Marie T. Greally

1.3k total citations
19 papers, 499 citations indexed

About

Marie T. Greally is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Marie T. Greally has authored 19 papers receiving a total of 499 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Marie T. Greally's work include Connective tissue disorders research (5 papers), Genomics and Rare Diseases (3 papers) and Congenital heart defects research (3 papers). Marie T. Greally is often cited by papers focused on Connective tissue disorders research (5 papers), Genomics and Rare Diseases (3 papers) and Congenital heart defects research (3 papers). Marie T. Greally collaborates with scholars based in Ireland, United States and United Kingdom. Marie T. Greally's co-authors include Gianpiero L. Cavalleri, Stuart L. Rulten, Elijah Chaila, Sean Ennis, Peter H. Byers, Rocío Romero‐Granados, Arjan P.M. de Brouwer, Mark D. Ludman, Stephen M. Krane and Mary Atkinson and has published in prestigious journals such as Nature Genetics, Neurology and The American Journal of Human Genetics.

In The Last Decade

Marie T. Greally

18 papers receiving 486 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marie T. Greally Ireland 10 276 223 73 61 59 19 499
Edmond G. Lemire Canada 14 240 0.9× 202 0.9× 38 0.5× 66 1.1× 51 0.9× 42 616
Saghira Malik Sharif United Kingdom 10 343 1.2× 339 1.5× 38 0.5× 50 0.8× 96 1.6× 12 672
Lakshmi Mehta United States 16 403 1.5× 348 1.6× 27 0.4× 67 1.1× 57 1.0× 46 754
Fortunato Lonardo Italy 16 258 0.9× 350 1.6× 110 1.5× 28 0.5× 25 0.4× 52 645
Chin‐To Fong United States 11 282 1.0× 197 0.9× 44 0.6× 38 0.6× 138 2.3× 22 738
Stephanie Spranger Germany 14 509 1.8× 606 2.7× 34 0.5× 46 0.8× 60 1.0× 34 860
Satoru Sakazume Japan 17 314 1.1× 436 2.0× 32 0.4× 85 1.4× 36 0.6× 34 725
Franca Dagna‐Bricarelli Italy 13 229 0.8× 125 0.6× 51 0.7× 93 1.5× 26 0.4× 28 530
Chantal Missirian France 16 404 1.5× 418 1.9× 35 0.5× 30 0.5× 41 0.7× 39 720
Carolyn Applegate United States 17 328 1.2× 270 1.2× 41 0.6× 56 0.9× 32 0.5× 24 821

Countries citing papers authored by Marie T. Greally

Since Specialization
Citations

This map shows the geographic impact of Marie T. Greally'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 Marie T. Greally with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marie T. Greally more than expected).

Fields of papers citing papers by Marie T. Greally

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie T. Greally. 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 Marie T. Greally. The network helps show where Marie T. Greally may publish in the future.

Co-authorship network of co-authors of Marie T. Greally

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

All Works

19 of 19 papers shown
1.
Bhatia, Mehak, Gianpiero L. Cavalleri, Norman Delanty, et al.. (2022). Germline mosaicism in a family withMBD5haploinsufficiency. Molecular Case Studies. 8(7). a006253–a006253.
2.
Murphy, Mary, et al.. (2022). KBG syndrome mimicking genetic generalized epilepsy. Epilepsy & Behavior Reports. 19. 100545–100545. 4 indexed citations
3.
Delanty, Norman, Katherine A. Benson, Mark McCormack, et al.. (2019). Development of a genomics module within an epilepsy‐specific electronic health record: Toward genomic medicine in epilepsy care. Epilepsia. 60(8). 1670–1677. 5 indexed citations
4.
McMahon, Colin J., et al.. (2015). De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay. American Journal of Medical Genetics Part A. 167(5). 1134–1141. 16 indexed citations
5.
Gómez-Herreros, Fernando, Janneke Schuurs-Hoeijmakers, Mark McCormack, et al.. (2014). TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function. Nature Genetics. 46(5). 516–521. 115 indexed citations
6.
McMahon, Colin J., et al.. (2014). Chromosome 22q11.21 microduplication in association with hypoplastic left heart syndrome with hypoplastic pulmonary arteries. Cardiology in the Young. 25(1). 167–170. 3 indexed citations
7.
Greally, Marie T., et al.. (2014). Autosomal recessive cutis laxa type 2A (ARCL2A) mimicking Ehlers‐Danlos syndrome by its dermatological manifestations: Report of three affected patients. American Journal of Medical Genetics Part A. 164(5). 1245–1253. 9 indexed citations
8.
Greally, Marie T., Eve Robinson, Nicholas M. Allen, Donough J. O’Donovan, & John A. Crolla. (2014). De novo interstitial deletion 2q14.1q22.1: Is there a recognizable phenotype?. American Journal of Medical Genetics Part A. 164(12). 3194–3202. 8 indexed citations
9.
Zirn, Birgit, Luitgard Graul‐Neumann, M. Suckfüll, et al.. (2013). Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics. BMJ Open. 3(3). e001917–e001917. 38 indexed citations
10.
Maldergem, Lionel Van, Memnune Yüksel‐Apak, Hülya Kayserili, et al.. (2008). Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type. Neurology. 71(20). 1602–1608. 27 indexed citations
11.
Morgan, Neil V., Louise Brueton, P. Cox, et al.. (2006). Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome. The American Journal of Human Genetics. 79(2). 390–395. 98 indexed citations
12.
13.
Greally, Marie T., John C. Carey, Dianna M. Milewicz, et al.. (1998). Shprintzen-Goldberg syndrome: A clinical analysis. American Journal of Medical Genetics. 76(3). 202–212. 49 indexed citations
14.
Greally, Marie T., John C. Carey, Dianna M. Milewicz, et al.. (1998). Shprintzen‐Goldberg syndrome: A clinical analysis. American Journal of Medical Genetics. 76(3). 202–212. 6 indexed citations
15.
Byers, Peter H., Madeleine Duvic, Mary Atkinson, et al.. (1997). Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in theCOL1A1 andCOL1A2 genes of type I collagen. American Journal of Medical Genetics. 72(1). 94–105. 82 indexed citations
16.
Greally, Marie T., Tamison Jewett, Wilbur L. Smith, George D. Penick, & Roger A. Williamson. (1993). Lethal bone dysplasia in a fetus with manifestations of atelosteogenesis I and Boomerang dysplasia. American Journal of Medical Genetics. 47(7). 1086–1091. 17 indexed citations
17.
Mortimer, G., et al.. (1992). Acardius in a Triplet Pregnancy: Cytogenetic and Morphological Profile. Acta geneticae medicae et gemellologiae twin research. 41(1). 27–32. 6 indexed citations
18.
Cullen, Michael J., Marie T. Greally, & J. Greally. (1976). The XX male syndrome ‐A case report. Clinical Genetics. 10(2). 73–76. 3 indexed citations
19.
Kiely, E., Marie T. Greally, & J. Greally. (1972). On the significance of lymphoid cell infiltration in hypernephromas. Irish Journal of Medical Science (1971 -). 141(1). 108–111. 4 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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