A C Nicholls

2.6k citations

56 papers · 1.9k indexed · h-index 27

Genetics top 1%
Molecular Biology
Rheumatology top 2%
Neurology top 5%
Pulmonary and Respiratory Medicine top 10%

Co-authors: F M Pope P Narcisi H. N. Rydon Allan J. Richards Jane E. Oliver P. M. Hardy Darwin J. Prockop Jeanne C. Myers
Topics: Connective tissue disorders research (40 papers)Bone and Dental Protein Studies (12 papers)Dermatological and Skeletal Disorders (12 papers)
Cited by: Genetics Rheumatology Immunology and Allergy
Journals: The Lancet Journal of Biological Chemistry Annals of the New York Academy of Sciences
Partner nations: United Kingdom United States Netherlands

In The Last Decade

A C Nicholls

53 papers receiving 1.8k citations

Peers

Countries citing papers authored by A C Nicholls

Since Specialization

Citations

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

Fields of papers citing papers by A C Nicholls

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A C Nicholls. 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 A C Nicholls. The network helps show where A C Nicholls may publish in the future.

Co-authorship network of co-authors of A C Nicholls

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical and Genetic Heterogeneity of the Marfan Syndrome 2015 ·Current problems in dermatology ·F M Pope,A C Nicholls,R M Lewkonia,(unknown),D. E. Dorrance,Ariela Pomerance	0
2	A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II. 1998 ·Journal of Medical Genetics ·Allan J. Richards,Sophie G. Martin,A C Nicholls,J. B. Harrison,F M Pope,Nigel Burrows	60
3	A Point Mutation in an Intronic Branch Site Results in Aberrant Splicing of COL5A1 and in Ehlers-Danlos Syndrome Type II in Two British Families 1998 ·The American Journal of Human Genetics ·Nigel Burrows,A C Nicholls,Allan J. Richards,Craig Luccarini,J. B. Harrison,John R.W. Yates,F M Pope	69
4	Mutation in the carboxy-terminal propeptide of the proα1 (I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): Possible implications for protein folding 1996 ·Human Mutation ·Jane E. Oliver,Elizabeth M. Thompson,F M Pope,A C Nicholls	26
5	The Gene Encoding Collagen α1(V) (COL5A1) Is Linked to Mixed Ehlers-Danlos Syndrome Type I/II 1996 ·Journal of Investigative Dermatology ·Nigel Burrows,A C Nicholls,John R.W. Yates,(unknown),(unknown),Allan J. Richards,F M Pope	42
6	COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture 1996 ·British Journal of Dermatology ·F M Pope,(unknown),A C Nicholls,(unknown),Gerard Pals,Allan J. Richards	78
7	Splice site mutation causing deletion of exon 21 sequences from the proα2(I) chain of type I collagen in a patient with severe dentinogenesis imperfecta but very mild osteogenesis imperfecta 1996 ·Human Mutation ·A C Nicholls,Jane E. Oliver,Seamus McCarron,G B Winter,F M Pope	19
8	Evolution of spinal bone loss and biochemical markers of bone remodeling after menopause in normal women 1995 ·Calcified Tissue International ·J. Reeve,John Pearson,Angela M. Mitchell,(unknown),A C Nicholls,Jamie N. Justice,Elizabeth Hudson,L. Klenerman	27
9	Study of a type III collagen protein defect in a patient with ecchymotic EDS: importance of the analysis of non-cutaneous connective tissues 1992 ·Ghent University Academic Bibliography (Ghent University) ·Anne De Paepe,Lieve Nuytinck,A C Nicholls,P Narcisi,(unknown),(unknown)	1
10	A 27-bp deletion from one allele of the type III collagen gene (COL3A1) in a large family with Ehlers-Danlos syndrome type IV 1992 ·Human Genetics ·Allan J. Richards,J. C. Lloyd,P Narcisi,Philip N. Ward,A C Nicholls,Anne De Paepe,F M Pope	23
11	Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IV. 1992 ·Journal of Medical Genetics ·Lieve Nuytinck,P Narcisi,A C Nicholls,Jean‐Pierre Renard,F M Pope,Anne De Paepe	21
12	The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: Exon skipping caused by an 11-bp deletion from an intron in one COL1A2 allele 1992 ·Human Genetics ·A C Nicholls,Jane E. Oliver,David V. Renouf,(unknown),F M Pope	34
13	Type III collagen mutations cause fragile cerebral arteries 1991 ·British Journal of Neurosurgery ·F M Pope,B. E. Kendall,(unknown),Ravish Kapoor,W. I. McDonald,D. A. S. Compston,R. Mitchell,Daniel Hope,(unknown),John Dean,Alan Johnston,Patrick Lynch,Padmini Sarathchandra,P Narcisi,A C Nicholls,Allan J. Richards,(unknown)	45
14	Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen ?2(I) chain 1991 ·Human Genetics ·A C Nicholls,Jane E. Oliver,David V. Renouf,Jane McPheat,(unknown),F M Pope	28
15	Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta 1989 ·Clinical Genetics ·Elizabeth Williams,A C Nicholls,S. C. M. Daw,(unknown),L. Stefan Levin,B. G. Green,J. Mackenzie,(unknown),(unknown),F M Pope	20
16	Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree 1988 ·Human Genetics ·A C Nicholls,A. De Paepe,P Narcisi,Raymond Dalgleish,Filip De Keyser,(unknown),F M Pope	32
17	Spontaneous carotid cavernous fistula in Ehlers Danlos syndrome. 1988 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown),F M Pope,P Narcisi,A C Nicholls,B. E. Kendall,M D Hourihan,D. A. S. Compston	26
18	An abnormal collagen alpha chain containing cysteine in autosomal dominant osteogenesis imperfecta. 1984 ·BMJ ·A C Nicholls,F M Pope,(unknown)	27
19	Lethal osteogenesis imperfecta congenita and a 300 base pair gene deletion for an alpha 1(I)-like collagen. 1984 ·BMJ ·F M Pope,Kathryn S.E. Cheah,A C Nicholls,Albert Price,Frank Grosveld	25
20	The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. 1984 ·Journal of Medical Genetics ·A C Nicholls,(unknown),Henning Schloon,H. G. Lenard,S B Deak,Jeanne C. Myers,Darwin J. Prockop,(unknown),P Fryer,F M Pope	93

About A C Nicholls

A C Nicholls is a scholar working on Genetics, Rheumatology and Anatomy, having authored 56 papers that have together received 1.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (40 papers), Bone and Dental Protein Studies (12 papers) and Dermatological and Skeletal Disorders (12 papers). The work is most often cited by research in Genetics (1.2k citations), Rheumatology (506 citations) and Immunology and Allergy (182 citations). A C Nicholls has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include F M Pope, P Narcisi, H. N. Rydon, Allan J. Richards, Jane E. Oliver, P. M. Hardy, Darwin J. Prockop, Jeanne C. Myers, J. B. Harrison and Nigel Burrows. Their work appears in journals such as The Lancet, Journal of Biological Chemistry and Annals of the New York Academy of Sciences.

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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