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Amal Yussuf

Ambry Genetics (United States)(US)

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64

Papers

1.4K

Citations

15

h-index

21

i10-index

Amal Yussuf is an academic researcher from Ambry Genetics (United States). The author has contributed to research in topics: BRCA gene mutations in cancer & Genetic factors in colorectal cancer & Cancer Genomics and Diagnostics. The author has an h-index of 15, co-authored 55 publications.

ORCID: 0000-0002-7876-2713

Research Topics

BRCA gene mutations in cancer Genetic factors in colorectal cancer Cancer Genomics and Diagnostics Genomic variations and chromosomal abnormalities Genomics and Rare Diseases

Papers by this author

works

A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients

2019 · Genetics in Medicine · 212 citations

https://doi.org/10.1038/s41436-019-0633-8

Holly LaDuca Eric C. Polley Amal Yussuf Lily Hoang

Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer

2020 · JNCI Journal of the National Cancer Institute · 36 citations

https://doi.org/10.1093/jnci/djaa167

Siddhartha Yadav Holly LaDuca Eric C. Polley Chunling Hu

Suggested application of HER2+ breast tumor phenotype for germline <i>TP53</i> variant classification within ACMG/AMP guidelines

2020 · Human Mutation · 22 citations

https://doi.org/10.1002/humu.24060

Cristina Fortuño Jessica L. Mester Tina Pesaran Jeffrey N. Weitzel

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

2025 · Nature Communications · 10 citations

https://doi.org/10.1038/s41467-025-57077-1

Anton Safonov Tomoki Nomakuchi Elizabeth Chao Carolyn Horton

An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance

2022 · npj Genomic Medicine · 5 citations

https://doi.org/10.1038/s41525-022-00302-3

Edwin S. Iversen Gary Lipton Steven N. Hart Kun Y. Lee

Data from Functional and clinical characterization of variants of uncertain significance identifies a hotspot for inactivating missense variants in RAD51C

2024 · 0 citations

https://doi.org/10.1158/0008-5472.c.6769332.v2

Chunling Hu Anil Belur Nagaraj Hermela Shimelis Gemma Montalban

Research topics

topics

BRCA gene mutations in cancer

Genetic factors in colorectal cancer

Cancer Genomics and Diagnostics

Genomic variations and chromosomal abnormalities

Genomics and Rare Diseases

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