Lawrence Babb

2.7k total citations
20 papers, 262 citations indexed

About

Lawrence Babb is a scholar working on Genetics, Molecular Biology and History. According to data from OpenAlex, Lawrence Babb has authored 20 papers receiving a total of 262 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 4 papers in History. Recurrent topics in Lawrence Babb's work include Genomics and Rare Diseases (10 papers), Historical Studies on Reproduction, Gender, Health, and Societal Changes (4 papers) and Historical Psychiatry and Medical Practices (3 papers). Lawrence Babb is often cited by papers focused on Genomics and Rare Diseases (10 papers), Historical Studies on Reproduction, Gender, Health, and Societal Changes (4 papers) and Historical Psychiatry and Medical Practices (3 papers). Lawrence Babb collaborates with scholars based in United States, United Kingdom and Australia. Lawrence Babb's co-authors include Heidi L. Rehm, Samuel Aronson, Eugene Clark, Samantha Baxter, Matthew Varugheese, Victoria A. Joshi, Elaine Lyon, Lisa Farwell, Birgit Funke and Ronak Y. Patel and has published in prestigious journals such as Journal of the American Medical Informatics Association, Human Mutation and Genetics in Medicine.

In The Last Decade

Lawrence Babb

17 papers receiving 233 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lawrence Babb United States	8	147	66	57	32	25	20	262
Robert T. Clark United States	8	37 0.3×	52 0.8×	8 0.1×	10 0.3×	4 0.2×	23	281
R. R. Macdonald United Kingdom	10	44 0.3×	26 0.4×	6 0.1×	5 0.2×	52 2.1×	34	284
Karen Adamson United Kingdom	12	44 0.3×	65 1.0×	7 0.1×		27 1.1×	27	375
L. F. Ross United States	3	208 1.4×	54 0.8×	28 0.5×		70 2.8×	4	336
Elizabeth Emery United States	6	12 0.1×	36 0.5×	8 0.1×	14 0.4×	17 0.7×	37	191
Robin Lee United States	9	198 1.3×	30 0.5×	44 0.8×		40 1.6×	15	305
K. Yakovenko Israel	13	235 1.6×	83 1.3×	9 0.2×	2 0.1×	29 1.2×	23	404
Neus Gadea Spain	9	178 1.2×	78 1.2×	29 0.5×		31 1.2×	15	242
Kenny Beckman United States	3	98 0.7×	38 0.6×	25 0.4×		24 1.0×	3	187
Aaron Broun United States	8	41 0.3×	214 3.2×	43 0.8×		27 1.1×	12	360

Countries citing papers authored by Lawrence Babb

Since Specialization

Citations

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

Fields of papers citing papers by Lawrence Babb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lawrence Babb

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

All Works

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20 of 20 papers shown

Reardon, Brendan, Kori Kuzma, James Stevenson, et al.. (2024). 65. Creating a common language for categorical variants. Cancer Genetics. 286-287. S21–S21. 1 indexed citations

Dolin, Robert H., Bret S.E. Heale, Carla Álvarez, et al.. (2023). Sync for Genes Phase 5: Computable artifacts for sharing dynamically annotated FHIR‐formatted genomic variants. Learning Health Systems. 7(4). 3 indexed citations

Dalton, Karen, Heidi L. Rehm, Matt W. Wright, et al.. (2022). Accessing clinical-grade genomic classification data through the ClinGen Data Platform. PubMed. 28. 531–535.

Babb, Lawrence, Srikar Chamala, Melissa Cline, et al.. (2022). Development and application of a computable genotype model in the GA4GH Variation Representation Specification. PubMed. 28. 383–394. 2 indexed citations

Li, Binglan, Michelle Whirl‐Carrillo, Matt W. Wright, et al.. (2021). An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease Genetics. PubMed. 27. 385–396. 1 indexed citations

Dolman, Lena, Angela Page, Lawrence Babb, et al.. (2018). ClinGen advancing genomic data‐sharing standards as a GA4GH driver project. Human Mutation. 39(11). 1686–1689. 11 indexed citations

Patel, Ronak Y., Andrew R. Jackson, Chris Bizon, et al.. (2018). ClinGen Allele Registry links information about genetic variants. Human Mutation. 39(11). 1690–1701. 25 indexed citations

Aronson, Samuel, Lisa Mahanta, Eugene Clark, et al.. (2016). Information Technology Support for Clinical Genetic Testing within an Academic Medical Center. Journal of Personalized Medicine. 6(1). 4–4. 10 indexed citations

Wilcox, Allison R., Pamela M. Neri, Lynn A. Volk, et al.. (2013). A novel clinician interface to improve clinician access to up-to-date genetic results. Journal of the American Medical Informatics Association. 21(e1). e117–e121. 13 indexed citations

10.

Aronson, Samuel, Eugene Clark, Matthew Varugheese, et al.. (2012). Communicating new knowledge on previously reported genetic variants. Genetics in Medicine. 14(8). 713–719. 66 indexed citations

11.

Aronson, Samuel, Eugene Clark, Lawrence Babb, et al.. (2011). The GeneInsight suite: a platform to support laboratory and provider use of DNA-based genetic testing. Human Mutation. 32(5). 532–536. 53 indexed citations

12.

Babb, Lawrence. (1970). The Moral Cosmos of Paradise Lost. 5 indexed citations

13.

Babb, Lawrence, et al.. (1962). William Shakespeare and Robert Burton.. Shakespeare Quarterly. 13(4). 577–577.

14.

Babb, Lawrence, et al.. (1961). Sanity in Bedlam: A Study of Robert Burton's Anatomy of Melancholy.. Modern Language Notes. 76(2). 155–155. 6 indexed citations

15.

Babb, Lawrence, et al.. (1960). Shakespeare and The Faerie Queene.. Shakespeare Quarterly. 11(1). 81–81. 2 indexed citations

16.

Babb, Lawrence, et al.. (1955). Shakespeare Psychognostic: Character Evolution and Transformation.. Shakespeare Quarterly. 6(2). 190–190.

17.

Babb, Lawrence, et al.. (1952). The Elizabethan Malady: A Study of Melancholia in English Literature from 1580 to 1642. Books Abroad. 26(4). 396–396. 2 indexed citations

18.

Babb, Lawrence, et al.. (1952). The Elizabethan Malady. A Study of Melancholia in English Literature from 1580 to 1642. The Modern Language Review. 47(4). 571–571. 15 indexed citations

19.

Babb, Lawrence, et al.. (1952). The Elizabethan Malady: A Study of Melancholia in English Literature from 1580 to 1642.. Shakespeare Quarterly. 3(3). 275–275. 41 indexed citations

20.

Babb, Lawrence, et al.. (1952). The Elizabethan Malady: A Study of Melancholia in English Literature from 1580 to 1640. Journal of Aesthetics and Art Criticism. 11(2). 177–177. 6 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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