M. Murer‐Orlando

414 total citations
19 papers, 294 citations indexed

About

M. Murer‐Orlando is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Murer‐Orlando has authored 19 papers receiving a total of 294 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Murer‐Orlando's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Chromosomal and Genetic Variations (6 papers). M. Murer‐Orlando is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Chromosomal and Genetic Variations (6 papers). M. Murer‐Orlando collaborates with scholars based in United Kingdom and Canada. M. Murer‐Orlando's co-authors include C.-L. Richer, Manuel Buchwald, Alan C. Peterson, Rachel A. Gibson, Christopher G. Mathew, Si Lok, Martin L. Breitman, Lap‐Chee Tsui, P Jean and Régen Drouin and has published in prestigious journals such as Nature, Annals of the New York Academy of Sciences and Human Molecular Genetics.

In The Last Decade

M. Murer‐Orlando

18 papers receiving 279 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. Murer‐Orlando United Kingdom 11 200 118 68 43 32 19 294
T. M. Schroeder-Kurth Germany 7 227 1.1× 143 1.2× 135 2.0× 47 1.1× 54 1.7× 10 330
Osamu Miyoshi Japan 11 176 0.9× 116 1.0× 37 0.5× 74 1.7× 16 0.5× 22 278
Nadja Kokalj-Vokač Slovenia 11 276 1.4× 176 1.5× 73 1.1× 51 1.2× 55 1.7× 19 406
Joyce Andrade Brazil 7 195 1.0× 126 1.1× 53 0.8× 32 0.7× 52 1.6× 14 331
Asit B. Mukherjee United States 10 163 0.8× 115 1.0× 76 1.1× 31 0.7× 27 0.8× 25 329
Jennifer McDaid United Kingdom 8 271 1.4× 99 0.8× 24 0.4× 21 0.5× 29 0.9× 8 325
H. Komatsubara Japan 6 320 1.6× 139 1.2× 51 0.8× 12 0.3× 56 1.8× 7 419
Steven Schonberg United States 13 247 1.2× 147 1.2× 39 0.6× 111 2.6× 52 1.6× 19 422
N. A. Egolina Russia 9 282 1.4× 118 1.0× 98 1.4× 19 0.4× 107 3.3× 15 402
Jane M. vanWert United States 11 370 1.9× 158 1.3× 28 0.4× 17 0.4× 40 1.3× 12 446

Countries citing papers authored by M. Murer‐Orlando

Since Specialization
Citations

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

Fields of papers citing papers by M. Murer‐Orlando

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Murer‐Orlando. 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. Murer‐Orlando. The network helps show where M. Murer‐Orlando may publish in the future.

Co-authorship network of co-authors of M. Murer‐Orlando

This figure shows the co-authorship network connecting the top 25 collaborators of M. Murer‐Orlando. A scholar is included among the top collaborators of M. Murer‐Orlando 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. Murer‐Orlando. M. Murer‐Orlando 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.
Murer‐Orlando, M. & Valerie McGuire. (2003). Short-Term Chorionic Villi and Amniotic Fluid Cultures. Humana Press eBooks. 5. 75–82.
2.
Davies, Angela, et al.. (1994). An Improved Method for the Detection of Trisomy 21 in Uncultured Amniocytes by Fluorescence in Situ Hybridizationa. Annals of the New York Academy of Sciences. 731(1). 67–72. 3 indexed citations
3.
Davies, Angela, et al.. (1994). FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs.. Journal of Medical Genetics. 31(9). 679–685. 15 indexed citations
4.
Gibson, Rachel A., et al.. (1993). A nonsense mutation and exon skipping in the Fanconi anaemia group C gene. Human Molecular Genetics. 2(6). 797–799. 71 indexed citations
5.
Zahed, L., M. Murer‐Orlando, & Michel Vekemans. (1992). In situ hybridization studies for the detection of common aneuploidies in CVS. Prenatal Diagnosis. 12(6). 483–493. 13 indexed citations
6.
Murer‐Orlando, M., L. Zahed, & Zoe Docherty. (1990). Prenatal diagnosis of chromosome abnormalities. A comparison of the results of various techniques, with special emphasis on mosaicism.. PubMed. 83(1). 61–5. 1 indexed citations
7.
Murer‐Orlando, M., L. Zahed, & Zoe Docherty. (1990). Prenatal diagnosis of chromosome abnormalities. Genetica. 83(1). 61–65. 1 indexed citations
8.
Richer, Claude‐Lise, G. Bleau, Alcide Chapdelaine, et al.. (1989). A man with isochromosome Xq Klinefelter syndrome with lack of height increase and normal androgenization. American Journal of Medical Genetics. 32(1). 42–44. 14 indexed citations
9.
Zahed, L., M. Murer‐Orlando, & Martin Bobrow. (1989). The application of automated metaphase scanning to direct preparations of chorionic villi. Prenatal Diagnosis. 9(1). 7–17. 2 indexed citations
10.
Murer‐Orlando, M., Maura McGuire, L. Zahed, et al.. (1989). Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndrome.. Journal of Medical Genetics. 26(3). 174–178. 6 indexed citations
11.
Murer‐Orlando, M., Maura McGuire, L. Zahed, et al.. (1988). Chromosome banding in direct preparations of chorionic villi. Prenatal Diagnosis. 8(6). 461–469. 5 indexed citations
12.
Zahed, Laïla, M. Murer‐Orlando, & Martin Bobrow. (1988). Cell cycle studies in chorionic villi. Human Genetics. 80(2). 127–134. 11 indexed citations
13.
Murer‐Orlando, M., et al.. (1987). Differential regulation of γ-crystallin genes during mouse lens development. Developmental Biology. 119(1). 260–267. 52 indexed citations
14.
Murer‐Orlando, M. & Alan C. Peterson. (1985). In situ nick translation of human and mouse chromosomes detected with a biotinylated nucleotide. Experimental Cell Research. 157(2). 322–334. 28 indexed citations
15.
Richer, C.-L., Régen Drouin, M. Murer‐Orlando, & P Jean. (1983). High-resolution idiogram of Giemsa R-banded human prophase chromosomes. Canadian Journal of Genetics and Cytology. 25(6). 642–650. 12 indexed citations
16.
Murer‐Orlando, M. & C.-L. Richer. (1983). Heterochromatin heterogeneity in Chinese hamster sex bivalents. Cytogenetic and Genome Research. 35(3). 195–199. 19 indexed citations
17.
Richer, C.-L., M. Murer‐Orlando, & Régen Drouin. (1983). R-banding of human chromosomes by heat denaturation and Giemsa staining after amethopterin-synchronization. Canadian Journal of Genetics and Cytology. 25(3). 261–269. 13 indexed citations
18.
Richer, Claude‐Lise, et al.. (1981). Analysis of banding patterns in a case of ring chromosome 21. American Journal of Medical Genetics. 10(4). 323–331. 19 indexed citations
19.
Jean, P, et al.. (1979). Translocation 8;14 in an ataxia telangiectasia-derived cell line. Nature. 277(5691). 56–58. 9 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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