Katherine Holman

2.3k total citations
31 papers, 911 citations indexed

About

Katherine Holman is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Katherine Holman has authored 31 papers receiving a total of 911 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 4 papers in Nephrology. Recurrent topics in Katherine Holman's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Chromatin Dynamics (5 papers) and Connective tissue disorders research (4 papers). Katherine Holman is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Chromatin Dynamics (5 papers) and Connective tissue disorders research (4 papers). Katherine Holman collaborates with scholars based in Australia, United States and United Kingdom. Katherine Holman's co-authors include Bruce Bennetts, Lesley C. Adès, Robert I. Richards, Maggie Brett, Gladys Ho, G.R. Sutherland, Andrew J. Mallett, Andrew Biggin, Chirag Patel and Elizabeth Farnsworth and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Kidney International.

In The Last Decade

Katherine Holman

28 papers receiving 897 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katherine Holman Australia 15 529 522 150 76 74 31 911
Rodger Palmer United Kingdom 13 397 0.8× 494 0.9× 105 0.7× 27 0.4× 51 0.7× 20 915
A Seller United Kingdom 15 940 1.8× 797 1.5× 63 0.4× 438 5.8× 94 1.3× 24 1.7k
Sı̇bel Aylı̇n Uğur İşerı̇ Türkiye 13 283 0.5× 218 0.4× 146 1.0× 19 0.3× 20 0.3× 39 690
Florence Niel France 17 879 1.7× 241 0.5× 144 1.0× 279 3.7× 30 0.4× 24 1.3k
Yves Sznajer Belgium 19 623 1.2× 373 0.7× 136 0.9× 27 0.4× 39 0.5× 50 1.1k
Sumita Danda India 16 489 0.9× 269 0.5× 88 0.6× 16 0.2× 45 0.6× 122 1.0k
Sirpa Ala‐Mello Finland 17 498 0.9× 468 0.9× 88 0.6× 33 0.4× 15 0.2× 29 1.2k
Lakshmi Mehta United States 16 403 0.8× 348 0.7× 44 0.3× 21 0.3× 34 0.5× 46 754
Ann Haskins Olney United States 19 842 1.6× 716 1.4× 142 0.9× 37 0.5× 34 0.5× 43 1.4k
Sylvie Manouvrier‐Hanu France 18 504 1.0× 395 0.8× 46 0.3× 22 0.3× 22 0.3× 57 846

Countries citing papers authored by Katherine Holman

Since Specialization
Citations

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

Fields of papers citing papers by Katherine Holman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katherine Holman

This figure shows the co-authorship network connecting the top 25 collaborators of Katherine Holman. A scholar is included among the top collaborators of Katherine 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 Katherine Holman. Katherine Holman 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.
Holman, Katherine, Stephanie G. Harshman, Megan Kuhnle, et al.. (2025). Differences in Perceived Versus Actual Sensory Perception in Avoidant/Restrictive Food Intake Disorder. International Journal of Eating Disorders. 58(4). 703–713. 2 indexed citations
2.
Aulinas, Anna, Francesca Galbiati, C. Sue Carter, et al.. (2025). Arginine-Vasopressin Dynamics in Relation to Food Intake and 8-Week Intranasal Oxytocin Treatment in Adults With Obesity. The Journal of Clinical Endocrinology & Metabolism. 110(12). e3972–e3979. 1 indexed citations
3.
Moudgil, Rohit, et al.. (2025). Cardiovascular disease in people living with HIV: Risk assessment and management. Cleveland Clinic Journal of Medicine. 92(3). 159–167.
4.
Wright, Dale, Artur Darmanian, Luke St Heaps, et al.. (2023). Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism. American Journal of Medical Genetics Part A. 191(12). 2913–2920. 1 indexed citations
5.
Holman, Katherine, Gladys Ho, Elizabeth Farnsworth, et al.. (2021). Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. npj Genomic Medicine. 6(1). 20–20. 15 indexed citations
6.
Mallett, Andrew J., Catherine Quinlan, Chirag Patel, et al.. (2019). Precision Medicine Diagnostics for Rare Kidney Disease: Twitter as a Tool in Clinical Genomic Translation. Kidney Medicine. 1(5). 315–318. 5 indexed citations
7.
Hudson, Rebecca, Chirag Patel, Carmel M. Hawley, et al.. (2019). Adult-Diagnosed Nonsyndromic Nephronophthisis in Australian Families Caused by Biallelic NPHP4 Variants. American Journal of Kidney Diseases. 76(2). 282–287. 5 indexed citations
8.
Forbes, Thomas, Sara E. Howden, Kynan T. Lawlor, et al.. (2018). Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms. The American Journal of Human Genetics. 102(5). 816–831. 155 indexed citations
9.
Xu, Jordan, et al.. (2018). Disseminated cerebral toxoplasmosis in a patient with chronic lymphocytic leukemia. Journal of Clinical Neuroscience. 50. 127–128. 2 indexed citations
10.
Mallett, Andrew J., Hugh J. McCarthy, Gladys Ho, et al.. (2017). Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders. Kidney International. 92(6). 1493–1506. 57 indexed citations
11.
Adès, Lesley C., Kathleen E. Sullivan, Andrew Biggin, et al.. (2006). FBN1, TGFBR1, and the Marfan‐craniosynostosis/mental retardation disorders revisited. American Journal of Medical Genetics Part A. 140A(10). 1047–1058. 69 indexed citations
12.
Biggin, Andrew, Katherine Holman, Maggie Brett, Bruce Bennetts, & Lesley C. Adès. (2003). Detection of thirty novelFBN1mutations in patients with Marfan syndrome or a related fibrillinopathy. Human Mutation. 23(1). 99–99. 49 indexed citations
13.
Adès, Lesley C., et al.. (2002). Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations. American Journal of Medical Genetics. 109(4). 261–270. 21 indexed citations
14.
Davies, Roger P., Eric Haan, Katherine Holman, et al.. (1999). Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent. Clinical Dysmorphology. 8(4). 269???276–269???276. 15 indexed citations
15.
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
16.
Shen, Yang, Katherine Holman, Norman A. Doggett, et al.. (1993). Five dinucleotide repeat polymorphisms on human chromosome 16q24.2 – q24.3. Human Molecular Genetics. 2(9). 1504–1504. 1 indexed citations
17.
Callen, David F., Norman A. Doggett, Raymond L. Stallings, et al.. (1992). High-resolution cytogenetic-based physical map of human chromosome 16. Genomics. 13(4). 1178–1185. 44 indexed citations
18.
Richards, Robert I., Katherine Holman, K. Friend, et al.. (1992). Evidence of founder chromosomes in fragile X syndrome. Nature Genetics. 1(4). 257–260. 152 indexed citations
19.
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
20.
Richards, Robert I., Katherine Holman, Sharon Lane, Grant R. Sutherland, & David F. Callen. (1991). Human chromosome 16 physical map: Mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites. Genomics. 10(4). 1047–1052. 10 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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