Andrei Verner

13.4k citations
19 papers · 1.6k · h-index 18

Impact in

Papers in

    • Genomics and Chromatin Dynamics 4
    • Epigenetics and DNA Methylation 2
    • Connexins and lens biology 2
    • Genetic Syndromes and Imprinting 4
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Genetic Associations and Epidemiology 2

Andrei Verner

19 papers receiving 1.5k citations

Peers

Andrei Verner
Comparison fields: 5 of 89
  • Clinical Biochemistry 131
  • Psychiatry and Mental health 271
  • Genetics 464
  • Cellular and Molecular Neuroscience 268
  • Neurology 162
Replace Carlo Fusco with:
Carlo Fusco Italy
Syed Hosain United States
Atsuo Nezu Japan
Jacinta M. McMahon Australia
E Peeters Netherlands
Fang He China
Michael Freilinger Austria
Shin‐ichiro Hamano Japan
Sylviane Peudenier France
Steffen Syrbe Germany
Andrei Verner relative to Carlo Fusco Italy Carlo Fusco's profile →
Citations per field
00.5×1.5×2.1×
Carlo Fusco · 1×
Citations per year

Countries citing papers authored by Andrei Verner

Since Specialization
Citations

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

Fields of papers citing papers by Andrei Verner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

19 of 19 papers shown
#Work
1 2002497
2 2004213
3 2001209
4 2003156
5 200593
6 200161
7 200148
8 200038
9 199738
10 200434
11 200431
12 199524
13 199623
14 200623
15 199919
16 200319
17 200619
18 200018
19 200615

About Andrei Verner

Andrei Verner is a scholar working on Molecular Biology, Genetics, Surgery, Epidemiology and Oncology, having authored 19 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Genomics and Chromatin Dynamics (4 papers), Metabolism and Genetic Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Epigenetics and DNA Methylation (2 papers), Connexins and lens biology (2 papers), Asthma and respiratory diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). The work is most often cited by research in Clinical Biochemistry (131 citations), Psychiatry and Mental health (271 citations), Genetics (464 citations), Cellular and Molecular Neuroscience (268 citations) and Neurology (162 citations). Andrei Verner has collaborated with scholars based in Canada, United States and Costa Rica. Frequent co-authors include Guy A. Rouleau, Thomas J. Hudson, Lionel Carmant, Lidong Liu, Wei‐Yang Lu, Michel Vanasse, Yu Tian Wang, Patrick Cossette, Haiheng Dong and Anne Lortie. Their work appears in journals such as The American Journal of Human Genetics, Mammalian Genome, Nature Genetics, Genetics and Human Genetics.

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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