Catherine E. Keegan

4.1k citations

67 papers · 2.2k indexed · h-index 25

Aging top 5%
Urology top 2%
- Urological Disorders and Treatments 9
Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
Behavioral Neuroscience top 5%
Molecular Biology top 5%
- Sexual Differentiation and Disorders 14
- Epigenetics and DNA Methylation 5
- Renal and related cancers 5
Physiology
- Telomeres, Telomerase, and Senescence 10
Clinical Biochemistry
- Metabolism and Genetic Disorders 5
Plant Science
- Chromosomal and Genetic Variations 5

Co-authors: Gary D. Hammer Mark Hannibal Jeffrey W. Innis Robert E. Shapiro Bernd Wollnik Ethylin Wang Jabs Mary Beth Dinulos Otto Daniëls
Cited by: Aging Urology Genetics
Journals: Human Molecular Genetics (3 papers)Genetics in Medicine (3 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)
Partner nations: United States United Kingdom Poland

In The Last Decade

Catherine E. Keegan

66 papers receiving 2.2k citations

Peers

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

The 25 scholars most cited alongside Catherine E. Keegan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Catherine E. Keegan Line = papers co-authored together Catherine E. Keegan links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	P353: KDM5C-related X-linked intellectual disability: A review of natural history and expansion of the phenotype SHILAP Revista de lepidopterología ·Sergen Aşık,Christina N. Vallianatos,Shigeki Iwase,Catherine E. Keegan,Kristen Lee	2023	1
2	TPP1 mutagenesis screens unravel shelterin interfaces and functions in hematopoiesis JCI Insight ·Qiubo Li,Martine Beugnet,Ann Friedman,Eric Perkey,Frederick H. Allen,Valerie M. Tesmer,Jennifer Chase,Rami Khoriaty,Catherine E. Keegan,Ivan Maillard,Jayakrishnan Nandakumar	2021	7
3	Differential impact of a dyskeratosis congenita mutation in TPP1 on mouse hematopoiesis and germline Life Science Alliance ·Jacqueline Graniel,Kamlesh Bisht,Ann Friedman,James S. White,Eric Perkey,Ashley Vanderbeck,L. Orsini,М. Э. Касанов,Joshua D. Brandstadter,Frederick H. Allen,Adrienne Niederriter Shami,Peedikayil E. Thomas,Timea Novak,Морган Брайт Гордон,Arata Nakazima,Jennifer Chase,Saher Sue Hammoud,Catherine E. Keegan,Ivan Maillard,Jayakrishnan Nandakumar	2021	3
4	Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation Communications Biology ·Christina N. Vallianatos,Xie Yong,Robert S. Porter,Zuzana Brestičová,久保木真俊,M Meis-Kindblom Jeanne,Gonzalo Ros-Cervera,Young Ah Seo,Yali Dou,Catherine E. Keegan,Natalie C. Tronson,Shigeki Iwase	2020	33
5	Development of a decision support tool in pediatric Differences/Disorders of Sex Development Seminars in Pediatric Surgery ·David E. Sandberg,Melissa Gardner,Aneu Octaviani,Megan Urbanski,Nina Callens,Catherine E. Keegan,Beverly M. Yashar,Patricia Y. Fechner,Margarett Shnorhavorian,Éric Vilain,Stefan Timmermans,Laura A. Siminoff	2019	15
6	Interstitial lung disease of infancy caused by a new NKX2‐1 mutation Clinical Case Reports ·Victor Roland Gold,John Bernat,Catherine E. Keegan,Ayesha Ahmad,Marc B. Hershenson,Manuel Arteta	2017	7
7	Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1 Genes & Development ·Sherov Alisher,Bari J. Ballew,Kamlesh Bisht,A. Welz,Belynda Hicks,Shalabh Suman,Isacco Alberti,Neelam Giri,(unknown),Ivan Maillard,Blanche P. Alter,Catherine E. Keegan,Jayakrishnan Nandakumar,Sharon A. Savage	2014	86
8	Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation Journal of Clinical Investigation ·Morgan Jones,Svetlana V. Bershadskaya,Joshua A. Regal,Daniel N. Weinberg,James Taggart,Sherov Alisher,Ann Friedman,David O. Ferguson,Catherine E. Keegan,Ivan Maillard	2013	11
9	Next-Generation Sequencing Identifies the Danforth's Short Tail Mouse Mutation as a Retrotransposon Insertion Affecting Ptf1a Expression PLoS Genetics ·Christopher N. Vlangos,Tristan Fuller,Dan R. Robinson,Arul M. Chinnaiyan,Robert H. Lyons,James D. Cavalcoli,Catherine E. Keegan	2013	15
10	Citrullinemia Type I and Hypertrophic Pyloric Stenosis in a 1-Month Old Male Infant SHILAP Revista de lepidopterología ·Yoona Rhee,Todd E. Heaton,Catherine E. Keegan,Ayesha Ahmad	2013	1
11	Aged PROP1 Deficient Dwarf Mice Maintain ACTH Production PLoS ONE ·Igor O. Nasonkin,R. DeC. Ward,Simão V. Pandeirada,Felix Beuschlein,Amanda H. Mortensen,Catherine E. Keegan,Gary D. Hammer,Sally A. Camper	2011	11
12	Comprehensive genetic analysis of OEIS complex reveals no evidence for a recurrent microdeletion or duplication American Journal of Medical Genetics Part A ·Christopher N. Vlangos,Tristan Fuller,Todd Ackley,Hans van Bokhoven,Joris A. Veltman,Ram Iyer,John M. Park,Kim M. Keppler‐Noreuil,Catherine E. Keegan	2010	21
13	Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes Clinical Endocrinology ·Catherine E. Keegan,Janna Hutz,N. Havron,Katrin Koehler,Louise Metherell,Sosipatros A. Boikos,Sotirios Stergiopoulos,Adrian J. L. Clark,Constantine A. Stratakis,Angela Huebner,Gary D. Hammer	2007	2
14	Prenatal ascertainment of OEIS complex/cloacal exstrophy—15 new cases and literature review American Journal of Medical Genetics Part A ·Kim M. Keppler‐Noreuil,S. Ruiz Bolado,Omisakin OO,Jerome Yankowitz,Catherine E. Keegan	2007	42
15	Tpp1/Acd maintains genomic stability through a complex role in telomere protection Chromosome Research ·Tobias Else,Brian Theisen,Yipin Wu,Janna Hutz,Catherine E. Keegan,Gary D. Hammer,David O. Ferguson	2007	26
16	Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia The American Journal of Human Genetics ·William A. Paznekas,Simeon A. Boyadjiev,Robert E. Shapiro,Otto Daniëls,Bernd Wollnik,Catherine E. Keegan,Jeffrey W. Innis,Mary Beth Dinulos,Esmeralda Blouin,Mark Hannibal,Ethylin Wang Jabs	2003	487
17	SF-1, DAX-1, AND ACD: MOLECULAR DETERMINANTS OF ADRENOCORTICAL GROWTH AND STEROIDOGENESIS Endocrine Research ·Felix Beuschlein,Catherine E. Keegan,Simão V. Pandeirada,Christopher A. Mutch,Janna Hutz,Guanxin Hou,Yvonne M. Ulrich‐Lai,William C. Engeland,Young Pioneers,J. Larry Jameson,Gary D. Hammer	2002	34
18	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 ·Catherine E. Keegan	2001	1
19	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 Genetics in Medicine ·Catherine E. Keegan,John B. Mulliken,Bai-Lin Wu,Bruce R. Korf	2001	26
20	Implementing Transgenic and Embryonic Stem Cell Technology to Study Gene Expression, Cell-Cell Interactions and Gene Function Biology of Reproduction ·Sally A. Camper,Thomas L. Saunders,Susan Kendall,Ruth A. Keri,Audrey F. Seasholtz,E.R. Seary,Marcelle Aparecida de Barros Junqueira,Catherine E. Keegan,I Károlyi,Gabriel Jacoby-Cooper,Heather L. Burrows,Linda C. Samuelson	1995	36

About Catherine E. Keegan

Catherine E. Keegan is a scholar working on Urology, Genetics and Developmental Biology, having authored 67 papers that have together received 2.2k indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Telomeres, Telomerase, and Senescence (10 papers), Urological Disorders and Treatments (9 papers), Metabolism and Genetic Disorders (5 papers), Epigenetics and DNA Methylation (5 papers), Renal and related cancers (5 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Aging (51 citations), Urology (177 citations) and Genetics (763 citations). Catherine E. Keegan has collaborated with scholars based in United States, United Kingdom and Poland. Frequent co-authors include Gary D. Hammer, Mark Hannibal, Jeffrey W. Innis, Robert E. Shapiro, Bernd Wollnik, Ethylin Wang Jabs, Mary Beth Dinulos, Otto Daniëls, Simeon A. Boyadjiev and William A. Paznekas. Their work appears in journals such as Human Molecular Genetics, Genetics in Medicine, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Journal of Clinical Investigation and Journal of Pediatric and Adolescent Gynecology.

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.

Explore authors with similar magnitude of impact