Sandra Yang

956 total citations
13 papers, 245 citations indexed

About

Sandra Yang is a scholar working on Physiology, Genetics and Molecular Biology. According to data from OpenAlex, Sandra Yang has authored 13 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Physiology, 5 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Sandra Yang's work include Lysosomal Storage Disorders Research (5 papers), Glycogen Storage Diseases and Myoclonus (2 papers) and Genomics and Rare Diseases (2 papers). Sandra Yang is often cited by papers focused on Lysosomal Storage Disorders Research (5 papers), Glycogen Storage Diseases and Myoclonus (2 papers) and Genomics and Rare Diseases (2 papers). Sandra Yang collaborates with scholars based in United States, Switzerland and Canada. Sandra Yang's co-authors include Gilbert Vézina, Cynthia J. Tifft, Jane Juusola, Timothy W. Yu, Alan H. Beggs, Casie A. Genetti, Richard B. Parad, Kimberly A. Chapman, Grace E. VanNoy and Monica H. Wojcik and has published in prestigious journals such as Neurology, Bone and Genetics in Medicine.

In The Last Decade

Sandra Yang

13 papers receiving 243 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra Yang United States	8	91	85	65	39	37	13	245
Mauricio De Castro United States	9	78 0.9×	51 0.6×	73 1.1×	32 0.8×	16 0.4×	20	230
Fatma Tuba Eminoğlu Türkiye	8	28 0.3×	85 1.0×	63 1.0×	40 1.0×	58 1.6×	58	244
Ebru Canda Türkiye	9	29 0.3×	105 1.2×	56 0.9×	45 1.2×	77 2.1×	55	326
Marian Girgis Egypt	10	50 0.5×	95 1.1×	79 1.2×	45 1.2×	84 2.3×	27	246
Tanyel Zübarioğlu Türkiye	10	49 0.5×	108 1.3×	56 0.9×	32 0.8×	121 3.3×	52	281
Miguel Angel Alcántara‐Ortigoza Mexico	12	149 1.6×	163 1.9×	71 1.1×	78 2.0×	45 1.2×	57	386
Michelina Sibilio Italy	11	43 0.5×	88 1.0×	86 1.3×	10 0.3×	63 1.7×	19	253
Yolanda Lillquist Canada	10	39 0.4×	121 1.4×	46 0.7×	40 1.0×	146 3.9×	17	250
Catherine Lynn T. Silao Philippines	9	45 0.5×	79 0.9×	43 0.7×	85 2.2×	124 3.4×	33	287
Hatice Serap Sivri Türkiye	12	35 0.4×	107 1.3×	91 1.4×	26 0.7×	102 2.8×	26	269

Countries citing papers authored by Sandra Yang

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Yang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Yang

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

All Works

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13 of 13 papers shown

Yang, Sandra, et al.. (2023). A Multifaceted Intervention to Improve Teamwork on an Inpatient Pediatric Neurosurgery Service. The Joint Commission Journal on Quality and Patient Safety. 50(2). 104–115. 1 indexed citations

Ritter, Alyssa, Emma Bedoukian, Justin H. Berger, et al.. (2019). Clinical utility of exome sequencing in infantile heart failure. Genetics in Medicine. 22(2). 423–426. 13 indexed citations

Ferreira, Carlos R., Debra S. Regier, Kristen S. Pan, et al.. (2019). The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention. Bone. 131. 115142–115142. 7 indexed citations

Gubbels, Cynthia S., Grace E. VanNoy, Jill A. Madden, et al.. (2019). Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield. Genetics in Medicine. 22(4). 736–744. 79 indexed citations

Regier, Debra S., Hyuk‐Joon Kwon, Jean M. Johnston, et al.. (2015). MRI/MRS as a surrogate marker for clinical progression in GM1 gangliosidosis. American Journal of Medical Genetics Part A. 170(3). 634–644. 25 indexed citations

Li, Zejuan, Lucia Guidugli, Amy Knight Johnson, et al.. (2015). A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings. Journal of Human Genetics. 60(7). 363–369. 27 indexed citations

Yang, Sandra, et al.. (2015). Racial and ethnic disparities in health care–associated Clostridium difficile infections in the United States: State of the science. American Journal of Infection Control. 44(1). 91–96. 12 indexed citations

Yang, Sandra, et al.. (2015). Adverse Drug Event Prevention. American Journal of Medical Quality. 31(5). 476–485. 4 indexed citations

Fraser, Jamie L., Adeline Vanderver, Sandra Yang, et al.. (2014). Thiamine pyrophosphokinase deficiency causes a Leigh Disease like phenotype in a sibling pair: identification through whole exome sequencing and management strategies. Molecular Genetics and Metabolism Reports. 1. 66–70. 29 indexed citations

10.

Pierson, Tyler Mark, David A. Adams, Thomas C. Markello, et al.. (2012). Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM ₁ -gangliosidosis. Neurology. 79(2). 123–126. 23 indexed citations

11.

Maegawa, Gustavo, Paul L. M. van Giersbergen, Sandra Yang, et al.. (2009). Pharmacokinetics, safety and tolerability of miglustat in the treatment of pediatric patients with GM2 gangliosidosis. Molecular Genetics and Metabolism. 97(4). 284–291. 22 indexed citations

12.

Tifft, Cynthia J. & Sandra Yang. (2007). WITHDRAWN: 105 Treat type I Gaucher disease with miglustat: Experience with two patients. Molecular Genetics and Metabolism. 1 indexed citations

13.

Yang, Sandra, et al.. (1998). Consumer Perspectives on Genetic Testing, Research and Services for Ethnoculturally Diverse Populations. Public Health Genomics. 1(3). 118–123. 2 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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