K. Holman

8.7k total citations · 2 hit papers
19 papers, 2.1k citations indexed

About

K. Holman is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, K. Holman has authored 19 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Cognitive Neuroscience. Recurrent topics in K. Holman's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Autism Spectrum Disorder Research (4 papers). K. Holman is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Autism Spectrum Disorder Research (4 papers). K. Holman collaborates with scholars based in Australia, United States and France. K. Holman's co-authors include Robert I. Richards, G.R. Sutherland, Eric J. Kremer, Michael Lynch, Shuancang Yu, Melanie Pritchard, Elizabeth Baker, David Schlessinger, John C. Mulley and Stephen T. Warren and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Genetics.

In The Last Decade

K. Holman

19 papers receiving 2.1k 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.

Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n

1991 738 citations Eric J. Kremer, Melanie Pritchard et al. Science profile →
Fragile X Genotype Characterized by an Unstable Region of DNA

1991 644 citations Shuancang Yu, Melanie Pritchard et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Holman Australia	14	1.6k	1.5k	616	414	119	19	2.1k
Elisabetta Tabolacci Italy	21	848 0.5×	850 0.6×	394 0.6×	174 0.4×	71 0.6×	49	1.3k
Marie Mangelsdorf Australia	18	950 0.6×	1.1k 0.7×	138 0.2×	275 0.7×	57 0.5×	24	1.6k
Catherine B. Kunst United States	14	627 0.4×	768 0.5×	265 0.4×	251 0.6×	71 0.6×	14	1.3k
Stormy J. Chamberlain United States	25	1.3k 0.9×	2.1k 1.4×	270 0.4×	103 0.2×	58 0.5×	44	2.5k
Mark Bieda United States	13	358 0.2×	980 0.7×	175 0.3×	218 0.5×	66 0.6×	22	1.3k
Anneke T. Vulto-van Silfhout Netherlands	4	959 0.6×	656 0.5×	112 0.2×	129 0.3×	56 0.5×	4	1.3k
Gaia Colasante Italy	17	397 0.3×	846 0.6×	90 0.1×	412 1.0×	60 0.5×	26	1.3k
Jean‐Baptiste Rivière Canada	18	575 0.4×	591 0.4×	101 0.2×	145 0.4×	79 0.7×	36	1.2k
Kenji Amano Japan	19	360 0.2×	551 0.4×	108 0.2×	276 0.7×	147 1.2×	36	1.1k
Jacque Pak Kan Ip Hong Kong	15	312 0.2×	561 0.4×	237 0.4×	355 0.9×	55 0.5×	27	1.1k

Countries citing papers authored by K. Holman

Since Specialization

Citations

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

Fields of papers citing papers by K. Holman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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19 of 19 papers shown

Рогаев, Е. И., Robin Sherrington, Chenyan Wu, et al.. (1997). Analysis of the 5′ Sequence, Genomic Structure, and Alternative Splicing of thepresenilin-1Gene (PSEN1) Associated with Early Onset Alzheimer Disease. Genomics. 40(3). 415–424. 112 indexed citations

George‐Hyslop, Peter St, Е. И. Рогаев, Robin Sherrington, et al.. (1996). Two homologous genes associated with early onset familial Alzheimer's disease. Biological Psychiatry. 39(7). 562–562. 1 indexed citations

Nancarrow, J.K., K. Holman, Marie Mangelsdorf, et al.. (1995). Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus. Human Molecular Genetics. 4(3). 367–372. 33 indexed citations

Richards, Robert I., K. Holman, K. Friend, et al.. (1994). FRAXAC2 instability. Nature Genetics. 7(2). 122–122. 1 indexed citations

Richards, Robert I., Ikuko Kondo, K. Holman, et al.. (1994). Haplotype analysis at the FRAXA locus in the Japanese population. American Journal of Medical Genetics. 51(4). 412–416. 31 indexed citations

Nancarrow, J.K., Eric J. Kremer, K. Holman, et al.. (1994). Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis. Science. 264(5167). 1938–1941. 117 indexed citations

Shen, Yang, K. Holman, Norman A. Doggett, et al.. (1994). Dinucleotide repeat polumorphisms at the D16S525, D16S359. D16S531 and D16S522 loci. Human Molecular Genetics. 3(1). 210–210. 4 indexed citations

Aksentijevich, Ivona, Eran Pras, Luis Gruberg, et al.. (1993). Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.. PubMed. 53(2). 451–61. 25 indexed citations

Richards, Robert I., et al.. (1993). Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins. Human Molecular Genetics. 2(9). 1429–1435. 104 indexed citations

10.

Gedeon, Ági K., K. Holman, Robert I. Richards, & John C. Mulley. (1992). Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci. American Journal of Medical Genetics. 43(1-2). 255–260. 21 indexed citations

11.

Thompson, Andrew, Yang Shen, K. Holman, et al.. (1992). Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16. Genomics. 13(2). 402–408. 82 indexed citations

12.

Richards, Robert I., K. Holman, H.M. Kozman, et al.. (1991). Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.. Journal of Medical Genetics. 28(12). 818–823. 120 indexed citations

13.

Yu, Shuancang, Melanie Pritchard, Eric J. Kremer, et al.. (1991). Fragile X Genotype Characterized by an Unstable Region of DNA. Science. 252(5009). 1179–1181. 644 indexed citations breakdown →

14.

Phillips, Hilary A., V.J. Hyland, K. Holman, et al.. (1991). Dinucleotide repeat polymorphism at D16S287. Nucleic Acids Research. 19(23). 6664–6664. 8 indexed citations

15.

Kremer, Eric J., Melanie Pritchard, Michael Lynch, et al.. (1991). Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n. Science. 252(5013). 1711–1714. 738 indexed citations breakdown →

16.

Shen, Yang, K. Holman, Andrew Thompson, et al.. (1991). An STS at the D16S290 locus. Nucleic Acids Research. 19(20). 5793–5793. 3 indexed citations

17.

Shen, Yang, K. Holman, Andrew Thompson, et al.. (1991). Dinucleotide repeat polymorphism at the D16S288 locus. Nucleic Acids Research. 19(19). 5445–5445. 45 indexed citations

18.

Harris, Peter C., Sinoula Apostolou, Elizabeth Baker, et al.. (1991). A refined physical map of the long arm of human chromosome 16. Genomics. 10(2). 308–312. 13 indexed citations

19.

Richards, Robert I., Yang Shen, K. Holman, et al.. (1991). Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.. PubMed. 48(6). 1051–7. 38 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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