Gonzaludo N - Search Results

1

PARC report: a health-systems focus on reimbursement and patient access to pharmacogenomics testing.

L Rogers S, Keeling NJ, Giri J, Gonzaludo N, Jones JS, Glogowski E, Formea CM. L Rogers S, et al. Among authors: gonzaludo n. Pharmacogenomics. 2020 Jul;21(11):785-796. doi: 10.2217/pgs-2019-0192. Epub 2020 Aug 4. Pharmacogenomics. 2020. PMID: 32748688 Review.

2

Publisher Correction: Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data.

Chen X, Shen F, Gonzaludo N, Malhotra A, Rogert C, Taft RJ, Bentley DR, Eberle MA. Chen X, et al. Among authors: gonzaludo n. Pharmacogenomics J. 2022 Dec;22(5-6):308. doi: 10.1038/s41397-022-00287-3. Pharmacogenomics J. 2022. PMID: 36171418 Free PMC article. No abstract available.

3

Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data.

Chen X, Shen F, Gonzaludo N, Malhotra A, Rogert C, Taft RJ, Bentley DR, Eberle MA. Chen X, et al. Among authors: gonzaludo n. Pharmacogenomics J. 2021 Apr;21(2):251-261. doi: 10.1038/s41397-020-00205-5. Epub 2021 Jan 18. Pharmacogenomics J. 2021. PMID: 33462347 Free PMC article.

4

Estimating the burden and economic impact of pediatric genetic disease.

Gonzaludo N, Belmont JW, Gainullin VG, Taft RJ. Gonzaludo N, et al. Genet Med. 2019 Aug;21(8):1781-1789. doi: 10.1038/s41436-018-0398-5. Epub 2018 Dec 20. Genet Med. 2019. PMID: 30568310 Free PMC article.

5

Correction: Estimating the burden and economic impact of pediatric genetic disease.

Gonzaludo N, Belmont JW, Gainullin VG, Taft RJ. Gonzaludo N, et al. Genet Med. 2019 Sep;21(9):2161. doi: 10.1038/s41436-019-0458-5. Genet Med. 2019. PMID: 30760893 Free PMC article.

6

The diagnostic trajectory of infants and children with clinical features of genetic disease.

Schroeder BE, Gonzaludo N, Everson K, Than KS, Sullivan J, Taft RJ, Belmont JW. Schroeder BE, et al. Among authors: gonzaludo n. NPJ Genom Med. 2021 Nov 22;6(1):98. doi: 10.1038/s41525-021-00260-2. NPJ Genom Med. 2021. PMID: 34811359 Free PMC article.

7

CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project.

Gaedigk A, Boone EC, Scherer SE, Lee SB, Numanagić I, Sahinalp C, Smith JD, McGee S, Radhakrishnan A, Qin X, Wang WY, Farrow EG, Gonzaludo N, Halpern AL, Nickerson DA, Miller NA, Pratt VM, Kalman LV. Gaedigk A, et al. Among authors: gonzaludo n. J Mol Diagn. 2022 Apr;24(4):337-350. doi: 10.1016/j.jmoldx.2021.12.011. Epub 2022 Feb 5. J Mol Diagn. 2022. PMID: 35134542 Free PMC article.

8

Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis.

Wong KHY, Levy-Sakin M, Ma W, Gonzaludo N, Mak ACY, Vaka D, Poon A, Chu C, Lao R, Balamir M, Grenville Z, Wong N, Kane JP, Kwok PY, Malloy MJ, Pullinger CR. Wong KHY, et al. Among authors: gonzaludo n. Mol Genet Genomic Med. 2019 Dec;7(12):e1007. doi: 10.1002/mgg3.1007. Epub 2019 Oct 16. Mol Genet Genomic Med. 2019. PMID: 31617323 Free PMC article.

9

Cost-effectiveness of genome sequencing for diagnosing patients with undiagnosed rare genetic diseases.

Incerti D, Xu XM, Chou JW, Gonzaludo N, Belmont JW, Schroeder BE. Incerti D, et al. Among authors: gonzaludo n. Genet Med. 2022 Jan;24(1):109-118. doi: 10.1016/j.gim.2021.08.015. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906478 Free article. Review.

10

HGV2012: leveraging next-generation technology and large datasets to advance disease research.

Gonzaludo N, Zheng HX, Wang J, Chanock SJ, Jin L, Scherer S, Wijmenga C, Kwok PY, Brookes AJ. Gonzaludo N, et al. Hum Mutat. 2013 Apr;34(4):657-60. doi: 10.1002/humu.22270. Hum Mutat. 2013. PMID: 23315969 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

16 results

Search Page