Human Heredity

70.6k citations
3.4k papers · · active since 1951

Impact in

  • Genetics top 2%
    • Genetic Associations and Epidemiology
    • Forensic and Genetic Research
    • Genetic diversity and population structure
    • Genetic Mapping and Diversity in Plants and Animals
    • Genomics and Rare Diseases
    • Schizophrenia research and treatment

Papers in

    • Genetic Associations and Epidemiology 1.5k
    • Forensic and Genetic Research 735
    • Genetic diversity and population structure 602
    • Dermatoglyphics and Human Traits 126
    • Hemoglobinopathies and Related Disorders 119
    • Genomics and Rare Diseases 89

Human Heredity

3.3k papers receiving 65.4k citations

Peers

Human Heredity
Comparison fields: 5 of 216
  • Genetics 30k
  • Psychiatry and Mental health 4.5k
  • Pharmacy 834
  • Clinical Biochemistry 899
  • Pediatrics, Perinatology and Child Health 2.4k
Replace Frontiers in Endocrinology with:
Frontiers in Endocrinology China
European Journal of Endocrinology United States
Clinical Endocrinology United Kingdom
Nature Reviews Endocrinology United States
British Medical Bulletin United Kingdom
British Journal of Ophthalmology United Kingdom
Frontiers in Physiology United States
Molecular and Cellular Endocrinology United States
Trends in Endocrinology and Metabolism United States
International Journal of Cardiology United States
Human Heredity relative to Frontiers in Endocrinology China Frontiers in Endocrinology's profile →
Citations per field
00.5×2×2.9×
Frontiers in Endocrinology · 1×
Citations per year

Countries where authors publish in Human Heredity

Since Specialization
Citations

This map shows the geographic impact of research published in Human Heredity. 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 published in Human Heredity with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Human Heredity more than expected).

Fields of papers published in Human Heredity

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers published in Human Heredity. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers published in Human Heredity.

About Human Heredity

The 3.4k papers published in Human Heredity in the last decades have received a total of 70.6k indexed citations . Papers published in Human Heredity usually cover Genetics (2.3k papers), Clinical Biochemistry (102 papers), Hematology (267 papers), Genetics (142 papers) and Developmental Biology (30 papers) specifically the topics of Genetic Associations and Epidemiology (1.5k papers), Forensic and Genetic Research (735 papers), Genetic diversity and population structure (602 papers), Blood groups and transfusion (172 papers), Dermatoglyphics and Human Traits (126 papers), Hemoglobinopathies and Related Disorders (119 papers), Genomics and Rare Diseases (89 papers) and Neonatal Health and Biochemistry (88 papers). The most active scholars publishing in Human Heredity are Natalie C. Lippa, Saskia C. Sanderson, Myles S. Faith, Susan Carnell, Tanja V.E. Kral, Robert C. Elston, Jason H. Moore, Frank Dudbridge, Daniel Rabinowitz and Lars E. Beckman.

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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