Projects per year
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ASSOCIATE PROFESSOR | Medicine, Medical Genomics ASSOCIATE PROFESSOR | Genetics and Genomic Sciences
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Dive into the research topics where Noura Abul-Husn is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Projects
- 2 Active
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Uncovering early signals of hereditary TTR amyloidosis in minority populations at high genetic risk
Abul-Husn, N., Abul-husn, N. S., Kontorovich, A. A. R. & Kontorovich, A.
National Heart, Lung, and Blood Institute
1/04/21 → 31/03/23
Project: Research
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Genomic risk in clinic care to promote health equity in New York City patients
Kenny, E., Abul-Husn, N., Cho, J. H., Kenny, E. E., Murphy, B. T. & Abul-husn, N. N. S.
National Human Genome Research Institute
1/07/20 → 30/04/23
Project: Research
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Diverse and unselected adults with clinically relevant ACADS variants lack evidence of metabolic disease
Breilyn, M. S., Kenny, E. E. & Abul-Husn, N. S., Jan 2023, In: Molecular Genetics and Metabolism. 138, 1, 106971.Research output: Contribution to journal › Article › peer-review
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ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
ACMG Secondary Findings Working Group, Jul 2022, In: Genetics in Medicine. 24, 7, p. 1407-1414 8 p.Research output: Contribution to journal › Editorial
Open Access13 Scopus citations -
Addressing the routine failure to clinically identify monogenic cases of common disease
Murray, M. F., Khoury, M. J. & Abul-Husn, N. S., Dec 2022, In: Genome Medicine. 14, 1, 60.Research output: Contribution to journal › Comment/debate
Open Access -
CDH1 pathogenic variants and cancer risk in an unselected patient population
Bar-Mashiah, A., Soper, E. R., Cullina, S., Belbin, G. M., Kenny, E. E., Lucas, A. L. & Abul-Husn, N. S., Apr 2022, In: Familial Cancer. 21, 2, p. 235-239 5 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Detection of mosaic variants using genome sequencing in a large pediatric cohort
Odgis, J. A., Gallagher, K. M., Rehman, A. U., Marathe, P. N., Bonini, K. E., Sebastin, M., Di Biase, M., Brown, K., Kelly, N. R., Ramos, M. A., Thomas-Wilson, A., Guha, S., Okur, V., Ganapathi, M., Elkhoury, L., Edelmann, L., Zinberg, R. E., Abul-Husn, N. S., Diaz, G. A., Greally, J. M., & 6 others, 2022, (Accepted/In press) In: American Journal of Medical Genetics, Part A.Research output: Contribution to journal › Article › peer-review
Press / Media
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New Antihyperlipidemic Agents Findings Has Been Reported by Investigators at Icahn School of Medicine at Mount Sinai (Prescriber Adoption of Slco1b1 Genotype-guided Simvastatin Clinical Decision Support In a Clinical Pharmacogenetics Program)
Stuart Scott, Eva Waite, Noura Abul-Husn & Aniwaa Owusu Obeng
16/12/22
1 item of Media coverage
Press/Media
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Genetic Tests Can Identify Breast Cancer Risk. Why Is It So Hard to Interpret the Results?
1/12/22
1 item of Media coverage
Press/Media
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