Catherine E. Keegan

4.1k total citations
67 papers, 2.2k citations indexed

About

Catherine E. Keegan is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Catherine E. Keegan has authored 67 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 28 papers in Genetics and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Catherine E. Keegan's work include Sexual Differentiation and Disorders (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Telomeres, Telomerase, and Senescence (10 papers). Catherine E. Keegan is often cited by papers focused on Sexual Differentiation and Disorders (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Telomeres, Telomerase, and Senescence (10 papers). Catherine E. Keegan collaborates with scholars based in United States, United Kingdom and Poland. Catherine E. Keegan's co-authors include Gary D. Hammer, Mark Hannibal, Jeffrey W. Innis, Robert E. Shapiro, Bernd Wollnik, Mary Beth Dinulos, Simeon A. Boyadjiev, Ethylin Wang Jabs, Otto Daniëls and William A. Paznekas and has published in prestigious journals such as Journal of Clinical Investigation, Genes & Development and SHILAP Revista de lepidopterología.

In The Last Decade

Catherine E. Keegan

66 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine E. Keegan United States	25	1.6k	763	500	192	177	67	2.2k
M David France	27	1.4k 0.9×	555 0.7×	271 0.5×	247 1.3×	391 2.2×	68	2.2k
Marika Charalambous United Kingdom	22	1.7k 1.1×	1.0k 1.3×	254 0.5×	251 1.3×	169 1.0×	39	3.0k
Danielle Carmignac United Kingdom	27	743 0.5×	536 0.7×	566 1.1×	435 2.3×	25 0.1×	46	2.5k
Valérie Mitchell France	26	636 0.4×	414 0.5×	143 0.3×	266 1.4×	50 0.3×	80	1.9k
Tullio Barni Italy	25	476 0.3×	211 0.3×	193 0.4×	108 0.6×	71 0.4×	66	1.6k
Rüdiger Behr Germany	30	1.5k 0.9×	602 0.8×	136 0.3×	355 1.8×	30 0.2×	95	2.3k
Yoko Kameda Japan	27	872 0.6×	324 0.4×	138 0.3×	253 1.3×	42 0.2×	118	2.0k
Chijen R. Lin United States	16	2.2k 1.4×	834 1.1×	206 0.4×	263 1.4×	23 0.1×	19	3.8k
Yoshikatsu Uematsu Japan	9	622 0.4×	434 0.6×	72 0.1×	52 0.3×	62 0.4×	10	1.7k
Paulo Alberto Otto Brazil	25	885 0.6×	825 1.1×	113 0.2×	88 0.5×	37 0.2×	130	1.9k

Countries citing papers authored by Catherine E. Keegan

Since Specialization

Citations

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

Fields of papers citing papers by Catherine E. Keegan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine E. Keegan. 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 Catherine E. Keegan. The network helps show where Catherine E. Keegan may publish in the future.

Co-authorship network of co-authors of Catherine E. Keegan

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine E. Keegan. A scholar is included among the top collaborators of Catherine E. Keegan 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 Catherine E. Keegan. Catherine E. Keegan 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

Vallianatos, Christina N., et al.. (2023). P353: KDM5C-related X-linked intellectual disability: A review of natural history and expansion of the phenotype. SHILAP Revista de lepidopterología. 1(1). 100381–100381. 1 indexed citations

Friedman, Ann, Eric Perkey, Frederick H. Allen, et al.. (2021). TPP1 mutagenesis screens unravel shelterin interfaces and functions in hematopoiesis. JCI Insight. 6(9). 7 indexed citations

Graniel, Jacqueline, Kamlesh Bisht, Ann Friedman, et al.. (2021). Differential impact of a dyskeratosis congenita mutation in TPP1 on mouse hematopoiesis and germline. Life Science Alliance. 5(1). e202101208–e202101208. 3 indexed citations

Vallianatos, Christina N., Robert S. Porter, Young Ah Seo, et al.. (2020). Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation. Communications Biology. 3(1). 278–278. 33 indexed citations

Bernat, John, et al.. (2017). Interstitial lung disease of infancy caused by a new NKX2‐1 mutation. Clinical Case Reports. 5(6). 739–743. 7 indexed citations

Byers, Heather M., Patricia Y. Fechner, Ming Chen, et al.. (2017). Unexpected ethical dilemmas in sex assignment in 46,XY DSD due to 5‐alpha reductase type 2 deficiency. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(2). 260–267. 20 indexed citations

Reutter, Heiko, Kim M. Keppler‐Noreuil, Catherine E. Keegan, et al.. (2015). Genetics of Bladder-Exstrophy-Epispadias Complex (BEEC): Systematic Elucidation of Mendelian and Multifactorial Phenotypes. Current Genomics. 17(1). 4–13. 15 indexed citations

Ballew, Bari J., Kamlesh Bisht, Belynda Hicks, et al.. (2014). Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1. Genes & Development. 28(19). 2090–2102. 86 indexed citations

Jones, Morgan, Joshua A. Regal, Daniel N. Weinberg, et al.. (2013). Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation. Journal of Clinical Investigation. 124(1). 353–366. 11 indexed citations

10.

Rhee, Yoona, Todd E. Heaton, Catherine E. Keegan, & Ayesha Ahmad. (2013). Citrullinemia Type I and Hypertrophic Pyloric Stenosis in a 1-Month Old Male Infant. SHILAP Revista de lepidopterología. 3(1). e2–e2. 1 indexed citations

11.

Nasonkin, Igor O., R. DeC. Ward, Felix Beuschlein, et al.. (2011). Aged PROP1 Deficient Dwarf Mice Maintain ACTH Production. PLoS ONE. 6(12). e28355–e28355. 11 indexed citations

12.

Vlangos, Christopher N., Todd Ackley, Hans van Bokhoven, et al.. (2010). Comprehensive genetic analysis of OEIS complex reveals no evidence for a recurrent microdeletion or duplication. American Journal of Medical Genetics Part A. 155(1). 38–49. 21 indexed citations

13.

Ou, Zhishuo, Jonathan S. Berg, Hagith Yonath, et al.. (2008). Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes. Genetics in Medicine. 10(4). 267–277. 139 indexed citations

14.

Keegan, Catherine E., Janna Hutz, Katrin Koehler, et al.. (2007). Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes. Clinical Endocrinology. 67(2). 168–174. 2 indexed citations

15.

Buchman, Steven R., et al.. (2006). Craniofacial dyssynostosis in two boys with apparently normal cognitive development. American Journal of Medical Genetics Part A. 140A(12). 1333–1336. 3 indexed citations

16.

Paznekas, William A., Simeon A. Boyadjiev, Robert E. Shapiro, et al.. (2003). Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia. The American Journal of Human Genetics. 72(2). 408–418. 487 indexed citations

17.

Beuschlein, Felix, Christopher A. Mutch, Yvonne M. Ulrich‐Lai, et al.. (2002). Steroidogenic Factor-1 Is Essential for Compensatory Adrenal Growth Following Unilateral Adrenalectomy. Endocrinology. 143(8). 3122–3135. 77 indexed citations

18.

Keegan, Catherine E.. (2001). Townes-Brocks : syndrome versus expanded spectrum hemifacial microsomia : review of eight patients and further evidence of a "hot spot" for mutation in the SALL1 gene. Human Genetics. 3. 310–313. 1 indexed citations

19.

Camper, Sally A., Thomas L. Saunders, Susan Kendall, et al.. (1995). Implementing Transgenic and Embryonic Stem Cell Technology to Study Gene Expression, Cell-Cell Interactions and Gene Function. Biology of Reproduction. 52(2). 246–257. 36 indexed citations

20.

Al‐Shawaf, Talha, James A. Brown, & Catherine E. Keegan. (1992). Retention of fetal bones 8 years following termination of pregnancy. Ultrasound in Obstetrics and Gynecology. 2(1). 61–63. 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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