A. Ghazani

发表

Determining the size and shape dependence of gold nanoparticle uptake into mammalian cells.

Arezou A Ghazani, Warren C W Chan, B Devika Chithrani, 2006, Nano letters.

Issadore Micro-Hall Detector Ultrasensitive Clinical Enumeration of Rare Cells ex Vivo Using a

David Issadore, Hakho Lee, Ralph Weissleder, 2012 .

Molecular characterization of scant lung tumor cells using iron-oxide nanoparticles and micro-nuclear magnetic resonance.

Cesar M. Castro, Hakho Lee, Amita Sharma, 2014, Nanomedicine : nanotechnology, biology, and medicine.

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories

Joshua L. Deignan, W. Chung, N. Spinner, 2016, Genetics in Medicine.

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.

Matthew S. Lebo, Aleksandar Milosavljevic, Heidi L Rehm, 2016, American journal of human genetics.

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.

Matthew S. Lebo, Aleksandar Milosavljevic, Heidi L Rehm, 2016, American journal of human genetics.

Assessing the effect of surface chemistry on gold nanorod uptake, toxicity, and gene expression in mammalian cells.

Arezou A Ghazani, Tanya S. Hauck, Warren C W Chan, 2008, Small.

Comparison of Whole Genome Amplification Methods for Analysis of DNA Extracted from Microdissected Early Breast Lesions in Formalin-Fixed Paraffin-Embedded Tissue

I. Jurisica, D. McCready, A. Ghazani, 2012, ISRN oncology.

Pathogenicity of VHL variants in families with non-syndromic von Hippel-Lindau phenotypes: An integrated evaluation of germline and somatic genomic results.

Danielle K. Manning, T. Choueiri, J. Garber, 2021, European journal of medical genetics.

Unexpected Pathogenic RET p.V804M Variant Leads to the Clinical Diagnosis and Management of Medullary Thyroid Carcinoma

J. Garber, E. Marqusee, H. Rana, 2020, The American journal of case reports.

Comparison of select cancer biomarkers in human circulating and bulk tumor cells using magnetic nanoparticles and a miniaturized micro-NMR system.

Mari Mino-Kenudson, Hakho Lee, Ralph Weissleder, 2013, Nanomedicine : nanotechnology, biology, and medicine.

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience

Yaping Yang, Katrina A B Goddard, Kathryn M Porter, 2018, Molecular genetics & genomic medicine.

An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes

Danielle K. Manning, J. Garber, H. Rana, 2022, Frontiers in Oncology.

Erratum: Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716300593) (10.1016/j.ajhg.2016.03.024))

Robert C. Green, Michael O. Dorschner, Matthew S. Lebo, 2016 .

An optimized protocol for evaluating pathogenicity of VHL germline variants in patients suspected with von Hippel-Lindau syndrome: Using somatic genome to inform the role of germline variants

Danielle K. Manning, J. Garber, N. Lindeman, 2022, MethodsX.

Concurrent Pathogenic Variants of BRCA1, MUTYH and CHEK2 in a Hereditary Cancer Family.

H. Rana, A. Ghazani, J. Yıldız, 2022, Cancer genetics.

Miniaturized nuclear magnetic resonance platform for detection and profiling of circulating tumor cells.

David Issadore, Hakho Lee, Ralph Weissleder, 2014, Lab on a chip.

The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine

Nikhil Wagle, Amaro Taylor-Weiner, Brendan Reardon, 2016, Genome Medicine.

Real-time Genomic Characterization of Advanced Pancreatic Cancer to Enable Precision Medicine.

Nicholas D. Camarda, Jeffrey W. Miller, W. Hahn, 2018, Cancer discovery.

High throughput Detection of Molecular Targets in Cancer Using Nanoparticles: Application in Diagnostics

A. Ghazani, 2009 .

Assessment of genomic alterations in non-syndromic von Hippel-Lindau: Insight from integrating somatic and germline next generation sequencing genomic data.

Danielle K. Manning, J. Garber, N. Lindeman, 2021, Data in brief.

Novel Pathogenic Germline Variant of the Adenomatous Polyposis Coli (APC) Gene, p.S2627Gfs*12 Identified in a Mild Phenotype of APC-Associated Polyposis: A Case Report

Danielle K. Manning, J. Garber, N. Lindeman, 2020, The American journal of case reports.

Limited tissue fixation times and whole genomic amplification do not impact array CGH profiles

A. Ghazani, N. Arneson, S. Done, 2006, Journal of Clinical Pathology.

Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study

Carrie Cibulskis, Nikhil Wagle, Steven Joffe, 2017, Genetics in Medicine.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2018, Genetics in Medicine.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2019, Genetics in Medicine.

Ultrasensitive Clinical Enumeration of Rare Cells ex Vivo Using a Micro-Hall Detector

Cesar M. Castro, Hakho Lee, Jaehoon Chung, 2012, Science Translational Medicine.

Vulvar Melanoma in association with germline MITF p.E318K variant.

J. Garber, N. Lindeman, H. Rana, 2022, Cancer genetics.

Point of care assessment of melanoma tumor signaling and metastatic burden from μNMR analysis of tumor fine needle aspirates and peripheral blood.

Hakho Lee, R. Weissleder, R. Sullivan, 2017, Nanomedicine : nanotechnology, biology, and medicine.

Genomic alterations in sporadic synchronous primary breast cancer using array and metaphase comparative genomic hybridization.

J. Squire, M. Pintilie, J. Bayani, 2007, Neoplasia.

High throughput quantification of protein expression of cancer antigens in tissue microarray using quantum dot nanocrystals.

Arezou A Ghazani, Brian C Wilson, Warren C W Chan, 2006, Nano letters.

Cellular imaging and surface marker labeling of hematopoietic cells using quantum dot bioconjugates.

Arezou A Ghazani, Warren C W Chan, Sawitri Mardyani, 2006, Laboratory hematology : official publication of the International Society for Laboratory Hematology.

AnFiSA: An open-source computational platform for the analysis of sequencing data for rare genetic disease

S. Sunyaev, C. Morton, M. Bouzinier, 2021, medRxiv.

Sensitive and direct detection of circulating tumor cells by multimarker µ-nuclear magnetic resonance.

Hakho Lee, Ralph Weissleder, Arezou A Ghazani, 2012, Neoplasia.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2019, Genetics in Medicine.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, K. Goddard, L. Hindorff, 2018, Genetics in Medicine.

Development and evaluation of INT2GRATE: a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome

H. Rana, L. Sholl, A. Ghazani, 2024, Frontiers in oncology.