Can Apacik

486 total citations
7 papers, 159 citations indexed

About

Can Apacik is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Can Apacik has authored 7 papers receiving a total of 159 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Can Apacik's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (3 papers). Can Apacik is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (3 papers). Can Apacik collaborates with scholars based in Germany and France. Can Apacik's co-authors include S. Stengel‐Rutkowski, Jutta Müller‐Navia, Simone Schuffenhauer, Antje Wirtz, Jan Murken, Sabine Uhrig, Monika Cohen, Thomas Cremer, Cornelia Daumer‐Haas and Christine Fauth and has published in prestigious journals such as The American Journal of Human Genetics, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Can Apacik

7 papers receiving 140 citations

Peers

Can Apacik

GENET

PS

PPCH

MB

CR

Heidi Whitby United States

Erin B. Kaminsky United States

Christina Kelbova Germany

M.R. Guichaoua France

Jole Messa Italy

Christine A Joyce United Kingdom

A. Polityko Germany

Angela Nietzel Germany

Theresa Naluai-Cecchini United States

Meryl Altree Australia

Heidi Whitby United States

Can Apacik

167 ×1.1

GENET

57 ×0.7

PS

79 ×1.2

PPCH

83 ×1.5

MB

7 ×0.5

CR

Citations per year, relative to Can Apacik Can Apacik (= 1×) peers Heidi Whitby

Countries citing papers authored by Can Apacik

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Can Apacik

This figure shows the co-authorship network connecting the top 25 collaborators of Can Apacik. A scholar is included among the top collaborators of Can Apacik 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 Can Apacik. Can Apacik is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Uhrig, Sabine, Simone Schuffenhauer, Christine Fauth, et al.. (1999). Multiplex-FISH for Pre- and Postnatal Diagnostic Applications. The American Journal of Human Genetics. 65(2). 448–462. 72 indexed citations

2.

Eggermann, Thomas, Regine Schubert, Hartmut Engels, et al.. (1999). Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.. PubMed. 42(2). 75–80. 12 indexed citations

3.

Eggermann, Thomas, Hartmut Engels, Can Apacik, et al.. (1997). Tetrasomy 18p caused by paternal meiotic nondisjunction.. PubMed. 5(3). 175–7. 16 indexed citations

4.

Eggermann, Thomas, Hartmut Engels, Can Apacik, et al.. (1997). Tetrasomy 18p Caused by Paternal Meiotic Nondisjunction. European Journal of Human Genetics. 5(3). 175–177. 16 indexed citations

5.

Apacik, Can, Maimon M. Cohen, Barbara Schmucker, et al.. (1996). Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12 → q13.3) inherited from the mother. Clinical Genetics. 50(2). 63–73. 19 indexed citations

6.

Stengel‐Rutkowski, S., et al.. (1993). The fragile-X phenotype. Computer assisted analysis of the dysmorphological features and discrimination from the Sotos phenotype.. PubMed. 4(1). 51–8. 5 indexed citations

7.

Stengel‐Rutkowski, S., Konrad Lohse, Christopher D. Herzog, et al.. (1992). Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk. Clinical Genetics. 42(4). 178–185. 19 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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