R De Mey

590 total citations
15 papers, 405 citations indexed

About

R De Mey is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, R De Mey has authored 15 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Epidemiology. Recurrent topics in R De Mey's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Chromosomal and Genetic Variations (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). R De Mey is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Chromosomal and Genetic Variations (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). R De Mey collaborates with scholars based in United Kingdom, Hungary and Canada. R De Mey's co-authors include S Collyer, W. H. Price, J.E. Wilson, A D Carothers, Lawrence J. Whalley, Andrew D. Carothers, M. S. NEWTON, Iain M. Johnstone, P.J.L. Cook and K.E. Buckton and has published in prestigious journals such as The British Journal of Psychiatry, British Journal of Cancer and Journal of Epidemiology & Community Health.

In The Last Decade

R De Mey

15 papers receiving 363 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R De Mey United Kingdom	10	249	120	83	51	51	15	405
A. Amante Italy	10	62 0.2×	90 0.8×	77 0.9×	37 0.7×	54 1.1×	36	311
Vickie Hannig United States	12	185 0.7×	175 1.5×	83 1.0×	36 0.7×	24 0.5×	19	494
J. A. Batch Australia	10	194 0.8×	183 1.5×	51 0.6×	38 0.7×	33 0.6×	16	448
J J Heinrich Argentina	13	134 0.5×	145 1.2×	51 0.6×	42 0.8×	19 0.4×	35	425
Naoto Shimura Japan	10	148 0.6×	258 2.1×	92 1.1×	114 2.2×	25 0.5×	32	501
Jiří Šantavý Czechia	9	137 0.6×	141 1.2×	76 0.9×	35 0.7×	38 0.7×	17	439
K L Garver United States	10	186 0.7×	94 0.8×	118 1.4×	77 1.5×	16 0.3×	12	616
N. E. Skakkeb�k Denmark	11	115 0.5×	166 1.4×	34 0.4×	34 0.7×	23 0.5×	13	404
Judd Hl United States	10	222 0.9×	67 0.6×	31 0.4×	69 1.4×	27 0.5×	15	508
Michael Zinger United States	7	62 0.2×	61 0.5×	64 0.8×	109 2.1×	24 0.5×	11	387

Countries citing papers authored by R De Mey

Since Specialization

Citations

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

Fields of papers citing papers by R De Mey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R De Mey. 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 R De Mey. The network helps show where R De Mey may publish in the future.

Co-authorship network of co-authors of R De Mey

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

All Works

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15 of 15 papers shown

Starr, John M., et al.. (2001). Parental Causes of Death in Stroke. Cerebrovascular Diseases. 11(1). 65–70. 8 indexed citations

Liede, Alexander, Brian Cohen, Rosemarie Davidson, et al.. (2000). Evidence of a founder BRCA1 mutation in Scotland. British Journal of Cancer. 82(3). 705–711. 23 indexed citations

Carothers, Andrew D., R De Mey, M. G. Daker, et al.. (1989). An aetiological study of isochromosome‐X Turner's syndrome. Clinical Genetics. 36(1). 53–58. 4 indexed citations

Mey, R De, et al.. (1987). Public records and recognition of genetic disease in Scotland. Clinical Genetics. 31(3). 125–131. 10 indexed citations

Price, W. H., et al.. (1987). Mortality and causes of death in females with extra X chromosomes and males with extra Y chromosomes.. Journal of Epidemiology & Community Health. 41(1). 1–4. 5 indexed citations

Price, W. H., et al.. (1986). Mortality ratios, life expectancy, and causes of death in patients with Turner's syndrome.. Journal of Epidemiology & Community Health. 40(2). 97–102. 119 indexed citations

Price, W. H., et al.. (1985). Causes of death in X chromatin positive males (Klinefelter's syndrome).. Journal of Epidemiology & Community Health. 39(4). 330–336. 44 indexed citations

Price, W. H., et al.. (1985). Mortality ratios and life expectancy in X chromatin positive males.. Journal of Epidemiology & Community Health. 39(1). 33–38. 9 indexed citations

Carothers, Andrew D., et al.. (1984). An aetiological study of 290 XXY males, with special reference to the role of paternal age. Human Genetics. 68(3). 248–253. 14 indexed citations

10.

Carothers, Andrew D., et al.. (1982). The effect of variant chromosomes on reproductive fitness in man. Clinical Genetics. 21(4). 280–289. 14 indexed citations

11.

Whalley, Lawrence J., et al.. (1982). A Study of Familial Factors in Alzheimer's Disease. The British Journal of Psychiatry. 140(3). 249–256. 71 indexed citations

12.

Carothers, A D, R De Mey, S Collyer, et al.. (1980). A collaborative study of the aetiology of Turner Syndrome. Annals of Human Genetics. 43(4). 355–368. 24 indexed citations

13.

Carothers, A D, et al.. (1978). Parental age and birth order in the aetiology of some sex chromosome aneuploidies. Annals of Human Genetics. 41(3). 277–287. 44 indexed citations

14.

Cook, P.J.L., et al.. (1977). On the orientation of the Rh: El₁ linkage group. Annals of Human Genetics. 41(2). 157–162. 12 indexed citations

15.

Buckton, K.E., M. S. NEWTON, I Lauder, et al.. (1975). Familial transmission of a (21q22q) translocation. Cytogenetic and Genome Research. 15(2). 103–111. 4 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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