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Personal journeys to and in human genetics and dysmorphology.
Schwartz, Charles E; Aylsworth, Arthur S; Allanson, Judith; Battaglia, Agatino; Carey, John C; Curry, Cynthia J; Davies, Kay E; Eichler, Evan E; Graham, John M; Hall, Bryan; Hall, Judith G; Holmes, Lewis B; Hoyme, H Eugene; Hunter, Alasdair; Innis, Jeffrey; Johnson, John; Keppler-Noreuil, Kim M; Leroy, Jules G; Moore, Cynthia; Nelson, David L; Neri, Giovanni; Opitz, John M; Picketts, David; Raymond, F Lucy; Shalev, Stavit Allon; Stevenson, Roger E; Stumpel, Connie T R M; Sutherland, Grant; Viskochil, David H; Weaver, David D; Zackai, Elaine H.
Afiliación
  • Schwartz CE; Senior Research Scientist Emeritus, Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Aylsworth AS; Emeritus Professor of Pediatrics and Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Allanson J; Professor of Paediatrics, University of Ottawa, Ottawa, Canada.
  • Battaglia A; Clinical Geneticist, Children's Hospital of Eastern Ontario (Retired), Ottawa, Canada.
  • Carey JC; Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, Pisa, Italy.
  • Curry CJ; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Davies KE; Professor of Pediatrics, Emerita, UCSF, Adjunct Professor of Pediatrics, Stanford, Medical Director Genetic Medicine, Community Regional Medical Center, Fresno, California, USA.
  • Eichler EE; Department of Physiology, Anatomy and Genetics, MDUK Oxford Neuromuscular Centre, Oxford, UK.
  • Graham JM; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, USA.
  • Hall B; Howard Hughes Medical Institute, University of Washington, Seattle, Washington, USA.
  • Hall JG; Professor Emeritus, Division of Medical Genetics, Department of Pediatrics, Cedars-Sinai Medical Center, and David Geffen School of Medicine, University of California, Los Angeles (UCLA), Los Angeles, California, USA.
  • Holmes LB; Emeritus, Department of Pediatrics, University of Kentucky, Lexington, Kentucky, USA.
  • Hoyme HE; University of British Columbia and Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
  • Hunter A; Department of Pediatrics and Medical Genetics, British Columbia Children's Hospital, Vancouver, Canada.
  • Innis J; Emeritus Chief, Medical Genetics and Metabolism Unit, Mass General for Children; Professor of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.
  • Johnson J; Medical Director, Sanford Children's Genomic Medicine Consortium, Senior Advisor, Sanford Imagenetics, Sanford Health, Emeritus Professor and Past Chair, Department of Pediatrics, University of South Dakota Sanford School of Medicine, Sioux Falls, South Dakota, USA.
  • Keppler-Noreuil KM; Adjunct Professor and Medical Director, Genetic Counseling Graduate Program, Augustana University, Sioux Falls, South Dakota, USA.
  • Leroy JG; Extraordinary Professor of Psychiatry, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
  • Moore C; Emeritus Clinical Geneticist, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Nelson DL; Staff Physician, Pediatric Genetics, Golisano Children's Hospital of Southwest Florida, Fort Myers, Florida, USA.
  • Neri G; Professor Emeritus of Human Genetics, Pediatrics and Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Opitz JM; Emeritus Clinical Geneticist, Department of Medical Genetics, Shodair Hospital, Helena, Montana, USA.
  • Picketts D; Professor of Pediatrics Division of Genetics & Metabolism, Program Director, Medical Genetics & Genomics Residency Training Program, Co-Director of the UW NORD Center of Excellence for Rare Diseases, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
  • Raymond FL; Professor Emeritus, Ghent University School of Medicine, Ghent, Belgium.
  • Shalev SA; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control, Atlanta, Georgia, USA.
  • Stevenson RE; Department of Molecular and Human Genetics, Jan and Dan Duncan Neurological Research Institute, Baylor College of Medicine, Houston, Texas, USA.
  • Stumpel CTRM; Institute of Genomic Medicine, Catholic University School of Medicine, Rome, Italy.
  • Sutherland G; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Viskochil DH; Senior Scientist, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Weaver DD; Professor, Departments of Medicine, Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Zackai EH; Department of Medical Genetics, University of Cambridge, Cambridge, England.
Am J Med Genet A ; 194(6): e63514, 2024 06.
Article en En | MEDLINE | ID: mdl-38329159
ABSTRACT
Genetics has become a critical component of medicine over the past five to six decades. Alongside genetics, a relatively new discipline, dysmorphology, has also begun to play an important role in providing critically important diagnoses to individuals and families. Both have become indispensable to unraveling rare diseases. Almost every medical specialty relies on individuals experienced in these specialties to provide diagnoses for patients who present themselves to other doctors. Additionally, both specialties have become reliant on molecular geneticists to identify genes associated with human disorders. Many of the medical geneticists, dysmorphologists, and molecular geneticists traveled a circuitous route before arriving at the position they occupied. The purpose of collecting the memoirs contained in this article was to convey to the reader that many of the individuals who contributed to the advancement of genetics and dysmorphology since the late 1960s/early 1970s traveled along a journey based on many chances taken, replying to the necessities they faced along the way before finding full enjoyment in the practice of medical and human genetics or dysmorphology. Additionally, and of equal importance, all exhibited an ability to evolve with their field of expertise as human genetics became human genomics with the development of novel technologies.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genética Médica Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genética Médica Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos