Ny Hoang
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 2
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- Autism Spectrum Disorder Research 10
- Co-authors
- Stephen W. Scherer (12 shared papers)Han G. Brunner (1 shared paper)Christa Lese Martin (1 shared paper)David H. Ledbetter (1 shared paper)Lisa M. Prock (1 shared paper)Siddharth Srivastava (1 shared paper)Thomas Frazier (1 shared paper)Robin Hansen (1 shared paper)
- Journals
- npj Genomic Medicine (4 papers)European Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)Journal of Neurodevelopmental Disorders (1 paper)Genetics in Medicine (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Ny Hoang
19 papers receiving 603 citations
Ny Hoang's Hit Papers
Peers
Comparison fields: 5 of 64
- Genetics 477
- Cognitive Neuroscience 215
- Pediatrics, Perinatology and Child Health 61
- Psychiatry and Mental health 42
- Molecular Biology 162
Countries citing papers authored by Ny Hoang
This map shows the geographic impact of Ny Hoang'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 Ny Hoang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ny Hoang more than expected).
Fields of papers citing papers by Ny Hoang
This network shows the impact of papers produced by Ny Hoang. 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 Ny Hoang. The network helps show where Ny Hoang may publish in the future.
Co-authors
The 25 scholars most cited alongside Ny Hoang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders Hit paper breakdown → | 2019 | 367 |
| 2 | 2017 | 33 | |
| 3 | 2015 | 33 | |
| 4 | 2019 | 29 | |
| 5 | 2017 | 29 | |
| 6 | 2017 | 26 | |
| 7 | 2018 | 19 | |
| 8 | 2020 | 17 | |
| 9 | 2014 | 17 | |
| 10 | 2021 | 17 | |
| 11 | 2024 | 6 | |
| 12 | 2023 | 4 | |
| 13 | 2017 | 3 | |
| 14 | 2022 | 3 | |
| 15 | 2024 | 1 | |
| 16 | 2025 | 1 | |
| 17 | 2023 | 1 | |
| 18 | 2017 | 1 | |
| 19 | 2022 | 1 | |
| 20 | 2024 | 0 |
About Ny Hoang
Ny Hoang is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 20 papers that have together received 608 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Autism Spectrum Disorder Research (10 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (8 papers), Congenital heart defects research (7 papers), Prenatal Screening and Diagnostics (2 papers), BRCA gene mutations in cancer (2 papers) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (477 citations), Cognitive Neuroscience (215 citations), Pediatrics, Perinatology and Child Health (61 citations), Psychiatry and Mental health (42 citations) and Molecular Biology (162 citations). Ny Hoang has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Stephen W. Scherer, Han G. Brunner, Christa Lese Martin, David H. Ledbetter, Lisa M. Prock, Siddharth Srivastava, Thomas Frazier, Robin Hansen, Jamie Love‐Nichols and Mustafa Şahin. Their work appears in journals such as npj Genomic Medicine, European Journal of Human Genetics, Journal of Medical Genetics, Journal of Neurodevelopmental Disorders and Genetics in Medicine.
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.