Christian P. Schaaf
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders 39
- Genomic variations and chromosomal abnormalities 31
- Genetic Syndromes and Imprinting 24
- Genomics and Rare Diseases 19
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research 17
- Molecular Biology top 5%
- Congenital heart defects research 12
- Epigenetics and DNA Methylation 11
- Biochemistry top 5%
- Developmental Neuroscience top 10%
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- Metabolism and Genetic Disorders 8
- Co-authors
- Arthur L. BeaudetMadelyn A. GillentineJiani YinHuda Y. ZoghbiAnkita PatelMichael D. FountainSau Wai CheungJoanna Wiszniewska
- Journals
- Clinical Genetics (4 papers)Human Mutation (4 papers)European Journal of Human Genetics (3 papers)
- Partner nations
- United StatesGermanyPoland
In The Last Decade
Christian P. Schaaf
117 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 128
- Genetics 1.9k
- Cognitive Neuroscience 612
- Molecular Biology 1.9k
- Biochemistry 139
- Developmental Neuroscience 59
Countries citing papers authored by Christian P. Schaaf
This map shows the geographic impact of Christian P. Schaaf'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 Christian P. Schaaf with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christian P. Schaaf more than expected).
Fields of papers citing papers by Christian P. Schaaf
This network shows the impact of papers produced by Christian P. Schaaf. 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 Christian P. Schaaf. The network helps show where Christian P. Schaaf may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Christian P. Schaaf, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2025 | 0 | |
| 3 | 2025 | 2 | |
| 4 | 2024 | 1 | |
| 5 | 2024 | 10 | |
| 6 | 2024 | 2 | |
| 7 | 2024 | 0 | |
| 8 | 2024 | 3 | |
| 9 | 2023 | 1 | |
| 10 | 2023 | 10 | |
| 11 | 2022 | 10 | |
| 12 | 2022 | 49 | |
| 13 | 2022 | 2 | |
| 14 | 2021 | 6 | |
| 15 | 2021 | 12 | |
| 16 | 2019 | 16 | |
| 17 | 2019 | 26 | |
| 18 | 2018 | 12 | |
| 19 | Xq28 Duplication Syndrome, Int22h1/Int22h2 Mediated | 2016 | 4 |
| 20 | 2011 | 111 |
About Christian P. Schaaf
Christian P. Schaaf is a scholar working on Genetics, Clinical Biochemistry and Molecular Biology, having authored 126 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (39 papers), Genomic variations and chromosomal abnormalities (31 papers), Genetic Syndromes and Imprinting (24 papers), Genomics and Rare Diseases (19 papers), Autism Spectrum Disorder Research (17 papers), Congenital heart defects research (12 papers), Epigenetics and DNA Methylation (11 papers) and Metabolism and Genetic Disorders (8 papers). The work is most often cited by research in Genetics (1.9k citations), Cognitive Neuroscience (612 citations) and Molecular Biology (1.9k citations). Christian P. Schaaf has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Arthur L. Beaudet, Madelyn A. Gillentine, Jiani Yin, Huda Y. Zoghbi, Ankita Patel, Michael D. Fountain, Sau Wai Cheung, Joanna Wiszniewska, Fan Xia and James R. Lupski. Their work appears in journals such as Clinical Genetics, Human Mutation, European Journal of Human Genetics, The American Journal of Human Genetics and Human Molecular 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.