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Mindin (SPON2) Is Essential for Cutaneous Fibrogenesis in a Mouse Model of Systemic Sclerosis.
Rana I, Kataria S, Tan TL, Hajam EY, Kashyap DK, Saha D, Ajnabi J, Paul S, Jayappa S, Ananthan ASHP, Kumar P, Zaarour RF, Haarshaadri J, Kansagara G, Rizvi A, Zirmire RK, Badarinath K, Khedkar SU, Chandra Y, Samuel R, George R, Danda D, Jacob PM, Dey R, Dhandapany PS, He YW, Varga J, Varghese S, Jamora C. Rana I, et al. Among authors: dhandapany ps. J Invest Dermatol. 2023 May;143(5):699-710.e10. doi: 10.1016/j.jid.2022.10.011. Epub 2022 Dec 15. J Invest Dermatol. 2023. PMID: 36528128 Free article.
Novel MYBPC3 Mutations in Indian Population with Cardiomyopathies.
Rani DS, Kasala A, Dhandapany PS, Muthusami U, Kunnoth S, Rathinavel A, Ayapati DR, Thangaraj K. Rani DS, et al. Among authors: dhandapany ps. Pharmgenomics Pers Med. 2023 Sep 20;16:883-893. doi: 10.2147/PGPM.S407179. eCollection 2023. Pharmgenomics Pers Med. 2023. PMID: 37750083 Free PMC article.
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy.
Lesurf R, Said A, Akinrinade O, Breckpot J, Delfosse K, Liu T, Yao R, Persad G, McKenna F, Noche RR, Oliveros W, Mattioli K, Shah S, Miron A, Yang Q, Meng G, Yue MCS, Sung WWL, Thiruvahindrapuram B, Lougheed J, Oechslin E, Mondal T, Bergin L, Smythe J, Jayappa S, Rao VJ, Shenthar J, Dhandapany PS, Semsarian C, Weintraub RG, Bagnall RD, Ingles J; Genomics England Research Consortium; Melé M, Maass PG, Ellis J, Scherer SW, Mital S. Lesurf R, et al. Among authors: dhandapany ps. NPJ Genom Med. 2022 Mar 14;7(1):18. doi: 10.1038/s41525-022-00288-y. NPJ Genom Med. 2022. PMID: 35288587 Free PMC article.
Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy.
Rani DS, Vijaya Kumar A, Nallari P, Sampathkumar K, Dhandapany PS, Narasimhan C, Rathinavel A, Thangaraj K. Rani DS, et al. Among authors: dhandapany ps. CJC Open. 2021 Aug 8;4(1):1-11. doi: 10.1016/j.cjco.2021.07.020. eCollection 2022 Jan. CJC Open. 2021. PMID: 35072022 Free PMC article.
Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy.
Jain PK, Jayappa S, Sairam T, Mittal A, Paul S, Rao VJ, Chittora H, Kashyap DK, Palakodeti D, Thangaraj K, Shenthar J, Koranchery R, Rajendran R, Alireza H, Mohanan KS, Rathinavel A, Dhandapany PS. Jain PK, et al. Among authors: dhandapany ps. J Med Genet. 2022 Oct;59(10):984-992. doi: 10.1136/jmedgenet-2021-107866. Epub 2021 Dec 16. J Med Genet. 2022. PMID: 34916228
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