Resham Ejaz

646 total citations
16 papers, 132 citations indexed

About

Resham Ejaz is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Resham Ejaz has authored 16 papers receiving a total of 132 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Resham Ejaz's work include Fetal and Pediatric Neurological Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Tuberous Sclerosis Complex Research (2 papers). Resham Ejaz is often cited by papers focused on Fetal and Pediatric Neurological Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Tuberous Sclerosis Complex Research (2 papers). Resham Ejaz collaborates with scholars based in Canada, Australia and United States. Resham Ejaz's co-authors include Riyana Babul‐Hirji, David Chitayat, Pekka Kannus, Graeme Nimmo, Dawn Cordeiro, Saadet Mercimek‐Andrews, Martine Tétreault, Lijia Huang, Taila Hartley and Yujin Suk and has published in prestigious journals such as Neurology, Journal of Thrombosis and Haemostasis and Journal of Surgical Oncology.

In The Last Decade

Resham Ejaz

14 papers receiving 128 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Resham Ejaz Canada	7	55	42	19	19	17	16	132
Natalya Karp Canada	8	53 1.0×	46 1.1×	23 1.2×	7 0.4×	16 0.9×	14	134
Aisha Al Shamsi United Arab Emirates	6	67 1.2×	35 0.8×	18 0.9×	10 0.5×	11 0.6×	13	129
Paula Morris United States	7	54 1.0×	34 0.8×	15 0.8×	11 0.6×	5 0.3×	12	179
Delphine Héron France	8	90 1.6×	74 1.8×	10 0.5×	10 0.5×	23 1.4×	15	214
Theresa Brunet Germany	7	54 1.0×	47 1.1×	7 0.4×	7 0.4×	8 0.5×	24	110
Dennis W. Bartholomew United States	8	121 2.2×	48 1.1×	52 2.7×	8 0.4×	12 0.7×	17	192
Tariq Faquih Saudi Arabia	6	72 1.3×	44 1.0×	6 0.3×	6 0.3×	32 1.9×	6	148
Cristina Skrypnyk Bahrain	8	95 1.7×	28 0.7×	9 0.5×	9 0.5×	8 0.5×	17	155
Özgür Kırbıyık Türkiye	8	109 2.0×	83 2.0×	6 0.3×	9 0.5×	28 1.6×	40	211
Bianca Russell United States	7	77 1.4×	71 1.7×	3 0.2×	18 0.9×	9 0.5×	18	142

Countries citing papers authored by Resham Ejaz

Since Specialization

Citations

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

Fields of papers citing papers by Resham Ejaz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Resham Ejaz

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

All Works

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16 of 16 papers shown

Ejaz, Resham, et al.. (2024). Severe Epilepsy in an Individual With a TSC2 R905Q Variant Prompting Late Diagnosis in Affected Family Members. Pediatric Neurology. 161. 158–161. 1 indexed citations

Suk, Yujin, et al.. (2024). The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future Directions. Genes. 15(3). 332–332. 18 indexed citations

McConkey, Haley, Nina Stein, Eric Chater‐Diehl, et al.. (2024). Diagnosis of TET3‐Related Beck–Fahrner Syndrome in an Individual With Chorioretinal and Iris Colobomata Using a DNA Methylation Signature. American Journal of Medical Genetics Part A. 197(2). e63864–e63864.

Ejaz, Resham, et al.. (2022). Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant. BMJ Case Reports. 15(12). e248995–e248995. 1 indexed citations

RamachandranNair, Rajesh, et al.. (2021). Pathogenic DNM1 Gene Variant Presenting With Unusually Nonsevere Neurodevelopmental Phenotype: A Case Report. Neurology Genetics. 7(5). e618–e618. 6 indexed citations

Mithoowani, Siraj, Resham Ejaz, Emily Sirotich, et al.. (2020). Management of major bleeds in patients with immune thrombocytopenia. Journal of Thrombosis and Haemostasis. 18(7). 1783–1790. 20 indexed citations

Sabatini, Peter, et al.. (2018). Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant. Molecular Cytogenetics. 11(1). 50–50. 9 indexed citations

Ejaz, Resham, Shiyi Chen, Amanda Carnevale, et al.. (2018). Impact of Mobility Device Use on Quality of Life in Children With Friedreich Ataxia. Journal of Child Neurology. 33(6). 397–404. 3 indexed citations

Ejaz, Resham, Anath C. Lionel, Susan Blaser, et al.. (2017). De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay. American Journal of Medical Genetics Part A. 173(10). 2725–2730. 11 indexed citations

10.

Nimmo, Graeme, Resham Ejaz, Dawn Cordeiro, Pekka Kannus, & Saadet Mercimek‐Andrews. (2017). Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiency. American Journal of Medical Genetics Part A. 176(2). 399–403. 21 indexed citations

11.

Samuel, Nardin, Resham Ejaz, Josh Silver, et al.. (2017). Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit gene. Journal of Surgical Oncology. 117(2). 160–162. 4 indexed citations

12.

Ejaz, Resham, Melissa Carter, & Karen W. Gripp. (2016). Lateral Meningocele Syndrome.

13.

Ejaz, Resham, Wen Qin, Lijia Huang, et al.. (2016). Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation. American Journal of Medical Genetics Part A. 170(4). 1070–1075. 20 indexed citations

14.

Ejaz, Resham, Riyana Babul‐Hirji, & David Chitayat. (2016). The evolving features of Nicolaides–Baraitser syndrome – a clinical report of a 20‐year follow‐up. Clinical Case Reports. 4(4). 351–355. 12 indexed citations

15.

Ejaz, Resham, et al.. (2016). Child Neurology: Diencephalic syndrome–like presentation of a cervicomedullary brainstem tumor. Neurology. 87(21). e248–e251. 5 indexed citations

16.

Ejaz, Resham, Tom Leibson, & Gideon Koren. (2014). Selective serotonin reuptake inhibitor discontinuation during pregnancy: at what risk?. PubMed. 60(12). 1105–6. 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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