Brant C. Hendrickson

1.5k total citations · 1 hit paper
15 papers, 935 citations indexed

About

Brant C. Hendrickson is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Brant C. Hendrickson has authored 15 papers receiving a total of 935 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Brant C. Hendrickson's work include BRCA gene mutations in cancer (8 papers), CRISPR and Genetic Engineering (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Brant C. Hendrickson is often cited by papers focused on BRCA gene mutations in cancer (8 papers), CRISPR and Genetic Engineering (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Brant C. Hendrickson collaborates with scholars based in United States, Germany and Norway. Brant C. Hendrickson's co-authors include Thomas Scholl, Viatcheslav R. Akmaev, Hui Zhu, Elaine A. Sugarman, Kerry L. Flynn, Narasimhan Nagan, Elizabeth M. Rohlfs, Zhaoqing Zhou, Bernice A. Allitto and Thaddeus Judkins and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and Cancer Research.

In The Last Decade

Brant C. Hendrickson

15 papers receiving 907 citations

Hit Papers

Pan-ethnic carrier screening and prenatal diagnosis for s... 2011 2026 2016 2021 2011 100 200 300 400
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.

  1. Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens
    2011 457 citations Elaine A. Sugarman, Narasimhan Nagan et al. European Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brant C. Hendrickson United States 10 524 435 317 291 173 15 935
Gail Norbury United Kingdom 15 402 0.8× 21 0.0× 166 0.5× 305 1.0× 159 0.9× 28 956
Linda Sutherland United Kingdom 10 572 1.1× 39 0.1× 116 0.4× 75 0.3× 29 0.2× 19 727
Nicole Yeager United States 8 251 0.5× 31 0.1× 153 0.5× 70 0.2× 30 0.2× 11 541
Nathalie Brison Belgium 16 271 0.5× 25 0.1× 323 1.0× 46 0.2× 110 0.6× 31 813
Volkhard Rippe Germany 13 401 0.8× 24 0.1× 99 0.3× 56 0.2× 68 0.4× 26 673
Hiroshi Tamada Japan 14 298 0.6× 26 0.1× 81 0.3× 120 0.4× 52 0.3× 19 550
Anna L. Furmanski United Kingdom 17 375 0.7× 44 0.1× 94 0.3× 88 0.3× 71 0.4× 24 596
Nicolas Hebert France 9 311 0.6× 157 0.4× 34 0.1× 141 0.5× 21 0.1× 20 654
Lutz Garbes Germany 11 500 1.0× 421 1.0× 265 0.8× 162 0.6× 5 0.0× 13 751
Michele Clemens United States 15 298 0.6× 69 0.2× 394 1.2× 123 0.4× 27 0.2× 25 625

Countries citing papers authored by Brant C. Hendrickson

Since Specialization
Citations

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

Fields of papers citing papers by Brant C. Hendrickson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brant C. Hendrickson. 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 Brant C. Hendrickson. The network helps show where Brant C. Hendrickson may publish in the future.

Co-authorship network of co-authors of Brant C. Hendrickson

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

All Works

15 of 15 papers shown
1.
Leo, Angela, A. M. Walker, Matthew S. Lebo, et al.. (2012). A GC-Wave Correction Algorithm that Improves the Analytical Performance of aCGH. Journal of Molecular Diagnostics. 14(6). 550–559. 6 indexed citations
2.
Sugarman, Elaine A., Narasimhan Nagan, Hui Zhu, et al.. (2011). Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens. European Journal of Human Genetics. 20(1). 27–32. 457 indexed citations breakdown →
3.
Dallosso, Anthony R., Kristilyn Eliason, Brant C. Hendrickson, et al.. (2008). Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas. Cancer Research. 68(2). 358–363. 68 indexed citations
4.
Leclair, Benoît, Robert C. Shaler, George R. Carmody, et al.. (2007). Bioinformatics and Human Identification in Mass Fatality Incidents: The World Trade Center Disaster*. Journal of Forensic Sciences. 52(4). 806–819. 30 indexed citations
5.
Weitzel, Jeffrey N., Veronica I. Lagos, Josef Herzog, et al.. (2007). Evidence for Common Ancestral Origin of a Recurring BRCA1 Genomic Rearrangement Identified in High-Risk Hispanic Families. Cancer Epidemiology Biomarkers & Prevention. 16(8). 1615–1620. 72 indexed citations
6.
Balmañà, Judith, David H. Stockwell, Ewout W. Steyerberg, et al.. (2006). Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome. JAMA. 296(12). 1469–1469. 135 indexed citations
7.
Judkins, Thaddeus, Brant C. Hendrickson, Amie M. Deffenbaugh, & Thomas Scholl. (2005). Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 573(1-2). 168–179. 17 indexed citations
8.
Ward, Benjamin D., Brant C. Hendrickson, Thaddeus Judkins, et al.. (2005). A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with Widely Dispersed Primer Sets. Journal of Molecular Diagnostics. 7(1). 139–142. 8 indexed citations
9.
Hendrickson, Brant C., Thaddeus Judkins, Benjamin D. Ward, et al.. (2005). Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families. Genes Chromosomes and Cancer. 43(3). 309–313. 43 indexed citations
10.
Judkins, Thaddeus, Brant C. Hendrickson, Amie M. Deffenbaugh, et al.. (2005). Application of Embryonic Lethal or Other Obvious Phenotypes to Characterize the Clinical Significance of Genetic Variants Found in Trans with Known Deleterious Mutations. Cancer Research. 65(21). 10096–10103. 51 indexed citations
11.
Hendrickson, Brant C., et al.. (2004). Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification.. PubMed. 45(4). 457–60. 9 indexed citations
12.
13.
Nielsen, David R., Brant C. Hendrickson, Michael T. Pyne, et al.. (2003). A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A→C is a mutation. Journal of Human Genetics. 48(8). 399–403. 13 indexed citations
14.
Hendrickson, Brant C., et al.. (2003). Application of haplotype pair analysis for the identification of hemizygous loci. Journal of Medical Genetics. 40(5). 346–347. 6 indexed citations
15.
Pyne, Michael T., et al.. (2000). The BRCA2 genetic variant IVS7 + 2T → G is a mutation. Journal of Human Genetics. 45(6). 351–357. 19 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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