James T. Lu

25.3k total citations
26 papers, 843 citations indexed

About

James T. Lu is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, James T. Lu has authored 26 papers receiving a total of 843 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 5 papers in Cancer Research and 4 papers in Molecular Biology. Recurrent topics in James T. Lu's work include Genomics and Rare Diseases (10 papers), Genetic Associations and Epidemiology (6 papers) and Connective tissue disorders research (5 papers). James T. Lu is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genetic Associations and Epidemiology (6 papers) and Connective tissue disorders research (5 papers). James T. Lu collaborates with scholars based in United States, Canada and United Kingdom. James T. Lu's co-authors include Philippe M. Campeau, Richard A. Gibbs, Brendan Lee, Floris Foijer, Björn Bakker, Bram Boeckx, Don W. Cleveland, Michelle S. Levine, Benjamin Vitre and Andrew J. Holland and has published in prestigious journals such as New England Journal of Medicine, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

James T. Lu

25 papers receiving 833 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James T. Lu United States 14 417 407 230 127 106 26 843
Anjana Saxena United States 18 315 0.8× 781 1.9× 68 0.3× 132 1.0× 106 1.0× 40 1.2k
Rhonda E. Schnur United States 20 333 0.8× 505 1.2× 261 1.1× 50 0.4× 23 0.2× 52 919
Tõnis Org Estonia 15 221 0.5× 582 1.4× 103 0.4× 73 0.6× 74 0.7× 26 1.3k
Cynthia Rothblum‐Oviatt United States 9 120 0.3× 613 1.5× 111 0.5× 181 1.4× 143 1.3× 12 847
Joy L. Little United States 12 123 0.3× 512 1.3× 138 0.6× 137 1.1× 244 2.3× 13 846
Jeffery Stevens United States 5 230 0.6× 552 1.4× 64 0.3× 159 1.3× 63 0.6× 5 819
S. P. Lucia Italy 17 166 0.4× 600 1.5× 69 0.3× 142 1.1× 71 0.7× 50 833
M. Rivière Belgium 15 238 0.6× 588 1.4× 51 0.2× 85 0.7× 69 0.7× 42 775
Timothy Hefferon United States 12 536 1.3× 537 1.3× 39 0.2× 44 0.3× 78 0.7× 20 886
Huiping Shi China 15 224 0.5× 321 0.8× 113 0.5× 51 0.4× 41 0.4× 54 754

Countries citing papers authored by James T. Lu

Since Specialization
Citations

This map shows the geographic impact of James T. Lu'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 T. Lu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James T. Lu more than expected).

Fields of papers citing papers by James T. Lu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James T. Lu

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

All Works

20 of 20 papers shown
1.
Elhanan, Gai, Iva Neveux, Shaun Dabe, et al.. (2022). Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record. Frontiers in Genetics. 13. 866169–866169. 6 indexed citations
2.
Read, Robert W., Karen Schlauch, Vincent C. Lombardi, et al.. (2021). Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. Frontiers in Genetics. 12. 639418–639418. 9 indexed citations
3.
Barrett, Kelly M. Schiabor, Alexandre Bolze, Yunyun Ni, et al.. (2021). Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records. Genetics in Medicine. 23(12). 2300–2308. 8 indexed citations
4.
Cirulli, Elizabeth T., Simon White, Robert W. Read, et al.. (2020). Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts. Nature Communications. 11(1). 542–542. 76 indexed citations
5.
Dunaway, Keith W., Erick Loomis, Stephen Riffle, et al.. (2019). Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world. Journal of Genetic Counseling. 28(2). 456–465. 18 indexed citations
6.
Lu, James T., Matthew J. Ferber, Jill Hagenkord, et al.. (2018). Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing. Journal of Molecular Diagnostics. 21(1). 3–12. 18 indexed citations
7.
Liu, Wei, James T. Lu, V. Reid Sutton, et al.. (2017). A non-mosaic PORCN mutation in a male with severe congenital anomalies overlapping focal dermal hypoplasia. Molecular Genetics and Metabolism Reports. 12. 57–61. 9 indexed citations
8.
Levine, Michelle S., Björn Bakker, Bram Boeckx, et al.. (2017). Centrosome Amplification Is Sufficient to Promote Spontaneous Tumorigenesis in Mammals. Developmental Cell. 40(3). 313–322.e5. 265 indexed citations
9.
Patel, Ronak M., David Liu, Claudia Gonzaga‐Jauregui, et al.. (2017). An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and aTUBB3mutation. Molecular Case Studies. 3(2). a000984–a000984. 15 indexed citations
10.
Machol, Keren, Mahim Jain, Mohammed Almannai, et al.. (2016). Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies. American Journal of Medical Genetics Part A. 173(3). 733–739. 8 indexed citations
11.
Lu, James T., Kenneth T. Kishida, Josepheen De Asis‐Cruz, et al.. (2015). Single-Stimulus Functional MRI Produces a Neural Individual Difference Measure for Autism Spectrum Disorder. Clinical Psychological Science. 3(3). 422–432. 13 indexed citations
12.
Rajagopal, Abbhirami, Débora Braslavsky, James T. Lu, et al.. (2014). Exome Sequencing Identifies a Novel Homozygous Mutation in the Phosphate Transporter SLC34A1 in Hypophosphatemia and Nephrocalcinosis. The Journal of Clinical Endocrinology & Metabolism. 99(11). E2451–E2456. 36 indexed citations
13.
Lu, James T., Philippe M. Campeau, & Brendan Lee. (2014). Genotype–Phenotype Correlation — Promiscuity in the Era of Next-Generation Sequencing. New England Journal of Medicine. 371(7). 593–596. 64 indexed citations
14.
Sule, Gautam, Philippe M. Campeau, Sandesh C.S. Nagamani, et al.. (2013). Next-generation sequencing for disorders of low and high bone mineral density. Osteoporosis International. 24(8). 2253–2259. 40 indexed citations
15.
Wang, Yibin, James T. Lu, Jin Yu, Richard A. Gibbs, & Fuli Yu. (2013). An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data. Genome Research. 23(5). 833–842. 65 indexed citations
16.
Grover, Monica, Philippe M. Campeau, Caressa Lietman, et al.. (2013). Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM 5 gene. Journal of Bone and Mineral Research. 28(11). 2333–2337. 22 indexed citations
17.
Shapiro, Jay R., Caressa Lietman, Monica Grover, et al.. (2013). Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM 5 Mutation. Journal of Bone and Mineral Research. 28(7). 1523–1530. 61 indexed citations
18.
Burrage, Lindsay C., James T. Lu, David S. Liu, et al.. (2013). Early childhood presentation of Czech dysplasia. Clinical Dysmorphology. 22(2). 76–80. 6 indexed citations
19.
Campeau, Philippe M., James T. Lu, Gautam Sule, et al.. (2012). Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis. Human Molecular Genetics. 21(22). 4904–4909. 65 indexed citations
20.
Lu, James T., Yibin Wang, Richard A. Gibbs, & Fuli Yu. (2012). Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms. Genome biology. 13(2). R15–R15. 25 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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