K. Kidd

3.4k total citations
16 papers, 972 citations indexed

About

K. Kidd is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, K. Kidd has authored 16 papers receiving a total of 972 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in K. Kidd's work include Genetic Associations and Epidemiology (2 papers), Obsessive-Compulsive Spectrum Disorders (2 papers) and Autism Spectrum Disorder Research (2 papers). K. Kidd is often cited by papers focused on Genetic Associations and Epidemiology (2 papers), Obsessive-Compulsive Spectrum Disorders (2 papers) and Autism Spectrum Disorder Research (2 papers). K. Kidd collaborates with scholars based in United States, Japan and Sweden. K. Kidd's co-authors include A.J. Pakstis, Judith R. Kidd, Fong‐Ming Chang, Kenneth J. Livak, Jean-Marc Lalouel, P.M. Conneally, N.E. Morton, J. Ott, Janice A. Egeland and J.R. Kidd and has published in prestigious journals such as Proceedings of the National Academy of Sciences, American Journal of Psychiatry and Human Molecular Genetics.

In The Last Decade

K. Kidd

16 papers receiving 923 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Kidd United States	12	356	309	200	167	140	16	972
Jay B. Lichter United States	13	556 1.6×	264 0.9×	342 1.7×	250 1.5×	123 0.9×	28	1.3k
Hugh Gurling United Kingdom	24	531 1.5×	681 2.2×	251 1.3×	318 1.9×	221 1.6×	64	1.6k
J. Loftus United Kingdom	16	260 0.7×	404 1.3×	74 0.4×	303 1.8×	148 1.1×	36	948
H.-J. M�ller Germany	14	185 0.5×	141 0.5×	134 0.7×	268 1.6×	72 0.5×	19	855
Sandra Leistner‐Segal Brazil	22	276 0.8×	190 0.6×	220 1.1×	133 0.8×	99 0.7×	88	1.6k
Hans W. Moises Germany	22	339 1.0×	410 1.3×	417 2.1×	447 2.7×	139 1.0×	38	1.5k
Maxim V. Myakishev United States	10	759 2.1×	600 1.9×	302 1.5×	162 1.0×	172 1.2×	12	1.4k
D E Comings United States	16	588 1.7×	244 0.8×	268 1.3×	178 1.1×	207 1.5×	26	1.4k
Ciara Fahey Ireland	19	572 1.6×	286 0.9×	136 0.7×	99 0.6×	254 1.8×	25	1.2k
Michael Escamilla United States	24	398 1.1×	536 1.7×	168 0.8×	360 2.2×	181 1.3×	62	1.4k

Countries citing papers authored by K. Kidd

Since Specialization

Citations

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

Fields of papers citing papers by K. Kidd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Kidd

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

All Works

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16 of 16 papers shown

Patin, Étienne, Christine Harmant, K. Kidd, et al.. (2006). Sub-Saharan African coding sequence variation and haplotype diversity at theNAT2gene. Human Mutation. 27(7). 720–720. 57 indexed citations

Asplund, Anna, Anna Gustafsson, Norbert Wikonkál, et al.. (2005). PTCH codon 1315 polymorphism and risk for nonmelanoma skin cancer. British Journal of Dermatology. 152(5). 868–873. 25 indexed citations

Gu, Shuang‐Xi, A.J. Pakstis, & K. Kidd. (2005). HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations. Computer applications in the biosciences. 21(20). 3938–3939. 23 indexed citations

Sirugo, Giorgio, Amos S. Deinard, J.R. Kidd, & K. Kidd. (1997). Survey of Maximum CTG/CAG Repeat Lengths in Humans and Non-Human Primates: Total Genome Scan in Populations Using the Repeat Expansion Detection Method. Human Molecular Genetics. 6(3). 403–408. 21 indexed citations

Chang, Fong‐Ming, Judith R. Kidd, Kenneth J. Livak, A.J. Pakstis, & K. Kidd. (1996). The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus. Human Genetics. 98(1). 91–101. 369 indexed citations

Gelernter, Joel, James F. Leckman, David L. Pauls, K. Kidd, & Roger Kurlan. (1995). Dopamine D2 Receptor and Tourette's Syndrome-Reply. Archives of Neurology. 52(5). 442–443. 2 indexed citations

Barr, Cathy L., James L. Kennedy, Carmela M. Castiglione, et al.. (1994). Linkage Study of a Susceptibility Locus for Schizophrenia in the Pseudoautosomal Region. Schizophrenia Bulletin. 20(2). 277–286. 17 indexed citations

Miller, Robert, et al.. (1989). The HGM10 information management system. Cytogenetic and Genome Research. 51(1-4). 3–7. 2 indexed citations

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

10.

Pauls, David L., D J Cohen, K. Kidd, & James F. Leckman. (1988). Tourette syndrome and neuropsychiatric disorders: is there a genetic relationship?. PubMed. 43(2). 206–17. 36 indexed citations

11.

Conneally, P.M., et al.. (1985). Report of the committee on methods of linkage analysis and reporting. Cytogenetic and Genome Research. 40(1-4). 356–359. 282 indexed citations

12.

Darby, John, J.R. Kidd, R S Sparkes, et al.. (1985). Linkage relationships of the gene for the β subunit of nerve growth factor (<i>NGFB</i>) with other chromosome 1 marker loci. Cytogenetic and Genome Research. 39(2). 158–160. 8 indexed citations

13.

Kidd, K., Janice A. Egeland, Lyndall Molthan, et al.. (1984). Amish study, IV: Genetic linkage study of pedigrees of bipolar probands. American Journal of Psychiatry. 141(9). 1042–1048. 55 indexed citations

14.

Egeland, Janice A., et al.. (1984). Amish study, V: Lithium-sodium countertransport and catechol O- methyltransferase in pedigrees of bipolar probands. American Journal of Psychiatry. 141(9). 1049–1054. 19 indexed citations

15.

Gerhard, Daniela S., K. Kidd, J.R. Kidd, Janice A. Egeland, & David E. Housman. (1984). Identification of a recent recombination event within the human beta-globin gene cluster.. Proceedings of the National Academy of Sciences. 81(24). 7875–7879. 31 indexed citations

16.

Rushton, Alan R., et al.. (1980). Penetrance estimates and recurrence risks for fibromuscular dysplasia. Clinical Genetics. 17(2). 115–116. 22 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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