Sandra Ratnavadivel

Title(s)Postdoctoral Scholar, Medicine
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
La Jolla CA 92093
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details 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. Generation of a TMEM43 knockout human induced pluripotent stem cell line (HDZi003-A-1) using CRISPR/Cas9. Stem Cell Res. 2024 Apr; 76:103354. Ratnavadivel S, Dammeier J, Gaertner A, de Toledo MAS, Zenke M, Gummert J, Bloch Rasmussen T, Klinke N, Jürgens K, Meyer H, Paululat A, Milting H. PMID: 38430734.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    2. A Drosophila melanogaster model for TMEM43-related arrhythmogenic right ventricular cardiomyopathy type 5. Cell Mol Life Sci. 2022 Jul 22; 79(8):444. Klinke N, Meyer H, Ratnavadivel S, Reinhardt M, Heinisch JJ, Malmendal A, Milting H, Paululat A. PMID: 35869176; PMCID: PMC9307560.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals
    3. The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3. Biomedicines. 2021 Oct 05; 9(10). Brodehl A, Hain C, Flottmann F, Ratnavadivel S, Gaertner A, Klauke B, Kalinowski J, Körperich H, Gummert J, Paluszkiewicz L, Deutsch MA, Milting H. PMID: 34680517; PMCID: PMC8533191.
      View in: PubMed   Mentions: 11  
    4. The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy. Can J Cardiol. 2021 06; 37(6):857-866. Protonotarios A, Brodehl A, Asimaki A, Jager J, Quinn E, Stanasiuk C, Ratnavadivel S, Futema M, Akhtar MM, Gossios TD, Ashworth M, Savvatis K, Walhorn V, Anselmetti D, Elliott PM, Syrris P, Milting H, Lopes LR. PMID: 33290826.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    5. Human pluripotent stem cell line (HDZi001-A) derived from a patient carrying the ARVC-5 associated mutation TMEM43-p.S358L. Stem Cell Res. 2020 10; 48:101957. Ratnavadivel S, Szymanski de Toledo M, Rasmussen TB, Šaric T, Gummert J, Zenke M, Milting H. PMID: 32858485.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    6. Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction. J Clin Med. 2020 Mar 29; 9(4). Kubánek M, Schimerová T, Piherová L, Brodehl A, Krebsová A, Ratnavadivel S, Stanasiuk C, Hansíková H, Zeman J, Palecek T, Houštek J, Drahota Z, Nusková H, Mikešová J, Zámecník J, Macek M, Ridzon P, Malusková J, Stránecký V, Melenovský V, Milting H, Kmoch S. PMID: 32235386; PMCID: PMC7231262.
      View in: PubMed   Mentions: 18  
    7. Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect. Genes (Basel). 2019 11 11; 10(11). Brodehl A, Pour Hakimi SA, Stanasiuk C, Ratnavadivel S, Hendig D, Gaertner A, Gerull B, Gummert J, Paluszkiewicz L, Milting H. PMID: 31718026; PMCID: PMC6896098.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCells
    8. Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies. Int J Mol Sci. 2019 Sep 06; 20(18). Brodehl A, Ebbinghaus H, Deutsch MA, Gummert J, Gärtner A, Ratnavadivel S, Milting H. PMID: 31489928; PMCID: PMC6770343.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansAnimalsCells