Moira Crosier

2.3k total citations
29 papers, 833 citations indexed

About

Moira Crosier is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Moira Crosier has authored 29 papers receiving a total of 833 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 10 papers in Genetics and 3 papers in Ophthalmology. Recurrent topics in Moira Crosier's work include DNA Repair Mechanisms (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Molecular Biology Techniques and Applications (4 papers). Moira Crosier is often cited by papers focused on DNA Repair Mechanisms (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Molecular Biology Techniques and Applications (4 papers). Moira Crosier collaborates with scholars based in United Kingdom, United States and Japan. Moira Crosier's co-authors include Susan Lindsay, John A.L. Armour, Irène Gottlob, A.J. Jeffreys, Bruce R. Westley, Anthony D. Hill, Rachel Straussberg, Ganeshwaran H. Mochida, Robert Hill and Christopher A. Walsh and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Cell Biology.

In The Last Decade

Moira Crosier

28 papers receiving 813 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Moira Crosier United Kingdom 15 554 239 111 98 68 29 833
Tarja Joensuu Finland 19 670 1.2× 344 1.4× 134 1.2× 261 2.7× 24 0.4× 31 1.3k
Gabriele Dekomien Germany 21 586 1.1× 301 1.3× 96 0.9× 134 1.4× 24 0.4× 65 1.1k
Saskia Biskup Germany 17 771 1.4× 358 1.5× 49 0.4× 99 1.0× 127 1.9× 37 1.1k
Eeva‐Marja Sankila Finland 18 811 1.5× 198 0.8× 115 1.0× 141 1.4× 15 0.2× 38 1.1k
David E. Bergstrom United States 13 440 0.8× 206 0.9× 100 0.9× 41 0.4× 13 0.2× 22 825
Haris Kokotas Greece 14 363 0.7× 107 0.4× 101 0.9× 29 0.3× 27 0.4× 31 637
Soo Kyung Koo South Korea 15 503 0.9× 99 0.4× 87 0.8× 47 0.5× 61 0.9× 28 743
Shahid Y. Khan United States 17 636 1.1× 113 0.5× 146 1.3× 64 0.7× 16 0.2× 38 958
Inga Ebermann Germany 15 845 1.5× 232 1.0× 162 1.5× 144 1.5× 10 0.1× 19 1.1k
Brian P. Brooks United States 22 884 1.6× 360 1.5× 35 0.3× 390 4.0× 26 0.4× 73 1.4k

Countries citing papers authored by Moira Crosier

Since Specialization
Citations

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

Fields of papers citing papers by Moira Crosier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moira Crosier

This figure shows the co-authorship network connecting the top 25 collaborators of Moira Crosier. A scholar is included among the top collaborators of Moira Crosier 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 Moira Crosier. Moira Crosier 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.
Dorgau, Birthe, Joseph Collin, Agata Rozanska, et al.. (2024). Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina. Nature Communications. 15(1). 3567–3567. 16 indexed citations
2.
Anderson, Robert H., Wouter H. Lamers, Jill P. J. M. Hikspoors, et al.. (2023). Development of the arterial roots and ventricular outflow tracts. Journal of Anatomy. 244(3). 497–513. 13 indexed citations
3.
Queen, Rachel, Moira Crosier, Lorraine Eley, et al.. (2023). Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves. PLoS Genetics. 19(11). e1010777–e1010777. 6 indexed citations
4.
5.
Chacko, Lejo Johnson, Saïd Assou, József Dudás, et al.. (2021). Transcriptome-Wide Analysis Reveals a Role for Extracellular Matrix and Integrin Receptor Genes in Otic Neurosensory Differentiation from Human iPSCs. International Journal of Molecular Sciences. 22(19). 10849–10849. 9 indexed citations
6.
Floros, Vasileios I., Angela Pyle, Sabine Dietmann, et al.. (2018). Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos. Nature Cell Biology. 20(2). 144–151. 151 indexed citations
7.
Kist, Ralf, et al.. (2014). The Formation of Endoderm-Derived Taste Sensory Organs Requires a Pax9-Dependent Expansion of Embryonic Taste Bud Progenitor Cells. PLoS Genetics. 10(10). e1004709–e1004709. 28 indexed citations
8.
Thomas, Mervyn G., Moira Crosier, Susan Lindsay, et al.. (2014). Abnormal retinal development associated with FRMD7 mutations. Human Molecular Genetics. 23(15). 4086–4093. 51 indexed citations
9.
Thomas, Mervyn G., Moira Crosier, Susan Lindsay, et al.. (2012). Retinal Changes In Idiopathic Infantile Nystagmus Associated With FRMD7 Mutations. Investigative Ophthalmology & Visual Science. 53(14). 520–520. 1 indexed citations
10.
Cuthbert, Gavin, et al.. (2012). Origin of trisomy: no evidence to support the ovarian mosaicism theory. Prenatal Diagnosis. 32(7). 668–673. 6 indexed citations
11.
Crosier, Moira, et al.. (2010). Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy. Brain Research Bulletin. 83(6). 374–379. 9 indexed citations
12.
Mochida, Ganeshwaran H., Muhammad Mahajnah, Anthony D. Hill, et al.. (2009). A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly. The American Journal of Human Genetics. 85(6). 897–902. 107 indexed citations
13.
Bartesaghi, Stefano, Moira Crosier, Susan Lindsay, et al.. (2009). The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development. Human Molecular Genetics. 19(2). 342–351. 57 indexed citations
14.
Crosier, Moira, et al.. (1999). Differences in Ki67 and c-erbB2 expression between screen-detected and true interval breast cancers.. PubMed. 5(10). 2682–8. 40 indexed citations
15.
Armour, John A.L., Moira Crosier, & A.J. Jeffreys. (1996). Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110). Annals of Human Genetics. 60(1). 11–20. 17 indexed citations
16.
Armour, John A.L., Moira Crosier, S Malcolm, Juliana C.N. Chan, & A.J. Jeffreys. (1995). Human minisatellite loci composed of interspersed GGA-GGT triplet repeats. Proceedings of the Royal Society B Biological Sciences. 261(1362). 345–349. 4 indexed citations
17.
Royle, Nicola J., John A.L. Armour, Moira Crosier, & A.J. Jeffreys. (1993). Abnormal Segregation of Alleles in CEPH Pedigree DNAs Arising from Allele Loss in Lymphoblastoid DNA. Genomics. 15(1). 119–122. 10 indexed citations
18.
Armour, John A.L., Moira Crosier, & Alec J. Jeffreys. (1992). Human minisatellite alleles detectable only after PCR amplification. Genomics. 12(1). 116–124. 19 indexed citations
19.
Jeffreys, A.J., Nicola J. Royle, I. Patel, et al.. (1991). Principles and Recent Advances in Human DNA Fingerprinting. Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions. 58. 1–19. 37 indexed citations
20.
Crosier, Moira, John A.L. Armour, & A.J. Jeffreys. (1991). A highly polymorphic minisatellite (pMS627) on chromsome 14 (D14S44). Nucleic Acids Research. 19(19). 5446–5446. 2 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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