Connection

LIESBETH VOSSAERT to Humans

This is a "connection" page, showing publications LIESBETH VOSSAERT has written about Humans.
Connection Strength

0.212
  1. Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing. Prenat Diagn. 2022 05; 42(6):686-696.
    View in: PubMed
    Score: 0.022
  2. Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis. Am J Hum Genet. 2019 12 05; 105(6):1262-1273.
    View in: PubMed
    Score: 0.018
  3. Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing. Prenat Diagn. 2018 12; 38(13):1069-1078.
    View in: PubMed
    Score: 0.017
  4. Identification of histone H3 clipping activity in human embryonic stem cells. Stem Cell Res. 2014 Jul; 13(1):123-34.
    View in: PubMed
    Score: 0.012
  5. Reference loci for RT-qPCR analysis of differentiating human embryonic stem cells. BMC Mol Biol. 2013 Sep 12; 14:21.
    View in: PubMed
    Score: 0.012
  6. Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage. Clin Chem. 2025 Jan 03; 71(1):141-154.
    View in: PubMed
    Score: 0.007
  7. Untargeted metabolomics analysis as a potential screening tool for 3-methylglutaconic aciduria syndromes. Mol Genet Metab. 2025 Mar; 144(3):109009.
    View in: PubMed
    Score: 0.006
  8. Family Lore, a Variant of Uncertain Significance, and?CADASIL. Am J Med Genet C Semin Med Genet. 2024 Nov; 196(2-3):e32117.
    View in: PubMed
    Score: 0.006
  9. MED12 Loss-of-Function Variants as a Cause of Congenital Diaphragmatic Hernia in Females With Hardikar Syndrome and Nonspecific Intellectual Disability. Am J Med Genet A. 2025 Jan; 197(1):e63868.
    View in: PubMed
    Score: 0.006
  10. Recurrent carotid paragangliomas in a syndromic patient with a heterozygous missense variant in DNA Methyltransferase 3 Alpha. Am J Med Genet A. 2025 Jan; 197(1):e63849.
    View in: PubMed
    Score: 0.006
  11. Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnoses. Cancer Genet. 2024 Nov; 288-289:5-9.
    View in: PubMed
    Score: 0.006
  12. Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clin Genet. 2024 Jul; 106(1):95-101.
    View in: PubMed
    Score: 0.006
  13. Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102.
    View in: PubMed
    Score: 0.006
  14. Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss. Mol Genet Genomic Med. 2024 Feb; 12(2):e2404.
    View in: PubMed
    Score: 0.006
  15. A familial deletion of 10p12.1 associated with thrombocytopenia. Am J Med Genet A. 2024 01; 194(1):77-81.
    View in: PubMed
    Score: 0.006
  16. Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved population. Mol Genet Genomic Med. 2023 Dec; 11(12):e2272.
    View in: PubMed
    Score: 0.006
  17. Cell-based Noninvasive Prenatal Testing (cbNIPT)-A Review on the Current Developments and Future Prospects. Clin Obstet Gynecol. 2023 09 01; 66(3):636-648.
    View in: PubMed
    Score: 0.006
  18. Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory. Genet Med. 2023 06; 25(6):100830.
    View in: PubMed
    Score: 0.006
  19. Circulating trophoblast numbers as a potential marker for pregnancy complications. Prenat Diagn. 2022 08; 42(9):1182-1189.
    View in: PubMed
    Score: 0.005
  20. Overview and recent developments in cell-based noninvasive prenatal testing. Prenat Diagn. 2021 Sep; 41(10):1202-1214.
    View in: PubMed
    Score: 0.005
  21. Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT. PLoS One. 2021; 16(4):e0249695.
    View in: PubMed
    Score: 0.005
  22. The effect of maternal body mass index and gestational age on circulating trophoblast yield in cell-based noninvasive prenatal testing. Prenat Diagn. 2020 10; 40(11):1383-1389.
    View in: PubMed
    Score: 0.005
  23. Comparison of fractionation proteomics for local SWATH library building. Proteomics. 2017 Aug; 17(15-16).
    View in: PubMed
    Score: 0.004
  24. Extracting histones for the specific purpose of label-free MS. Proteomics. 2016 12; 16(23):2937-2944.
    View in: PubMed
    Score: 0.004
  25. Evidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing. Prenat Diagn. 2016 Nov; 36(11):1009-1019.
    View in: PubMed
    Score: 0.004
  26. Assessing the impact of minimizing arginine conversion in fully defined SILAC culture medium in human embryonic stem cells. Proteomics. 2016 10; 16(20):2605-2614.
    View in: PubMed
    Score: 0.004
  27. Histone proteolysis: a proposal for categorization into 'clipping' and 'degradation'. Bioessays. 2015 Jan; 37(1):70-9.
    View in: PubMed
    Score: 0.003
  28. Detailed method description for noninvasive monitoring of differentiation status of human embryonic stem cells. Anal Biochem. 2014 Sep 15; 461:60-6.
    View in: PubMed
    Score: 0.003
  29. Quantitative proteomics to characterize specific histone H2A proteolysis in chronic lymphocytic leukemia and the myeloid THP-1 cell line. Int J Mol Sci. 2014 May 27; 15(6):9407-21.
    View in: PubMed
    Score: 0.003
  30. Neutrophil Elastase in the capacity of the "H2A-specific protease". Int J Biochem Cell Biol. 2014 Jun; 51:39-44.
    View in: PubMed
    Score: 0.003
  31. Influence of activin A supplementation during human embryonic stem cell derivation on germ cell differentiation potential. Stem Cells Dev. 2013 Dec 01; 22(23):3141-55.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.