Rizwan Naeem

1.0k total citations
31 papers, 700 citations indexed

About

Rizwan Naeem is a scholar working on Molecular Biology, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rizwan Naeem has authored 31 papers receiving a total of 700 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Hematology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rizwan Naeem's work include Prenatal Screening and Diagnostics (8 papers), Acute Myeloid Leukemia Research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Rizwan Naeem is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Acute Myeloid Leukemia Research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Rizwan Naeem collaborates with scholars based in United States, Tanzania and Germany. Rizwan Naeem's co-authors include Joseph M. Corson, Jonathan A. Fletcher, Jonathan A. Fletcher, Stephen P. Naber, Sheng Xiao, Marcia L. Lux, S.‐F. Huang, Rushdia Z. Yusuf, John Hicks and Louise C. Strong and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and JNCI Journal of the National Cancer Institute.

In The Last Decade

Rizwan Naeem

28 papers receiving 676 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rizwan Naeem United States 15 198 194 164 142 141 31 700
Jacqueline R. Batanian United States 15 92 0.5× 206 1.1× 82 0.5× 113 0.8× 52 0.4× 56 568
Klaus Fenchel Germany 14 164 0.8× 258 1.3× 340 2.1× 133 0.9× 48 0.3× 31 855
Annet Simons Netherlands 17 145 0.7× 239 1.2× 144 0.9× 153 1.1× 149 1.1× 29 800
C. Cullinane United Kingdom 19 378 1.9× 428 2.2× 175 1.1× 33 0.2× 81 0.6× 33 1.0k
TS Ganesan United Kingdom 14 91 0.5× 319 1.6× 149 0.9× 215 1.5× 55 0.4× 23 942
Yasumasa Monobe Japan 13 154 0.8× 188 1.0× 199 1.2× 43 0.3× 31 0.2× 75 856
Ken Gatter United States 16 114 0.6× 80 0.4× 158 1.0× 130 0.9× 78 0.6× 31 498
J.P. Vannier France 10 78 0.4× 203 1.0× 185 1.1× 76 0.5× 42 0.3× 26 659
Ki-Wai Chik Hong Kong 10 106 0.5× 256 1.3× 142 0.9× 117 0.8× 28 0.2× 15 746
Mary Ann Perle United States 15 178 0.9× 298 1.5× 163 1.0× 30 0.2× 62 0.4× 42 713

Countries citing papers authored by Rizwan Naeem

Since Specialization
Citations

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

Fields of papers citing papers by Rizwan Naeem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rizwan Naeem

This figure shows the co-authorship network connecting the top 25 collaborators of Rizwan Naeem. A scholar is included among the top collaborators of Rizwan Naeem 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 Rizwan Naeem. Rizwan Naeem 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.
Rehman, Majeed Ur, et al.. (2024). Spirulina spp. occurrence and association with physico-environmental factors of water bodies available in Kohat, Pakistan. International Journal of Environmental Science and Technology. 22(8). 6747–6758. 1 indexed citations
2.
Ahmed, Syed A., et al.. (2024). Developing medical genetics in a low-income country: Unveiling the journey of the Pakistani Society of Medical Genetics and Genomics (PSMG). SHILAP Revista de lepidopterología. 2(Suppl 2). 101883–101883. 1 indexed citations
3.
Ustun, Berrin, et al.. (2023). PIK3CA-related overgrowth spectrum (PROS) presenting as isolated macrodactyly. Journal of Surgical Case Reports. 2023(10). rjad549–rjad549.
4.
5.
Azad, Abul Kalam, et al.. (2020). De novo mosaic and partial monosomy of chromosome 21 in a case with superior vena cava duplication. Molecular Cytogenetics. 13(1). 45–45.
6.
Naeem, Rizwan, D. Goldstein, Mark H. Einstein, et al.. (2017). SurePath Specimens Versus ThinPrep Specimen Types on the COBAS 4800 Platform: High-Risk HPV Status and Cytology Correlation in an Ethnically Diverse Bronx Population. Laboratory Medicine. 48(3). 207–213. 7 indexed citations
7.
Talwalkar, Sameer S., C. Cameron Yin, Rizwan Naeem, et al.. (2010). Myelodysplastic Syndromes Arising in Patients With Germline TP53 Mutation and Li-Fraumeni Syndrome. Archives of Pathology & Laboratory Medicine. 134(7). 1010–1015. 36 indexed citations
8.
Habeebu, Sultan S., et al.. (2009). Molecular Monitoring of 8p11 Myeloproliferative Syndrome in an Infant. Journal of Pediatric Hematology/Oncology. 31(11). 879–883. 8 indexed citations
9.
Rabin, Karen R., Tsz‐Kwong Man, Alexander Yu, et al.. (2008). Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia. Pediatric Blood & Cancer. 51(2). 171–177. 18 indexed citations
10.
Park, Hong Seok, Weon Seo Park, Jolanta Bondaruk, et al.. (2008). Quantitation of Aurora Kinase A Gene Copy Number in Urine Sediments and Bladder Cancer Detection. JNCI Journal of the National Cancer Institute. 100(19). 1401–1411. 58 indexed citations
11.
Curry, Choladda V., Megan K. Dishop, John Hicks, et al.. (2008). Clear cell sarcoma of soft tissue: diagnostic utility of fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction. Journal of Cutaneous Pathology. 35(4). 411–417. 11 indexed citations
12.
Meyer, Claus, Eric Kowarz, Rolf Marschalek, et al.. (2007). C/EBPβ suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL. Cancer Genetics and Cytogenetics. 177(2). 108–114. 13 indexed citations
13.
Qazilbash, Muzaffar H., Rima M. Saliba, Bilal Ahmed, et al.. (2007). Deletion of the Short Arm of Chromosome 1 (del 1p) is a Strong Predictor of Poor Outcome in Myeloma Patients Undergoing an Autotransplant. Biology of Blood and Marrow Transplantation. 13(9). 1066–1072. 35 indexed citations
14.
15.
Marconi, Sharon, et al.. (2002). Role of Liver Biopsy in the Diagnosis of Hepatic Iron Overload in the Era of Genetic Testing. American Journal of Clinical Pathology. 118(1). 73–81. 14 indexed citations
16.
Yusuf, Rukh & Rizwan Naeem. (2001). Cytogenetic studies of spontaneous miscarriages: a seven year study to compare significance of primary vs. secondary culture methods for assessment of fetal karyotype yield and maternal cell contamination.. PubMed. 5(2). 121–31. 3 indexed citations
17.
Naeem, Rizwan, et al.. (2000). De novo translocation (8;12) and frontofacionasal dysplasia in a newborn boy. American Journal of Medical Genetics. 94(3). 179–183. 3 indexed citations
18.
Naeem, Rizwan, et al.. (1998). Reproduction in a patient with trisomy 8 mosaicism: Case report and literature review. American Journal of Medical Genetics. 75(4). 382–385. 12 indexed citations
19.
Naeem, Rizwan, Samuel Singer, & Jonathan A. Fletcher. (1995). Translocation t(8;13)(p11;q11‐12) in stem cell leukemia/lymphoma of t‐cell and myeloid lineages. Genes Chromosomes and Cancer. 12(2). 148–151. 15 indexed citations
20.
Fletcher, Jonathan A., Rizwan Naeem, Sheng Xiao, & Joseph M. Corson. (1995). Chromosome aberrations in desmoid tumors Trisomy 8 may be a predictor of recurrence. Cancer Genetics and Cytogenetics. 79(2). 139–143. 73 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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