Andy Peiffer

19 papers receiving 2.5k citations

Andy Peiffer's Hit Papers

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns 1998 · 939 citations
9390+9+19Years since publication250500750

Peers

Andy Peiffer
Comparison fields: 5 of 101
  • Ophthalmology 535
  • Behavioral Neuroscience 177
  • Cellular and Molecular Neuroscience 806
  • Psychiatry and Mental health 575
  • Biological Psychiatry 61
Replace Hideki Mochizuki with:
Hideki Mochizuki Japan
Stephanie Ohlraun Germany
Dawn L. Thiselton United States
Roberto Gradini Italy
Junko Imaki Japan
Michael R. Pranzatelli United States
Gavin Hudson United Kingdom
Caroline L. Speck United States
Antje Grosche Germany
Andy Peiffer relative to Hideki Mochizuki Japan Hideki Mochizuki's profile →
Citations per field
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Citations per year

Countries citing papers authored by Andy Peiffer

Since Specialization
Citations

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

Fields of papers citing papers by Andy Peiffer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

19 of 19 papers shown
#Work
1
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
Hit paper breakdown →
1998939
2
Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular Degeneration
Hit paper breakdown →
1997687
3 2009203
4 1999131
5 1991121
6 2003112
7 199870
8 200755
9 198754
10 199144
11 200237
12 200330
13 199418
14 199917
15
Modulation of glucocorticoid receptor gene expression in the thymus by the sex steroid hormone milieu and correlation with sexual dimorphism of immune response
199416
16 20109
17 20177
18 19845
19
Genes for rare idiopathic generalized epilepsies: BFNC.
19992

About Andy Peiffer

Andy Peiffer is a scholar working on Genetics, Molecular Biology, Endocrinology, Diabetes and Metabolism, Behavioral Neuroscience and Cardiology and Cardiovascular Medicine, having authored 19 papers that have together received 2.6k indexed citations. Recurring topics across this work include Hormonal Regulation and Hypertension (4 papers), Estrogen and related hormone effects (4 papers), Stress Responses and Cortisol (3 papers), Metabolism and Genetic Disorders (2 papers), Epilepsy research and treatment (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Retinal Imaging and Analysis (2 papers) and Retinal Diseases and Treatments (2 papers). The work is most often cited by research in Ophthalmology (535 citations), Behavioral Neuroscience (177 citations), Cellular and Molecular Neuroscience (806 citations), Psychiatry and Mental health (575 citations) and Biological Psychiatry (61 citations). Andy Peiffer has collaborated with scholars based in United States, Canada and Belgium. Frequent co-authors include Mark Leppert, Nicholas Barden, Mark Leppert, Nanda A. Singh, Carole Charlier, Robin J. Leach, Thomas G. Quattlebaum, Dora Stauffer, Gabriel M. Ronen and Jerome V. Murphy. Their work appears in journals such as Biochemical and Biophysical Research Communications, Nature Genetics, PLoS Currents, PLoS 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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