J.R. Kidd

5.7k total citations · 2 hit papers
41 papers, 4.2k citations indexed

About

J.R. Kidd is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, J.R. Kidd has authored 41 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 18 papers in Molecular Biology and 4 papers in Epidemiology. Recurrent topics in J.R. Kidd's work include Genetic Associations and Epidemiology (10 papers), Forensic and Genetic Research (7 papers) and Genetic diversity and population structure (5 papers). J.R. Kidd is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Forensic and Genetic Research (7 papers) and Genetic diversity and population structure (5 papers). J.R. Kidd collaborates with scholars based in United States, Canada and Japan. J.R. Kidd's co-authors include A. Bowcock, Kenneth K. Kídd, L. L. Cavalli‐Sforza, Andrés Ruiz‐Linares, James Tomfohrde, Eric Minch, A.J. Pakstis, William C. Speed, Sarah A. Tishkoff and T Jenkins and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

J.R. Kidd

41 papers receiving 4.0k 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.

High resolution of human evolutionary trees with polymorphic microsatellites

1994 1.5k citations J.R. Kidd et al. profile →
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins

1996 452 citations Sarah A. Tishkoff, William C. Speed et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J.R. Kidd United States	21	2.3k	1.2k	434	336	317	41	4.2k
Jeffrey Rogers United States	41	1.3k 0.6×	1.7k 1.4×	392 0.9×	338 1.0×	347 1.1×	179	5.7k
Andrés Ruiz‐Linares United Kingdom	34	2.9k 1.3×	1.2k 1.0×	506 1.2×	280 0.8×	201 0.6×	109	5.1k
Ranjan Deka United States	44	3.4k 1.5×	2.1k 1.7×	304 0.7×	335 1.0×	562 1.8×	159	6.9k
Jeffrey C. Long United States	37	2.9k 1.3×	959 0.8×	420 1.0×	493 1.5×	364 1.1×	70	5.9k
Shashaank Vattikuti United States	10	4.3k 1.9×	1.9k 1.6×	657 1.5×	130 0.4×	452 1.4×	11	7.1k
Bernard Jalabert France	38	3.0k 1.3×	1.5k 1.2×	178 0.4×	613 1.8×	151 0.5×	86	10.5k
Jaume Bertranpetit Spain	60	6.2k 2.7×	2.8k 2.3×	372 0.9×	390 1.2×	292 0.9×	223	10.0k
Christopher Chang United States	12	4.4k 1.9×	1.9k 1.6×	664 1.5×	101 0.3×	473 1.5×	26	7.3k
Ariel Darvasi Israel	35	3.3k 1.4×	1.6k 1.4×	1.4k 3.2×	339 1.0×	215 0.7×	77	5.6k
Anjali K. Henders Australia	35	3.3k 1.5×	1.8k 1.5×	498 1.1×	258 0.8×	359 1.1×	83	6.5k

Countries citing papers authored by J.R. Kidd

Since Specialization

Citations

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

Fields of papers citing papers by J.R. Kidd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.R. Kidd. 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 J.R. Kidd. The network helps show where J.R. Kidd may publish in the future.

Co-authorship network of co-authors of J.R. Kidd

This figure shows the co-authorship network connecting the top 25 collaborators of J.R. Kidd. A scholar is included among the top collaborators of J.R. Kidd 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 J.R. Kidd. J.R. Kidd 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

Rajeevan, Haseena, et al.. (2011). ALFRED: an allele frequency resource for research and teaching. Nucleic Acids Research. 40(D1). D1010–D1015. 75 indexed citations

Mukherjee, N., A.J. Pakstis, Shagufta Khaliq, et al.. (2008). Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene. The Pharmacogenomics Journal. 8(5). 349–356. 19 indexed citations

Mukherjee, N., Kenneth K. Kídd, A.J. Pakstis, et al.. (2008). The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase. Molecular Psychiatry. 15(2). 216–225. 48 indexed citations

Paschou, Peristera, Yu Feng, A.J. Pakstis, et al.. (2004). Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region. The American Journal of Human Genetics. 75(4). 545–560. 45 indexed citations

Kídd, Kenneth K., A.J. Pakstis, William C. Speed, & J.R. Kidd. (2004). Understanding Human DNA Sequence Variation. Journal of Heredity. 95(5). 406–420. 63 indexed citations

Palmatier, Meg A., A.J. Pakstis, William C. Speed, et al.. (2004). COMT haplotypes suggest P2 promoter region relevance for schizophrenia. Molecular Psychiatry. 9(9). 859–870. 59 indexed citations

Osier, Michael V., R.B. Lu, A.J. Pakstis, et al.. (2003). Possible epistatic role of ADH7 in the protection against alcoholism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 126B(1). 19–22. 32 indexed citations

Tishkoff, Sarah A., A.J. Pakstis, Mark Stoneking, et al.. (2000). Short Tandem-Repeat Polymorphism/Alu Haplotype Variation at the PLAT Locus: Implications for Modern Human Origins. The American Journal of Human Genetics. 67(4). 901–925. 74 indexed citations

Zhao, Hongyu, A.J. Pakstis, J.R. Kidd, & Kenneth K. Kídd. (1999). Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association. Annals of Human Genetics. 63(2). 167–179. 30 indexed citations

10.

Tishkoff, Sarah A., A Goldman, Francesc Calafell, et al.. (1998). A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations. The American Journal of Human Genetics. 62(6). 1389–1402. 149 indexed citations

11.

Novoradovsky, Alexey, J.R. Kidd, Kenneth K. Kídd, & David Goldman. (1995). Apparent monomorphism of ALDH2 in seven American Indian populations. Alcohol. 12(2). 163–167. 11 indexed citations

12.

Pakstis, A.J., Peter Heutink, David L. Pauls, et al.. (1991). Progress in the search for genetic linkage with Tourette syndrome: An exclusion map covering more than 50% of the autosomal genome. PubMed Central. 21 indexed citations

13.

Kidd, J.R., Francis L. Black, Karin Weiss, I. Balazs, & Kenneth K. Kídd. (1991). Studies of three Amerindian populations using nuclear DNA polymorphisms.. PubMed. 63(6). 775–94. 86 indexed citations

14.

Miki, T., Isamu Nishisho, H Tateishi, et al.. (1988). D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4. Genomics. 3(1). 78–81. 3 indexed citations

15.

Wu, Jia Qian, Vijaya Ramesh, J.R. Kidd, et al.. (1988). The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10. Cytogenetic and Genome Research. 48(2). 126–127. 9 indexed citations

16.

Farrer, Lindsay A., Paul J. Goodfellow, Shirley M. Myers, et al.. (1987). An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.. Europe PMC (PubMed Central). 40(4). 329–37. 10 indexed citations

17.

Goodfellow, Paul J., Alessandra M.V. Duncan, Lindsay A. Farrer, et al.. (1987). Localization and linkage of three polymorphic DNA sequences on human chromosome 20. Cytogenetic and Genome Research. 44(2-3). 112–117. 18 indexed citations

18.

Pletcher, Beth A., Toshiyuki Takeuchi, & J.R. Kidd. (1987). A PPY cDNA clone identifies a frequent RFLP. Nucleic Acids Research. 15(18). 7650–7650. 1 indexed citations

19.

Pakstis, A.J., J.R. Kidd, Carmela M. Castiglione, R S Sparkes, & Kenneth K. Kídd. (1986). Close linkage of <i>MT2P1 </i>with <i>GC </i>on chromosome 4. Cytogenetic and Genome Research. 41(3). 189–190. 12 indexed citations

20.

Kidd, J.R., George J. Dizikes, W W Grody, Stephen D. Cederbaum, & K.K. Kidd. (1986). A PvuII RFLP for the human liver arginase (ARG1) gene. Nucleic Acids Research. 14(23). 9544–9544. 4 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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