Andrew Green

24.1k total citations · 2 hit papers
226 papers, 8.6k citations indexed

About

Andrew Green is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andrew Green has authored 226 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 57 papers in Genetics and 27 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andrew Green's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (13 papers) and Urological Disorders and Treatments (12 papers). Andrew Green is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (13 papers) and Urological Disorders and Treatments (12 papers). Andrew Green collaborates with scholars based in United Kingdom, Ireland and United States. Andrew Green's co-authors include John R.W. Yates, Alan Wise, Fiona H. Marshall, Steven M. Foord, Piers C. Emson, Neil J. Fraser, Ashley Barnes, Julia H. White, G. H. Disney and Martin J. Main and has published in prestigious journals such as Nature, Science and The Lancet.

In The Last Decade

Andrew Green

214 papers receiving 8.3k 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.

Heterodimerization is required for the formation of a functional GABAB receptor

1998 972 citations Andrew Green et al. profile →
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

2006 518 citations Matthew Greenway, Peter M. Andersen et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew Green United Kingdom	47	3.5k	1.6k	1.5k	951	928	226	8.6k
Philip Thomas United States	71	8.6k 2.4×	2.0k 1.3×	1.5k 1.1×	1.6k 1.7×	638 0.7×	227	16.5k
Ying Xia China	58	3.8k 1.1×	2.1k 1.3×	387 0.3×	1.0k 1.1×	586 0.6×	337	11.4k
Bor Luen Tang Singapore	51	4.5k 1.3×	1.2k 0.8×	567 0.4×	1.4k 1.5×	435 0.5×	242	9.3k
Shigeo Okabe Japan	53	5.1k 1.4×	4.2k 2.6×	706 0.5×	1.2k 1.3×	608 0.7×	211	11.7k
Aaron B. Bowman United States	44	3.1k 0.9×	1.6k 1.0×	563 0.4×	685 0.7×	652 0.7×	150	7.8k
Jane E. Lamerdin United States	29	4.7k 1.3×	863 0.5×	939 0.6×	503 0.5×	382 0.4×	47	7.9k
Yongqing Zhang China	58	5.5k 1.6×	1.2k 0.8×	1.3k 0.9×	960 1.0×	182 0.2×	354	13.2k
Bruce A. Buchholz United States	37	3.5k 1.0×	679 0.4×	769 0.5×	1.7k 1.8×	211 0.2×	123	9.5k
Massimo Gulisano Italy	41	3.7k 1.0×	924 0.6×	1.1k 0.7×	613 0.6×	320 0.3×	206	7.0k
Lucia Migliore Italy	53	3.1k 0.9×	347 0.2×	637 0.4×	976 1.0×	523 0.6×	167	7.5k

Countries citing papers authored by Andrew Green

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Green

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Green

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

Green, Andrew, et al.. (2025). Novel STAG2 variant expands Mullegama-Klein-Martinez Syndrome phenotype. European Journal of Medical Genetics. 76. 105024–105024.

Sarker, Biddut K., Dennis E. Walker, Gary W. Hughes, et al.. (2025). Temperature dependent characterization of 140–180 nm AlGaN/GaN HEMTs using DC and small-signal RF measurements. Applied Physics Letters. 127(8).

Ahmed, Shaikh, Ahmad E. Islam, Daniel M. Dryden, et al.. (2024). Theoretical Power Figure-of-Merit in β -Ga₂O₃ Lateral Power Transistors Determined Using Physics-Based TCAD Simulation. IEEE Transactions on Electron Devices. 71(9). 5305–5312. 3 indexed citations

Sherwood, Kitty, Lynn Martin, Archie Campbell, et al.. (2023). Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair. Nature Communications. 14(1). 3636–3636. 7 indexed citations

Ren, Zhongjie, A F M Anhar Uddin Bhuiyan, Zixuan Feng, et al.. (2022). β-Ga2O3 FinFETs with ultra-low hysteresis by plasma-free metal-assisted chemical etching. Applied Physics Letters. 121(5). 36 indexed citations

Green, Andrew, et al.. (2021). An unusual case of tetralogy of Fallot with an absent pulmonary valve associated with a retro-aortic innominate vein in a patient with a 16p12.2 microdeletion. Cardiology in the Young. 31(5). 836–837. 5 indexed citations

Duignan, Sophie, et al.. (2021). Nicolaides–Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion. Cardiology in the Young. 32(5). 821–823. 3 indexed citations

Green, Andrew. (2020). A tribute to some of the doctors who died from COVID-19. The Lancet. 396(10264). 1720–1729. 7 indexed citations

Darlow, John M., Rebecca Darlay, Mark G. Dobson, et al.. (2017). Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. Scientific Reports. 7(1). 14595–14595. 11 indexed citations

10.

Kagami, Masayo, Maureen J. O’Sullivan, Andrew Green, et al.. (2010). The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers. PLoS Genetics. 6(6). e1000992–e1000992. 174 indexed citations

11.

Rodbard, Helena W., Andrew Green, Kathleen M. Fox, & Susan Grandy. (2010). Impact of type 2 diabetes mellitus on prescription medication burden and out-of-pocket healthcare expenses. Diabetes Research and Clinical Practice. 87(3). 360–365. 29 indexed citations

12.

Pitcher, R. S., Andrew Green, Anna Brzostek, et al.. (2007). NHEJ protects mycobacteria in stationary phase against the harmful effects of desiccation. DNA repair. 6(9). 1271–1276. 73 indexed citations

13.

Doherty, Liam, John Kiely, Paul Deegan, et al.. (2007). Late-onset central hypoventilation syndrome: a family genetic study. European Respiratory Journal. 29(2). 312–316. 38 indexed citations

14.

O’Çonnell, Susan, Kenneth R. Butler, Joe McMenamin, Mary Waldron, & Andrew Green. (2006). Genetic conditions in the Irish Roma gypsy population.. PubMed. 98(10). 246–7. 2 indexed citations

15.

Greenway, Matthew, Peter M. Andersen, Carsten Russ, et al.. (2006). ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. Nature Genetics. 38(4). 411–413. 518 indexed citations breakdown →

16.

Solari, Valeria, Sean Ennis, Akihiro Yoneda, et al.. (2003). Mutation analysis of the RET gene in total intestinal aganglionosis by wave DNA fragment analysis system. Journal of Pediatric Surgery. 38(3). 497–501. 14 indexed citations

17.

Daly, Peter A., Andrew Green, W. Ormiston, et al.. (2003). Predictive testing for BRCA1 and 2 mutations: a male contribution. Annals of Oncology. 14(4). 549–553. 32 indexed citations

18.

Maselli, Ricardo A., Jonathan B. Jaspan, Betty Soliven, et al.. (1989). Comparison of sympathetic skin response with quantitative sudomotor axon reflex test in diabetic neuropathy. Muscle & Nerve. 12(5). 420–423. 66 indexed citations

19.

O’Meara, Yvonne, Andrew Green, M. Carmody, et al.. (1989). Recurrent Glomerulonephritis in Renal Transplants: Fourteen Years' Experience. Nephrology Dialysis Transplantation. 4(8). 730–734. 54 indexed citations

20.

Green, Andrew. (1962). Drugs and Foetal Abnormalities. BMJ. 2(5301). 407.1–407. 1 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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