Sue Holder

857 total citations
12 papers, 573 citations indexed

About

Sue Holder is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Sue Holder has authored 12 papers receiving a total of 573 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Surgery, 4 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Sue Holder's work include Congenital limb and hand anomalies (1 paper), Hair Growth and Disorders (1 paper) and Hedgehog Signaling Pathway Studies (1 paper). Sue Holder is often cited by papers focused on Congenital limb and hand anomalies (1 paper), Hair Growth and Disorders (1 paper) and Hedgehog Signaling Pathway Studies (1 paper). Sue Holder collaborates with scholars based in United Kingdom, United States and Germany. Sue Holder's co-authors include Vera Beyer, Thomas Haaf, Ira Schwaab, Ruben van’t Slot, Martin Poot, Barbara K. Burton, Helen Stewart, Michael A. Simpson, William Drake and Muriel Holder‐Espinasse and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Medicine & Science in Sports & Exercise.

In The Last Decade

Sue Holder

12 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sue Holder United Kingdom 7 318 228 64 62 57 12 573
Eileen K. Sawyer United States 16 187 0.6× 179 0.8× 45 0.7× 25 0.4× 46 0.8× 36 654
Ciliu Zhang China 11 263 0.8× 69 0.3× 10 0.2× 56 0.9× 17 0.3× 41 572
Josh Mahlios United States 8 265 0.8× 153 0.7× 47 0.7× 18 0.3× 138 2.4× 8 597
Deepa Pai United States 10 254 0.8× 413 1.8× 14 0.2× 129 2.1× 306 5.4× 15 773
Walter Oleschko Arruda Brazil 16 253 0.8× 29 0.1× 12 0.2× 42 0.7× 16 0.3× 67 692
M Medina Spain 10 145 0.5× 110 0.5× 11 0.2× 88 1.4× 24 0.4× 31 434
Mona Lindström Sweden 11 225 0.7× 57 0.3× 36 0.6× 65 1.0× 8 0.1× 21 402
Osman Demırhan Türkiye 14 222 0.7× 235 1.0× 5 0.1× 59 1.0× 30 0.5× 72 662
Julie Vogt United Kingdom 14 234 0.7× 200 0.9× 5 0.1× 51 0.8× 23 0.4× 25 476
Yaping Yang United States 16 322 1.0× 292 1.3× 4 0.1× 39 0.6× 24 0.4× 37 654

Countries citing papers authored by Sue Holder

Since Specialization
Citations

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

Fields of papers citing papers by Sue Holder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sue Holder

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

All Works

12 of 12 papers shown
1.
Simpson, Michael A., Melita Irving, Esra Asilmaz, et al.. (2011). Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss. Nature Genetics. 43(4). 303–305. 218 indexed citations
2.
Vogt, Julie, Neil V. Morgan, Laurence Bonhomme‐Faivre, et al.. (2011). CHRNG genotype–phenotype correlations in the multiple pterygium syndromes. Journal of Medical Genetics. 49(1). 21–26. 30 indexed citations
3.
Brugha, Rossa, et al.. (2011). Genitopatellar syndrome. Clinical Dysmorphology. 20(3). 163–165. 5 indexed citations
4.
Hanson, Dan, Philip Murray, Amit Sud, et al.. (2009). The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1. The American Journal of Human Genetics. 84(6). 801–806. 81 indexed citations
5.
Poot, Martin, Vera Beyer, Ira Schwaab, et al.. (2009). Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics. 11(1). 81–89. 96 indexed citations
6.
Nik‐Zainal, Serena, et al.. (2008). Keipert syndrome: two further cases and review of the literature. Clinical Dysmorphology. 17(3). 169–175. 2 indexed citations
7.
Petrides, George A., et al.. (2008). Caudal appendage in focal dermal hypoplasia (Goltz syndrome). Clinical Dysmorphology. 17(2). 129–131. 4 indexed citations
8.
Zolkipli, Zarazuela, Cheryl Longman, S. Brown, et al.. (2003). Skeletal muscle involvement in infantile systemic hyalinosis. European Journal of Paediatric Neurology. 7(6). 401–406. 6 indexed citations
9.
Holder, Sue, et al.. (2002). Isolated non‐compaction of the ventricular myocardium: prenatal diagnosis and natural history. Ultrasound in Obstetrics and Gynecology. 21(1). 75–80. 22 indexed citations
10.
Blair, S. N., Yongcun Cheng, Sue Holder, Carolyn E. Barlow, & James B. Kampert. (2001). PHYSICAL ACTIVITY OR CARDIORESPIRATORY FITNESS. Medicine & Science in Sports & Exercise. 33(5). S275–S275. 43 indexed citations
11.
Leidig‐Bruckner, G., Bernd Limberg, Dieter Felsenberg, et al.. (2000). Sex Difference in the Validity of Vertebral Deformities as an Index of Prevalent Vertebral Osteoporotic Fractures: A Population Survey of Older Men and Women. Osteoporosis International. 11(2). 102–119. 64 indexed citations
12.

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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