Isabel M. Hanson

8.8k total citations · 2 hit papers
44 papers, 5.2k citations indexed

About

Isabel M. Hanson is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Isabel M. Hanson has authored 44 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 17 papers in Genetics and 9 papers in Immunology. Recurrent topics in Isabel M. Hanson's work include Developmental Biology and Gene Regulation (24 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Renal and related cancers (6 papers). Isabel M. Hanson is often cited by papers focused on Developmental Biology and Gene Regulation (24 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Renal and related cancers (6 papers). Isabel M. Hanson collaborates with scholars based in United Kingdom, United States and Italy. Isabel M. Hanson's co-authors include Veronica van Heyningen, Tim Jordan, John Trowsdale, Nicholas D. Hastie, Jane Prosser, Robert E. Hill, Ian Mockridge, Adrian Kelly, Stephan Beck and Anne Seawright and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Isabel M. Hanson

44 papers receiving 5.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mouse Small eye results from mutations in a paired-like homeobox-containing gene

1991 984 citations Robert E. Hill, Jack Favor et al. Nature profile →
Sequences encoded in the class II region of the MHC related to the 'ABC' superfamily of transporters

1990 624 citations John Trowsdale, Isabel M. Hanson et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Isabel M. Hanson United Kingdom	29	3.8k	1.7k	675	610	435	44	5.2k
Zbyněk Kozmík Czechia	39	3.7k 1.0×	922 0.5×	238 0.4×	606 1.0×	157 0.4×	114	5.0k
Kunio Yasuda Japan	35	3.8k 1.0×	1.1k 0.6×	303 0.4×	213 0.3×	204 0.5×	78	4.5k
Chris F. Inglehearn United Kingdom	42	3.7k 1.0×	947 0.6×	760 1.1×	222 0.4×	1.0k 2.4×	138	5.2k
Milan Jamrich United States	42	4.4k 1.1×	1.3k 0.7×	261 0.4×	202 0.3×	262 0.6×	87	5.3k
Elfride De Baere Belgium	39	3.1k 0.8×	1.8k 1.1×	228 0.3×	478 0.8×	986 2.3×	153	4.4k
Philip J. Gage United States	31	2.4k 0.6×	1.0k 0.6×	529 0.8×	243 0.4×	290 0.7×	52	3.7k
Kirk W. Beisel United States	42	2.7k 0.7×	439 0.3×	406 0.6×	1.1k 1.9×	110 0.3×	123	6.6k
Isao Matsuo Japan	39	4.0k 1.1×	1.2k 0.7×	151 0.2×	257 0.4×	144 0.3×	70	5.2k
Gregory M. Acland United States	44	5.3k 1.4×	3.0k 1.8×	597 0.9×	188 0.3×	1.8k 4.1×	153	7.1k
Yusuke Kamachi Japan	32	4.2k 1.1×	1.7k 1.0×	173 0.3×	330 0.5×	69 0.2×	58	5.2k

Countries citing papers authored by Isabel M. Hanson

Since Specialization

Citations

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

Fields of papers citing papers by Isabel M. Hanson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabel M. Hanson

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Ansari, Morad, Jacqueline K. Rainger, Jennie Murray, et al.. (2014). A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX. European Journal of Medical Genetics. 57(10). 587–595. 16 indexed citations

Henderson, Richard A., Kathy Williamson, Michael W. Clarke, et al.. (2007). Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia. European Journal of Human Genetics. 15(8). 898–901. 30 indexed citations

Hanson, Isabel M., et al.. (2005). A screen for proteins that interact with PAX6: C-terminal mutations disrupt interaction with HOMER3, DNCL1 and TRIM11. BMC Genetics. 6(1). 43–43. 18 indexed citations

Tzoulaki, Ioanna, Ian White, & Isabel M. Hanson. (2005). PAX6 mutations: genotype-phenotype correlations. BMC Genetics. 6(1). 27–27. 167 indexed citations

Hanson, Isabel M., et al.. (2003). A novel PAX6 gene mutation in an Indian aniridia patient.. PubMed. 9. 205–9. 15 indexed citations

Mitchell, Tejal N., S. L. Free, Kathleen A. Williamson, et al.. (2003). Polymicrogyria and absence of pineal gland due to PAX6 mutation. Annals of Neurology. 53(5). 658–663. 130 indexed citations

Churchill, A, Isabel M. Hanson, & Alexander F. Markham. (2000). Prenatal diagnosis of aniridia11The authors have no proprietary interest in the development or marketing of the techniques mentioned in this article.. Ophthalmology. 107(6). 1153–1156. 20 indexed citations

Hanson, Isabel M.. (1999). Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations. Human Molecular Genetics. 8(2). 165–172. 147 indexed citations

Hammond, Katherine L., et al.. (1999). Human (DACH) and Mouse (Dach) Homologues ofDrosophila dachshundMap to Chromosomes 13q22 and 14E3, Respectively. Genomics. 55(2). 252–253. 8 indexed citations

10.

Hammond, Katherine L., Isabel M. Hanson, Alison G. M. Brown, Laura A. Lettice, & Robert E. Hill. (1998). Mammalian and Drosophila dachshund genes are related to the Ski proto-oncogene and are expressed in eye and limb. Mechanisms of Development. 74(1-2). 121–131. 120 indexed citations

11.

Axton, Richard A, et al.. (1998). A new set of primers for mutation analysis of the human PAX6 gene. Human Mutation. 12(2). 128–134. 26 indexed citations

12.

Hanson, Isabel M. & Veronica van Heyningen. (1995). Pax6: more than meets the eye. Trends in Genetics. 11(7). 268–272. 159 indexed citations

13.

Hanson, Isabel M., Judy Fletcher, Tim Jordan, et al.. (1994). Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly. Nature Genetics. 6(2). 168–173. 381 indexed citations

14.

Hill, Ruaraidh & Isabel M. Hanson. (1992). Molecular genetics of the Pax gene family. Current Opinion in Cell Biology. 4(6). 967–972. 35 indexed citations

15.

Beck, Stephan, Isabel M. Hanson, Adrian P. Kelly, Darryl Pappin, & John Trowsdale. (1992). A homologue of the Drosophila female sterile homeotic (fsh) gene in the class II region of the human MHC. DNA sequence. 2(4). 203–210. 79 indexed citations

16.

Hanson, Isabel M., Anne Seawright, & Veronica van Heyningen. (1992). The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13–p14. Genomics. 13(4). 1331–1333. 67 indexed citations

17.

Hill, Robert E., Jack Favor, Brigid L.M. Hogan, et al.. (1991). Mouse Small eye results from mutations in a paired-like homeobox-containing gene. Nature. 354(6354). 522–525. 984 indexed citations breakdown →

18.

Hanson, Isabel M., Jiannis Ragoussis, & John Trowsdale. (1991). Organization of the human HLA-class-II region. International Journal of Cancer. 47(S6). 18–19. 1 indexed citations

19.

Trowsdale, John, et al.. (1990). Sequences encoded in the class II region of the MHC related to the 'ABC' superfamily of transporters. Nature. 348(6303). 741–744. 624 indexed citations breakdown →

20.

Hanson, Isabel M., Patricia Gorman, Vincent Chi Hang Lui, et al.. (1989). The human α2(XI) collagen gene (COL11A2) maps to the centromeric border of the major histocompatibility complex on chromosome 6. Genomics. 5(4). 925–931. 29 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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