M.R. Whittle

1.2k total citations
19 papers, 220 citations indexed

About

M.R. Whittle is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, M.R. Whittle has authored 19 papers receiving a total of 220 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Ecology. Recurrent topics in M.R. Whittle's work include Forensic and Genetic Research (11 papers), Molecular Biology Techniques and Applications (8 papers) and Genetic Associations and Epidemiology (5 papers). M.R. Whittle is often cited by papers focused on Forensic and Genetic Research (11 papers), Molecular Biology Techniques and Applications (8 papers) and Genetic Associations and Epidemiology (5 papers). M.R. Whittle collaborates with scholars based in Brazil, Spain and Argentina. M.R. Whittle's co-authors include Carlos Alberto de Bragança Pereira, Telba Irony, Hongyu Sun, Denilce R. Sumita, Sujuan Liu, Yinming Zhang, Mariz Vainzof, Maria Rita Passos‐Bueno, Mayana Zatz and Suely Kazue Nagahashi Marie and has published in prestigious journals such as Genetics, The American Journal of Human Genetics and Transfusion.

In The Last Decade

M.R. Whittle

19 papers receiving 209 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M.R. Whittle Brazil 9 142 108 22 18 17 19 220
Jiashun Xiao China 8 101 0.7× 111 1.0× 4 0.2× 12 0.7× 3 0.2× 14 206
Manuel García‐Magariños Spain 12 372 2.6× 283 2.6× 27 1.2× 9 0.5× 3 0.2× 18 497
Xiaowei Zhan United States 5 146 1.0× 75 0.7× 5 0.2× 2 0.1× 3 0.2× 6 202
François Van Lishout Belgium 9 140 1.0× 113 1.0× 4 0.2× 6 0.4× 15 215
Arunabha Majumdar United States 9 167 1.2× 168 1.6× 1 0.0× 5 0.3× 5 0.3× 16 287
Gengqian Zhang China 11 157 1.1× 244 2.3× 33 1.5× 5 0.3× 36 318
Derek E. Kelly United States 6 78 0.5× 91 0.8× 23 1.0× 4 0.2× 4 0.2× 7 202
Adeline Vigouroux France 7 146 1.0× 157 1.5× 21 1.2× 8 239
Dominic Nelson Canada 5 149 1.0× 46 0.4× 6 0.3× 1 0.1× 2 0.1× 6 215
B. Hoste Belgium 7 98 0.7× 101 0.9× 8 0.4× 14 0.8× 15 178

Countries citing papers authored by M.R. Whittle

Since Specialization
Citations

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

Fields of papers citing papers by M.R. Whittle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M.R. Whittle

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

All Works

19 of 19 papers shown
1.
Whittle, M.R., et al.. (2020). Noninvasive prenatal paternity determination using microhaplotypes: a pilot study. BMC Medical Genomics. 13(1). 157–157. 2 indexed citations
2.
Whittle, M.R., et al.. (2017). Routine implementation of noninvasive prenatal paternity testing with STRs. Forensic science international. Genetics supplement series. 6. e233–e234. 2 indexed citations
3.
Sumita, Denilce R., et al.. (2013). Development and use of a single-tube four dye, 21plex direct PCR autosomal STR loci amplification assay for human identification and relationship testing. Forensic science international. Genetics supplement series. 4(1). e264–e265. 1 indexed citations
4.
Sun, Hongyu, Sujuan Liu, Yinming Zhang, & M.R. Whittle. (2013). Comparison of southern Chinese Han and Brazilian Caucasian mutation rates at autosomal short tandem repeat loci used in human forensic genetics. International Journal of Legal Medicine. 128(1). 1–9. 26 indexed citations
5.
Whittle, M.R., et al.. (2011). Use of matrix standards for new fluorophores in capillary sequencers. Forensic science international. Genetics supplement series. 3(1). e73–e74. 2 indexed citations
6.
Sumita, Denilce R., et al.. (2011). Use of universal reporter primers in multiplex PCR of autosomal loci. Forensic science international. Genetics supplement series. 3(1). e71–e72. 2 indexed citations
7.
Whittle, M.R., et al.. (2009). Paternity investigation experience with a 40 autosomal SNP panel. Forensic science international. Genetics supplement series. 2(1). 149–150. 1 indexed citations
8.
Sumita, Denilce R. & M.R. Whittle. (2009). Updated allelic structures of the DXS10135 and DXS10078 STR loci. Forensic science international. Genetics supplement series. 2(1). 51–52. 4 indexed citations
9.
Sánchez‐Diz, Paula, Cı́ntia Alves, Elizeu Fagundes de Carvalho, et al.. (2008). Population and segregation data on 17 Y-STRs: results of a GEP-ISFG collaborative study. International Journal of Legal Medicine. 122(6). 529–533. 29 indexed citations
10.
Whittle, M.R. & Denilce R. Sumita. (2008). Quadruplex real-time PCR for forensic DNA quantitation. Forensic science international. Genetics supplement series. 1(1). 86–88. 1 indexed citations
11.
Whittle, M.R., et al.. (2007). Use of X‐linked short tandem repeat loci in routine parentage casework. Transfusion. 47(6). 1050–1053. 8 indexed citations
12.
Pereira, Carlos Alberto de Bragança, et al.. (2006). Genuine Bayesian multiallelic significance test for the Hardy-Weinberg equilibrium law.. PubMed. 5(4). 619–31. 8 indexed citations
13.
Whittle, M.R., et al.. (2005). Efficient mispriming during apolipoprotein E genotyping. Jornal Brasileiro de Patologia e Medicina Laboratorial. 41(1). 4 indexed citations
14.
Sánchez‐Diz, Paula, Leonor Gusmão, Sandra Beleza, et al.. (2003). Results of the GEP-ISFG collaborative study on two Y-STRs tetraplexes: GEPY I (DYS461, GATA C4, DYS437 and DYS438) and GEPY II (DYS460, GATA A10, GATA H4 and DYS439). Forensic Science International. 135(2). 158–162. 11 indexed citations
15.
Gusmão, Leonor, Paula Sánchez‐Diz, Cı́ntia Alves, et al.. (2003). Results of the GEP-ISFG collaborative study on the Y chromosome STRs GATA A10, GATA C4, GATA H4, DYS437, DYS438, DYS439, DYS460 and DYS461: population data. Forensic Science International. 135(2). 150–157. 10 indexed citations
16.
Whittle, M.R., et al.. (2003). Updated Brazilian genetic data, together with mutation rates, on 19 STR loci, including D10S1237.. Forensic Science International. 139(2-3). 207–210. 18 indexed citations
17.
Irony, Telba, et al.. (2001). An Unconditional Exact Test for the Hardy-Weinberg Equilibrium Law: Sample-Space Ordering Using the Bayes Factor. Genetics. 158(2). 875–883. 37 indexed citations
18.
Escamilla, Michael, Erin Roche, Laura Almasy, et al.. (2000). A Minimalist Approach to Gene Mapping: Locating the Gene for Acheiropodia, by Homozygosity Analysis. The American Journal of Human Genetics. 66(6). 1995–2000. 12 indexed citations
19.
Passos‐Bueno, Maria Rita, Suely Kazue Nagahashi Marie, Mário Luiz Ribeiro Monteiro, et al.. (1994). Knobloch syndrome in a large Brazilian consanguineous family: Confirmation of autosomal recessive inheritance. American Journal of Medical Genetics. 52(2). 170–173. 42 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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