Risultati della ricerca - Nathanson, Katherine

Using genetics and genomics strategies to personalize therapy for cancer: focus on melanoma di Nathanson, Katherine L.

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Pheochromocytoma and Paraganglioma: Understanding the Complexities of the Genetic Background di Fishbein, Lauren, Nathanson, Katherine L.

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Molecular Testing in Melanoma di Wilson, Melissa Ann, Nathanson, Katherine L.

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Hereditary Renal Cancer Syndromes di Haas, Naomi B., Nathanson, Katherine L.

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Common breast cancer risk variants in the post-COGS era: a comprehensive review di Maxwell, Kara N, Nathanson, Katherine L

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Genetic Changes Associated with Testicular Cancer Susceptibility di Pyle, Louise C., Nathanson, Katherine L.

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A Practical Guide for Evaluating Gonadal Germ Cell Tumor Predisposition in Differences of Sex Development di Pyle, Louise C., Nathanson, Katherine L.

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Resolving ATM Haplotypes in Whites di Letrero, Richard, Weber, Barbara L., Nathanson, Katherine L.

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Two Decades After BRCA: Setting Paradigms in Personalized Cancer Care and Prevention di Couch, Fergus J., Nathanson, Katherine L., Offit, Kenneth

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Biallelic TSC gene inactivation in tuberous sclerosis complex di Crino, Peter B., Aronica, Eleonora, Baltuch, Gordon, Nathanson, Katherine L.

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Filaggrin sequencing and bioinformatics tools di Margolis, David J., Mitra, Nandita, Wubbenhorst, Bradley, Nathanson, Katherine L.

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Genomic Biomarkers for Breast Cancer Risk di Walsh, Michael F., Nathanson, Katherine L., Couch, Fergus J., Offit, Kenneth

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ALLELE-SPECIFIC COPY NUMBER ESTIMATION BY WHOLE EXOME SEQUENCING di Chen, Hao, Jiang, Yuchao, Maxwell, Kara N., Nathanson, Katherine L., Zhang, Nancy

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From Race-Based to Precision Oncology: Leveraging Behavioral Economics and the Electronic Health Record to Advance Health Equity in Cancer Care di Lau-Min, Kelsey S., Guerra, Carmen E., Nathanson, Katherine L., Bekelman, Justin E.

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Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing di Fishbein, Lauren, Merrill, Shana, Fraker, Douglas L., Cohen, Debbie L., Nathanson, Katherine L.

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HNPCC-Associated Pheochromocytoma: Expanding the Tumor Spectrum di Riff, Brian P., Katona, Bryson, Wilkerson, Myra, Nathanson, Katherine L., Metz, David C.

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A Practical Approach to Adjusting for Population Stratification in Genome-wide Association Studies: Principal Components And Propensity Scores (PCAPS) di Zhao, Huaqing, Mitra, Nandita, Kanetsky, Peter A., Nathanson, Katherine L., Rebbeck, Timothy R.

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Using a Machine Learning Approach to Identify Low-Frequency and Rare FLG Alleles Associated with Remission of Atopic Dermatitis di Berna, Ronald, Mitra, Nandita, Hoffstad, Ole, Wubbenhorst, Bradley, Nathanson, Katherine L., Margolis, David J.

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Uncommon variants in FLG2 and TCHHL1 are associated with remission of atopic dermatitis in a large longitudinal US cohort di Berna, Ronald, Mitra, Nandita, Hoffstad, Ole, Wubbenhorst, Bradley, Nathanson, Katherine L., Margolis, David J.

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CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing di Jiang, Yuchao, Wang, Rujin, Urrutia, Eugene, Anastopoulos, Ioannis N., Nathanson, Katherine L., Zhang, Nancy R.

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