Chad Haynes

8.8k total citations · 3 hit papers
30 papers, 6.4k citations indexed

About

Chad Haynes is a scholar working on Molecular Biology, Genetics and Biochemistry. According to data from OpenAlex, Chad Haynes has authored 30 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 15 papers in Genetics and 3 papers in Biochemistry. Recurrent topics in Chad Haynes's work include Genetic Associations and Epidemiology (13 papers), Gene expression and cancer classification (8 papers) and Bioinformatics and Genomic Networks (5 papers). Chad Haynes is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Gene expression and cancer classification (8 papers) and Bioinformatics and Genomic Networks (5 papers). Chad Haynes collaborates with scholars based in United States, Russia and China. Chad Haynes's co-authors include Jürg Ott, Alice K. Henning, Robert J. Klein, Josephine Hoh, John Paul SanGiovanni, Caroline J. Zeiss, Michael B. Bracken, Emily Y. Chew, Frederick L. Ferris and Jen-Yue Tsai and has published in prestigious journals such as Science, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

Chad Haynes

30 papers receiving 6.2k 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.

Complement Factor H Polymorphism in Age-Related Macular Degeneration

2005 3.3k citations Robert J. Klein, Caroline J. Zeiss et al. Science profile →
Structural basis of biological nitrogen fixation

2005 673 citations Douglas C. Rees, F. Akif Tezcan et al. Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences profile →
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

1991 597 citations Chad Haynes et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chad Haynes United States	20	2.8k	1.7k	1.5k	1.1k	694	30	6.4k
Kazuhiko Yoshida Japan	40	2.4k 0.9×	923 0.5×	250 0.2×	546 0.5×	596 0.9×	370	6.4k
Joseph R. Casey Canada	46	4.7k 1.7×	351 0.2×	325 0.2×	624 0.6×	259 0.4×	128	7.8k
Masaru Miyagi United States	37	3.8k 1.3×	1.4k 0.8×	249 0.2×	583 0.5×	659 0.9×	128	5.9k
Leonard M. Hjelmeland United States	36	3.4k 1.2×	1.5k 0.9×	267 0.2×	834 0.8×	278 0.4×	97	5.5k
Bennett Van Houten United States	71	12.3k 4.4×	198 0.1×	1.8k 1.2×	308 0.3×	824 1.2×	232	16.8k
Henrik Vorum Denmark	41	3.7k 1.3×	762 0.4×	413 0.3×	730 0.7×	791 1.1×	221	7.2k
J. Mark Petrash United States	44	3.0k 1.1×	524 0.3×	275 0.2×	311 0.3×	173 0.2×	123	6.2k
Weitong Huang China	48	4.9k 1.7×	258 0.1×	339 0.2×	1.3k 1.2×	1.0k 1.5×	216	9.4k
Mridul Mukherji United States	21	6.2k 2.2×	144 0.1×	1.5k 1.0×	395 0.4×	440 0.6×	40	9.3k
Jacques Demaille France	49	4.8k 1.7×	145 0.1×	591 0.4×	238 0.2×	608 0.9×	175	7.4k

Countries citing papers authored by Chad Haynes

Since Specialization

Citations

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

Fields of papers citing papers by Chad Haynes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chad Haynes

This figure shows the co-authorship network connecting the top 25 collaborators of Chad Haynes. A scholar is included among the top collaborators of Chad Haynes 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 Chad Haynes. Chad Haynes 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

Pitsawong, Warintra, Chad Haynes, Ronald L. Koder, David W. Rodgers, & Anne‐Frances Miller. (2017). Mechanism-Informed Refinement Reveals Altered Substrate-Binding Mode for Catalytically Competent Nitroreductase. Structure. 25(7). 978–987.e4. 26 indexed citations

Londoño, Douglas, Chad Haynes, Francisco M. De La Vega, Stephen J. Finch, & Derek Gordon. (2010). A Cost-Effective Statistical Method to Correct for Differential Genotype Misclassification When Performing Case-Control Genetic Association. Human Heredity. 70(2). 102–108. 3 indexed citations

Radivojac, Predrag, Vladimir Vacic, Chad Haynes, et al.. (2009). Identification, analysis, and prediction of protein ubiquitination sites. Proteins Structure Function and Bioinformatics. 78(2). 365–380. 459 indexed citations

Matthews, Abigail G., et al.. (2008). Collapsing SNP Genotypes in Case-Control Genome-Wide Association Studies Increases the Type I Error Rate and Power. Statistical Applications in Genetics and Molecular Biology. 7(1). Article23–Article23. 12 indexed citations

Petukhova, Lynn, Amalia Martı́nez-Mir, Lawrence Shapiro, et al.. (2008). Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation. Genomics. 92(5). 273–278. 23 indexed citations

Martı́nez-Mir, Amalia, Abraham Zlotogorski, Derek Gordon, et al.. (2007). Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata. The American Journal of Human Genetics. 80(2). 316–328. 103 indexed citations

Gordon, Derek, Chad Haynes, Yaning Yang, Patricia L. Kramer, & Stephen J. Finch. (2007). Linear trend tests for case–control genetic association that incorporate random phenotype and genotype misclassification error. Genetic Epidemiology. 31(8). 853–870. 25 indexed citations

Nielsen, David A., et al.. (2007). The BiolAD-DB System. Molecular Diagnosis & Therapy. 11(1). 15–19. 2 indexed citations

Haynes, Chad, Christopher J. Oldfield, Fei Ji, et al.. (2006). Intrinsic Disorder Is a Common Feature of Hub Proteins from Four Eukaryotic Interactomes. PLoS Computational Biology. 2(8). e100–e100. 463 indexed citations

10.

Gordon, Derek, Chad Haynes, Stephen J. Finch, & Abraham M. Brown. (2006). Increase in Linkage Information by Stratification of Pedigree Data into Gold-Standard and Standard Diagnoses: Application to the NIMH Alzheimer Disease Genetics Initiative Dataset. Human Heredity. 61(2). 97–103. 8 indexed citations

11.

Barral, Sandra, Chad Haynes, Millicent Stone, & Derek Gordon. (2006). LRTae: improving statistical power for genetic association with case/control data when phenotype and/or genotype misclassification errors are present. BMC Genetics. 7(1). 24–24. 11 indexed citations

12.

Ji, Fei, Yaning Yang, Chad Haynes, Stephen J. Finch, & Derek Gordon. (2006). Computing Asymptotic Power and Sample Size for Case-Control Genetic Association Studies in the Presence of Phenotype and/or Genotype Misclassification Errors. Statistical Applications in Genetics and Molecular Biology. 4(1). Article37–Article37. 22 indexed citations

13.

Ahn, Kwangmi, et al.. (2006). The Effects of SNP Genotyping Errors on the Power of The Cochran‐Armitage Linear Trend Test for Case/Control Association Studies. Annals of Human Genetics. 71(2). 249–261. 28 indexed citations

14.

Klein, Robert J., Caroline J. Zeiss, Emily Y. Chew, et al.. (2005). Complement Factor H Polymorphism in Age-Related Macular Degeneration. Science. 308(5720). 385–389. 3275 indexed citations breakdown →

15.

Rees, Douglas C., F. Akif Tezcan, Chad Haynes, et al.. (2005). Structural basis of biological nitrogen fixation. Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences. 363(1829). 971–984. 673 indexed citations breakdown →

16.

Barral, Sandra, Chad Haynes, Mark A. Levenstien, & Derek Gordon. (2005). Precision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statistics. BMC Genetics. 6(S1). S150–S150. 11 indexed citations

17.

Edwards, Brian J., Chad Haynes, Mark A. Levenstien, Stephen J. Finch, & Derek Gordon. (2005). Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies. BMC Genetics. 6(1). 18–18. 76 indexed citations

18.

Kang, Sun Jung, Stephen J. Finch, Chad Haynes, & Derek Gordon. (2004). Quantifying the Percent Increase in Minimum Sample Size for SNP Genotyping Errors in Genetic Model-Based Association Studies. Human Heredity. 58(3-4). 139–144. 33 indexed citations

19.

Gordon, Derek, Yaning Yang, Chad Haynes, et al.. (2004). Increasing Power for Tests of Genetic Association in the Presence of Phenotype and/or Genotype Error by Use of Double-Sampling. Statistical Applications in Genetics and Molecular Biology. 3(1). 1–32. 56 indexed citations

20.

Haynes, Chad, Ronald L. Koder, Anne‐Frances Miller, & David W. Rodgers. (2002). Structures of Nitroreductase in Three States. Journal of Biological Chemistry. 277(13). 11513–11520. 137 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.

Explore authors with similar magnitude of impact