Elisabeth King, RN, FNP, AOCNP, AGN is a nurse practitioner and the senior manager of Genomic Cancer Risk Counseling in the Division of Clinical Cancer Genomics at City of Hope. Ms. King joined City of Hope in 2018 from Texas Oncology, where she helped lead and support the Advanced Practice Provider and Genetics programs throughout the state. She is a family nurse practitioner and also holds advanced nursing certifications in oncology and genetics. She received her bachelor’s degree in biology with a focus on genetics and biotechnology from University of Texas at Austin. She earned her master’s degree in nursing at Frontier Nursing University. King is an alumnus and clinical faculty member of the City of Hope Intensive Course in Cancer Risk Assessment.

RACHELLE MANOOKIAN, MS, CGC is a licensed and board-certified cancer genetic counselor specializing in pediatric oncology at Children’s Hospital Los Angeles (CHLA). She was previously with the Division of Clinical Cancer Genomics at City of Hope, and before that, a general genetic counselor at the VA Medical Center serving six VA hospitals via telehealth. She has a special interest in genitourinary cancers. She brings her growing expertise in medical education to her role as an adjunct faculty member for the Keck Graduate Institute Genetic Counseling and Genomic Data Analytics master’s programs. She serves as a faculty mentor, graduate capstone supervisor, and rotation supervisor for current genetic counseling students. She is actively engaged in the Fanconi anemia community and has been a volunteer at Camp Sunshine Fanconi Anemia week since 2016, and she is a two-time nominee of the Heart of Genetic Counseling Award from the National Society of Genetic Counselors

BITA NEHORAY, MS, CGC, is a licensed board-certified genetic counselor specializing in cancer genetics. She received her Master’s degree in Human Genetics and Genetic Counseling from Stanford University. Ms. Nehoray joined the City of Hope Division of Clinical Cancer Genomics in 2012. As a Senior Genetic Counselor she provides cancer genetics services for patients and families suspected to have a hereditary predisposition to cancer, with a focus in Li-Fraumeni syndrome and Clonal Hematopoiesis of Indeterminate Potential. Current research projects include understanding cancer risk, penetrance, prevalence, and clinical outcomes for individuals with TP53 pathogenic variants as part of the LiFT UP study, evaluating the spectrum of germline variants in Israeli breast cancer patients, and assessing community-based provider experiences with polygenic risk scores in genetic cancer risk assessment. She also serves on the genetic counseling advisory committee for the Li-Fraumeni Syndrome Association and is a member of the ClinGen TP53 Variant Curation Expert Panel. She is fluent in Spanish and Farsi and is committed to advancing the provision of cancer genetics services to medically underserved and culturally diverse populations. She is faculty for the City of Hope Intensive Course in Genetic Cancer Risk Assessment. She is an active member of the National Society of Genetic Counselors, Southern California Genetic Counselors, and the American Society of Human Genetics.

RACHELLE MANOOKIAN, MS, CGC is a licensed and board-certified cancer genetic counselor specializing in pediatric oncology at Children’s Hospital Los Angeles (CHLA). She was previously with the Division of Clinical Cancer Genomics at City of Hope, and before that, a general genetic counselor at the VA Medical Center serving six VA hospitals via telehealth. She has a special interest in genitourinary cancers. She brings her growing expertise in medical education to her role as an adjunct faculty member for the Keck Graduate Institute Genetic Counseling and Genomic Data Analytics master’s programs. She serves as a faculty mentor, graduate capstone supervisor, and rotation supervisor for current genetic counseling students. She is actively engaged in the Fanconi anemia community and has been a volunteer at Camp Sunshine Fanconi Anemia week since 2016, and she is a two-time nominee of the Heart of Genetic Counseling Award from the National Society of Genetic Counselors

Dr. Padma Sheila Rajagopal received her M.D. at Columbia University’s College of Physicians and Surgeons, during which she also received an M.P.H. in quantitative methods with a focus on genetic epidemiology at the Harvard School of Public Health. She completed her internal medicine residency training at the University of Pittsburgh and a fellowship in hematology/oncology with an additional fellowship year focused on cancer genetics at the University of Chicago, where she received an M.Sc. in biomedical informatics. Dr. Rajagopal is a recipient of the Ruth L. Kirschstein F32 Postdoctoral Fellowship and the American Society of Clinical Oncology / Breast Cancer Research Foundation Conquer Cancer Young Investigator Award.

Dr. Rajagopal’s laboratory focuses on how characterizing genomic and transcriptomic interactions between germline variants / inherited cancer syndromes and somatic development in tumors can improve clinical prediction and prognostication in patients with cancer. Her current research focuses on using transcriptomics to characterize breast cancers and treatment responses in patients with hereditary cancer syndromes.

COLIN PRITCHARD, MD, PhD, is a Professor of Laboratory Medicine and Pathology at the University of Washington and Program Director for Cancer Precision Diagnostics for the Brotman Baty Institute for Precision Medicine. He also serves as the Co-Director of the Genetics and Solid Tumors Laboratory that services the Fred Hutchinson Cancer Center. The Pritchard laboratory focuses on oncology molecular diagnostics, particularly the source and utility of cell-free nucleic acid biomarkers in blood, and the development of innovative molecular diagnostics for the identification of DNA repair gene mutations that can guide therapeutic decision-making. His clinical work focuses on applications of next-generation sequencing gene panels for cancer risk assessment and precision treatment. He has led the development and implementation of the ColoSeq™ Lynch and Polyposis Syndrome Panel and the UW-OncoPlex™ Cancer Gene Panel in current clinical use for cancer patients and their families. He is a longstanding distinguished faculty member of the City of Hope Clinical Cancer Genomics Community of Practice. In 2021 Dr. Pritchard was awarded the C2 Catalyst for Precision Medicine Award from Scientific American.

ALLISON W. KURIAN, M.D., M.Sc., is a Professor of Medicine and of Epidemiology and Population Health at Stanford University. She is Associate Chief of the Division of Oncology, Director of the Stanford Women’s Clinical Cancer Genetics Program, and Co-Leader of the Stanford Cancer Institute Population Sciences Program. Dr. Kurian’s research is designed to understand cancer burden and improve cancer treatment quality at the population level, with a focus on identifying women with elevated breast and gynecologic cancer risk, and on the development and evaluation of novel techniques for early cancer detection and risk reduction. She leads epidemiologic studies of cancer risk factors, clinical trials of novel approaches to cancer risk reduction, and decision analyses of strategies to improve cancer outcomes. Her research has been supported by grants from the National Institutes of Health, California Breast Cancer Research Program, Komen for the Cure Foundation, Breast Cancer Research Foundation, and others. Dr. Kurian’s work has been honored by Impact Awards of the National Consortium of Breast Centers and the BRCA Foundation, selection as a Komen Scholar and election to the American Society of Clinical Investigation. Dr. Kurian also contributes her extensive expertise to the City of Hope Clinical Cancer Genomics Community of Practice as a distinguished faculty member.

Lisa Madlensky, PhD, is a board-certified genetic counselor who provides cancer risk assessment and genetic counseling for patients and their families. She helps people investigate their family health history, navigate the genetic testing process, and understand and adapt to the medical or psychological implications of genetic diseases.

As director of the Family Cancer Genetics Program at Moores Cancer Center at UC San Diego Health, Dr. Madlensky helps ensure that patients and families with an increased risk of cancer receive outstanding care, with a focus on cancer prevention and early detection.

In addition to her clinical activities, Dr. Madlensky is a researcher at Moores Cancer Center. Her work centers on cancer prevention in those at increased risk of disease because of their family history or genetic predisposition. Her research themes include clinical genetic testing and follow-up for families with Lynch Syndrome and BRCA1/2 mutations; the public health implications of cancer genetic testing; quality of life in those at increased risk of cancer; the integration of cancer risk assessment into family practice; and family-level cancer prevention.

Dr. Madlensky earned her doctoral degree from the University of Toronto Institute of Health Policy, Management and Evaluation. She obtained a Master of Science in genetic counseling from McGill University in Montreal Canada.

BITA NEHORAY, MS, CGC, is a licensed board-certified genetic counselor specializing in cancer genetics. She received her Master’s degree in Human Genetics and Genetic Counseling from Stanford University. Ms. Nehoray joined the City of Hope Division of Clinical Cancer Genomics in 2012. As a Senior Genetic Counselor she provides cancer genetics services for patients and families suspected to have a hereditary predisposition to cancer, with a focus in Li-Fraumeni syndrome and Clonal Hematopoiesis of Indeterminate Potential. Current research projects include understanding cancer risk, penetrance, prevalence, and clinical outcomes for individuals with TP53 pathogenic variants as part of the LiFT UP study, evaluating the spectrum of germline variants in Israeli breast cancer patients, and assessing community-based provider experiences with polygenic risk scores in genetic cancer risk assessment. She also serves on the genetic counseling advisory committee for the Li-Fraumeni Syndrome Association and is a member of the ClinGen TP53 Variant Curation Expert Panel. She is fluent in Spanish and Farsi and is committed to advancing the provision of cancer genetics services to medically underserved and culturally diverse populations. She is faculty for the City of Hope Intensive Course in Genetic Cancer Risk Assessment. She is an active member of the National Society of Genetic Counselors, Southern California Genetic Counselors, and the American Society of Human Genetics.

SUSAN SHEHAYEB, MS, CGC, is a licensed board-certified genetic counselor specializing in cancer genetics with the Division of Clinical Cancer Genomics at City of Hope National Medical Center. She is fluent in Arabic and has competency in Spanish. She has a Master of Science degree in genetic counseling from University of California Irvine. Ms. Shehayeb's clinical role has centered on widening patient access to genetic counseling and testing throughout the City of Hope network and on genetics representation and expertise in the setting of gynecologic oncology. Her past research has focused on lifestyle choices in the context of hereditary cancer testing, hereditary causes of multiple breast cancers, and hereditary gynecologic cancers. Her special interests include hereditary gynecologic cancers and hereditary genodermatoses, furthering education of providers in the setting of genomic cancer risk assessment, and advocacy for diversity and equity in the field of cancer genetics. She is a faculty member of the City of Hope Intensive Course in Genetic Cancer Risk Assessment, and a member of the National Society of Genetic Counselors and the Southern California Genetic Counselors.

Lisa Madlensky, PhD, is a board-certified genetic counselor who provides cancer risk assessment and genetic counseling for patients and their families. She helps people investigate their family health history, navigate the genetic testing process, and understand and adapt to the medical or psychological implications of genetic diseases.

As director of the Family Cancer Genetics Program at Moores Cancer Center at UC San Diego Health, Dr. Madlensky helps ensure that patients and families with an increased risk of cancer receive outstanding care, with a focus on cancer prevention and early detection.

In addition to her clinical activities, Dr. Madlensky is a researcher at Moores Cancer Center. Her work centers on cancer prevention in those at increased risk of disease because of their family history or genetic predisposition. Her research themes include clinical genetic testing and follow-up for families with Lynch Syndrome and BRCA1/2 mutations; the public health implications of cancer genetic testing; quality of life in those at increased risk of cancer; the integration of cancer risk assessment into family practice; and family-level cancer prevention.

Dr. Madlensky earned her doctoral degree from the University of Toronto Institute of Health Policy, Management and Evaluation. She obtained a Master of Science in genetic counseling from McGill University in Montreal Canada.

Julie Culver, MS, LCGC, CCRP is a licensed genetic counselor and Clinical Instructor specializing in cancer genetics. She received her Master’s degree at the University of Michigan in Ann Arbor in 1994. Ms. Culver then worked in Cancer Prevention and Public Health at the University of Washington and the Fred Hutchinson Cancer Research in Seattle for almost a decade. In 2004, she joined the City of Hope Division of Clinical Cancer Genetics where worked for 8 years and served as the Assistant Director of the Cancer Screening & Prevention Program Network and conducted research pertaining to hereditary breast and ovarian cancer and decision-making for woman carrying deleterious BRCA mutations and variants of uncertain significance. In 2012, she moved to the USC Norris Cancer Comprehensive Cancer Center where she currently serves on the faculty of Medical Oncology and is the lead genetic counselor. Her research pertains to hereditary cancer panel testing, cancer risk perception, and medical decision-making following genetic testing. She has served on the faculty for the City of Hope Intensive Course and taught cancer risk assessment to health professionals and students since 2004.

BITA NEHORAY, MS, CGC, is a licensed board-certified genetic counselor specializing in cancer genetics. She received her Master’s degree in Human Genetics and Genetic Counseling from Stanford University. Ms. Nehoray joined the City of Hope Division of Clinical Cancer Genomics in 2012. As a Senior Genetic Counselor she provides cancer genetics services for patients and families suspected to have a hereditary predisposition to cancer, with a focus in Li-Fraumeni syndrome and Clonal Hematopoiesis of Indeterminate Potential. Current research projects include understanding cancer risk, penetrance, prevalence, and clinical outcomes for individuals with TP53 pathogenic variants as part of the LiFT UP study, evaluating the spectrum of germline variants in Israeli breast cancer patients, and assessing community-based provider experiences with polygenic risk scores in genetic cancer risk assessment. She also serves on the genetic counseling advisory committee for the Li-Fraumeni Syndrome Association and is a member of the ClinGen TP53 Variant Curation Expert Panel. She is fluent in Spanish and Farsi and is committed to advancing the provision of cancer genetics services to medically underserved and culturally diverse populations. She is faculty for the City of Hope Intensive Course in Genetic Cancer Risk Assessment. She is an active member of the National Society of Genetic Counselors, Southern California Genetic Counselors, and the American Society of Human Genetics.

Sonia S. Kupfer is an Assistant Professor of Medicine in the Section of Gastroenterology at the University of Chicago Medical Center, Chicago, IL. She is the Director of the Gastrointestinal Cancer Risk and Prevention Clinic and co-Director of the Comprehensive Cancer Risk and Prevention clinic at the University of Chicago. She is funded by a K08 career development award from the NIH/NCI to study colorectal cancer genetic susceptibility variants in African Americans. Dr. Kupfer is also currently investigating genetics related to chemopreventive agents for colorectal cancer, notably vitamin D. In addition to her translational research, Dr. Kupfer is actively engaged in clinical studies in high-risk colorectal cancer primarily Lynch syndrome. Her clinical work focuses on hereditary GI cancer evaluation, testing and management. She also has served as co-Director of two CME conferences on genomics. Dr. Kupfer received her undergraduate degree from Yale University and then completed medical school, residency, chief residency and gastroenterology fellowship training at the University of Chicago. She is originally from a northern suburb of Chicago and currently resides in the Hyde Park area with her husband, an art dealer, and her two children.

HEATHER HAMPEL, MS, CGC, is a Professor in the Department of Medical Oncology and Therapeutics Research and Associate Director of the Division of Cancer Genomics at City of Hope National Cancer Center. She co-leads the administration of more than 20 genetic counselors, 6 GCAs, and additional support staff who provide genetic cancer risk assessment through the City of Hope enterprise and more than 20 CRAs, LVNs and CRNs on the Precision Medicine consent team. Her research focuses on Lynch syndrome and universal tumor screening for Lynch syndrome. She has >190 publications on the prevalence of Lynch syndrome among colorectal and endometrial cancer patients, the best testing protocols, cost-effectiveness, and referral guidelines for cancer genetics. She was on the Board of Directors for the American Board of Genetic Counseling from 2006-2011, serving as President in 2009 and 2010. She has been on the Steering Committee of the National Colorectal Cancer Roundtable since 2016. She was on the Council of the Collaborative Group of the Americas on Inherited Colorectal Cancer from 2016-2019, serving as president in 2017-2018. She served as the Secretary/Treasurer of the National Society of Genetic Counselors in 2022. She was awarded the Natalie Weissberger Paul National Achievement Award from the National Society of Genetic Counselors in 2023.

Dr. Idos is a board-certified gastroenterologist and trained cancer geneticist, who specializes in the care of patients with Lynch syndrome, FAP (familial adenomatous polyposis) and other inherited syndromes. The goal of his research is to find new ways to prevent cancer and to improve treatment and care for cancer patients.

A UCLA graduate, Dr. Idos has a master’s degree from Keck School of Medicine of USC. He received his medical degree at University of Vermont, continued his residency training at USC and completed his gastroenterology fellowship at Brigham and Women’s Hospital at Harvard. Dr. Idos is an associate clinical professor in Division of Gastroenterology and leads one of the largest multicenter studies examining the benefits and harms of “multiplex” gene panel testing. His research also focuses on the evaluation of novel technologies with the goal of providing new tools for hereditary cancer risk assessment and the development of novel cellular models to elucidate the fundamental mechanisms of microsatellite instability and Lynch syndrome.

Sonia S. Kupfer is an Assistant Professor of Medicine in the Section of Gastroenterology at the University of Chicago Medical Center, Chicago, IL. She is the Director of the Gastrointestinal Cancer Risk and Prevention Clinic and co-Director of the Comprehensive Cancer Risk and Prevention clinic at the University of Chicago. She is funded by a K08 career development award from the NIH/NCI to study colorectal cancer genetic susceptibility variants in African Americans. Dr. Kupfer is also currently investigating genetics related to chemopreventive agents for colorectal cancer, notably vitamin D. In addition to her translational research, Dr. Kupfer is actively engaged in clinical studies in high-risk colorectal cancer primarily Lynch syndrome. Her clinical work focuses on hereditary GI cancer evaluation, testing and management. She also has served as co-Director of two CME conferences on genomics. Dr. Kupfer received her undergraduate degree from Yale University and then completed medical school, residency, chief residency and gastroenterology fellowship training at the University of Chicago. She is originally from a northern suburb of Chicago and currently resides in the Hyde Park area with her husband, an art dealer, and her two children.

RACHELLE MANOOKIAN, MS, CGC is a licensed and board-certified cancer genetic counselor specializing in pediatric oncology at Children’s Hospital Los Angeles (CHLA). She was previously with the Division of Clinical Cancer Genomics at City of Hope, and before that, a general genetic counselor at the VA Medical Center serving six VA hospitals via telehealth. She has a special interest in genitourinary cancers. She brings her growing expertise in medical education to her role as an adjunct faculty member for the Keck Graduate Institute Genetic Counseling and Genomic Data Analytics master’s programs. She serves as a faculty mentor, graduate capstone supervisor, and rotation supervisor for current genetic counseling students. She is actively engaged in the Fanconi anemia community and has been a volunteer at Camp Sunshine Fanconi Anemia week since 2016, and she is a two-time nominee of the Heart of Genetic Counseling Award from the National Society of Genetic Counselors

Dr. Park is an assistant professor in the department of Medical Oncology and Therapeutics Research and Population Sciences at City of Hope National Medical Center. Dr. Park graduated medical school from The College of Osteopathic Medicine of the Pacific at Western University of Health Sciences in Pomona, California. She completed her internal medicine residency program at Kaiser Permanente-Fontana. During her internal medicine training, she developed deep interest in genetics and pursued medical genetics training at University of California, Irvine. She is board certified in Internal Medicine and clinical genetics and genomics.

Dr. Else’s primary appointment is with the Division of Metabolism, Endocrinology and Diabetes, but he currently serves as the Interim Chief of the Division of Genetics in Medicine in the Dept. of Internal Medicine. He received his MD degree from the University of Hamburg, Germany. He pursued his clinical training at the University of Hamburg (Residency: Internal Medicine) and the University of Michigan (Residency: Internal Medicine, Fellowship: Endocrinology). His main research interests are the genetics of endocrine tumors. Dr. Else’s clinical practice focuses on the care for patients with benign and malignant endocrine tumors, particularly pheochromocytoma, adrenocortical tumors and neuroendocrine tumors as well as accompanying hormone excess syndromes (e.g Cushing syndrome, primary aldosteronism). Dr. Else has a particular interest in taking care of patients with hereditary syndromes that predispose to the development of endocrine tumors (e.g. Multiple Endocrine Neoplasia (MEN) type 1, MEN2A & MEN2B, Hereditary Paraganglioma Syndrome). He attends the Multidisciplinary Endocrine Oncology Clinic, where patients with tumors receive diagnostic procedures and treatment. In addition, he is part of the Cancer Genetics Clinic, which evaluates patients for hereditary syndromes and facilitates regular exams and surveillance for patients at risk for endocrine tumors.