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Year | Number of Results |
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2022 | 3 |
2023 | 2 |
2024 | 0 |
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Page 1
Recommendations for clinical interpretation of variants found in non-coding regions of the genome.
Genome Med. 2022 Jul 19;14(1):73. doi: 10.1186/s13073-022-01073-3.
Genome Med. 2022.
PMID: 35850704
Free PMC article.
The Need for Inclusive Genomic Research.
Krishnan N, Ingles J.
Krishnan N, et al.
Circ Genom Precis Med. 2022 Apr;15(2):e003736. doi: 10.1161/CIRCGEN.122.003736. Epub 2022 Mar 21.
Circ Genom Precis Med. 2022.
PMID: 35311525
No abstract available.
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Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.
Josephs KS, Roberts AM, Theotokis P, Walsh R, Ostrowski PJ, Edwards M, Fleming A, Thaxton C, Roberts JD, Care M, Zareba W, Adler A, Sturm AC, Tadros R, Novelli V, Owens E, Bronicki L, Jarinova O, Callewaert B, Peters S, Lumbers T, Jordan E, Asatryan B, Krishnan N, Hershberger RE, Chahal CAA, Landstrom AP, James C, McNally EM, Judge DP, van Tintelen P, Wilde A, Gollob M, Ingles J, Ware JS.
Josephs KS, et al. Among authors: krishnan n.
Genome Med. 2023 Oct 23;15(1):86. doi: 10.1186/s13073-023-01246-8.
Genome Med. 2023.
PMID: 37872640
Free PMC article.
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Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.
Josephs KS, Roberts AM, Theotokis P, Walsh R, Ostrowski PJ, Edwards M, Fleming A, Thaxton C, Roberts JD, Care M, Zareba W, Adler A, Sturm AC, Tadros R, Novelli V, Owens E, Bronicki L, Jarinova O, Callewaert B, Peters S, Lumbers T, Jordan E, Asatryan B, Krishnan N, Hershberger RE, Chahal CAA, Landstrom AP, James C, McNally EM, Judge DP, van Tintelen P, Wilde A, Gollob M, Ingles J, Ware JS.
Josephs KS, et al. Among authors: krishnan n.
medRxiv [Preprint]. 2023 Apr 3:2023.04.03.23287612. doi: 10.1101/2023.04.03.23287612.
medRxiv. 2023.
PMID: 37066275
Free PMC article.
Updated.
Preprint.
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The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic.
Stafford F, Krishnan N, Richardson E, Butters A, Hespe S, Burns C, Gray B, Medi C, Nowak N, Isbister JC, Raju H, Richmond D, Ryan MP, Singer ES, Sy RW, Yeates L, Bagnall RD, Semsarian C, Ingles J.
Stafford F, et al. Among authors: krishnan n.
Genome Med. 2022 Dec 28;14(1):145. doi: 10.1186/s13073-022-01149-0.
Genome Med. 2022.
PMID: 36578016
Free PMC article.
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