M. Anwar Iqbal

2.2k total citations
63 papers, 1.5k citations indexed

About

M. Anwar Iqbal is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, M. Anwar Iqbal has authored 63 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 21 papers in Molecular Biology and 18 papers in Hematology. Recurrent topics in M. Anwar Iqbal's work include Genomic variations and chromosomal abnormalities (19 papers), Acute Myeloid Leukemia Research (15 papers) and Prenatal Screening and Diagnostics (9 papers). M. Anwar Iqbal is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Acute Myeloid Leukemia Research (15 papers) and Prenatal Screening and Diagnostics (9 papers). M. Anwar Iqbal collaborates with scholars based in United States, Saudi Arabia and Canada. M. Anwar Iqbal's co-authors include Carl L. Schildkraut, E H Brown, K S Hatton, Veena Dhar, Diana Maas, Ronald E. Verrall, Jay E. Valinsky, Auṣāf Aḥmad, Dixie L. Mager and George T. Roberts and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

M. Anwar Iqbal

60 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Anwar Iqbal United States 20 787 367 222 207 125 63 1.5k
Ariadni Mavrou Greece 24 626 0.8× 458 1.2× 120 0.5× 103 0.5× 84 0.7× 94 1.7k
Katsunori Aoki Japan 20 630 0.8× 145 0.4× 120 0.5× 118 0.6× 173 1.4× 69 1.4k
Jasenka Wagner Croatia 23 397 0.5× 209 0.6× 307 1.4× 91 0.4× 246 2.0× 66 1.4k
Véronique David France 19 523 0.7× 406 1.1× 408 1.8× 127 0.6× 56 0.4× 40 1.6k
Laurence Cuisset France 25 2.1k 2.6× 297 0.8× 510 2.3× 232 1.1× 34 0.3× 62 2.5k
Mara Giordano Italy 20 503 0.6× 371 1.0× 37 0.2× 111 0.5× 81 0.6× 83 1.3k
Éric Piver France 19 379 0.5× 598 1.6× 99 0.4× 228 1.1× 95 0.8× 51 1.5k
Nobuhiro Suzumori Japan 23 570 0.7× 461 1.3× 95 0.4× 128 0.6× 86 0.7× 82 2.1k
Marie‐Pierre Audrézet France 26 794 1.0× 924 2.5× 108 0.5× 260 1.3× 98 0.8× 69 2.0k
Mariko Eguchi Japan 24 832 1.1× 170 0.5× 845 3.8× 143 0.7× 306 2.4× 123 2.1k

Countries citing papers authored by M. Anwar Iqbal

Since Specialization
Citations

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

Fields of papers citing papers by M. Anwar Iqbal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Anwar Iqbal. 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 M. Anwar Iqbal. The network helps show where M. Anwar Iqbal may publish in the future.

Co-authorship network of co-authors of M. Anwar Iqbal

This figure shows the co-authorship network connecting the top 25 collaborators of M. Anwar Iqbal. A scholar is included among the top collaborators of M. Anwar Iqbal 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 M. Anwar Iqbal. M. Anwar Iqbal 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.
Broeckel, Ulrich, M. Anwar Iqbal, Brynn Levy, et al.. (2024). Detection of Constitutional Structural Variants by Optical Genome Mapping. Journal of Molecular Diagnostics. 26(3). 213–226. 8 indexed citations
2.
Pang, Andy Wing Chun, Karena Kosco, Nikhil Sahajpal, et al.. (2023). Analytic Validation of Optical Genome Mapping in Hematological Malignancies. Biomedicines. 11(12). 3263–3263. 7 indexed citations
3.
Iqbal, M. Anwar, et al.. (2023). Prenatal Evaluation of a Fetal Cystic Hygroma: An Unexpected Finding of a De Novo Fetal BRCA1 Deletion Case Report. SHILAP Revista de lepidopterología. 4(4). 242–247. 1 indexed citations
4.
Iqbal, M. Anwar, Ulrich Broeckel, Brynn Levy, et al.. (2023). Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases. Journal of Molecular Diagnostics. 25(3). 175–188. 23 indexed citations
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Fong, Chin‐To, et al.. (2021). Allelic and dosage effects of NHS in X-linked cataract and Nance–Horan syndrome: a family study and literature review. Molecular Cytogenetics. 14(1). 48–48. 5 indexed citations
7.
Fong, Chin‐To, et al.. (2020). Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review. Molecular Cytogenetics. 13(1). 40–40. 6 indexed citations
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Marques, Mayra A., José R. Pinto, Adolfo H. Moraes, et al.. (2017). Allosteric Transmission along a Loosely Structured Backbone Allows a Cardiac Troponin C Mutant to Function with Only One Ca2+ Ion. Journal of Biological Chemistry. 292(6). 2379–2394. 14 indexed citations
10.
Aḥmad, Auṣāf, Soumyaroop Bhattacharya, Arthi Sridhar, M. Anwar Iqbal, & Thomas J. Mariani. (2016). Recurrent copy number variants associated with bronchopulmonary dysplasia. Pediatric Research. 79(6). 940–945. 7 indexed citations
11.
Vargas, Hugo M., et al.. (2012). A 4.5 Mb terminal deletion of chromosome 12p helps further define a psychosis-associated locus. European Journal of Medical Genetics. 55(10). 573–576. 8 indexed citations
12.
Velinov, Milen, et al.. (2012). A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split‐hand/split‐foot malformation. American Journal of Medical Genetics Part A. 158A(12). 3201–3206. 9 indexed citations
13.
Al‐Owain, Mohammed, Namik Kaya, Hamad Alzaidan, et al.. (2010). Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy. Journal of Immunology Research. 2010(1). 586342–586342. 12 indexed citations
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Iqbal, M. Anwar, et al.. (2004). Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patients. Annals of Saudi Medicine. 24(5). 368–372. 18 indexed citations
17.
Iqbal, M. Anwar, et al.. (1999). Use of FISH technique in the diagnosis of chromosomal syndromes. Eastern Mediterranean Health Journal. 5(6). 1218–1224. 1 indexed citations
18.
Iqbal, M. Anwar, Mohammed Akhtar, & Muhammad Ali. (1996). Cytogenetic findings in renal cell carcinoma. Human Pathology. 27(9). 949–954. 20 indexed citations
19.
Dhar, Veena, Dixie L. Mager, M. Anwar Iqbal, & Carl L. Schildkraut. (1988). The coordinate replication of the human beta-globin gene domain reflects its transcriptional activity and nuclease hypersensitivity.. Molecular and Cellular Biology. 8(11). 4958–4965. 66 indexed citations
20.
Brown, E H, et al.. (1987). Rate of Replication of the Murine Immunoglobulin Heavy-Chain Locus: Evidence that the Region is Part of a Single Replicon. Molecular and Cellular Biology. 7(1). 450–457. 37 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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