Pedram Razavi

ORCID: 0000-0003-4236-0576
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About
Contact & Profiles
Research Areas
  • Cancer Genomics and Diagnostics
  • Advanced Breast Cancer Therapies
  • Advancements in Semiconductor Devices and Circuit Design
  • Semiconductor materials and devices
  • Lung Cancer Treatments and Mutations
  • Genetic factors in colorectal cancer
  • HER2/EGFR in Cancer Research
  • PI3K/AKT/mTOR signaling in cancer
  • Nanowire Synthesis and Applications
  • Lung Cancer Research Studies
  • Breast Cancer Treatment Studies
  • Pancreatic and Hepatic Oncology Research
  • Metabolism, Diabetes, and Cancer
  • Protein Degradation and Inhibitors
  • Cancer-related Molecular Pathways
  • Histone Deacetylase Inhibitors Research
  • Multiple and Secondary Primary Cancers
  • Estrogen and related hormone effects
  • BRCA gene mutations in cancer
  • Cancer Treatment and Pharmacology
  • COVID-19 and healthcare impacts
  • Epigenetics and DNA Methylation
  • Integrated Circuits and Semiconductor Failure Analysis
  • Cancer Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research

Memorial Sloan Kettering Cancer Center
2016-2025

Cornell University
2017-2024

Kettering University
2016-2024

University of California, San Diego
2021-2023

Weill Cornell Medicine
2022

Moores Cancer Center
2021

Icahn School of Medicine at Mount Sinai
2020

Eli Lilly (United States)
2020

Faculty of 1000 (United States)
2020

ORCID
2020

Ahmet Zehir Ryma Benayed Ronak Shah Aijazuddin Syed Sumit Middha and 95 more Hyunjae R. Kim Preethi Srinivasan Jianjiong Gao Debyani Chakravarty Sean M. Devlin Matthew D. Hellmann David Barron Alison M. Schram Meera Hameed Snjezana Doğan Dara S. Ross Jaclyn F. Hechtman Deborah F. DeLair JinJuan Yao Diana Mandelker Donavan T. Cheng Raghu Chandramohan Abhinita Mohanty Ryan Ptashkin Gowtham Jayakumaran Meera Prasad Mustafa Syed Anoop Balakrishnan Rema Zhen Y. Liu Khédoudja Nafa Laetitia Borsu Justyna Sadowska Jacklyn Casanova Ruben Bacares Iwona Kiecka Anna Razumova Julie B Son Lisa Stewart Tessara Baldi Kerry Mullaney Hikmat Al‐Ahmadie Efsevia Vakiani Adam Abeshouse Alexander Penson Philip Jonsson Niedzica Camacho Matthew T. Chang Helen Won Benjamin Groß Ritika Kundra Zachary Heins Hsiao‐Wei Chen Sarah Phillips Hongxin Zhang Jiaojiao Wang Angelica Ochoa Jonathan Wills Michael Eubank Stacy B. Thomas Stuart M. Gardos Dalicia N. Reales Jesse Galle Robert Durany Roy Cambria Wassim Abida Andrea Cercek Darren R. Feldman Mrinal M. Gounder A. Ari Hakimi James J. Harding Gopa Iyer Yelena Y. Janjigian Emmet Jordan Ciara M. Kelly Maeve A. Lowery Luc G.T. Morris Antonio Omuro Nitya Raj Pedram Razavi Alexander N. Shoushtari Neerav Shukla Tara E. Soumerai Anna M. Varghese Rona Yaeger Jonathan Coleman Bernard H. Bochner Gregory J. Riely Leonard B. Saltz Howard I. Scher Paul Sabbatini Mark E. Robson David S. Klimstra Barry S. Taylor José Baselga Nikolaus Schultz David M. Hyman Maria E. Arcila David B. Solit Marc Ladanyi Michael F. Berger

10.1038/nm.4333 article EN Nature Medicine 2017-05-08

<para xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"> This paper investigates the temperature dependence of main electrical parameters junctionless (JL) silicon nanowire transistors. Direct comparison is made to (trigate) MOSFETs. Variation such as threshold voltage and <emphasis emphasistype="smcaps">on</emphasis>– emphasistype="smcaps">off</emphasis> current characteristics analyzed. The JL FET has a lager variation with than standard inversion-...

10.1109/ted.2009.2039093 article EN IEEE Transactions on Electron Devices 2010-01-29

Abstract Most mutations in cancer are rare, which complicates the identification of therapeutically significant and thus limits clinical impact genomic profiling patients with cancer. Here, we analyzed 24,592 cancers including 10,336 prospectively sequenced advanced disease to identify mutant residues arising more frequently than expected absence selection. We identified 1,165 statistically hotspot 80% arose 1 1,000 or fewer patients. Of 55 recurrent in-frame indels, validated that novel...

10.1158/2159-8290.cd-17-0321 article EN Cancer Discovery 2017-12-16

Abstract Recent studies have identified somatic ESR1 mutations in patients with metastatic breast cancer and found some of them to promote estrogen-independent activation the receptor. The degree which all recurrent mutants can drive activities reduced sensitivity ER antagonists like fulvestrant is not established. In this report, we characterize spectrum from more than 900 patients. were detected 10%, D538G being most frequent (36%), followed by Y537S (14%). Several novel, activating also...

10.1158/2159-8290.cd-15-1523 article EN Cancer Discovery 2016-12-17

The electric field perpendicular to the current flow is found be significantly lower in junctionless transistors than regular inversion-mode or accumulation-mode field-effect transistors. Since inversion channel mobility metal-oxide-semionductor reduced by this field, low transistor may give them an advantage terms of drive for nanometer-scale complementary metal-oxide semiconductor applications. This observation still applies when quantum confinement present.

10.1063/1.3299014 article EN Applied Physics Letters 2010-02-15

This paper presents the evaluation of analog properties nMOS junctionless (JL) multigate transistors, comparing their performance with those exhibited by inversion-mode (IM) trigate devices similar dimensions. The study has been performed for operating in saturation as single-transistor amplifiers, and we have considered dependence on fin width <i xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">W</i> <sub...

10.1109/ted.2011.2157826 article EN IEEE Transactions on Electron Devices 2011-06-29

Seeing double can be a good thing Many human breast cancers harbor activating mutations in PIK3CA , the gene coding for catalytic subunit of phosphoinositide 3-kinase (PI3K). Clinical trials are underway to evaluate efficacy PI3K inhibitors cancer patients. Vasan et al. found unexpectedly that subset not one—but two— mutations, and occur on same allele (see Perspective by Toker). In model systems, hyperactivate signaling enhance tumor growth. Preliminary analysis clinical trial data suggests...

10.1126/science.aaw9032 article EN Science 2019-11-08

Amplification of and oncogenic mutations in ERBB2, the gene encoding HER2 receptor tyrosine kinase, promote hyperactivation tumor growth. Here we demonstrate that ubiquitination internalization, rather than its overexpression, are key mechanisms underlying endocytosis consequent efficacy anti-HER2 antibody-drug conjugates (ADC) ado-trastuzumab emtansine (T-DM1) trastuzumab deruxtecan (T-DXd) lung cancer cell lines patient-derived xenograft models. These data translated into a 51% response...

10.1158/2159-8290.cd-20-0215 article EN Cancer Discovery 2020-03-25

Cyclin-dependent kinases 4 and 6 (CDK4/6) represent a major therapeutic vulnerability for breast cancer. The are clinically targeted via ATP competitive inhibitors (CDK4/6i); however, drug resistance commonly emerges over time. To understand CDK4/6i resistance, we surveyed 1,300 cancers identified several genetic alterations (e.g., FAT1, PTEN, or ARID1A loss) converging on upregulation of CDK6. Mechanistically, demonstrate CDK6 causes by inducing binding CDK inhibitor INK4 proteins...

10.1158/2159-8290.cd-20-1726 article EN cc-by-nc-nd Cancer Discovery 2021-09-20

Circulating cell-free DNA from blood plasma of cancer patients can be used to non-invasively interrogate somatic tumor alterations. Here we develop MSK-ACCESS (Memorial Sloan Kettering - Analysis cfDNA Examine Somatic Status), an NGS assay for detection very low frequency alterations in 129 genes. Analytical validation demonstrated 92% sensitivity de-novo mutation calling down 0.5% allele and 99% a priori profiling. To evaluate the performance MSK-ACCESS, report results 681 prospective...

10.1038/s41467-021-24109-5 article EN cc-by Nature Communications 2021-06-18

Public neoantigens (NeoAgs) represent an elite class of shared cancer-specific epitopes derived from recurrently mutated driver genes. Here we describe a high-throughput platform combining single-cell transcriptomic and T cell receptor (TCR) sequencing to establish whether mutant PIK3CA, among the most frequently genomically altered oncogenes, generates immunogenic public NeoAg. Using this strategy, developed panel TCRs that recognize endogenously processed neopeptide encompassing common...

10.1038/s41591-022-01786-3 article EN cc-by Nature Medicine 2022-04-28

Conduction mechanisms in junctionless nanowire transistors (gated resistors) are compared to inversion-mode and accumulation-mode MOS devices. The device uses bulk conduction instead of surface channel. current drive is controlled by doping concentration not gate capacitance. variation threshold voltage with physical parameters intrinsic performance analyzed. A scheme proposed for the fabrication devices on silicon.

10.1109/essderc.2010.5618216 article EN Proceedings of the European Solid State Device Research Conference 2010-09-01
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