Hatip Aydın

1.2k total citations
13 papers, 164 citations indexed

About

Hatip Aydın is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Hatip Aydın has authored 13 papers receiving a total of 164 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Hatip Aydın's work include Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (3 papers) and Connective tissue disorders research (3 papers). Hatip Aydın is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (3 papers) and Connective tissue disorders research (3 papers). Hatip Aydın collaborates with scholars based in Türkiye and United States. Hatip Aydın's co-authors include Ali̇ Karaman, Arda Çetinkaya, James R. Lupski, Bilgen Bilge Geçkinli, Beyhan Tüysüz, Hugo J. Bellen, Marjorie Withers, Ghayda Mirzaa, Priya S. Shah and Sedat Işıkay and has published in prestigious journals such as Developmental Cell, European Journal of Human Genetics and Mutation Research/Genetic Toxicology and Environmental Mutagenesis.

In The Last Decade

Hatip Aydın

12 papers receiving 161 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Hatip Aydın Türkiye	6	79	50	29	20	18	13	164
Jessica Douglas United States	9	94 1.2×	134 2.7×	23 0.8×	31 1.6×	23 1.3×	12	225
Pu-Yao Zhang China	8	184 2.3×	30 0.6×	64 2.2×	15 0.8×	20 1.1×	10	262
Jacob Malte Jensen Denmark	8	112 1.4×	87 1.7×	24 0.8×	39 1.9×	10 0.6×	9	207
Sandra Batista United States	4	90 1.1×	36 0.7×	15 0.5×	34 1.7×	11 0.6×	5	180
Stephanie K. Jones United States	7	187 2.4×	23 0.5×	12 0.4×	36 1.8×	14 0.8×	13	264
Auke B.C. Otten United States	9	218 2.8×	24 0.5×	30 1.0×	47 2.4×	27 1.5×	12	284
Nathalie Da Silva France	10	155 2.0×	58 1.2×	47 1.6×	8 0.4×	12 0.7×	21	320
Bilgen Bilge Geçkinli Türkiye	7	74 0.9×	54 1.1×	42 1.4×	6 0.3×	18 1.0×	18	151
Angad Johar Australia	9	83 1.1×	91 1.8×	25 0.9×	12 0.6×	5 0.3×	14	245
Luisina Ongaro Canada	11	153 1.9×	63 1.3×	72 2.5×	24 1.2×	13 0.7×	27	289

Countries citing papers authored by Hatip Aydın

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Hatip Aydın

This figure shows the co-authorship network connecting the top 25 collaborators of Hatip Aydın. A scholar is included among the top collaborators of Hatip Aydın based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hatip Aydın. Hatip Aydın is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Link, Nichole, Hyung-Lok Chung, Angad Jolly, et al.. (2019). Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause Microcephaly. Developmental Cell. 51(6). 713–729.e6. 66 indexed citations

Aydın, Hatip, et al.. (2016). Anensefalide Gebelerin Folat ve Vitamin B12 Düzeyleri ile Faktör V Leiden, Faktör II G20210A, MTHFR C667T ve MTHFR A1298C Polimorfizlerinin Önemi. DergiPark (Istanbul University). 3(3). 112–116.

Çebi, Alper Han, et al.. (2016). 22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS.. PubMed. 27(1). 43–9. 3 indexed citations

Bayram, Yavuz, Hatip Aydın, Tomasz Gambin, et al.. (2015). Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral‐facial‐digital syndrome type VI. American Journal of Medical Genetics Part A. 167(9). 2132–2137. 9 indexed citations

Aydın, Hatip, et al.. (2015). CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33.. PubMed. 26(4). 393–400. 7 indexed citations

Karaman, Ali̇, et al.. (2015). DNA damage is increased in lymphocytes of patients with metabolic syndrome. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 782. 30–35. 43 indexed citations

Aydın, Hatip, et al.. (2015). MICROARRAY DELINEATION OF DE NOVO DUPLICATION 1q32q42 IN A CHILD SHOWING MULTIPLE ANOMALIES AND DYSMORPHISM.. PubMed. 26(2). 181–6. 1 indexed citations

Mutlu, Gül Yeşiltepe, et al.. (2014). Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report. Journal of Pediatric Endocrinology and Metabolism. 28(1-2). 207–10. 5 indexed citations

Pehli̇van, Davut, Ender Karaca, Hatip Aydın, et al.. (2014). Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia. European Journal of Human Genetics. 22(9). 1145–1148. 13 indexed citations

10.

Aydın, Hatip, et al.. (2013). Tetrasomy 12p presenting with long appendix: a prenatal case.. PubMed. 24(4). 439–40. 3 indexed citations

11.

Seven, Mehmet, Erkan Koparir, Alper Gezdirici, et al.. (2013). A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve–Melchior–Clausen syndrome. Clinical Dysmorphology. 23(1). 1–7. 7 indexed citations

12.

Çine, Naci, et al.. (2011). A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.. PubMed. 22(1). 11–9. 3 indexed citations

13.

Loeys, Bart, et al.. (2010). A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutation.. PubMed. 21(2). 225–32. 4 indexed citations

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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