Lisa McKie

1.4k total citations
24 papers, 702 citations indexed

About

Lisa McKie is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Lisa McKie has authored 24 papers receiving a total of 702 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Cell Biology and 8 papers in Genetics. Recurrent topics in Lisa McKie's work include Retinal Development and Disorders (11 papers), melanin and skin pigmentation (4 papers) and Photoreceptor and optogenetics research (3 papers). Lisa McKie is often cited by papers focused on Retinal Development and Disorders (11 papers), melanin and skin pigmentation (4 papers) and Photoreceptor and optogenetics research (3 papers). Lisa McKie collaborates with scholars based in United Kingdom, United States and Germany. Lisa McKie's co-authors include Ian J. Jackson, Sally H. Cross, Katrine West, Alan Hart, Margaret Keighren, Angela Lee, Shoumo Bhattacharya, Jürgen E. Schneider, Joanne Morgan and David G. Brownstein and has published in prestigious journals such as Nature Communications, Scientific Reports and Journal of Cell Science.

In The Last Decade

Lisa McKie

22 papers receiving 696 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lisa McKie United Kingdom	13	433	218	128	87	85	24	702
Marisa Zallocchi United States	17	456 1.1×	71 0.3×	79 0.6×	142 1.6×	41 0.5×	35	755
Lixing W. Reneker United States	23	934 2.2×	220 1.0×	153 1.2×	39 0.4×	215 2.5×	46	1.3k
Loreto Cuitiño Chile	11	332 0.8×	220 1.0×	83 0.6×	19 0.2×	56 0.7×	17	753
Jungmook Lyu South Korea	17	757 1.7×	82 0.4×	108 0.8×	38 0.4×	85 1.0×	43	1.0k
Mingchu Xu United States	19	623 1.4×	92 0.4×	182 1.4×	14 0.2×	184 2.2×	28	760
Annabel Christ Germany	14	321 0.7×	97 0.4×	101 0.8×	8 0.1×	50 0.6×	18	556
Olivier Lorentz France	7	547 1.3×	45 0.2×	275 2.1×	27 0.3×	120 1.4×	9	792
Sachiko Aono Japan	17	556 1.3×	489 2.2×	138 1.1×	82 0.9×	27 0.3×	36	996
Arif O. Khan Saudi Arabia	19	721 1.7×	114 0.5×	299 2.3×	23 0.3×	343 4.0×	74	960

Countries citing papers authored by Lisa McKie

Since Specialization

Citations

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

Fields of papers citing papers by Lisa McKie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa McKie

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

Newton, Fay, et al.. (2025). Autophagy disruption and mitochondrial stress precede photoreceptor necroptosis in multiple mouse models of inherited retinal disorders. Nature Communications. 16(1). 4024–4024.

Budd, Peter S., Darren W. Logan, Margaret Keighren, et al.. (2025). A Dominant Mutation in G_αs‐Protein Increases Hair Pigmentation. Pigment Cell & Melanoma Research. 38(3). e70025–e70025.

Megaw, Roly, Zhixian Zhang, Fay Newton, et al.. (2024). Ciliary tip actin dynamics regulate photoreceptor outer segment integrity. Nature Communications. 15(1). 4316–4316. 8 indexed citations

Hall, Emma A., Dhivya Kumar, Suzanna L. Prosser, et al.. (2023). Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis. eLife. 12. 28 indexed citations

Tingaud‐Sequeira, Angèle, Vincent Michaud, Benoı̂t Pinson, et al.. (2022). The Dct−/− Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism. Genes. 13(7). 1164–1164. 4 indexed citations

Stanton, Chloë M., Camilla Drake, Philippe Gautier, et al.. (2021). A mouse model of brittle cornea syndrome caused by mutation in Zfp469. Disease Models & Mechanisms. 14(9). 11 indexed citations

Cross, Sally H., Lisa McKie, Toby W. Hurd, et al.. (2020). The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification. PLoS Genetics. 16(4). e1008583–e1008583. 13 indexed citations

Pennamen, Perrine, Angèle Tingaud‐Sequeira, Iveta Gažová, et al.. (2020). Dopachrome tautomerase variants in patients with oculocutaneous albinism. Genetics in Medicine. 23(3). 479–487. 36 indexed citations

McKie, Lisa, Margaret Keighren, Luis Sánchez‐Pulido, et al.. (2020). Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function. Scientific Reports. 10(1). 437–437. 1 indexed citations

10.

Cross, Sally H., Lisa McKie, Margaret Keighren, et al.. (2019). Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse. Investigative Ophthalmology & Visual Science. 60(8). 2875–2875. 12 indexed citations

11.

Carter, Roderick N., Lisa McKie, Peter S. Budd, et al.. (2018). Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function. Disease Models & Mechanisms. 11(12). 20 indexed citations

12.

Cross, Sally H., Danilo G. Macalinao, Lisa McKie, et al.. (2014). A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation. PLoS Genetics. 10(5). e1004359–e1004359. 23 indexed citations

13.

Douvaras, Panagiotis, Weijia Liu, Richard L. Mort, et al.. (2012). Normal X-inactivation mosaicism in corneas of heterozygous Flna Dilp2/+ female mice-a model of human Filamin A (FLNA) diseases. BMC Research Notes. 5(1). 122–122. 1 indexed citations

14.

Cross, Sally H., Lisa McKie, West Km, et al.. (2010). The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype. Human Molecular Genetics. 20(2). 223–234. 12 indexed citations

15.

Mill, Pleasantine, Angela Lee, Yuko Fukata, et al.. (2009). Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation. PLoS Genetics. 5(11). e1000748–e1000748. 77 indexed citations

16.

Cross, Sally H., Alan Hart, Joanne Morgan, et al.. (2009). 06-P022 Rwhs is a mouse model for Bochdalek congenital diaphragmatic hernia in humans. Mechanisms of Development. 126. S126–S126. 1 indexed citations

17.

Lang, Bing, Lei Zhao, Li Cai, et al.. (2009). GABAergic amacrine cells and visual function are reduced in PAC1 transgenic mice. Neuropharmacology. 58(1). 215–225. 9 indexed citations

18.

Hart, Alan, Joanne Morgan, Jürgen E. Schneider, et al.. (2006). Cardiac malformations and midline skeletal defects in mice lacking filamin A. Human Molecular Genetics. 15(16). 2457–2467. 130 indexed citations

19.

Agtmael, Tom Van, Ursula Schlötzer‐Schrehardt, Lisa McKie, et al.. (2005). Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy. Human Molecular Genetics. 14(21). 3161–3168. 116 indexed citations

20.

Hart, Alan, Lisa McKie, James P. Morgan, et al.. (2005). Genotype–Phenotype Correlation of MousePde6bMutations. Investigative Ophthalmology & Visual Science. 46(9). 3443–3443. 71 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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