Wayne Gottlieb

948 citations
11 papers · 818 · h-index 8

Impact in

    • Sperm and Testicular Function
  • Genetics top 5%
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Sperm and Testicular Function 4
    • Genetic Syndromes and Imprinting 6
    • Genomic variations and chromosomal abnormalities 2
    • Animal Genetics and Reproduction 1
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1

Wayne Gottlieb

11 papers receiving 786 citations

Peers

Wayne Gottlieb
Comparison fields: 5 of 69
  • Reproductive Medicine 168
  • Genetics 533
  • Pediatrics, Perinatology and Child Health 209
  • Physiology 27
  • Molecular Biology 377
Replace Hazel L. Kinnell with:
Hazel L. Kinnell United Kingdom
Nancy A. Telford United States
B Delobel France
Takuya Wakai Japan
Jacqueline F. Ackland United States
Seiji Kito Japan
Vladimiro Calvari Italy
Junko Tomikawa Japan
Parimal S. Nathwani Canada
Aurélie Dipietromaria France
Wayne Gottlieb relative to Hazel L. Kinnell United Kingdom Hazel L. Kinnell's profile →
Citations per field
00.5×2×2.7×
Hazel L. Kinnell · 1×
Citations per year

Countries citing papers authored by Wayne Gottlieb

Since Specialization
Citations

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

Fields of papers citing papers by Wayne Gottlieb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 1992232
2 1999218
3 1988133
4 199264
5 198962
6 198840
7 199333
8 198725
9 19946
10
Chromosome breakage in Prader-Willi and Angelman syndrome deletions may involve recombination between a repeat at the proximal and distal breakpoints
19944
11 20071

About Wayne Gottlieb

Wayne Gottlieb is a scholar working on Reproductive Medicine, Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Physiology, having authored 11 papers that have together received 818 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), Sperm and Testicular Function (4 papers), Prenatal Screening and Diagnostics (3 papers), Reproductive Biology and Fertility (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Animal Genetics and Reproduction (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Reproductive Medicine (168 citations), Genetics (533 citations), Pediatrics, Perinatology and Child Health (209 citations), Physiology (27 citations) and Molecular Biology (377 citations). Wayne Gottlieb has collaborated with scholars based in United States. Frequent co-authors include Stanley Meizel, Robert D. Nicholls, Peter K. Rogan, Ashley I. Yudin, Paul G. Fitzgerald, Maria J. Mascari, Alec J. Jeffreys, David A. Waller, Roger L. Ladda and Merlin G. Butler. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics, New England Journal of Medicine, Annals of Neurology and Journal of Andrology.

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