Harrison Brand

27.1k total citations · 1 hit paper
22 papers, 1.4k citations indexed

About

Harrison Brand is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Harrison Brand has authored 22 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Harrison Brand's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and CRISPR and Genetic Engineering (5 papers). Harrison Brand is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and CRISPR and Genetic Engineering (5 papers). Harrison Brand collaborates with scholars based in United States, Australia and United Kingdom. Harrison Brand's co-authors include Michael E. Talkowski, Ryan L. Collins, Chad A. Cowan, Kiran Musunuru, Ashok Ragavendran, Serkan Erdin, Qiurong Ding, Adrian Veres, Bridget S. Gosis and Alexei Stortchevoi and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Harrison Brand

21 papers receiving 1.4k 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.

Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9

2014 379 citations Pankaj Kumar Mandal, Leonardo M. R. Ferreira et al. Cell stem cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Harrison Brand United States	15	1.1k	596	146	117	117	22	1.4k
Alexei Stortchevoi United States	12	828 0.8×	335 0.6×	159 1.1×	115 1.0×	57 0.5×	18	988
Nicole M. Bode United States	9	1.2k 1.1×	424 0.7×	181 1.2×	41 0.4×	53 0.5×	11	1.5k
Caroline Rooryck France	25	1.0k 1.0×	668 1.1×	85 0.6×	40 0.3×	62 0.5×	75	1.9k
Joffrey Mianné France	9	1.2k 1.1×	282 0.5×	53 0.4×	26 0.2×	181 1.5×	19	1.4k
Matthew C. LaFave United States	14	1.1k 1.0×	535 0.9×	113 0.8×	43 0.4×	72 0.6×	22	1.4k
Kendell Clement United States	23	2.8k 2.6×	680 1.1×	171 1.2×	19 0.2×	192 1.6×	41	3.0k
Sumedha G. Penheiter United States	10	992 0.9×	221 0.4×	109 0.7×	19 0.2×	65 0.6×	15	1.3k
Jarryd M. Campbell United States	9	874 0.8×	276 0.5×	38 0.3×	19 0.2×	81 0.7×	13	1.1k
Michael C. Gundry United States	14	978 0.9×	210 0.4×	124 0.8×	19 0.2×	53 0.5×	24	1.2k
Shoukhrat Mitalipov United States	31	2.6k 2.4×	574 1.0×	37 0.3×	52 0.4×	37 0.3×	65	3.1k

Countries citing papers authored by Harrison Brand

Since Specialization

Citations

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

Fields of papers citing papers by Harrison Brand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harrison Brand

This figure shows the co-authorship network connecting the top 25 collaborators of Harrison Brand. A scholar is included among the top collaborators of Harrison Brand 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 Harrison Brand. Harrison Brand 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:

20 of 20 papers shown

1.

Robinson, Kelsey, Sarah W. Curtis, Justin Paschall, et al.. (2025). Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios. The American Journal of Human Genetics. 112(11). 2679–2692.

2.

Duyzend, Michael, Pilar Cacheiro, Julius O.B. Jacobsen, et al.. (2024). Improving prenatal diagnosis through standards and aggregation. Prenatal Diagnosis. 44(4). 454–464. 3 indexed citations

3.

Robinson, Kelsey, Wasiu Lanre Adeyemo, Terri H. Beaty, et al.. (2024). Genome-wide study of gene-by-sex interactions identifies risks for cleft palate. Human Genetics. 143(11). 1341–1352. 2 indexed citations

4.

Babadi, Mehrtash, Jack Fu, Samuel K. Lee, et al.. (2023). GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data. Nature Genetics. 55(9). 1589–1597. 35 indexed citations

5.

Zhao, Boxun, Jill A. Madden, Jasmine Lin, et al.. (2022). A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene. European Journal of Human Genetics. 30(9). 1083–1087. 10 indexed citations

6.

Belyeu, Jonathan R., Harrison Brand, Harold Wang, et al.. (2021). De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families. The American Journal of Human Genetics. 108(4). 597–607. 50 indexed citations

7.

Kousi, Maria, Onuralp Söylemez, Niki Mourtzi, et al.. (2020). Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy. Nature Genetics. 52(11). 1145–1150. 21 indexed citations

8.

Stamou, Maria, Shi‐Yan Ng, Harrison Brand, et al.. (2019). A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator. The Journal of Clinical Endocrinology & Metabolism. 105(3). e231–e244. 23 indexed citations

9.

Werling, Donna M., Harrison Brand, Joon‐Yong An, et al.. (2019). LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES. European Neuropsychopharmacology. 29. S784–S785. 2 indexed citations

10.

Wang, Chen‐Yu, Harrison Brand, Natalie D. Shaw, Michael E. Talkowski, & Jeannie T. Lee. (2019). Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in Humans. Genetics. 213(2). 685–703. 3 indexed citations

11.

Huang, Yanbo, Harrison Brand, Ruifang Sui, et al.. (2016). Cotton Yield Estimation Using Very High-Resolution Digital Images Acquired with a Low-Cost Small Unmanned Aerial Vehicle. Transactions of the ASABE. 59(6). 1563–1574. 38 indexed citations

12.

Wolf, Zena, Harrison Brand, John R. Shaffer, et al.. (2015). Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate. PLoS Genetics. 11(3). e1005059–e1005059. 83 indexed citations

13.

Brand, Harrison, Ryan L. Collins, Carrie Hanscom, et al.. (2015). Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. The American Journal of Human Genetics. 97(1). 170–176. 37 indexed citations

14.

Veres, Adrian, Bridget S. Gosis, Qiurong Ding, et al.. (2014). Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing. Cell stem cell. 15(1). 27–30. 378 indexed citations

15.

Veres, Adrian, Bridget S. Gosis, Qiurong Ding, et al.. (2014). Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing. Cell stem cell. 15(2). 254–254. 19 indexed citations

16.

Mandal, Pankaj Kumar, Leonardo M. R. Ferreira, Ryan L. Collins, et al.. (2014). Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9. Cell stem cell. 15(5). 643–652. 379 indexed citations breakdown →

17.

Brand, Harrison, Vamsee Pillalamarri, Ryan L. Collins, et al.. (2014). Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders. The American Journal of Human Genetics. 95(4). 454–461. 27 indexed citations

18.

Sugathan, Aarathi, Marta Biagioli, Christelle Golzio, et al.. (2014). CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. Proceedings of the National Academy of Sciences. 111(42). E4468–77. 227 indexed citations

19.

Brand, Harrison, Brenda Diergaarde, Michael R. O’Connell, David C. Whitcomb, & Randall E. Brand. (2013). Variation in the γ-Glutamyltransferase 1 Gene and Risk of Chronic Pancreatitis. Pancreas. 42(5). 836–840. 21 indexed citations

20.

Backer, Joseph M., Carl V. Hamby, John Pizzonia, et al.. (2009). Chaperone-Targeting Cytotoxin and Endoplasmic Reticulum Stress-Inducing Drug Synergize to Kill Cancer Cells. Neoplasia. 11(11). 1165–IN11. 48 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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