Valeh Hadavi

1.7k total citations
17 papers, 425 citations indexed

About

Valeh Hadavi is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Valeh Hadavi has authored 17 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Hematology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Valeh Hadavi's work include Hemoglobinopathies and Related Disorders (10 papers), Iron Metabolism and Disorders (10 papers) and Prenatal Screening and Diagnostics (4 papers). Valeh Hadavi is often cited by papers focused on Hemoglobinopathies and Related Disorders (10 papers), Iron Metabolism and Disorders (10 papers) and Prenatal Screening and Diagnostics (4 papers). Valeh Hadavi collaborates with scholars based in Iran, Singapore and United States. Valeh Hadavi's co-authors include Hossein Najmabadi, Roxana Kariminejad, Christian Oberkanins, Hai‐Yang Law, Kimia Kahrizi, Farkhondeh Behjati, Masoud Garshasbi, Hans Hilger Ropers, Andreas W. Kuß and Andreas Tzschach and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Valeh Hadavi

17 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Valeh Hadavi Iran	11	252	228	98	97	70	17	425
V. Faà Italy	14	234 0.9×	164 0.7×	94 1.0×	145 1.5×	88 1.3×	20	489
M Patterson Canada	12	359 1.4×	262 1.1×	60 0.6×	148 1.5×	90 1.3×	27	505
Anindita Basak Türkiye	8	198 0.8×	140 0.6×	63 0.6×	188 1.9×	45 0.6×	14	363
Cong Peng China	5	167 0.7×	90 0.4×	38 0.4×	160 1.6×	74 1.1×	12	290
Maria Suciu United Kingdom	4	180 0.7×	77 0.3×	52 0.5×	236 2.4×	144 2.1×	6	388
G. Mérault France	12	226 0.9×	152 0.7×	43 0.4×	123 1.3×	48 0.7×	22	366
Meihuan Chen China	8	155 0.6×	124 0.5×	71 0.7×	70 0.7×	70 1.0×	49	257
Brian Gibbs United States	5	36 0.1×	98 0.4×	98 1.0×	123 1.3×	33 0.5×	8	254
G. V. Sciarratta Italy	11	292 1.2×	193 0.8×	54 0.6×	108 1.1×	88 1.3×	27	387
G Fioretti Italy	14	188 0.7×	133 0.6×	128 1.3×	131 1.4×	73 1.0×	28	402

Countries citing papers authored by Valeh Hadavi

Since Specialization

Citations

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

Fields of papers citing papers by Valeh Hadavi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valeh Hadavi

This figure shows the co-authorship network connecting the top 25 collaborators of Valeh Hadavi. A scholar is included among the top collaborators of Valeh Hadavi 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 Valeh Hadavi. Valeh Hadavi 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

Hafezi‐Nejad, Nima, Mohsen Khosravi, Ariana Kariminejad, et al.. (2014). Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience. Hemoglobin. 38(3). 153–157. 8 indexed citations

Mahdavi, Mohammad Reza, et al.. (2012). Report of haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran.. PubMed. 62(4). 396–8. 5 indexed citations

Azarkeivan, Azita, et al.. (2011). Genotype-Phenotype Correlation In Iranian Patients With Hb H Disease. Hemoglobin. 35(1). 40–46. 16 indexed citations

Neishabury, Maryam, et al.. (2010). A REPORT OF 8 CASES WITH HEMOGLOBIN H DISEASE IN AN IRANIAN FAMILY. Pediatric Hematology and Oncology. 27(5). 405–412. 3 indexed citations

Tamaddoni, Ahmad, Valeh Hadavi, Navid Almadani, et al.. (2009). α-Thalassemia Mutation Analyses in Mazandaran Province, North Iran. Hemoglobin. 33(2). 115–123. 40 indexed citations

Hadavi, Valeh, Nima Hafezi‐Nejad, Fatemeh Eskandari, et al.. (2009). α-Thalassemia Mutations in Gilan Province, North Iran. Hemoglobin. 33(3-4). 235–241. 31 indexed citations

Hasanzad, Mandana, Roxana Kariminejad, Valeh Hadavi, et al.. (2009). Deletions in the Survival Motor Neuron Gene in Iranian Patients with Spinal Muscular Atrophy. Annals of the Academy of Medicine Singapore. 38(2). 139–141. 4 indexed citations

Nikuei, Pooneh, et al.. (2008). Prenatal Diagnosis for β-Thalassemia Major in the Iranian Province of Hormozgan. Hemoglobin. 32(6). 539–545. 14 indexed citations

Garshasbi, Masoud, Valeh Hadavi, Kimia Kahrizi, et al.. (2008). A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation. The American Journal of Human Genetics. 82(5). 1158–1164. 106 indexed citations

10.

Hafezi‐Nejad, Nima, Valeh Hadavi, Christian Oberkanins, et al.. (2008). α-Thalassemia Mutations in Khuzestan Province, Southwest Iran. Hemoglobin. 32(6). 546–552. 30 indexed citations

11.

Hadavi, Valeh, Amir Hossein Taromchi, Mahdi Malekpour, et al.. (2007). Elucidating the spectrum of -thalassemia mutations in Iran. Haematologica. 92(7). 992–993. 52 indexed citations

12.

Salipante, Stephen J., Kathleen F. Benson, Valeh Hadavi, et al.. (2007). Double de novo mutations ofELA2 in cyclic and severe congenital neutropenia. Human Mutation. 28(9). 874–881. 26 indexed citations

13.

Najmabadi, Hossein, Alireza Ghamari, Farhad Sahebjam, et al.. (2006). Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran. Public Health Genomics. 9(2). 93–97. 58 indexed citations

14.

Hadavi, Valeh, et al.. (2005). AN INVESTIGATION OF HUMAN APOLIPOPROTEIN E POLYMORPHISMS IN MULTIPLE SCLEROSIS PATIENTS OF IRAN. The Medical Journal of The Islamic Republic of Iran. 18(4). 297–301. 1 indexed citations

15.

Hadavi, Valeh, et al.. (2004). Association of apolipoprotein E polymorphism with susceptibility to multiple sclerosis. Iranian Journal of Biotechnology. 2(1). 49–54. 1 indexed citations

16.

Chaleshtori, Morteza Hashemzadeh, et al.. (2002). "Deafness –Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population". SHILAP Revista de lepidopterología. 31(34). 75–79. 19 indexed citations

17.

Farhud, D.D., Valeh Hadavi, & Hassan Sadighi. (2000). EPIDEMIOLOGY OF NEURAL TUBE DEFECTS IN THE WORLD AND IRAN. SHILAP Revista de lepidopterología. 11 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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