Herman M. Slatis

613 total citations
25 papers, 473 citations indexed

About

Herman M. Slatis is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Herman M. Slatis has authored 25 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Genetics. Recurrent topics in Herman M. Slatis's work include Metabolism and Genetic Disorders (3 papers), Hearing Impairment and Communication (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Herman M. Slatis is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Hearing Impairment and Communication (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Herman M. Slatis collaborates with scholars based in United States, Canada and Papua New Guinea. Herman M. Slatis's co-authors include John Stanley, Alexander Sokoloff, David Yi‐Yung Hsia, Batsheva Bonné‐Tamir, M B Katznelson, J. W. Boyes, F. Walker, Arthur G. Steinberg, Asher Finkel and E. A. Schwinghamer and has published in prestigious journals such as Science, JAMA and Ecology.

In The Last Decade

Herman M. Slatis

25 papers receiving 372 citations

Peers

Herman M. Slatis
Comparison fields: 5 of 107
  • Genetics 178
  • Molecular Biology 107
  • Plant Science 60
  • Pediatrics, Perinatology and Child Health 51
  • Ecology, Evolution, Behavior and Systematics 41
Replace Krishna R. Dronamraju with:
Krishna R. Dronamraju United States
Robert Semeonoff United Kingdom
L. B. Jorde United States
Lydia E. Brownhill United States
John Shield Australia
H. Krzanowska Poland
Jim A. Mossman United States
R. B. Campbell United States
Leang C. Sieu United States
Sean P. Flaherty Australia
Krishna R. Dronamraju United States View profile →
Citations per field, relative to Herman M. Slatis
Herman M. Slatis · 1×
Citations per year, relative to Herman M. Slatis
Herman M. Slatis · 1×

Countries citing papers authored by Herman M. Slatis

Since Specialization
Citations

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

Fields of papers citing papers by Herman M. Slatis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Herman M. Slatis. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Herman M. Slatis. The network helps show where Herman M. Slatis may publish in the future.

Co-authorship network of co-authors of Herman M. Slatis

This figure shows the co-authorship network connecting the top 25 collaborators of Herman M. Slatis. A scholar is included among the top collaborators of Herman M. Slatis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Herman M. Slatis. Herman M. Slatis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
# Work Indexed citations
1
The inheritance of fingerprint patterns.
31
2 2
3 30
4
THE STUDY OF NORMAL VARIATION IN MAN. I. INTERRELATIONS OF ADIPOSITY, ANCESTRY, AND BLOOD TYPE.
6
5
Hairy pinna of the ear in Israeli populations.
20
6 16
7
The use of purebred dogs in research. Problems of genetics.
2
8
Outline of Human Genetics
6
9 44
10 75
11
Consanguineous marriages in the Chicago region.
56
12 6
13 28
14
Comments on the rate of mutation to chondrodystrophy in man.
12
15 4
16 8
17
A method of estimating the frequency of abnormal autosomal recessive genes in man.
12
18 15
19
Seasonal variation in the American live birth sex ratio.
32
20
The measurement of linkage in heredity.
1

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 authors with similar magnitude of impact

Rankless by CCL
2026