Meera Warby

756 total citations
11 papers, 183 citations indexed

About

Meera Warby is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Meera Warby has authored 11 papers receiving a total of 183 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Meera Warby's work include BRCA gene mutations in cancer (7 papers), Genomics and Rare Diseases (4 papers) and Childhood Cancer Survivors' Quality of Life (3 papers). Meera Warby is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Genomics and Rare Diseases (4 papers) and Childhood Cancer Survivors' Quality of Life (3 papers). Meera Warby collaborates with scholars based in Australia, Canada and United States. Meera Warby's co-authors include Kathy Tucker, Claire E. Wakefield, Janine Vetsch, Brittany C. McGill, Richard J. Cohn, David S. Ziegler, Alison Metcalfe, Tracey O’Brien, Andrea Farkas Patenaude and Veronica Quinn and has published in prestigious journals such as Cancer, Neuro-Oncology and Seminars in Oncology.

In The Last Decade

Meera Warby

10 papers receiving 182 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Meera Warby Australia	9	102	90	33	25	18	11	183
Stacy J. Hines‐Dowell United States	7	109 1.1×	57 0.6×	22 0.7×	39 1.6×	13 0.7×	10	156
Emily A. Quinn United States	7	90 0.9×	55 0.6×	24 0.7×	34 1.4×	16 0.9×	13	159
João Silva Portugal	9	94 0.9×	24 0.3×	19 0.6×	64 2.6×	24 1.3×	27	213
Regina Nuccio United States	5	80 0.8×	56 0.6×	20 0.6×	11 0.4×	12 0.7×	9	117
Naz Khan United Kingdom	10	94 0.9×	27 0.3×	24 0.7×	38 1.5×	42 2.3×	21	241
Ulrik Kristoffer Stoltze Denmark	8	55 0.5×	39 0.4×	24 0.7×	73 2.9×	14 0.8×	19	137
Marian J. Gilmore United States	10	151 1.5×	76 0.8×	65 2.0×	14 0.6×	30 1.7×	25	267
Daniela Lico Italy	12	44 0.4×	53 0.6×	99 3.0×	29 1.2×	21 1.2×	23	513
Lucinda Freeman Australia	9	70 0.7×	33 0.4×	30 0.9×	24 1.0×	16 0.9×	26	207
Meagan Farmer United States	8	107 1.0×	43 0.5×	22 0.7×	30 1.2×	12 0.7×	12	161

Countries citing papers authored by Meera Warby

Since Specialization

Citations

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

Fields of papers citing papers by Meera Warby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meera Warby

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

All Works

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11 of 11 papers shown

Fuentes-Bolanos, Noemi, Loretta M. S. Lau, Meera Warby, et al.. (2024). HGG-50. LOW GRADE GLIOMA CAUGHT IN TRANSFORMATION: UTILITY OF COMPREHENSIVE GENOMIC PROFILING IN PEDIATRIC LI FRAUMENI SYNDROME ASSOCIATED HIGH-GRADE GLIOMA. Neuro-Oncology. 26(Supplement_4). 0–0.

McGill, Brittany C., Claire E. Wakefield, Kathy Tucker, et al.. (2023). Parents’ expectations, preferences, and recall of germline findings in a childhood cancer precision medicine trial. Cancer. 129(22). 3620–3632. 12 indexed citations

Robertson, Eden G., Kate Hetherington, David S. Ziegler, et al.. (2022). What’s in a Name? Parents’ and Healthcare Professionals’ Preferred Terminology for Pathogenic Variants in Childhood Cancer Predisposition Genes. Journal of Personalized Medicine. 12(8). 1327–1327. 4 indexed citations

McGill, Brittany C., Claire E. Wakefield, Kate Hetherington, et al.. (2020). “Balancing Expectations with Actual Realities”: Conversations with Clinicians and Scientists in the First Year of a High-Risk Childhood Cancer Precision Medicine Trial. Journal of Personalized Medicine. 10(1). 9–9. 24 indexed citations

Vetsch, Janine, Claire E. Wakefield, Meera Warby, et al.. (2019). Healthcare professionals’ attitudes toward cancer precision medicine: A systematic review. Seminars in Oncology. 46(3). 291–303. 19 indexed citations

Rampersaud, Evadnie, David S. Ziegler, Ilaria Iacobucci, et al.. (2019). Germline deletion of ETV6 in familial acute lymphoblastic leukemia. Blood Advances. 3(7). 1039–1046. 18 indexed citations

McGill, Brittany C., Claire E. Wakefield, Janine Vetsch, et al.. (2019). “I remember how I felt, but I don't remember the gene”: Families’ experiences of cancer‐related genetic testing in childhood. Pediatric Blood & Cancer. 66(8). e27762–e27762. 30 indexed citations

Weber, Martin, Louise Jackett, Charles Chan, et al.. (2018). Oral malignant gastrointestinal neuroectodermal tumour with junctional component mimicking mucosal melanoma. Pathology. 50(6). 648–653. 11 indexed citations

Vetsch, Janine, Claire E. Wakefield, Meera Warby, et al.. (2018). Cancer-Related Genetic Testing and Personalized Medicine for Adolescents: A Narrative Review of Impact and Understanding. Journal of Adolescent and Young Adult Oncology. 7(3). 259–262. 19 indexed citations

10.

Warby, Meera, Claire E. Wakefield, Janine Vetsch, & Kathy Tucker. (2018). Families’ and health care professionals’ attitudes towards Li‐Fraumeni syndrome testing in children: A systematic review. Clinical Genetics. 95(1). 140–150. 11 indexed citations

11.

McGill, Brittany C., Veronica Quinn, Kathy Tucker, et al.. (2017). Parents’ attitudes toward genetic testing of children for health conditions: A systematic review. Clinical Genetics. 92(6). 569–578. 35 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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