Stephan Ripke

127.6k citations
107 papers · 10.2k · 5 hit papers · h-index 37

Impact in

  • Genetics top 0.1%
    • Genetic Associations and Epidemiology
    • Genetic Mapping and Diversity in Plants and Animals
    • Genetics and Neurodevelopmental Disorders
    • Genetic and phenotypic traits in livestock
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genetic Associations and Epidemiology 47
    • Genetics and Neurodevelopmental Disorders 10
    • Genomic variations and chromosomal abnormalities 10
    • Neural and Behavioral Psychology Studies 7
    • Autism Spectrum Disorder Research 6

Stephan Ripke

100 papers receiving 10.0k citations

Stephan Ripke's Hit Papers

Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment 2020 · 802 citations
8020+6+12Years since publication50010001.5k2.0k2.5k

Peers

Stephan Ripke
Comparison fields: 5 of 160
  • Biological Psychiatry 387
  • Genetics 4.5k
  • Psychiatry and Mental health 922
  • Cognitive Neuroscience 1.2k
  • Behavioral Neuroscience 189
Replace Cathryn M. Lewis with:
Cathryn M. Lewis United Kingdom
Howard J. Edenberg United States
Laura Almasy United States
John Blangero United States
David M. Hougaard Denmark
Kazuhiko Nakamura Japan
Martin Schalling Sweden
Lisa Jones United Kingdom
Bertram Müller‐Myhsok Germany
Tadao Arinami Japan
Stephan Ripke relative to Cathryn M. Lewis United Kingdom Cathryn M. Lewis's profile →
Citations per field
00.5×1.5×2.0×
Cathryn M. Lewis · 1×
Citations per year

Countries citing papers authored by Stephan Ripke

Since Specialization
Citations

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

Fields of papers citing papers by Stephan Ripke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 107 papers — load more, or switch the sort, to bring in the rest.

#Work
1
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Hit paper breakdown →
20152647
2
GenABEL: an R library for genome-wide association analysis
Hit paper breakdown →
20071325
3
Most genetic risk for autism resides with common variation
Hit paper breakdown →
2014840
4
Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment
Hit paper breakdown →
2020802
5
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
Hit paper breakdown →
2012398
6 2008290
7 2013246
8 2011243
9 2009230
10 2015225
11 2017192
12 2012177
13 2014148
14 2015120
15 2014120
16 2018108
17 201698
18 201592
19 201389
20 201586

About Stephan Ripke

Stephan Ripke is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Experimental and Cognitive Psychology and Clinical Psychology, having authored 107 papers that have together received 10.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (47 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (10 papers), Neural and Behavioral Psychology Studies (7 papers), Child and Adolescent Psychosocial and Emotional Development (7 papers), Neuroendocrine regulation and behavior (6 papers), Bipolar Disorder and Treatment (6 papers) and Autism Spectrum Disorder Research (6 papers). The work is most often cited by research in Biological Psychiatry (387 citations), Genetics (4.5k citations), Psychiatry and Mental health (922 citations), Cognitive Neuroscience (1.2k citations) and Behavioral Neuroscience (189 citations). Stephan Ripke has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Jian Yang, Yurii S. Aulchenko, Aaron Isaacs, Cornelia M. van Duijn, Mark J. Daly, Po‐Ru Loh, Alkes L. Price, Hilary K. Finucane, Brendan Bulik‐Sullivan and Naomi R. Wray. Their work appears in journals such as European Neuropsychopharmacology, Molecular Psychiatry, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Biological Psychiatry and Nature 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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