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        <title>Cassa Lab</title>
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        <dc:date>2018-04-05T21:44:33+00:00</dc:date>
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        <title>Contact Information</title>
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        <description>Contact Information


Harvard Medical School New Research Building
Brigham and Women’s Hospital, Division of Genetics
77 Avenue Louis Pasteur, Room 464
Boston, MA 02115ccassa _at_ hms.harvard.edu
Phone: 617-525-4757
Fax:   617-525-4705</description>
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        <dc:date>2024-09-12T19:20:47+00:00</dc:date>
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        <title>Opportunities</title>
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        <description>Opportunities

Graduate Students

We currently have openings for funded graduate student positions, for individuals who are already admitted to a graduate program at Harvard Medical School within the Harvard Integrated Life Science programs, or Harvard University. Please email CV and statement of interest to ccassa@bwh.harvard.edu.</description>
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        <dc:date>2026-03-02T23:55:58+00:00</dc:date>
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        <title>Selected Recent Publications</title>
        <link>https://genetics.bwh.harvard.edu/wiki/!cassa/publications?rev=1772495758&amp;do=diff</link>
        <description>Selected Recent Publications
Cassa CA&lt;https://doi.org/10.64898/2026.02.28.26347206&gt;Cassa C&lt;https://doi.org/10.1101/2024.12.31.24319792&gt;Cassa CACassa CA&lt;https://doi.org/10.1016/j.xgen.2024.100667&gt;&lt;https://doi.org/10.1038/s41588-024-01726-6&gt;Cassa CACassa CA&lt;https://doi.org/10.1101/2023.01.06.23284281&gt;Cassa, CA&lt;https://t.co/mOD0P53Ppn&gt;Cassa CA&lt;https://doi.org/10.1016/j.xgen.2023.100304&gt;Cassa CA*, &lt;https://elifesciences.org/articles/74970&gt;&lt;https://doi.org/10.7554/eLife.74970&gt;Cassa CA&lt;https://doi.org…</description>
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        <dc:date>2016-08-15T20:27:47+00:00</dc:date>
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        <title>Research</title>
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        <description>Research

The Cassa Research Group conducts predictive analytic research in two major application areas: the pathogenicity assessment of genomic variants and the clinical application of predictive algorithms in genomics. These applications draw on approaches to enable unprecedented extraction of information from existing data sources.</description>
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        <description>Clintegrate: Integrated predictions of clinical risk 

Clintegrate provides clinical risk assessments that are personalized for individuals who carry genetic variants in well-known disease genes such as BRCA1 and LDLR. Many healthy people carry genetic variants in these disease genes, yet the risk of developing the related disorder is low for most of them.</description>
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        <title>Home</title>
        <link>https://genetics.bwh.harvard.edu/wiki/!cassa/start?rev=1675115941&amp;do=diff</link>
        <description>Home

Research

Our research group studies the statistical genetics of Mendelian disorders. We focus on two major application areas: methods to assess the pathogenicity of individual genomic variants, and methods to predict the clinical impact of such variants in the context of an individual&#039;s existing clinical and genetic risk factors.</description>
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