Gavin Kelsey

17.7k citations
155 papers · 12.2k indexed · 5 hit papers · h-index 60

Impact in

Papers in

Gavin Kelsey

153 papers receiving 12.1k citations

Hit Papers

scNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells 2018 · 437 citations
4372002202620102018250500750

Peers

Gavin Kelsey
Comparison fields: 5 of 140
  • Genetics 5.6k
  • Pediatrics, Perinatology and Child Health 3.4k
  • Molecular Biology 9.6k
  • Obstetrics and Gynecology 660
  • Cancer Research 1.2k
Replace Robert Feil with:
Robert Feil France
Simon Andrews United Kingdom
Marisa S. Bartolomei United States
Jörn Walter Germany
Felix Krueger United Kingdom
Bernhard Horsthemke Germany
Hongcang Gu United States
Timothy H. Bestor United States
Dirk Schübeler Switzerland
En Li United States
Gavin Kelsey relative to Robert Feil France Robert Feil's profile →
Citations per field
00.5×1.5×
Robert Feil · 1×
Citations per year

Countries citing papers authored by Gavin Kelsey

Since Specialization
Citations

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

Fields of papers citing papers by Gavin Kelsey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown
#Work
1 20250
2 20250
3 202412
4 20242
5 202218
6 20228
7 202139
8 202137
9 202033
10 202033
11
scNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells
Hit paper breakdown →
2018437
12 201854
13 2017174
14
Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity
Hit paper breakdown →
2016510
15 2006202
16 200654
17 2005245
18 2004120
19 19968
20 198817

About Gavin Kelsey

Gavin Kelsey is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Reproductive Medicine and Public Health, Environmental and Occupational Health, having authored 155 papers that have together received 12.2k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (111 papers), Genetic Syndromes and Imprinting (86 papers), Prenatal Screening and Diagnostics (40 papers), Reproductive Biology and Fertility (15 papers), Genomics and Chromatin Dynamics (14 papers), Pancreatic function and diabetes (13 papers), Cancer-related gene regulation (10 papers) and Single-cell and spatial transcriptomics (9 papers). The work is most often cited by research in Genetics (5.6k citations), Pediatrics, Perinatology and Child Health (3.4k citations), Molecular Biology (9.6k citations), Obstetrics and Gynecology (660 citations) and Cancer Research (1.2k citations). Gavin Kelsey has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Wolf Reik, Sébastien A. Smallwood, Wendy Dean, Miguel Constância, Felix Krueger, Oliver Stegle, Simon Andrews, Heather Lee, Stephen J. Clark and Robert Feil. Their work appears in journals such as Clinical Epigenetics, Genes & Development, Nature, Proceedings of the National Academy of Sciences and Mammalian Genome.

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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