David Millar

7.0k citations

60 papers · 4.8k indexed · 2 hit papers · h-index 24

Impact in

Hematology top 1%
- Blood Coagulation and Thrombosis Mechanisms
- Hemophilia Treatment and Research
Molecular Biology top 2%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics

Papers in ⓘ

Pulmonary and Respiratory Medicine 25
- Neonatal Respiratory Health Research 18
- Respiratory Support and Mechanisms 11
Hematology 21
- Blood Coagulation and Thrombosis Mechanisms 13
- Hemophilia Treatment and Research 12

Co-authors: Marianne Frommer (1 shared paper)Cheryl Paul (1 shared paper)Fujiko Watt (1 shared paper)Christina M. Collis (1 shared paper)G. W. GRIGG (1 shared paper)Peter L. Molloy (1 shared paper)D.N. Cooper (24 shared papers)Haresh Kirpalani (15 shared papers)
Journals: Human Genetics (11 papers)Cochrane Database of Systematic Reviews (5 papers)Thrombosis and Haemostasis (4 papers)Nucleic Acids Research (3 papers)The Journal of Pediatrics (2 papers)
Partner nations: United Kingdom United States Canada

In The Last Decade

David Millar

58 papers receiving 4.7k citations

Hit Papers

align trajectories log scale

The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting 2020 · 410 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2020 Human Genetics
1992 Proceedings of the National Academy of Sciences

Peers

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-authors

The 25 scholars most cited alongside David Millar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Millar Line = papers co-authored together David Millar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 60 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proceedings of the National Academy of Sciences ·Marianne Frommer, Louise E. McDonald, David Millar, Christina M. Collis, Fujiko Watt, G. W. GRIGG, Peter L. Molloy, Cheryl Paul Hit paper breakdown →	1992	2449
2	The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting Human Genetics ·Peter D. Stenson, Matthew Mort, Edward V. Ball, Molly Chapman, Katy Evans, Luı́sa Azevedo, Matthew Hayden, Sally Heywood, David Millar, Andrew D. Phillips, D.N. Cooper Hit paper breakdown →	2020	410
3	Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA Nucleic Acids Research ·P. Warnecke, Clare Stirzaker, J R Melki, David Millar, Christine Paul, Susan J. Clark	1997	307
4	Antithrombin Mutation Database: 2nd (1997) Update Thrombosis and Haemostasis ·David A. Lane, Trevor A. Bayston, R.J. Olds, Alison Fitches, D.N. Cooper, David Millar, Kristin Jochmans, David J. Perry, Kenji Okajima, Swee Lay Thein, Joseph Emmerich	1997	193
5	A Trial Comparing Noninvasive Ventilation Strategies in Preterm Infants New England Journal of Medicine ·Haresh Kirpalani, David Millar, Brigitte Lemyre, Bradley A. Yoder, Aaron Chiu, Robin S. Roberts	2013	169
6	Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition Nucleic Acids Research ·Edward G. D. Tuddenham, R. Schwaab, J. Seehafer, David Millar, Jane Gitschier, Miyoko Higuchi, Sanjay I. Bidichandani, J. M. Connor, Leon W. Hoyer, Akira Yoshioka, I R Peake, K. Olek, H H Kazazian, J. M. Lavergne, F. Giannelli, Stylianos E. Antonarakis, D.N. Cooper	1994	120
7	Inherited Factor VII Deficiency: Molecular Genetics and Pathophysiology Thrombosis and Haemostasis ·D.N. Cooper, David Millar, Adam Wacey, David W. Banner, Edward G. D. Tuddenham	1997	115
8	Molecular analysis of the genotype-phenotype relationship in factor X deficiency Human Genetics ·David Millar, Linda Elliston, P. Deex, Michael Krawczak, A. I. Wacey, J. Reynaud, H. Karel Nieuwenhuis, Paula Bolton‐Maggs, P. M. Mannucci, Joan Carles Reverter, P G Cachia, John Pasi, D. Mark Layton, D.N. Cooper	2000	105
9	Human growth hormone 1 (GH1) gene expression: Complex haplotype-dependent influence of polymorphic variation in the proximal promoter and locus control region Human Mutation ·Martin Horan, David Millar, Jürgen Hedderich, Geraint F. Lewis, Vicky Newsway, Neil Mo, Linda Fryklund, Annie Procter, Michael Krawczak, D.N. Cooper	2003	88
10	Glycosylation of Threonine of the Repeating Unit of RNA Polymerase II with β-Linked N-Acetylglucosame Leads to a Turnlike Structure Journal of the American Chemical Society ·Eric E. Simanek, Dee‐Hua Huang, Laura B. Pasternack, Timothy Machajewski, Oliver Seitz, David Millar, H. Jane Dyson, Chi‐Huey Wong	1998	61
11	Inherited Factor X Deficiency: Molecular Genetics and Pathophysiology Thrombosis and Haemostasis ·D.N. Cooper, David Millar, Adam Wacey, Susan Pemberton, Edward G. D. Tuddenham	1997	50
12	Evidence-Based Neonatal Drug Therapy for Prevention of Bronchopulmonary Dysplasia in Very-Low-Birth-Weight Infants Neonatology ·Barbara Schmidt, Robin Roberts, David Millar, Haresh Kirpalani	2008	43
13	Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition Nucleic Acids Research ·Edward G. D. Tuddenham, R. Schwaab, J. Seehafer, David Millar, Jane Gitschier, Miyoko Higuchi, S. Bidichandani, J.M. Connor, Leon W. Hoyer, A. Yoshioka, I R Peake, K. Olek, H H Kazazian, J. M. Lavergne, F. Giannelli, Stylianos E. Antonarakis, D.N. Cooper	1994	42
14	Characterisation of a functional intronic polymorphism in the human growth hormone (GHI) gene Human Genomics ·David Millar, Martin Horan, Nadia Chuzhanova, D.N. Cooper	2010	42
15	NTNG1 mutations are a rare cause of Rett syndrome American Journal of Medical Genetics Part A ·Hayley Archer, Julie Evans, David Millar, Peter Thompson, Alison Kerr, Helen Leonard, John Christodoulou, David Ravine, L. Lazarou, Lucy Grove, Christopher Verity, Sharon D. Whatley, Daniela T. Pilz, Julian R. Sampson, Angus Clarke	2006	38
16	Noninvasive respiratory support for neonates Current Opinion in Pediatrics ·Sara B. DeMauro, David Millar, Haresh Kirpalani	2014	36
17	Normal blood cell values in the early mid‐trimester fetus Prenatal Diagnosis ·David Millar, L. R. Davis, Charles H. Rodeck, K. H. Nicolaides, R.S. Mibashan	1985	35
18	The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene Human Genetics ·David Millar, Ricarda A. Steinbrecher, Kerstin Wieland, C Grundy, U. Martinowitz, Michael Krawczak, Barbara Zoll, D. H. Whitmore, J Stephenson, R.S. Mibashan, V V Kakkar, D.N. Cooper	1990	34
19	PRENATAL DIAGNOSIS OF GLANZMANN'S THROMBASTHENIA The Lancet ·Uri Seligsohn, R.S. Mibashan, Charles H. Rodeck, K. H. Nicolaides, David Millar, BS Coller	1985	32
20	Fetal haematology in rhesus isoimmunisation. BMJ ·K. H. Nicolaides, Charles H. Rodeck, David Millar, R.S. Mibashan	1985	31

About David Millar

David Millar is a scholar working on Pulmonary and Respiratory Medicine, Hematology, Surgery, Molecular Biology and Genetics, having authored 60 papers that have together received 4.8k indexed citations. Recurring topics across this work include Neonatal Respiratory Health Research (18 papers), Blood Coagulation and Thrombosis Mechanisms (13 papers), Hemophilia Treatment and Research (12 papers), Respiratory Support and Mechanisms (11 papers), Congenital Diaphragmatic Hernia Studies (10 papers), Cancer-related gene regulation (7 papers), Genetic Syndromes and Imprinting (5 papers) and Neuroscience of respiration and sleep (5 papers). The work is most often cited by research in Hematology (809 citations), Molecular Biology (3.1k citations), Genetics (992 citations), Internal Medicine (129 citations) and Endocrine and Autonomic Systems (208 citations). David Millar has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Marianne Frommer, Cheryl Paul, Fujiko Watt, Christina M. Collis, G. W. GRIGG, Peter L. Molloy, D.N. Cooper, Haresh Kirpalani, Christine Paul and P. Warnecke. Their work appears in journals such as Human Genetics, Cochrane Database of Systematic Reviews, Thrombosis and Haemostasis, Nucleic Acids Research and The Journal of Pediatrics.

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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