Deborah Ruddy

5.7k total citations
11 papers, 594 citations indexed

About

Deborah Ruddy is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Deborah Ruddy has authored 11 papers receiving a total of 594 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Cell Biology and 3 papers in Physiology. Recurrent topics in Deborah Ruddy's work include Skin and Cellular Biology Research (2 papers), RNA regulation and disease (2 papers) and Alzheimer's disease research and treatments (2 papers). Deborah Ruddy is often cited by papers focused on Skin and Cellular Biology Research (2 papers), RNA regulation and disease (2 papers) and Alzheimer's disease research and treatments (2 papers). Deborah Ruddy collaborates with scholars based in United Kingdom, United States and Germany. Deborah Ruddy's co-authors include Teepu Siddique, Frank Baas, Vianney de Jong, Ammar Al‐Chalabi, Christopher E. Shaw, Caroline Vance, Bradley Smith, Helenius J. Schelhaas, Jemeen Sreedharan and Benno Küsters and has published in prestigious journals such as Brain, The American Journal of Human Genetics and Muscle & Nerve.

In The Last Decade

Deborah Ruddy

11 papers receiving 579 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Deborah Ruddy United Kingdom	8	338	237	149	125	118	11	594
Judith Hartley United Kingdom	9	387 1.1×	178 0.8×	202 1.4×	100 0.8×	161 1.4×	12	591
Paulo Victor Sgobbi de Souza Brazil	14	277 0.8×	250 1.1×	179 1.2×	168 1.3×	47 0.4×	82	707
M. Parton United Kingdom	13	320 0.9×	193 0.8×	198 1.3×	89 0.7×	50 0.4×	26	588
Andreas Sommacal Switzerland	7	453 1.3×	329 1.4×	290 1.9×	57 0.5×	64 0.5×	7	613
Denise Griffiths United States	7	86 0.3×	146 0.6×	73 0.5×	26 0.2×	157 1.3×	8	341
Benjamin D. Canan United States	15	73 0.2×	559 2.4×	101 0.7×	34 0.3×	101 0.9×	30	812
Marina Siebert Brazil	14	109 0.3×	146 0.6×	41 0.3×	50 0.4×	236 2.0×	51	581
Ana Kolicheski United States	11	82 0.2×	105 0.4×	51 0.3×	98 0.8×	100 0.8×	18	343
Sohyun L. McElroy United States	8	160 0.5×	299 1.3×	90 0.6×	68 0.5×	57 0.5×	12	494

Countries citing papers authored by Deborah Ruddy

Since Specialization

Citations

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

Fields of papers citing papers by Deborah Ruddy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deborah Ruddy

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

All Works

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11 of 11 papers shown

Halliday, Dorothy, Helen Hanson, Deborah Ruddy, et al.. (2021). Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel–Lindau Disease. Genes. 12(9). 1414–1414. 5 indexed citations

Southgate, Laura, Maja Sukalo, Edward J. Taylor, et al.. (2015). Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams–Oliver Syndrome With Variable Cardiac Anomalies. Circulation Cardiovascular Genetics. 8(4). 572–581. 70 indexed citations

Sukalo, Maja, Hülya Kayserili, Dietmar Müller, et al.. (2015). DOCK6Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies. Human Mutation. 36(6). 593–598. 35 indexed citations

Tan, S. Veronica, Werner J. Z’Graggen, Delphine Boërio, et al.. (2013). Chloride channels in myotonia congenita assessed by velocity recovery cycles. Muscle & Nerve. 49(6). 845–857. 30 indexed citations

Dolan, Siobhan M., Shanna Cox, Naomi K. Tepper, et al.. (2012). Pharmacists' knowledge, attitudes, and practices regarding influenza vaccination and treatment of pregnant women. Journal of the American Pharmacists Association. 52(1). 43–56. 21 indexed citations

McClelland, Verity M., Thomas Cullup, István Bódi, et al.. (2010). Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy. American Journal of Medical Genetics Part A. 152A(3). 741–747. 35 indexed citations

Snape, Katie, Deborah Ruddy, Martin Zenker, et al.. (2009). The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects. American Journal of Medical Genetics Part A. 149A(8). 1860–1881. 70 indexed citations

Turnbull, Clare, Deborah Ruddy, & Angela Barnicoat. (2009). Nasopharyngeal teratoma and diaphragmatic hernia: no longer a random association but a new syndrome?. Clinical Dysmorphology. 18(3). 131–134. 2 indexed citations

Naughton, Michael, et al.. (2007). Educating Practically Wise Professionals. 4(2). 437–457. 1 indexed citations

10.

Vance, Caroline, Ammar Al‐Chalabi, Deborah Ruddy, et al.. (2006). Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3. Brain. 129(4). 868–876. 269 indexed citations

11.

Ruddy, Deborah, M. Parton, Ammar Al‐Chalabi, et al.. (2003). Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16q. The American Journal of Human Genetics. 73(2). 390–396. 56 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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