Hatip Aydın
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 5
- Connective tissue disorders research 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Genomics and Rare Diseases 1
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- RNA modifications and cancer 3
- Co-authors
- Ali̇ Karaman (6 shared papers)Arda Çetinkaya (2 shared papers)James R. Lupski (3 shared papers)Bilgen Bilge Geçkinli (3 shared papers)Beyhan Tüysüz (1 shared paper)Burak Tepe (1 shared paper)Marjorie Withers (1 shared paper)Benjamin R. Arenkiel (1 shared paper)
- Journals
- European Journal of Human Genetics (1 paper)Developmental Cell (1 paper)Mutation Research/Genetic Toxicology and Environmental Mutagenesis (1 paper)American Journal of Medical Genetics Part A (1 paper)Journal of Pediatric Endocrinology and Metabolism (1 paper)
- Partner nations
- TürkiyeUnited States
In The Last Decade
Hatip Aydın
12 papers receiving 170 citations
Peers
Comparison fields: 5 of 58
- Genetics 50
- Aging 3
- Cancer Research 19
- Cell Biology 21
- Molecular Biology 78
Countries citing papers authored by Hatip Aydın
This map shows the geographic impact of Hatip Aydın'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 Hatip Aydın with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hatip Aydın more than expected).
Fields of papers citing papers by Hatip Aydın
This network shows the impact of papers produced by Hatip Aydın. 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 Hatip Aydın. The network helps show where Hatip Aydın may publish in the future.
Co-authors
The 25 scholars most cited alongside Hatip Aydın, 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 | 2019 | 73 | |
| 2 | 2015 | 43 | |
| 3 | 2014 | 14 | |
| 4 | 2015 | 9 | |
| 5 | CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33. | 2015 | 8 |
| 6 | 2013 | 7 | |
| 7 | 2014 | 6 | |
| 8 | A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutation. | 2010 | 4 |
| 9 | A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome. | 2011 | 4 |
| 10 | Tetrasomy 12p presenting with long appendix: a prenatal case. | 2013 | 3 |
| 11 | 22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS. | 2016 | 3 |
| 12 | MICROARRAY DELINEATION OF DE NOVO DUPLICATION 1q32q42 IN A CHILD SHOWING MULTIPLE ANOMALIES AND DYSMORPHISM. | 2015 | 1 |
| 13 | Anensefalide Gebelerin Folat ve Vitamin B12 Düzeyleri ile Faktör V Leiden, Faktör II G20210A, MTHFR C667T ve MTHFR A1298C Polimorfizlerinin Önemi | 2016 | 0 |
About Hatip Aydın
Hatip Aydın is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Pediatrics, Perinatology and Child Health, having authored 13 papers that have together received 175 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (3 papers), Connective tissue disorders research (3 papers), Pediatric Hepatobiliary Diseases and Treatments (2 papers), Folate and B Vitamins Research (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Genomics and Rare Diseases (1 paper) and Fatty Acid Research and Health (1 paper). The work is most often cited by research in Genetics (50 citations), Aging (3 citations), Cancer Research (19 citations), Cell Biology (21 citations) and Molecular Biology (78 citations). Hatip Aydın has collaborated with scholars based in Türkiye and United States. Frequent co-authors include Ali̇ Karaman, Arda Çetinkaya, James R. Lupski, Bilgen Bilge Geçkinli, Beyhan Tüysüz, Burak Tepe, Marjorie Withers, Benjamin R. Arenkiel, Hugo J. Bellen and Sedat Işıkay. Their work appears in journals such as European Journal of Human Genetics, Developmental Cell, Mutation Research/Genetic Toxicology and Environmental Mutagenesis, American Journal of Medical Genetics Part A and Journal of Pediatric Endocrinology and Metabolism.
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.