James Hyland

2.5k citations

26 papers · 853 indexed · h-index 15

Immunology and Allergy top 5%
- Cell Adhesion Molecules Research 7
Genetics top 5%
- Connective tissue disorders research 20
- Neurogenetic and Muscular Disorders Research 3
Rheumatology top 5%
- Osteoarthritis Treatment and Mechanisms 2
Cancer Research
Pulmonary and Respiratory Medicine
- Aortic Disease and Treatment Approaches 2
Oncology
- Bone health and treatments 3
Developmental Biology
- Congenital limb and hand anomalies 2
Molecular Biology
- Porphyrin Metabolism and Disorders 2

Co-authors: Leena Ala‐Kokko Kari I. Kivirikko Raili Myllylä Darwin J. Prockop Beat Steinmann Peter Royce Pertti Ritvaniemi Dianna M. Milewicz
Cited by: Immunology and Allergy Genetics Rheumatology
Partner nations: United States Finland Germany

In The Last Decade

James Hyland

25 papers receiving 822 citations

Peers

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

The 25 scholars most cited alongside James Hyland, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with James Hyland Line = papers co-authored together James Hyland links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Review of Attributes and Outcomes of Hospitalized Patients with Alcohol Withdrawal H. R. Desai,James Hyland,Erica Paulos,Eric K. Shaw,Nayda Parisio-Poldiak,Maulikkumar Patel	2024	0
2	Clinical report: Two patients with atelosteogenesis type I caused by missense mutations affecting the same FLNB residue Ben C. Li,Jacob S. Hogue,Meg Eilers,Pavni Mehrotra,James Hyland,Tara Holm,Tracy Prosen,Anne Slavotinek	2013	3
3	A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene: Figure 1 Ola Khalifa,Faiqa Imtiaz,Rabab Allam,Zuhair N. Al‐Hassnan,Amal Al‐Hemidan,Khalid Al-Mane,Gheid Abuharb,Ameera Balobaid,Nadia Sakati,James Hyland,Mohammed Al‐Owain	2012	14
4	Ectopia lentis as the presenting and primary feature in Marfan syndrome Neda Zadeh,Jonathan A. Bernstein,Anna Kaisa Niemi,Sarah Dugan,Andrea Kwan,David Liang,James Hyland,H. Eugene Hoyme,Louanne Hudgins,Melanie A. Manning	2011	35
5	A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome Stuart G. Baker,Carol Booth,Corrine Fillman,Michael J. Shapiro,Michael P. Blair,James Hyland,Leena Ala‐Kokko	2011	67
6	De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction Dianna M. Milewicz,John R. Østergaard,Leena Ala‐Kokko,Nadia Khan,Dorothy K. Grange,Roberto Mendoza‐Londono,Timothy J. Bradley,Ann Haskins Olney,Lesley C. Adès,Joseph F. Maher,Dongchuan Guo,L. Maximilian Buja,Dong Kim,James Hyland,Ellen S. Regalado	2010	178
7	Genotype–phenotype correlation in DTDST dysplasias: Atelosteogenesis type II and diastrophic dysplasia variant in one family Ellen Dwyer,James Hyland,Peggy Modaff,Richard M. Pauli	2010	17
8	Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension Wouter I. Schievink,Ora Gordon,James Hyland,Leena Ala‐Kokko	2008	6
9	Novel Fibrillin 1 Mutation in a Case of Neonatal Marfan Syndrome: The Increasing Importance of Early Recognition Jamie S. Sutherell,Yuri A. Zárate,Bradley T. Tinkle,Larry W. Markham,Linda Cripe,James Hyland,David P. Witte,Robert J. Hopkin,Robert B. Hinton	2007	16
10	COL2A1–related skeletal dysplasias with predominant metaphyseal involvement Kerstin Walter,Mojca Tansek,Edward S. Tobias,Shiro Ikegawa,Paul Coucke,James Hyland,Geert Mortier,Tsutomu Iwaya,Gen Nishimura,Andrea Superti‐Furga,Sheila Unger	2006	25
11	A NOVEL MUTATION IN INTRON 11 OF THE COL2A1 GENE IN A PATIENT WITH TYPE 1 STICKLER SYNDROME Loh-Shan Leung,James Hyland,Alistair A. Young,Morton F. Goldberg,James T. Handa	2006	4
12	A dominantly inherited spondylometaphyseal dysplasia with “corner fractures” and congenital scoliosis V. Reid Sutton,James Hyland,William A. Phillips,Alan E Schlesinger,Paula W. Brill	2005	6
13	Lack of correlation between the type ofCOL1A1orCOL1A2mutation and hearing loss in osteogenesis imperfecta patients Heini Hartikka,Kaija Kuurila,Jarmo Körkkö,Ilkka Kaitila,Reidar Grénman,Seppo Pynnönen,James Hyland,Leena Ala‐Kokko	2004	65
14	A compound heterozygote patient with Ehlers-Danlos syndrome type VI has a deletion in one allele and a splicing defect in the other allele of the lysyl hydroxylase gene Birgitta Pousi,Timo Hautala,James Hyland,Jukka Schröter,Beate Eckes,Kari I. Kivirikko,Raili Myllylä	1998	23
15	Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16. Gerard Tromp,Helena Kuivaniemi,Steven Raphael,Leena Ala‐Kokko,Angela M. Christiano,Eileen L. Considine,Rohini Dhulipala,James Hyland,Anu Jokinen,Sirpa Kivirikko,R Korn,Swarna Madhatheri,Seamus McCarron,Lea Pulkkinen,Hope H. Punnett,Koichiro Shimoya,Loretta D. Spotila,A. Rosemary Tate,Charlene J. Williams	1996	105
16	Identification of col2a1 gene mutations in patients with chondrodysplasias and familial osteoarthritis Pertti Ritvaniemi,Jarmo Körkkö,Jacky Bonaventure,Miikka Vikkula,James Hyland,Petteri Paassilta,Ilkka Kaitila,Helena Kääriäinen,Boris P. Sokolov,Markku Hakala,Pertti Mannismäki,E. M. Meerson,Tero Klemola,Charlene J. Williams,Leena Peltonen,Kari I. Kivirikko,Darwin J. Prockop,Leena Ala‐Kokko	1995	50
17	A Fourth Example Suggests That Premature Termination Codons in the COL2A1 Gene Are a Common Cause of the Stickler Syndrome: Analysis of the COL2A1 Gene by Denaturing Gradient Gel Electrophoresis Pertti Ritvaniemi,James Hyland,Jaakko Ignatius,Kari I. Kivirikko,Darwin J. Prockop,Leena Ala‐Kokko	1993	63
18	A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers–Danlos syndrome type VI James Hyland,Leena Ala‐Kokko,Peter Royce,Beat Steinmann,Kari I. Kivirikko,Raili Myllylä	1992	83
19	Expression of a human cartilage procollagen gene (COL2A1) in mouse 3T3 cells Leena Ala‐Kokko,James Hyland,Chris Smith,Kari I. Kivirikko,Sergio A. Jiménez,D.J. Prockop	1991	39
20	Mutations in Human Procollagen Genes Darwin J. Prockop,Anne S. Olsen,Sirpa Kontusaari,James Hyland,Leena Ala‐Kokko,Nagaswami Vasan,ELISABETH BARTON,Susan J. Buck,KATHLEEN HARRISON,ROBERT L. BRENT	1990	15

About James Hyland

James Hyland is a scholar working on Immunology and Allergy, Developmental Biology and Genetics, having authored 26 papers that have together received 853 indexed citations. Recurring topics across this work include Connective tissue disorders research (20 papers), Cell Adhesion Molecules Research (7 papers), Bone health and treatments (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Congenital limb and hand anomalies (2 papers), Porphyrin Metabolism and Disorders (2 papers), Aortic Disease and Treatment Approaches (2 papers) and Osteoarthritis Treatment and Mechanisms (2 papers). The work is most often cited by research in Immunology and Allergy (115 citations), Genetics (493 citations) and Rheumatology (229 citations). James Hyland has collaborated with scholars based in United States, Finland and Germany. Frequent 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.

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