With a focus on translational medicine, the Institutes at the Icahn School of medicine at Mount Sinai facilitate interactions within and across disciplines in order to advance research, ensure quality education, and promote breakthroughs in clinical care.
For inquiries about research collaboration please contact James Faghmous, PhD.
Mount Sinai’s strategic plan provides a road map for major investments in research and infrastructure to establish a series of new Institutes, including The Charles Bronfman Institute for Personalized Medicine (IPM).
The Institute is dedicated to advancing personalized health and health care with three core objectives:
- Provide clinical and translational investigators with greater and easier access to high quality, standardized biospecimen collections, linked with full clinical information.
- Provide an academic research home and technology support for discovering clinically important genotype-phenotype associations through interdisciplinary, translational genomics programs.
- Facilitate clinical development of gene-based diagnostics and risk assessment algorithms and evaluate their impact on health care delivery at the patient and population level.
IPM is home to research faculty pursuing studies in the clinical areas of pharmacogenomics, obesity and metabolic traits, cardiovascular and kidney disease. Institute faculty generates innovations and new paradigms in mapping of complex traits in diverse populations, clinical knowledge representation and phenomics, and personalized medicine clinical decision support.
Headed by Judy Cho,MD, IPM provides full and sole support for the IPM BioMe Biobank Program including the Biobank Informatics and Genomic Data Analysis Services Center (BIGDASC).
BioMe™ Biobank Program
To discover better treatments, researchers are seeking to unravel the complexity of disease at the most basic level through “molecular” studies. The donation of samples from many thousands of individuals is essential to such studies. BioMe is a biobank program of the Charles Bronfman Institute for Personalized Medicine at Mount Sinai. BioMe is dedicated to advancing the application of human blood-derived biospecimen and clinical data to life science research to accelerate the development of personalized healthcare and medical solutions.
Since September 2007, over 33,000 Mount Sinai Health System patients have enrolled in the Electronic Medical Record-linked BioMe Biobank Program. It is designed to generate a large collection of DNA and plasma samples, and phenotypic (questionnaire-based and EMR-linked) and genomic data, that are stored in a way that protects patient’s privacy. The three major self-reported racial/ethnic populations include 32% EA (European Ancestry), 24% AA (African Ancestry, 35% HA (Hispanic Ancestry). At the same time, it enables research to be performed on de-identified, comprehensive, electronic clinical information extracted from the Mount Sinai Data Warehouse (MSDW).
IPM represents Mount Sinai as a member site to several large NIH-funded research networks, including the IGNITE Implementing GeNomics In pracTicE Network, Population Architecture Using Genomics and Epidemiology (PAGE), Phase II, eMERGE II Network (electronic medical records and genomics), the eMERGE-Pharmacogenetics Research Network (PGRN) research partnership, the CKD Biomarker Consortium, among others.
The BioMe Biobank Program contributes under collaborative agreements with international research consortia and collaborations, including:
- GIANT (Genetic Investigation of Anthropometric Traits) – GWAS data contributed for discovery analysis for anthropometric traits from all BioMe™ participants and workgroup participation
- COGENT BP (Continental Origins and Genetic Epidemiology Network) – GWAS data for BP from African American BioMe™ participants contributed for discovery analysis
- GHBP (Genomics in Hispanics for Blood Pressure) – GWAS data for BP from Hispanics contributed for discovery analysis
- Massachusetts Institute of Technology Computer Science and Artificial Intelligence Laboratory (John Guttag): Predictive Modelling and Personalized Health Decision Support Tools
- Genetics of Obesity and related traits in African Americans – GWAS data of BMI from African Americans BioMe™ participants contributed for discovery and follow up analysis and workgroup participation
- African American Type 2 Diabetes Genetics Consortium – GWAS data of T2D from African American BioMe™ participants contributed for analysis
- CHARGE (Cohorts for Heart and Aging Research In Genomic Epidemiology) – Exome chip date contributed for analysis of BP from all BioMe™ participants
- CKDGen (CKD Genetics Consortium) – GWAS data contributed for discovery analysis and workgroup participation
- CKDGen (CKD Genetics Consortium) – Exome chip data contributed for analysis of BP from all BioMe™ participants
- GLGC (Global Lipids Genetics Consortium) – Exome chip data contributed for discovery analysis of all lipids from all BioMe™ participants
- GLGC (Global Lipids Genetics Consortium) – Exome chip data contributed for follow-up analysis of CAD from all African American BioMe™ participants
- ESP-LDL (Exome Sequencing Projects LDL Cholesterol) – Exome chip data contributed for follow-up analysis of LDL from all BioMe™ participants
- MAGIC (Meta-Analyses of Glucose and Insulin-related traits Consortium) – Exome chip data contributed for discovery analysis of HbA1c from all BioMe™ participants
- CHARGE (Cohorts for Heart and Aging Research In Genomic Epidemiology) – Exome chip data contributed for discovery analysis of Glycaemic traits from all BioMe™ participants
- CHARGE (Cohorts for Heart and Aging Research In Genomic Epidemiology) – Exome chip data contributed for follow-up analysis of Amyloidoses from all BioMe™ participants
- MEDIA MEta-analysis of type 2 DIabetes in African Americans (MEDIA) Consortium – GWAS data contributed for discovery analysis of T2D from African American BioMe™ participants.
- TranscenD (TRANS-ethnic Evaluation of vitamin D) – GWAS data contributed for discovery analysis of Vitamin D from all BioMe™ participants.
- Lipids in HA – GWAS data contributed for discovery analysis of Lipids from all Hispanic American BioMe™ participants.
- AAGILE (African American Glucose and Insulin Genetic Epidemiology (AAGILE) Consortium) – GWAS data contributed for discovery analysis of HbA1c and glucose from all African American BioMe™ participants.
- DIAGRAM+ and GOT2D (Genetics of Type 2 Diabetes) – GWAS data contributed for follow-up analysis of T2D from all BioMe™ participants.
- BP in HA GWAS data contributed for discovery analysis of BP from all Hispanic American BioMe™ participants.
- ICBP (International Consortium for Blood Pressure) – GWAS data contributed for discovery analysis of BP from all European American BioMe™ participants.
- Anthropometric Traits in HA – GWAS data contributed for discovery analysis of Anthropometric Traits from all Hispanic American BioMe™ participants.
- T2D Genes – Targeted sequencing for follow-up analysis of T2D from all European American BioMe™ participants.
Visit the Charles Bronfman Institute for Personalized Medicine or email the Charles Bronfman Institute for Personalized Medicine for more information.
Last Updated: January 28, 2016
The mission of the Mindich Child Health and Development Institute (MCHDI) is to enable translational research of diseases affecting infants, children and adolescents by assembling outstanding physician-scientists and scientists in an intellectually rich and supportive environment, which fosters collaborative scientific investigation as well as the training of the next generation of scientific leaders for pediatric medicine.
The MCHDI is dedicated to translational research with an emphasis on genomic and environmental studies to better understand the pathogenesis of prevalent pediatric conditions and diseases. Leveraging Mount Sinai's leadership in genetics and genomics sciences, as well as environmental medicine, the MCHDI has focused on the following areas of research emphasis to maximize its impact on new discoveries:
- Asthma and Allergy
- Cardiovascular Diseases
- Neurodevelopmental Disorders
- Obesity and Diabetes
- Other Childhood Diseases
Last Update: September 24, 2015
ConduITS the Institutes for Translational Sciences was established in 2009 when Mount Sinai received a prestigious Clinical and Translational Science Award (CTSA) from the National Institutes of Health. To read more, please visit ConduITS.
Center for Therapeutic Antibody Development
The Center for Therapeutic Antibody Development (CTAD) offers assistance and expertise to investigators requesting the preparation of monoclonal antibodies to a desired antigen. The monoclonal antibodies can be made in mouse model systems or using human blood and a baiting system. The hybridoma production includes the immunization of animals, cell fusions, screening via ELISA, cloning, isotyping, and cryopreservation. The facility also offers peptide linkage to carrier molecules, genetic immunizations, additional screening options such as transient transfection immunostaining, and large-scale growth of hybridoma supernatant for antibody purification. Antibodies are generated using a protein or peptides antigen for immunization or by using only the DNA encoding the protein (genetic immunizations) or by viruses expressing proteins of interest on their surfaces. CTAD specializes in the production of mAb to cell surface proteins including GPCRs. Unique strategies for production of this type of antibody have been developed in CTAD.
Last Update: September 23, 2015
Medicinal Chemistry Core
The Medicinal Chemistry Program of the Experimental Therapeutics Institute aims to become a resource available to basic and clinical research investigators at Mount Sinai who are interested in employing small molecule chemistry to furnish research tools or to develop new experimental small molecule therapeutics. Chemists in the Program will be operating in a newly renovated medicinal chemistry laboratory space located in the Icahn Medical Institute Building and in an environment conducive to interdisciplinary research, for example with biophysical (x-ray, NMR) and computational researchers; this capitalizes on existing strengths within Icahn School of Medicine.
To initiate the search for novel small molecule agents, research groups will run HTS assays in conjunction with the ETI’s Translational Chemical Biology Center. The Center’s compound collection currently comprises approximately 115,000 lead-like small molecule compounds (see the TCBC description for details) and when screening hits have been identified medicinal chemists will be available to work collaboratively with the research teams in three progressively more interdisciplinary phases:
- Hit confirmation and resupply - Data from an HTS campaign will be triaged to eliminate false positives or artifacts: compound purity from the active wells will be assessed, and material re-synthesized, scaled-up and purified. Hit compounds may then be interrogated in detail in the screening assay or other follow-up assays as appropriate to confirm useful levels of activity.
- Hit to Lead Chemistry - Confirmed hits will then be assessed and ranked based on a number of factors in addition to potency, particularly chemical tractability. A chemically tractable lead will be of reasonably low molecular weight structure (<500 Da), which is amenable to rapid analog synthesis to facilitate exploration of structure activity relationships. Depending on the molecular type additional analogs may be available from commercial sources, or parallel libraries will be designed and synthesized to explore various sites for modification and improvement of the structure. A successful screening campaign will yield three or four tractable lead series suitable for this type for early exploration. Compound series where potency and selectivity can be usefully modulated will be characterized in more detail with respect to drug-like properties, and where appropriate with respect to predictive pharmacology models generated by the Systems Pharmacology Core (see the SPCC description for details). Medicinal chemists, together with biologists and pharmacologists will also work with Mount Sinai’s OTBD to develop a strategy to define and protect intellectual property on novel composition of matter. In vitro leads of this type may serve as research tools for interrogation of novel disease targets or as jumping off points for further optimization.
- Lead Optimization - Based on an assessment of biochemical potency, cell based activity, overall physicochemical profile and input from models from the SPBCC, one series may be selected for further optimization. The objectives of the lead optimization are to increase potency in cell-based assays and to test molecules in more downstream in vitro and in vivo functional assays. In vitro ADME parameters such as microsomal stability and physical properties such as aqueous solubility will be monitored as leads progress. When an adequate balance of potency and physicochemical properties is achieved, initial rodent PK (IV, ip and oral) will be obtained in conjunction with scientists in the Pharmacokinetics and Pharmacodynamics Core of the ETI (see the PCC description for details). At this stage in lead optimization broader pharmacological profiling of leads is appropriate: for example selectivity profiling versus panels of receptors and enzymes. Early in vitro safety parameters may also be assessed, for example hERG channel or CYP450 activity. These assays may identify additional parameters that require optimization or influence go/no decisions on continued optimization; they will also provide input for model development by the SPBCC on novel experimental therapeutics discovered at the institute.
Optimized leads produced by the ETI will have in vivo efficacy in animal models (either disease or biomarker), at an acceptable dose and route of administration, with no obvious toxicity or metabolic liabilities. Medicinal chemistry is central to the design and synthesis of these leads, and chemists will interact with scientists in the TCBC, SPBCC and PPC of the ETI as projects progress.
Last Update: May 24, 2012
Molecular Informatics Core
The Molecular Informatics Core (MIC) facilitates sophisticated use of molecular structure information by providing access to databases, state-of-the-art software, and expert support for protein sequence and structure analysis, protein structure modeling, characterization of protein-ligand interactions, and virtual screening. The MIC staff assists researchers with the development and execution of computational strategies to address specific research questions. Working closely with other core facilities of the Experimental Therapeutics Institute (ETI) at Mount Sinai, in particular the Integrated Screening Core, the MIC will support target characterization, lead discovery, and lead optimization.
Target characterization services include: protein structure modeling for target proteins, identification and prioritization of ligand binding sites in protein structures, and modeling of protein-ligand complexes. In the area of lead discovery the MIC offers small-molecule virtual screening and docking, including high-throughput computational screening of small-molecule libraries, containing more than 4,000,000 compounds, against experimental and predicted target protein structures; construction of targeted libraries for HT chemical screening based on virtual screening results; targeted docking of selected compounds into experimental and predicted target protein structures. For lead optimization the MIC offers services to model and characterize protein-ligand interactions, identification of affinity and selectivity determining residues in the target protein, and support for structure-based refinement of protein-ligand interactions to enhance affinity and selectivity.
Last Update: March 22, 2012
Pluripotent Stem Cell (PSC) Core Facility
The study of human embryonic stem cells (hESCs) and Induced Pluripotent Stem Cells (iPSC) collectively referred to as pluripotent stem cells and their differentiation into specific lineages provides an extraordinary opportunity to study the cellular / molecular mechanisms regulating pluripotency and differentiation. It also offers a potentially unlimited source of numerous cell types for drug screening and cell-based therapies. The Pluripotent Stem Cell Shared Resource Facility has been established to facilitate the transfer of this technology to the Mount Sinai community and other institutions. The objectives of this facility are:
- To generate induced pluripotent stem cells using the latest transgene-free Sendai virus and mRNA/micro RNA technology.
- To provide undifferentiated PSCs, mouse embryonic fibroblasts (MEFs) and/or hematopoietic, cardiac and endoderm progenitors.
- To train faculty, postdoctoral fellows and students in the maintenance and the differentiation of pluripotent stem cells.
- To provide tested media / reagents necessary for the maintenance as well as the differentiation of pluripotent stem cells at discounted prices.
- To karyotype and bank hESC and iPSC stocks.
- To generate gene targeted hESC lines and iPSC lines.
- To assist PIs with pilot projects.
Last Update: May 13, 2014
Systems Pharmacology-Bioinformatics and Computational Systems Biology Core
The Systems Pharmacology-Bioinformatics and Computational Systems Biology Core assists Mount Sinai investigators with analyzing their genomics and proteomics datasets such as those collected by RNA-seq, cDNA microarray, ChIP-seq, IP/MS proteomics, SILAC phosphoproteomics or exome sequencing. The Core has the capabilities of visualizing cellular networks from lists of differentially expressed genes/proteins identified experimentally or considered as disease gene lists using the tools developed in-house. The Systems Pharmacology-Bioinformatics and Computational Systems Biology Core also has the capabilities of performing gene-set enrichment analyses using data collected from ENCODE, the Epigenomics Roadmap, KEGG, BioCarta, WikiPathways, Reactome, The Gene Ontology, MGI Mammalian Phenotype Browser, LINCS Connectivity Map, OMIM, BioGPS, CCLE, PFAM and InterPro and more. Such analyses can be performed by the popular tools Enrichr, ChEA and KEA. In addition, the Core has the capabilities of building customized web-portals dedicated to specific projects for interactive data exploration and data analysis on the web.
Last Update: September 23, 2015
The Friedman Brain Institute is an interdisciplinary hub for defining the mechanisms underlying brain and nervous system diseases and for translating those findings into preventative or restorative interventions. The Institute is focused on three major areas of investigation where Mount Sinai can be truly transformative: neural injury and repair, cognition, and neuropsychiatry. The Institute will be judged by its success in advancing brain repair, developing new ways to advance cognition, and improving the treatment of neuropsychiatric disorders.
The Brain Institute's work spans basic molecular and genetic research of nervous system disorders, from animal models to investigations of human populations in the clinic. New knowledge from animal studies will drive clinical investigations, while new insight from clinical studies will help guide more basic exploration into the underlying mechanisms. This broad-based approach incorporates a wide range of state-of-the-art methodologies and coordinates efforts among numerous departments at the Icahn School of Medicine, including neuroscience, neurology, psychiatry, neurosurgery, pharmacology, geriatrics, ophthalmology, and rehabilitative medicine.
Mount Sinai has been recognized as a leader in brain research and treatment for over a century. It has been at the forefront of the rapidly evolving discipline of basic neuroscience, while its longstanding reputation for excellence in clinical neurology, neurosurgery, psychiatry, ophthalmology, and rehabilitative medicine has continued to grow.
Last Update: September 23, 2015
The Global Health and Emerging Pathogens Institute is the nucleus of Mount Sinai’s work on infectious diseases and the pathogens that cause them. The Institute, based in New York City, builds on Mount Sinai’s internationally recognized expertise in RNA virus research and encompasses ongoing research on the molecular pathogenesis of influenza, HIV, and dengue and Ebola viruses, as well as on hepatitis C and West Nile.
The innate component of the immune response is a rapid one, in which the body recognizes and fights off general classes of infectious agents. Mount Sinai has been at the forefront of current research, identifying viral factors that inhibit innate immune responses and showing how such factors contribute to the pathogenesis of the virus. Global Health and Emerging Pathogens Institute expertise in virology will prove invaluable as we work to develop robust vaccines and antiviral drugs that save people lives.
The Global Health and Emerging Pathogens Institute is focused on expanding Mount Sinai’s world-renowned programs in RNA viruses. Our strategy serves as a model for developing new programs to study other viruses, specially zoonotic and emerging viruses, including MERS and Zika viruses. These viruses blur the line between animal and human viruses and do not respect country borders, consistent with the concept “one world, one health, one medicine”, linking human, animal and environmental health. The Institute is also developing research programs driven by local and global public health needs. One emerging area of interest is the impact of host genetics and of the microbiome in virus disease.
Last Update: June 9, 2016
The Immunology Institute at Icahn School of Medicine brings together and fosters collaboration between faculty members in multiple disciplines and departments who conduct research in immunology, allergy, inflammation, and transplantation. The overall goal is to provide an institutional mechanism to enhance research collaborations, education, and clinical translation of basic research in immune mediated diseases, exploring and dissecting disease pathways with the intention of developing novel therapeutic approaches.
Last Update: September 23, 2015
The Institute for Genomics and Multiscale Biology at the Icahn School of Medicine is a "core technology institute", which enables Mount Sinai Researchers to carry out cutting-edge genomic-based basic and translational research that brings state of the art high throughput genomic technologies under one roof to provide a centralized resource to carry out large scale genomic studies. The Genomic institute has three core units: The Genomics Core, the Proteomics/Metabolomics Core, and the Computational Genomics Core. Each core has state-of-the-art equipment, technical and analytical infrastructure manned and run by highly skilled and knowledgeable technical and scientific staff to facilitate sophisticated genomic, proteomic and metabolomic research. Eric Schadt, PhD Chair of the Department of Genetics and Genomic Sciences, directs the Institute. Andrew Kasarskis, PhD is the Co-Director of the Institute.
The Genomics Core:
Apart from housing the standard Sanger Sequencing facility, the Genomics Core provides the latest next generation sequencing and microarray technologies. The Genomics Core currently operates multiple next generation sequencing platforms: 4 Illumina HiSeqs, one MiSeq, one Pac Bio RS system. Two Astro platforms that are the latest high tech models over the RS system will be commissioned by the end of 2012. The Genomics Core facility is directed by Milind Mahajan, PhD and has 12 full time staff including three PhD level staff appointments. The day-to-day production, R&D operation, and scientific and business oversight of Genomics Core are handled by Milind Mahajan, PhD and Andrew Kasarskis. All necessary infrastructures such as high performance computation and bioinformatics support are already in place. The types of high throughput sequencing projects that are being routinely carried out include preparation of Seq-libraries followed by sequencing for RNA-seq, CHIP-seq, and small RNA Seq, targeted gene selection sequencing and whole exome and genomic sequencing from variety of clinical and non-clinical samples from different biological sources.
Microarray Technology is offered for Genome Wide Association Studies, Pharmocogenetics, Genomics, Methylation, candidate gene, and genotyping analyses. The Core has extensive experience and expertise in genotyping and expression array analysis on Affymetrix and Illumina platforms. Currently, the Core uses the Illumina platform for genotyping employing the Golden Gate assay as well as OmniExpress, OmniQuad2.5, and Omni2.5-8 arrays. The Core has all the necessary liquid robotic automation systems, a HiScan and Bead Express system to carry out wide range of sample volumes. With the existing latest state of the art equipment and facilities, the current capacity is to process up to 600 samples per week.
Quantitative PCR analysis for small-scale gene expression quantitation and detection of single nucleotide polymorphisms is available using an Applied Biosystem 7900HT with associated robotics for accurate reaction set-up using a Biomek FX for automated liquid handeling. Automated, high throughput nucleic acid purification from blood, tissue or bacteria is performed in a 96 well format using a Qiagen Universal BioRobot. To assess the quality of nucleic acids, the Genomic Institute has an Agilent Bioanalyzer 2100.
The Genomic Institute has ample computing power, and software developed in-house that is described below and listed in the Major Equipment document. The data are processed on a 360-core compute cluster with 128GB of RAM available on each node (with ~50 cores per node). Additional servers, with large amounts of RAM, bring up the total amount of available RAM to 1.2 TB. A 400 TB networked storage device from Isilon provides ample storage for the sequencing data. The storage and computer clusters are connected to each other through a 10G interconnect. A special server from Avere provides tiered data access, with frequently used files being cached for rapid access. An externally accessible website is hosted on two mirrored servers, with load balancing controlled by an F5 load-balancer. Nodes on the compute cluster are pre-loaded with all of the necessary software to perform routine analysis of high-throughput sequencing data and are regularly updated with the latest public genomic data resources. Several tools, for analysis and data exploration, have been developed in-house. These are deployed as browser-based tools backed by distributed web-services that help maintain performance and availability. The servers are housed in two 42U racks with ample power and air-conditioning. Both power and air-conditioning have backup, ensuring 24/7 operation. A dedicated system administrator helps keep the software up to-date. In addition, two programmers/analysts develop software and analyze data.
Scientific Computing Infrastructure:
Mount Sinai has committed over $50M to its scientific computational and data cyberinfrastructure, recognizing that a well-designed and managed infrastructure empowers its scientists and researchers to be more productive and effective. This significant investment includes professional staff, expertise, hardware, software and a new computational and data facility dedicated to scientific computing. Mount Sinai closely collaborates and partners with other facilities and vendors, to keep its cyberinfrastructure and services state-of-the-art. The staff follows the communities’ best practices and procedures to ensure that the computing and data services are the most efficient and effective for the researchers.
Mount Sinai’s robust computing and data cyberinfrastructure has been designed for the rapid and accurate ingest of the sequencer output and high performance post-processing and analysis by the computational cluster and affiliated file systems and storage. The cyberinfrastructure resources have been tailored specifically to handle the computational and data workflow from the sequencer, including a high bandwidth network.
The computing and data center at Mount Sinai contains over 10,000 square-feet of space. It offers several complementary resources, including an SGI Altix 1300 cluster with 816 CPU cores, 64 Nehalem-class nodes with Quad Data Rate (QDR) Infiniband connectivity and 38 nodes with Double Data Rate (DDR) Infiniband. All of those nodes are attached to 65 Terabytes of Lustre-based high-speed shared storage. The software and programming environments are the best of breed, and include community standards such as Linux and MPI. The clusters also run resource managers and schedulers optimized for the job workload, optimized to process as many jobs as possible for the highest overall machine utilization, job throughput and job success rate. The clusters are operated with over 95% uptime, using scalable and reproducible configuration management techniques. The machines are also monitored for security.
High Performance Computing (HPC) Cluster:
The new High Performance Computing cluster and storage will be installed at the beginning of March 2012, and expect to open the cluster up for general access in mid-April 2012. The resource expansion is specifically designed for applications in learning and modeling biological networks, application of Bayesian analysis frameworks more generally, second and third-generation sequence analysis, modeling the kinetics of DNA synthesis to detect 6-methyladenosine, 4- and 5-methylcytosine, 8-oxoguanine and other modified nucleotides. The hardware accessible for analysis includes systems optimized for embarrassingly parallel jobs such as QTL analyses that are CPU bound as well as parallel jobs such as Bayesian network reconstruction that are memory bound. In addition, there is support for jobs requiring substantial shared memory, such as all-by-all comparisons or splice-form specific RNA-seq results to generate isoform-specific coexpression networks, an n2 problem with an estimated between 100,000 and 200,000 for most tissues. High-availability storage is provided to support both very large files and very large numbers of small files in these analyses. In summary, the compute infrastructure is designed to be flexible to allow both exact mathematical models of high complexity and heuristic machine learning approaches to be explored in addressing biological hypotheses in an iterative and complementary way.
Last Update: April 16, 2012
The Institute for Medical Education (IME) was established in 2001 to promote and advance innovative medical education and scholarship as well as recognize and reward our outstanding educators. The IME serves the vital need in our institution of creating, educating, mentoring, and retaining the best educators for our students, residents, and faculty. Fostering the success of our educators includes recognizing and rewarding those who display dedication and excellence in their work and providing programs that develop and reinforce their scholarship, teaching skills, and successful promotion. In doing so, we create a network of dedicated educators that contributes its knowledge and experience back to this community by serving as teachers and mentors. Our activities have positioned the Institute as a center for teaching and learning excellence across the Mount Sinai health system.
The scope of the IME goals encompasses promoting scholarship and dissemination of innovative medical education approaches, acknowledging and rewarding our accomplished educators, creating faculty development opportunities for all teaching faculty and supporting career advancement of medical educators in academia. Specifically, the IME aims to:
- Recognize and reward excellence in education and teaching
- Facilitate the academic promotion of educators
- Support skills development in teaching, learning and medical education research
- Promote the dissemination of innovative medical education scholarship
- Create an educational community whose members inform and support one another
Last Update: March 23, 2016
The Institute for Translational Epidemiology, headed by Emanuela Taioli, MD, PhD takes advantage of Mount Sinai's extraordinary strengths in both research and practice in basic, clinical and preventive disciplines to foster the development of cutting-edge, multidisciplinary epidemiology research projects in the clinic, in the community, and in collaborating institutions across the world. The mission of the Institute for Translational Epidemiology is to develop and facilitate highly collaborative translational and interdisciplinary research integrating population studies, genomic and proteomic research, with the ultimate purpose of spearheading changes in clinical practice, improvement in disease treatment, disease outcome and patients’ quality of life. Epidemiology rese arch has greatly contributed in the last 60 years to improving our knowledge in many areas of medicine, which in turn has entailed major changes in clinical and preventive practices. Exciting transformations have occurred to Epidemiology in the 21st century, and this is reflected by the new popular terminology “Integrative Epidemiology”, a definition that describes the discipline as cohesive; interdisciplinary, collaborative, multilevel, where new technologies and alternatives to classic study designs become the leading forces to transformation. Epidemiologists are now in the position to integrate genetic and genomic data, social factors, built environment, large electronic clinical data, to predict individual disease risk, response to treatment and prognosis. All the elements for a successful Integrative Epidemiology Program are present at Mount Sinai. The Institute has several Concentration Areas (CA) of research: Chronic Disease Epidemiology (cancer, CVD, diabetes, and neurologic conditions); Mental Health Epidemiology; Infectious Disease Epidemiology; Social Epidemiology; Occupational Epidemiology; Epidemiologic Methods (Biostatistics, High throughput analyses, bioinformatics), Life course Epidemiology, Molecular and Genetic Epidemiology.
The Institute collaborates closely with the Department of Population Health Science and Policy and the Department of Preventive Medicine, as well as a variety of other Mount Sinai entities in building the research portfolio. In addition, training and education is part of the research portfolio.
Visit the Institute for Translational Epidemiology for more information.
Last Update: June 9, 2016
The mission of the Icahn School of Medicine Mount Sinai Diabetes, Obesity and Metabolism Institute is to develop better therapeutic and prevention strategies for types 1 and 2 diabetes, obesity, diabetes, and the metabolic syndrome through basic and clinical research.
Six areas form the core of the Metabolism Institute's research enterprise: (1) Pancreatic Beta Cell Regeneration and Replacement. (2) Type 1 Diabetes Immunopatholobiology Research Program, in collaboration with the Immunology Institute. (3) The Genetics and Genomics of Diabetes in collaboration with the Institute for Genomics and Multiscale Biology and the Charles Bronfman Institute for Personalized Medicine. (4) CNS Control of Metabolism. (5) Fuel Metabolism and Signal Transduction in skeletal muscle, liver, pancreatic beta cells and the adipocyte. (6) Complications of Diabetes: vascular, renal, and neuropathic. (7) Clinical Research in Type 1 Diabetes, Type 2 Diabetes, Obesity and Bariatric Surgery in collaboration with the Mount Sinai CTSA. (8) Community Based Prevention, Diabetes Research and Epidemiology. (9) Diabetes and Cancer research.
The Research Cores within and used by the Diabetes, Obesity and Metabolism Institute include mouse metabolic and histopathologic phenotyping, high-throughput screening and drug discovery, human and animal imaging, cell biological imaging, proteomics, next-gen sequencing, epigenomics, monoclonal antibody generation, microsurgery, among many others.
Finally, we share an NIH/NIDDK-supported joint Albert Einstein College of Medicine and Mount Sinai Diabetes Research Center (ES-DRC), with multiple cores, including a Human Islet and Adenoviral Core (HIAC) based at Mount Sinai. Complete information is available at Einstein-Mount Sinai Diabetes Research Center.
Last Update: September 23, 2015
As one of the largest and most comprehensive adult and pediatric abdominal transplantation centers in the world, the Recanati/Miller Transplantation Institute (RMTI) at The Mount Sinai Health System is committed to outstanding patient care, research, and educational programs. Our transplant services for adults and children include kidney, liver, pancreas, and intestinal organ transplant. In addition, RMTI has one of the largest living donor programs in the United States. Through our Zweig Family Center for Living Donation, we provide the best in medical, surgical, and psychological care to living organ donors. Additionally, we provide comprehensive, personalized treatment and compassionate care to people with a wide variety of liver/bile duct and pancreatic diseases, including cancers affecting these organs.
We bring together a distinguished team of surgeons, physicians, and other healthcare professionals to support patients with end stage disease in every step of their care up to and including transplantation. RMTI team members view transplantation as one step in the continuum of patient care. Our multidisciplinary approach ensures that patients benefit from the expertise of multiple specialists, who understand their unique needs.
Having performed more than 5,500 liver, kidney, pancreas, and intestinal transplants over 40 years, we have a rich history of innovation and excellence in the field of organ transplantation. One of the key factors in our success is close collaboration between our physicians and the scientists who conduct state-of-the-art research here. It enables us to provide leading-edge technologies and the most up-to-date therapies to our patients, including individuals with complex medical needs. For example, RMTI researchers working side-by-side with our clinical teams have made great strides in increasing the eligibility of patients previously denied kidney / pancreas transplants due to medical conditions, such as Hepatitis B, Hepatitis C, and HIV.
At RMTI, we offer a full spectrum of abdominal organ transplantation programs and services, including: adult and pediatric liver disease and transplantation, adult and pediatric kidney transplantation, adult pancreas transplantation and intestinal rehabilitation and transplantation.
Last update: June 12, 2014
Under the leadership of Steven Burakoff, MD the Tisch Cancer Institute (TCI) was awarded National Cancer Institute (NCI) designation in 2015. The mission of the TCI is to advance the field of cancer research, treatment and prevention and to facilitate the availability of these advancements to our communities so as to extend and improve the lives of cancer patients and their families. To accomplish this mission, the TCI has four research programs: Cancer Immunology, which addresses anti-tumor immunity and fosters the development of cancer vaccines; Cancer Mechanisms, which seeks to understand the biology of cancer cell development; Liver Cancer, whose focus is to discover novel approaches to diagnose and treat liver cancer; and Cancer Prevention and Control, which addresses the important aspects of primary and secondary cancer prevention. Cancer Institute members span across multiple departments in the medical center and work collaboratively within and across these multidisciplinary research programs. To facilitate pertinent clinical research, the Tisch Cancer Institute provides oversight of all clinical trials through its Protocol Review and Monitoring Committee and its centralized database of clinical trial protocols and enrollments. As of February 2016, cancer grant awards exceeded $68 million in direct costs, and in 2015, there were 136 open therapeutic clinical trials that enrolled a total of 385 new patients.
As part of its mission, the Tisch Cancer Institute supports several Shared Resources and Facilities that are critical to cancer research. These include clinical resources such as the Cancer Clinical Trials Office and Cancer Biostatistics core, as well as many basic sciences resources, including the Flow Cytometry, Mouse Genetics, and Microscopy cores. In addition, the TCI provides competitive Research Awards to both basic, clinical, and population cancer scientists to facilitate new insights into cancer biology, prevention and treatment.
Last update: June 1, 2016
The Translational and Molecular Imaging Institute (TMII) serves as a research catalyst for a new generation of translational and molecular imaging methodologies. It offers researchers highly efficient, cost-effective services for commonly used imaging tests, without the usual institutional overhead. TMII provides expertise for developing and validating new procedures and encourages interdisciplinary collaborations that help close the gaps between clinical and preclinical studies. Through its targeted seminars, research fellowships, publications, and other training programs, TMII educates researchers, postdoctoral fellows, students, and technicians about biomedical imaging advances and options.
TMII is responsible for coordinating and executing all in vivo imaging research at Mount Sinai. Currently, TMII has over 50 members with expertise in all aspects of translational imaging research, from image acquisition to image analysis. Mount Sinai and TMII have entered into a strategic partnership with Siemens Medical Systems to support its effort in translational research. Housed in approximately 20,000 square feet in the new Hess Center for Science and Medicine, are state-of-the-art Siemens systems, including a whole-body 7T actively shielded MR scanner, a fully integrated simultaneous MR(3T)/PET mMR system, a 3T MR Skyra scanner and a novel dual-source Somatom Force CT for faster and lower dose imaging. These systems will be available for human and large animal research. In addition, TMII will have access to a variety of Siemens systems that will be managed by the Department of Radiology at Mount Sinai, including a 1.5T MR Aera scanner, a PET/CT(40) Biograph mCT, and a multidetector CT Somatom Definition Flash.
TMII also provides preclinical imaging services performed on a variety of small animal scanners, including a 9.4T (89mm bore size) Bruker vertical bore system, a 7.0T Bruker (154mm bore size) horizontal bore scanner, a micro-PET/CT (TBD), a biophotonic IVIS spectrum, a near-IR imager from Dr. John Frangioni, and a micro ultrasound Vevo 2100 from VisualSonics. All of these imaging systems will be equipped with a variety of peripherals for physiological monitoring, physiological gating, fmri experiments, drug infusion and anesthesia delivery.
TMII has a data center in the new Center for Science and Medicine that contains a dedicated server room hosting a larger Mac Server Cluster of 2 x 16TB of initial online storage with direct connectivity to all of the imaging modalities. TMII XNAT serves as the central point for research data transfer, archive, and sharing. TMII XNAT is built upon a secure database, supports automated pipelines for processing managed data, and provides tools for exploring the data. Currently TMII XNAT runs on two mirrored Linux servers with 60TB storage space on each. It can host more than 15,000 image sessions with backups. In addition, TMII offers an image analysis room equipped with a large viewing display and more than 15 high-performance workstations to facilitate learning and image analysis as well as a nanomedicine laboratory for the design, synthesis and evaluation of novel imaging probes and drug delivery systems.
Updated: September 29, 2015