Tracy Brandt

2.7k total citations
14 papers, 581 citations indexed

About

Tracy Brandt is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Tracy Brandt has authored 14 papers receiving a total of 581 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Tracy Brandt's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Tracy Brandt is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Tracy Brandt collaborates with scholars based in United States, Spain and Costa Rica. Tracy Brandt's co-authors include Lisa Edelmann, Gabriele Richard, Amanda Lindy, Anita Shanmugham, Elizabeth Butler, Kyle Retterer, Dianalee McKnight, Ninette Cohen, Stuart A. Scott and Gökçe Törüner and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Epilepsia.

In The Last Decade

Tracy Brandt

13 papers receiving 577 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tracy Brandt United States	10	399	286	93	82	73	14	581
Chantal Missirian France	16	418 1.0×	404 1.4×	17 0.2×	100 1.2×	41 0.6×	39	720
Cristina da Silva United States	12	218 0.5×	225 0.8×	68 0.7×	22 0.3×	38 0.5×	19	528
Rebecca I. Torene United States	10	206 0.5×	165 0.6×	56 0.6×	56 0.7×	19 0.3×	20	506
Mónica Rosello Spain	14	360 0.9×	295 1.0×	22 0.2×	95 1.2×	12 0.2×	41	535
Deborah Morrogh United Kingdom	9	299 0.7×	247 0.9×	78 0.8×	29 0.4×	36 0.5×	13	542
Maria Descartes United States	16	431 1.1×	399 1.4×	12 0.1×	94 1.1×	72 1.0×	34	720
Yaping Yang United States	16	292 0.7×	322 1.1×	16 0.2×	84 1.0×	37 0.5×	37	654
Michele Traversa Italy	11	232 0.6×	183 0.6×	33 0.4×	45 0.5×	10 0.1×	16	393
Birgitte Bertelsen Denmark	13	195 0.5×	244 0.9×	13 0.1×	29 0.4×	56 0.8×	26	525
Joanna Wiszniewska United States	12	360 0.9×	348 1.2×	12 0.1×	106 1.3×	16 0.2×	22	607

Countries citing papers authored by Tracy Brandt

Since Specialization

Citations

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

Fields of papers citing papers by Tracy Brandt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tracy Brandt

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

All Works

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14 of 14 papers shown

Oetjens, Matthew T., Alexander S. F. Berry, Andrés Moreno-De-Luca, et al.. (2025). Monogenic disorders associated with motor speech phenotypes in children and adolescents undergoing clinical exome sequencing. Genetics in Medicine. 27(4). 101374–101374. 2 indexed citations

Torene, Rebecca I., et al.. (2025). A scalable approach for genomic-first rare disorder detection in a healthcare-based population. The American Journal of Human Genetics. 112(11). 2565–2577.

Brandt, Tracy, Laura M. Sack, Dolores Arjona, et al.. (2019). Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants. Genetics in Medicine. 22(2). 336–344. 88 indexed citations

Parente, Daniel J., Stephanie M. Morris, Robert C. McKinstry, et al.. (2019). Sorting nexin 27 (SNX27) variants associated with seizures, developmental delay, behavioral disturbance, and subcortical brain abnormalities. Clinical Genetics. 97(3). 437–446. 8 indexed citations

Lindy, Amanda, Elizabeth Butler, Anita Shanmugham, et al.. (2018). Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders. Epilepsia. 59(5). 1062–1071. 190 indexed citations

Linderman, Michael D., Tracy Brandt, Lisa Edelmann, et al.. (2014). Analytical validation of whole exome and whole genome sequencing for clinical applications. BMC Medical Genomics. 7(1). 20–20. 57 indexed citations

Brandt, Tracy, et al.. (2013). 46,XY disorder of sex development and developmental delay associated with a novel 9q33.3 microdeletion encompassing NR5A1. European Journal of Medical Genetics. 56(11). 619–623. 14 indexed citations

Liang, Li, Jonathan J. Edwards, Tracy Brandt, et al.. (2013). Effect of Copy Number Variants on Outcomes for Infants With Single Ventricle Heart Defects. Circulation Cardiovascular Genetics. 6(5). 444–451. 73 indexed citations

Webb, Bryn D., Tracy Brandt, Chaim Jalas, et al.. (2013). A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population. Clinical Genetics. 86(2). 155–160. 12 indexed citations

10.

Brandt, Tracy, David Grodberg, Lakshmi Mehta, et al.. (2012). Complex autism spectrum disorder in a patient with a 17q12 microduplication. American Journal of Medical Genetics Part A. 158A(5). 1170–1177. 14 indexed citations

11.

Scott, Stuart A., Ninette Cohen, Tracy Brandt, et al.. (2010). Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization. Genetics in Medicine. 12(2). 85–92. 62 indexed citations

12.

McInnes, L. Alison, Marion Pilorge, Tracy Brandt, et al.. (2010). A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region. Molecular Autism. 1(1). 5–5. 38 indexed citations

13.

Scott, Stuart A., et al.. (2010). Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome. Human Molecular Genetics. 19(17). 3383–3393. 18 indexed citations

14.

Brandt, Tracy & Victor G. Corces. (2008). The Lawc protein is required for proper transcription by RNA polymerase II in Drosophila. Molecular Genetics and Genomics. 280(5). 385–396. 5 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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