David C. Ward

1.5k total citations · 1 hit paper
19 papers, 1.3k citations indexed

About

David C. Ward is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, David C. Ward has authored 19 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in David C. Ward's work include DNA Repair Mechanisms (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Congenital heart defects research (2 papers). David C. Ward is often cited by papers focused on DNA Repair Mechanisms (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Congenital heart defects research (2 papers). David C. Ward collaborates with scholars based in United States, India and Canada. David C. Ward's co-authors include D. Gary Gilliland, G. F. Barker, Scott W. Hiebert, Elaine Morgan, Susana C. Raimondi, Stefan K. Bohlander, Janet D. Rowley, Patricia Bray‐Ward, Todd R. Golub and Joan C. Menninger and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Immunology.

In The Last Decade

David C. Ward

19 papers receiving 1.2k citations

Hit Papers

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22... 1995 2026 2005 2015 1995 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David C. Ward United States 15 805 402 268 267 120 19 1.3k
Ellen Magenis United States 18 694 0.9× 215 0.5× 141 0.5× 815 3.1× 101 0.8× 31 1.4k
Sandra Ruf Germany 14 1.1k 1.4× 163 0.4× 185 0.7× 397 1.5× 40 0.3× 20 1.8k
Sylvie Taviaux France 21 992 1.2× 152 0.4× 55 0.2× 312 1.2× 237 2.0× 42 1.5k
Reinhard Grausenburger Austria 14 702 0.9× 195 0.5× 207 0.8× 92 0.3× 106 0.9× 25 1.1k
Jayne Y. Hehir‐Kwa Netherlands 24 854 1.1× 218 0.5× 262 1.0× 1.1k 4.1× 49 0.4× 53 1.9k
Marguerite Prieur France 22 789 1.0× 85 0.2× 295 1.1× 740 2.8× 23 0.2× 33 1.5k
Joseph C. Giacalone United States 19 1.3k 1.6× 59 0.1× 79 0.3× 463 1.7× 149 1.2× 37 1.7k
Gordana Raca United States 18 586 0.7× 138 0.3× 133 0.5× 1.1k 4.0× 37 0.3× 62 1.7k
Dominick Amato Canada 16 341 0.4× 275 0.7× 51 0.2× 128 0.5× 109 0.9× 42 1.1k
Udo Trautmann Germany 23 930 1.2× 94 0.2× 80 0.3× 1.1k 3.9× 31 0.3× 65 1.7k

Countries citing papers authored by David C. Ward

Since Specialization
Citations

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

Fields of papers citing papers by David C. Ward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David C. Ward

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

All Works

19 of 19 papers shown
1.
Ghosh, Bidyut, Harris C. Jacobs, Leanne M. Wiedemann, et al.. (1999). Genomic structure, cDNA mapping, and chromosomal localization of the mouse homeobox gene, Hex. Mammalian Genome. 10(10). 1023–1025. 13 indexed citations
2.
Ward, David C., et al.. (1999). Genetics of Childhood Disorders: VI. FISH, FISH, and More FISH. Journal of the American Academy of Child & Adolescent Psychiatry. 38(9). 1200–1202. 2 indexed citations
3.
Thomson, R. Brent, et al.. (1998). cDNA Cloning and Chromosomal Localization of the Human and Mouse Isoforms of Ksp-Cadherin. Genomics. 51(3). 445–451. 38 indexed citations
4.
Sirugo, Giorgio, et al.. (1996). Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization. Nature Genetics. 12(2). 183–185. 30 indexed citations
5.
Golub, Todd R., G. F. Barker, Stefan K. Bohlander, et al.. (1995). Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.. Proceedings of the National Academy of Sciences. 92(11). 4917–4921. 604 indexed citations breakdown →
6.
Haaf, Thomas & David C. Ward. (1994). High resolution ordering of YAC contigs using extended chromatin and chromosomes. Human Molecular Genetics. 3(4). 629–633. 50 indexed citations
7.
Chai, Karl X., David C. Ward, Julie Chao, & Lee Chao. (1994). Molecular Cloning, Sequence Analysis, and Chromosomal Localization of the Human Protease Inhibitor 4 (Kallistatin) Gene (PI4). Genomics. 23(2). 370–378. 25 indexed citations
8.
Narayan, Deepak, Trushna Desai, Amy Banks, et al.. (1994). Localization of the Human Cytoplasmic Dynein Heavy Chain (DNECL) to 14qter by Fluorescence in Situ Hybridization. Genomics. 22(3). 660–661. 9 indexed citations
9.
Lu-Kuo, Jennifer M., David C. Ward, & Richard A. Spritz. (1993). Fluorescence in Situ Hybridization Mapping of 25 Markers on Distal Human Chromosome 2q Surrounding the Human Waardenburg Syndrome, Type I (WS1) Locus (PAX3 Gene). Genomics. 16(1). 173–179. 32 indexed citations
10.
Ried, Thomas, et al.. (1993). Localization of a Highly Conserved Human Potassium Channel Gene (NGK2-KV4; KCNC1) to Chromosome 11p15. Genomics. 15(2). 405–411. 30 indexed citations
11.
Wilson, Gaye Lynn, et al.. (1993). Genomic structure and chromosomal mapping of the human CD22 gene. The Journal of Immunology. 150(11). 5013–5024. 45 indexed citations
12.
Stallings, R. L., Norman A. Doggett, Katsuzumi Okumura, & David C. Ward. (1992). Chromosome 16-specific repetitive DNA sequences that map to chromosomal regions known to undergo breakage/ rearrangement in leukemia cells. Genomics. 13(2). 332–338. 22 indexed citations
13.
Harrison, Lynn, et al.. (1992). Human apurinic endonuclease gene (APE): structure and genomic mapping (chromosome 1 4q11.2 - 12). Human Molecular Genetics. 1(9). 677–680. 25 indexed citations
15.
Wagstaff, John, Joan H.M. Knoll, J Fleming, et al.. (1991). Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.. PubMed. 49(2). 330–7. 155 indexed citations
16.
Rudy, Bernardo, Kikuo Sen, Eleazar Vega‐Saenz de Miera, et al.. (1991). Cloning of a human cDNA expressing a high voltage‐activating. Tea‐sensitive, type‐a K+ channel which maps to chromosome 1 band p21. Journal of Neuroscience Research. 29(3). 401–412. 56 indexed citations
17.
Boyce, Frederick M., Patrick W. Kleyn, Linda M. Brzustowicz, et al.. (1991). Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.. Proceedings of the National Academy of Sciences. 88(17). 7873–7876. 43 indexed citations
18.
Wilson, John T., et al.. (1985). Use of biotinylated probes for detecting sickle cell anemia.. PubMed. 31(7). 1203–6. 12 indexed citations
19.
McFarland, Ross A., et al.. (1960). Dark Adaptation as a Function of Age: I. A Statistical Analysis. Journal of Gerontology. 15(2). 149–154. 65 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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