Can Apacik
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 4
- Genetic Syndromes and Imprinting 3
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Prenatal Screening and Diagnostics 4
- Co-authors
- S. Stengel‐Rutkowski (6 shared papers)Jutta Müller‐Navia (3 shared papers)Simone Schuffenhauer (2 shared papers)Christine Fauth (1 shared paper)Monika Cohen (1 shared paper)Sabine Uhrig (1 shared paper)Jan Murken (1 shared paper)Hartmut Engels (3 shared papers)
In The Last Decade
Can Apacik
7 papers receiving 139 citations
Peers
Comparison fields: 5 of 21
- Genetics 142
- Pediatrics, Perinatology and Child Health 51
- Plant Science 75
- Developmental Biology 3
- Molecular Biology 51
Countries citing papers authored by Can Apacik
This map shows the geographic impact of Can Apacik'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 Can Apacik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Can Apacik more than expected).
Fields of papers citing papers by Can Apacik
This network shows the impact of papers produced by Can Apacik. 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 Can Apacik. The network helps show where Can Apacik may publish in the future.
Co-authors
The 24 scholars most cited alongside Can Apacik, 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 | 1999 | 71 | |
| 2 | 1996 | 19 | |
| 3 | 1992 | 19 | |
| 4 | 1997 | 16 | |
| 5 | Tetrasomy 18p caused by paternal meiotic nondisjunction. | 1997 | 16 |
| 6 | Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature. | 1999 | 12 |
| 7 | The fragile-X phenotype. Computer assisted analysis of the dysmorphological features and discrimination from the Sotos phenotype. | 1993 | 5 |
About Can Apacik
Can Apacik is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Infectious Diseases, having authored 7 papers that have together received 158 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Chromosomal and Genetic Variations (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), RNA regulation and disease (1 paper) and Renal and related cancers (1 paper). The work is most often cited by research in Genetics (142 citations), Pediatrics, Perinatology and Child Health (51 citations), Plant Science (75 citations), Developmental Biology (3 citations) and Molecular Biology (51 citations). Can Apacik has collaborated with scholars based in Germany and France. Frequent co-authors include S. Stengel‐Rutkowski, Jutta Müller‐Navia, Simone Schuffenhauer, Christine Fauth, Monika Cohen, Sabine Uhrig, Jan Murken, Hartmut Engels, Cornelia Daumer‐Haas and Gesa Schwanitz. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, European Journal of Human Genetics and PubMed.
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.