Louise Tee

5.8k total citations
31 papers, 1.5k citations indexed

About

Louise Tee is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Louise Tee has authored 31 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Louise Tee's work include Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (4 papers) and Prenatal Screening and Diagnostics (4 papers). Louise Tee is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (4 papers) and Prenatal Screening and Diagnostics (4 papers). Louise Tee collaborates with scholars based in United Kingdom, United States and Netherlands. Louise Tee's co-authors include Eamonn R. Maher, Shanaz Pasha, Esther Meyer, Paul D.P. Pharoah, Alison M. Dunning, Wolf Reik, Derek Lim, Fatimah Rahman, Gail Kirby and Fiona MacDonald and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and Blood.

In The Last Decade

Louise Tee

31 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Louise Tee United Kingdom	18	801	781	349	176	153	31	1.5k
Almuth Caliebe Germany	23	655 0.8×	678 0.9×	324 0.9×	96 0.5×	113 0.7×	66	1.4k
Sabrina Giglio Italy	29	1.5k 1.8×	1.3k 1.7×	422 1.2×	79 0.4×	111 0.7×	116	2.6k
Sascha Tierling Germany	24	1.2k 1.5×	516 0.7×	258 0.7×	152 0.9×	64 0.4×	56	2.0k
Dusica Babovic‐Vuksanovic United States	27	863 1.1×	540 0.7×	144 0.4×	118 0.7×	48 0.3×	99	2.2k
Boleslaw Goldman Israel	22	746 0.9×	575 0.7×	246 0.7×	63 0.4×	94 0.6×	74	1.7k
Nico Ruf Germany	13	1.2k 1.4×	849 1.1×	352 1.0×	53 0.3×	100 0.7×	16	1.6k
Julie Désir Belgium	19	676 0.8×	529 0.7×	119 0.3×	85 0.5×	154 1.0×	46	1.4k
Sharon Zeligson Israel	19	731 0.9×	281 0.4×	166 0.5×	97 0.6×	122 0.8×	41	1.3k
Céline Schaeffer Italy	20	1.3k 1.6×	544 0.7×	184 0.5×	83 0.5×	37 0.2×	32	2.0k
Béatrice Conne Switzerland	20	921 1.1×	409 0.5×	88 0.3×	95 0.5×	230 1.5×	30	1.9k

Countries citing papers authored by Louise Tee

Since Specialization

Citations

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

Fields of papers citing papers by Louise Tee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Tee

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

Wragg, Joseph W., Yavor Hadzhiev, Kasun Wanigasooriya, et al.. (2023). Intra-promoter switch of transcription initiation sites in proliferation signaling-dependent RNA metabolism. Nature Structural & Molecular Biology. 30(12). 1970–1984. 1 indexed citations

Pickles, Oliver, Kasun Wanigasooriya, Anetta Ptasinska, et al.. (2023). MHC Class II is Induced by IFNγ and Follows Three Distinct Patterns of Expression in Colorectal Cancer Organoids. Cancer Research Communications. 3(8). 1501–1513. 6 indexed citations

Wanigasooriya, Kasun, João D. Barros‐Silva, Louise Tee, et al.. (2022). Patient Derived Organoids Confirm That PI3K/AKT Signalling Is an Escape Pathway for Radioresistance and a Target for Therapy in Rectal Cancer. Frontiers in Oncology. 12. 920444–920444. 11 indexed citations

Mori, Jun, Zoltán Nagy, Christopher W. Smith, et al.. (2018). Maintenance of murine platelet homeostasis by the kinase Csk and phosphatase CD148. Blood. 131(10). 1122–1144. 32 indexed citations

Willet, Joseph D. P., Helen Griffin, Neil V. Morgan, et al.. (2016). Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency. Journal of Clinical Immunology. 36(2). 117–122. 51 indexed citations

Tee, Louise, et al.. (2015). The intake and quality of breakfast consumption in adolescents attending public secondary schools in the North West province, South Africa. South African Journal of Clinical Nutrition. 28(2). 81–88. 15 indexed citations

Ibrahim, Abdulla, Gail Kirby, Carol Hardy, et al.. (2014). Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects. Clinical Epigenetics. 6(1). 11–11. 87 indexed citations

Tee, Louise, Derek Lim, Renuka Dias, et al.. (2013). Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology. Clinical Epigenetics. 5(1). 23–23. 31 indexed citations

Morgan, Neil V., Jane Hartley, Kenneth D.R. Setchell, et al.. (2013). A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver disease. Orphanet Journal of Rare Diseases. 8(1). 74–74. 17 indexed citations

10.

Meyer, Esther, Manju A. Kurian, Neil V. Morgan, et al.. (2011). Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease. Molecular Genetics and Metabolism. 104(4). 637–643. 18 indexed citations

11.

Hartley, Jane, Nicholas C. Zachos, Ban B. Dawood, et al.. (2010). Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy). Gastroenterology. 138(7). 2388–2398.e2. 96 indexed citations

12.

Meyer, Esther, Christopher J. Ricketts, Neil V. Morgan, et al.. (2010). Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome). The American Journal of Human Genetics. 86(3). 471–478. 46 indexed citations

13.

Joyce, Sarah, Louise Tee, Aiysha Abid, et al.. (2010). Locus heterogeneity and Knobloch syndrome. American Journal of Medical Genetics Part A. 152A(11). 2880–2881. 12 indexed citations

14.

Kurian, Manju A., Juan Zhen, Shuyuan Cheng, et al.. (2009). Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia. Journal of Clinical Investigation. 119(6). 1595–603. 148 indexed citations

15.

Meyer, Esther, Derek Lim, Shanaz Pasha, et al.. (2009). Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome). PLoS Genetics. 5(3). e1000423–e1000423. 183 indexed citations

16.

Bowdin, Sarah, Louise Tee, Gail Kirby, et al.. (2008). Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies. Human Reproduction. 24(3). 741–747. 160 indexed citations

17.

Forshew, Tim, Colin A. Johnson, Shagufta Khaliq, et al.. (2005). Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations. Human Genetics. 117(5). 452–459. 66 indexed citations

18.

Dunning, Alison M., Mitch Dowsett, Catherine S. Healey, et al.. (2004). Polymorphisms Associated With Circulating Sex Hormone Levels in Postmenopausal Women. JNCI Journal of the National Cancer Institute. 96(12). 936–945. 278 indexed citations

19.

Neuhausen, Susan L., Alison M. Dunning, Linda Steele, et al.. (2003). Role of CHEK2*1100delC in unselected series of non‐BRCA1/2 male breast cancers. International Journal of Cancer. 108(3). 477–478. 41 indexed citations

20.

Chang‐Claude, Jenny, Alison M. Dunning, Udo Schnitzbauer, et al.. (2002). The patched polymorphism Pro1315Leu (C3944T) may modulate the association between use of oral contraceptives and breast cancer risk. International Journal of Cancer. 103(6). 779–783. 61 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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