S.A. Latt

6.4k citations
73 papers · 5.2k · 2 hit papers · h-index 34

Impact in

  • Genetics top 1%
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Carcinogens and Genotoxicity Assessment

Papers in

    • DNA and Nucleic Acid Chemistry 20
    • DNA Repair Mechanisms 12
    • Genomics and Chromatin Dynamics 9
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
    • Genomic variations and chromosomal abnormalities 10
    • Animal Genetics and Reproduction 7

S.A. Latt

71 papers receiving 4.8k citations

S.A. Latt's Hit Papers

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion 1989 · 458 citations
4580+16+32Years since publication200400600

Peers

S.A. Latt
Comparison fields: 5 of 169
  • Genetics 1.4k
  • Cancer Research 632
  • Molecular Biology 3.0k
  • Biophysics 206
  • Pediatrics, Perinatology and Child Health 538
Replace Ger van den Engh with:
Ger van den Engh United States
Minoru S.H. Ko United States
Rolf Zeller Switzerland
Tomoko Watanabe Japan
Keiji Suzuki Japan
Heather Lee Australia
Zhijin Wu United States
Nils R. Ringertz Sweden
Robert E. Hill United Kingdom
Yasushi Okazaki Japan
S.A. Latt relative to Ger van den Engh United States Ger van den Engh's profile →
Citations per field
00.5×2.6×
Ger van den Engh · 1×
Citations per year

Countries citing papers authored by S.A. Latt

Since Specialization
Citations

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

Fields of papers citing papers by S.A. Latt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S.A. Latt. 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 S.A. Latt. The network helps show where S.A. Latt may publish in the future.

Co-authors

The 25 scholars most cited alongside S.A. Latt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S.A. Latt Line = papers co-authored together S.A. Latt links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Automatic measurement of sister chromatid exchange frequency.
Hit paper breakdown →
1977710
2
Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
Hit paper breakdown →
1989458
3 1985383
4 1990347
5 1976327
6 1975243
7 1985181
8 1965155
9 1975140
10 1986138
11
Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy.
1976121
12 1983108
13 1986100
14
Sister chromatid exchange analysis.
198098
15 197192
16 198388
17 198786
18 198286
19 197777
20 198575

About S.A. Latt

S.A. Latt is a scholar working on Molecular Biology, Genetics, Plant Science, Oncology and Cancer Research, having authored 73 papers that have together received 5.2k indexed citations. Recurring topics across this work include DNA and Nucleic Acid Chemistry (20 papers), Chromosomal and Genetic Variations (17 papers), DNA Repair Mechanisms (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Genomic variations and chromosomal abnormalities (10 papers), Genomics and Chromatin Dynamics (9 papers), Animal Genetics and Reproduction (7 papers) and Carcinogens and Genotoxicity Assessment (7 papers). The work is most often cited by research in Genetics (1.4k citations), Cancer Research (632 citations), Molecular Biology (3.0k citations), Biophysics (206 citations) and Pediatrics, Perinatology and Child Health (538 citations). S.A. Latt has collaborated with scholars based in United States, Hungary and Finland. Frequent co-authors include Gail Stetten, Joan H.M. Knoll, Louis M. Kunkel, Bert L. Vallée, Rhona Schreck, L. Juergens, H.F. Willard, M. Lalande, Park S. Gerald and Anthony P. Monaco. Their work appears in journals such as Journal of Histochemistry & Cytochemistry, Experimental Cell Research, Proceedings of the National Academy of Sciences, Human Genetics and Molecular and Cellular Biology.

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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