédric Coulonges, et al.
The Journal of Investigative Dermatology|June 26, 2009
An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disordersTiphaine Oudot, Fabienne Lesueur, Mickaël Guedj, et al.
Scientific Reports|July 1, 2026
A comprehensive urine workflow enables robust methylation and fragmentation analysis of cell-free DNAFlorence Mauger, Nouara Oussada, Caroline Horgues, et al.
Diabetes|July 18, 2008
G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetesDavid-Alexandre Trégouet, Per-Henrik Groop, Steven McGinn, et al.
BMC Genomics|July 29, 2025
Interlaboratory evaluation of high molecular weight DNA extraction methods for long-read sequencing and structural variant analysisAlison S Devonshire, Jordi Morata, Claire Jubin, et al.
Human Mutation|April 25, 2018
Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140Véronique Geoffroy, Corinne Stoetzel, Sophie Scheidecker, et al.
EMBO Molecular Medicine|June 6, 2020
Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stressAriane Kröll-Hermi, Frédéric Ebstein, Corinne Stoetzel, et al.
New Biotechnology|October 31, 2015
New technologies for DNA analysis--a review of the READNA ProjectSteven McGinn, David Bauer, Thomas Brefort, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 2