G. Nozari

732 total citations
18 papers, 547 citations indexed

About

G. Nozari is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, G. Nozari has authored 18 papers receiving a total of 547 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in G. Nozari's work include Hemoglobinopathies and Related Disorders (11 papers), Erythrocyte Function and Pathophysiology (5 papers) and Hemoglobin structure and function (5 papers). G. Nozari is often cited by papers focused on Hemoglobinopathies and Related Disorders (11 papers), Erythrocyte Function and Pathophysiology (5 papers) and Hemoglobin structure and function (5 papers). G. Nozari collaborates with scholars based in United States, Iran and United Kingdom. G. Nozari's co-authors include Steve S. Sommer, Qiang Liu, S. Rahbar, R. Bruce Wallace, Frank K. Fujimura, Vũ Quốc Huy Nguyễn, April Mengos, Carolyn H. Buzin, H. Lehmann and Richard A. Gatti and has published in prestigious journals such as Blood, Analytical Biochemistry and FEBS Letters.

In The Last Decade

G. Nozari

18 papers receiving 530 citations

Peers

G. Nozari

MB

HEMAT

GENET

CR

Scott C. Crable United States

Lois B. Wilson United States

K Ohyashiki Japan

A.J. Montandon United Kingdom

Stella J. Nylund Finland

Katarzyna E. Kolodziej Netherlands

Manabu Shimoyama Japan

G. Salvo Italy

Kimberly R. Blahnik United States

Ji Yoo Kim Japan

Scott C. Crable United States

G. Nozari

446 ×1.3

MB

99 ×0.3

HEMAT

124 ×1.1

GENET

111 ×1.5

GENET

37 ×1.0

CR

Citations per year, relative to G. Nozari G. Nozari (= 1×) peers Scott C. Crable

Countries citing papers authored by G. Nozari

Since Specialization

Citations

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

Fields of papers citing papers by G. Nozari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Nozari

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

All Works

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18 of 18 papers shown

1.

Buzin, Carolyn H., Richard A. Gatti, Vũ Quốc Huy Nguyễn, et al.. (2003). Comprehensive scanning of theATM gene with DOVAM-S. Human Mutation. 21(2). 123–131. 39 indexed citations

2.

Buzin, Carolyn H., Vũ Quốc Huy Nguyễn, G. Nozari, et al.. (2000). Scanning by DOVAM-S Detects All Unique Sequence Changes in Blinded Analyses: Evidence that the Scanning Conditions Are Generic. BioTechniques. 28(4). 746–753. 35 indexed citations

3.

Feng, Jinong, Carolyn H. Buzin, G. Nozari, et al.. (1999). Detection of Virtually All Mutations-SSCP (DOVAM-S): A Rapid Method for Mutation Scanning with Virtually 100% Sensitivity. BioTechniques. 26(5). 932–942. 51 indexed citations

4.

Liu, Qiang, G. Nozari, & Steve S. Sommer. (1998). Single-Tube Polymerase Chain Reaction for Rapid Diagnosis of the Inversion Hotspot of Mutation in Hemophilia A. Blood. 92(4). 1458–1459. 127 indexed citations

5.

Liu, Qiang, G. Nozari, & Steve S. Sommer. (1998). Single-Tube Polymerase Chain Reaction for Rapid Diagnosis of the Inversion Hotspot of Mutation in Hemophilia A. Blood. 92(4). 1458–1459. 148 indexed citations

6.

Rahbar, S., et al.. (1997). HB Watts [α74(EF3) OR α75(EF4)ASP→0]: A Shortened α Chain Variant Due to the Deletion of Three Nucleotides in Exon 2 of the α2-Globin Gene. Hemoglobin. 21(4). 321–330. 10 indexed citations

7.

Nozari, G., et al.. (1995). Molecular Analyses of β-Thalassa in Iran. Hemoglobin. 19(6). 425–431. 29 indexed citations

8.

Nozari, G., et al.. (1993). Splice Junction [IVS-II-1 (G→C)] Thalassemia; A New Mutation Detected in an Iranian Patient. Hemoglobin. 17(3). 279–283. 1 indexed citations

9.

Rahbar, S. & G. Nozari. (1993). A Novel Initiation Codon Mutation (ATG→ATT) in a β-Thalassemia Patient. Hemoglobin. 17(6). 557–562. 5 indexed citations

10.

Rahbar, S., et al.. (1992). Association of HB Hope [β 136(H14)GLY→ASP] and α-THALASSEMIA-2 (3.7 KB Deletion) Causing Severe Microcytic Anemia. Hemoglobin. 16(5). 421–425. 10 indexed citations

11.

Wu, Dan Y., et al.. (1989). Direct Analysis of Single Nucleotide Variation in Human DNA and RNA Using In Situ Dot Hybridization. DNA. 8(2). 135–142. 16 indexed citations

12.

Rahbar, S., G. Nozari, Ram Chillar, & R. Bruce Wallace. (1988). Further Evidence for a Post-Translational Phenomenon in the Interaction of α-Thalassemia with Sickle Cell Trait. Hemoglobin. 12(1). 71–76. 5 indexed citations

13.

Nozari, G., S. Rahbar, & R. Bruce Wallace. (1988). Haplotype analysis of the human β-globin gene complex using multiple locus specific oligonucleotide probes. Analytical Biochemistry. 172(1). 180–184. 2 indexed citations

14.

Nozari, G., S. Rahbar, & R. Bruce Wallace. (1986). Discrimination among the transcripts of the allelic human β-globin genes βA, βS and βC using oligodeoxynucleotide hybridization probes. Gene. 43(1-2). 23–28. 30 indexed citations

15.

Rahbar, S., et al.. (1979). Haemoglobin Avicenna (β47 (CD6) Asp → Ala). A new abnormal haemoglobin. Biochimica et Biophysica Acta (BBA) - Protein Structure. 576(2). 466–470. 6 indexed citations

16.

Casey, R., Pamela A.M. Kynoch, A. Lang, et al.. (1978). Double Heterozygosity for Two Unstable Haemoglobins: Hb Sydney (β67[E11] Val→Ala) and Hb Coventry (β141[H19] Leu Deleted). British Journal of Haematology. 38(2). 195–209. 17 indexed citations

17.

Nozari, G., S. Rahbar, & H. Lehmann. (1978). Haemoglobin coventry (β 141 deleted) in iran. FEBS Letters. 95(1). 88–90. 3 indexed citations

18.

Nozari, G., et al.. (1977). Hemoglobin Setif (α94 (G1) ASP → TYR) in Iran a Report of 9 Cases. Hemoglobin. 1(3). 289–292. 13 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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