Search

Your search keyword '"Johansson, Lennart"' showing total 1,063 results

Search Constraints

Start Over You searched for: Author "Johansson, Lennart" Remove constraint Author: "Johansson, Lennart"
1,063 results on '"Johansson, Lennart"'

Search Results

1. Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

4. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

5. MOLGENIS VIP: an open-source and modular pipeline for high-throughput and integrated DNA variant analysis

8. Comparing Sequence-Based and Literature-Based Pathogenicity Scoring Methods for Human Variants

9. Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy

11. Stationsbyen og glokaliseringen:- fra Jylland til Småland

12. Clinical Value of EGFR Copy Number Gain Determined by Amplicon-Based Targeted Next Generation Sequencing in Patients with EGFR-Mutated NSCLC

14. Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy.

15. Cas9-directed long-read sequencing to resolve optical genome mapping findings in leukemia diagnostics

16. Ten quick tips for building FAIR workflows

17. Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching

18. PB1701: REPLACING THE CURRENT METHODS IN LEUKEMIA DIAGNOSTICS WITH OPTICAL GENOME MAPPING AND CAS9-DIRECTED NANOPORE SEQUENCING.

22. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

23. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

24. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

25. Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching

26. CINECA GDPR and FAIR compliant Diagnostic Services D5.3

27. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

29. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

33. Cancer Stem Cells and Radiation

35. Radiation Induced Cell Deaths

37. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

38. Diagnostic dosimetry

41. Low Detection Rates of Genetic FH in Cohort of Patients With Severe Hypercholesterolemia in the United Arabic Emirates

44. Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patients

45. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

46. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

47. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

Catalog

Books, media, physical & digital resources