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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2018 | 3 |
2020 | 1 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
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Page 1
Systematic Functional Annotation of Somatic Mutations in Cancer.
Cancer Cell. 2018 Mar 12;33(3):450-462.e10. doi: 10.1016/j.ccell.2018.01.021.
Cancer Cell. 2018.
PMID: 29533785
Free PMC article.
Comprehensive Molecular Characterization of the Hippo Signaling Pathway in Cancer.
Wang Y, Xu X, Maglic D, Dill MT, Mojumdar K, Ng PK, Jeong KJ, Tsang YH, Moreno D, Bhavana VH, Peng X, Ge Z, Chen H, Li J, Chen Z, Zhang H, Han L, Du D, Creighton CJ, Mills GB; Cancer Genome Atlas Research Network; Camargo F, Liang H.
Wang Y, et al. Among authors: bhavana vh.
Cell Rep. 2018 Oct 30;25(5):1304-1317.e5. doi: 10.1016/j.celrep.2018.10.001.
Cell Rep. 2018.
PMID: 30380420
Free PMC article.
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Nitric Oxide Production and Effects in Group B Streptococcus Chorioamnionitis.
Keith MF, Gopalakrishna KP, Bhavana VH, Hillebrand GH, Elder JL, Megli CJ, Sadovsky Y, Hooven TA.
Keith MF, et al. Among authors: bhavana vh.
Pathogens. 2022 Sep 28;11(10):1115. doi: 10.3390/pathogens11101115.
Pathogens. 2022.
PMID: 36297171
Free PMC article.
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Differential expression of MAGEA6 toggles autophagy to promote pancreatic cancer progression.
Tsang YH, Wang Y, Kong K, Grzeskowiak C, Zagorodna O, Dogruluk T, Lu H, Villafane N, Bhavana VH, Moreno D, Elsea SH, Liang H, Mills GB, Scott KL.
Tsang YH, et al. Among authors: bhavana vh.
Elife. 2020 Apr 9;9:e48963. doi: 10.7554/eLife.48963.
Elife. 2020.
PMID: 32270762
Free PMC article.
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Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features.
Luo X, Schoch K, Jangam SV, Bhavana VH, Graves HK, Kansagra S, Jasien JM, Stong N, Keren B, Mignot C, Ravelli C; Undiagnosed Diseases Network; Bellen HJ, Wangler MF, Shashi V, Yamamoto S.
Luo X, et al. Among authors: bhavana vh.
Hum Mol Genet. 2021 Jun 26;30(14):1283-1292. doi: 10.1093/hmg/ddab110.
Hum Mol Genet. 2021.
PMID: 33864376
Free PMC article.
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Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
Liu N, Schoch K, Luo X, Pena LDM, Bhavana VH, Kukolich MK, Stringer S, Powis Z, Radtke K, Mroske C, Deak KL, McDonald MT, McConkie-Rosell A, Markert ML, Kranz PG, Stong N, Need AC, Bick D, Amaral MD, Worthey EA, Levy S; Undiagnosed Diseases Network (UDN); Wangler MF, Bellen HJ, Shashi V, Yamamoto S.
Liu N, et al. Among authors: bhavana vh.
Hum Mol Genet. 2018 Jul 15;27(14):2454-2465. doi: 10.1093/hmg/ddy146.
Hum Mol Genet. 2018.
PMID: 29726930
Free PMC article.
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