James C. Mullikin

89.5k total citations · 2 hit papers
122 papers, 8.0k citations indexed

About

James C. Mullikin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, James C. Mullikin has authored 122 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 50 papers in Genetics and 15 papers in Cancer Research. Recurrent topics in James C. Mullikin's work include Genomics and Phylogenetic Studies (25 papers), Chromosomal and Genetic Variations (13 papers) and RNA and protein synthesis mechanisms (12 papers). James C. Mullikin is often cited by papers focused on Genomics and Phylogenetic Studies (25 papers), Chromosomal and Genetic Variations (13 papers) and RNA and protein synthesis mechanisms (12 papers). James C. Mullikin collaborates with scholars based in United States, United Kingdom and Netherlands. James C. Mullikin's co-authors include Zemin Ning, Anthony J. Cox, Jamie K. Teer, Stephen W. Hartley, David Reich, Nancy F. Hansen, Leslie G. Biesecker, Joseph F. Ryan, Alon Keinan and Eric S. Lander and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

James C. Mullikin

122 papers receiving 7.8k 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.

SSAHA: A Fast Search Method for Large DNA Databases

2001 715 citations Zemin Ning, Anthony J. Cox et al. Genome Research profile →
The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution

2013 487 citations Christine E. Schnitzler, Tyra G. Wolfsberg et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James C. Mullikin United States	46	4.4k	2.9k	789	781	621	122	8.0k
Junhyong Kim United States	48	4.6k 1.1×	2.1k 0.7×	733 0.9×	705 0.9×	537 0.9×	139	8.4k
Tyra G. Wolfsberg United States	32	5.5k 1.2×	1.4k 0.5×	462 0.6×	610 0.8×	354 0.6×	68	7.9k
Daniel J. Richter United States	22	2.6k 0.6×	2.7k 0.9×	612 0.8×	244 0.3×	477 0.8×	34	5.7k
Carol J. Bult United States	48	6.2k 1.4×	3.0k 1.0×	1.9k 2.4×	749 1.0×	622 1.0×	144	11.3k
Carsten Russ United States	35	5.7k 1.3×	2.0k 0.7×	796 1.0×	1.4k 1.8×	161 0.3×	56	8.3k
Arend Sidow United States	36	6.5k 1.5×	2.4k 0.8×	1.2k 1.6×	894 1.1×	107 0.2×	62	8.6k
Andreas D. Baxevanis United States	39	3.7k 0.8×	1.3k 0.4×	386 0.5×	291 0.4×	924 1.5×	111	5.9k
Nick Patterson United States	33	3.8k 0.9×	6.1k 2.1×	1.1k 1.4×	445 0.6×	749 1.2×	46	10.1k
Joshua M. Akey United States	49	4.8k 1.1×	7.0k 2.4×	1.0k 1.3×	731 0.9×	375 0.6×	111	11.4k
Joseph K. Pickrell United States	31	4.2k 0.9×	5.7k 2.0×	601 0.8×	775 1.0×	267 0.4×	52	9.3k

Countries citing papers authored by James C. Mullikin

Since Specialization

Citations

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

Fields of papers citing papers by James C. Mullikin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James C. Mullikin

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

All Works

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20 of 20 papers shown

Sanders, Steven M., Anh‐Dao Nguyen, Sergey Koren, et al.. (2022). A family of unusual immunoglobulin superfamily genes in an invertebrate histocompatibility complex. Proceedings of the National Academy of Sciences. 119(40). e2207374119–e2207374119. 14 indexed citations

Sood, Raman, Qun Wang, Morgan Park, et al.. (2020). Clinical and genomic analysis of a large Chinese family with familial cortical myoclonic tremor with epilepsy and SAMD12 intronic repeat expansion. Epilepsia Open. 6(1). 102–111. 11 indexed citations

Chen, Zelin, Yoshihiro Omori, Sergey Koren, et al.. (2019). De novo assembly of the goldfish ( Carassius auratus ) genome and the evolution of genes after whole-genome duplication. Science Advances. 5(6). eaav0547–eaav0547. 138 indexed citations

Pemov, Alexander, Nancy F. Hansen, Sivasish Sindiri, et al.. (2019). Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1–associated atypical neurofibromas. Neuro-Oncology. 21(8). 981–992. 69 indexed citations

Coon, Steven L., Lynne A. Holtzclaw, Joseph C. Mays, et al.. (2019). Single Cell Sequencing of the Pineal Gland: The Next Chapter. Frontiers in Endocrinology. 10. 590–590. 10 indexed citations

Brooks, Brian P., Wadih M. Zein, A. Thompson, et al.. (2018). Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center. Ophthalmology. 125(12). 1937–1952. 41 indexed citations

Dewan, Ramita, Alexander Pemov, Evgenia Pak, et al.. (2017). First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation. BMC Cancer. 17(1). 127–127. 13 indexed citations

Hartley, Stephen W., et al.. (2016). Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural Regulation. PLoS ONE. 11(9). e0163590–e0163590. 8 indexed citations

Winter, Jean M., Derek Gildea, Jonathan Andreas, et al.. (2016). Mapping Complex Traits in a Diversity Outbred F1 Mouse Population Identifies Germline Modifiers of Metastasis in Human Prostate Cancer. Cell Systems. 4(1). 31–45.e6. 38 indexed citations

10.

Perera, Erasmo M., Dawn E. Watkins‐Chow, Nancy F. Hansen, et al.. (2015). The transcription factors Ets1 and Sox10 interact during murine melanocyte development. Developmental Biology. 407(2). 300–312. 15 indexed citations

11.

Johnston, Jennifer J., Katie L. Lewis, David Ng, et al.. (2015). Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations. The American Journal of Human Genetics. 96(6). 913–925. 43 indexed citations

12.

Cherukuri, Praveen F., Valerie V. Maduro, Kevin Lam, et al.. (2015). Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data. BMC Genomics. 16(1). 998–998. 5 indexed citations

13.

Johnston, Jennifer J., Wendy S. Rubinstein, Flavia M. Facio, et al.. (2012). Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes. The American Journal of Human Genetics. 91(1). 97–108. 155 indexed citations

14.

Rees, Matthew G., David Ng, Clesson Turner, et al.. (2011). Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes. Journal of Clinical Investigation. 122(1). 205–217. 36 indexed citations

15.

Johnston, Jennifer J., Jamie K. Teer, Praveen F. Cherukuri, et al.. (2010). Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate. The American Journal of Human Genetics. 86(5). 743–748. 120 indexed citations

16.

Teer, Jamie K. & James C. Mullikin. (2010). Exome sequencing: the sweet spot before whole genomes. Human Molecular Genetics. 19(R2). R145–R151. 203 indexed citations

17.

Sun, Jing, James C. Mullikin, Nick Patterson, & David Reich. (2009). Microsatellites Are Molecular Clocks That Support Accurate Inferences about History. Molecular Biology and Evolution. 26(5). 1017–1027. 58 indexed citations

18.

Reich, David, S. F. Schaffner, Mark J. Daly, et al.. (2002). Human genome sequence variation and the influence of gene history, mutation and recombination. Nature Genetics. 32(1). 135–142. 226 indexed citations

19.

Ning, Zemin, Anthony J. Cox, & James C. Mullikin. (2001). SSAHA: A Fast Search Method for Large DNA Databases. Genome Research. 11(10). 1725–1729. 715 indexed citations breakdown →

20.

Young, Ian, et al.. (1993). Depth-of-Focus in Microscopy. Research Repository (Delft University of Technology). 28 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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