Tim Footz

1.2k total citations
36 papers, 728 citations indexed

About

Tim Footz is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Tim Footz has authored 36 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Ophthalmology and 7 papers in Genetics. Recurrent topics in Tim Footz's work include Glaucoma and retinal disorders (7 papers), Developmental Biology and Gene Regulation (6 papers) and Retinal Development and Disorders (5 papers). Tim Footz is often cited by papers focused on Glaucoma and retinal disorders (7 papers), Developmental Biology and Gene Regulation (6 papers) and Retinal Development and Disorders (5 papers). Tim Footz collaborates with scholars based in Canada, United States and Germany. Tim Footz's co-authors include Michael A. Walter, Anastassia Voronova, Fred B. Berry, C. Backhouse, Vincent Raymond, W. Ted Allison, Ordan J. Lehmann, Martin J. Somerville, Robert Ritch and Farideh Mirzayans and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Tim Footz

36 papers receiving 722 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tim Footz Canada	17	446	190	130	84	72	36	728
Umberto Di Vicino Italy	16	779 1.7×	262 1.4×	153 1.2×	68 0.8×	23 0.3×	22	949
Akiko Suga Japan	10	603 1.4×	63 0.3×	134 1.0×	58 0.7×	67 0.9×	16	716
Daniela Sanges Italy	12	768 1.7×	148 0.8×	218 1.7×	124 1.5×	16 0.2×	12	861
Jessica Gumerson United States	11	574 1.3×	92 0.5×	91 0.7×	149 1.8×	25 0.3×	16	647
Felix Tonagel Germany	14	772 1.7×	119 0.6×	347 2.7×	97 1.2×	38 0.5×	33	1.0k
Sarah Decembrini Switzerland	14	621 1.4×	50 0.3×	152 1.2×	64 0.8×	42 0.6×	18	777
Pilar Villacampa Spain	13	344 0.8×	200 1.1×	141 1.1×	104 1.2×	13 0.2×	21	762
J. Brett Stanton United States	15	669 1.5×	170 0.9×	296 2.3×	135 1.6×	26 0.4×	22	869
Oliver Puk Germany	17	404 0.9×	158 0.8×	186 1.4×	47 0.6×	15 0.2×	30	681
Conor M. Ramsden United Kingdom	11	712 1.6×	82 0.4×	271 2.1×	43 0.5×	61 0.8×	23	842

Countries citing papers authored by Tim Footz

Since Specialization

Citations

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

Fields of papers citing papers by Tim Footz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tim Footz

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

Almeida, Monique Marylin Alves de, Danny Galleguillos, Maryam Nakhaei‐Nejad, et al.. (2023). Fractalkine enhances oligodendrocyte regeneration and remyelination in a demyelination mouse model. Stem Cell Reports. 18(2). 519–533. 21 indexed citations

Almeida, Monique Marylin Alves de, Yutong Li, Tim Footz, et al.. (2021). Fractalkine signaling regulates oligodendroglial cell genesis from SVZ precursor cells. Stem Cell Reports. 16(8). 1968–1984. 20 indexed citations

Vidal‐García, Marta, J. David Aponte, Tim Footz, et al.. (2021). The Chromatin Regulator Ankrd11 Controls Palate and Cranial Bone Development. Frontiers in Cell and Developmental Biology. 9. 645386–645386. 22 indexed citations

Almeida, Monique Marylin Alves de, Tim Footz, Jorge M. David, et al.. (2021). Agathisflavone Modifies Microglial Activation State and Myelination in Organotypic Cerebellar Slices Culture. Journal of Neuroimmune Pharmacology. 17(1-2). 206–217. 6 indexed citations

Ghosh, Sunita, et al.. (2021). FOXQ1 is Differentially Expressed Across Breast Cancer Subtypes with Low Expression Associated with Poor Overall Survival. Breast Cancer Targets and Therapy. Volume 13. 171–188. 13 indexed citations

Footz, Tim, et al.. (2019). Regulation of CNS precursor function by neuronal chemokines. Neuroscience Letters. 715. 134533–134533. 45 indexed citations

Footz, Tim, Michael A. Walter, Amelia Aránega, et al.. (2018). A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation. The American Journal of Cardiology. 123(5). 787–793. 15 indexed citations

Doucette, Lance P., et al.. (2017). FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25. PLoS ONE. 12(6). e0178518–e0178518. 8 indexed citations

Footz, Tim, et al.. (2014). Analysis of Exocytosis Regulation by Transcription Factor FOXC1 and its Role in Axenfeld-Rieger Syndrome Pathogenesis. Investigative Ophthalmology & Visual Science. 55(13). 3802–3802. 1 indexed citations

10.

Asai-Coakwell, Mika, Periasamy Sundaresan, Tim Footz, et al.. (2009). Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies. Human Molecular Genetics. 19(2). 287–298. 117 indexed citations

11.

Itō, Yoko, Fred B. Berry, Tim Footz, Arif O. Khan, & Michael A. Walter. (2008). Molecular Characterization of a Novel FOXC1 Mutation Found in a Patient With Aniridia. Investigative Ophthalmology & Visual Science. 49(13). 1653–1653. 1 indexed citations

12.

Sharan, Sapna, Farideh Mirzayans, Tim Footz, Michael A. Walter, & Alex V. Levin. (2008). Elliptical anterior iris stromal defects associated with PAX6 gene sequence changes. Journal of American Association for Pediatric Ophthalmology and Strabismus. 12(4). 340–343.e2. 8 indexed citations

13.

Berry, Fred B., Matthew A. Lines, Tim Footz, et al.. (2006). Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis. Human Molecular Genetics. 15(6). 905–919. 7 indexed citations

14.

Tamimi, Yahya, Jonathan M. Skarie, Tim Footz, et al.. (2006). FGF19 is a target for FOXC1 regulation in ciliary body-derived cells. Human Molecular Genetics. 15(21). 3229–3240. 36 indexed citations

15.

Footz, Tim, et al.. (2004). Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis. The Analyst. 129(1). 25–25. 25 indexed citations

16.

Backhouse, C., Tim Footz, Sophia Adamia, & L M Pilarski. (2004). Microfluidic chips for the molecular analysis of human cancer. 93. 377–382. 3 indexed citations

17.

Footz, Tim, et al.. (2003). Heteroduplex-Based Genotyping with Microchip Electrophoresis and dHPLC. Genetic Testing. 7(4). 283–293. 20 indexed citations

18.

Footz, Tim, et al.. (2003). Three duplicons form a novel chimeric transcription unit in the pericentromeric region of chromosome 22q11. Human Genetics. 112(1). 57–61. 12 indexed citations

19.

Footz, Tim, Sybille Wunsam, Stephen C. Kulak, et al.. (2001). Sample purification on a microfluidic device. Electrophoresis. 22(18). 3868–3875. 29 indexed citations

20.

Footz, Tim, Bruce W. Birren, Satoshi Minoshima, et al.. (1998). The Gene for Death Agonist BID Maps to the Region of Human 22q11.2 Duplicated in Cat Eye Syndrome Chromosomes and to Mouse Chromosome 6. Genomics. 51(3). 472–475. 13 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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