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LIESBETH VOSSAERT

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Molecular & Human Genetics
Address2450 HOLCOMBE
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Duarte R, Vossaert L, Darilek SA, Rose C, Schauer E, Parobek C, Bland E, Machol K, Mizerik E, Murali CN. Family Lore, a Variant of Uncertain Significance, and?CADASIL. Am J Med Genet C Semin Med Genet. 2024 Oct 20; e32117. PMID: 39428697.
      Citations:    Fields:    
    2. Kao EC, Mizerik EA, Bacino CA, Dai H, Vossaert L, Scott DA. 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. 2024 Aug 30; e63868. PMID: 39215511.
      Citations:    Fields:    
    3. German RJ, Vuocolo B, Vossaert L, Saba L, Fletcher R, Tedder ML, Sadikovic B, Kerkhof J, Wangler M, Bacino CA, Texome Project. Recurrent carotid paragangliomas in a syndromic patient with a heterozygous missense variant in DNA Methyltransferase 3 Alpha. Am J Med Genet A. 2024 Aug 21; e63849. PMID: 39166703.
      Citations:    Fields:    
    4. Kumar RD, Vossaert L, Bi W, Owen N, Rau RE, Helber HL, Sasa G, Reuther J, Roy A, Fisher KE. Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnoses. Cancer Genet. 2024 Aug 15; 288-289:5-9. PMID: 39178500.
      Citations:    Fields:    
    5. Parobek CM, Zemet R, Shanahan MA, Burnett BA, Mizerik E, Rosenfeld JA, Vossaert L, Clark SL, Hunter JV, Lalani SR. Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clin Genet. 2024 Jul; 106(1):95-101. PMID: 38545656; PMCID: PMC11147704.
      Citations:    Fields:    Translation:Humans
    6. Vuocolo B, German RJ, Lalani SR, Murali CN, Bacino CA, Baskin S, Littlejohn R, Odom JD, McLean S, Schmid C, Nutter M, Stuebben M, Magness E, Juarez O, El Achi D, Mitchell B, Glinton KE, Robak L, Nagamani SC, Saba L, Ritenour A, Zhang L, Streff H, Chan K, Kemere KJ, Carter K, Texome Project, Owen N, Vossaert L, Liu P, Bellen H, Wangler M, Vuocolo B, German RJ, Lalani SR, Murali CN, Bacino CA, Baskin S, Littlejohn R, Odom JD, McLean S, Schmid C, Nutter M, Stuebben M, Magness E, Juarez O, El Achi D, Mitchell B, Glinton KE, Robak L, Nagamani SCS, Ritenour A, Zhang L, Streff H, Chan K, Kemere KJ, Carter K, Owen N, Vossaert L, Liu P, Bellen H, Wangler MF. Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102. PMID: 38431799; PMCID: PMC11161315.
      Citations:    Fields:    Translation:Humans
    7. German RJ, Vuocolo B, Vossaert L, Owen N, Lewis RA, Saba L, Texome Project, Wangler MF, Nagamani S. 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. PMID: 38404254; PMCID: PMC10895382.
      Citations: 1     Fields:    Translation:Humans
    8. Manohar S, Gofin Y, Streff H, Vossaert L, Camacho P, Murali CN. A familial deletion of 10p12.1 associated with thrombocytopenia. Am J Med Genet A. 2024 01; 194(1):77-81. PMID: 37746810.
      Citations:    Fields:    Translation:Humans
    9. Ford CP, Littlejohn RO, German R, Vuocolo B, Aceves J, Vossaert L, Owen N, Wangler M, Schmid CA, Texome Project. 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. PMID: 37614148; PMCID: PMC10724509.
      Citations: 1     Fields:    Translation:Humans
    10. Maktabi MA, Vossaert L, Van den Veyver IB. 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. PMID: 37650673; PMCID: PMC10491429.
      Citations:    Fields:    Translation:Humans
    11. Meng L, Attali R, Talmy T, Regev Y, Mizrahi N, Smirin-Yosef P, Vossaert L, Taborda C, Santana M, Machol I, Xiao R, Dai H, Eng C, Xia F, Tzur S. Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory. Genet Med. 2023 06; 25(6):100830. PMID: 36939041.
      Citations: 1     Fields:    Translation:Humans
    12. Crovetti B, Maktabi MA, Erfani H, Panchalee T, Wang Q, Vossaert L, Van den Veyver I. Circulating trophoblast numbers as a potential marker for pregnancy complications. Prenat Diagn. 2022 08; 42(9):1182-1189. PMID: 35765264; PMCID: PMC9710861.
      Citations:    Fields:    
    13. Liu P, Vossaert L. Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing. Prenat Diagn. 2022 05; 42(6):686-696. PMID: 35416301; PMCID: PMC10014115.
      Citations:    Fields:    Translation:Humans
    14. Okur V, Chen Z, Vossaert L, Peacock S, Rosenfeld J, Zhao L, Du H, Calamaro E, Gerard A, Zhao S, Kelsay J, Lahr A, Mighton C, Porter HM, Siemon A, Silver J, Svihovec S, Fong CT, Grant CL, Lerner-Ellis J, Manickam K, Madan-Khetarpal S, McCandless SE, Morel CF, Schaefer GB, Berry-Kravis EM, Gates R, Gomez-Ospina N, Qiu G, Zhang TJ, Wu Z, Meng L, Liu P, Scott DA, Lupski JR, Eng CM, Wu N, Yuan B. De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities. NPJ Genom Med. 2021 Dec 07; 6(1):104. PMID: 34876591; PMCID: PMC8651650.
      Citations:    
    15. Chakchouk I, Vossaert L, Zemet R, Van den Veyver IB. Overview and recent developments in cell-based noninvasive prenatal testing. Prenat Diagn. 2021 Sep; 41(10):1202-1214. PMID: 33974713; PMCID: PMC9355411.
      Citations:    Fields:    Translation:HumansCells
    16. Zhuo X, Wang Q, Vossaert L, Salman R, Kim A, Van den Veyver I, Breman A, Beaudet A. 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. PMID: 33857205; PMCID: PMC8049273.
      Citations:    Fields:    Translation:HumansCells
    17. Panchalee T, Vossaert L, Wang Q, Crovetti BR, McCombs AK, Wapner RJ, Van den Veyver IB, Beaudet AL. 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. PMID: 32452065; PMCID: PMC7688572.
      Citations:    Fields:    Translation:HumansCells
    18. Vossaert L, Wang Q, Salman R, McCombs AK, Patel V, Qu C, Mancini MA, Edwards DP, Malovannaya A, Liu P, Shaw CA, Levy B, Wapner RJ, Bi W, Breman AM, Van den Veyver IB, Beaudet AL. 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. PMID: 31785788; PMCID: PMC6904821.
      Citations: 17     Fields:    Translation:HumansCells
    19. Vossaert L, Wang Q, Salman R, Zhuo X, Qu C, Henke D, Seubert R, Chow J, U'ren L, Enright B, Stilwell J, Kaldjian E, Yang Y, Shaw C, Levy B, Wapner R, Breman A, Van den Veyver I, Beaudet A. Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing. Prenat Diagn. 2018 12; 38(13):1069-1078. PMID: 30357877; PMCID: PMC6587831.
      Citations: 21     Fields:    Translation:HumansCells
    20. Govaert E, Van Steendam K, Willems S, Vossaert L, Dhaenens M, Deforce D. Comparison of fractionation proteomics for local SWATH library building. Proteomics. 2017 Aug; 17(15-16). PMID: 28664598; PMCID: PMC5601298.
      Citations: 5     Fields:    Translation:HumansCells
    21. Govaert E, Van Steendam K, Scheerlinck E, Vossaert L, Meert P, Stella M, Willems S, De Clerck L, Dhaenens M, Deforce D. Extracting histones for the specific purpose of label-free MS. Proteomics. 2016 12; 16(23):2937-2944. PMID: 27718312; PMCID: PMC5157773.
      Citations: 8     Fields:    Translation:HumansCells
    22. Breman AM, Chow JC, U'Ren L, Normand EA, Qdaisat S, Zhao L, Henke DM, Chen R, Shaw CA, Jackson L, Yang Y, Vossaert L, Needham RH, Chang EJ, Campton D, Werbin JL, Seubert RC, Van den Veyver IB, Stilwell JL, Kaldjian EP, Beaudet AL. Evidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing. Prenat Diagn. 2016 Nov; 36(11):1009-1019. PMID: 27616633; PMCID: PMC5129580.
      Citations: 26     Fields:    Translation:HumansCellsCTClinical Trials
    23. Scheerlinck E, Van Steendam K, Daled S, Govaert E, Vossaert L, Meert P, Van Nieuwerburgh F, Van Soom A, Peelman L, De Sutter P, Dhaenens M, Deforce D, Heindryckx B. 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. PMID: 27392809; PMCID: PMC5096064.
      Citations: 2     Fields:    Translation:HumansCells
    24. Dhaenens M, Glibert P, Meert P, Vossaert L, Deforce D. Histone proteolysis: a proposal for categorization into 'clipping' and 'degradation'. Bioessays. 2015 Jan; 37(1):70-9. PMID: 25350939; PMCID: PMC4305269.
      Citations: 27     Fields:    Translation:HumansAnimalsCells
    25. Scheerlinck E, Van Steendam K, Vandewoestyne M, Lepez T, Gobin V, Meert P, Vossaert L, Van Nieuwerburgh F, Van Soom A, Peelman L, De Sutter P, Dhaenens M, Deforce D, Heindryckx B. Detailed method description for noninvasive monitoring of differentiation status of human embryonic stem cells. Anal Biochem. 2014 Sep 15; 461:60-6. PMID: 24909445.
      Citations: 2     Fields:    Translation:HumansAnimalsCells
    26. Glibert P, Vossaert L, Van Steendam K, Lambrecht S, Van Nieuwerburgh F, Offner F, Kipps T, Dhaenens M, Deforce D. 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. PMID: 24871368; PMCID: PMC4100102.
      Citations: 6     Fields:    Translation:HumansCells
    27. Vossaert L, Meert P, Scheerlinck E, Glibert P, Van Roy N, De Sutter P, Dhaenens M, Deforce D, Heindryckx B. Identification of histone H3 clipping activity in human embryonic stem cells. Stem Cell Res. 2014 Jul; 13(1):123-34. PMID: 24874291.
      Citations: 22     Fields:    Translation:HumansAnimalsCells
    28. Dhaenens M, Glibert P, Lambrecht S, Vossaert L, Van Steendam K, Elewaut D, Deforce D. Neutrophil Elastase in the capacity of the "H2A-specific protease". Int J Biochem Cell Biol. 2014 Jun; 51:39-44. PMID: 24685679.
      Citations: 6     Fields:    Translation:HumansAnimals
    29. Vossaert L, O'Leary T, Van Neste C, Vandesompele J, De Sutter P, Deforce D, Heindryckx B. Reference loci for RT-qPCR analysis of differentiating human embryonic stem cells. BMC Mol Biol. 2013 Sep 12; 14:21. PMID: 24028740; PMCID: PMC3848990.
      Citations: 17     Fields:    Translation:HumansCells
    30. Duggal G, Warrier S, O'Leary T, Van der Jeught M, Lierman S, Vossaert L, Deroo T, Deforce D, Chuva de Sousa Lopes SM, De Sutter P, Heindryckx B. 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. PMID: 23829223; PMCID: PMC3856713.
      Citations: 7     Fields:    Translation:HumansAnimalsCells
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