D. David

2.6k total citations
53 papers, 1.7k citations indexed

About

D. David is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, D. David has authored 53 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Genetics and 14 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in D. David's work include Hemophilia Treatment and Research (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Cancer-related gene regulation (7 papers). D. David is often cited by papers focused on Hemophilia Treatment and Research (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Cancer-related gene regulation (7 papers). D. David collaborates with scholars based in Portugal, United States and Mozambique. D. David's co-authors include Ilan Kutz, Katia Dayan, Simcha Meisel, Yaron Arbel, Thomas A. Mellman, Maria Guida Boavida, Beatrice Nolan, Andreas Gal, Masahito Naito and Eric L. Michelson and has published in prestigious journals such as The Lancet, Circulation and Nature Genetics.

In The Last Decade

D. David

51 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. David Portugal 17 594 478 292 200 164 53 1.7k
José Luís Carrasco Spain 26 419 0.7× 294 0.6× 97 0.3× 94 0.5× 607 3.7× 127 2.2k
M. Heras Spain 20 677 1.1× 78 0.2× 72 0.2× 106 0.5× 194 1.2× 57 1.6k
Christopher W. Smith United Kingdom 19 116 0.2× 253 0.5× 71 0.2× 47 0.2× 197 1.2× 36 1.4k
Markus Kraemer Germany 27 104 0.2× 171 0.4× 127 0.4× 55 0.3× 175 1.1× 89 2.3k
Jan Aarseth Norway 27 96 0.2× 183 0.4× 72 0.2× 59 0.3× 75 0.5× 66 2.1k
J. C. Christian United States 25 324 0.5× 514 1.1× 521 1.8× 26 0.1× 40 0.2× 52 2.0k
Grace S. Lee United States 22 66 0.1× 531 1.1× 73 0.3× 101 0.5× 48 0.3× 67 1.6k
Bernhard Saller Germany 32 222 0.4× 460 1.0× 371 1.3× 81 0.4× 67 0.4× 95 3.2k
John B. Walker Canada 13 142 0.2× 154 0.3× 82 0.3× 37 0.2× 262 1.6× 21 1.6k
Cavit Boz Türkiye 21 245 0.4× 110 0.2× 23 0.1× 141 0.7× 91 0.6× 75 1.4k

Countries citing papers authored by D. David

Since Specialization
Citations

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

Fields of papers citing papers by D. David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. David

This figure shows the co-authorship network connecting the top 25 collaborators of D. David. A scholar is included among the top collaborators of D. David 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 D. David. D. David is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Marques, Bárbara, et al.. (2021). SVInterpreter: A Comprehensive Topologically Associated Domain-Based Clinical Outcome Prediction Tool for Balanced and Unbalanced Structural Variants. Frontiers in Genetics. 12. 757170–757170. 6 indexed citations
3.
4.
Lengyel, Anna, Henriett Pikó, D. David, et al.. (2020). Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature. European Journal of Medical Genetics. 63(10). 104027–104027. 5 indexed citations
5.
David, D., Deepti Anand, Brian Gloss, et al.. (2018). Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentis. Experimental Eye Research. 168. 161–170. 5 indexed citations
6.
Hadzsiev, Kinga, D. David, Gyula Szabó, et al.. (2014). Partial Trisomy of the Pericentromeric Region of Chromosome 5 in a Girl with Binder Phenotype. Cytogenetic and Genome Research. 144(3). 190–195. 14 indexed citations
7.
David, D., Bárbara Marques, Cristina Ferreira, et al.. (2009). Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1–q14.2. European Journal of Human Genetics. 17(8). 1024–1033. 14 indexed citations
8.
David, D., Célia Ventura, Margarida Maria de Castro Antunes, et al.. (2006). The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patients.. PubMed. 91(6). 840–3. 25 indexed citations
9.
Shukla, Sandeep Kumar, Elizabeth McPherson, Nader Ghebranious, et al.. (2005). An analysis of PAX1 in the development of vertebral malformations. Clinical Genetics. 68(5). 448–453. 45 indexed citations
10.
David, D., et al.. (2003). Analysis of the consequences of premature termination codons within factor VIII coding sequences. Journal of Thrombosis and Haemostasis. 1(1). 139–146. 13 indexed citations
11.
David, D., Joana Cardoso, Bárbara Marques, et al.. (2003). Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGFβ2 in the pathogenesis of Peters’ anomaly. Genomics. 81(5). 489–503. 29 indexed citations
12.
David, D., Evgueni L. Saenko, Daniel J. D. Johnson, et al.. (2001). Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM−) and G1948D (CRMr). British Journal of Haematology. 113(3). 604–615. 8 indexed citations
13.
Araújo, Fernando, et al.. (1999). Genetic Risk Factors in Acute Coronary Disease. Pathophysiology of Haemostasis and Thrombosis. 29(4). 212–218. 23 indexed citations
14.
David, D., et al.. (1998). Five novel factor IX mutations in unrelated hemophilia B patients. Human Mutation. 11(S1). S301–S303. 2 indexed citations
15.
David, D., Ulrike Orth, H. Heilbronner, & Andreas Gal. (1996). A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndrome. Human Mutation. 7(2). 181–182. 3 indexed citations
16.
Karin, J., et al.. (1996). The effects of lidocaine on cardiac parasympathetic control in normal subjects and in subjects after myocardial infarction. Clinical Autonomic Research. 6(6). 313–319. 5 indexed citations
17.
David, D., M. R. A. LALLOZ, R. Schwaab, et al.. (1994). Analysis of the essential sequences of the factor VIII gene in twelve haemophilia A patients by single-stranded conformation polymorphism. Blood Coagulation & Fibrinolysis. 5(2). 257–264. 29 indexed citations
18.
David, D., et al.. (1993). Single-strand conformation polymorphism (SSCP) analysis of the molecular pathology of hemophilia B. Human Mutation. 2(5). 355–361. 10 indexed citations
19.
Meisel, Simcha, et al.. (1991). Effect of Iraqi missile war on incidence of acute myocardial infarction and sudden death in Israeli civilians. The Lancet. 338(8768). 660–661. 293 indexed citations
20.
Hasin, Yonathan, D. David, & S. Rogel. (1976). Diagnostic and therapeutic assessment by telephone electrocardiographic monitoring of ambulatory patients.. BMJ. 2(6036). 609–612. 31 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by José Luís Carrasco Breakdown of academic impact, for papers by M. Heras Breakdown of academic impact, for papers by Christopher W. Smith Breakdown of academic impact, for papers by Markus Kraemer Breakdown of academic impact, for papers by Jan Aarseth Breakdown of academic impact, for papers by J. C. Christian Breakdown of academic impact, for papers by Grace S. Lee Breakdown of academic impact, for papers by Bernhard Saller Breakdown of academic impact, for papers by John B. Walker Breakdown of academic impact, for papers by Cavit Boz
Rankless by CCL
2026