H.M. Kozman

885 total citations
23 papers, 706 citations indexed

About

H.M. Kozman is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, H.M. Kozman has authored 23 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in H.M. Kozman's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and RNA regulation and disease (3 papers). H.M. Kozman is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and RNA regulation and disease (3 papers). H.M. Kozman collaborates with scholars based in Australia, United States and United Kingdom. H.M. Kozman's co-authors include John C. Mulley, Robert I. Richards, G.R. Sutherland, K. Holman, David F. Callen, Ági K. Gedeon, Michael Lynch, Andrew Thompson, Eric J. Kremer and Melanie Pritchard and has published in prestigious journals such as Science, Nucleic Acids Research and The American Journal of Human Genetics.

In The Last Decade

H.M. Kozman

23 papers receiving 695 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H.M. Kozman Australia 15 483 356 112 86 82 23 706
Julia Parrish United States 13 414 0.9× 348 1.0× 12 0.1× 71 0.8× 36 0.4× 19 695
Shehla Mohammed United Kingdom 12 497 1.0× 248 0.7× 34 0.3× 22 0.3× 19 0.2× 25 680
Rachel Flomen United Kingdom 12 370 0.8× 180 0.5× 16 0.1× 114 1.3× 20 0.2× 17 583
Angus Dobbie United Kingdom 12 402 0.8× 284 0.8× 27 0.2× 21 0.2× 23 0.3× 20 675
Anne Puech United States 15 604 1.3× 351 1.0× 24 0.2× 31 0.4× 21 0.3× 25 851
Lauren Gehman United States 7 716 1.5× 107 0.3× 25 0.2× 80 0.9× 28 0.3× 11 938
Sérgio B. Sousa Portugal 12 351 0.7× 359 1.0× 14 0.1× 34 0.4× 32 0.4× 37 594
G.R. Sutherland Australia 16 396 0.8× 355 1.0× 7 0.1× 110 1.3× 110 1.3× 22 703
Ton van Essen Netherlands 11 474 1.0× 324 0.9× 10 0.1× 60 0.7× 39 0.5× 13 726

Countries citing papers authored by H.M. Kozman

Since Specialization
Citations

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

Fields of papers citing papers by H.M. Kozman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.M. Kozman. 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 H.M. Kozman. The network helps show where H.M. Kozman may publish in the future.

Co-authorship network of co-authors of H.M. Kozman

This figure shows the co-authorship network connecting the top 25 collaborators of H.M. Kozman. A scholar is included among the top collaborators of H.M. Kozman 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 H.M. Kozman. H.M. Kozman 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.
Gedeon, Ági K., H.M. Kozman, Hazel M. Robinson, et al.. (1996). Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann syndrome. American Journal of Medical Genetics. 64(1). 63–68. 12 indexed citations
2.
Callen, David F., Sharon Lane, H.M. Kozman, et al.. (1995). Integration of Transcript and Genetic Maps of Chromosome 16 at Near-1-Mb Resolution: Demonstration of a “Hot Spot” for Recombination at 16p12. Genomics. 29(2). 503–511. 30 indexed citations
3.
Mulley, J.C., H.M. Kozman, & G.R. Sutherland. (1994). The CEPH consortium linkage map of human chromosome 16. The American Journal of Human Genetics. 55. 1 indexed citations
4.
Donnelly, Andrew J., K.H. Andy Choo, H.M. Kozman, et al.. (1994). Regional localisation of a non‐specific X‐linked mental retardation gene (MRX19) to Xp22. American Journal of Medical Genetics. 51(4). 581–585. 26 indexed citations
5.
Shen, Yang, H.M. Kozman, Andrew Thompson, et al.. (1994). A PCR-Based Genetic Linkage Map of Human Chromosome 16. Genomics. 22(1). 68–76. 28 indexed citations
6.
Donnelly, Andrew J., H.M. Kozman, Ági K. Gedeon, et al.. (1994). A Linkage Map of Microsatellite Markers on the Human X Chromosome. Genomics. 20(3). 363–370. 29 indexed citations
7.
Edwards, Matthew, Richard J. Roberts, M. W. Partington, et al.. (1994). Clinical and linkage study of a large family with simple ectopia lentis linked to FBN1. American Journal of Medical Genetics. 53(1). 65–71. 18 indexed citations
8.
Gedeon, Ági K., John C. Mulley, H.M. Kozman, Andrew J. Donnelly, & M. W. Partington. (1994). Localisation of the gene for X‐linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X‐linked cutaneous amyloidosis. American Journal of Medical Genetics. 52(1). 75–78. 13 indexed citations
9.
Mitchison, Hannah M., Peter E.M. Taschner, Angela O'Rawe, et al.. (1994). Genetic Mapping of the Batten Disease Locus (CLN3) to the Interval D16S288-D16S383 by Analysis of Haplotypes and Allelic Association. Genomics. 22(2). 465–468. 27 indexed citations
10.
Mitchison, Hannah M., Andrew Thompson, John C. Mulley, et al.. (1993). Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci. Genomics. 16(2). 455–460. 43 indexed citations
11.
Phillips, Hilary A., Andrew Thompson, H.M. Kozman, G.R. Sutherland, & J.C. Mulley. (1993). A microsatellite marker within the duplicated D16S79 locus has a null allele: significance for linkage mapping. Cytogenetic and Genome Research. 64(3-4). 131–132. 12 indexed citations
12.
Mulley, John C., H.M. Kozman, Hilary A. Phillips, et al.. (1993). Refined genetic localization for central core disease.. PubMed. 52(2). 398–405. 38 indexed citations
13.
Beggs, Alan H., Hilary A. Phillips, H.M. Kozman, et al.. (1992). A (CA)n repeat polymorphism for the human skeletal muscle α-actinin gene ACTN2 and its localization on the linkage map of chromosome 1. Genomics. 13(4). 1314–1315. 10 indexed citations
14.
Cox, Timothy C., H.M. Kozman, Wendy H. Raskind, Brian K. May, & John C. Mulley. (1992). Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemia. Human Molecular Genetics. 1(8). 639–641. 31 indexed citations
15.
Richards, Robert I., Katherine Holman, Yang Shen, et al.. (1991). Human glandular kallikrein genes: Genetic and physical mapping of the KLK1 locus using a highly polymorphic microsatellite PCR marker. Genomics. 11(1). 77–82. 23 indexed citations
16.
Kozman, H.M., Ági K. Gedeon, S.A. Whitmore, et al.. (1991). Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1. Genomics. 11(3). 756–759. 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.
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
19.
Kozman, H.M., et al.. (1989). Molecular genetic evidence for common pathogenesis of childhood and adult Wilms' tumor. Cancer Genetics and Cytogenetics. 38(1). 121–125. 4 indexed citations
20.
Suthers, G K, David F. Callen, V.J. Hyland, et al.. (1989). A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA ). Science. 246(4935). 1298–1300. 54 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Julia Parrish Breakdown of academic impact, for papers by Shehla Mohammed Breakdown of academic impact, for papers by Rachel Flomen Breakdown of academic impact, for papers by Angus Dobbie Breakdown of academic impact, for papers by Anne Puech Breakdown of academic impact, for papers by Lauren Gehman Breakdown of academic impact, for papers by Sérgio B. Sousa Breakdown of academic impact, for papers by G.R. Sutherland Breakdown of academic impact, for papers by Ton van Essen
Rankless by CCL
2026