Karen David

1.1k total citations
9 papers, 183 citations indexed

About

Karen David is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Karen David has authored 9 papers receiving a total of 183 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Surgery. Recurrent topics in Karen David's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Congenital Anomalies and Fetal Surgery (2 papers). Karen David is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Congenital Anomalies and Fetal Surgery (2 papers). Karen David collaborates with scholars based in United States and South Korea. Karen David's co-authors include Kurt Hirschhorn, Sara Kaffe, Lillian Y. F. Hsu, Lawrence R. Shapiro, Edmund C. Jenkins, Ernest Lieber, Dorothy Warburton, Alan Shanske, Peter Benn and Ralph E. Moloshok and has published in prestigious journals such as The Lancet, Journal of Medical Genetics and Pediatric Research.

In The Last Decade

Karen David

8 papers receiving 165 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karen David United States 6 130 105 44 42 38 9 183
Françoise Girard‐Lemaire France 8 140 1.1× 98 0.9× 31 0.7× 81 1.9× 21 0.6× 12 194
Marijo Kent United States 7 87 0.7× 48 0.5× 18 0.4× 43 1.0× 27 0.7× 9 165
Chen‐Chi Lee Taiwan 11 230 1.8× 183 1.7× 40 0.9× 69 1.6× 62 1.6× 23 270
Rhonda Spiro United States 8 249 1.9× 120 1.1× 41 0.9× 120 2.9× 38 1.0× 8 286
G. Nocera Italy 6 72 0.6× 85 0.8× 30 0.7× 39 0.9× 18 0.5× 11 152
L Zergollern Croatia 6 95 0.7× 39 0.4× 14 0.3× 44 1.0× 30 0.8× 25 143
L. Memo Italy 7 150 1.2× 77 0.7× 15 0.3× 131 3.1× 60 1.6× 11 241
J. Lespinasse France 12 195 1.5× 162 1.5× 16 0.4× 69 1.6× 108 2.8× 25 310
Céline Pebrel‐Richard France 7 91 0.7× 39 0.4× 26 0.6× 69 1.6× 20 0.5× 20 138
David M. deKretser Australia 6 133 1.0× 34 0.3× 28 0.6× 117 2.8× 19 0.5× 10 278

Countries citing papers authored by Karen David

Since Specialization
Citations

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

Fields of papers citing papers by Karen David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen David

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

All Works

9 of 9 papers shown
1.
David, Karen, et al.. (1993). Prenatal Diagnosis of a Neurenteric Cyst by Magnetic Resonance Imaging. American Journal of Perinatology. 10(4). 304–306. 19 indexed citations
2.
Hsu, Lillian Y. F., Sara Kaffe, Edmund C. Jenkins, et al.. (1992). Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenatal Diagnosis. 12(7). 555–573. 105 indexed citations
3.
Greig, Fenella, et al.. (1985). Duplication 11 (q22----qter) in an infant. A case report with review.. PubMed. 28(3). 185–8. 10 indexed citations
4.
Hsu, L Y, et al.. (1978). Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism. Journal of Medical Genetics. 15(3). 222–226. 22 indexed citations
5.
David, Karen, et al.. (1978). Prenatal diagnosis of 5p‐. Clinical Genetics. 13(2). 224–228. 4 indexed citations
6.
Hsu, Lillian Y. F., Sara Kaffe, Lynn Godmilow, et al.. (1978). Prenatal cytogenetic diagnosis: First 1,000 successful cases. American Journal of Medical Genetics. 2(4). 365–383. 15 indexed citations
7.
David, Karen, et al.. (1977). MONOSOMY“ RE-EVALUATED. Pediatric Research. 11(4). 454–454. 1 indexed citations
8.
David, Karen, et al.. (1977). THE NUMBER OF C-BANDS OF HUMAN ISOCHROMOSOME Xqi AND THEIR REIATIONSHIP TO 45,X MOSAICISM. Pediatric Research. 11(4). 457–457. 6 indexed citations
9.
David, Karen, et al.. (1976). IDENTIFICATION OF MACROPHAGES IN AMNIOTIC-FLUID CELL CULTURES. The Lancet. 307(7973). 1349–1349. 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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