Karen L. David

2.0k total citations
14 papers, 899 citations indexed

About

Karen L. David is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karen L. David has authored 14 papers receiving a total of 899 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karen L. David's work include BRCA gene mutations in cancer (3 papers), Ethics and Legal Issues in Pediatric Healthcare (3 papers) and Genomics and Rare Diseases (2 papers). Karen L. David is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Ethics and Legal Issues in Pediatric Healthcare (3 papers) and Genomics and Rare Diseases (2 papers). Karen L. David collaborates with scholars based in United States, Belgium and Israel. Karen L. David's co-authors include Howard M. Saal, L. F. Ross, Rebecca Rae Anderson, Carolyn M. Wilson, Catherine Rehder, Hutton M. Kearney, Helga V. Toriello, Betsy Hirsch, Graciela Moya and Nicole Van Regemorter and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Urology and Journal of Medical Genetics.

In The Last Decade

Karen L. David

14 papers receiving 863 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karen L. David United States	12	491	263	226	127	78	14	899
Florence Fellmann Switzerland	18	691 1.4×	417 1.6×	188 0.8×	227 1.8×	28 0.4×	54	1.4k
Siddharth Banka United Kingdom	18	480 1.0×	339 1.3×	69 0.3×	59 0.5×	34 0.4×	55	991
Ivan Macciocca Australia	16	319 0.6×	211 0.8×	80 0.4×	66 0.5×	47 0.6×	36	928
Jodi D. Hoffman United States	18	365 0.7×	215 0.8×	119 0.5×	48 0.4×	15 0.2×	33	654
Christine M. Armour Canada	20	435 0.9×	340 1.3×	358 1.6×	86 0.7×	9 0.1×	52	923
Richard H. Scott United Kingdom	21	676 1.4×	760 2.9×	363 1.6×	89 0.7×	13 0.2×	42	1.5k
Tanya N. Nelson Canada	21	450 0.9×	308 1.2×	276 1.2×	126 1.0×	6 0.1×	51	1.0k
Amanda L. Bergner United States	14	227 0.5×	101 0.4×	70 0.3×	63 0.5×	21 0.3×	32	640
Maria Cristina Rosatelli Italy	30	472 1.0×	425 1.6×	665 2.9×	58 0.5×	16 0.2×	105	2.4k
Sophia B. Hufnagel United States	6	805 1.6×	286 1.1×	142 0.6×	169 1.3×	14 0.2×	6	1.1k

Countries citing papers authored by Karen L. David

Since Specialization

Citations

This map shows the geographic impact of Karen L. 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 L. 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 L. David more than expected).

Fields of papers citing papers by Karen L. David

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen L. David

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

All Works

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14 of 14 papers shown

David, Karen L., Robert G. Best, Joshua L. Deignan, et al.. (2018). Patient re-contact after revision of genomic test results: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 21(4). 769–771. 85 indexed citations

Bartoshesky, Louis, et al.. (2018). Pediatric clinical exome/genome sequencing and the engagement process: encouraging active conversation with the older child and adolescent: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(7). 692–694. 26 indexed citations

Hardee, Isabel, Ariane Soldatos, Mariska Davids, et al.. (2017). Defective ciliogenesis in INPP5E‐related Joubert syndrome. American Journal of Medical Genetics Part A. 173(12). 3231–3237. 19 indexed citations

David, Karen L., et al.. (2016). Alacrima as a Harbinger of Adrenal Insufficiency in a Child with Allgrove (AAA) Syndrome. American Journal of Case Reports. 17. 703–706. 20 indexed citations

Leung, Samuel, et al.. (2016). A Case of Beare-Stevenson Syndrome with Unusual Manifestations. American Journal of Case Reports. 17. 254–258. 4 indexed citations

Wentzensen, Ingrid M., Jennifer J. Johnston, Kim M. Keppler‐Noreuil, et al.. (2015). Exome sequencing identifies novel mutations in C5orf42 in patients with Joubert syndrome with oral–facial–digital anomalies. Human Genome Variation. 2(1). 15045–15045. 18 indexed citations

Weh, Eric, Linda M. Reis, Hannah C. Happ, et al.. (2014). Whole exome sequence analysis of Peters anomaly. Human Genetics. 133(12). 1497–1511. 53 indexed citations

Ross, L. F., Howard M. Saal, Karen L. David, & Rebecca Rae Anderson. (2013). Technical report: ethical and policy issues in genetic testing and screening of children. Genetics in Medicine. 15(3). 234–245. 309 indexed citations

Rehder, Catherine, Karen L. David, Betsy Hirsch, et al.. (2013). American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing. Genetics in Medicine. 15(2). 150–152. 114 indexed citations

10.

Lee, Ka, Bradley R. Williams, H. Ferguson, et al.. (2009). PTPN11analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings. Clinical Genetics. 75(2). 190–194. 58 indexed citations

11.

Désir, Julie, Graciela Moya, Orit Reish, et al.. (2007). Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy. Journal of Medical Genetics. 44(5). 322–326. 119 indexed citations

12.

Tanner, Stephan M., Cihan Öner, Mualla Çetin, et al.. (2005). Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene. Proceedings of the National Academy of Sciences. 102(11). 4130–4133. 60 indexed citations

13.

David, Karen L., et al.. (1993). Involvement of rabbis in counseling and referral for genetic conditions: results of a survey.. PubMed. 53(6). 1359–65. 11 indexed citations

14.

Castells, Salvador, et al.. (1983). Deficiency of androgen receptors in male pseudohermaphroditism. Urology. 21(2). 168–171. 3 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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