Dianne Gerrelli

4.1k total citations
47 papers, 2.2k citations indexed

About

Dianne Gerrelli is a scholar working on Molecular Biology, Genetics and Small Animals. According to data from OpenAlex, Dianne Gerrelli has authored 47 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 16 papers in Genetics and 8 papers in Small Animals. Recurrent topics in Dianne Gerrelli's work include Developmental Biology and Gene Regulation (9 papers), Helminth infection and control (7 papers) and Hedgehog Signaling Pathway Studies (6 papers). Dianne Gerrelli is often cited by papers focused on Developmental Biology and Gene Regulation (9 papers), Helminth infection and control (7 papers) and Hedgehog Signaling Pathway Studies (6 papers). Dianne Gerrelli collaborates with scholars based in United Kingdom, United States and Canada. Dianne Gerrelli's co-authors include Andrew J. Copp, Nicholas D. E. Greene, Patricia Ybot‐González, D. Ε. Jacobs, M. Fox, Massimo Signore, Patricia Cogram, Dawn Savery, Clare Faux and H. W. M. van Straaten and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Dianne Gerrelli

46 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dianne Gerrelli United Kingdom	27	1.4k	801	350	223	179	47	2.2k
Henry J. Baker United States	28	990 0.7×	391 0.5×	390 1.1×	74 0.3×	210 1.2×	63	2.0k
Ryuzo Torii Japan	25	783 0.6×	260 0.3×	85 0.2×	171 0.8×	150 0.8×	96	2.0k
Cathryn S. Mellersh United Kingdom	28	1.9k 1.4×	1.8k 2.2×	341 1.0×	170 0.8×	89 0.5×	102	3.3k
Duncan B. Sparrow Australia	36	3.0k 2.2×	982 1.2×	249 0.7×	36 0.2×	390 2.2×	70	3.8k
E. J. Sanders Canada	30	1.6k 1.2×	699 0.9×	410 1.2×	12 0.1×	203 1.1×	103	2.6k
Kenji Tanigaki Japan	29	2.7k 2.0×	420 0.5×	408 1.2×	93 0.4×	294 1.6×	47	4.8k
Laurent Tiret France	22	880 0.6×	277 0.3×	320 0.9×	56 0.3×	107 0.6×	71	1.6k
H.‐Dieter Dellmann United States	22	399 0.3×	120 0.1×	179 0.5×	81 0.4×	137 0.8×	67	1.8k
Daniel J. Bernard Canada	36	1.8k 1.3×	729 0.9×	83 0.2×	26 0.1×	91 0.5×	145	3.9k
Benoît Robert France	36	2.8k 2.0×	784 1.0×	247 0.7×	11 0.0×	230 1.3×	77	3.9k

Countries citing papers authored by Dianne Gerrelli

Since Specialization

Citations

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

Fields of papers citing papers by Dianne Gerrelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dianne Gerrelli

This figure shows the co-authorship network connecting the top 25 collaborators of Dianne Gerrelli. A scholar is included among the top collaborators of Dianne Gerrelli 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 Dianne Gerrelli. Dianne Gerrelli 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

Holt, Richard, Fabiola Ceroni, Dorine A. Bax, et al.. (2017). New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders. Scientific Reports. 7(1). 7975–7975. 11 indexed citations

Lindsay, Susan, Yaobo Xu, Steven Lisgo, et al.. (2016). HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development. Frontiers in Neuroanatomy. 10. 86–86. 54 indexed citations

Davidson, Alice E., Dianne Gerrelli, Roberta Rizzo, et al.. (2016). Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis. The American Journal of Human Genetics. 99(6). 1338–1352. 38 indexed citations

McCabe, Mark J., Carles Gaston‐Massuet, Vaitsa Tziaferi, et al.. (2011). NovelFGF8Mutations Associated with Recessive Holoprosencephaly, Craniofacial Defects, and Hypothalamo-Pituitary Dysfunction. The Journal of Clinical Endocrinology & Metabolism. 96(10). E1709–E1718. 97 indexed citations

Pagnamenta, A. T., Hamza Khan, Susan Walker, et al.. (2010). Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of Medical Genetics. 48(1). 48–54. 76 indexed citations

Twigg, Stephen R.F., Sarah L. Versnel, Gudrun Nürnberg, et al.. (2009). Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene. The American Journal of Human Genetics. 84(5). 698–705. 93 indexed citations

Gestri, Gaia, Robert J. Osborne, Alexander W. Wyatt, et al.. (2009). Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators. Human Genetics. 126(6). 791–803. 60 indexed citations

Duggan, Anne, et al.. (2008). Transient expression of the conserved zinc finger gene INSM1 in progenitors and nascent neurons throughout embryonic and adult neurogenesis. The Journal of Comparative Neurology. 507(4). 1497–1520. 57 indexed citations

Kelberman, Daniel, Sandra C. de Castro, Heike Biebermann, et al.. (2008). Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. Human Molecular Genetics. 17(14). 2150–2159. 65 indexed citations

10.

Ybot‐González, Patricia, Dawn Savery, Dianne Gerrelli, et al.. (2007). Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure. Development. 134(4). 789–799. 260 indexed citations

11.

Dawe, Helen R., Andrew R. Cullinane, Dianne Gerrelli, et al.. (2006). The Meckel–Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. Human Molecular Genetics. 16(2). 173–186. 202 indexed citations

12.

Gerrelli, Dianne, Stéphan Gasca, Elizabeth L. Berg, et al.. (2003). Cordon-bleu is a conserved gene involved in neural tube formation. Developmental Biology. 262(1). 16–31. 73 indexed citations

13.

Copp, Andrew J., Patricia Cogram, Angeleen Fleming, et al.. (2003). Neurulation and Neural Tube Closure Defects. Humana Press eBooks. 136. 135–160. 33 indexed citations

14.

Murdoch, J., Kit Doudney, Dianne Gerrelli, et al.. (2003). Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia. Molecular and Cellular Neuroscience. 22(1). 62–74. 9 indexed citations

15.

Ybot‐González, Patricia, Patricia Cogram, Dianne Gerrelli, & Andrew J. Copp. (2002). Sonic hedgehog and the molecular regulation of mouse neural tube closure. Development. 129(10). 2507–2517. 129 indexed citations

16.

Greene, Nicholas D. E., Dianne Gerrelli, H. W. M. van Straaten, & Andrew J. Copp. (1998). Abnormalities of floor plate, notochord and somite differentiation in the loop-tail (Lp) mouse: a model of severe neural tube defects. Mechanisms of Development. 73(1). 59–72. 113 indexed citations

17.

Fleming, Angeleen, Dianne Gerrelli, Nicholas D. E. Greene, & Andrew J. Copp. (1997). Mechanisms of normal and abnormal neurulation: evidence from embryo culture studies. The International Journal of Developmental Biology. 41(2). 199–212. 28 indexed citations

18.

Gerrelli, Dianne, John Huntriss, & D.S. Latchman. (1994). Antagonistic Effects of Retinoic Acid and Thyroid Hormone on the Expression of the Tissue-specific Splicing Protein SmN in a Clonal Cell Line Derived from Rat Heart. Journal of Molecular and Cellular Cardiology. 26(6). 713–719. 22 indexed citations

19.

Gerrelli, Dianne, et al.. (1991). Cloning and sequencing of a mouse embryonal carcinoma cell mRNA encoding the tissue specific RNA splicing protein SmN. Nucleic Acids Research. 19(23). 6642–6642. 7 indexed citations

20.

Fox, M., et al.. (1988). Use of blood gastrin assay in the diagnosis of ovine haemonchiasis. Veterinary Record. 122(6). 136–137. 16 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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