David Millar

7.0k total citations · 2 hit papers
60 papers, 4.8k citations indexed

About

David Millar is a scholar working on Pulmonary and Respiratory Medicine, Hematology and Surgery. According to data from OpenAlex, David Millar has authored 60 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Pulmonary and Respiratory Medicine, 21 papers in Hematology and 12 papers in Surgery. Recurrent topics in David Millar's work include Neonatal Respiratory Health Research (18 papers), Blood Coagulation and Thrombosis Mechanisms (13 papers) and Hemophilia Treatment and Research (12 papers). David Millar is often cited by papers focused on Neonatal Respiratory Health Research (18 papers), Blood Coagulation and Thrombosis Mechanisms (13 papers) and Hemophilia Treatment and Research (12 papers). David Millar collaborates with scholars based in United Kingdom, United States and Canada. David Millar's co-authors include Fujiko Watt, Marianne Frommer, Cheryl Paul, Christina M. Collis, Peter L. Molloy, G. W. GRIGG, D.N. Cooper, Haresh Kirpalani, Clare Stirzaker and P. Warnecke and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

David Millar

58 papers receiving 4.7k 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.

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands.

1992 2.4k citations David Millar et al. profile →
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting

2020 410 citations Peter D. Stenson, Matthew Mort et al. Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Millar United Kingdom	24	3.1k	992	809	617	355	60	4.8k
Christos Kittas Greece	40	3.3k 1.1×	557 0.6×	255 0.3×	586 0.9×	783 2.2×	202	6.7k
M Massobrio Italy	43	1.5k 0.5×	799 0.8×	427 0.5×	498 0.8×	697 2.0×	185	8.1k
William A. Pastor United States	29	7.9k 2.6×	1.5k 1.6×	484 0.6×	244 0.4×	670 1.9×	59	9.1k
Christopher I. Amos United States	42	2.2k 0.7×	1.8k 1.8×	138 0.2×	510 0.8×	682 1.9×	101	6.1k
Torben A. Kruse Denmark	39	2.7k 0.9×	1.1k 1.1×	441 0.5×	313 0.5×	979 2.8×	214	5.2k
Yehudit Bergman Israel	38	6.3k 2.1×	1.5k 1.5×	197 0.2×	227 0.4×	845 2.4×	73	7.9k
Hideo Hamaguchi Japan	34	1.1k 0.4×	634 0.6×	294 0.4×	229 0.4×	242 0.7×	155	4.3k
François Fuks Belgium	42	9.4k 3.1×	2.1k 2.1×	695 0.9×	438 0.7×	1.6k 4.5×	83	11.0k
Jaroslav Jelı́nek United States	49	5.8k 1.9×	980 1.0×	2.3k 2.8×	715 1.2×	1.3k 3.7×	159	8.3k
Shinsuke Ito Japan	20	6.7k 2.2×	1.2k 1.3×	340 0.4×	184 0.3×	638 1.8×	33	7.3k

Countries citing papers authored by David Millar

Since Specialization

Citations

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

Fields of papers citing papers by David Millar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Millar

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

Stenson, Peter D., Matthew Mort, Edward V. Ball, et al.. (2020). The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting. Human Genetics. 139(10). 1197–1207. 410 indexed citations breakdown →

Waite, Adrian J., David Millar, & Angus Clarke. (2020). The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 gene. Stem Cell Research. 49. 102018–102018. 1 indexed citations

Bamat, Nicolas A., James P. Guevara, Matthew Bryan, et al.. (2017). Variation in Positive End-Expiratory Pressure Levels for Mechanically Ventilated Extremely Low Birth Weight Infants. The Journal of Pediatrics. 194. 28–33.e5. 8 indexed citations

Seligsohn, Uri, R.S. Mibashan, C. H. Rodeck, et al.. (2015). Prevention Program of Type I Glanzmann Thrombasthenia in Israel: Prenatal Diagnosis. Current studies in hematology and blood transfusion. 174–179.

DeMauro, Sara B., David Millar, & Haresh Kirpalani. (2014). Noninvasive respiratory support for neonates. Current Opinion in Pediatrics. 26(2). 157–162. 36 indexed citations

Murgiano, Leonardo, David Millar, Elise Glen, et al.. (2013). A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti. PLoS ONE. 8(12). e81625–e81625. 11 indexed citations

Kirpalani, Haresh, David Millar, Brigitte Lemyre, et al.. (2013). A Trial Comparing Noninvasive Ventilation Strategies in Preterm Infants. New England Journal of Medicine. 369(7). 611–620. 169 indexed citations

Millar, David, Martin Horan, Nadia Chuzhanova, & D.N. Cooper. (2010). Characterisation of a functional intronic polymorphism in the human growth hormone (GHI) gene. Human Genomics. 4(5). 289–289. 42 indexed citations

Millar, David, Mark Lewis, Martin Horan, et al.. (2008). Growth hormone (GH1) gene variation and the growth hormone receptor (GHR) exon 3 deletion polymorphism in a West-African population. Molecular and Cellular Endocrinology. 296(1-2). 18–25. 11 indexed citations

10.

Dolovich, Myrna, et al.. (2005). LUNG DEPOSITION OF QVAR (HFA134A-BDP) IN NEWBORN INFANTS WITH BRONCHOPULMONARY DYSPLASIA (BPD). CHEST Journal. 128(4). 351S–351S. 2 indexed citations

11.

Horan, Martin, David Millar, Jürgen Hedderich, et al.. (2003). Human growth hormone 1 (GH1) gene expression: Complex haplotype-dependent influence of polymorphic variation in the proximal promoter and locus control region. Human Mutation. 21(4). 408–423. 88 indexed citations

12.

Ariffin, Hany, et al.. (2003). Prenatal Exclusion of Severe Factor VII Deficiency. Journal of Pediatric Hematology/Oncology. 25(5). 418–420. 9 indexed citations

13.

Warnecke, P., et al.. (1997). Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA. Nucleic Acids Research. 25(21). 4422–4426. 307 indexed citations

14.

Tuddenham, Edward G. D., R. Schwaab, David Millar, et al.. (1994). Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Research. 22(22). 4851–4868. 42 indexed citations

15.

Millar, David, et al.. (1993). A novel point mutation (Val 297???Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic disease. Blood Coagulation & Fibrinolysis. 4(4). 631–634. 4 indexed citations

16.

Grundy, C, et al.. (1992). A novel missense mutation in the antithrombin III gene (Ser349→Pro) causing recurrent venous thrombosis. Human Genetics. 88(6). 707–708. 7 indexed citations

17.

Millar, David, et al.. (1991). Carrier detection in haemophilia A by direct analysis of factor VIII gene lesions. Human Genetics. 87(1). 99–100. 1 indexed citations

18.

Jedlička, Pavel, Steven Greer, David Millar, et al.. (1990). Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus. Human Genetics. 85(3). 315–8. 2 indexed citations

19.

Nicolaides, K. H., Charles H. Rodeck, David Millar, & R.S. Mibashan. (1985). Fetal haematology in rhesus isoimmunisation.. BMJ. 290(6469). 661–663. 31 indexed citations

20.

Millar, David, et al.. (1983). FETAL HAEMOPHILIA AND ALLIED BLEEDING DISORDERS. British Medical Bulletin. 39(4). 392–398. 4 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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