Sarah Ng

11.5k citations
33 papers · 6.1k indexed · 5 hit papers · h-index 20

Impact in

  • Genetics top 0.5%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic Associations and Epidemiology
    • Cancer Genomics and Diagnostics

Papers in

    • Cancer-related molecular mechanisms research 4
    • Cancer Genomics and Diagnostics 4
    • RNA modifications and cancer 10
    • Genomics and Phylogenetic Studies 5
    • RNA and protein synthesis mechanisms 5
    • Single-cell and spatial transcriptomics 3

Sarah Ng

31 papers receiving 6.0k citations

Hit Papers

Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore 2021 · 197 citations
19720092026201420204008001.2k

Peers

Sarah Ng
Comparison fields: 5 of 162
  • Genetics 3.1k
  • Cancer Research 1.0k
  • Molecular Biology 3.5k
  • Clinical Biochemistry 159
  • Cognitive Neuroscience 410
Replace Choli Lee with:
Choli Lee United States
Christa Lese Martin United States
Lars Feuk Sweden
Alexander Hoischen Netherlands
Christian Gilissen Netherlands
Brian J. O’Roak United States
Alexandre Reymond Switzerland
Paweł Stankiewicz United States
Abigail W. Bigham United States
Anita Rauch Germany
Sarah Ng relative to Choli Lee United States Choli Lee's profile →
Citations per field
00.5×1.5×
Choli Lee · 1×
Citations per year

Countries citing papers authored by Sarah Ng

Since Specialization
Citations

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

Fields of papers citing papers by Sarah Ng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sarah Ng, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sarah Ng Line = papers co-authored together Sarah Ng links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20212
2
Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore
Hit paper breakdown →
2021197
3 202079
4 20201
5 20207
6 202052
7 201817
8 20151
9 201438
10
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
Hit paper breakdown →
2011806
11 201179
12
Exome sequencing as a tool for Mendelian disease gene discovery
Hit paper breakdown →
20111120
13 201170
14 2010161
15 200976
16 2009206
17
Exome sequencing identifies the cause of a mendelian disorder
Hit paper breakdown →
20091303
18 200670
19 200535
20 20046

About Sarah Ng

Sarah Ng is a scholar working on Cancer Research, Molecular Biology, Genetics, Computer Science Applications and Human-Computer Interaction, having authored 33 papers that have together received 6.1k indexed citations. Recurring topics across this work include RNA modifications and cancer (10 papers), Genomics and Phylogenetic Studies (5 papers), RNA and protein synthesis mechanisms (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer-related molecular mechanisms research (4 papers), Cancer Genomics and Diagnostics (4 papers), Genomics and Rare Diseases (3 papers) and Single-cell and spatial transcriptomics (3 papers). The work is most often cited by research in Genetics (3.1k citations), Cancer Research (1.0k citations), Molecular Biology (3.5k citations), Clinical Biochemistry (159 citations) and Cognitive Neuroscience (410 citations). Sarah Ng has collaborated with scholars based in United States, Singapore and United Kingdom. Frequent co-authors include Jay Shendure, Deborah A. Nickerson, Michael J. Bamshad, Abigail W. Bigham, Choli Lee, Holly K. Tabor, Evan E. Eichler, Mary J. Emond, Emily H. Turner and Paul Shannon. Their work appears in journals such as Nature Biotechnology, Cancer Research, Nature Genetics, Proceedings of the National Academy of Sciences and Scientific Reports.

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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