Shu Yau

2.4k total citations
10 papers, 258 citations indexed

About

Shu Yau is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Shu Yau has authored 10 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in Shu Yau's work include Genomics and Rare Diseases (3 papers), Autophagy in Disease and Therapy (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). Shu Yau is often cited by papers focused on Genomics and Rare Diseases (3 papers), Autophagy in Disease and Therapy (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). Shu Yau collaborates with scholars based in United Kingdom, United States and Italy. Shu Yau's co-authors include Chiara Fallerini, Michel van Geel, Helen Storey, Arthur van den Wijngaard, Francesca Mari, Francesco Cetta, H.J.M. Smeets, Francesca Ariani, Alessandra Renieri and Frances Flinter and has published in prestigious journals such as The Journal of Pediatrics, British Journal of Haematology and Journal of Medical Genetics.

In The Last Decade

Shu Yau

10 papers receiving 242 citations

Peers

Shu Yau

MB

GENET

IA

HEMAT

GENET

Margherita Baldassarri Italy

Dorothée Cailley France

Marijn F. Stokman Netherlands

Teresa Parrella United States

Jason P. Twohig United Kingdom

Natália D. Linhares Brazil

Maryam Abiri Iran

Alison Colley Australia

Ken Saida Japan

Barbara A. Benson United States

Margherita Baldassarri Italy

Shu Yau

120 ×0.9

MB

91 ×1.0

GENET

61 ×0.8

IA

32 ×0.7

HEMAT

17 ×0.4

GENET

Citations per year, relative to Shu Yau Shu Yau (= 1×) peers Margherita Baldassarri

Countries citing papers authored by Shu Yau

Since Specialization

Citations

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

Fields of papers citing papers by Shu Yau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shu Yau

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

All Works

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10 of 10 papers shown

1.

Sabir, Ataf, Jameela Sheikh, Alistair Calder, et al.. (2021). Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era. BMC Medical Genomics. 14(1). 148–148. 11 indexed citations

2.

Silcock, Lee, Shu Yau, Yvonne Daniel, et al.. (2020). A novel non‐invasive prenatal sickle cell disease test for all at‐risk pregnancies. British Journal of Haematology. 190(1). 119–124. 24 indexed citations

3.

Vontell, Regina, Veena G. Supramaniam, Alice Davidson, et al.. (2019). Post-mortem Characterisation of a Case With an ACTG1 Variant, Agenesis of the Corpus Callosum and Neuronal Heterotopia. Frontiers in Physiology. 10. 623–623. 13 indexed citations

4.

Aartsma‐Rus, Annemieke, Madhuri Hegde, Tawfeg Ben‐Omran, et al.. (2018). Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy. The Journal of Pediatrics. 204. 305–313.e14. 23 indexed citations

5.

Touraine, Renaud, Annie Laquerrière, Florent Marguet, et al.. (2017). Autopsy findings in EPG5‐related Vici syndrome with antenatal onset. American Journal of Medical Genetics Part A. 173(9). 2522–2527. 6 indexed citations

6.

Hamilton, Mark, Ruth Newbury‐Ecob, Muriel Holder‐Espinasse, et al.. (2016). Rubinstein–Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum. Clinical Dysmorphology. 25(4). 135–145. 36 indexed citations

7.

Mencarelli, Maria Antonietta, Laurence Heidet, Helen Storey, et al.. (2015). Evidence of digenic inheritance in Alport syndrome. Journal of Medical Genetics. 52(3). 163–174. 107 indexed citations

8.

Cullup, Thomas, Carlo Dionisi‐Vici, Ay Lin Kho, et al.. (2013). Clinical utility gene card for: Vici Syndrome. European Journal of Human Genetics. 22(3). 435–435. 14 indexed citations

9.

Ellard, Sian, et al.. (2009). Semi-Automated Unidirectional Sequence Analysis for Mutation Detection in a Clinical Diagnostic Setting. Genetic Testing and Molecular Biomarkers. 13(3). 381–386. 20 indexed citations

10.

Ellard, Sian, Ruth Charlton, Shu Yau, et al.. (2009). Practice guidelines for Sanger Sequencing Analysis and Interpretation.. Royal Devon and Exeter Research Repository (Royal Devon and Exeter). 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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