James Hyland

2.5k total citations
26 papers, 853 citations indexed

About

James Hyland is a scholar working on Genetics, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, James Hyland has authored 26 papers receiving a total of 853 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Immunology and Allergy. Recurrent topics in James Hyland's work include Connective tissue disorders research (20 papers), Cell Adhesion Molecules Research (7 papers) and Bone health and treatments (3 papers). James Hyland is often cited by papers focused on Connective tissue disorders research (20 papers), Cell Adhesion Molecules Research (7 papers) and Bone health and treatments (3 papers). James Hyland collaborates with scholars based in United States, Finland and Germany. James Hyland's co-authors include Leena Ala‐Kokko, Kari I. Kivirikko, Raili Myllylä, Darwin J. Prockop, Beat Steinmann, Peter Royce, Pertti Ritvaniemi, Dianna M. Milewicz, Ann Haskins Olney and Roberto Mendoza‐Londono and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

James Hyland

25 papers receiving 822 citations

Peers

James Hyland
Glen Taylor United States
J. Spranger Germany
Jan M. Cobben Netherlands
B. Kerry Maddox United States
Edward G. Cleary Australia
Ruth M. Liberfarb United States
Marjolijn Renard Belgium
Stephen P. Henry United States
D L Rimoin United States
Mateusz Kolanczyk Germany
Glen Taylor United States
James Hyland
Citations per year, relative to James Hyland James Hyland (= 1×) peers Glen Taylor

Countries citing papers authored by James Hyland

Since Specialization
Citations

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

Fields of papers citing papers by James Hyland

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Hyland

This figure shows the co-authorship network connecting the top 25 collaborators of James Hyland. A scholar is included among the top collaborators of James Hyland 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 James Hyland. James Hyland 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.
Hyland, James, et al.. (2024). Review of Attributes and Outcomes of Hospitalized Patients with Alcohol Withdrawal. Journal of Community Hospital Internal Medicine Perspectives. 14(6). 35–42.
2.
Hogue, Jacob S., et al.. (2013). Clinical report: Two patients with atelosteogenesis type I caused by missense mutations affecting the same FLNB residue. American Journal of Medical Genetics Part A. 161(3). 619–625. 3 indexed citations
3.
Khalifa, Ola, Faiqa Imtiaz, Zuhair N. Al‐Hassnan, et al.. (2012). A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene: Figure 1. Journal of Medical Genetics. 49(4). 246–248. 14 indexed citations
4.
Zadeh, Neda, Jonathan A. Bernstein, Sarah Dugan, et al.. (2011). Ectopia lentis as the presenting and primary feature in Marfan syndrome. American Journal of Medical Genetics Part A. 155(11). 2661–2668. 35 indexed citations
5.
Baker, Stuart G., Carol Booth, Michael J. Shapiro, et al.. (2011). A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome. American Journal of Medical Genetics Part A. 155(7). 1668–1672. 67 indexed citations
6.
Milewicz, Dianna M., John R. Østergaard, Leena Ala‐Kokko, et al.. (2010). De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction. American Journal of Medical Genetics Part A. 152A(10). 2437–2443. 178 indexed citations
7.
Dwyer, Ellen, James Hyland, Peggy Modaff, & Richard M. Pauli. (2010). Genotype–phenotype correlation in DTDST dysplasias: Atelosteogenesis type II and diastrophic dysplasia variant in one family. American Journal of Medical Genetics Part A. 152A(12). 3043–3050. 17 indexed citations
8.
Schievink, Wouter I., Ora Gordon, James Hyland, & Leena Ala‐Kokko. (2008). Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension. The Journal of Headache and Pain. 9(2). 99–102. 6 indexed citations
9.
Zárate, Yuri A., Larry W. Markham, Linda Cripe, et al.. (2007). Novel Fibrillin 1 Mutation in a Case of Neonatal Marfan Syndrome: The Increasing Importance of Early Recognition. Congenital Heart Disease. 2(5). 342–346. 16 indexed citations
10.
Walter, Kerstin, Edward S. Tobias, Shiro Ikegawa, et al.. (2006). COL2A1–related skeletal dysplasias with predominant metaphyseal involvement. American Journal of Medical Genetics Part A. 143A(2). 161–167. 25 indexed citations
11.
Leung, Loh-Shan, James Hyland, Alistair A. Young, Morton F. Goldberg, & James T. Handa. (2006). A NOVEL MUTATION IN INTRON 11 OF THE COL2A1 GENE IN A PATIENT WITH TYPE 1 STICKLER SYNDROME. Retina. 26(1). 106–109. 4 indexed citations
12.
Sutton, V. Reid, et al.. (2005). A dominantly inherited spondylometaphyseal dysplasia with “corner fractures” and congenital scoliosis. American Journal of Medical Genetics Part A. 133A(2). 209–212. 6 indexed citations
13.
Kuurila, Kaija, Jarmo Körkkö, Ilkka Kaitila, et al.. (2004). Lack of correlation between the type ofCOL1A1orCOL1A2mutation and hearing loss in osteogenesis imperfecta patients. Human Mutation. 24(2). 147–154. 65 indexed citations
14.
15.
Tromp, Gerard, Helena Kuivaniemi, Steven Raphael, et al.. (1996). Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16.. PubMed. 59(5). 1097–107. 105 indexed citations
16.
Ritvaniemi, Pertti, Jarmo Körkkö, Jacky Bonaventure, et al.. (1995). Identification of col2a1 gene mutations in patients with chondrodysplasias and familial osteoarthritis. Arthritis & Rheumatism. 38(7). 999–1004. 50 indexed citations
17.
18.
Hyland, James, Leena Ala‐Kokko, Peter Royce, et al.. (1992). A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers–Danlos syndrome type VI. Nature Genetics. 2(3). 228–231. 83 indexed citations
19.
Ala‐Kokko, Leena, James Hyland, Chris Smith, et al.. (1991). Expression of a human cartilage procollagen gene (COL2A1) in mouse 3T3 cells. Journal of Biological Chemistry. 266(22). 14175–14178. 39 indexed citations
20.
Prockop, Darwin J., Anne S. Olsen, Sirpa Kontusaari, et al.. (1990). Mutations in Human Procollagen Genes. Annals of the New York Academy of Sciences. 580(1). 330–339. 15 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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