Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2019/02/01
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Journal
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Indian UGC (journal)
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Refrences59
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Citations34
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Jan M. Friedman
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Yvonne Bombard
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Martina C. Cornel
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Conrad V. Fernandez
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Anne K. Junker
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Sharon E. Plon
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Zornitza Stark
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Bartha Maria Knoppers
Cite
Friedman, Jan M., et al. “Genome-Wide Sequencing in Acutely Ill Infants: Genomic medicine’s Critical Application?”. Genetics in Medicine, vol. 21, no. 2, 2019, pp. 498-04, https://doi.org/10.1038/s41436-018-0055-z.
Friedman, J. M., Bombard, Y., Cornel, M. C., Fernandez, C. V., Junker, A. K., Plon, S. E., Stark, Z., & Knoppers, B. M. (2019). Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?. Genetics in Medicine, 21(2), 498-504. https://doi.org/10.1038/s41436-018-0055-z
Friedman, Jan M., Yvonne Bombard, Martina C. Cornel, Conrad V. Fernandez, Anne K. Junker, Sharon E. Plon, Zornitza Stark, and Bartha Maria Knoppers. “Genome-Wide Sequencing in Acutely Ill Infants: Genomic medicine’s Critical Application?”. Genetics in Medicine 21, no. 2 (2019): 498-504. https://doi.org/10.1038/s41436-018-0055-z.
Friedman JM, Bombard Y, Cornel MC, Fernandez CV, Junker AK, Plon SE, et al. Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?. Genetics in Medicine. 2019;21(2):498-504.
Journal Categories
Medicine
Medicine (General)
Medicine
Medicine (General)
Medical technology
Science
Biology (General)
Genetics
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Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| JAK1 gain-of-function causes an autosomal dominant immune dysregulatory and hypereosinophilic syndrome | Journal of Allergy and Clinical Immunology |
| 89 | 2017 |
| The limitations of QALY: a literature review | Journal of Stem Cell Research & Therapy | 2016 | ||
| ACCE: a model process for evaluating data on emerging genetic tests | 2003 | |||
| Methods guide for medical test reviews | 2012 | |||
| 10.17226/24632 |
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child? | Genetics in Medicine |
| 2024 | |
| Hospital-level variation in genetic testing in children’s hospitals’ neonatal intensive care units from 2016 to 2021 | Genetics in Medicine |
| 6 | 2023 |
BLEND: a fast, memory-efficient and accurate mechanism to find fuzzy seed matches in genome analysis | NAR Genomics and Bioinformatics |
| 8 | 2023 |
Whole Genome Sequencing in Era of Newborn Screening | OBM Genetics | 2023 | ||
| Measures of Utility Among Studies of Genomic Medicine for Critically Ill Infants | JAMA Network Open |
| 16 | 2022 |
Citations Analysis
The category
Science: Biology (General): Genetics 18
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled ClinGen advancing genomic data‐sharing standards as a GA4GH driver project and was published in 2018. The most recent citation comes from a 2024 study titled Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?. This article reached its peak citation in 2022, with 11 citations. It has been cited in 22 different journals, 22% of which are open access. Among related journals, the Genetics in Medicine cited this research the most, with 5 citations. The chart below illustrates the annual citation trends for this article.