Sunday M. Stray

4.9k total citations · 1 hit paper
14 papers, 2.2k citations indexed

About

Sunday M. Stray is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Sunday M. Stray has authored 14 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Hematology. Recurrent topics in Sunday M. Stray's work include BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (4 papers) and Hemoglobinopathies and Related Disorders (4 papers). Sunday M. Stray is often cited by papers focused on BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (4 papers) and Hemoglobinopathies and Related Disorders (4 papers). Sunday M. Stray collaborates with scholars based in United States, Israel and Slovakia. Sunday M. Stray's co-authors include Tom Walsh, Mary‐Claire King, Ming K. Lee, Silvia Casadei, Elizabeth M. Swisher, Jessica B. Mandell, Alex S. Nord, Christopher C. Pennil, Anne Thornton and Barbara M. Norquist and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JAMA and Journal of Clinical Investigation.

In The Last Decade

Sunday M. Stray

14 papers receiving 2.1k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

2011 662 citations Tom Walsh, Silvia Casadei et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sunday M. Stray United States	11	1.3k	921	499	465	428	14	2.2k
Christopher C. Oakes United States	27	344 0.3×	1.7k 1.9×	698 1.4×	252 0.5×	281 0.7×	67	2.5k
Bernard Peissel Italy	21	948 0.7×	942 1.0×	208 0.4×	253 0.5×	265 0.6×	63	1.7k
M.H. Skolnick United States	14	824 0.6×	558 0.6×	255 0.5×	401 0.9×	413 1.0×	22	1.8k
Maria Grazia Tibiletti Italy	29	503 0.4×	838 0.9×	469 0.9×	812 1.7×	810 1.9×	93	2.3k
Janet M. Cowan United States	25	553 0.4×	1.1k 1.2×	305 0.6×	508 1.1×	169 0.4×	56	2.0k
Ronald J. deLeeuw Canada	19	745 0.6×	795 0.9×	342 0.7×	956 2.1×	362 0.8×	22	2.5k
Syed M. Jalal United States	28	1.0k 0.8×	1.3k 1.4×	163 0.3×	310 0.7×	317 0.7×	71	2.6k
Sheila Seal United Kingdom	25	3.3k 2.6×	2.9k 3.1×	1.3k 2.5×	962 2.1×	903 2.1×	30	4.9k
Wendy N. Cooper United Kingdom	26	499 0.4×	1.6k 1.8×	383 0.8×	200 0.4×	109 0.3×	34	2.3k
Francesca Megiorni Italy	25	341 0.3×	988 1.1×	382 0.8×	154 0.3×	112 0.3×	65	2.1k

Countries citing papers authored by Sunday M. Stray

Since Specialization

Citations

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

Fields of papers citing papers by Sunday M. Stray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sunday M. Stray

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

All Works

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14 of 14 papers shown

Pennil, Christopher C., Silvia Casadei, Kathy Agnew, et al.. (2012). Loss of function germline mutations in RAD51D in women with ovarian carcinoma. Gynecologic Oncology. 127(3). 552–555. 28 indexed citations

Walsh, Tom, Silvia Casadei, Ming K. Lee, et al.. (2011). Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proceedings of the National Academy of Sciences. 108(44). 18032–18037. 662 indexed citations breakdown →

Pierce, Sarah B., Cailyn H. Spurrell, Jessica B. Mandell, et al.. (2011). Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria. Proceedings of the National Academy of Sciences. 108(45). 18313–18317. 11 indexed citations

Casadei, Silvia, Barbara M. Norquist, Tom Walsh, et al.. (2011). Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer. Cancer Research. 71(6). 2222–2229. 182 indexed citations

Nord, Alex S., Wendy Roeb, Diane E. Dickel, et al.. (2011). Reduced transcript expression of genes affected by inherited and de novo CNVs in autism. European Journal of Human Genetics. 19(6). 727–731. 89 indexed citations

Walsh, Tom, Ming K. Lee, Silvia Casadei, et al.. (2010). Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing. Proceedings of the National Academy of Sciences. 107(28). 12629–12633. 325 indexed citations

Shahin, Hashem, Tom Walsh, Amal Abu Rayyan, et al.. (2009). Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. European Journal of Human Genetics. 18(4). 407–413. 69 indexed citations

Walsh, Tom, Silvia Casadei, Elizabeth M. Swisher, et al.. (2006). Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer. JAMA. 295(12). 1379–1379. 469 indexed citations

Reiner, Alex P., Sunday M. Stray, & Arthur R. Thompson. (1992). Three missense mutations in arg codons of the factor viii genes of mild to moderately severe hemophilia a patients. Thrombosis Research. 66(1). 93–99. 9 indexed citations

10.

Ca, Finch, et al.. (1986). Plasma ferritin determination as a diagnostic tool.. PubMed. 145(5). 657–63. 182 indexed citations

11.

Celada, Antonio, Sunday M. Stray, Murali Sivarajan, & C. A. Finch. (1984). Iron supply for erythropoiesis in the rabbit.. Journal of Clinical Investigation. 74(1). 161–164. 2 indexed citations

12.

Pippard, M. J. & Sunday M. Stray. (1982). Simple Assay For Urinary Iron after Desferrioxamine Therapy. American Journal of Clinical Pathology. 77(3). 324–327. 9 indexed citations

13.

Stray, Sunday M., et al.. (1981). The relationship between plasma iron and plasma iron turnover in the rat. Blood. 57(2). 239–242. 15 indexed citations

14.

Milder, Michael S., James D. Cook, Sunday M. Stray, & Clement A. Finch. (1980). Idiopathic Hemochromatosis, an Interim Report. Medicine. 59(1). 34–49. 165 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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