David Schlessinger

22.9k citations
61 papers · 3.7k · 2 hit papers · h-index 31

Impact in

  • Genetics top 0.5%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • RNA and protein synthesis mechanisms
    • Genomics and Chromatin Dynamics

Papers in

    • RNA and protein synthesis mechanisms 9
    • Genomics and Chromatin Dynamics 6
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
    • Genetics and Neurodevelopmental Disorders 6
    • Bacterial Genetics and Biotechnology 5
    • Genetic Associations and Epidemiology 5
    • Genomic variations and chromosomal abnormalities 5

David Schlessinger

57 papers receiving 3.6k citations

David Schlessinger's Hit Papers

Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n 1991 · 738 citations
7380+11+23Years since publication200400600

Peers

David Schlessinger
Comparison fields: 5 of 130
  • Genetics 2.1k
  • Molecular Biology 2.2k
  • Cognitive Neuroscience 522
  • Cellular and Molecular Neuroscience 407
  • Biological Psychiatry 42
Replace Mark Lathrop with:
Mark Lathrop France
Thierry Bienvenu France
Atsushi Yoshiki Japan
Tiziano Pramparo United States
Claude Moraine France
Thomas Eggermann Germany
Dietrich Stephan United States
Brian J. O’Roak United States
Xinsheng Nan United Kingdom
Pietro Chiurazzi Italy
David Schlessinger relative to Mark Lathrop France Mark Lathrop's profile →
Citations per field
00.5×1.5×2.0×
Mark Lathrop · 1×
Citations per year

Countries citing papers authored by David Schlessinger

Since Specialization
Citations

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

Fields of papers citing papers by David Schlessinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Schlessinger. 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 David Schlessinger. The network helps show where David Schlessinger may publish in the future.

Co-authors

The 25 scholars most cited alongside David Schlessinger, 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 David Schlessinger Line = papers co-authored together David Schlessinger links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 61 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n
Hit paper breakdown →
1991738
2
Fragile X Genotype Characterized by an Unstable Region of DNA
Hit paper breakdown →
1991641
3 2007255
4 2009185
5 1989113
6 1996110
7 199191
8
Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes.
199083
9 199882
10 199676
11 199375
12 199075
13 200564
14
Report of the sixth international workshop on X chromosome mapping 1995
199564
15 199061
16 201361
17 201161
18 198859
19 199758
20 199553

About David Schlessinger

David Schlessinger is a scholar working on Molecular Biology, Genetics, Plant Science, Ecology and Immunology, having authored 61 papers that have together received 3.7k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (13 papers), RNA and protein synthesis mechanisms (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Chromatin Dynamics (6 papers), Bacterial Genetics and Biotechnology (5 papers), Genetic Associations and Epidemiology (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Genetics (2.1k citations), Molecular Biology (2.2k citations), Cognitive Neuroscience (522 citations), Cellular and Molecular Neuroscience (407 citations) and Biological Psychiatry (42 citations). David Schlessinger has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include G.R. Sutherland, Shuancang Yu, Elizabeth Baker, K. Holman, Michael Lynch, Melanie Pritchard, Eric J. Kremer, Stephen T. Warren, Robert I. Richards and Michele D’Urso. Their work appears in journals such as Genomics, Human Molecular Genetics, Gene, Nucleic Acids Research and Journal of Bacteriology.

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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