Silicom Summit 2010




       
       
Edward Abrahams, Ph.D. Executive Director Personalized Medicine Coalition    
       
Edward Abrahams, Ph.D., is executive director of the Personalized Medicine Coalition (PMC). Representing a broad spectrum of academic, industrial, patient, provider and payer communities, PMC seeks to advance the understanding and adoption of personalized medicine concepts and products for the benefit of patients. It has grown from its original 18 founding members in November 2004 to over 160 today. Previously he was Executive Director of the Pennsylvania Biotechnology Association, where he spearheaded the successful effort that led to the Commonwealth of Pennsylvania’s investment of $200 million to commercialize biotechnology in the state. Earlier he had been Assistant Vice President for Federal Relations at the University of Pennsylvania and held a senior administrative position at Brown University. Dr. Abrahams worked for seven years for the U.S. Congress, including as a legislative assistant to Senator Lloyd Bentsen, an economist for the Joint Economic Committee under the chairmanship of Representative Lee Hamilton, and as a AAAS Congressional Fellow for the House Committee on the Interior.
 
     
Kenneth A. Berlin President and Chief Executive Officer Rosetta Genomics      
         
Prior to his appointment as president and CEO of Rosetta Genomics, since July 2007, Mr. Berlin served as worldwide General Manager at cellular and molecular cancer diagnostics developer, Veridex, LLC, a Johnson & Johnson (NYSE: JNJ) company. Under his leadership the organization grew to over 100 employees, and he spearheaded the launch of three cancer diagnostic products, the acquisition of its cellular diagnostics partner, and delivered significant growth in sales as Veridex transitioned from a research and development entity to a commercial provider of oncology diagnostic products and services. During Mr. Berlin’s tenure, Veridex received numerous awards including recognition from the Cleveland Clinic and Prix Galien for the use of its innovative CellSearch® technology in the fight against cancer. Mr. Berlin joined Johnson & Johnson in 1994 and served as corporate counsel for six years. He led and participated on the legal team that oversaw several mergers, acquisitions, divestitures and commercial transactions across Johnson & Johnson. He then held positions of increasing responsibility within Johnson & Johnson and a number of its subsidiary companies. From 2001 until 2004 he served as vice president, licensing and new business development in the pharmaceuticals group, and from 2004 until 2007 was worldwide vice president, franchise development, Ortho-Clinical Diagnostics. He has been responsible for numerous licensing and/or research collaboration deals in metabolic disease, cardiovascular disease, oncology, CNS and women’s health, including the ex-U.S. license to Millennium Pharmaceutical’s VELCADE, a first-in-class, oncology therapeutic with reported sales outside the U.S. in excess of $750 million in 2008.
   
     
       
Daniel Chelsky, Ph.D. Chief Scientific Officer, Caprion Proteomics    
       

Dan brings to Caprion Proteomics deep industrial experience in applying the CellCarta® proteomics platform to drug target and biomarker discovery. Prior to joining the Company, Dan was President and General Manager of BioSignal Packard Inc. (a division of Perkin Elmer), where he oversaw the development of novel technologies and reagents for drug discovery and genomics research, including the AlphaScreenTM and BRET2TM technologies and product lines. Dan also spent five years at Pharmacopeia where, as Senior Director of Biology, his team identified many lead compounds from Pharmacopeia’s million member combinatorial chemistry libraries that resulted in multiple compounds in the clinic. His previous experience also includes positions at Onyx Pharmaceuticals and the DuPont Merck Pharmaceutical Company in cancer research. Dan received his B.Sc. from the University of California at Santa Barbara and his Ph.D. in Chemistry from the University Of Oregon Institute of Molecular Biology and was an American Cancer Society fellow at the University of California at Berkeley.

 
 
       
Maureen Cronin, Ph.D. Vice President, Translational Research, Genomic Health, Inc.    
       

Dr. Cronin’s current position is Vice President of Translational Research at Genomic Health, Inc.  There she heads a team responsible for conducting initial feasibility research for new product concepts encompassing both technical and biological aspects of each concept including laboratory processes, automation systems, and data management with bioinformatics and biostatistical analyses.   All product concepts are focused on applying genomic biomarkers to provide clinically relevant molecular pathology tests for patient and physician clients.  Programs focus on delivering high throughput, high-performance, innovative, first-in-class medical products in a regulated reference laboratory environment.  Dr. Cronin brings 20 years of R&D experience in biotechnology companies focused on applying cutting edge technology to clinical diagnostics including ACLARA BioSciences, Protogene Laboratories and, Affymetrix where she played a key role in developing DNA microarray (GeneChipä) technology.  Dr. Cronin’s Ph.D. in Molecular Pharmacology is from the University of California, San Diego and her undergraduate education from the University of California, Davis.

 
     
       
Asif Dhar, MD Chief Medical Informatics Officer, Deloitte LLP    
       

Dr. Dhar is Deloitte’s Chief Medical Informatics Officer. He helps clients develop innovative strategies to improve clinical outcomes and therapeutic discovery. His translational informatics work is helping clients discover new approaches to optimize clinical R&D with breakthrough information management approaches. He has been retained by numerous provider systems, Cancer Centers, Life Science companies and Governmental Agencies to define translational research programs. Dr. Dhar is also a Senior Fellow with the Deloitte Center for Health Solutions. He developed the Center’s perspective on the ROI for Personalized Medicine with the Personalized Medicine Coalition which was presented at the American Association for the Advancement of Science. Dr. Dhar has deep functional and management experience that spans public and private sector clients. He has provided senior leadership for numerous Electronic Health Record (EHR) implementations in the US, Canada, and the UK. He has also helped design enterprise data warehousing solutions, clinical discovery applications, and quality improvement programs at large integrated delivery networks and academic medical institutions. Dr. Dhar has a deep experience in developing clinical and research informatics programs. He is a Senior Advisor to the FDA’s Enterprise Architecture team. He also has provided biomedical informatics advisory services for the National Cancer Institute (NCI) and has served on multiple study sections for the NIH National Human Genome Research Institute. Dr. Dhar holds a Medical Degree from the University of Illinois, a Masters in Business Administration degree from the University Of Chicago Booth School Of Business, and a Bachelor in Arts degree from the University of Chicago.

 
     
       
Michael A. Goldman, Ph.D. Department of Biology Prof. & Chair San Francisco State University  
       
Dr. Goldman did his undergraduate work in Biology at the University of Rochester and obtained a Ph.D. in evolutionary biology at Purdue University in 1981. He completed fellowships in Medical Genetics at Baylor College of Medicine in Houston and at the University of Washington in Seattle. He joined the faculty at San Francisco State University in 1988, where he is now Professor and Chair of the Department of Biology. He teaches human genetics at the graduate level, general genetics for biology majors, developmental biology for Cell & Molecular Biology majors, and an interdisciplinary course on the ethical issues in science and technology. Dr. Goldman's research is in chromatin structure and the regulation of gene expression during mammalian development. Of special interest is the relationship between chromosome structural elements called nuclear matrix attachment regions (MARs) as boundaries of functional chromatin domains, studied through molecular methods and bioinformatics. He sees the public understanding of science as a key need if science and society are to thrive, and has talked about various issues like stem cell biology for TV and radio call-in audiences. He has written Op-Ed pieces for the Los Angeles Times, the Sacramento Bee, and the San Francisco Chronicle as well a professional papers appearing in Science and Nature Genetics. Thinking that the public learns much about science and bioethics from fiction, he reviews novels addressing various aspects of genetic science and its implications, in venues like Nature, Science, Nature Genetics and the San Francisco Chronicle.
 
     
       
Richard Deane Hockett, M.D. Chief Medical Officer Affymetrix    
       
Richard D. Hockett’s current position is Chief Medical Officer, Affymetrix, Santa Clara, CA.  His responsibilities include translation of genomics technologies, medical and regulatory affairs.  Special areas of focus are molecular diagnostics, clinical application of technology, and biomarker strategies.  Prior to joining Affymetrix, Dr. Hockett was a Medical Fellow II, Group Leader for Genomic Medicine at Eli Lilly and Company, where he developed the pharmacogenomic program and oversaw the application of genetic biomarkers to clinical drug development.  While there he was instrumental in developing the DMET analysis system.    Prior to joining Lilly, Dr. Hockett was employed by the University of Alabama at Birmingham in the Department of Pathology, where he oversaw the Clinical Immunology and Molecular Diagnostic Laboratories.  His research interests have been in the areas of Developmental Immunology and HIV disease.  Dr. Hockett received his M.D. degree from the University of Minnesota, and did his residency in Clinical Pathology at Washington University, St. Louis.
 
   
       
Eddy Karnieli MD Prof. & Director, Inst. Endocrinology, Diabetes & Metabolism Rambam Medical Center Director, Galil Center for Telemedicine, Medical Informatics & Personalized Medicine RB Rappaport Faculty of Medicine - Technion
 
     

Professor Eddy Karnieli is a graduate of the Rappaport Faculty of Medicine at the Technion– Israel Institute of Technology in Haifa.He obtained clinical training in Internal Medicine and Endocrinology at the Rambam Medical Center and did his Post-Doctoral Fellowship in Diabetes, Obesity and Endocrinology at the National Institutes of Health in Bethesda, Maryland.
He was a visiting scholar at the University of California at San Diego and at the National Institutes of Health. He is currently the Director of the Institute of Endocrinology, Diabetes and Metabolism at the Rambam Medical Center. Professor Karnieli's main research interests are the molecular mechanisms for regulating cellular glucose uptake and transporters and their implications in diabetes, obesity and insulin resistance; Gene therapy modalities to trans-differentiate human cells toward beta-cells as a potential cure for type 1 diabetes; Medical informatics, telemedicine and personalized medicine. He has published about 70 peer reviewed papers and reviews.Professor Karnieli serves on the editorial board of several scientific journals and review boards. Professor Karnieli is a retired Colonel from the Israel Defense Forces Medical Corps and is a former Deputy Director of the Rambam Medical Center.

 
     
     
Peter M. Kash President & Partner Two River Group Holdings, LLC    
       

Mr. Kash is a co-founder and Partner of Two River. Since September 2004, Mr. Kash has served as the President of Two River's managing member, Two River Group Management, LLC, and served as its Chairman until April 2008. Mr. Kash is also the President and Chairman of Riverbank Capital Securities, Inc., a FINRA member broker dealer ("Riverbank") that has raised over $200 million since its inception in September 2005, including more than $80 million for Two River's Portfolio Companies. From 1992 until 2004, Mr. Kash was a Senior Managing Director of Paramount BioCapital, Inc., a FINRA member broker dealer, and Paramount BioCapital Investments, LLC, a biotechnology focused venture capital company. Mr. Kash also served as a member of the General Partner of the Orion Biomedical Fund, LP, a private equity fund. Mr. Kash currently serves as Chairman of the Board of Directors of Nile Therapeutics, Inc. (NASDAQ:NLTX) and as a director of Arno Therapeutics, Inc. (OTCBB:LRRI.OB), and Danube Pharmaceuticals, Inc. He was also a co-founder and former Vice Chairman of Javelin Pharmaceuticals, Inc. (AMEX:JAV). Mr. Kash served as an Adjunct Professor of Entrepreneurship and International Venture Capital at the Wharton School of Business at the University of Pennsylvania from 1996-2000. He was also Entrepreneur in Residence at Pace University and at Ball State University in May 2002. Mr. Kash served as a Professor of Entrepreneurship at the Sy Syms School of Business from 2003-2005, as well as Visiting Professor of Entrepreneurship at the Graduate School of Business at Nihon University in Tokyo. He is also the author of two books: Make Your Own Luck (2001 Prentice Hall), and Freedom From Disease (2008 - St. Martin's Press). Mr. Kash currently serves on the Board of Keren-Or, a charity for blind and multi-handicapped children, and is active in a variety of other charities, including Kids Kicking Cancer and Cancer Schmancer. He earned his B.S. in Management Science from SUNY Binghamton and his M.B.A. in Banking and International Finance from Pace University. He is currently writing his thesis for his Doctorate of Education.

 
   
     
Raphael Lehrer, Ph.D. Head of Personalized Oncology Services CollabRX  
     
Raphael Lehrer directs CollabRx ONE, our personalized oncology research service. Previously, Dr. Lehrer was the Executive Director of Strategic Alliances for Gene Logic's Drug Repositioning and Selection Business where he negotiated alliances with pharmaceutical companies to discover new therapeutic uses for their compounds that have failed in late-stage clinical trials. In earlier positions at Gene Logic, he played a key role in formulating strategy for the company; evaluating, acquiring, and integrating the preclinical CRO business; and in adding service-based offerings to Gene Logic's toxicogenomics business. Prior to joining Gene Logic, Dr. Lehrer worked at The Boston Consulting Group, where he supported top-ten pharmaceutical clients on a variety of R&D and commercial issues, including formulating licensing strategies, clinical development process design, regulatory processes, post-merger integration, and outsourcing strategies. Additionally, Dr. Lehrer was a key contributor to BCG's positioning paper on the impact of genomics on pharmaceutical R&D. Dr. Lehrer holds a B.S. degree in Physics from Yale University and a Ph.D. degree in Physics from Harvard University, where he was awarded the Maurice Goldhaber Prize for best theoretical physics student.
 
   
       
Andrew Marshall Chief Editor (New York), Nature Biotechnology    
       
 
Andy obtained his PhD and postdoctoral experience in molecular biology and microbiology at King's College London. Before joining Nature Biotechnology in 1996, he was Editor of Current Opinion in Biotechnology for four years. He has written numerous articles and editorials on science and technology for the popular media, including The Economist, and for trade publications. As well as frequently speaking on biotechnology issues at international meetings, he regularly organizes conferences and symposia for Nature Publishing Group in the biotechnology area.
 
   
     
Irene Norstedt Head of Sector for Medicines for the Future European Commission  
     

Irene Norstedt has been working with various aspects of European Life Sciences research at the European Commission since 1996. She is currently Head of Sector for Medicines for the Future with key focus is on Personalized Medicine. Before that she was one of the key drivers for setting up the Innovative Medicines Initiative (IMI), a public private partnership between the EC and the Pharmaceutical industry. Previous responsibilities at the EC have primarily focussed on Small and Medium size Enterprises and industry aspects of biotechnology and health research at European level. Before starting her job in Brussels she worked for BIAcore AB in Uppsala, Sweden. There she had several positions including Business Development for the Drug Discovery and Food Analysis areas and Technical Services Manager. She has also worked as Assistant Technical Attaché at the Swedish Embassy in London. She has an MSc degree from the Royal Institute for Technology in Stockholm.

 
   
     
David O’Reilly Senior Vice President, Proteus Biomedical  
     
David O’Reilly is Senior Vice President, Corporate Development of Proteus Biomedical, developer of ingestible and implantable technologies that are the foundation for the development of the company’s intelligent medical products. Prior to joining Proteus, he was president of Catalyst Biosciences, a company developing novel therapeutic protein products based on engineered proteases. Mr. O’Reilly was chief business officer and part of the founding management team at Iconix Biosciences, a leading chemogenomics company. Prior to Iconix, Mr. O’Reilly was an executive at ARIAD Pharmaceuticals, Inc., where he was responsible for partnerships and licenses with pharmaceutical, biotechnology and academic organizations. He also managed the strategic development of ARIAD’s gene therapy subsidiary, ARIAD Gene Therapeutics, Inc. Mr. O’Reilly is a graduate of Wesleyan University, where he was named the school’s Gilbert H. Clee Scholar, and Harvard Business School, where he received an MBA with Distinction.
 
   
     
Ron Ribitzky, M.D. CEO R & D Ribitzky  
     
Dr. Ron Ribitzky is a physician executive in healthcare I.T. and life-sciences Informatics. With a track record of accelerating innovation from idea to practice; charging ahead of the technology curve, and leading multi-national cross-functional teams, Ron has a unique experience bringing together clinical insight, technology leadership, and global perspectives to drive innovation, shape strategy and execute throughout the product, solution, and service life cycle. Following 10 years in clinical practice, Ron’s informatics career developed from Sr. Programmer Analyst to Director of Applications and Research Computing at Boston Children’s Hospital; CIO at UMass Medical Center; Sr. Director Medical Sales Support, VP Prototype Development, and VP Advanced Research at Eclipsys; Sr. Healthcare Strategist and Marketing Campaign Manager for Mobile Point of Care Worldwide at Intel. Ron served as Co-Pi in ARPA National Medical Center Information Collaborative, and advisor to AT&T on the U.S. Department of Commerce/NIST National Medical Practice Knowledge Bank. Ron guided the development of the American College of Cardiology’s National Cardiovascular Data Registry, and led SAIC’ Semantic Integration Team at Kaiser Permanente’s National Clinical Information System. His academic appointments included Visiting Scientist at IBM and Weizmann Institute; Research Fellow, Medical Informatics at Harvard; Assistant Professor at UMass; and Assistant Professor, Center for Clinical Evaluation Sciences at Emory School of Public Health. He published, presented, and led workshops around the world in industry, academia, marketing, and sales events. Boards and committees include HIMSS EHR Usability Workgroup Leadership Council; CPRI Framework for Evaluating Electronic Health Records; NSF Center for Intelligent Information Retrieval; and ACSIOM, a technology transfer corporation. Ron holds a U.S. patent on component-based object-relational database infrastructure and user interface. He founded R&D Ribitzky, a healthcare I.T. and informatics firm in 1988. Ron earned his M.D. degree from the Sackler School of Medicine, Tel-Aviv University.
 
   
     
Doina Roman, M.D. Senior Medical Director Translational Medicine Takeda Pharmaceuticals  
     
Doina Roman, MD, is Senior Medical Director in Translational Medicine Sciences at Takeda Global Research & Development. In her role Dr. Roman leads and develops translational medicine and early clinical development strategies across multiple therapeutic areas utilizing relevant modalities such as biomarker driven development decision, modeling, imaging, emerging new technologies and statistical approaches. Before Joining Takeda Pharmaceuticals North America, Inc. Dr. Roman held several director positions at Pfizer Global Research and Development, most recently in the Clinical Development Group developing drugs in the pain and inflammation therapeutic areas. Prior to Pfizer she worked for Parke-Davis/ Warner Lambert, in the Clinical Pharmacology and Experimental Medicine Department. Dr. Roman is a graduate in Medicine from the Medical School University of Targu- Mures, Romania. Following training in Internal Medicine, she began her career in the pharmaceutical field at the Ohio State University, Clinical Pharmacology Department. In her career to date, Dr. Roman has a strong focus on translational medicine research by facilitating and improving drug development.
 
   
       
David Sidransky, M.D. Chairman, Champions Biotechnology    
     

David Sidransky, M.D. was appointed the Chairman of the Board of Directors in October, 2007. Dr. Sidransky is a renowned oncologist and research scientist named and profiled by TIME magazine in 2001 as one of the top physicians and scientists in America, recognized for his work with early detection of cancer. Since 1994, Dr. Sidransky has been the Director of the Head and Neck Cancer Research Division at Johns Hopkins University School of Medicine and Professor of Oncology, Otolaryngology, Cellular & Molecular Medicine, Urology, Genetics, and Pathology at John Hopkins University and Hospital. Dr. Sidransky is one of the most highly cited researchers in clinical and medical journals in the world, in the field of oncology during the past decade, with over 300 peer-reviewed publications. He has contributed more than 40 cancer reviews and chapters. Dr. Sidransky is a founder of a number of biotechnology companies and holds numerous biotechnology patents. He has served as Vice Chairman of the Board of Directors, and was, until the merger with Eli Lilly, a director of ImClone Systems, Inc., a global biopharmaceutical company committed to advancing oncology care. He is the Chairman of Alfacell Corporation and serves on the Board of Directors of Xenomics. He is serving and has served on scientific advisory boards of MedImmune, Roche, Amgen and Veridex, LLC (a Johnson & Johnson diagnostic company), among others. Dr. Sidransky serves as Director (2005-2008) of American Association for Cancer Research (AACR). He was the chairperson of AACR International Conferences (2006 and 2007) on Molecular Diagnostics in Cancer Therapeutic Development: Maximizing Opportunities for Personalized Treatment. Dr. Sidransky is the recipient of a number of awards and honors, including the 1997 Sarstedt International Prize from the German Society of Clinical Chemistry, the 1998 Alton Ochsner Award Relating Smoking and Health by the American College of Chest Physicians and the 2004 Hinda and Richard Rosenthal Award from the American Association of Cancer Research. Dr. Sidransky received a B.A. from Brandeis University and M.D. from the Baylor College of Medicine.

 
     
       

Jayson Slotnik Health Policy Specialist, Foley Hoag

 
       

Jayson Slotnik serves as Counsel in the firm’s Government Strategies practice, where he advises clients on Medicare and Medicaid coverage, as well as reimbursement and coding issues covering medical devices, diagnostic tests, drugs, and biologics. Prior to joining Foley Hoag LLP, he worked as an Associate for other nationally renowned law firms advising both payors and innovators pertaining to Medicare and Medicaid payment and coverage issues. Previously, Jayson served as the initial Director of Medicare and Medicaid Reimbursement at the Biotechnology Industry Organization (BIO), the principal trade organization for the global biotech industry, handling matters relating to insurance coverage, coding and payment of drugs and biologics. He regularly represented the industry before the Center for Medicare and Medicaid Services, as well as Congress regarding coverage and reimbursement issues. In addition, Jayson advised BIO members on business development issues and worked with the membership and affiliate groups to develop innovator friendly policies related to complex diagnostic tests and other medical therapies. Prior to law school, Jayson gained extensive private sector healthcare experience. He worked as an epidemiologist designing scientific studies demonstrating clinical effectiveness of client products. As a senior analyst for a legislative firm, he monitored Medicaid and Medicare programs for healthcare technology clients with an eye towards expanding access to clients' therapies. He started his career as a reimbursement analyst for a pharmaceutical consulting firm counseling pharmaceutical and biotechnology companies on Medicare, Medicaid and other government reimbursement policies.

 
     
       

Keith Strier Principal & Partner, Health Sciences & Government Practice, Deloitte LLP

 
       

Keith Strier is a Principal/Partner with Health Sciences & Government Practice of Deloitte LLP and serves in numerous roles including Co-Leader, Health Informatics and Senior Fellow in Deloitte’s Washington, DC-based healthcare think tank, Center for Health Solutions. Keith advises Ministries of Health and Multi-National Corporations alike on biomedical innovation, personalized healthcare, translational medicine and globalization themes such as medical tourism and cross-border collaboration. Keith has been a Guest Faculty at the Harvard Medical School / MIT Health Science Technology Program, lecturing on healthcare innovation, since 2002. He also serves as a Strategic Advisor to Harvard Medical School’s Center for BioMedical Informatics. Keith has been a guest speaker at many prominent US academic institutions, including UCLA’s LA BioMedical Research Institute, UC Irvine’s Healthcare MBA Program, USC’s Global BioBusiness Initiative, UC Berkeley’s BioExec Institute, Claremont’s Keck School of Applied Sciences and at the Mayo Clinic’s Inaugural Symposium on Innovation in Healthcare. Internationally, Keith has been an invited speaker at the Summit on Information Systems in Translational Research at Seoul National University in Seoul, South Korea (2008), at Peking Union Medical Center in Beijing, China (2009) and at Amgen’s 2nd annual Oncology and Hematology Conference in Istanbul, Turkey (2010). Mr. Strier has a Bachelor’s of Science in Industrial & Labor Relations with Honors from Cornell University (1993) and a Law Degree from New York University’s School of Law (1996).

 
     
       

Patrick Terry, CEO of Technic Solutions, Co-Founder of Genomic Health, Founder of Personalized Medicine Coalition

 
     
Patrick F. Terry is a social entrepreneur who has founded a series of philanthropic, research, and commercial organizations based on the life sciences, applied technology, and social-network theory. He is the co-founded of Genomic Health [NASDAQ: GHDX], and former Director at the pioneering personalized medicine company based in California. His perspective is forged from personal and family experiences with genetic disease, cancer, and extensive work in the patient advocacy community. He has published dozens of peer-reviewed scientific papers, articles, and book chapters in the fields of genetics, rare disease, and personalized medicine. Some of his recent activities included leadership positions on numerous trade associations, professional societies, corporate boards, and federal advisory bodies. He has experience doing hands-on bench science, coordinating genetics research, conducting research on rare diseases, and managing a life sciences patent portfolio. He has received many honors and awards in the business and scientific communities in the U.S. and internationally. He has dedicated his career to helping people and advancing a patient-centered perspective in research, product development, and delivery of care. He is currently a Director at Sirius Genomics, TcLand Expression, BioLogos Foundation, and GRAND Therapeutics. Patrick has also founded the following organizations: Personalized Medicine Coalition, 21st Century Medicine Coalition, PXE International, Genetic Alliance BioBank, International Genetic Alliance, European Personalized Medicine Diagnostic Association, and GRAND Therapeutics.
 
   
     

Alan H.B. Wu, Ph.D. Professor of Laboratory Medicine, UCSF Pathology & Laboratory Medicine

 
       
Dr. Wu is Chief of Clinical Chemistry and Toxicology at San Francisco General Hospital and Professor of Laboratory Medicine, University of California, San Francisco. He received B.S. degrees in chemistry and biology at Purdue University, West Lafayette, Indiana, and a Ph.D. degree in analytical chemistry at the University of Illinois, Champaign-Urbana, Illinois. He completed a postdoctoral fellowship in clinical chemistry at Hartford Hospital. He is certified by the American Board of Clinical Chemistry in Clinical Chemistry and Toxicological Chemistry. Dr. Wu’s research interest has been in three areas within the field of clinical chemistry laboratory. He has been involved at the national and international levels with development and use of biochemical markers for cardiovascular disease including CK-MB, myoglobin, troponin, B-type natriuretic peptide, and markers of myocardial ischemia, and stroke. As also has a long history of analytical, clinical, and forensic toxicology. In both of these areas, Dr. Wu has co-authored the National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines. More recently, Dr. Wu has developed research and clinical programs in pharmacogenomics in support of the UCSF clinical pharmacogenomics laboratory. Among the areas of interest include pharmacogenomics for anticoagulants, especially warfarin, chemotherapeutics (tamoxefin, irinotecan), and drugs that can induce hypersensitivity reactions (abacavir, anticonvulsants).
 
     
       
 BOOT CAMP SPEAKERS  
     
Amos Barzilay Venture Consultant, Walden International  
     
Until recently, Dr. Barzilay was the interim CEO of CollabRx, a biotechnology company whose goal is to help oncologists develop customized therapies for cancer patients who are unresponsive to standard treatments.  Dr. Barzilay is a Venture Consultant and was a General Partner with Walden International, a global Venture Capital firm with over $2 billion under management. At Walden Dr. Barzilay led several investments in innovative software companies and served on their boards. Prior to joining Walden Dr. Barzilay was Vice President & General Manager, Content and Supplier Solutions in Commerce One. Dr. Barzilay joined Commerce One as part of Commerce One's acquisition of Mergent Systems in January 2000. Dr. Barzilay was a co-founder, chairman, and CEO of Mergent Systems, a business-to-business e-commerce infrastructure start-up. Prior to Mergent, Dr. Barzilay held a variety of senior management positions including General Manager of C*ATS,  senior marketing executive at Informix and CEO at Syntelligence Systems. Prior to Syntelligence, Dr. Barzilay was an AI researcher at Xerox Parc. Dr. Barzilay has an engineering degree from the Technion in Israel and an M.B.A. and Ph.D. degree from the University of Pittsburgh.
 
     
     
Benny Schnaider Co-Founder & former CEO, Qumranet (acquired by Redhat)  
     

Benny Schnaider was Qumranet's CEO and a Co-Founder. The company was acquired by Redhat in 2008. Benny was CEO and Co-Founder of PentaCom Ltd. a provider of networking products which was acquired by Cisco in 2000. Benny also co-founded and served on the Board of Directors for P-Cube, a developer of IP service control platforms, which was acquired by Cisco in 2004. Over the past 30 years, Benny has held senior management, engineering and strategic roles at many Silicon-Valley based companies including Cisco Systems, Amdahl/Fujitsu, Hitachi, IDT, Sun Microsystems and 3Com. Benny holds a Masters degree in Engineering Management from Santa Clara University, and a B.Sc in Computer Engineering from the Technion (Israel Institute of technology).

 

 
     
     
Steve Blank Lecturer, UC Berkeley, Stanford University  
     

Steve Blank is a retired serial entrepreneur and has been a founder or participant in eight Silicon Valley startups since 1978. After he retired, he wrote a book about building early stage companies:  Four Steps to the Epiphany. He's moved from being an entrepreneur to teaching entrepreneurship to both undergraduate and graduate students at U.C. Berkeley, Stanford University and the Columbia University/Berkeley Joint Executive MBA program. The “Customer Development” model that he developed in his book is one of the core themes for these classes. In 2009 he was awarded the Stanford University Undergraduate Teaching Award in the department of Management Science and Engineering.

 
     
     
Eli Sternheim Co-founder, President & CEO, interHDL (acquired by Avant! Corp.)  
     

Eli Sternheim has more than 25 years of experience in engineering, management, entrepreneurship, business and investment. He received his B.Sc. in EE from the Technion, and M.Sc. and Ph.D. in EE from Carnegie Mellon University. Dr. Sternheim has worked for a few startups, such as Trilogy, Zoran and Nexgen (later went public and was acquired by AMD). In 1991 Dr. Sternheim co-founded interHDL, an EDA company where he was the president and CEO. He wrote the book "Digital Design and Synthesis with Verilog HDL" and served as the chairman of the Architectural Committee for Open Verilog International (OVI). InterHDL was sold to Avant! corporation. Since 1995 Dr. Sternheim has been investing in high-tech startups and currently holds a portfolio of a few dozen companies. In 1999, he joined Redwood VP as a Venture Partner.

 
     
     
Joseph Bach Partner, Nixon Peabody  
     
Mr. Bach has more than a decade of legal experience in all aspects of intellectual property law, including patent prosecution and litigation. Joseph has developed methodologies for, and counsels clients on, efficiently building and managing effective patent portfolios. Joseph has successfully handled and managed cases in a broad range of technologies and has litigation experience before the International Trade Commission and federal courts. Joseph was formerly Senior Director of Intellectual Property at Applied Materials, where he was responsible for all aspects of the company's intellectual property internationally. He hold a law degree from the Duke University School of Law and a B.S. Engineering and Applied Science from California Institute of Technology (Caltech).
 




     
 
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