Brooke Smith

1.4k total citations · 1 hit paper
8 papers, 975 citations indexed

About

Brooke Smith is a scholar working on Genetics, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Brooke Smith has authored 8 papers receiving a total of 975 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Infectious Diseases and 2 papers in Molecular Biology. Recurrent topics in Brooke Smith's work include Genomic variations and chromosomal abnormalities (3 papers), Antifungal resistance and susceptibility (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Brooke Smith is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Antifungal resistance and susceptibility (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Brooke Smith collaborates with scholars based in United States, Czechia and Germany. Brooke Smith's co-authors include M. William Lensch, Phillip F. Chance, Norisada Matsunami, Thomas D. Bird, Phillip D. Swanson, Christine M. Distèche, Shannon J. Odelberg, Kathleen A. Leppig, L. Ballard and Hans Werner Müller and has published in prestigious journals such as Cell, Nature Genetics and Frontiers in Microbiology.

In The Last Decade

Brooke Smith

8 papers receiving 949 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.

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1993 606 citations Phillip F. Chance, Kathleen A. Leppig et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brooke Smith United States	7	719	302	263	256	150	8	975
Ina Zorn Netherlands	8	678 0.9×	264 0.9×	180 0.7×	239 0.9×	40 0.3×	9	776
Akihiro Hashiguchi Japan	16	498 0.7×	204 0.7×	317 1.2×	178 0.7×	81 0.5×	79	822
Ashraf U. Mannan India	16	242 0.3×	129 0.4×	273 1.0×	60 0.2×	131 0.9×	32	630
Takao Honda Japan	15	308 0.4×	55 0.2×	510 1.9×	109 0.4×	372 2.5×	24	1.1k
James Powell United States	4	244 0.3×	72 0.2×	182 0.7×	232 0.9×	52 0.3×	6	568
B. Wilburn United States	9	552 0.8×	39 0.1×	607 2.3×	228 0.9×	95 0.6×	12	921
Artem Kaplan United States	5	188 0.3×	63 0.2×	283 1.1×	301 1.2×	32 0.2×	6	640
Aneeza Kim United States	6	246 0.3×	56 0.2×	314 1.2×	179 0.7×	34 0.2×	10	520
Marco Onorati Italy	14	294 0.4×	47 0.2×	525 2.0×	67 0.3×	40 0.3×	29	728
Armida Faella United States	10	122 0.2×	85 0.3×	426 1.6×	122 0.5×	332 2.2×	14	793

Countries citing papers authored by Brooke Smith

Since Specialization

Citations

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

Fields of papers citing papers by Brooke Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brooke Smith

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Oh, Soon-Hwan, Brooke Smith, Vít Hubka, et al.. (2021). Pursuing Advances in DNA Sequencing Technology to Solve a Complex Genomic Jigsaw Puzzle: The Agglutinin-Like Sequence (ALS) Genes of Candida tropicalis. Frontiers in Microbiology. 11. 594531–594531. 11 indexed citations

2.

Smith, Brooke, Andrew N. Miller, Bart L. Staker, et al.. (2019). Agglutinin-Like Sequence (ALS) Genes in the Candida parapsilosis Species Complex: Blurring the Boundaries Between Gene Families That Encode Cell-Wall Proteins. Frontiers in Microbiology. 10. 781–781. 29 indexed citations

3.

Millan, Francisca, Megan T. Cho, Kyle Retterer, et al.. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American Journal of Medical Genetics Part A. 170(7). 1791–1798. 42 indexed citations

4.

Stolerman, Elliot, Brooke Smith, Alka Chaubey, & Julie R. Jones. (2016). CHD8 intragenic deletion associated with autism spectrum disorder. European Journal of Medical Genetics. 59(4). 189–194. 20 indexed citations

5.

Manners, Prudence, et al.. (2015). Joint Aspiration for Acute Hemarthrosis in Children Receiving Factor VIII Prophylaxis for Severe Hemophilia: 11-year Safety Data. The Journal of Rheumatology. 42(5). 885–890. 18 indexed citations

6.

Everman, David B., R. Curtis Rogers, Barbara R. DuPont, et al.. (2009). Microcephaly and Congenital Grouped Pigmentation of the Retinal Pigment Epithelium Associated with Submicroscopic Deletions of 13q33.3-q34 and 11p15.4. Ophthalmic Genetics. 30(3). 136–141. 3 indexed citations

7.

Chance, Phillip F., Kathleen A. Leppig, M. William Lensch, et al.. (1993). DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell. 72(1). 143–151. 606 indexed citations breakdown →

8.

Matsunami, Norisada, Brooke Smith, L. Ballard, et al.. (1992). Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1A. Nature Genetics. 1(3). 176–179. 246 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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