Download
s41431-020-00785-7.pdf 420,41KB
WeightNameValue
1000 Titel
  • Origins of human genetics. A personal perspective
1000 Autor/in
  1. Passarge, Eberhard |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-02-04
1000 Erschienen in
1000 Quellenangabe
  • 29(7):1038-1044
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41431-020-00785-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298510/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Genetics evolved as a field of science after 1900 with new theories being derived from experiments obtained in fruit flies, bacteria, and viruses. This personal account suggests that the origins of human genetics can best be traced to the years 1949 to 1959. Several genetic scientific advances in genetics in 1949 yielded results directly relating to humans for the first time, except for a few earlier observations. In 1949 the first textbook of human genetics was published, the American Journal of Human Genetics was founded, and in the previous year the American Society of Human Genetics. In 1940 in Britain a textbook entitled Introduction to Medical Genetics served as a foundation for introducing genetic aspects into medicine. The introduction of new methods for analyzing chromosomes and new biochemical assays using cultured cells in 1959 and subsequent years revealed that many human diseases, including cancer, have genetic causes. It became possible to arrive at a precise cause-related genetic diagnosis. As a result the risk of occurrence or re-occurrence of a disease within a family could be assessed correctly. Genetic counseling as a new concept became a basis for improved patient care. Taken together the advances in medically orientated genetic research and patient care since 1949 have resulted in human genetics being both, a basic medical and a basic biological science. Prior to 1949 genetics was not generally viewed in a medical context. Although monogenic human diseases were recognized in 1902, their occurrence and distribution were considered mainly at the population level.
1000 Sacherschließung
lokal Genetic Association Studies/methods [MeSH]
lokal Genetic Predisposition to Disease [MeSH]
lokal Genetic Association Studies/history [MeSH]
lokal Genetic Diseases, Inborn/therapy [MeSH]
lokal Humans [MeSH]
lokal Genetics, Medical/history [MeSH]
lokal Genetic Diseases, Inborn/diagnosis [MeSH]
lokal Viewpoint
lokal Biomedical Research/history [MeSH]
lokal Genetics, Medical/trends [MeSH]
lokal Genetics
lokal Alleles [MeSH]
lokal Genetic Diseases, Inborn/genetics [MeSH]
lokal History, 20th Century [MeSH]
lokal Genetic Association Studies/trends [MeSH]
lokal Genetic counselling
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-2093-8042
1000 Hinweis
  • DeepGreen-ID: 462a12c595dd499b8f2567c31a889c0c ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Dateien
  1. Origins of human genetics. A personal perspective
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6442798.rdf
1000 Erstellt am 2023-04-26T15:45:52.323+0200
1000 Erstellt von 322
1000 beschreibt frl:6442798
1000 Zuletzt bearbeitet Thu Oct 19 13:26:21 CEST 2023
1000 Objekt bearb. Thu Oct 19 13:26:21 CEST 2023
1000 Vgl. frl:6442798
1000 Oai Id
  1. oai:frl.publisso.de:frl:6442798 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

View source