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Andreas Laner

Showing results (11-20 of 48) with videos related to

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Human Mutation|February 13, 2020
Critical assessment of secondary findings in genes linked to primary arrhythmia syndromesIsabel Diebold, Ulrike Schön, Florentine Scharf, et al.
Familial Cancer|May 3, 2025
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?Morghan C Lucas, Thomas Keßler, Florentine Scharf, et al.
Familial Cancer|May 15, 2022
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational studyTeresa M Neuhann, Katharina Haub, Verena Steinke-Lange, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Biallelic MUTYH mutations can mimic Lynch syndromeMonika Morak, Barbara Heidenreich, Gisela Keller, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|April 23, 2015
Phosphatidylinositol 3-kinase (PI3K) signalling regulates insulin-like-growth factor binding protein-2 (IGFBP-2) production in human adipocytesFranziska Wilhelm, Franziska Kässner, Gordian Schmid, et al.
Genetics in Medicine Open|March 3, 2025
Reclassification of VUS in <i>BRCA1</i> and <i>BRCA2</i> using the new <i>BRCA1</i>/<i>BRCA2</i> ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification systemAnna Benet-Pagès, Andreas Laner, Luis R Nassar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Gene delivery systems--gene therapy vectors for cystic fibrosisDaniel Klink, Dirk Schindelhauer, Andreas Laner, et al.
BMC Medical Genomics|April 1, 2021
HPO-driven virtual gene panel: a new efficient approach in molecular autopsy of sudden unexplained deathUlrike Schön, Anna Holzer, Andreas Laner, et al.
Genes|January 26, 2024
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)Alexander German, Jelena Jukic, Andreas Laner, et al.
Familial Cancer|February 1, 2020
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnosticsMonika Morak, Verena Steinke-Lange, Trisari Massdorf, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Human Mutation|February 13, 2020
Critical assessment of secondary findings in genes linked to primary arrhythmia syndromesIsabel Diebold, Ulrike Schön, Florentine Scharf, et al.
Familial Cancer|May 3, 2025
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?Morghan C Lucas, Thomas Keßler, Florentine Scharf, et al.
Familial Cancer|May 15, 2022
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational studyTeresa M Neuhann, Katharina Haub, Verena Steinke-Lange, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Biallelic MUTYH mutations can mimic Lynch syndromeMonika Morak, Barbara Heidenreich, Gisela Keller, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|April 23, 2015
Phosphatidylinositol 3-kinase (PI3K) signalling regulates insulin-like-growth factor binding protein-2 (IGFBP-2) production in human adipocytesFranziska Wilhelm, Franziska Kässner, Gordian Schmid, et al.
Genetics in Medicine Open|March 3, 2025
Reclassification of VUS in <i>BRCA1</i> and <i>BRCA2</i> using the new <i>BRCA1</i>/<i>BRCA2</i> ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification systemAnna Benet-Pagès, Andreas Laner, Luis R Nassar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Gene delivery systems--gene therapy vectors for cystic fibrosisDaniel Klink, Dirk Schindelhauer, Andreas Laner, et al.
BMC Medical Genomics|April 1, 2021
HPO-driven virtual gene panel: a new efficient approach in molecular autopsy of sudden unexplained deathUlrike Schön, Anna Holzer, Andreas Laner, et al.
Genes|January 26, 2024
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)Alexander German, Jelena Jukic, Andreas Laner, et al.
Familial Cancer|February 1, 2020
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnosticsMonika Morak, Verena Steinke-Lange, Trisari Massdorf, et al.
Pageof 5