Human Heredity

65.5k citations
3.4k papers · indexed · active since 1950

Impact in

  • Genetics top 2%
    • Genetic Associations and Epidemiology
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetic and phenotypic traits in livestock
    • Genomic variations and chromosomal abnormalities
    • Hemoglobinopathies and Related Disorders
    • Forensic and Genetic Research
  • Pharmacy top 5%

Papers in

    • Genetic Associations and Epidemiology 619
    • Genetic Mapping and Diversity in Plants and Animals 349
    • Hemoglobinopathies and Related Disorders 237
    • Genetic and phenotypic traits in livestock 208
    • Genomic variations and chromosomal abnormalities 167
    • Blood groups and transfusion 278

Human Heredity

3.0k papers receiving 57.8k citations

Peers

Human Heredity
Comparison fields: 5 of 227
  • Genetics 24.4k
  • Pharmacy 1.8k
  • Genetics 3.8k
  • Hematology 3.9k
  • Pediatrics, Perinatology and Child Health 4.9k
Replace Annals of Medicine with:
Annals of Medicine China
Scandinavian Journal of Gastroenterology Sweden
British Medical Bulletin United Kingdom
Current Opinion in Pediatrics United States
Annual Review of Medicine United States
Medical Hypotheses United States
Frontiers in Pediatrics China
Journal of Endocrinological Investigation Italy
Nature Reviews Endocrinology United States
Orphanet Journal of Rare Diseases United States
Human Heredity relative to Annals of Medicine China Annals of Medicine's profile →
Citations per field
00.5×2.6×
Annals of Medicine · 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 65.5k indexed citations . Papers published in Human Heredity usually cover Genetics (1.3k papers), Hematology (429 papers), Genetics (294 papers), Clinical Biochemistry (117 papers) and Pediatrics, Perinatology and Child Health (293 papers) specifically the topics of Genetic Associations and Epidemiology (619 papers), Genetic Mapping and Diversity in Plants and Animals (349 papers), Blood groups and transfusion (278 papers), Hemoglobinopathies and Related Disorders (237 papers), Erythrocyte Function and Pathophysiology (221 papers), Genetic and phenotypic traits in livestock (208 papers), Neonatal Health and Biochemistry (173 papers) and Genomic variations and chromosomal abnormalities (167 papers). The most active scholars publishing in Human Heredity are Natalie Lippa, Saskia C. Sanderson, Myles S. Faith, Susan Carnell, Tanja V.E. Kral, Robert C. Elston, Jason A. Stewart, Jason H. Moore, Frank Dudbridge and Daniel Rabinowitz.

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.

Explore journals with similar magnitude of impact

Rankless by CCL
2026