H. Serap Kalkanoğlu

637 total citations
17 papers, 216 citations indexed

About

H. Serap Kalkanoğlu is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H. Serap Kalkanoğlu has authored 17 papers receiving a total of 216 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Clinical Biochemistry, 8 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H. Serap Kalkanoğlu's work include Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (4 papers) and Neonatal Health and Biochemistry (4 papers). H. Serap Kalkanoğlu is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (4 papers) and Neonatal Health and Biochemistry (4 papers). H. Serap Kalkanoğlu collaborates with scholars based in Türkiye, Denmark and Germany. H. Serap Kalkanoğlu's co-authors include Turgay Coşkun, Ayşegül Tokatlı, Ali Dursun, İ Özalp, Gülden Köksal, Anne Romstad, Flemming Güttler, Embiya Dilber, R. Öner and Alpay Çeliker and has published in prestigious journals such as Journal of Clinical Pathology, Atherosclerosis and Human Genetics.

In The Last Decade

H. Serap Kalkanoğlu

17 papers receiving 209 citations

Peers

H. Serap Kalkanoğlu

PHYSI

PPCH

RHEUM

Nawal Makhseed Kuwait

Sylvia Stoeckler-Ipsiroglu Austria

Patrícia Janeiro Portugal

Friederike Hörster Germany

Jose Luis Puerta Spain

Joanna Taybert Poland

Sommer Gaughan United States

Takeyori Saheki Japan

Angela Hosack Canada

Ute Spiekerkötter Germany

Nawal Makhseed Kuwait

H. Serap Kalkanoğlu

104 ×0.9

167 ×1.8

53 ×1.2

PHYSI

51 ×1.2

PPCH

66 ×1.6

RHEUM

Citations per year, relative to H. Serap Kalkanoğlu H. Serap Kalkanoğlu (= 1×) peers Nawal Makhseed

Countries citing papers authored by H. Serap Kalkanoğlu

Since Specialization

Citations

This map shows the geographic impact of H. Serap Kalkanoğlu'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 H. Serap Kalkanoğlu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H. Serap Kalkanoğlu more than expected).

Fields of papers citing papers by H. Serap Kalkanoğlu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. Serap Kalkanoğlu. 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 H. Serap Kalkanoğlu. The network helps show where H. Serap Kalkanoğlu may publish in the future.

Co-authorship network of co-authors of H. Serap Kalkanoğlu

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

All Works

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17 of 17 papers shown

Ichida, Kimiyoshi, Halil İbrahim Aydın, Makoto Hosoyamada, et al.. (2006). A Turkish Case with Molybdenum Cofactor Deficiency. Nucleosides Nucleotides & Nucleic Acids. 25(9-11). 1087–1091. 9 indexed citations

Kalkanoğlu, H. Serap, Kirsten Ahring, Lisbeth Birk Møller, et al.. (2005). Behavioural effects of phenylalanine‐free amino acid tablet supplementation in intellectually disabled adults with untreated phenylketonuria. Acta Paediatrica. 94(9). 1218–1222. 20 indexed citations

Sozen, Mert, Ros Whittall, Cihan Öner, et al.. (2005). The molecular basis of familial hypercholesterolaemia in Turkish patients. Atherosclerosis. 180(1). 63–71. 34 indexed citations

Yalçın, Sıddika Songül, et al.. (2005). The effect of oral L‐carnitine supplementation on the lipid profiles of hyperlipidaemic children. Acta Paediatrica. 94(6). 711–716. 4 indexed citations

Olcay, Lale, Esra Erdemlı, Mehmet Kesımer, et al.. (2005). High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluation. Journal of Clinical Pathology. 58(9). 939–945. 9 indexed citations

Kalkanoğlu, H. Serap, et al.. (2005). Four-Month-Old Infant With Focal Segmental Glomerulosclerosis and Mitochondrial DNA Deletion. Journal of Child Neurology. 20(1). 83–84. 4 indexed citations

Yalçın, Sıddika Songül, et al.. (2005). The effect of oral L-carnitine supplementation on the lipid profiles of hyperlipidaemic children. Acta Paediatrica. 94(6). 711–716. 2 indexed citations

Kalkanoğlu, H. Serap, et al.. (2004). A Boy With Spastic Paraparesis and Dyspnea. Journal of Child Neurology. 19(5). 397–398. 7 indexed citations

Dilber, Embiya, Alpay Çeliker, Tevfik Karagöz, & H. Serap Kalkanoğlu. (2002). Permanent Transfemoral Pacemaker Implantation in a Child with Maroteaux Lamy Syndrome. Pacing and Clinical Electrophysiology. 25(12). 1784–1785. 14 indexed citations

10.

Dursun, Ali, Marco Henneke, Rıza Köksal Özgül, et al.. (2002). Maple syrup urine disease: Mutation analysis in Turkish patients. Journal of Inherited Metabolic Disease. 25(2). 89–97. 16 indexed citations

11.

Kalkanoğlu, H. Serap, Anne Romstad, Turgay Coşkun, & Flemming Güttler. (2001). Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis. Prenatal Diagnosis. 21(10). 868–870. 4 indexed citations

12.

Dursun, Ali, H. Serap Kalkanoğlu, Turgay Coşkun, et al.. (2001). Mutation analysis in Turkish patients with hereditary fructose intolerance. Journal of Inherited Metabolic Disease. 24(5). 523–526. 9 indexed citations

13.

Özalp, İ, Turgay Coşkun, Ayşegül Tokatlı, et al.. (2001). Newborn PKU screening in Turkey: at present and organization for future.. PubMed. 43(2). 97–101. 54 indexed citations

14.

Kalkanoğlu, H. Serap, Turgay Coşkun, Sultan Durmuş Aydoğdu, Ayşegül Tokatlı, & Aytemiz Gürgey. (2001). Factor V Leiden mutation in Turkish patients with homozygous cystathionine β‐synthase deficiency. Journal of Inherited Metabolic Disease. 24(3). 367–369. 3 indexed citations

15.

Yılmaz, Engin, Francesco Calı̀, Valentino Romano, et al.. (2000). Molecular basis of mild hyperphenylalaninaemia in Turkey. Journal of Inherited Metabolic Disease. 23(5). 523–525. 9 indexed citations

16.

Kalkanoğlu, H. Serap, Deniz Anadol, Engin Yılmaz, & Turgay Coşkun. (2000). Phenylketonuria and cystic fibrosis in the same patient. Pediatrics International. 42(1). 92–93. 2 indexed citations

17.

Romstad, Anne, H. Serap Kalkanoğlu, Turgay Coşkun, et al.. (2000). Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE). Human Genetics. 107(6). 546–553. 16 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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