Jagirdar K - Search Results

1

Point mutation in p14^ARF -specific exon 1β of CDKN2A causing familial melanoma and astrocytoma.

McInerney-Leo AM, Wheeler L, Sturm RA, Tan JM, Harris JE, Anderson L, Jagirdar K, Brown MA, Leo PJ, Soyer HP, Duncan EL. McInerney-Leo AM, et al. Among authors: jagirdar k. Br J Dermatol. 2018 Apr;178(4):e263-e264. doi: 10.1111/bjd.16275. Epub 2018 Feb 19. Br J Dermatol. 2018. PMID: 29278422 No abstract available.

2

The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls.

McMeniman EK, Duffy DL, Jagirdar K, Lee KJ, Peach E, McInerney-Leo AM, De'Ambrosis B, Rayner JE, Smithers BM, Soyer HP, Sturm RA. McMeniman EK, et al. Among authors: jagirdar k. Br J Dermatol. 2020 Aug;183(2):357-366. doi: 10.1111/bjd.18777. Epub 2020 Feb 5. Br J Dermatol. 2020. PMID: 31794051

3

CDKN2A testing threshold in a high-risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk.

McMeniman EK, Peach E, Lee KJ, Yanes T, Jagirdar K, Stark MS, Soyer HP, Duffy DL, McInerney-Leo AM, Sturm RA. McMeniman EK, et al. Among authors: jagirdar k. J Eur Acad Dermatol Venereol. 2020 Dec;34(12):e797-e798. doi: 10.1111/jdv.16627. Epub 2020 Jul 9. J Eur Acad Dermatol Venereol. 2020. PMID: 32386439 No abstract available.

4

Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: a cross-sectional study.

Lee S, Duffy DL, McClenahan P, Lee KJ, McEniery E, Burke B, Jagirdar K, Martin NG, Sturm RA, Soyer HP, Schaider H. Lee S, et al. Among authors: jagirdar k. Br J Dermatol. 2016 Feb;174(2):356-63. doi: 10.1111/bjd.14291. Epub 2016 Jan 22. Br J Dermatol. 2016. PMID: 26871925

5

The BRAF and NRAS mutation prevalence in dermoscopic subtypes of acquired naevi reveals constitutive mitogen-activated protein kinase pathway activation.

Tan JM, Tom LN, Jagirdar K, Lambie D, Schaider H, Sturm RA, Soyer HP, Stark MS. Tan JM, et al. Among authors: jagirdar k. Br J Dermatol. 2018 Jan;178(1):191-197. doi: 10.1111/bjd.15809. Epub 2017 Dec 18. Br J Dermatol. 2018. PMID: 28714107

6

Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case-control study.

Laino AM, Berry EG, Jagirdar K, Lee KJ, Duffy DL, Soyer HP, Sturm RA. Laino AM, et al. Among authors: jagirdar k. Br J Dermatol. 2018 May;178(5):1119-1127. doi: 10.1111/bjd.16323. Epub 2018 Apr 6. Br J Dermatol. 2018. PMID: 29315480

7

Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients.

Rayner JE, McMeniman EK, Duffy DL, De'Ambrosis B, Smithers BM, Jagirdar K, Lee KJ, Soyer HP, Sturm RA. Rayner JE, et al. Among authors: jagirdar k. J Eur Acad Dermatol Venereol. 2019 Jun;33(6):1076-1083. doi: 10.1111/jdv.15446. Epub 2019 Mar 15. J Eur Acad Dermatol Venereol. 2019. PMID: 30680790

8

High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk.

Duffy DL, Lee KJ, Jagirdar K, Pflugfelder A, Stark MS, McMeniman EK, Soyer HP, Sturm RA. Duffy DL, et al. Among authors: jagirdar k. Br J Dermatol. 2019 Nov;181(5):1009-1016. doi: 10.1111/bjd.17833. Epub 2019 Jul 17. Br J Dermatol. 2019. PMID: 30820946

9

BRAF wild-type melanoma in situ arising in a BRAF V600E mutant dysplastic nevus.

Tan JM, Lin LL, Lambie D, Flewell-Smith R, Jagirdar K, Schaider H, Sturm RA, Prow TW, Soyer HP. Tan JM, et al. Among authors: jagirdar k. JAMA Dermatol. 2015 Apr;151(4):417-21. doi: 10.1001/jamadermatol.2014.3775. JAMA Dermatol. 2015. PMID: 25607474 Free article.

10

High incidence of primary melanomas in an MC1R RHC homozygote/CDKN2A mutant genotype patient.

Sinnya S, Jagirdar K, De'Ambrosis B, McMeniman E, Sturm RA, Soyer HP. Sinnya S, et al. Among authors: jagirdar k. Arch Dermatol Res. 2015 Oct;307(8):741-5. doi: 10.1007/s00403-015-1582-y. Epub 2015 Jun 24. Arch Dermatol Res. 2015. PMID: 26103950

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