Richard Lao

490 total citations
7 papers, 117 citations indexed

About

Richard Lao is a scholar working on Genetics, Genetics and Surgery. According to data from OpenAlex, Richard Lao has authored 7 papers receiving a total of 117 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Genetics and 1 paper in Surgery. Recurrent topics in Richard Lao's work include Congenital Ear and Nasal Anomalies (4 papers), Ocular Disorders and Treatments (3 papers) and Craniofacial Disorders and Treatments (2 papers). Richard Lao is often cited by papers focused on Congenital Ear and Nasal Anomalies (4 papers), Ocular Disorders and Treatments (3 papers) and Craniofacial Disorders and Treatments (2 papers). Richard Lao collaborates with scholars based in United States, Qatar and India. Richard Lao's co-authors include Pui–Yan Kwok, Eunice Wan, Paul Ling-Fung Tang, Anne Slavotinek, Alex Choi, Tanya Bardakjian, Gary M. Shaw, Adele Schneider, Dedeepya Vaka and Flavia Chen and has published in prestigious journals such as Human Molecular Genetics, Experimental Eye Research and Human Mutation.

In The Last Decade

Richard Lao

6 papers receiving 117 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Richard Lao United States	4	68	51	23	18	14	7	117
Constance Wells France	7	61 0.9×	49 1.0×	20 0.9×	12 0.7×	6 0.4×	11	124
Arjan Bouman Netherlands	8	73 1.1×	68 1.3×	6 0.3×	11 0.6×	7 0.5×	14	146
Moiz Bootwalla United States	7	47 0.7×	72 1.4×	17 0.7×	5 0.3×	13 0.9×	10	153
Pauline Grogan Italy	2	110 1.6×	48 0.9×	5 0.2×	55 3.1×	75 5.4×	3	180
Mafalda Mucciolo Italy	8	73 1.1×	88 1.7×	8 0.3×	21 1.2×	24 1.7×	21	158
Keren Machol United States	6	21 0.3×	58 1.1×	17 0.7×	5 0.3×	12 0.9×	11	123
Shaoying Yang China	9	49 0.7×	31 0.6×	26 1.1×	5 0.3×	45 3.2×	20	138
Becky Treacy United Kingdom	5	139 2.0×	60 1.2×	8 0.3×	9 0.5×	2 0.1×	5	195
Flore Zufferey Switzerland	5	67 1.0×	67 1.3×	6 0.3×	17 0.9×	16 1.1×	5	150
Christopher M. Kirton United Kingdom	4	15 0.2×	63 1.2×	7 0.3×	8 0.4×	36 2.6×	7	124

Countries citing papers authored by Richard Lao

Since Specialization

Citations

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

Fields of papers citing papers by Richard Lao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richard Lao

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

All Works

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7 of 7 papers shown

1.

Wong, K., Michal Levy‐Sakin, Nina Gonzaludo, et al.. (2019). Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis. Molecular Genetics & Genomic Medicine. 7(12). e1007–e1007. 3 indexed citations

2.

Bardakjian, Tanya, Di Wu, Richard Lao, et al.. (2017). A recurrent, non-penetrant sequence variant, p.Arg266Cys in Growth/Differentiation Factor 3 (GDF3) in a female with unilateral anophthalmia and skeletal anomalies. American Journal of Ophthalmology Case Reports. 7. 102–106. 2 indexed citations

3.

Bassaganyas, Laia, Dedeepya Vaka, Eunice Wan, et al.. (2017). Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification. Human Mutation. 39(1). 167–171. 26 indexed citations

4.

Ullah, Ehsan, Muhammad Arif Nadeem Saqib, Neelam Shah, et al.. (2016). Genetic analysis of consanguineous families presenting with congenital ocular defects. Experimental Eye Research. 146. 163–171. 16 indexed citations

5.

Wu, Di, Shyamali Mandal, Alex Choi, et al.. (2015). DLX4is associated with orofacial clefting and abnormal jaw development. Human Molecular Genetics. 24(15). 4340–4352. 30 indexed citations

6.

Choi, Alex, Richard Lao, Paul Ling-Fung Tang, et al.. (2014). Novel mutations in PXDN cause microphthalmia and anterior segment dysgenesis. European Journal of Human Genetics. 23(3). 337–341. 40 indexed citations

7.

Lao, Richard, et al.. (2002). The Twisted-Pair Telephone Transmission Line.

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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