Hereditary Disease Foundation

259 papers and 8.7k indexed citations

About

In recent decades, authors affiliated with Hereditary Disease Foundation have published 259 papers, which have received a total of 8.7k indexed citations. Scholars at this organization have produced 57 papers in Molecular Biology, 54 papers in Genetics and 40 papers in Cellular and Molecular Neuroscience on the topics of Genetic Neurodegenerative Diseases (33 papers), BRCA gene mutations in cancer (22 papers) and Mitochondrial Function and Pathology (21 papers). Their work is cited by papers focused on Molecular Biology (3.4k citations), Cellular and Molecular Neuroscience (2.7k citations) and Genetics (1.9k citations). Authors at Hereditary Disease Foundation collaborate with scholars in United States, Hungary and United Kingdom and have published in prestigious journals including Nature, Science and Cell. Some of Hereditary Disease Foundation's most productive authors include Andrew E. Czeizel, Nancy S. Wexler, Hans F. A. Vasen, James F. Gusella, P. Michael Conneally, Rudolph E. Tanzi, Mary Anne Anderson, Anne B. Young, Ira Shoulson and Ernesto Bonilla.

In The Last Decade

Hereditary Disease Foundation

241 papers receiving 8.6k citations

Fields of papers published by authors at Hereditary Disease Foundation

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers affiliated with Hereditary Disease Foundation at the time of their publication. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers affiliated with Hereditary Disease Foundation at the time of their publication.

Countries citing scholars working at Hereditary Disease Foundation

Since Specialization
Citations

This map shows the geographic impact of research produced by authors working at Hereditary Disease Foundation. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by papers produced at Hereditary Disease Foundation with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hereditary Disease Foundation more than expected).

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar’s output or impact.

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2026