Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Genetic Diseases, Inborn

"Genetic Diseases, Inborn" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.


This graph shows the total number of publications written about "Genetic Diseases, Inborn" by people in Harvard Catalyst Profiles by year, and whether "Genetic Diseases, Inborn" was a major or minor topic of these publication.
Bar chart showing 308 publications over 30 distinct years, with a maximum of 25 publications in 2016
To see the data from this visualization as text, click here.
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Funded by the NIH/NCATS Clinical and Translational Science Award (CTSA) program, grant number UL1TR001102, and through institutional support from Harvard University, Harvard Medical School, Harvard T.H. Chan School of Public Health, Beth Israel Deaconess Medical Center, Boston Children's Hospital, Brigham and Women's Hospital, Massachusetts General Hospital and the Dana Farber Cancer Institute.