Andreas Laner
Munich, BY, Germany
Last Updated: 09/26/2026
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Found 44 publications
Improving genetic diagnosis of hereditary tumor syndromes: From expanded gene panels to functional genomics.
Journal: International journal of cancer
Published: October 14, 2025
Validation structures for sequence variants of uncertain significance in hereditary cancer.
Journal: European journal of human genetics : EJHG
Published: October 14, 2025
Next-Generation Sequencing in Congenital Eye Malformations: Identification of Genetic Causes and Comparison of Different Panel-Based Diagnostic Strategies.
Journal: International journal of molecular sciences
Published: September 10, 2025
From Expert Judgment to Structured Guidelines: A Brief History and Bright Future of DNA Variant Interpretation.
Journal: Annals of human genetics
Published: January 31, 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?
Journal: Familial cancer
Published: November 25, 2024
Joint analysis of germline genetic data from over 29,000 cases with suspected hereditary breast and ovarian cancer (HBOC) as part of the NASGE initiative.
Journal: Breast (Edinburgh, Scotland)
Published: October 28, 2024
Blood biomarker fingerprints in a cohort of patients with CHRNE-related congenital myasthenic syndrome.
Journal: Acta neuropathologica communications
Published: October 14, 2024
Systematic large-scale application of ClinGen InSiGHT APC -specific ACMG/AMP variant classification criteria substantially alleviates the burden of variants of uncertain significance in ClinVar and LOVD databases.
Journal: medRxiv : the preprint server for health sciences
Published: May 15, 2024
Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS.
Journal: American journal of human genetics
Published: April 14, 2024
Novel Genetic and Biochemical Insights into the Spectrum of NEFL-Associated Phenotypes.
Journal: Journal of neuromuscular diseases
Published: April 05, 2024
Reclassification of VUS in BRCA1 and BRCA2 using the new BRCA1/BRCA2 ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification system.
Journal: Genetics in medicine open
Published: March 04, 2024
Last Updated: 09/26/2026