ScholarIQanswers from OpenAlex
Genomics and Rare Diseases
TopicLeading institutions, researchers & key papers
Genomics and Rare Diseases is a topic indexed in ScholarIQ from OpenAlex.
What is known about Genomics and Rare Diseases?
ScholarIQrecord summary
This cluster of papers focuses on the standards, guidelines, and tools for interpreting genetic variants, particularly in the context of clinical genomics and Mendelian disorders. It includes topics such as pathogenicity prediction, functional annotations, sequence interpretation, and the use of exome sequencing for identifying disease-causing variants.
How many works does Genomics and Rare Diseases have?
ScholarIQindexed works
Genomics and Rare Diseases has 67,380 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Genomics and Rare Diseases have?
ScholarIQcitation count
Genomics and Rare Diseases has 814,068 citations in the OpenAlex counts ScholarIQ stores.
What is the OpenAlex record for Genomics and Rare Diseases?
ScholarIQopenalex
The OpenAlex for Genomics and Rare Diseases is on the source record.
Who are the most-cited researchers behind Genomics and Rare Diseases?
ScholarIQtop researchers by citations
Where is Genomics and Rare Diseases research published, and who funds it?
ScholarIQvenues & funding sources
TOP JOURNALS
No journal data available yet.
TOP FUNDERS
National Science Foundation—
NIH—
Wellcome Trust—
European Research Council—
Funder breakdown is a member featureSign up free to unlock
Who collaborates most closely around Genomics and Rare Diseases?
ScholarIQco-authorship network
United States
100%