Kathy Mann

1.9k total citations
41 papers, 1.3k citations indexed

About

Kathy Mann is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Kathy Mann has authored 41 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 26 papers in Pediatrics, Perinatology and Child Health and 13 papers in Plant Science. Recurrent topics in Kathy Mann's work include Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (19 papers) and Chromosomal and Genetic Variations (13 papers). Kathy Mann is often cited by papers focused on Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (19 papers) and Chromosomal and Genetic Variations (13 papers). Kathy Mann collaborates with scholars based in United Kingdom, Australia and Canada. Kathy Mann's co-authors include Caroline Mackie Ogilvie, Zoe Docherty, Celia Donaghue, Shu C. Yau, Joo Wook Ahn, Stephen Abbs, Paul N. Scriven, Alison Hills, Roland G. Roberts and Angharad M. Roberts and has published in prestigious journals such as Nature, The Lancet and Blood.

In The Last Decade

Kathy Mann

41 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kathy Mann United Kingdom 22 862 800 330 172 126 41 1.3k
Vincenzo Cirigliano Spain 18 550 0.6× 817 1.0× 210 0.6× 91 0.5× 111 0.9× 46 1.0k
Avirachan T. Tharapel United States 19 976 1.1× 881 1.1× 443 1.3× 274 1.6× 162 1.3× 61 1.5k
Iris Bartels Germany 20 643 0.7× 738 0.9× 305 0.9× 206 1.2× 130 1.0× 69 1.3k
Amber N. Pursley United States 20 1.1k 1.3× 690 0.9× 498 1.5× 250 1.5× 61 0.5× 28 1.4k
Cindy Melotte Belgium 19 813 0.9× 840 1.1× 566 1.7× 291 1.7× 80 0.6× 32 1.5k
Voula Velissariou Greece 17 444 0.5× 390 0.5× 354 1.1× 78 0.5× 55 0.4× 40 784
Anıl Biricik Italy 18 614 0.7× 1.2k 1.5× 315 1.0× 87 0.5× 146 1.2× 41 1.5k
Joy D.A. Delhanty United Kingdom 17 290 0.3× 423 0.5× 267 0.8× 60 0.3× 128 1.0× 30 796
Don Leigh Australia 15 387 0.4× 548 0.7× 329 1.0× 57 0.3× 126 1.0× 43 933
Marta Rodríguez de Alba Spain 19 316 0.4× 566 0.7× 285 0.9× 35 0.2× 64 0.5× 42 889

Countries citing papers authored by Kathy Mann

Since Specialization
Citations

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

Fields of papers citing papers by Kathy Mann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kathy Mann. 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 Kathy Mann. The network helps show where Kathy Mann may publish in the future.

Co-authorship network of co-authors of Kathy Mann

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

All Works

20 of 20 papers shown
1.
Sakka, Sophia, Kathy Mann, Katherine Lachlan, et al.. (2020). Haematological chimerism masquerading as disorder of sex development. Clinical Endocrinology. 92(5). 487–489. 1 indexed citations
2.
Togneri, Fiona S., et al.. (2020). Cytogenomic results following high-chance non-invasive prenatal testing: a UK national audit. Genetics Research. 102. e7–e7. 3 indexed citations
3.
Mann, Kathy, Erwin Petek, & Barbara Pertl. (2018). Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCR. Methods in molecular biology. 1885. 139–160. 1 indexed citations
4.
Leeuw, Nicole de, Kathy Mann, Heleen Schuring‐Blom, et al.. (2018). European guidelines for constitutional cytogenomic analysis. European Journal of Human Genetics. 27(1). 1–16. 92 indexed citations
5.
Donaghue, Celia, et al.. (2017). Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data. Molecular Cytogenetics. 10(1). 12–12. 17 indexed citations
6.
7.
Mann, Kathy & Caroline Mackie Ogilvie. (2012). QF‐PCR: application, overview and review of the literature. Prenatal Diagnosis. 32(4). 309–314. 47 indexed citations
8.
9.
Hills, Alison, Celia Donaghue, Jonathan J. Waters, et al.. (2010). QF‐PCR as a stand‐alone test for prenatal samples: the first 2 years' experience in the London region. Prenatal Diagnosis. 30(6). 509–517. 57 indexed citations
10.
Donaghue, Celia, et al.. (2009). Combined QF‐PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis. Prenatal Diagnosis. 30(2). 133–137. 32 indexed citations
11.
Ogilvie, Caroline Mackie, et al.. (2009). A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report. Molecular Cytogenetics. 2(1). 9–9. 21 indexed citations
12.
13.
Waters, Jonathan J., Kathy Mann, Caroline Mackie Ogilvie, et al.. (2007). Complete discrepancy between QF‐PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS. Prenatal Diagnosis. 27(4). 332–339. 27 indexed citations
14.
Donaghue, Celia, Kathy Mann, Zoe Docherty, & Caroline Mackie Ogilvie. (2005). Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis. Prenatal Diagnosis. 25(1). 65–72. 76 indexed citations
15.
Mann, Kathy, et al.. (2005). Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping. Prenatal Diagnosis. 25(1). 79–83. 45 indexed citations
16.
Spence, Jennifer M., Walter Mills, Kathy Mann, Clare Huxley, & Christine J. Farr. (2005). Increased missegregation and chromosome loss with decreasing chromosome size in vertebrate cells. Chromosoma. 115(1). 60–74. 31 indexed citations
17.
Mann, Kathy, et al.. (2004). Strategies for the rapid prenatal diagnosis of chromosome aneuploidy. European Journal of Human Genetics. 12(11). 907–915. 112 indexed citations
18.
Mann, Kathy. (2004). Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence-PCR. Humana Press eBooks. 92. 141–156. 6 indexed citations
19.
Donaghue, Celia, Angharad M. Roberts, Kathy Mann, & Caroline Mackie Ogilvie. (2003). Development and targeted application of a rapid QF‐PCR test for sex chromosome imbalance. Prenatal Diagnosis. 23(3). 201–210. 53 indexed citations
20.
Mann, Kathy, Stephen Abbs, Shu C. Yau, et al.. (2001). Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis. The Lancet. 358(9287). 1057–1061. 160 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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