Carol A. Crowe

2.3k total citations
28 papers, 904 citations indexed

About

Carol A. Crowe is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Carol A. Crowe has authored 28 papers receiving a total of 904 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Carol A. Crowe's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Muscle Physiology and Disorders (4 papers). Carol A. Crowe is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Muscle Physiology and Disorders (4 papers). Carol A. Crowe collaborates with scholars based in United States, Canada and United Kingdom. Carol A. Crowe's co-authors include Stuart Schwartz, Mark A. Micale, Jeffrey M. Conroy, Laurie A. Christ, Ken Inoue, Cornelius F. Boerkoel, Joram Sawady, Konstantin Shilo, James R. Lupski and Dimitri P. Agamanolis and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and Annals of Neurology.

In The Last Decade

Carol A. Crowe

27 papers receiving 872 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carol A. Crowe United States 17 582 318 136 119 100 28 904
Stavit A. Shalev Israel 19 519 0.9× 416 1.3× 84 0.6× 107 0.9× 108 1.1× 44 962
Caroline Astbury United States 17 483 0.8× 427 1.3× 142 1.0× 95 0.8× 46 0.5× 54 1.0k
Yvonne J. Vos Netherlands 19 520 0.9× 240 0.8× 111 0.8× 103 0.9× 111 1.1× 42 1.0k
B. Le Marec France 19 506 0.9× 474 1.5× 150 1.1× 115 1.0× 63 0.6× 67 1.0k
Loydie A. Jerome‐Majewska Canada 17 979 1.7× 319 1.0× 144 1.1× 105 0.9× 95 0.9× 40 1.3k
Ann Haskins Olney United States 19 842 1.4× 716 2.3× 214 1.6× 169 1.4× 65 0.7× 43 1.4k
Judith A. Skinner United Kingdom 12 963 1.7× 418 1.3× 80 0.6× 100 0.8× 74 0.7× 15 1.1k
Shu C. Yau United Kingdom 10 399 0.7× 335 1.1× 270 2.0× 79 0.7× 22 0.2× 15 719
Rodger Palmer United Kingdom 13 397 0.7× 494 1.6× 79 0.6× 76 0.6× 69 0.7× 20 915
H. Enders Germany 18 899 1.5× 933 2.9× 313 2.3× 100 0.8× 101 1.0× 40 1.5k

Countries citing papers authored by Carol A. Crowe

Since Specialization
Citations

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

Fields of papers citing papers by Carol A. Crowe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carol A. Crowe. 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 Carol A. Crowe. The network helps show where Carol A. Crowe may publish in the future.

Co-authorship network of co-authors of Carol A. Crowe

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

All Works

20 of 20 papers shown
1.
Ashwath, Mahi L., Irwin B. Jacobs, Carol A. Crowe, et al.. (2014). Left Ventricular Dysfunction in Duchenne Muscular Dystrophy and Genotype. The American Journal of Cardiology. 114(2). 284–289. 50 indexed citations
2.
3.
Slavin, Thomas P., Noam Lazebnik, Dinah Clark, et al.. (2012). Germline mosaicism in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 158A(6). 1481–1485. 23 indexed citations
4.
Birnkrant, David J., Mahi L. Ashwath, Garey Noritz, et al.. (2010). Cardiac and Pulmonary Function Variability in Duchenne/Becker Muscular Dystrophy: An Initial Report. Journal of Child Neurology. 25(9). 1110–1115. 24 indexed citations
5.
Scharner, Juergen, Charlotte A. Brown, Matthew Bower, et al.. (2010). Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations. Human Mutation. 32(2). 152–167. 55 indexed citations
6.
Oshima, Junko, Daniel B. Magner, Jennifer A. Lee, et al.. (2009). Regional genomic instability predisposes to complex dystrophin gene rearrangements. Human Genetics. 126(3). 411–423. 40 indexed citations
7.
Alkhouri, Naim, Barbara Kaplan, Marsha Kay, et al.. (2008). Johanson-Blizzard syndrome with mild phenotypic features confirmed by UBR1 gene testing. World Journal of Gastroenterology. 14(44). 6863–6863. 27 indexed citations
8.
Tay, S K, Sara Shanske, Carol A. Crowe, et al.. (2005). Clinical and Genetic Features in Two Families With MELAS and the T3271C Mutation in Mitochondrial DNA. Journal of Child Neurology. 20(2). 142–146. 9 indexed citations
9.
Nesbit, M. Andrew, Michael R. Bowl, Brian Harding, et al.. (2004). Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome. Journal of Biological Chemistry. 279(21). 22624–22634. 122 indexed citations
10.
Chang, Susie, Carol A. Crowe, & Elias I. Traboulsi. (2004). Brown syndrome associated with velocardiofacial syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 8(3). 290–292. 5 indexed citations
11.
12.
Inoue, Ken, Konstantin Shilo, Cornelius F. Boerkoel, et al.. (2002). Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg–Hirschsprung disease: Phenotypes linked by SOX10 mutation. Annals of Neurology. 52(6). 836–842. 96 indexed citations
13.
Scacheri, Peter C., Elizabeth M. Gillanders, S. H. Subramony, et al.. (2002). Novel mutations in collagen VI genes. Neurology. 58(4). 593–602. 79 indexed citations
14.
Brown, Charlotte A., Kimberly Q. McKinney, Carol A. Crowe, et al.. (2001). Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy. American Journal of Medical Genetics. 102(4). 359–367. 90 indexed citations
15.
Christ, Laurie A., Carol A. Crowe, Mark A. Micale, Jeffrey M. Conroy, & Stuart Schwartz. (1999). Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome. The American Journal of Human Genetics. 65(5). 1387–1395. 74 indexed citations
16.
Pollin, Toni I., William B. Dobyns, Carol A. Crowe, et al.. (1999). Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller‐Dieker syndrome (MDS) critical region in chromosome 17p13.3. American Journal of Medical Genetics. 85(4). 369–375.
17.
Pollin, Toni I., William B. Dobyns, Carol A. Crowe, et al.. (1999). Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3. American Journal of Medical Genetics. 85(4). 369–375. 5 indexed citations
18.
Crowe, Carol A., et al.. (1996). A case of acute hepatitis B occurring four months after multiple rape. International Journal of STD & AIDS. 7(2). 133–134. 3 indexed citations
19.
Micale, Mark A., et al.. (1995). Parental origin of de novo chromosome 9 deletions in del(9p) syndrome. American Journal of Medical Genetics. 57(1). 79–81. 18 indexed citations
20.
Fujimoto, Atsuko, Judith Allanson, Carol A. Crowe, Mark Lipson, & Virginia P. Johnson. (1992). Natural history of mosaic trisomy 14 syndrome. American Journal of Medical Genetics. 44(2). 189–196. 37 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Stavit A. Shalev Breakdown of academic impact, for papers by Caroline Astbury Breakdown of academic impact, for papers by Yvonne J. Vos Breakdown of academic impact, for papers by B. Le Marec Breakdown of academic impact, for papers by Loydie A. Jerome‐Majewska Breakdown of academic impact, for papers by Ann Haskins Olney Breakdown of academic impact, for papers by Judith A. Skinner Breakdown of academic impact, for papers by Shu C. Yau Breakdown of academic impact, for papers by Rodger Palmer Breakdown of academic impact, for papers by H. Enders
Rankless by CCL
2026