Nathalie Chami

One Gustave L. Levy Place
10029-6574 New York
United States

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23 Article
2 Review article
1 Comment/debate

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
The BioBank Japan Project, Regeneron Genetics Center & DBDS Genomic Consortium, Mar 2025, In: Nature Genetics. 57, 3, p. 539-547 9 p., 11303.
Research output: Contribution to journal › Article › peer-review
13 Scopus citations
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, 11 Apr 2025, In: Nature Communications. 16, 1, p. 3470 1 p.
Research output: Contribution to journal › Article › peer-review
1 Scopus citations
Determinants of mosaic chromosomal alteration fitness
Pershad, Y., Mack, T., Poisner, H., Jakubek, Y. A., Stilp, A. M., Mitchell, B. D., Lewis, J. P., Boerwinkle, E., Loos, R. J. F., Chami, N., Wang, Z., Barnes, K., Pankratz, N., Fornage, M., Redline, S., Psaty, B. M., Bis, J. C., Shojaie, A., Silverman, E. K. & Cho, M. H. & 24 others, Yun, J. H., DeMeo, D., Levy, D., Johnson, A. D., Mathias, R. A., Taub, M. A., Arnett, D., North, K. E., Raffield, L. M., Carson, A. P., Doyle, M. F., Rich, S. S., Rotter, J. I., Guo, X., Cox, N. J., Roden, D. M., Franceschini, N., Desai, P., Reiner, A. P., Auer, P. L., Scheet, P. A., Jaiswal, S., Weinstock, J. S. & Bick, A. G., Dec 2024, In: Nature Communications. 15, 1, 3800.
Research output: Contribution to journal › Article › peer-review
5 Scopus citations
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2024, In: Nature Communications. 15, 1, 8549.
Research output: Contribution to journal › Article › peer-review
12 Scopus citations
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, 27 Apr 2023, In: Nature. 616, 7958, p. 755-763 9 p.
Research output: Contribution to journal › Article › peer-review

Open Access
61 Scopus citations

Recent Research from Broad Institute Highlight Findings in Atrial Fibrillation (Meta-analysis of Genome-wide Associations and Polygenic Risk Prediction for Atrial Fibrillation In More Than 180,000 Cases)
Smit, R. & Chami, N.
28/04/25
1 item of Media coverage
Press/Media
Broad Institute of Harvard & MIT Reports Findings in Life Science (A Statistical Framework for Multi-trait Rare Variant Analysis In Large-scale Whole-genome Sequencing Studies)
Kenny, E., Chami, N. & Nadkarni, G.
4/04/25
1 item of Media coverage
Press/Media

Nathalie Chami

Fingerprint

Collaborations and top research areas from the last five years

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Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

Determinants of mosaic chromosomal alteration fitness

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Recent Research from Broad Institute Highlight Findings in Atrial Fibrillation (Meta-analysis of Genome-wide Associations and Polygenic Risk Prediction for Atrial Fibrillation In More Than 180,000 Cases)

Broad Institute of Harvard & MIT Reports Findings in Life Science (A Statistical Framework for Multi-trait Rare Variant Analysis In Large-scale Whole-genome Sequencing Studies)

Nathalie Chami

Fingerprint

Collaborations and top research areas from the last five years

Research output

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

Determinants of mosaic chromosomal alteration fitness

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Press/Media

Recent Research from Broad Institute Highlight Findings in Atrial Fibrillation (Meta-analysis of Genome-wide Associations and Polygenic Risk Prediction for Atrial Fibrillation In More Than 180,000 Cases)

Broad Institute of Harvard & MIT Reports Findings in Life Science (A Statistical Framework for Multi-trait Rare Variant Analysis In Large-scale Whole-genome Sequencing Studies)