Tracy L. Trotter

1.5k total citations · 1 hit paper
19 papers, 821 citations indexed

About

Tracy L. Trotter is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and General Health Professions. According to data from OpenAlex, Tracy L. Trotter has authored 19 papers receiving a total of 821 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in General Health Professions. Recurrent topics in Tracy L. Trotter's work include BRCA gene mutations in cancer (8 papers), Genomics and Rare Diseases (5 papers) and Ethics and Legal Issues in Pediatric Healthcare (5 papers). Tracy L. Trotter is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Genomics and Rare Diseases (5 papers) and Ethics and Legal Issues in Pediatric Healthcare (5 papers). Tracy L. Trotter collaborates with scholars based in United States, Uganda and France. Tracy L. Trotter's co-authors include Judith G. Hall, Marilyn J. Bull, Stephanie L. Santoro, Celanie K. Christensen, Randall W. Grout, Helen Martin, Angela E. Scheuerle, Joan M. Stoler, Emily Chen and Susan A. Berry and has published in prestigious journals such as PEDIATRICS, Genetics in Medicine and Journal of Molecular Diagnostics.

In The Last Decade

Tracy L. Trotter

18 papers receiving 784 citations

Hit Papers

align trajectories sort by overperformance

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.

Health Supervision for Children and Adolescents With Down Syndrome

2022 129 citations Marilyn J. Bull, Tracy L. Trotter et al. PEDIATRICS profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tracy L. Trotter United States	13	400	144	142	141	137	19	821
Ettore Piro Italy	21	287 0.7×	83 0.6×	165 1.2×	271 1.9×	253 1.8×	85	936
Assunta Albanese United Kingdom	20	338 0.8×	88 0.6×	137 1.0×	279 2.0×	446 3.3×	46	1.2k
Juliane Léger France	15	357 0.9×	87 0.6×	69 0.5×	315 2.2×	320 2.3×	26	1.1k
Donatella Capalbo Italy	25	302 0.8×	60 0.4×	87 0.6×	244 1.7×	338 2.5×	72	1.6k
Helen Spoudeas United Kingdom	21	177 0.4×	203 1.4×	110 0.8×	409 2.9×	202 1.5×	59	1.3k
Maria Francesca Messina Italy	21	285 0.7×	102 0.7×	74 0.5×	125 0.9×	215 1.6×	63	1.0k
Pat Mahachoklertwattana Thailand	20	133 0.3×	104 0.7×	65 0.5×	215 1.5×	254 1.9×	82	1.2k
Amanda L. Bergner United States	14	227 0.6×	63 0.4×	59 0.4×	70 0.5×	101 0.7×	32	640
Delphine Zénaty France	18	522 1.3×	92 0.6×	54 0.4×	168 1.2×	438 3.2×	34	1000
Gönül Öçal Türkiye	18	397 1.0×	85 0.6×	52 0.4×	158 1.1×	468 3.4×	102	1.2k

Countries citing papers authored by Tracy L. Trotter

Since Specialization

Citations

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

Fields of papers citing papers by Tracy L. Trotter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tracy L. Trotter. 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 Tracy L. Trotter. The network helps show where Tracy L. Trotter may publish in the future.

Co-authorship network of co-authors of Tracy L. Trotter

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

All Works

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19 of 19 papers shown

Hartnett, M. J., Michele A. Lloyd-Puryear, Norma P. Tavakoli, et al.. (2022). Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot. International Journal of Neonatal Screening. 8(4). 50–50. 12 indexed citations

Bull, Marilyn J., Tracy L. Trotter, Stephanie L. Santoro, Celanie K. Christensen, & Randall W. Grout. (2022). Health Supervision for Children and Adolescents With Down Syndrome. PEDIATRICS. 149(5). 129 indexed citations breakdown →

Bonkowsky, Joshua L., Stephanie Keller, Jamie K. Capal, et al.. (2021). Leukodystrophies in Children: Diagnosis, Care, and Treatment. PEDIATRICS. 148(3). 8 indexed citations

Bean, Lora Jh, Maren T. Scheuner, Michael F. Murray, et al.. (2021). DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(6). 979–988. 18 indexed citations

Hoover‐Fong, Julie, Charles I. Scott, Marilyn C. Jones, et al.. (2020). Health Supervision for People With Achondroplasia. PEDIATRICS. 145(6). 70 indexed citations

Morris, Colleen A., Stephen R. Braddock, Emily Chen, et al.. (2020). Health Care Supervision for Children With Williams Syndrome. PEDIATRICS. 145(2). 55 indexed citations

McGregor, Tracy L., Susan A. Berry, Katrina M. Dipple, et al.. (2020). Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency. PEDIATRICS. 147(1). 2 indexed citations

Miller, David T., Debra Freedenberg, Elizabeth K. Schorry, et al.. (2019). Health Supervision for Children With Neurofibromatosis Type 1. PEDIATRICS. 143(5). 117 indexed citations

Lloyd-Puryear, Michele A., Thomas O. Crawford, Amy Brower, et al.. (2018). Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations. International Journal of Neonatal Screening. 4(1). 6–6. 5 indexed citations

10.

Saul, Robert A., et al.. (2017). Survey of family history taking and genetic testing in pediatric practice. Journal of Community Genetics. 8(2). 109–115. 20 indexed citations

11.

Scott, Joan & Tracy L. Trotter. (2013). Primary Care and Genetics and Genomics. PEDIATRICS. 132(Supplement_3). S231–S237. 23 indexed citations

12.

Trotter, Tracy L., Alan R. Fleischman, R. Rodney Howell, & Michele A. Lloyd-Puryear. (2011). Secretary's Advisory Committee on Heritable Disorders in Newborns and Children response to the President's Council on Bioethics report: The changing moral focus of newborn screening. Genetics in Medicine. 13(4). 301–304. 11 indexed citations

13.

Calonge, Ned, Nancy Green, Piero Rinaldo, et al.. (2010). Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children. Genetics in Medicine. 12(3). 153–159. 64 indexed citations

14.

Kemper, Alex R., Tracy L. Trotter, Michele A. Lloyd-Puryear, et al.. (2010). A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: Recommendations of the United States Secretary for Health and Human Services Advisory Committee on Heritable Disorders in Newborns and Children. Genetics in Medicine. 12(2). 77–80. 37 indexed citations

15.

Lubin, Ira M., Margaret M. McGovern, Susan J. Gross, et al.. (2009). Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report. Journal of Molecular Diagnostics. 11(2). 162–171. 41 indexed citations

16.

Lubin, Ira M., Michele Caggana, Carolyn M. Constantin, et al.. (2008). Ordering Molecular Genetic Tests and Reporting Results. Journal of Molecular Diagnostics. 10(5). 459–468. 23 indexed citations

17.

Trotter, Tracy L. & Helen Martin. (2007). Family History in Pediatric Primary Care. PEDIATRICS. 120(SUPPLEMENT_2). S60–S65. 36 indexed citations

18.

Pagon, Roberta A & Tracy L. Trotter. (2007). Genetic testing: when to test and when to refer. Paediatrics and Child Health. 17(9). 367–370.

19.

Trotter, Tracy L. & Judith G. Hall. (2005). Health Supervision for Children With Achondroplasia. PEDIATRICS. 116(3). 771–783. 150 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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