Amy Yang

1.3k total citations
28 papers, 841 citations indexed

About

Amy Yang is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Amy Yang has authored 28 papers receiving a total of 841 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 10 papers in Physiology. Recurrent topics in Amy Yang's work include Lysosomal Storage Disorders Research (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (5 papers). Amy Yang is often cited by papers focused on Lysosomal Storage Disorders Research (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (5 papers). Amy Yang collaborates with scholars based in United States, Mexico and Brazil. Amy Yang's co-authors include Steven J. Frucht, Pichet Termsarasab, Yitzchak Frank, Alexander Kolevzon, Joseph D. Buxbaum, A. Ting Wang, Lisa Edelmann, Robert J. Desnick, David Grodberg and Roberto Canitano and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Amy Yang

25 papers receiving 815 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amy Yang United States 14 414 367 194 193 93 28 841
Katherine Lachlan United Kingdom 19 659 1.6× 869 2.4× 122 0.6× 104 0.5× 69 0.7× 45 1.4k
Carlos Eduardo Steiner Brazil 15 203 0.5× 157 0.4× 143 0.7× 145 0.8× 65 0.7× 58 586
Jean‐Baptiste Rivière Canada 18 575 1.4× 591 1.6× 101 0.5× 79 0.4× 141 1.5× 36 1.2k
Angela Peron Italy 18 365 0.9× 261 0.7× 127 0.7× 344 1.8× 29 0.3× 54 827
Sunita Venkateswaran Canada 15 261 0.6× 333 0.9× 51 0.3× 65 0.3× 81 0.9× 33 769
Alexandre Dionne‐Laporte Canada 15 391 0.9× 436 1.2× 65 0.3× 59 0.3× 68 0.7× 32 905
Muhammad Mahajnah Israel 16 281 0.7× 391 1.1× 59 0.3× 47 0.2× 126 1.4× 55 831
Katrin Õunap Estonia 25 857 2.1× 1.0k 2.8× 72 0.4× 191 1.0× 126 1.4× 106 1.8k
Alexandra Afenjar France 16 621 1.5× 521 1.4× 69 0.4× 55 0.3× 96 1.0× 42 1.0k
Abdul Noor Canada 20 620 1.5× 823 2.2× 145 0.7× 32 0.2× 75 0.8× 42 1.4k

Countries citing papers authored by Amy Yang

Since Specialization
Citations

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

Fields of papers citing papers by Amy Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Yang

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

All Works

20 of 20 papers shown
1.
Reyes, Emily de los, Lenora Lehwald, Erika F. Augustine, et al.. (2020). Intracerebroventricular Cerliponase Alfa for Neuronal Ceroid Lipofuscinosis Type 2 Disease: Clinical Practice Considerations From US Clinics. Pediatric Neurology. 110. 64–70. 15 indexed citations
2.
Yang, Amy, et al.. (2020). The N370S/R496H genotype in type 1 Gaucher disease – Natural history and implications for pre symptomatic diagnosis and counseling. Molecular Genetics and Metabolism Reports. 22. 100567–100567. 4 indexed citations
3.
Yau, Mabel, Amy Yang, Christopher Romero, et al.. (2019). Primary Cortisol Deficiency and Growth Hormone Deficiency in a Neonate With Hypoglycemia: Coincidence or Consequence?. Journal of the Endocrine Society. 3(4). 838–846. 1 indexed citations
4.
Wasserstein, Melissa, Michele Caggana, Sean M. Bailey, et al.. (2018). The New York pilot newborn screening program for lysosomal storage diseases: Report of the First 65,000 Infants. Genetics in Medicine. 21(3). 631–640. 108 indexed citations
5.
6.
Schussler, Edith, Amy Yang, Jonathan J. Lyons, Joshua D. Milner, & Julie Wang. (2017). Persistent tryptase elevation in a patient with Gaucher disease. The Journal of Allergy and Clinical Immunology In Practice. 6(2). 697–699. 11 indexed citations
7.
Yang, Amy, Hetanshi Naik, Christopher Liong, et al.. (2017). Parkinson's disease prevalence in Fabry disease: A survey study. Molecular Genetics and Metabolism Reports. 14. 27–30. 32 indexed citations
8.
Yang, Amy, Louise Bier, Jessica Overbey, et al.. (2016). Early manifestations of type 1 Gaucher disease in presymptomatic children diagnosed after parental carrier screening. Genetics in Medicine. 19(6). 652–658. 17 indexed citations
9.
Termsarasab, Pichet, Amy Yang, & Steven J. Frucht. (2015). Myoclonus in Ataxia–Telangiectasia. Tremor and Other Hyperkinetic Movements. 5(0). 298–298. 9 indexed citations
10.
Termsarasab, Pichet, Amy Yang, & Steven J. Frucht. (2015). Intermediate Phenotypes of <i>ATP1A3</i> Mutations: Phenotype–Genotype Correlations. Tremor and Other Hyperkinetic Movements. 5(0). 336–336. 19 indexed citations
11.
Termsarasab, Pichet, Amy Yang, & Steven J. Frucht. (2015). Intermediate Phenotypes of ATP1A3 Mutations: Phenotype–Genotype Correlations. SHILAP Revista de lepidopterología. 5. 336–336. 22 indexed citations
12.
Kolevzon, A lexander, Lauren Bush, A. Ting Wang, et al.. (2014). Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring. Journal of Neurodevelopmental Disorders. 6(1). 39–39. 118 indexed citations
13.
Termsarasab, Pichet, et al.. (2014). Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion. Tremor and Other Hyperkinetic Movements. 4(0). 274–274. 15 indexed citations
14.
Khattab, Ahmed, Tony Yuen, Mabel Yau, et al.. (2014). Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiency. Journal of Pediatric Endocrinology and Metabolism. 28(5-6). 623–8. 26 indexed citations
15.
Soorya, Latha, A lexander Kolevzon, Jessica Zweifach, et al.. (2013). Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency. Molecular Autism. 4(1). 18–18. 236 indexed citations
16.
Yang, Amy, Bobby G. Ng, Steven A. Moore, et al.. (2013). Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy. Molecular Genetics and Metabolism. 110(3). 345–351. 65 indexed citations
17.
Wierenga, Klaas J., Zhijie Jiang, Amy Yang, John J. Mulvihill, & Nicholas F. Tsinoremas. (2012). A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents. Genetics in Medicine. 15(5). 354–360. 58 indexed citations
18.
Magro, Cynthia M., Amy Yang, & Garth Fraga. (2012). Blastic Marginal Zone Lymphoma. American Journal of Dermatopathology. 35(3). 319–326. 26 indexed citations
19.
20.
Bokhoven, Hans van, John A. McGrath, Jacopo Celli, et al.. (2000). P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation.. The American Journal of Human Genetics. 67(4). 41–41. 6 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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