M. G. Daker

1.4k total citations
28 papers, 538 citations indexed

About

M. G. Daker is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, M. G. Daker has authored 28 papers receiving a total of 538 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Plant Science and 9 papers in Molecular Biology. Recurrent topics in M. G. Daker's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chromosomal and Genetic Variations (5 papers) and Prenatal Screening and Diagnostics (4 papers). M. G. Daker is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chromosomal and Genetic Variations (5 papers) and Prenatal Screening and Diagnostics (4 papers). M. G. Daker collaborates with scholars based in United Kingdom, Canada and New Zealand. M. G. Daker's co-authors include Eva Alberman, P. A. Jacobs, Alison Fordyce, Anthony J. Swerdlow, Valerie Beral, C Hermon, Sheila Youings, David Mutton, P. E. Polani and Boleslaw Goldman and has published in prestigious journals such as Nature, Human Molecular Genetics and British Journal of Dermatology.

In The Last Decade

M. G. Daker

28 papers receiving 498 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. G. Daker United Kingdom	13	333	225	113	82	47	28	538
Lisskulla Sylvén Sweden	10	455 1.4×	231 1.0×	36 0.3×	53 0.6×	61 1.3×	12	653
Elke Back Germany	15	576 1.7×	456 2.0×	247 2.2×	138 1.7×	58 1.2×	36	829
Sandra Monfort Spain	13	364 1.1×	264 1.2×	50 0.4×	94 1.1×	49 1.0×	41	530
Annelyse Mertz Germany	9	752 2.3×	663 2.9×	174 1.5×	53 0.6×	89 1.9×	9	947
D A Couzin United Kingdom	12	226 0.7×	135 0.6×	117 1.0×	124 1.5×	17 0.4×	23	367
M. Winkelmann Germany	7	739 2.2×	638 2.8×	162 1.4×	49 0.6×	88 1.9×	7	923
Vanna Pecile Italy	17	499 1.5×	443 2.0×	112 1.0×	175 2.1×	17 0.4×	54	825
Elisabeth A. Keitges United States	11	439 1.3×	249 1.1×	105 0.9×	85 1.0×	35 0.7×	13	529
Maxine J. Sutcliffe United States	13	375 1.1×	316 1.4×	129 1.1×	130 1.6×	80 1.7×	27	676
W Rosenkranz Austria	17	473 1.4×	318 1.4×	159 1.4×	137 1.7×	7 0.1×	58	729

Countries citing papers authored by M. G. Daker

Since Specialization

Citations

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

Fields of papers citing papers by M. G. Daker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. G. Daker

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

All Works

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20 of 20 papers shown

Swerdlow, Anthony J., C Hermon, P. A. Jacobs, et al.. (2001). Mortality and cancer incidence in persons with numerical sex chromosome abnormalities: a cohort study. Annals of Human Genetics. 65(2). 177–188. 144 indexed citations

Ogilvie, Caroline Mackie, et al.. (2000). Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. American Journal of Medical Genetics. 96(1). 15–15. 1 indexed citations

Seller, Mary J., et al.. (1998). Trisomy 9 in an embryo with spina bifida. Clinical Dysmorphology. 7(3). 217–219. 6 indexed citations

Daker, M. G., et al.. (1998). FISH analysis in patients with clinical diagnosis of Williams syndrome. Acta Paediatrica. 87(1). 48–53. 21 indexed citations

Daker, M. G., et al.. (1998). FISH analysis in patients with clinical diagnosis of Williams syndrome*. Acta Paediatrica. 87(1). 48–53. 2 indexed citations

Hirst, Mark C., Angela Barnicoat, Geraldine Flynn, et al.. (1993). The identification of a third fragile site, FRAXF, in Xq27 — q28 distal to both FRAXA and FRAXE. Human Molecular Genetics. 2(2). 197–200. 55 indexed citations

Wilson, J. Bastow, et al.. (1990). A phenetic comparison of someFumaria spp. (Fumariaceae). Plant Systematics and Evolution. 172(1-4). 51–63. 2 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

Giannelli, F., Andrew H. Morris, Christine Garrett, et al.. (1987). Genetic heterogeneity of X‐linked mental retardation with fragile X Association of tight linkage to factor IX and incomplete penetrance in males. Annals of Human Genetics. 51(2). 107–124. 10 indexed citations

10.

Daker, M. G., et al.. (1985). Acute myeloid leukaemia after treatment with razoxane. British Journal of Dermatology. 113(2). 131–134. 12 indexed citations

11.

Daker, M. G.. (1983). Chorionic tissue biopsy in the first trimester of pregnancy. BJOG An International Journal of Obstetrics & Gynaecology. 90(3). 193–195. 4 indexed citations

12.

Goldman, Boleslaw, et al.. (1982). Clinical and cytogenetic aspects of X‐chromosome deletions. Clinical Genetics. 21(1). 36–52. 49 indexed citations

13.

Cook, P.J.L., R H Lindenbaum, Riitta Salonen, et al.. (1981). The MNSs blood groups of families with chromosome 4 rearrangements. Annals of Human Genetics. 45(1). 39–47. 23 indexed citations

14.

Hancock, J. L. & M. G. Daker. (1981). Testicular hypoplasia in a boar with abnormal sex chromosome constitution (39 XXY). Reproduction. 61(2). 395–397. 18 indexed citations

15.

Daker, M. G.. (1979). Prospective Chromosomal Study of 30 Patients Undergoing 90y Synovectomy. Lara D. Veeken. XVIII(suppl). 41–44. 6 indexed citations

16.

Doyle, David, et al.. (1977). A CLINICAL AND PROSPECTIVE CHROMOSOMAL STUDY OF YTTRIUM-90 SYNOVECTOMY. Lara D. Veeken. 16(4). 217–222. 15 indexed citations

17.

Creasy, M. R., John A. Crolla, & M. G. Daker. (1974). A familial reciprocal translocation between three chromosomes. Human Genetics. 24(4). 303–308. 16 indexed citations

18.

Mutton, David & M. G. Daker. (1973). Pericentric Inversion of Chromosome 9. Nature New Biology. 241(107). 80–80. 33 indexed citations

19.

Daker, M. G. & Keith Jones. (1970). The Chromosomes of Orchids: V: Stanhopeinae Benth. (Gongorinae Auct.). Kew Bulletin. 24(3). 457–457. 1 indexed citations

20.

Jones, Keith & M. G. Daker. (1968). The Chromosomes of Orchids: III. Catasetinae Schltr.. Kew Bulletin. 22(3). 421–421. 12 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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