Regina Regan

11.3k total citations
27 papers, 2.5k citations indexed

About

Regina Regan is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Regina Regan has authored 27 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Regina Regan's work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Chromosomal and Genetic Variations (8 papers). Regina Regan is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Chromosomal and Genetic Variations (8 papers). Regina Regan collaborates with scholars based in United Kingdom, United States and Netherlands. Regina Regan's co-authors include Samantha J.L. Knight, Jonathan Flint, Robert E. Kearney, Sharon W. Horsley, A Nicod, N. M. Lawrie, D. L. N. Cardy, Andrew J. Sharp, Raoul C. M. Hennekam and Robin M. Winter and has published in prestigious journals such as The Lancet, Nature Genetics and PLoS ONE.

In The Last Decade

Regina Regan

27 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Regina Regan United Kingdom 18 2.1k 1.2k 778 472 118 27 2.5k
Bassem A. Bejjani United States 36 2.6k 1.2× 1.8k 1.4× 577 0.7× 1.0k 2.1× 71 0.6× 83 4.1k
Willy M. Nillesen Netherlands 23 1.3k 0.6× 1.3k 1.0× 247 0.3× 271 0.6× 44 0.4× 42 2.2k
Roberto Ciccone Italy 23 956 0.5× 681 0.6× 270 0.3× 283 0.6× 43 0.4× 51 1.4k
Maria Isabel Melaragno Brazil 20 893 0.4× 592 0.5× 270 0.3× 221 0.5× 40 0.3× 117 1.3k
Steven Van Vooren Belgium 16 1.3k 0.6× 1.2k 1.0× 187 0.2× 247 0.5× 25 0.2× 25 2.0k
Elizabeth Roeder United States 21 972 0.5× 1.2k 1.0× 158 0.2× 346 0.7× 37 0.3× 37 1.9k
Evica Rajcan‐Separovic Canada 24 770 0.4× 775 0.6× 178 0.2× 386 0.8× 32 0.3× 58 1.6k
H F Willard United States 22 804 0.4× 1.2k 1.0× 545 0.7× 124 0.3× 130 1.1× 28 1.8k
Victoria Mok Siu Canada 25 868 0.4× 1.3k 1.0× 152 0.2× 138 0.3× 61 0.5× 73 1.9k
P. Pearson Netherlands 21 710 0.3× 879 0.7× 276 0.4× 144 0.3× 60 0.5× 50 1.6k

Countries citing papers authored by Regina Regan

Since Specialization
Citations

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

Fields of papers citing papers by Regina Regan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Regina Regan

This figure shows the co-authorship network connecting the top 25 collaborators of Regina Regan. A scholar is included among the top collaborators of Regina Regan 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 Regina Regan. Regina Regan 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.
Casey, Jillian P., Paul McGettigan, Niamh Lynam‐Lennon, et al.. (2012). Identification of a mutation in LARS as a novel cause of infantile hepatopathy. Molecular Genetics and Metabolism. 106(3). 351–358. 68 indexed citations
2.
Magalhães, Tiago R., Jillian P. Casey, Judith Conroy, et al.. (2012). HGDP and HapMap Analysis by Ancestry Mapper Reveals Local and Global Population Relationships. PLoS ONE. 7(11). e49438–e49438. 9 indexed citations
3.
Casey, Jillian P., Riki Kawaguchi, Hui Sun, et al.. (2011). First implication ofSTRA6mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to theSTRA6phenotype. Human Mutation. 32(12). 1417–1426. 64 indexed citations
4.
Lynch, Sally Ann, Nicola Foulds, Ann‐Charlotte Thuresson, et al.. (2011). The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth. European Journal of Human Genetics. 19(5). 534–539. 33 indexed citations
5.
Ballabio, Erica, Regina Regan, Jochen Harbott, et al.. (2011). Genomic Imbalances Are Confined to Non-Proliferating Cells in Paediatric Patients with Acute Myeloid Leukaemia and a Normal or Incomplete Karyotype. PLoS ONE. 6(6). e20607–e20607. 3 indexed citations
6.
Hannes, Femke, Andrew J. Sharp, Heather C. Mefford, et al.. (2008). Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. Journal of Medical Genetics. 46(4). 223–232. 207 indexed citations
7.
Wordsworth, Sarah, James Buchanan, Regina Regan, et al.. (2007). Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom. PubMed. 1(1-2). 35–45. 27 indexed citations
8.
Sharp, Andrew J., Rebecca R. Selzer, Joris A. Veltman, et al.. (2007). Characterization of a recurrent 15q24 microdeletion syndrome. Human Molecular Genetics. 16(5). 567–572. 129 indexed citations
9.
Koolen, David A., Erik A. Sistermans, Samantha J.L. Knight, et al.. (2007). Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches. European Journal of Human Genetics. 16(3). 395–400. 12 indexed citations
10.
Sharp, Andrew J., Rebecca R. Selzer, Ze Cheng, et al.. (2006). Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nature Genetics. 38(9). 1038–1042. 429 indexed citations
11.
Koolen, David A., Lisenka E.L.M. Vissers, Rolph Pfundt, et al.. (2006). A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nature Genetics. 38(9). 999–1001. 305 indexed citations
12.
Vries, Bert B.A. de, Melissa Lees, Samantha J.L. Knight, et al.. (2001). Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13). American Journal of Medical Genetics. 99(4). 314–319. 18 indexed citations
13.
Sismani, Carolina, et al.. (2001). Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay. European Journal of Human Genetics. 9(7). 527–532. 53 indexed citations
14.
Knight, Samantha J.L., Christa M. Lese, Kathrin S. Precht, et al.. (2000). An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture. The American Journal of Human Genetics. 67(2). 320–332. 237 indexed citations
15.
Shannon, Nora, et al.. (2000). Navajo poikiloderma with cyclic neutropenia in Turkish children, clinical description and exclusion of linkage to the Rothmund Thomson RECQL4 gene. The American Journal of Human Genetics. 67(4). 124–124. 1 indexed citations
16.
Knight, Samantha J.L., et al.. (2000). Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3. Developmental Medicine & Child Neurology. 42(3). 201–206. 29 indexed citations
17.
Knight, Samantha J.L., Regina Regan, A Nicod, et al.. (1999). Subtle chromosomal rearrangements in children with unexplained mental retardation. The Lancet. 354(9191). 1676–1681. 325 indexed citations
18.
Beier, David R., Kenneth Smith, Robert E. Kearney, et al.. (1997). cDNA Cloning of a Humandishevelled DVL-3Gene, Mapping to 3q27, and Expression in Human Breast and Colon Carcinomas. Biochemical and Biophysical Research Communications. 239(2). 510–516. 18 indexed citations
19.
Tinberg, Harold M., et al.. (1978). Mallory bodies: isolation of hepatocellular hyalin and electrophoretic resolution of polypeptide components.. PubMed. 39(5). 483–90. 33 indexed citations
20.
Regan, Regina, et al.. (1976). The influence of surface rugosity on haemolysis occurring in tubing.. PubMed. 11(3). 91–4. 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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