İ Özalp

1.3k total citations
77 papers, 961 citations indexed

About

İ Özalp is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, İ Özalp has authored 77 papers receiving a total of 961 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Clinical Biochemistry, 26 papers in Molecular Biology and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in İ Özalp's work include Metabolism and Genetic Disorders (38 papers), Neonatal Health and Biochemistry (12 papers) and Folate and B Vitamins Research (9 papers). İ Özalp is often cited by papers focused on Metabolism and Genetic Disorders (38 papers), Neonatal Health and Biochemistry (12 papers) and Folate and B Vitamins Research (9 papers). İ Özalp collaborates with scholars based in Türkiye, United States and Germany. İ Özalp's co-authors include Turgay Coşkun, Ayşegül Tokatlı, Kraisid Tontisirin, Meral Özgüç, Vernon R. Young, V. R. Young, N. S. Scrimshaw, Nevin S. Scrimshaw, H. Serap Kalkanoğlu and Barry Wolf and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Nutrition and The Journal of Pediatrics.

In The Last Decade

İ Özalp

75 papers receiving 899 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
İ Özalp Türkiye 17 452 321 198 183 175 77 961
Nicholas Ah Mew United States 23 799 1.8× 712 2.2× 65 0.3× 266 1.5× 259 1.5× 53 1.3k
H. Ghadimi United States 14 298 0.7× 231 0.7× 63 0.3× 111 0.6× 133 0.8× 32 711
Phyllis B. Acosta United States 19 777 1.7× 322 1.0× 129 0.7× 472 2.6× 191 1.1× 58 1.1k
L.‐O. Norée Sweden 9 187 0.4× 164 0.5× 304 1.5× 300 1.6× 56 0.3× 11 804
Richard W. Vilter United States 13 98 0.2× 194 0.6× 45 0.2× 109 0.6× 51 0.3× 36 810
Tohru Inouye United States 13 136 0.3× 335 1.0× 99 0.5× 162 0.9× 73 0.4× 21 967
Claude Allard Canada 16 51 0.1× 316 1.0× 84 0.4× 235 1.3× 38 0.2× 38 945
L Stanková United States 17 52 0.1× 185 0.6× 92 0.5× 117 0.6× 53 0.3× 33 890
F. Schønheyder Denmark 11 91 0.2× 170 0.5× 117 0.6× 129 0.7× 64 0.4× 29 484
F. W. Schmidt Germany 15 45 0.1× 148 0.5× 54 0.3× 148 0.8× 30 0.2× 52 904

Countries citing papers authored by İ Özalp

Since Specialization
Citations

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

Fields of papers citing papers by İ Özalp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by İ Özalp. 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 İ Özalp. The network helps show where İ Özalp may publish in the future.

Co-authorship network of co-authors of İ Özalp

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

All Works

20 of 20 papers shown
1.
Terzioglu, Mügen, Ayşegül Tokatlı, Turgay Coşkun, et al.. (2002). Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B. Human Mutation. 19(2). 184–185. 21 indexed citations
2.
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
3.
Blanton, Susan H., Arti Pandya, Walter E. Nance, et al.. (1999). Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations. Human Heredity. 50(2). 102–111. 8 indexed citations
4.
Seyrantepe, Volkan, Meral Özgüç, Turgay Coşkun, İ Özalp, & Juergen Reichardt. (1999). Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Human Mutation. 13(4). 339–339. 7 indexed citations
5.
Wolf, Barry, Robert J. Pomponio, Ira T. Lott, et al.. (1998). Delayed-onset profound biotinidase deficiency. The Journal of Pediatrics. 132(2). 362–365. 54 indexed citations
6.
Kılıç, İlknur, İ Özalp, Turgay Coşkun, et al.. (1998). The Effect of Zinc-Supplemented Bread Consumption on School Children with Asymptomatic Zinc Deficiency. Journal of Pediatric Gastroenterology and Nutrition. 26(2). 167–171. 28 indexed citations
7.
Tokatlı, Ayşegül, Turgay Coşkun, & İ Özalp. (1998). Isovaleric acidemia. Clinical presentation of 6 cases.. PubMed. 40(1). 111–9. 8 indexed citations
8.
9.
Gürgey, Aytemiz, İ Özalp, Agnès Rötig, et al.. (1996). A case of Pearson syndrome associated with multiple renal cysts. Pediatric Nephrology. 10(5). 637–638. 32 indexed citations
10.
Yordam, N, Ali S. Çalıkoğlu, Şükrü Hatun, et al.. (1995). Screening for congenital hypothyroidism in Turkey. European Journal of Pediatrics. 154(8). 614–616. 35 indexed citations
11.
Yurdakök, Murat, et al.. (1995). Cerebrospinal fluid amino acid levels in newborn infants with intracranial hemorrhage. Pediatrics International. 37(6). 694–696. 2 indexed citations
12.
Şahin, Gönül, et al.. (1995). Aluminum content of infant formulas used in Turkey. Biological Trace Element Research. 50(1). 87–96. 10 indexed citations
13.
Özgüç, Meral, Engin Yılmaz, Hayat Erdem‐Yurter, et al.. (1994). Allele frequencies of Mp6D‐9 and GATT markers in 32 Turkish cystic fibrosis families. Clinical Genetics. 45(5). 266–268.
14.
Özalp, İ, Turgay Coşkun, Meral Özgüç, et al.. (1994). Genetic and neurological evaluation of untreated and late‐treated patients with phenylketonuria. Journal of Inherited Metabolic Disease. 17(3). 371–371. 4 indexed citations
15.
Ataman, Mehmet Bozkurt, et al.. (1992). Biotidinase deficiency: a rare cause of laryngeal stridor. International Journal of Pediatric Otorhinolaryngology. 23(3). 281–284. 3 indexed citations
16.
Coşkun, Turgay, et al.. (1990). Scleroderma-like skin lesions in two patients with phenylketonuria. European Journal of Pediatrics. 150(2). 109–110. 4 indexed citations
17.
Büyükgebiz, Benal, et al.. (1990). Investigation of Serum Vitamin A Levels of Children who had a History of Recurrent Diarrhoea and Acute Respiratory Infections in Ankara. Journal of Tropical Pediatrics. 36(5). 251–255. 14 indexed citations
18.
Lichter‐Konecki, Uta, Magdalena Schlotter, Meral Özgüç, et al.. (1989). DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population. Human Genetics. 81(4). 373–376. 28 indexed citations
19.
Özalp, İ, et al.. (1977). A case of Hartnup disorder with hypoalbuminemia and edema.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 19(1-2). 73–7. 1 indexed citations
20.
Özme, Şencan, Meltem Refıker Ege, İ Özalp, & G Ciliv. (1977). Serum lipids and lipoproteins in children from families with early coronary heart disease.. SHILAP Revista de lepidopterología. 19(1-2). 67–72. 1 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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