Tessa Homfray

14.3k total citations · 1 hit paper
69 papers, 5.8k citations indexed

About

Tessa Homfray is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tessa Homfray has authored 69 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 24 papers in Genetics and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tessa Homfray's work include Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (9 papers) and Cardiovascular Effects of Exercise (8 papers). Tessa Homfray is often cited by papers focused on Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (9 papers) and Cardiovascular Effects of Exercise (8 papers). Tessa Homfray collaborates with scholars based in United Kingdom, United States and Italy. Tessa Homfray's co-authors include Matthew E. Hurles, D. Wénzel, Magdalena Renner, Andrew P. Jackson, Carol-Anne Martin, Josef Penninger, Louise S. Bicknell, Juergen A. Knoblich, Madeline A. Lancaster and B. Thilaganathan and has published in prestigious journals such as Nature, The Lancet and Circulation.

In The Last Decade

Tessa Homfray

65 papers receiving 5.7k 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.

Cerebral organoids model human brain development and microcephaly

2013 3.6k citations Madeline A. Lancaster, Magdalena Renner 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
Tessa Homfray United Kingdom	25	3.3k	1.3k	1.1k	787	651	69	5.8k
D. Wénzel Germany	19	2.9k 0.9×	1.4k 1.0×	439 0.4×	867 1.1×	441 0.7×	59	4.8k
Miodrag Stojković Germany	58	7.5k 2.2×	878 0.7×	2.2k 2.0×	813 1.0×	467 0.7×	167	11.2k
In‐Hyun Park United States	35	5.8k 1.7×	946 0.7×	1.1k 1.0×	854 1.1×	319 0.5×	89	7.1k
Benjamin Reubinoff Israel	44	7.8k 2.3×	1.3k 1.0×	1.1k 1.0×	1.3k 1.6×	406 0.6×	115	10.1k
Rona S. Carroll United States	52	3.2k 1.0×	654 0.5×	1.2k 1.0×	651 0.8×	1.2k 1.9×	150	7.6k
Carol-Anne Martin United Kingdom	5	3.5k 1.0×	1.3k 1.0×	523 0.5×	747 0.9×	763 1.2×	7	5.2k
Edwin S. Monuki United States	39	2.9k 0.9×	1.0k 0.8×	726 0.7×	1.5k 1.9×	178 0.3×	89	5.6k
Louise S. Bicknell New Zealand	14	2.9k 0.9×	1.3k 1.0×	567 0.5×	751 1.0×	464 0.7×	28	4.3k
In-Hyun Park United States	26	7.0k 2.1×	1.0k 0.8×	838 0.8×	941 1.2×	462 0.7×	32	8.1k
Philip H. Schwartz United States	29	2.1k 0.6×	657 0.5×	699 0.6×	723 0.9×	211 0.3×	78	3.7k

Countries citing papers authored by Tessa Homfray

Since Specialization

Citations

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

Fields of papers citing papers by Tessa Homfray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tessa Homfray

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

Homfray, Tessa, Ranjit Akolekar, Srividhya Sankaran, et al.. (2024). Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort. Prenatal Diagnosis. 45(1). 15–26.

Jokela, Manu, Meriel McEntagart, Tessa Homfray, et al.. (2023). The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum. Journal of Medical Genetics. 60(9). 866–873. 8 indexed citations

Kumar, Ajith, Angela F. Brady, Tessa Homfray, et al.. (2022). Expanding the phenotype of TAB2 variants and literature review. American Journal of Medical Genetics Part A. 188(11). 3331–3342. 6 indexed citations

Eeles, Rosalind A., et al.. (2022). Whole genome germline sequencing: Its role in general health screening in family practice, the first study in the UK.. Journal of Clinical Oncology. 40(16_suppl). 10510–10510.

Hazekamp, Mark G., David J. Barron, Joanna Szymkiewicz–Dangel, et al.. (2021). Consensus document on optimal management of patients with common arterial trunk. Cardiology in the Young. 31(6). 915–939. 2 indexed citations

Homfray, Tessa, et al.. (2020). Fetal hydrops – a review and a clinical approach to identifying the cause. Expert Opinion on Orphan Drugs. 8(2-3). 51–66. 7 indexed citations

Ramachandran, Vijaya, et al.. (2020). Case report: targeted whole exome sequencing enables the first prenatal diagnosis of the lethal skeletal dysplasia Osteocraniostenosis. BMC Medical Genetics. 21(1). 7–7. 7 indexed citations

Robertus, Jan Lukas, et al.. (2020). ATGL Deficiency-Induced Triglyceride Deposit Cardiomyovasculopathy Requiring Heart Transplant. SHILAP Revista de lepidopterología. 2(5). 760–763. 4 indexed citations

Haworth, A., Eva Serra, Janna Kenny, et al.. (2020). A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review. BJOG An International Journal of Obstetrics & Gynaecology. 128(6). 1012–1019. 29 indexed citations

10.

King, Daniel A., Alejandro Sifrim, Tomas Fitzgerald, et al.. (2017). Detection of structural mosaicism from targeted and whole-genome sequencing data. Genome Research. 27(10). 1704–1714. 38 indexed citations

11.

Vigneswaran, Trisha V., Tessa Homfray, Lindsey D. Allan, John Simpson, & Vita Zidere. (2017). Persistently elevated nuchal translucency and the fetal heart. The Journal of Maternal-Fetal & Neonatal Medicine. 31(18). 2376–2380. 8 indexed citations

12.

Rea, Gillian, Tessa Homfray, Jan Till, et al.. (2016). Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11. Molecular Case Studies. 3(1). a001271–a001271. 11 indexed citations

13.

Lancaster, Madeline A., Magdalena Renner, Carol-Anne Martin, et al.. (2013). Cerebral organoids model human brain development and microcephaly. Nature. 501(7467). 373–379. 3647 indexed citations breakdown →

14.

Bhuiyan, Zahurul A., Tarek Momenah, Qiuming Gong, et al.. (2008). Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation. Heart Rhythm. 5(4). 553–561. 47 indexed citations

15.

Lin, Lin, Pascal Philibert, Bruno Ferraz‐de‐Souza, et al.. (2007). Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function. The Journal of Clinical Endocrinology & Metabolism. 92(3). 991–999. 150 indexed citations

16.

Forzano, Francesca, et al.. (2007). Posterior fossa malformation in fetuses: a report of 56 further cases and a review of the literature. Prenatal Diagnosis. 27(6). 495–501. 41 indexed citations

17.

Schwärzler, P., Tessa Homfray, J. P. Bernard, John M. Bland, & Y. Ville. (2003). Late onset microcephaly: failure of prenatal diagnosis. Ultrasound in Obstetrics and Gynecology. 22(6). 640–642. 17 indexed citations

18.

Lees, C., Tessa Homfray, & K. H. Nicolaides. (2001). Prenatal ultrasound diagnosis of Leroy I cell disease. Ultrasound in Obstetrics and Gynecology. 18(3). 275–276. 3 indexed citations

19.

Crosby, Andrew H., Steven Jeffery, Tessa Homfray, Rohan Taylor, & Michael A. Patton. (1999). Prenatal Diagnosis and the Subsequent Mutation Analysis in a Family with Carbohydrate-Deficient Glycoprotein Type I Syndrome: Growing Evidence to Support Founder Effects within CDG1 Populations. Genetic Testing. 3(3). 305–307. 3 indexed citations

20.

Beck, N E, Ian Tomlinson, Tessa Homfray, et al.. (1997). Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas. Gut. 41(2). 235–238. 17 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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