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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2015 2
2017 1
2018 2
2020 1
2021 4
2022 2
2023 2
2024 1

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14 results

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Page 1
Molecular genetic studies of complete hydatidiform moles.
Carey L, Nash BM, Wright DC. Carey L, et al. Among authors: nash bm. Transl Pediatr. 2015 Apr;4(2):181-8. doi: 10.3978/j.issn.2224-4336.2015.04.02. Transl Pediatr. 2015. PMID: 26835372 Free PMC article. Review.
MERTK retinopathy: biomarkers assessing vision loss.
Sakti DH, Cornish EE, Mustafic N, Zaheer A, Retsas S, Rajagopalan S, Chung CW, Ewans L, McCluskey P, Nash BM, Jamieson RV, Grigg JR. Sakti DH, et al. Among authors: nash bm. Ophthalmic Genet. 2021 Dec;42(6):706-716. doi: 10.1080/13816810.2021.1955278. Epub 2021 Jul 22. Ophthalmic Genet. 2021. PMID: 34289798
Genome sequencing in congenital cataracts improves diagnostic yield.
Ma A, Grigg JR, Flaherty M, Smith J, Minoche AE, Cowley MJ, Nash BM, Ho G, Gayagay T, Lai T, Farnsworth E, Hackett EL, Slater K, Wong K, Holman KJ, Jenkins G, Cheng A, Martin F, Brown NJ, Leighton SE, Amor DJ, Goel H, Dinger ME, Bennetts B, Jamieson RV. Ma A, et al. Among authors: nash bm. Hum Mutat. 2021 Sep;42(9):1173-1183. doi: 10.1002/humu.24240. Epub 2021 Jun 15. Hum Mutat. 2021. PMID: 34101287
Natural history and biomarkers of KCNV2-associated retinopathy.
Sakti DH, Cornish EE, Ali H, Retsas S, Raza M, Saakova N, Carvalho LS, Nash BM, Jamieson RV, Grigg JR. Sakti DH, et al. Among authors: nash bm. Clin Exp Ophthalmol. 2024 Mar 5. doi: 10.1111/ceo.14373. Online ahead of print. Clin Exp Ophthalmol. 2024. PMID: 38443311
NMNAT1 variants cause cone and cone-rod dystrophy.
Nash BM, Symes R, Goel H, Dinger ME, Bennetts B, Grigg JR, Jamieson RV. Nash BM, et al. Eur J Hum Genet. 2018 Mar;26(3):428-433. doi: 10.1038/s41431-017-0029-7. Epub 2017 Nov 28. Eur J Hum Genet. 2018. PMID: 29184169 Free PMC article.
Revealing hidden genetic diagnoses in the ocular anterior segment disorders.
Ma A, Yousoof S, Grigg JR, Flaherty M, Minoche AE, Cowley MJ, Nash BM, Ho G, Gayagay T, Lai T, Farnsworth E, Hackett EL, Fisk K, Wong K, Holman KJ, Jenkins G, Cheng A, Martin F, Karaconji T, Elder JE, Enriquez A, Wilson M, Amor DJ, Stutterd CA, Kamien B, Nelson J, Dinger ME, Bennetts B, Jamieson RV. Ma A, et al. Among authors: nash bm. Genet Med. 2020 Oct;22(10):1623-1632. doi: 10.1038/s41436-020-0854-x. Epub 2020 Jun 5. Genet Med. 2020. PMID: 32499604 Free PMC article.
14 results