Janet Davison Rowley was an American human geneticist and the first scientist to identify a chromosomal translocation as the cause of leukemia and other cancers, thus proving that cancer is a genetic disease. Rowley spent the majority of her life working in Chicago and received many awards and honors throughout her life, recognizing her achievements and contributions in the area of genetics.
Ahmad Said Teebi was a Palestinian, born in Lebanon, clinical geneticist who studied and practiced in several countries, ending his career in Canada and the United States.
The Pritzker School of Medicine is the M.D.-granting unit of the Biological Sciences Division of the University of Chicago. It is located on the university's main campus in the historic Hyde Park neighborhood of Chicago and matriculated its first class in 1927. The medical school offers a full-time Doctor of Medicine degree program, joint degree programs, graduate medical education, and continuing medical education.
Oliver Smithies was a British-American geneticist and physical biochemist. He is known for introducing starch as a medium for gel electrophoresis in 1955, and for the discovery, simultaneously with Mario Capecchi and Martin Evans, of the technique of homologous recombination of transgenic DNA with genomic DNA, a much more reliable method of altering animal genomes than previously used, and the technique behind gene targeting and knockout mice. He received the Nobel Prize in Physiology or Medicine in 2007 for his genetics work.
R. Ellen Magenis was an American pediatrician, medical geneticist and cytogeneticist.
Robert Martin Jacobson is the medical director of the Population Health Science Program of the Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery. He is a previous chair of the Department of Pediatric and Adolescent Medicine at the Mayo Clinic and a full professor of pediatrics at the Mayo Clinic School of Medicine in Rochester, Minnesota. He still regularly sees young patients as a member of the Division of Community Pediatric and Adolescent Medicine. His research area is in vaccinology, with a focus on delivery, effectiveness, and adverse consequences. He is also involved with the Clinical Research Training Program in the Mayo Clinic School of Medicine, where he concentrates on teaching evidence-based medicine.
Arthur L. Horwich is an American biologist and Sterling Professor of Genetics and Pediatrics at the Yale School of Medicine. Horwich has also been a Howard Hughes Medical Institute investigator since 1990. His research into protein folding uncovered the action of chaperonins, protein complexes that assist the folding of other proteins; Horwich first published this work in 1989.
Jack William Szostak is a Canadian American biologist of Polish British descent, Nobel Prize laureate, university professor at the University of Chicago, former Professor of Genetics at Harvard Medical School, and Alexander Rich Distinguished Investigator at Massachusetts General Hospital, Boston. Szostak has made significant contributions to the field of genetics. His achievement helped scientists to map the location of genes in mammals and to develop techniques for manipulating genes. His research findings in this area are also instrumental to the Human Genome Project. He was awarded the 2009 Nobel Prize for Physiology or Medicine, along with Elizabeth Blackburn and Carol W. Greider, for the discovery of how chromosomes are protected by telomeres.
Yong Poovorawan is a professor of pediatrics at the Faculty of Medicine of Chulalongkorn University in Bangkok, Thailand. He is known for research in the fields of pediatric hepatology, viral hepatitis and virology, and avian influenza.
James Edward Bowman Jr. was an American physician and specialist in pathology, hematology, and genetics. He was a professor of pathology and genetics at the Pritzker School of Medicine at the University of Chicago. He published more than ninety works across the fields of human genetics; population genetics; and ethical, legal and public policy issues in human genetics. He received many awards, including the Chicago African American History Makers Award and recognition from the Hastings Center and Stanford’s Kaiser Family Foundation, and Howard University.
Barton Childs was an American pediatrician and geneticist. He was born in Chicago, Illinois, and graduated from Williams College in 1938. In 1942, he received his M.D. from Johns Hopkins University. Following military service in World War II, he returned to Johns Hopkins for a residency in pediatrics. After a fellowship at Boston Children's Hospital in Boston, he returned to Johns Hopkins University in 1949, where he remained until his retirement in 1981. He remained a professor emeritus in the Department of Pediatrics at The Johns Hopkins University School of Medicine until his death.
Alan Edward Guttmacher, M.D. was the director of the National Institute of Child Health (NICHD), one of the 27 institutes and centers that comprise the National Institutes of Health (NIH). In that capacity, he oversaw the institute’s activities as the focal point at the NIH for research in pediatric health and development, maternal health, reproductive health, intellectual and developmental disabilities, and rehabilitation medicine, among other areas.
The University of Utah School of Medicine is located on the upper campus of the University of Utah in Salt Lake City, Utah. It was founded in 1905 and is currently the only MD-granting medical school in the state of Utah.
Olufunmilayo I. Olopade is a Nigerian hematology oncologist, Associate Dean for Global Health and Walter L. Palmer Distinguished Service Professor in Medicine and Human Genetics at the University of Chicago. She also serves as director of the University of Chicago Hospital's Cancer Risk Clinic.
David Rosenblatt is a Canadian medical geneticist, pediatrician, and professor in the departments of Human Genetics, Medicine, Pediatrics, and Biology at McGill University in Montreal, Quebec, where he was the chairman of the Department of Human Genetics from 2001 to 2013. He is known for his contributions to the field of inborn errors of folate and vitamin B12 metabolism.
Douglas Cecil Wallace is a geneticist and evolutionary biologist at the University of Pennsylvania and the Children's Hospital of Philadelphia in Pennsylvania. He pioneered the use of human mitochondrial DNA as a molecular marker.
Gerardo Jiménez Sánchez is a Mexican-born pediatrician, scientist and businessman. Along with David Valle and Barton Childs, he completed the first medical analysis of the human genome. He was founder and director of the first National Institute of Genomic Medicine in Latin America (INMEGEN) and leader of the team that developed the Genomic Map of the Mexican Population.
John M. Opitz is a German-American medical geneticist and professor at the University of Utah School of Medicine. He is best known for rediscovering the concept of the developmental field in humans and for his detection and delineation of many genetic syndromes, several now known as the "Opitz syndromes" including Smith–Lemli–Opitz syndrome (SLOS), Opitz–Kaveggia syndrome (FGS1), Opitz G/BBB syndrome, Bohring–Opitz syndrome, and other autosomal and X-linked conditions. He is founder of the Wisconsin Clinical Genetics Center, the American Journal of Medical Genetics, and was a cofounder of the American College and American Board of Medical Genetics.
Terri L. Young is an American pediatric ophthalmologist.
Sheldon Clark Reed was an American biologist and geneticist who coined the term genetic counseling and advocated for the wider use of genetic counseling as a means to educate the public.
