2015 Archived Content
Speaker Biographies
Sylvia L. Asa, M.D., Ph.D., Laboratory Medicine Program, University Health Network; Senior Scientist, Ontario Cancer Institute; Professor, Laboratory Medicine & Pathobiology, University of Toronto
Dr. Sylvia Asa is Professor in the Department of Laboratory Medicine and Pathobiology at the University of Toronto and recently completed 15 years as the Pathologist-in-Chief and Medical Director of the Laboratory Medicine Program at the University Health Network. A Clinician-Scientist with a focus on Endocrine Pathology, her research aims to identify the basis for development of endocrine tumors, to improve diagnostic tests and to identify targets for therapy of those diseases. She has published more than 400 scientific articles, written four books, co-edited five books and written more than 100 book chapters. As head of the largest academic pathology department in Canada, Dr. Asa made innovative changes to the practice of the discipline, with emphasis on subspecialization, automation, biobanking, electronic initiatives and digital pathology.
Sassan
M. Azad, Project Manager, Clinical, Translational & Biobanking Research
Office, Toronto Lung Transplant Program, Toronto General Hospital, University
Health Network
For the past 10
years, Sassan has been working as acting manager and Clinical Research
Associate (CRA) in the division of Thoracic Surgery & Lung Transplantation
at University Health Network (Toronto, Canada). Sassan’s duties and
responsibilities include clinical trial management, database management and
biobanking management all within the Toronto Lung Transplant Program. Sassan’s
job as liaison/bridge is to act as a hub transitioning basic research (bench)
to clinical applications (bedside) by providing the high-quality and accurate
data and biospecimens to support current and future research proposals.
Amit
Bar-Or, M.D., FRCPC, Professor, Neurology & Neurosurgery; Director,
Experimental Therapeutics Program and Scientific Director, Clinical Research
Unit, Montreal Neurological Institute, McGill University
A
neurologist and neuroimmunologist at the Montreal Neurological Institute (MNI),
McGill University, Dr. Bar-Or’s laboratory studies basic principles of
immune-regulation, immune-neural interaction and neural-glial interaction, and
roles in physiologic processes, inflammatory injury and repair in the human
central nervous system. His clinical focus is MS and he is currently the
President of the Canadian Consortium of MS Clinics. He also serves as Director,
Experimental Therapeutics Program and Scientific Director, Clinical Research
Unit at the MNI. Dr. Bar-Or coordinates a number of multicenter national and
international translational research initiatives. An overarching theme is
translation of basic lab discoveries towards development and understanding of
novel experimental therapies and biomarkers for patients with autoimmune and
neurological diseases. Dr. Bar-Or serves on the several journal editorial
boards and serves on the scientific/advisory boards of the Guthy-Jackson
Greater-Good Foundation (NMO research); the Accelerated Cure Project; the
ACTRIMS, ISNI and FOCIS organizations; and as Speaker of the Scientific
Advisory, German National MS/Neuroimmunology Kompetenz Network. Following undergraduate work in biopsychology
at McMaster University, Dr. Bar-Or received his medical degree cum laude from McGill University, then
pursued Neurology residency and Fellowship training in Neuroimmunology at
Harvard University where he also completed the Harvard/MIT Clinical
Investigator Training Program (CITP).
Mary Kay Belota, MA, MT(ASCP)SBB, CQA(ASQ), Consultant, Consulting Services Division, AABB
Mary Kay Belota, Consultant, brings over 25 years’ experience in cellular therapy, blood center operations and transfusion medicine to AABB’s Consulting Services Division. With such diverse experience, she is well versed in accreditation and licensure requirements, to include FDA’s cGMP and cGTP. Building organizational capacity, Mary Kay integrates standards and regulations with workplace protocols to achieve patient-centered, quality-driven operations. Prior to joining AABB, Mary Kay was the technical supervisor with the St. Louis Cord Blood Bank in St. Louis, MO, serving as the manufacturing subject matter expert during their successful application for FDA licensure. As the laboratory director of the GMP Facility at Washington University in St. Louis, Mary Kay focused on the development of quality systems for this translational research program. She gained Director-level experience in blood center operations with the American Red Cross Missouri-Illinois Region, responsible for collections, manufacturing, donor testing and blood product inventory management. Mary Kay managed the transfusion service at St. Louis University Hospital, a tertiary care teaching facility. Mary Kay received her Bachelor of Science degree in Medical Technology from West Virginia University and is certified as a Specialist in Blood Banking by the American Society for Clinical Pathology. She graduated from Washington University in St. Louis with a Master of Arts in Human Resources Management.
Marianna
J. Bledsoe, MA, Adjunct Assistant Professor, Department of Clinical Research and
Leadership, George Washington University School of Medicine and Health
Sciences; Co-Chair, Science Policy Committee, ISBER
Marianna is
a science policy consultant and Adjunct Assistant Professor in both the
Department of Pathology and the Department of Clinical Research and Leadership
at George Washington University School of Medicine and Health Sciences. She is
also Deputy Editor for Biopreservation and Biobanking. Involved in
biobanking for nearly 20 years, Marianna managed numerous biobanks at the National
Cancer Institute and the Department of Veterans Affairs. As Deputy Associate
Director of the Clinical Research Policy Analysis and Coordination Program in
the Office of Science Policy, Office the Director, NIH, she helped develop biobanking policies nationally and internationally. These
included the HHS Secretary’s Advisory Committee for Human Research Protections
recommendations on specimen research, the Council of Europe Recommendations on
Human Biological Materials(2006), the Organization for Economic Cooperation and
Development Guidelines on Human Biobanks and Genetic Research Databases, the
NCI Best Practices for Human Specimen Resources and International Society for
Biological and Environmental Repositories (ISBER) 2012 Best Practices
for Repositories. Marianna was ISBER President 2007. She serves on their Board
of Directors and co-chairs the ISBER Science Policy Committee. She received the
2012 ISBER Distinguished Leadership and Service Award, and the 2013 ISBER
Special Act or Service Award.
Dawn E.
Bowles, Ph.D., Assistant Professor, Department of Surgery, Division of Surgical
Sciences and Co-Director, Duke Human Heart Repository
Dawn E. Bowles, Ph.D., is an Assistant
Professor in the Department of Surgery, Division of Surgical Sciences, and
Co-Director of the Duke Human Heart Repository. Her research is focused on
discovery, testing and translation of novel therapeutic modalities for cardiac
injury and end-stage heart failure. With Dr. Carmelo Milano, M.D., Dr. Bowles
has developed a cardiac transplantation biorepository that is heavily
integrated into their research on improving cardiac transplant outcomes.
Beth Bradford, Client Support Project Manager, BioProcessing Solutions Alliance (BSA)
As Client Support Project Manager of the BioProcessing Solutions Alliance, Beth Bradford serves as a lead manager of client projects and is responsible for ensuring client requirements, on-time deliverables and customer satisfaction. After years of client relationship management, she is recognized as a subject matter expert in establishing a client governance structure while utilizing project management tools and best practices to ensure overall success of client programs. With a strong background in the FDA-regulated biopharmaceutical industries, Bradford has developed a deep appreciation for high ethical standards, product integrity and process compliance. She possesses extensive experience with project execution in fast-paced, contracted services environments through identification of key performance metrics and process improvement initiatives. Bradford earned an MBA from Washington University, St. Louis, and has a BA in Chemistry from Indiana University, Bloomington.
Andrew Brooks, Ph.D., COO, RUCDR Infinite Biologics; Associate Professor, Genetics, Rutgers University
Dr. Brooks is the Chief Operating Officer
of RUCDR Infinite Biologics and Director of the Bionomics Research and
Technology Center at Rutgers University. He is also one of the founding members
of the Bioprocessing Solutions Alliance. Dr. Brooks is a molecular
neuroscientist whose research focuses on deciphering the molecular mechanisms
that underlie memory and learning. Dr. Brooks is a well-recognized genomicist
and has been involved in the development and implementation of cutting-edge
molecular-based technologies for nucleic acid and protein analyses.
Rex L. Chisholm, Ph.D., Vice Dean, Scientific Affairs and Graduate
Education; Adam and Richard T. Lind Professor, Medical Genetics, Northwestern University
Feinberg School of Medicine
Dr. Chisholm is the Adam and Richard T. Lind Professor of
Medical Genetics in the Feinberg School of Medicine and professor of Cell and
Molecular Biology and Surgery. He was the founding Director of the Center for
Genetic Medicine. Since 2007 he has served as Vice Dean for Scientific Affairs
in the Feinberg School. In October 2012 he was also appointed Associate Vice
President for Research of Northwestern University. A faculty member at
Northwestern University since 1984, Chisholm is author of over 100 scientific
publications. His research focuses on genomics and bioinformatics. Chisholm
leads a major DNA biobanking effort at Northwestern University, NUgene (www.nugene.org). NUgene enrolls research
participants in a study focused on investigating the genetic contributions to
human disease, therapeutic outcomes and gene-environment interactions. NUgene
is a participant in the NHGRI-funded eMERGE network (www.gwas.net) – a network of electronic medical
record (EHR) linked biobanks. The goal of his current eMERGE network project is
to establish a program for genomics-informed personalized medicine in
partnership with Northwestern’s health care affiliates. He is Principal
Investigator of dictyBase (www.dictyBase.org), the NIH-funded genome database for
the cellular slime mold Dictyostelium and is an NHGRI-funded member of the gene
Ontology Consortium (www.geneontology.org).
His research has been supported by the National Institutes of Health, the
American Cancer Society, American Heart Association and the Department of
Defense.
Rajiv Dhir, M.D., MBA, Chief, Pathology, Shadyside Hospital,
University of Pittsburgh Health Systems
Rajiv
Dhir, M.D., MBA, is a practicing pathologist and currently serves as the Chief
of Pathology at Shadyside Hospital, one of the flagship hospitals of the
University of Pittsburgh. He is a board-certified pathologist with subspecialty
fellowship training in Genitourinary pathology. He has served as the director
of the GU center of excellence at the University of Pittsburgh for the past
nine years. Dr. Dhir’s interests include the molecular changes in bladder,
renal and prostate carcinogenesis. He has been involved in numerous clinical,
basic and translational projects focused on GU diseases and has been a
recipient of NIH/NCI grants in this area. His major focus of interest is the
identification and validation of novel targets for diagnostic, prognostic and
therapeutic use. Dr. Dhir has been the Medical Director of the Health Sciences
Tissue Bank of the University of Pittsburgh since 1997. He oversees the tissue
and biological specimen collection at the four flagship hospitals of the
University of Pittsburgh Health Systems. This Tissue Resource has developed
into a large resource for basic and translational research at the University of
Pittsburgh as well collaborative research with investigators outside the
University of Pittsburgh. This facility is a designated core facility for the
University of Pittsburgh and the University of Pittsburgh Cancer Institute and
supports many institutional, national and international initiatives. The
University of Pittsburgh was one of the largest contributors to the TCGA
effort. Dr. Dhir was also one of the participants in the RAND report on Tissue
Banking and has been an invited member of the Marble Arch group, an
international consortium of Tissue Bankers. He has published 10 book chapters,
has over 145 peer-reviewed publications and has over 100 published abstracts.
Heidi Elmoazzen, Ph.D., Director, National Public Cord Blood Bank
Dr. Heidi Elmoazzen
currently works at Canadian Blood Services where she is the Director of the
National Public Cord Blood Bank. She is responsible for leading the Cord Blood
Project Team in the establishment and successful national implementation of the
National Public Cord Blood Bank. Dr. Elmoazzen obtained her Ph.D. in Medical
Sciences from the University of Alberta with a concentration in cryobiology.
She then went on to do a postdoctoral fellowship at Harvard Medical School and
Massachusetts General Hospital in Boston, USA. Following her fellowship, in
2010, she became an instructor at Harvard Medical School and an Assistant in
Bioengineering in the Department of Surgery and Obstetrics and Gynecology. Her
area of research was focused on fertility preservation and developing novel
biopreservation techniques for stem cells and reproductive cells. Her main
areas of expertise and experience include bio-preservation, stem cell banking
and translational medicine. She has
published two book chapters on stem cell preservation as well as over 20
journal papers. She has over 70 contributed and invited presentations at
various national and international meetings.
Neil
Fleshner, M.D., MPH, FRCSC, Chair, Urology,
Department of Surgery, University of Toronto; Head, Urology, University
Health Network; Director, GU BioBank, Princess Margaret Cancer Centre
Dr.
Fleshner is Chair of Urology at the University of Toronto as well as Chief of
Urology at the University Health Network. He has achieved an international
reputation as a talented cancer researcher who has made significant
contributions in the field of urologic oncology. His current research
priorities include translational, clinical and health services research and he
has published over 250 articles in these areas. Dr. Fleshner conceptualized,
developed and continues to oversee a highly successful uro-oncology BioBank
that is a central resource for research discovery in proteomics and genomics
with the goal of personalizing medicine and ultimately improving outcome for GU
oncology patients. He has also played a major role in the establishment of a
Canadian research network to foster biologic research across the country from
coast to coast.
Gord Glendon, MSc, Research Project Director, Ontario Familial Breast Cancer Registry, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Princess Margaret Hospital, University Health Network
Mr. Glendon has an Honours Bachelor of Science degree in Genetics from the University of Western Ontario and a Master’s in Genetic Counselling from McGill University. He has worked in the field of familial predisposition to cancer for over 20 years. His time has been spent in both the clinical and research realms, initially as a genetic counsellor and more recently as the Research Project Director of the Ontario Familial Breast Cancer Registry. His research interest lies in the impact of the presence of cancer upon families and the clinical application of evolving genetic technology. In the last five years he has been co-author on over 50 publications regarding genetic predisposition to breast cancer.
Nickolas
Greer, CSO, Rissali LLC
Nickolas
Greer is a CSO of Rissali – a biopreservation company based in Missouri, USA.
His research is focused on developing novel methods for cryopreservation of
live cells and tissues, including the innovative approach for freezing under
pressure recently published in Cryobiology
journal. Mr. Greer holds degrees in Mechanical Engineering and Biology.
Aaron Hansen, BSc, MBBS (Hons), FRACP, Medical Oncologist, Princess Margaret Cancer Centre
Dr. Aaron Hansen is a medical oncologist at the Princess Margaret Cancer Centre and he is an assistant professor in the Department of Medicine at the University of Toronto. His research interests include clinical genomics and experimental therapeutics. As a clinician investigator he has developed several studies under the flagship Clinical Genomics Program at the Princess Margaret involving next-generation sequencing of archived samples, in addition to fresh tissue, cytology and blood specimens to identify actionable somatic mutations that may select patients for treatment on early phase clinical trials. Some of his work has also included evaluating tumor heterogeneity in the clinic and he has more recently expanded his translational interests to include immune profiling on archived tissue samples. Dr. Hansen is currently involved in developing several immune therapies on phase I trials and he is part of the newly formed immune-oncology program at Princess Margaret.
Marianne K. Henderson, MS, CPC,
Chief, Division of Cancer Epidemiology & Genetics, Office of Division
Operations and Analysis and the Center for Global Health, National Cancer
Institute, National Institutes of Health; Chair, Organizing
Advisory Committee, ISBER
Ms. Henderson is the Chief, Office of
Division Operations and Analysis in the Division of Cancer Epidemiology and
Genetics of the U.S. National Cancer Institute. She also lends her expertise as
an advisor to the NCI Center for Global Health for biobanking. She trained in
Zoology and Marine Ecology at the University of Maryland, College Park. She has
postgraduate training in molecular biology and genetics. In her role in DCEG,
she is responsible and involved in program operations, project and contract
management, fiscal and scientific reporting; strategic planning; technology
transfer; development and oversight of computing contract management; and
laboratory/biorepository infrastructure planning for large-scale molecular
epidemiology studies for the Division. She is a founding member of the NCI
Biospecimen Coordinating Committee established by the NCI Biorepositories and
Biospecimen Research Branch (BBRB) (née OBBR) and participated in the
development and revision of the first and second editions of NCI’s Best
Practices for Biospecimen Resources. Since 1999, she has been a member of the
International Society for Biological and Environmental Repositories (ISBER) and
served as ISBER President 2011-2012. Marianne is currently the Chair of the
ISBER Organizing Advisory Committee. She is also a member of the BBMRI-LPC SEAB
and BBMRI.se Advisory Boards; member of the U.S. Interagency Working Group on
Scientific Collections; Steering committee member of the International Agency
on Cancer’s LMIC Biobank and Cohort Network
(BCNet); and the U.S.-France Working Group on Large Scale Infrastructure for
Life Sciences. Ms. Henderson is actively involved in human biospecimen
management process improvements in processing, handling, technology transfer
and repository automation.
Galen Hostetter, M.D., Associate Director, Pathology Core, Van Andel
Research Institute
Galen is a research pathologist at the Van Andel Institute with >15 years’ experience in research applications with human pathology and cancer focus on analyte validation on tissue specimens, including paraffin tissue adaptation. His work is highly collaborative and incorporates sophisticated technologies that include microarray and NGS experiments as well as multiplexed tissue-based assays. Tissue microarray (TMA) technology, a proven high-value and low-tech tool in translational cancer research, was validated by Dr. Hostetter and his colleagues as an NIH fellow in the Kallioniemi/Trent lab in the late 1990’s. The design and use of TMAs remains an integral function in assay optimization of novel biomarkers in Dr. Hostetter’s laboratory. More recently, contributions to the Program for Biospecimen Science at VARI include design of animal-based studies to assess pre-analytic variables and effect on RNA integrity by multimodality platforms including whole transcriptome RNA-seq.
Anthony
M. Joshua, MBBS, Ph.D., Staff Oncologist/Affiliate Scientist, Princess Margaret
Cancer Centre
Dr. Anthony
Joshua completed his medical oncology training at the Royal Prince Alfred
hospital in Sydney, Australia before moving to Toronto to complete a Ph.D.
under the supervision of Dr. Jeremy Squire in prostatic carcinogenesis. He has
since joined the Department of Medical Oncology at Princess Margaret Hospital,
specialising in genito-urinary malignancy and melanoma. He is currently an
Assistant Professor with the University of Toronto and a clinician-scientist at
the University Health Network. His research interests include (I) Understanding
Phenotype to Genotype correlations and as such he co-leads the Princess
Margaret Cancer Centre Rapid Autopsy Program and the Exceptional responders
Program, (II) the unfolded protein response (working with Dr. Brad Wouters),
(III) autophagy in prostate cancer, (IV) mechanisms of enzalutamide resistance
in prostate cancer immunotherapy and (IV) translational research in GU and
melanoma. He has currently published over 50 articles in his areas of interest
to date.
Devon D. Kelly, Director, OHSU Knight BioLibrary, Oregon
Health & Science University, Knight Cancer Institute
Devon Kelly
is the Director of the OHSU Knight BioLibrary at the Oregon Health and Science
University. She earned her BA in Zoology from the George Washington University,
and an MSc in Forensic Science, from the University of New Haven. Devon is a
molecular biologist by training with over 15 years’ experience in specimen
repository management, 10 years within pharmacogenetics research and five years
in basic research. Currently Devon is responsible for oversight of tissue
collections and related regulatory affairs, standardizing oncology sample and
data repository practices, and in developing strategies that allow value
creation of the Knight BioLibrary. Devon is a member of the International
Society of Biological and Environmental Repositories, and has gained
accreditation of her biobank from the College of American Pathologists.
Jonathan Y.H. Loh, Ph.D.,
Assistant Professor, Department of Biological Sciences, National University of
Singapore, A*STAR Institute of Molecular and Cell Biology
Jonathan Y.H. Loh, Ph.D., is an Assistant Professor at the National
University of Singapore. His research is focused on identification of novel
mechanisms and development of innovative technologies in cell fate
transformation. Recently his lab pioneered the use blood cells for defined
factor somatic cell reprogramming. This technique greatly facilitates the development
of global iPSCs biobanking.
Koren Mann, Ph.D., Assistant Professor, Oncology, Lady Davis
Institute for Medical Research, McGill University
Dr. Koren K. Mann is an Assistant Professor of Oncology at
McGill University and an Investigator at the Lady Davis Institute for Medical
Research. As part of the Lymphoma Translational Research Group, she performs
correlative studies in the context of clinical trials in diffuse large B-cell
lymphoma. Her lab is interested in the molecular basis of drug resistance
and overcoming this with targeted novel therapies. In addition, her lab has an
interest in the environmental toxicology of metals, including arsenic and
tungsten.
Veronique
Neumeister, M.D., Laboratory Director, Specialized Translational Services Lab,
Department of Pathology, Yale University School of Medicine
Veronique Neumeister is the Laboratory Director
of the Specialized Translational Services Lab at Yale University, School of
Medicine, Department of Pathology. She completed Medical School at the
University of Vienna, Austria, followed by a Surgery Residency in Vienna, Austria.
At Yale since 2007, Veronique has been involved in breast cancer and
biospecimen research with a focus on automated quantitative in situ biomarker analyses and its
application. The Specialized Translational Services Lab (STSL) has been part
of the Yale Pathology Tissue Services (YPTS) since 2013. This lab is a
CLIA-certified institution offering services to academic and non-academic
entities. Veronique focuses on in situ
assessment and quantification of proteins and non-coding RNAs, on
standardization of optimal tissue processing and development of new companion
diagnostic tests.
Annmarie Nowak, Coordinator & Director, Data Bank and
Biorepository, Biobanking Systems Integration Cancer Prevention and Population
Science, Roswell Park Cancer Institute
Annmarie
Nowak is the Coordinator and Director of Biobanking Systems Integration for the
Data Bank and BioRepository at Roswell Park Cancer Institute in Buffalo, New
York. She works with other RPCI biobanks and the clinical investigators to
coordinate, manage and execute requests for biospecimens and data. A Systems
Analyst with a focus on Information Technology in Cancer Research, she was lead
analyst on the design and implementation of the Laboratory Information
Management System (LIMS) in the DBBR and other core resources. She has over 20
years of experience in laboratory technology, data management, application
design, data processing and reporting. Her qualifications are based upon a
unique background in Medical Technology, Programming and Biology.
Jeffrey Otto, MBA, Ph.D., National Director, Center for Translational
Research, Institute for Research and Innovation, Catholic Health Initiatives
Dr. Otto is the National Director of Catholic
Health Initiatives Center for Translational Research - an organization that he
has led since its inception in 2009. Prior to CHI, he has held leadership roles
at Perlegen, Sequenom and Genaisance Pharmaceuticals. He has a Ph.D. in biology
from Marquette University and an MBA from NYIT.
Michael H. A. Roehrl, M.D., Ph.D., Director, UHN Program in
BioSpecimen Sciences, University Health Network and University of Toronto
Dr. Roehrl is
Director of the BioSpecimen Sciences Program (BSP) at University Health Network
in Toronto. He is a practicing academic physician-scientist who is dually
board-certified in both anatomic pathology and laboratory medicine. In
addition, he is a Principal Investigator at the Ontario Cancer Institute, where
he studies novel genomic and proteomic biomarkers of colorectal and pancreatic
cancers using a variety of biophysical (mass spectrometric) and bioinformatics
approaches. Dr. Roehrl’s BSP is one of the largest academic programs of its
kind in North America and has pioneered a number of research specimen data
management tools as well as rapid intraoperative procurement and unique rapid
research autopsy program.
Sherilyn J.
Sawyer, Ph.D., Scientific Director, BWH/Harvard Cohorts Biorepository, Channing
Division of Network Medicine, Brigham and Women’s Hospital
Dr. Sherilyn Sawyer is the Director of the
Cohorts Biorepository at the Channing Division of Network Medicine, which
contains approximately 3 million biospecimens representing the Nurses’ Health
Study, Health Professionals Follow Up Study and Growing Up Today cohorts, among
others. Prior to joining the BWH team in 2012, Dr. Sawyer was a Health Science
Administrator with the Office of Biorepositories and Biospecimen Research at
the National Cancer Institute. Her responsibilities included a major role in
the design and implementation of the caHUB program and technical oversight of
caHUB central operations. In addition, Dr. Sawyer served as the co-director of
Biospecimen Acquisitions for the Genotype Tissue Expression (GTEx) Roadmap
Initiative. Dr. Sawyer is a molecular biologist with expertise in cell
signaling and regulation of RNA expression. She earned her Ph.D. in Molecular
Biology, Cell Biology and Biochemistry from Boston University and a BS in
Molecular Biology from the University of Nevada-Reno.
Brent
Schacter, M.D., FRCPC, Principal Investigator, CTRNet; Professor, Department of
Internal Medicine, Section of Hematology/Oncology, College of Medicine,
University of Manitoba/CancerCare Manitoba; President-Elect, ISBER
Dr. Schacter is the President-Elect of ISBER (International Society for Biological and Environmental Biorepositories), a Professor in the Department of Internal Medicine of the University of
Manitoba and member of the Department of Medical Oncology and Hematology at
CancerCare Manitoba. From 1993 to 2003 he was President and CEO of CancerCare
Manitoba. He then became CEO of the Canadian Association of Provincial Cancer
Agencies (CAPCA) from 2003 until 2008. He was a member and then Co-Chair of the
Steering Committee of the Canadian Strategy for Cancer Control (CSCC) from 1999 to 2002 and Co-Vice Chair of the
Council for the CSCC from 2004 to
2006. He is the Principal Investigator on the Canadian Tissue Repository
Network (CTRNet, www.ctrnet.ca) Program
Grant from CIHR-ICR, which has launched the Canadian Tumour Biobank
Certification Program and which has received $ 6.3 million in funding from the
Canadian Institutes of Health Research-Institute of Cancer Research since 2004.
Dr. Schacter is currently the Co-Chair of the Canadian Task Force on AYA
(Adolescents and Young Adults) Oncology.
Christina Schröder, Ph.D, Head, Metabiobanks CRIP, Fraunhofer
Institute for Cell Therapy and Immunology
Christina Schröder is head of the group Metabiobanks CRIP at the
Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (IZI-BB) in Potsdam, Germany. Serving Fraunhofer since 2007, she has coordinated the Central
Research Infrastructure for molecular Pathology (CRIP). Meanwhile, her group
has developed further metabiobanks, including the “Projektportal im Deutschen
Biobanken-Register” (P2B2) as a pilot for the German BBMRI node, and – most
recently – the virtual biobank “DPKK-Biobank” for the German Prostate Cancer
Consortium. Dr. Schröder is a Councilor of the European, Middle Asian and
African Society for Biopreservation and Biobanking (ESBB), and an expert
registered with the German Institute of Standardization (DIN) and the
International Organization for Standardization (ISO).
Teresa Selander, Manager,
Biospecimen Repository and Processing Laboratory, Lunenfeld-Tanenbaum Research
Institute, Mount Sinai Hospital
Teresa has been helping investigators obtain accurate,
well-annotated and high-quality biospecimens for their research needs since 1998. She has been involved in the customized processing,
storage and distribution of biospecimens for over 20 different research studies
that range in both the number of samples and in complexity.
Dana Spence, Ph.D., Associate Professor, Department of Chemistry,
Michigan State University
Dr. Spence received his BS degree in chemistry from Grand Valley State University in Allendale, MI in 1992 and his Ph.D. in Analytical Chemistry from Michigan State University in 1997. He has been on the chemistry department faculty at Saint Louis University (1997-2004) and Wayne State University (2004-2007). Currently, he is a Professor of Chemistry and Professor of Cell and Molecular Biology at Michigan State University. Dr. Spence’s group, consisting of chemistry and biochemistry Ph.D. candidates, is interested in the development of biotechnological tools to facilitate understanding of the role of the red blood cell in the life sciences. Current efforts focus on revitalizing C-peptide as a replacement therapeutic for diabetes, investigating the unique metabolism of red cells obtained from people with multiple sclerosis, and improving red cells for use in transfusion medicine.
K. Stephen Suh, Ph.D.,
Director, Genomics and Biomarkers Program, John Theurer Cancer Center,
Hackensack University Medical Center
As scientific director of
the Tissue Bank, K. Stephen Suh, Ph.D., manages The Cancer Center’s Tissue
Repository and the Genomics and Biomarkers Program for multiple human cancer
types. Dr. Suh’s laboratory focuses on personalized medicine topics, including population
screening diagnostics, biomarkers-driven patient selection and precision drugs
for optimal clinical outcome and reducing healthcare costs. Dr. Suh has been
conducting research in molecular and cell biology, animal
modeling/translational science, biobanking and clinical science for over 25
years.
Daniel B. Thiel, Public Health Researcher, Health Services Organization
and Policy, University of Michigan School of Public Health
Daniel Thiel (MA, Philosophy Stony Brook
University; Doctoral Student, Health Management and Policy, University of
Michigan) is a doctoral student broadly interested in the ethical, legal,
social and policy implications of genomics and the introduction of genomics
into public health, clinical medicine and clinical research. Over the past five
years, as Assistant Director of the Life Sciences and Society Program (UM,
School of Public Health), Mr. Thiel has worked with an interdisciplinary team
of researchers to explore issues of community engagement, informed consent and
public preferences regarding biobanking in the state of Michigan. The work
presented here is made possible by support from NIH grants (5RC1HG005439 and R01-HD-067264) and the University of Michigan.
Suzanne
Vercauteren, M.D., Ph.D., FRCPC, Head, Division of Hematopathology, BC
Children’s Hospital and Clinical Assistant Professor, Pathology and Laboratory
Medicine, University of British Columbia
Suzanne Vercauteren is the Head of the
Division of Hematopathology at BC Children’s Hospital and is Director of the BC
Children’s Hospital BioBank. She is a Clinical Assistant Professor in the
Department of Pathology and Laboratory Medicine at the University of British
Columbia. Suzanne is also on the board of the management committee of the
Canadian Tumour Repository Network.
Kerry R. Wiles, Program Director, Cooperative Human Tissue Network
and Vanderbilt University Medical Center Tissue Repository, Vanderbilt
University
Kerry Wiles
is the Director for the Cooperative Human Tissue Network (CHTN) Western
Division at Vanderbilt University Medical Center under the direction of Mary
Kay Washington, M.D., Ph.D. Ms. Wiles received her BS degree from Pittsburgh
State University (Kansas) and has completed 20 hours towards an MS degree with
an emphasis on genetics-molecular biology and microbiology. She has over 15
years of “wet bench” research experience in genetic mapping, association
studies, tissue culture, MALDI-TOF /SNP genotyping and analysis, sequencing,
microsatellite library creation and robotics and over 20 years’ experience as a
project and laboratory manager. Ms. Wiles began her scientific career at the
University of Iowa working on genetic mapping of chromosome X and 4 and
association studies of BFLS and FSH. Ms. Wiles also studied the role of Beta
defensins in normal human lung, diseased lung (cystic fibrosis) and skin using
animal models. Ms. Wiles continued her scientific career at the National
Institutes of Health under the direction of Dr. Francis Collins, National Human
Genome Research Institute-NHGRI (FUSION) and was involved in NIDDM research
using a large Finnish cohort. In 2002, Ms. Wiles was recruited by Dr.
Washington to be the project manager/coordinator of CHTN Western Division at
Vanderbilt University Medical Center. Ms. Wiles is a certified Lean Six Sigma
Black Belt and has over seven years’ experience in Six Sigma and Lean Six
Sigma.