Frishman D - Search Results

1

Identification of novel hereditary cancer genes by whole exome sequencing.

Sokolenko AP, Suspitsin EN, Kuligina ESh, Bizin IV, Frishman D, Imyanitov EN. Sokolenko AP, et al. Among authors: frishman d. Cancer Lett. 2015 Dec 28;369(2):274-88. doi: 10.1016/j.canlet.2015.09.014. Epub 2015 Sep 30. Cancer Lett. 2015. PMID: 26427841 Review.

2

Genome-wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma.

Smida J, Xu H, Zhang Y, Baumhoer D, Ribi S, Kovac M, von Luettichau I, Bielack S, O'Leary VB, Leib-Mösch C, Frishman D, Nathrath M. Smida J, et al. Among authors: frishman d. Int J Cancer. 2017 Aug 15;141(4):816-828. doi: 10.1002/ijc.30778. Epub 2017 May 25. Int J Cancer. 2017. PMID: 28494505 Free article.

3

MutHTP: mutations in human transmembrane proteins.

Kulandaisamy A, Binny Priya S, Sakthivel R, Tarnovskaya S, Bizin I, Hönigschmid P, Frishman D, Gromiha MM. Kulandaisamy A, et al. Among authors: frishman d. Bioinformatics. 2018 Jul 1;34(13):2325-2326. doi: 10.1093/bioinformatics/bty054. Bioinformatics. 2018. PMID: 29401218

4

Prediction of disease-associated mutations in the transmembrane regions of proteins with known 3D structure.

Popov P, Bizin I, Gromiha M, A K, Frishman D. Popov P, et al. Among authors: frishman d. PLoS One. 2019 Jul 10;14(7):e0219452. doi: 10.1371/journal.pone.0219452. eCollection 2019. PLoS One. 2019. PMID: 31291347 Free PMC article.

5

Edgetic perturbation signatures represent known and novel cancer biomarkers.

Kataka E, Zaucha J, Frishman G, Ruepp A, Frishman D. Kataka E, et al. Among authors: frishman g, frishman d. Sci Rep. 2020 Mar 9;10(1):4350. doi: 10.1038/s41598-020-61422-3. Sci Rep. 2020. PMID: 32152446 Free PMC article.

6

Differential expression analysis of human endogenous retroviruses based on ENCODE RNA-seq data.

Haase K, Mösch A, Frishman D. Haase K, et al. Among authors: frishman d. BMC Med Genomics. 2015 Nov 3;8:71. doi: 10.1186/s12920-015-0146-5. BMC Med Genomics. 2015. PMID: 26530187 Free PMC article.

7

Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing.

Kostareva A, Kiselev A, Gudkova A, Frishman G, Ruepp A, Frishman D, Smolina N, Tarnovskaya S, Nilsson D, Zlotina A, Khodyuchenko T, Vershinina T, Pervunina T, Klyushina A, Kozlenok A, Sjoberg G, Golovljova I, Sejersen T, Shlyakhto E. Kostareva A, et al. Among authors: frishman g, frishman d. PLoS One. 2016 Sep 23;11(9):e0163362. doi: 10.1371/journal.pone.0163362. eCollection 2016. PLoS One. 2016. PMID: 27662471 Free PMC article.

8

Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy.

Tarnovskaya S, Kiselev A, Kostareva A, Frishman D. Tarnovskaya S, et al. Among authors: frishman d. Amino Acids. 2017 Nov;49(11):1815-1829. doi: 10.1007/s00726-017-2480-8. Epub 2017 Aug 22. Amino Acids. 2017. PMID: 28831623

9

Expitope 2.0: a tool to assess immunotherapeutic antigens for their potential cross-reactivity against naturally expressed proteins in human tissues.

Jaravine V, Mösch A, Raffegerst S, Schendel DJ, Frishman D. Jaravine V, et al. Among authors: frishman d. BMC Cancer. 2017 Dec 28;17(1):892. doi: 10.1186/s12885-017-3854-8. BMC Cancer. 2017. PMID: 29282079 Free PMC article.

10

Predicting novel disease mutations in the cardiac sodium channel.

Tarnovskaya SI, Korkosh VS, Zhorov BS, Frishman D. Tarnovskaya SI, et al. Among authors: frishman d. Biochem Biophys Res Commun. 2020 Jan 15;521(3):603-611. doi: 10.1016/j.bbrc.2019.10.142. Epub 2019 Oct 31. Biochem Biophys Res Commun. 2020. PMID: 31677787

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