Christopher Krapp

629 citations
16 papers · 414 · h-index 10

Impact in

    • Prenatal Screening and Diagnostics
    • Assisted Reproductive Technology and Twin Pregnancy
    • Birth, Development, and Health
    • Genetic Syndromes and Imprinting
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Epigenetics and DNA Methylation 8
    • Genetic Syndromes and Imprinting 5
    • Genetics and Neurodevelopmental Disorders 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2

Christopher Krapp

15 papers receiving 411 citations

Peers

Christopher Krapp
Comparison fields: 5 of 66
  • Pediatrics, Perinatology and Child Health 110
  • Genetics 151
  • Reproductive Medicine 32
  • Health, Toxicology and Mutagenesis 47
  • Molecular Biology 216
Replace Jin Hee Eum with:
Jin Hee Eum South Korea
Mathew Van de Pette United Kingdom
Hannah Demond United Kingdom
Eric de Waal United States
Soumaya Mougou Tunisia
Ashish Jain United States
Galyna Pliushch Germany
Huiru Cheng China
Zina Wen China
Keiko Shioda United States
Christopher Krapp relative to Jin Hee Eum South Korea Jin Hee Eum's profile →
Citations per field
00.5×2.6×
Jin Hee Eum · 1×
Citations per year

Countries citing papers authored by Christopher Krapp

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Krapp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

16 of 16 papers shown
#Work
1 2013118
2 201851
3 201845
4 201042
5 202036
6 201926
7 201122
8 200321
9 201220
10 202217
11 20227
12 20195
13 20232
14 20241
15 20251
16 20250

About Christopher Krapp

Christopher Krapp is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Oncology and Cancer Research, having authored 16 papers that have together received 414 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (8 papers), Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Prenatal Screening and Diagnostics (2 papers), Cancer-related molecular mechanisms research (2 papers), Plant Micronutrient Interactions and Effects (1 paper) and Chronic Myeloid Leukemia Treatments (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (110 citations), Genetics (151 citations), Reproductive Medicine (32 citations), Health, Toxicology and Mutagenesis (47 citations) and Molecular Biology (216 citations). Christopher Krapp has collaborated with scholars based in United States, South Korea and Chile. Frequent co-authors include Marisa S. Bartolomei, Paula Stein, Joanne L. Thorvaldsen, Christos Coutifaris, Teri Ord, Richard M. Schultz, Eric de Waal, Winifred Mak, Yemin Lan and Huntington F. Willard. Their work appears in journals such as Genetics, Molecular Cell, Annals of Oncology, Developmental Biology and Hormones and Behavior.

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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