Ny Hoang

3.5k total citations · 1 hit paper
20 papers, 608 citations indexed

About

Ny Hoang is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Ny Hoang has authored 20 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Cognitive Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Ny Hoang's work include Genomic variations and chromosomal abnormalities (12 papers), Autism Spectrum Disorder Research (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Ny Hoang is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Autism Spectrum Disorder Research (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Ny Hoang collaborates with scholars based in Canada, United States and United Kingdom. Ny Hoang's co-authors include Stephen W. Scherer, David T. Miller, Siddharth Srivastava, Thomas Frazier, Wendy K. Chung, Han G. Brunner, Lisa M. Prock, Jamie Love‐Nichols, Christa Lese Martin and Robin Hansen and has published in prestigious journals such as Neuropsychologia, Journal of Medical Genetics and Patient Education and Counseling.

In The Last Decade

Ny Hoang

19 papers receiving 603 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

2019 367 citations Siddharth Srivastava, Jamie Love‐Nichols et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ny Hoang Canada	10	477	215	162	61	42	20	608
Jacobine E. Buizer‐Voskamp Netherlands	14	507 1.1×	149 0.7×	340 2.1×	85 1.4×	38 0.9×	16	781
Rena Vanzo United States	14	302 0.6×	74 0.3×	186 1.1×	82 1.3×	15 0.4×	25	504
Daniel Moreno‐De‐Luca United States	9	413 0.9×	389 1.8×	179 1.1×	51 0.8×	63 1.5×	16	677
Sophia Docherty United Kingdom	13	197 0.4×	76 0.4×	176 1.1×	39 0.6×	36 0.9×	14	453
Michael Duyzend United States	8	383 0.8×	336 1.6×	276 1.7×	52 0.9×	51 1.2×	16	673
Corneliu Bodea United States	4	514 1.1×	563 2.6×	284 1.8×	31 0.5×	77 1.8×	5	809
Shunsuke Kataoka Japan	6	202 0.4×	280 1.3×	158 1.0×	84 1.4×	16 0.4×	7	508
Dina Manaa United States	2	501 1.1×	563 2.6×	270 1.7×	31 0.5×	77 1.8×	2	793
Keith W. Dunaway United States	16	410 0.9×	205 1.0×	472 2.9×	85 1.4×	21 0.5×	18	692
Carolin Purmann United States	7	542 1.1×	144 0.7×	419 2.6×	100 1.6×	14 0.3×	10	843

Countries citing papers authored by Ny Hoang

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Ny Hoang

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

All Works

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20 of 20 papers shown

Hoang, Ny, Jennifer Howe, Alana Iaboni, et al.. (2025). Clinical utility of genome sequencing in autism: illustrative examples from a genomic research study. Journal of Medical Genetics. 62(6). 413–421. 1 indexed citations

Hoang, Ny, et al.. (2024). Global developmental delay and a de novo deletion of the 16p13.13 region. BMJ Case Reports. 17(2). e251521–e251521. 1 indexed citations

Hoang, Ny, Elemi Breetvelt, Merit M. Tabbers, et al.. (2024). Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(8). e32999–e32999.

Summers, Jane, Danielle Baribeau, Ny Hoang, et al.. (2024). An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure. Journal of Neurodevelopmental Disorders. 16(1). 37–37. 6 indexed citations

Vorstman, Jacob, et al.. (2023). Support to caregivers who have received genetic information about neurodevelopmental and psychiatric vulnerability in their young children: A narrative review. Clinical Genetics. 104(2). 163–173. 4 indexed citations

Woodbury‐Smith, Marc, Lia D’Abate, Dimitri J. Stavropoulos, et al.. (2023). The Phenotypic variability of 16p11.2 distal BP2–BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples. Journal of Medical Genetics. 60(12). 1153–1160. 1 indexed citations

Baribeau, Danielle, Ny Hoang, Dimitri J. Stavropoulos, et al.. (2022). Developmental implications of genetic testing for physical indications. European Journal of Human Genetics. 30(11). 1297–1300. 3 indexed citations

Drmic, Irene, Sanne Jilderda, Ny Hoang, et al.. (2022). Neurodevelopmental functioning in probands and non‐proband carriers of 22q11.2 microduplication. American Journal of Medical Genetics Part A. 188(10). 2999–3008. 1 indexed citations

Hoang, Ny, Ryan K. C. Yuen, Jennifer Howe, et al.. (2021). Sleep phenotype of individuals with autism spectrum disorder bearing mutations in the PER2 circadian rhythm gene. American Journal of Medical Genetics Part A. 185(4). 1120–1130. 17 indexed citations

10.

Hoang, Ny, et al.. (2020). Not only memory: Investigating the sensitivity and specificity of the Mnemonic Similarity Task in older adults. Neuropsychologia. 149. 107670–107670. 17 indexed citations

11.

Chan, Ada J. S., Cheryl Cytrynbaum, Ny Hoang, et al.. (2019). Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants. npj Genomic Medicine. 4(1). 9–9. 29 indexed citations

12.

Srivastava, Siddharth, Jamie Love‐Nichols, Kira A. Dies, et al.. (2019). Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genetics in Medicine. 21(11). 2413–2421. 367 indexed citations breakdown →

13.

Hoang, Ny, Janet A. Buchanan, & Stephen W. Scherer. (2018). Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders. npj Genomic Medicine. 3(1). 27–27. 19 indexed citations

14.

Hoang, Ny, Cheryl Cytrynbaum, & Stephen W. Scherer. (2017). Communicating complex genomic information: A counselling approach derived from research experience with Autism Spectrum Disorder. Patient Education and Counseling. 101(2). 352–361. 26 indexed citations

15.

Woodbury‐Smith, Marc, Éric Deneault, Ryan K. C. Yuen, et al.. (2017). Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly. Molecular Autism. 8(1). 59–59. 33 indexed citations

16.

Hoang, Ny, Robin Z. Hayeems, Janet M. Davies, et al.. (2017). Does personal genome testing drive service utilization in an adult preventive medicine clinic?. Journal of Community Genetics. 8(3). 151–158. 3 indexed citations

17.

Jilderda, Sanne, Ny Hoang, Bhooma Thiruvahindrapuram, et al.. (2017). Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage. npj Genomic Medicine. 2(1). 28–28. 1 indexed citations

18.

Woodbury‐Smith, Marc, Rob Nicolson, Mehdi Zarrei, et al.. (2017). Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes. npj Genomic Medicine. 2(1). 29 indexed citations

19.

Hayeems, Robin Z., Riyana Babul‐Hirji, Ny Hoang, Rosanna Weksberg, & Cheryl Shuman. (2015). Parents’ Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling. Journal of Genetic Counseling. 25(2). 298–304. 33 indexed citations

20.

Hayeems, Robin Z., Ny Hoang, Sébastien Chénier, et al.. (2014). Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray. European Journal of Human Genetics. 23(9). 1135–1141. 17 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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